Memory cortex

The temporal lobe is the inferior middle portion of the cerebral cortex of both hemispheres. The temporal lobes are involved in the analysis of visual and acoustic information and in memory formation. The hippocampus is part of the inner, medial side of the temporal lobes. 

The pathologic hallmarks of the disease in the brain include neurofibrillary tangles and neuritic plaques made up of various proteins, which result in a shortage of the neurotransmitter acetylcholine. These are primarily located in brain regions involved in learning, memory, and emotional behaviors such as the cerebral cortex, hippocampus, basal forebrain, and amygdala.11... 

Cannabinoid receptors are expressed throughout the cerebral cortex and the hippocampus, and a subpopulation of these cells appear to show an unusually high level of activity. It is possible that cells in these areas modulate the sensory effects of cannabis, particularly the effects on perception, task performance and memory. In addition, the anticonvulsant properties of cannabis are believed to be mediated here. Parts of the hypothalamus show high levels of receptor sites for cannabinoids this may be related to hypothermia effects. High levels in the cerebellum may be related to mediating the property of cannabinoids that produces the reduction in ataxic (muscle co-ordination) symptoms in certain disorders (Herkenham et al., 1991). 

LTP has been shown in many parts of the brain but it has been most extensively studied in the hippocampus, a phy-logenetically old part of the cerebral cortex that in humans is embedded in the temporal horn and in rats and rabbits lies beneath the parietal and temporal neocortex (Fig. 15-3A). The hippocampus is essential for (declarative) memory formation in rats the role of hippocampus in acquisition of spatial information has been studied in... 

Amnesia patients showed the role of temporal lobe in memory. Almost at the same time of Penfield s studies, Brenda Milner of the Montreal Neurological Institute examined a patient, known by his initials as H. M., who had undergone bilateral surgical removal of the temporal lobe (medial temporal cortex, amygdala, and two-thirds of the hippocampus). The surgery was apparently a success... 

Fuster, J. M. Memory in the Cerebral Cortex. An Empirical Approach to Neural Networks in the Human and Nonhuman Primate. Cambridge, MA The MIT Press, 1994. 

Milad, M. R. and Quirk, G. J. Neurons in medial prefrontal cortex signal memory for fear extinction. Nature 420 70-74, 2002. 

To confirm their results and check for methodological problems, some studies have been carried out. As there was a probability that hypothermic conditions during temporary removal from dam may have affected the results, Pauluhn and Schmuck administered S-bioallethrin and deltamethrin to neonatal mice from postnatal day 10 to 16 under a hypo-, normo-, or hyperthermic environment, and measured the MAChR density at the age of 17 days [51]. Increase in MAChR in Cortex at PND 17 in animals treated with S-bioallethrin was observed. Meanwhile, no changes were observed in animals treated with deltamethrin. In addition, an enormous influence of environmental temperature on the density of MAChR receptors in the crude synaptