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Right Inferior Temporal Lobe

From: Neuropsychiatry, Neuropsychology, Clinical Neuroscience
by Rhawn Joseph, Ph.D.
(Academic Press, New York, 2000)


By Rhawn Joseph, Ph.D.


The temporal lobe is the most heterogenous of the four lobes of the human brain, as it consists of six layered neocortex, four to five layered mesocortex, and 3 layered allocortex, with the hippocampus and amygdala forming its limbic core.


As detailed in chapters, 5, 12, over the course of evolution the dorsally situated hippocampus became displaced and progressively assumed a ventral position, during the course of which it also contributed to the neocortical development of portions of the parietal, occipital and temporal lobe. Similarly, portions of the amygdala became increasingly cortical in structure, and together with the hippocampus, contributed to the evolution of the anterior, medial, superior, and lateral temporal lobes.

Because so much of the temporal lobe evolved from these limbic nuclei, unlike the other lobes, it consists of a mixture of allocortex, mesocortex, and neocortex, with allocortex and mesocortex being especially prominent in and around the medial-anterior inferiorally located uncus, beneath which and which abuts the amygdala and hippocampus.

Given the role of the amygdala and hippocampus in memory, emotion, attention, and the processing of complex auditory and visual stimuli, the temporal lobe became similarly organized (Gloor, 1997). Broadly considered, the neocortical surface of the temporal lobes can be subdivided into three main convolutions, the superior, middle, and inferior temporal gyri, which in turn are separated and distinguished by the sylvian fissure and the superior, middle, and inferior temporal sulci. Each of these subdivision performs different (albeit overlapping) functions, i.e. auditory, visual, and auditory-visual-affective perception including memory storage.

The inferior and medial temporal lobe harbors the amygdala and hippocampus, performs complex visual integrative activities including visual closure, and contains neurons which respond selectively to faces and complex geometric and visual stimuli (Gross & Graziano 1995; Nakamura et al. 1994; Rolls 1992; Tovee et al. 1994). The inferior and middle temporal lobes, are the recipients of one two diverging (dorsal and ventral) streams of visual input arising from within the occipital lobe and thalamus (Ungerlieder & Mishkin, 1982); i.e. the pulvinar and dorsal medial nucleus of the thalamus. The dorsal stream is more concerned with the detection of motion and movement, orientation, binocular disparity, whereas the ventral stream is concerned with the discrimination of shapes, textures, objects and faces, including individual faces (Baylis et al., 1985; Perrett et al., 1984, 1992). This information flows from the primary visual to visual association areas and is received and processed in the temporal lobes and is then shunted to parietal lobe, and to the amygdala and entorhinal cortex (the gateway to the hippocampus) where it may then be learned and stored in memory.


The temporal lobes, however, also receive extensive projections from the somesthetic and visual association areas, and processes gustatory, visceral, and olfactory sensations (Jones & Powell, 1970; Previc 1990; Seltzer & Pandya, 1978) including the feeling of hunger (Fisher 1994). Hence, the temporal lobes perform an exceedingly complex array of divergent and interrelated functions.


The basal temporal region can be subdivided into a medial, inferior, middle, and anterior and posterior zones, harbors the amygdala and hippocampus in its depths. These tissues are extensively interconnected, and project to the auditory association area, frontal convexity, and orbital region (Jones & Powell, 1970; Pandya & Kuypers, 1969). The inferior arcuate fasciculus in it's journey from the amygdala to Wernickes areas also passes through this neocortical auditory territory. Hence, when considered a whole, the inferior and middle temporal lobe is a complex multifunctional tissue which is functionally lateralized and has extensive visual and auditory and linguistic capabilities.

In general, the anterior basal temporal lobe is more involved in auditory functioning, whereas the posterior basal temporal lobe is more intimately concerned with the processing of higher level visual information including form recognition and (in the left temporal lobe) the reading of the written language. Indeed, this generalized dichotomy, first proposed in the 1990 edition of this text, has since been born out by a variety of functional imaging studies and is supported by lesions and neurosurgical stimulation studies.


Specifically, the left inferior-middle posterior temporal lobe (Brodmann's area 37), is located between the visual cortex and the anterior temporal cortex and becomes activated during a variety of language tasks, including reading and object and letter naming (Price, 1997). This has been demonstrated not only by functional imaging (Buchel et al., 1998; Price, 1997), but direct cortical recoding (Nobre et al., 1994), and electrical stimulation (Luders et al., 1986). In fact, both normal, cognitally blind, and late-blind subject display activity in this area (Buchel et al., 1998). For example, reading of concrete and abstract words activates the left posterior basal temporal lobe and the left frontal operculum (Buchel et al., 1998).


Hence, because of its role in language, when the middle temporal lobe is stimulated there can result aphasic abnormalities (Penfield & Rasmussen, 1950). Lesions involving this area are also associated with subtle disturbances involving language, including word finding difficulty, confrontive naming deficits, abnormalities in the maintanance of temporal order and sequence, as well as verbal memory impairments (Luria, 1980). Patients may suffer from reading and naming deficits (Rapcsak, et al., 1987); a condition referred to as phonological alexia. Moreover, patients with developmental dyslexia have been found to have abnormalities in this area (Rumsey et al., 1997).

As noted, left temporal lobe activity increases as word length increases. Hence, with injuries in this area, including the basal temporal lobe, patients may have difficulty recalling word lists or order of word presentation, such that the longer the list, the greater the difficulty. Hence, if a list of four words were read, the patient cannot repeat the correct order even after repeated presentations, although individuals words may be recalled correctly (Luria, 1980).

However, the nature of the disturbances depends on the exact location of the lesion (Coltheart, 1998; Miozzo & Caramazza, 1998), for as noted, the anterior and posterior and inferior and middle temporal lobes perform interrelated but also divergent functions. In general, the more posterior aspect is concerned with the visual aspects of perception and language, including reading and object naming. Indeed, the left posterior basal temporal lobe is a convergence zone for visual, auditory, and tactile information. Hence, patients may suffer from alexia as well as visual and tactile anomia if this area is injured (Rapcsak, et al., 1987). In addition, these structures are lateralized, and although both the right and left temporal lobe become activated by various language and reading tasks (reviewed in Price, 1997), the right basal temporal lobe is much more concerned with non-verbal visual functioning.


The middle temporal lobe, (MTL) like other structures throughout the brain, appears to be functionaly lateralized such that the right temporal region is more involved in visual and non-verbal auditory functioning, whereas the left MTL is more concerned with auditory-linguistic capabilities. Hence, whereas the auditory-linguistic zones appear to be more extensive within the left temporal lobe (and include portions of the posterior temporal region), the right MTL seems to be more associated with visual responsiveness. In general, however, the middle temporal gyrus of both hemispheres appear to contain visually responsive neurons (Beckers & Zeki 1995; Felleman & Kaas, 1974; Heit et al. 1990; Maunsell & Van Essen 1984; Selemon et al. 1994). Nevertheless, since there have been relatively few published studies of the effects of lesions or the functional capabilities of the middle temporal lobes in humans, notions regarding the extensiveness of auditory vs. visual lateralized representation are admittedly speculative.


Visual cells in the MTL receive direct projections from the striate cortex, area 17 and the association area 18 (Wall et al. 1982). This area in turns projects to the MTL of the opposite hemisphere via the corpus callosum, ipsilaterally to areas 17, 18, 19, the inferior temporal and the parietal-occipital cortex (Tigges et al., 1981; Wall et al., 1982), and maintains interconnections with the pulvinar, superior colliculus and pontine nuclei of the brainstem (Walls et al., 1982). Hence, this regions has connections with areas concerned with visual and visual attentional capabilities.


MTL neurons are sensitive to speed and direction of stimulus movement, motion, orientation, width, and disparity (Felleman & Kaas, 1984; Maunsell & Van Essen, 1983). However, most MTG neurons are not particular sensitive to the form of a stimulus--most preferring narrow stimuli (Albright et al. 1984; Maunsell & Van Essen, 1983). A large number of cells have binocular capabilities and respond to stimuli from either or both eyes. Hence, these cells are significantly involved in stereoscopic vision as well as determining distance.


Although not specialized for perception of form per se, via the combined analysis of width, orientation, speed and direction of movement these cells can process visual stimuli in a three-dimensional fashion, particularly in regard to trajectory, depth and position, i.e. if an object is near or far, approaching or withdrawing (Maunsell & Van essen, 1983).

Via its interconnections with the parietal-occipital lobe (an area involved in depth perception, visual fixation, and the visual-somesthetic guidance of movement) the MTL appears to provide visual guidance in regard to interactional object and body movement. That is, via the analysis of the flow of movement, local direction and speed, as well as the relative distances of objects, these neurons (in conjunction with area 7 cells) are important in guiding the movements of the body as well as the individuals limbs toward the object (Manunsell & Van Essen,1983).

The MTL maintains extensive interconnections with the inferior region and thus with limbic nuclei. It is probably via these connections that objects or conspecies of motivational significance can be discerned and attended to. That is, not only is the speed, movement, distance, etc. of a stimulus determined, but its emotional attributes (e.g. should it be feared, chased, eaten). Moreover, not just written words, but object recognition occurs in this area (in conjunction with the inferior temporal lobe), such that if injured, patients may suffer from agnosia (Giannokapoulos et al., 1999).


Tumors involving the middle temporal lobe have been associated with the development of auditory and visual hallucinations, dreamy states, and alterations in emotional functioning--particularly as the lesion encroaches on the inferior regions (Luria, 1980). Electrical stimulation also initiates the development of complex hallucinations and alterations in consciousness (Penfield & Roberts, 1959).


As noted, it is possible to very loosely define the anterior-inferior temporal lobes as auditory cortex, although neurons in this vicinity receive visual as well as somesthetic input.. Hence, the inferior temporal lobes can respond to auditory as well as emotionally and visually significant stimuli (Gloor, 1997; Nakamura et al., 1994; Tovee et al., 1994).

That the inferior temporal lobe (ITL) processes complex auditory, visual and emotional stimuli is probably a function of it being a derivative of the amygdala (see chapter 14) as well as visual cortex (Diamond 1973; Gloor, 1997). Visual and auditory functions also reflect its reception of extensive (upper visual field) projections from the optic radiations, highly processed input from the visual association areas in the occipital lobes of both cerebral hemispheres (via the corpus callosum), and fibers from the superior colliculus by way of the pulvinar of the thalamus (Chow, 1950; Kaas & Krubitzer 1991; Kuypers et al., 1965; Previc 1990; Rocha-Miranda et al. 1975).


Indeed, the neocortex of the ITL is specialized for receiving, analyzing, discriminating, recognizing and recalling complex visual information and is involved in attention and visually guided behavior (Gross & Graziano 1995; Gross et al. 1972; Tovee et al. 1994), including the recollection and learning of visual discriminations (Gross, 1972) and memory for objects and spatial locations (Nunn et al., 1999; Ploner et al., 1999). If the temporal lobe is injured, these functions become compromised.

For example, Kimura (1963) found that patients with right vs left temporal lobe injury were impaired when presented with overlapping nonsense shapes and then immediately tested for recognition. Likewise, Meier and French (1965), found that those with right vs left temporal lobe injuries were impaired when asked to make visual discriminations when presented with fragmented concentric circle patterns--skills which are also related to visual closure and gestalt formation. More recently, Nunn et al., (1999) found that right vs left temporal lobectomy patients were more impaired when required to remember and recognize toys and recall their location.

Cells in the ITL have very large, bilateral visual receptive fields which include the fovea, and many are sensitive to direction of stimulus movement, color, contrast, size, shape, orientation and are involved in the perception of three dimensional objects and the supramodal analysis of information already processed in the association areas (Eskander, et al. 1992; Gross & Graziano 1995; Gross, et al. 1972; Nakamura et al. 1994; Rolls, 1992; Sergent, et al.1990). Thus inferior temporal (IT) neurons appear to take part in the last stages of visual analysis for form recognition and receive terminal fibers from the primary and association visual areas (Gloor, 1997; Gross, et al. 1972; Ungerleider & Mishkin, 1982); that is, via the ventral visual stream. Indeed, a single neuron can respond to a combination of these features and many will fire selectively in response to particular shapes and faces (Eskander, et al. 1992; Gross, et al. 1972; Nakamura et al. 1994; Richmond, et al. 1983; Rolls, 1992; Sergent, et al.1990).


Overall, the ITL appears to be involved in the highest level of visual integration containing highly developed neurons which seem to be the end station of a hierarchical system which mediates the perception and recognition of specific and particular shapes and forms (Desimone & Schein, 1987; Gross & Graziano 1995; Nakamura et al. 1994; Richmond, et al. 1983; Rolls, 1992.) Indeed, in addition to the optic radiations, there is a pathway (the ventral stream) beginning in the primary visual cortex which passes through areas 18 and 19 and terminates in the ITL (Kuypers et al., 1965; Previc 1990). As information is passed from the primary to these association areas various features important in the identification of specific objects become progressively and hiarchically analyzed and increasingly complex associations are formed.


In fact, based on single cell recordings, some of these ITL neurons have been found to become particularly excited when presented with two dimensional patterns or three dimensional objects such as hands, brushes, and in particular, faces (Deismone & Gross, 1979; Gross et al., 1972; Nakamura et al. 1994; Richmond et al., 1983; Richmond et al.1987). A variety of different feature detectors are found and the majority probably act collectively so as code and assemble a particular shape, including the formation of gestalts and thus the performance of visual closure, particularly the right temporal region (see chapter 10). Via closure an individual can detect a partial stimulus and recognize that it is a face vs a rabbit.


Some cells are responsive to particular facial orientations, such as a profile, some respond to only parts of the face, such as eyes or a mouth, whereas others respond only to the entire face; i.e. a correctly organized facial gestalt. Interestingly, the ITL also contains neurons which will fire even to a scrambled face, so long as all the features are present (Gross et al., 1984). Moreover, some cells respond preferentially to familiar faces, to the faces of certain individuals, to specific emotions conveyed via the face, and the direction of the face including the direction of gaze--especially cells within the amygdala. Specifically, the left amygdala acts to discriminate the direction of another person's gaze, whereas the right amygdala becomes activated while making eye-to-eye contact (Kawashima, et al., 1999). Hence, these cells can determine if someone is looking at them, or looking at someone else, if the facial expression conveys threat, and if there is a hand moving toward or away from the subject or another person.

Hence, these cells are especially equipped for determining social signals and to read the emotions conveyed facially between two people. Interestingly, these same capacities were originally mediated by the olfactory system which in turn gave rise to the amygdala and promoted its differentiation and thus the development of the temporal lobe. In this regard it is also noteworthy that with the bilateral removal of the anterior inferior temporal lobe (thus destroying the amygdala as well as parts of the hippocampus), patients (and non-human primates) develop so called "psychic blindness," and will pick up and smell and taste whatever object captures their attention. In other words, being deprived of an amygdala that can process, visually, social and emotional signals, the amygdalectomized patient/primate reverts back to those behaviors typical of creatures that rely on smell.


As noted, abnormalities affecting the middle temporal lobe (area 37) can result in agnosic disturbances (Giannokapoulos et al., 1999). There are however, to major forms of agnosia, and different subtypes as well, which can be produced by damage to tissues mediating complex visual perception or lesions disconnecting the IPL, for example, from visual, somesthetic, or auditory input.

For example, one type of agnosia, "apperceptive visual agnosia" refers to a disturbance in perceptual and visual-motor integration, such that patients have difficulty copying or matching various objects. This latter form of agnosia has been associated with lesions to the parietal occipital cortex (Mizuno, et al., 1996), as well as to bilateral damage to the inferior-occipital cortex (Shelton, et al., 1994).

By contrast, associative visual agnosia, which is a deficit in naming, such that auditory equivalents cannot be matched to a visual perception, is associated with left inferior and middle temporal (area 37) occipital abnormalities (Giannokapoulos et al., 1999), which may be accompanied with alexia (Feinberg et al., 1994), as well as to lesions to and atrophy of the parietal occipital cortex (Mizuno, et al., 1996).

It is noteworthy that depending on the laterality and location of the injury, e.g., right vs left inferior/medial vs superior temporal lobe, patients may display category specific agnosias. For example, a 27-year old man I examined who had sustained a massive right inferior-posterior temporal lobe injury that also involved surgical removal, was able to recognize pictures of tools (he had been a carpenter) but could not recognize or correctly name pictures of animals and he could not correctly remember facial stimuli that he had been shown five minutes earlier and could not differentiate them from faces he had not seen. By contrast, a 43 year old woman who had been a waitress, and had developed a left inferior temporal lobe glioma that required surgical removal (coupled with chemotherapy) was able to recognize and name pictures of animals and could remember different pictures of faces, but had considerable difficulty recognizing and naming common household objects.

In this regard a 47-year old woman I examined who was subsequently found to have a calcium cyst growing from the skull into the right superior temporal lobe, was able to name pictures of animals, tools and household objects. However, she was almost completely unable to recognize and correctly name animal and humans sounds (e.g. a baby crying, a crowd cheering, a lion roaring) which had been briefly presented, but was better able to recognize non-living sounds such as a creaking door, or a hammer hammering--though these abilities were also compromised.

These findings, which require independent confirmation, raises the possibility that the temporal lobes are not only able to distinguish between living and non-living things including tools and faces, but that the right temporal lobe is specialized for perceiving living creatures (and the sounds they make) whereas the left is specialized for perceiving and naming non-living things, such as tools and household objects.


Attention and visual fixation involves the activation of neurons in the superior parietal and frontal eye fields, the midbrain colliculi, and thalamic nuclei--regions with which the ITL maintains interconnections (Gloor, 1997; Gross & Graziano 1995; Previc 1990). Attention, however, generally requires that visual fixation be focused. Since many ITL neurons maintain large bilateral visual fields, when engaged in visual fixation ITL these cells appear to become partly suppressed. That is, the area of the visual field they respond to becomes restricted to the fovea (Pevic 1990; Richmond et al., 1983). In this manner, ITL neurons become less responsive to other objects such as those in the periphery as the receptive field contracts around the object attended to.

Hence, ITL neurons seems to scan the entire visual field so as to alert the organism to objects of interest or motivational importance (via interconnections with limbic nuclei). When detected, the frontal eye fields, the superior parietal lobe, and subcortical neurons are activated triggering visual fixation. Simultaneously, ITL visual form recognition neurons are activated whereas those with wide non-specific visual fields are inhibited. In this manner, objects of interest are detected and fixated upon (e.g. Previc 1990).

Of adjunctive importance is the middle temporal lobe which in turn can analyze the velocity and direction of the objects movement so that the individual may approach, and, via interaction with cells in area 7, grasp and manipulate the object.



As based on functional imaging (Sergent, et al., 1992), the medial temporal lobe, the right parahippocampal gyrus (in conjunction with areas 19, 37, 36), and the inferior and middle temporal lobe becomes highly active when viewing and categorizing faces and other complex stimuli. Likwise, electrical stimulation of these areas can produce hallucinations and memories of faces of complex visual stimuli (Gloor, 1997; Halgren, 1992).

Damage or removal of the inferior temporal lobe results in loss of the ability to recognize faces, as well as creating severe disturbances involving visual discrimination learning and retention (Braun et al. 1994; Gross & Mishkin, 1977; Mishkin, 1972), and difficulty performing visual closure and recognizing incomplete figural stimuli (Kimura, 1963; Lansdell, 1968,1970). For example, primates with lesions in this vicinity, have severe difficulty learning to discriminate between different shapes and patterns and objects which differ in regard to size or color, although visual acuity is normal.

With damage to the right temporal-occipital region, there can result a severe disturbance in the ability to recognize the faces of friends, loved ones, or pets (Braun et al. 1994; DeRenzi, 1986; DeRenzi et. al., 1968; DeRenzi & Spinnler, 1966; Hanley et al. 1990; Hecaen & Angelergues, 1962; Landis et al., 1986; Levine, 1978; Whitely & Warrington, 1977l ) or to discriminate and identify even facial affect (Braun et al. 1994); a condition referred to as prosopagnosia. In fact, with gradual deterioration and degeneration of the right inferior temporal lobe, patients may suffer a progressive prosopagnosia (Evans et al. 1995). Some patients may in fact be unable to recognize their own face in the mirror. For example, one patient was unable to even discriminate between people on the basis of sex but instead had to relie on the presence of details, such as lipstick, rouge, hair length, a moustache, so as to make discriminations (Levine, 1978).

Presumably, the inability to recognize faces is due to the destruction of facial recognition neurons, including those within the amygdala (Young et al. 1995) and hippocampus (which becomes activated when memorizing faces, Kapur et al. 1995). However, because, at a neocortical level, global facial recognition cells appear to be in a minority whereas those specialized for analyzing facial parts are more numerous, the ability to recognize facial details is therefore more likely to be preserved following inferior temporal destruction -particularly if the left temporal lobe is spared.

Nevertheless, the association with the amygdala is particularly important, as facial stimuli are also social emotional stimuli, and facial recognition, for example, that of a friend or loved one, is generally associated with emotional feelings. Moreover it is via the face that emotional intent and affective states, including threat or fear, is conveyed--information that is processed by the amygdala (e.g. Morris et al., 1996). Hence, damage to the overlying temporal lobe may result in prosopagnosia, including an inability to recognize the face of friends or relatives, due to also to disconnection and an inability to attribute and associate the emotion of recognition to these facial stimuli. It is perhaps for this reason, that some patients with prosopagnosia are also unable to recognize their pets or their homes--the emotional significance of these stimuli can no longer be evoked. These stimuli are no longer personalized and thus cannot be recognized. Lateralization & Facial Recognition.

Although patients with prosopagnosia often suffer from bilateral injuries, in many cases the lesions are restricted to the right hemisphere (DeRenzi, 1986; DeRenzi et. al., 1968; DeRenzi & Spinnler, 1966; Evans et al. 1995; Hanley et al. 1990; Hecaen & Angelergues, 1962; Landis et al., 1986; Levine, 1978; Whitely & Warrington, 197l). Disturbances involving facial recognition do not usually occur with isolated left cerebral lesions. Indeed, the right hemisphere appears to be dominant in regard to the recognition of both familiar and unfamiliar faces as has been well demonstrated in numerous studies of brain injured as well as normal, intact individuals (Bradshaw et al. 1980; DeRenzi, 1982; DeRenzi et al.1968; DeRenzi & Spinnler, 1966; Evans et al. 1995; Geffen et al. 1971; Levy et al. 1972; Ley & Bryden, 1977; Hecaen & Angelergues, 1962). The left hemisphere, however, is involved in the recognition of famous faces (Marzi & Berlucchi, 1977; Rizzolatti, et al. 1971; Hanley et al. 1990).

Among neurosurgical patients, it has also been reported that electrical stimulation of the posterior right temporal gyrus disrupts visual-spatial memory for faces in general (Fried et al., 1982). Electrical stimulation of the posterior portion of the right middle temporal gyrus also results in an inability to correctly lable emotion faces.


When the ITL is damaged, in addition to prosopagnosia there may occur difficulty identifying various familiar stimuli and objects, e.g. utensils, cars, as well as differentiating among similar visual stimuli. Many patients also have difficulty with color recognition (Green & Lessell, 1977; Meadows, 1974b). Frequently these types of agnosic disturbances are related to left cerebral or bilateral dysfunction.


The IT is able to code for and learn new stimuli, can recall the code of the previous stimuli, and can make comparisons between what was perceived on one occasion versus another (Eskandar et al. 1992). This enables IT neurons to make judgments regarding temporal order; if the stimulus was first or second or last (Baylis, & Rolls, 1987; Eskander, et al. 1992). Thus, IT neurons can perform sequential analysis and can compare initial with previous visual representations (Eskandar et al. 1992). Hence, neurons in the IT are involved in form and facial recognition, discrimination, temporal-sequencing, and thus learning and memory for a variety of stimuli.

In addition, IT neurons are directly connected with the entorhinal cortex (Jones & Powel, 1970; Van Hoesen & Pandya, 1975b) -the "gateway to the hippocampus"- as well as to the amygdala (Amaral et al. 1987). Thus neurons located in the inferior temporal lobe are also involved in the maintenance of short term emotional, visual and cognitive memory, and many display heightened activity during delay periods while learning (Fuster & Jevey, 1981; Miyashita & Chang, 1988). Moreover, IT neurons are are also highly concerned with the behavioral context in which learning occurs (Baylis & Rolls, 1987; Gross, et al. 1979; Riches, et al. 1991).

For example, Eskandar, et al. (1992) found in their studies of electrophysiological activity that neurons in the inferior temporal gyrus convey information concerning current versus previous stimulus patterns and their behavioral context. IT neurons are therefore involved in remembering this information, matching it with previously learned information, and are capable of simultaneously transmitting these impressions (including contextual details) to other brain areas. However, IT neurons are also capable of discriminating between stimuli independent of context (Eskandar, et al., 1992).

Hence, IT neurons are involved in both encoding, storage, and recall and interact with the amygdala and hippocampus in regard to learning, memory and recognition. It is in this manner and through these interconnects that IT neurons are involved in emotional as well as non-emotional cognitive processing and memory storage. Conversely, with injuries to the inferior temporal lobe, visual and verbal memory functions suffer (see chapter 14).


The entorhinal, perirhinal, and parahippocampal neocortex are located in the inferior and medial temporal lobe and are adjacent to and richly interconnected with the hippocampus which is buried within its depths. Like the hippocampus and amygdala, the inferior and medial temporal lobes are involved in memory functioning (Gloor, 1990, 1997; Murray, 1992; Nunn et al., 1999; Ploner et al., 1999; Squire, 1992) and may in fact serve as neuronal memory depots that becomes activated during recognition (e.g. Brewer et al., 1998, Wagner et al., 1998).


As argued by Heit and colleagues (1990), "MTL firing patterns may contribute to the reactivation of neocortical circuits encoding a particular stimulus-context gestalt" which in turn makes recognition and retrieval possible. For example, the medial temporal lobe (MTL) becomes activated during recognition memory tasks including those involving words and faces (Heit et al. 1990). Indeed, the greater the activation, the greater is the likelihood that material will be remembered (e.g. Brewer et al., 1998; Wagner et al., 1998).

When the inferior and medial temporal lobe is electrically stimulated exceedingly vivid personal memories may be triggered and recalled (Gloor, 1990, 1992, 1997; Halgren 1992; Halgren, et al. 1978; Penfield, 1954; Penfield & Perot, 1963). Patients may report seeing a complex scene from their past or early childhood, including hearing conversations, seeing faces, experiencing somesthetic sensations, and related events. Curiously, however, these scenes do not move forward in time and are otherwise quite static (See Gloor, 1990, 1997; Halgren 1992), like a wide angle, multi-sensory snapshot.

Conversely, left MTL lesions results in recognition deficits for words (Milner & Teuber 1968), whereas those involving the right MTL disrupt memory for visual forms and faces (e.g. Hanley et al. 1990). However, the entorhinal cortex and hippocampus appear to be the crucial structures, whereas the neocortex may be the site where memories are stored. Consider, for example, patients who undergo "hippocampal removals" whereas the overlying neocortex is spared (Milner, 1990) and patients such as the famous H.M., who underwent bilateral mesial temporal removals: amygdala, hippocampus, entorhinal cortex (Milner, 1968). These patients (particularly those with right sided destruction) perform exceedingly poorly on visual recognition memory tests, including those involving recurring nonsense figures (Kimura, 1963) and human faces (Milner, 1990).

In that the inferior and inferior medial temporal lobes also contain neurons which are selectively sensitive to particular sensory features, and will fire in response to faces, hands, and geometric patterns and objects (Gross et al. 1979; Gross et al. 1972; Sergent et al. 1990), it is possible that not only are auditory and visual memories stored within the inferior temporal lobe, but that it may act as an associational warehouse (so to speak) from which particular auditory-visual images can be activated, retrieved and so that comparisons can be made. Through the neocortex the hippocampus and amygdala can gain access to particular perceptual images as well as store associated information via the aid and guidance of the neural circuits maintained in the entorhinal cortex and through which information is transmitted to both nuclei.

For example, the entorhinal cortex acts as a gateway via which information from the immediately adjacent perirhinal cortex (which sits above and is richly interconnected with the amygdala) and the parahippocampal gyrus (which receives visual, auditory and tactual neocortical information) is analyzed and is then transmitted into the hippocampus (see Horel et al. 1987; Issausti et al. 1987; Squire, 1992). It is also via the entorhinal area that the hippocampus receives amygdaloid projections (Carlsen et al., 1982; Gloor, 1955, 1997; Krettek & Price, 1976; Steward, 1977) and fibers from the orbital frontal and temporal lobes (Van Hoesen, et al., 1972). These neocortical regions are thus highly important in memory.

Squire (1992 p. 202) in fact argues that "the cortical structures adjacent to the hippocampus (entorhinal, perirhinal, and parahippocampal cortex) appear to participate with the hippocampus in a common memory function." He bases this argument on his review of numerous studies (many of which were conducted by Squire and Zola Morgan and colleagues) which indicate that severe memory impairments can result from lesions restricted to these cortical areas.


Although a variety of neurochemical and neuroanatomical regions are involved in the formulation of memory, it has long been known that damage or the neurosurgical removal of the temporal lobes can produce profound disturbances in the learning and recollection of verbal and visual stimuli (Milner, 1958; Kimura, 1963; Nunn et al., 1999; Ploner et al., 1999; Squire, 1987, 1992). For example, left temporal lobectomy, siezures or lesions involving the inferior temporal areas can moderately disrupt immediate and severely impair delayed memory for verbal passages, and the recall of verbal paried-associates, consonant trigrams, word lists and number sequences (Delaney et al. 1980; Meyer, 1959; Meyer & Yates,1955; Milner, 1958, 1968; Milner & Teuber, 1968; Weingartner, 1968). Similarly, severe anterograde and retrograde memory loss for verbal material has been noted when the anterior and posterior temporal regions (respectively) are electrically stimulated (Ojeman et al., 1968, 1971).

In contrast, right temporal lesions or lobectomy significantly impair recognition memory for tactile and recurring visual stimuli such as faces and meaningless designs, as well as memory for object position and orientation, and visual-pictorial stimuli (Corkin, 1965; Delaney et al., 1980; Evans et al. 1995; Kimura, 1963; Milner, 1968; Nunn et al., 1999; Ploner et al., 1999; Taylor, 1969). Electrical stimulation of the right anterior and posterior temporal region also causes respectively, severe anterograde and retrograde memory loss for designs and geometric stimuli, and impairs memory for faces Fried et al., 1982; Ojeman et al., 1968).

With bilateral removal of the inferior temporal region there results a condition which has been variably referred to as "psychic blindness" and the "Kluver-Bucy syndrome". However, as explained in chapter 13, this is due to destruction of the amygdala. If the mesial regions are removed, severe memory disturbances involving visual and auditory stimuli result such that the patient suffers a permanent anterograde amnesia, including facial processing impairments (Young et al. 1995).

Based on lesion, temporal lobectomy and electrical stimulation studies it thus appears that the anterior temporal region is more involved in initial consolidation storage phase of memory, whereas the posterior region is more involved in memory retrieval and recall. In addition, as based on event-related functional magnetic imaging (Brewer et al., 1998; Wagner et al., 1999), it appears that the temporal lobes directly interact with the frontal lobes in memorization and remembering. Indeed, the greater the activation of the frontal and temporal lobes (and associated tissues), the greater is the likelihood that subjects will remember whereas reduced activity is associated with forgetting. Hence, these areas interact to promote memory and retention. In consequence, if the frontal lobe is injured, and even if the temporal lobes are spared, patients may demonstrate significant memory loss --due to an inability to correctly search for and find the memory (see chapter 19).


Temporal lobe epilepsy is often associated with atrophy and sclerosis of the hippocampus in about 50% of such patients (Mathern, 1999; Mitchell et al., 1999), with yet others demonstrating sclerosis in the amygdala (Wolf & Blumcke 1999). In fact, according to Gloor (1997, p. 692), "studies on temporal lobe epilepsy provide evidence that the amygdala is involved inmany of the common symptoms and signs that occur in the course of temporal lobe seizures." Gloor (1997, p. 693), also argues that "hippocampal sclerosis is most likely a consequence of prolonged seizures or status epilepticus, particularly when occurring in early childhood and can therefore be regarded as a lesion induced by seizures rather than a causative agent." Gloor (1997) further suggests that the seizure is either produced by the amygdala, which then envelops the hippocampus, and/or that both must give rise to the seizure simultaneously. In support of this position are the findings of Feindel and Rasmussen (1991) who report 65 of 100 neurosurgery epilepsy patients in whom the amygdala and the hippocampus was removed showed a favorable outcome, whereas an equal number showed a favorable outcome if just the amygdala was removed and the hippocampus was spared.

Because the hippocampus and amygdala have the lowest seizure thresholds of all other brain structures, when injured they are thus highly likely to develop seizure activity and thus give rise to temporal lobe epilepsy.

There are a number of factors which can independently give rise to temporal lobe epilepsy (Kotagal & Luders, 1999; Mathern, 1999; Mitchell et al., 1999; Trimble, 1991; Wolf & Blumcke 1999). For example, incisural hernation at the time of brith is a major cause of amygdala injury and hippocampal sclerosis. Head injuries also cause injuries to the temporal region due to contusion from the bony structures in which it is encased. That is, if the head is struck, the inferior and anterior temporal regions may strike against the skull and may even be sheared due to rotational forces. Also middle ear infections are associated with disturbances involving the temporal lobe which result in TLE (Kotagal & Luders, 1999).

In addition, as detailed in chapter 30, severe and repeated early emotional trauma can in fact injure the immature hippocampus and temporal lobe, giving rise to a propensity to develop kindling as well as abnormal neural networks. This would make these individuals are more likely to develop psychotic and severe emotional and dissociative disorders.


Usually, during the course of a temporal lobe seizure, there are no abrupt and drastic alterations in motor activity such as tonic-clonic spasms (Kotagal & Luders, 1999; Trimble, 1991, 1996). However, some patients may simply cease to respond and stare blankly straight ahead, make licking or smacking movements of the lips, and/or fiddle with their clothing, as if picking up pieces of lint. Although conscious-awareness is lost, these patients are not unconscious. Rather, their mental state is one of absence. In fact, they may appear awake and conscious, although unable to speak or respond to questions, and behaviorally their actions seem semi-purposeful. Nevertheless, sometimes it is extremely obvious that they are experiencing a seizure, whereas in some cases an inexperienced observor may only have the impression that the person is acting somewhat odd.

Nevertheless, unless the patient has several different seizure foci, the same characteristic behavioral manifestations are elicited every time a patient has a seizure. The patient does not simply stare on one occasion and on the next begin rolling his eyes and cry out.



Some patients also note an aura immediately prior to seizure onset (Kotagal & Luders, 1999; Trimble, 1991, 1996). This may involve feelings of fear or anxiety, alterations in gastric motility, or unpleasant tastes or in particular, odors (e.g. burning rubber or feces), i.e. an olfactory aura (Gloor, 1997). Some patients may lick and repeatedly smack their lips.

Presumably, the experience of olfactory hallucinations is due to abnormal activation of the rhinencephalon (the "nose brain") and thus limbic nuclei such as the amygdala (Gloor, 1997). Possibly the licking and smacking movements are also due to activation of the amygdala and other limbic structures associated with food consumption. Changes in gastrict motility may be secondary to insular activation and/or limbic participation.

Automatisms associated with TLE occur in up to 75-95% of patients which is twice what occurs with lesions outside the temporal lobe (Kotagal & Luders, 1999; Trimble, 1991, 1996). Thse includes staring, searching, groping, lip smaking, spitting, gropoing, staring, salivation. Also laughing, cryng, hssing, gritting or gnasing of teeth, clenching the fist, confused talking, scraming, shouting, standing, wrunning, walking, kissing, and so on.

Common visceral reactions associated with TLE auras include feelings of a racing or flutering heart, incuding pounding or throbbing (Kotagal & Luders, 1999; Trimble, 1991, 1996) also there may be feelings of smothering or chocking. Body sensation include numbness, tenseness, pressure and heaviness. Ther may also be visual sensations such as macro or micro or of things be very hear or far (Gloor, 1997).

Feelings of strangeness or familiarity are also common (Gloor, 1997; Kotagal & Luders, 1999; Trimble, 1991, 1996). deja vue occurs in up to 20% of such patients, usually with right cerebral seizures within the temporal lobe. Some claim to have feelings like a desire to ge alone, or of wanting something but not knowing what.

Olfactory hallucinations are not uncommon and are usually quite disagreeable and include smells like burnign meat, fish, lime, acid fumes, burnign shit. There may also be gustatory sesatniosn which are also usually disagreeable coupled with very bad and bitter or metalic and sour tastes.

Fear is one of the most common feelings, which include feelings of panic, terror, or of soemting horrible about to happen (Daly, 1958; Gibbs, 1958; Penfield & Jasper, 1954; Williams, 1956). Some patients have experienced fear coupled with sexual sensations, including fear associated with a feeling of sexual climax, or feelings of being sexually pentrated following by orgasm then a loss of consciousness. Although one patient stated it was like "a red hot pocker being inserted into her vagina."

Hence, there are a vast range of aura and experiental phenomenon associated with temporal lobe epilepsy, many of which reflect the possible activation of those structures innervated by the amygdala. Not uncommonly these experiential phenomenon begin just before the seizure. In summary, these include fear, coupled with the remembrance of a fearful or traumatic memories, rising epigastric sensations, chest sensations, nausea, heart palpations, feelings of cold or warmth, shivering, pallor or flushing of the face, respiratory changes inlcuding apnea, salavation, belching, farting, sweating, and vaginal secretions in women which may be accompanied by sexual feelings or behaviors (Daly, 1958; Gloor, 1997; Penfield & Jasper, 1954; Remillard et al., 1983). Moreover, many of these same exact feelings and behaviors can be triggered by direct stimulation of the amygdala (Chapman, 1960; Chapman et al., 1954; Gloor, 1997; Halgren, 1992; Kaada, 1951, 1972), including deja vu--the feeling of familiarity/reminiscence.

In addition, patients may act out on these emotions and auras. There have been reported instances of patient's suddenly lashing out and even attempting to attack those close by, while in the midst of a seizure (Saint-Hilaire et al., 1980), and/or attacking, kicking, and destroying furniture and other objects (Ashford et al., 1980). Patient's have also behaved violently with direct stimulation of the amygdala (Mark et al., 1972), as have a variety of animal subjects (see chapter 13).

Others have responded with behaviors indicative of extreme fear, or conversely, extreme pleasure, including laughter and mirth. Moreover, some patients have acted out sexually during a seizure, such as by displaying their penis, or lying on the floor with legs spread and thrusting, even moaning with pleasure and experiencing libidinous feelings in the vagina and thighs, coupled with an orgasm (Currier, Little, Suess and Andy, 1971; Gloor, 1997; Remillard et al., 1983).


The primate amygdala is sexually differentiated (Nishizuka & Arai, 1981) and in conjunction with the overlying temporal lobe, is capable of detecting sexually significant stimuli, and can determine and detect gender differences such as male and female faces and the emotions they convey (Hasselmo, Rolls, & Baylis, 1989, Heit et al., 1988; Rolls, 1984). Because the amygdala is involved in sexuality and is sexually differentiated, activation of the amygdala can produce penile erection (Kling and Brothers, 1992; MacLean, 1990; Robinson and Mishkin, 1968; Stoffels et al., 1980) sexual feelings (Bancaud et al., 1970; Remillard et al., 1983), sensations of extreme pleasure (Olds and Forbes, 1981), memories of sexual intercourse (Gloor, 1986), as well as ovulation, uterine contractions, lactogenetic responses, and orgasm (Backman and Rossel, 1984; Currier et al., 1971; Freemon and Nevis,1969; Warneke, 1976; Remillard et al., 1983; Shealy and Peel, 1957).

By contrast, injuries to and/or seizure activity within the amygdala/temporal lobe may result in bizarre sexual changes, such as continuous masturbation and indiscriminate, often hypersexual hetero- and homosexual behaviors including attempts at sex with inanimate objects (Kling and Brothers, 1992; Kluver and Bucy, 1939; Pribram and Bagshaw 1953; Terzian and Ore, 1955). Hypersexuality following amygdala injury has been documented among numerous species, including cats and dogs (Blumer 1970; Kling and Brothers, 1992).

Humans with an abnormally activated or severely injured amygdala/temporal lobe may expose and manipulate their genitals (Leutmezer et al., 1999), masturbate in public, and attempt to have sex with family members or individuals of the same sex (Blumer, 1970; Kolarsky, Freund, Macheck, and Polak, 1967; Terzian and Ore, 1955). Moreover, abnormal activity involving the amygdala and overlying temporal lobe has been associated with the the development of hyposexuality (Taylor, 1971; Heirons and Saunders, 1966; Toon, Edem, Nanjee, and Wheeler, 1989), hypersexuality (Blumer, 1970) as well as homosexuality, transvestism, and thus confusion over sexual orientation (Davies and Morgenstern, 1960; Kolarsky et al., 1967). In fact, abnormal- or seizure activity within the amygdala or overlying temporal lobe may induce an individual to engage in "sexual intercourse" even in the absence of a partner. For example, Currier and colleagues (1971, p. 260) described a female temporal lobe seizure patient who was "sitting at the kitchen table with her daughter making out a shopping list" when she suffered a seizure. "She appeared dazed, slumped to the floor on her back, lifted her skirt, spread her knees and elevated her pelvis rhythmically. She made appropriate vocalizations for sexual intercourse such as: It feels so good...further, further."


In some instances patients with temporal lobe seizures (triggered perhaps by tumor) may display extremely odd and bizzare behaviors during the course of the seizure (Chen & Forster, 1973; Trimble 1991) For example, a number of authors have presented case reports of individuals who developed laughing (gelastic epilepsy), crying (dacrystic epilepsy), and/or running seizures (cursive epilepsy) -running apparently being triggered via amygdala-striatal activation (chapter 13, 16).

One patient's seizure consisted of suddenly bursting into laughter, rubbing his upper abdomen and running wildly about the room with an expression of fear on his face (Sethi & Rao, 1976). Another individual displayed paroxysmal attacks of weeping, sobbing, and mournful moaning (Offen et al., 1976). These behaviors were involuntary, however, and part of the seizure. Once consciousness returned, the patients would have no recollection of their actions.


The most common emotional reactions and sensations which occur secondary to or during the course of a temporal lobe seizure include feelings of fear, anxiety, depression, depersonalization, pleasure, unpleasure, and familiarity (Bear, 1979; Cendes, et al. 1994; Herman & Chhabria, 1980; Gloor, 1997; Gloor et al., 1982; Perez & Trimble, 1980; Trimble 1991; Slater & Beard 1963; Strauss et al., 1982; Weil, 1956; Williams, 1956), fear being the most frequently experienced. Many of these same feelings are also triggered by electrical stimulation of the temporal lobes, amygdala and hippocampus (Gloor, 1972, 1997; Gloor et al., 1982; Heath, 1964; Mullan & Penfield, 1959).

Depression (lasting from hours to weeks) may occur as an immediate sequela to the seizure, many patients also experiencing confusion. A depressive aura may also precede and thus hearld the coming of a seizure by hours or even days (Trimble 1991, 1996; Williams, 1956). This may be due in part to the role of the temporal lobe (and amygdala) is storing emotional and personal memories, including those with are negative, depressing and traumatic (Abrams & Taylor, 1979; Cimino, et al. 1991 Cohen, Penick & Tarter, 1974; Deglin & Nikolaenko, 1975; Shagass et al.,1979; Wexler, 1973) such that when activated, depressive moods and memories may be provoked. For example, Abrams and Taylor (1979) and Shagass et al. (1979) have found that depressed patients demonstrated more right vs left temporal lobe electrophysiological activity and EEG abnormalities. Moreover, others have argued that ECT administered to the right vs left temporal lobe is more likely to alleviate depressive symptoms (Cohen, et al, 1974; Deglin & Nikolaenko, 1975).

Rather than increased emotionality, some patients complain of emotional blocking, and feelings of emptiness: "feelings don't reach me anymore" (Weil, 1956). Presumably this is a consequence of limbic disconnection. That is, the siezure foci (or lesion) acts to deconnect the limbic areas from the temporal (or orbital frontal) lobes. In consequence, percepts and thoughts no longer come to be assigned emotional or motivational significance.


It has been reported by a number of neuroscientists that some patients who experience temporal lobe epilepsy, seizures, or related abnormalties sometimes experience very sexual as well as bizarre, unusual and fearful mental phenomenon including dissociative states, feelings of depersonalization, and hallucinogenic and dream-like recollections involving threatening men, naked women, sexual intercourse, religion, the experience of god, as well as demons and ghosts and pigs walking upright dressed as people (Bear 1979; Daly 1958; Gloor 1986, 1992; Halgren 1992; Horowitz et al. 1968; Penfield & Perot 1963; Slater & Beard 1963; Taylor 1972 1975; Trimble 1991; Weingarten, et al. 1977; Williams 1956). Moreover, some individuals report communing with spirits or receiving profound knowledge from the Hereafter, following temporal lobe activation (Daly 1958; MacLean 1990; Penfield & Perot 1963; Williams 1956).

One young many had repeated conversations with God. One day God informed this young man that he was Jesus Christ, could perform miracles and could fly. Believing that he was in fact The Christ, since god had told him so, he climbed upon a roof and leaped into the air, with disasterous results (Sommer 1880).

Intense activation of the temporal lobe, hippocampus, and amygdala has been repeatedly reported to give rise to a host of sexual, religious and spiritual experiences; and chronic hyperstimulation can induce an individual to become hyper-religious or visualize and experience ghosts, demons, angels, and even God, as well as claim demonic and angelic possession or the sensation of having left their body (Bear 1979; Daly 1958; Gloor 1986, 1992; Horowitz et al. 1968; MacLean 1990; Mesulam 1981; Penfield & Perot 1963; Schenk, & Bear 1981; Slater & Beard 1963; Subirana & Oller-Daurelia, 1953; Trimble 1991; Weingarten, et al. 1977; Williams 1956). Indeed, as detailed in chapter 9, the temporal lobe, amygdala and hippocampus enables humans to have religious, spiritual and mystical experiences (Bear 1979; Daly 1958; d'Aquili & Newberg 1993; Mesulam 1981; Trimble 1991).

In one case, a 37 year-old manager of a car dealership had been struck by a car while walking across a street, and was slammed against the pavement, striking his head. According to this fellow (GM), once he gained "consciousness" he realized he was standing next to his body, which was still lying in the street. He could see that his head was bloody, and he could see that he was unconscious and he could see other people rushing over to where he lay. However, this dissociative hallucination only lasted a few seconds, and then he was back in his body, regaining consciousness. GM states that his experience was a "revalation" and although he had never been religious, that he became very religious, and began reading the Bible, volunteering at a local church, and writing a religious column for a small local newspaper. He also began having repeated episodes where he would float beside his body. As his wife complained that he was repeatedly "blanking out" and as he was also having memory problems, he sought medical help, was referred for neuropsychological testing, which revealed significant disturbances of memory, and evidence of temporal lobe epilepsy. Subsequent EEG demosntrated bilateral spiking and theta activity over the temporal lobes.


Penfield and Perot (1963) describe several patients who during a seizure claimed they could see themselves in different situaitons. One woman stated that "it was though I were two persons, one watching, and the other having this happen to me," and that it was she who was doing the watching as if she was completely separated from her body. According to Penfield, "It was as though the patient were attending a play and was both actor and audience.

Other patients claim to have quite pleasent aurs and describe feelings such as elation, security, eternal harmony, immense joy, paradisiacal happiness, euphoria, completeness. Between .5 and 20% of such patients claim such feelings (Williams, 1956; Daly, 1958). One patient of Williams (1956) claimed that his attacks began with a "sudden feeling of extrreme well being involvign all my senses. I see a curtain of beautiful colors before my eyes and experience a pleasant but indescribable taste in my mouth. Objects feeling pleasurably warm. the room assumes vast proportions, and I feel as if in anothe world."

A patient described by Daly claimned his seizure felt like "a sunny day when your friends are all around you." He then felt disociated from his body, as if he were looking down upon himself and wathcing his actions.

Williams (1956) describes a patient who claimed that during an aura she experienced a feeling that she was being lifted up out of her body, coupled with a very pleasant sensation of eleation and the sensation that she was "just about to find out knowlede no one else shares, something to do with the line between life and death."

Subirana and Oller-Daurelia (1953) described two patients who experienced ecastic feelings of either "extrraordinary beatitude" or of paradise as if they had gone to heaven and noted that his fantastic feelings lasted for hours.

Other patients have noted that feelings and things suddenly become "cyrstal clear" or that they have a feeling of clairvoyance, or of having the truth revealed to them, or opf having achieved a sense of greater awareness and of a new awarness such that sounds, smells and visual objects seemd to have a greater meaning and sensibility.


Personality and psychiatric disorders have been frequently reported as a common associated complication among a small percentage of individuals (between 4.5 to 7%) with seizures-disorders localized to the temporal lobe (Harrison, 1999; Trimble 1991, 1996). Such patients may appear depressed, paranoid, hysterical, or suffering from schizophrenic-like symptomology (However, see Gold et al. 1994).


Some authors have argued that, like hallucinations, the nearer the seizure foci to the anterior temporal lobe, the greater the probability of significant psychiatric abnormality (Gibbs, 1951; Gloor 1992; Trimble 1991, 1996). Presumably this is a function of hyper-activation of underlying limbic structures and thus abnormal attribution of emotional significance to different afferent streams of perceptual experience (Bear, 1979).


It has been repeatedly reported that a significant minority of individuals with temporal lobe epilepsy suffer from prolonged and/or repeated instances of major psychopathology (Bruton et al. 1994; Buchsbaum, 1990; Falconer, 1973; Flor-Henry, 1969, 1983; Gibbs, 1951; Jensen & Larsen, 1979; Perez & Trimble 1980; Sherwin, 1977, 1981; Slater & beard, 1963; Taylor, 1972; Trimble 1991, 1996). Conversely, those with affective disturbances, e.g. mania, have been found to suffer from seizures involving the right temporal lobe (Bear et al., 1982; Falconer & Taylor, 1970; Flor-Henry, 1969; Trimble 1991, or right frontal lobe (chapter 19), although depression may be more likely with left vs right hemisphere injuries (see chapter 11).

Estimates of psychosis and affective disorders among individuals suffering from temporal lobe epilepsy, be it a single episode or chronic psychiatric condition have varied from 2-81%. Probably a more realistic figure is 3% to 7% (see Trimble, 1991, 1992, 1996).

There are several distinct neurological explanations for the association between temporal lobe damage and psychotic and affective disorders. As discussed in detail in previous chapter 10, the right hemisphere is dominant for most aspects of emotional functioning. Hence, when damaged or abnormally activated, such as from a seizure or chronic subclinical seizure activity, emotional functioning becomes altered and disturbed. Moreover, since the amygdala and hippocampus are often secondarily aroused (or hyperaroused), the possibility of abnormal emotionality is enhanced even further.

In this regard, Gloor et al., (1982) in a depth electrode stimulation study of patients suffering from epilepsy presented evidence indicating that all experiential and emotional alterations were encountered following right amygdala and hippocampal activation, with the majority of phenomenon elicited from the amygdala. As discussed in chapter 13, the limbic system seem to be lateralized and the right amygdala and hippocampus appear to be more involved in emotional functioning . Hence, abnormal activation of these nuclei (such as during the course of a temporal lobe seizure) are more likely to give rise to abnormal emotional reactions, with the exception of depression which is common with left frontal and left temporal lobe injuries.


In addition, some individuals with temporal lobe seizures may complain of emotional blunting. Hence, rather than a limbic hyperconnection, these individuals suffer from a disconnection; similar to what occurs with a left frontal injury.

It has also been repeatedly demonstrated in histological studies that the temporal lobe of schizophrenics are characterized by an excessive focal temporal lobe neuronal damage including gliosis (Akbarian et al. 1993; Bruder, et al., 1999; Bruton 1988; Bruton et al. 1990; Harrison, 1999; Kwon et al., 1999; Stevens 1982; Taylor 1972). Hence, these patients may experience auditory hallucinations and are more likely to demonstrate formal thought disorders and aphasic thinking including the production of neologisms and syntactical speech errors (Kwon et al., 1999), as well as emotional (or thought) blocking or blunting due to limbic system-temporal lobe disconnection (Perez & Trimble, 1980; Slater & Beard, 1963). As often occurs with receptive aphasia and left temporal lobe dysfunction, individuals suffering from schizphrenia may be unaware of their illness (Amador et al. 1994; Lysaker, et al., 1999; Wilson et al. 1986).

Hence, certain subgroups of schizophrenics display significant abnormalities involving speech processing, such that the semantic, temporal-sequential, and lexical aspects of speech organization and comprehension are disturbed and deviantly constructed (Chaika, 1982; Clark et al. 1994; Flor-Henry, 1983; Hoffman, 1986; Hoffman et al. 1986; Rutter, 1979). Indeed, significant similarities between schizophrenic discourse and aphasic abnormalties have been reported (Faber, Abrams, Taylor, Kasprisin et al. 1983). It is often difficult to determine what a schizophrenic individual may be talking about, particularly in that some of these individuals complain that what they say often differs from what they intended to say (Chapman, 1966). Temporal-sequentual (i.e. syntactical) abnormalities have also been noted in their ability to reason. The classic example being: "I am a virgin; the Virgin Mary was a virgin; therefore I am the Virgin Mary."

Hence, there is considerable evidence indicating that a significant relationship exists between abnormal left hemisphere and left temporal lobe functioning and schizophrenic language, thought and behavior. As detailed in chapter 19, the left frontal region and medial frontal cortices are also implicated in the genesis of schiophrenic-like abnormalities including catatonia (chapter 19).

However, in contrast to those with frontal lobe schizophrenia who are more likely to present with "negative" symptoms and emotional blunting, temporal lobe schziophrenics are likely to present with "positive" symptoms, including retention of the capacity to experience and express "warmth" (Crow, 1980; Crowe & Kuttner 1991). Emotional expression, however, tends to be abnormal, inappropriate or incongruent, and/or exaggerated (Bear & Fedio, 1977; Crow, 1980; Crowe & Kuttner 1991).

It has also been repeatedly reported that irritative lesions more greatly involves the lateral convexity of the left temporal lobe are he most likely to result in schizophrenic-like disturbances (DeLisi et al. 1991; Dauphinais et al. 1990; Flor-Henry 1983; Harrison, 1999; Perez et al. 1985; Rossi et al. 1990, 1991; Sherwin 1981). Given the role of the temporal lobe in language (and the fact that the superior temporal lobe is derived from amygdala and hippocampal tissue) it is also not uncommon for these individuals to demonstrate aphasic abnormalities in their thought and speech (Chaika, 1982; Clark et al. 1994; Flor-Henry, 1983; Hoffman, 1986; Hoffman et al. 1986; Perez & Trimble, 1980; Rutter, 1979; Slater & Beard, 1963).

However, the type and form of temporal lobe schizophrenia may differ dependent on which regions have been compromised. In some instances the amygdala and hippocampus are involved, (Bogerts et al. 1985; Brown et al. 1986; Falkai & Bogerts 1986) in which case memory and emotional functioning may be most severely effected, and patients may experience visual hallucinations. Temporal lobe schizophrenics with limbic involvement may behave violently and aggressively (Crow & Kuttner 1991; Lewis et al. 1982; Taylor 1969). They may also experience extreme feelings of religiousness (Bear, 1979, Trimble, 1991, 1992), fear, paranoia, and depression (Crow & Kuttner 1991; Perez & Trimble, 1980; Trimble, 1991, 1992), as well as hallucinations.

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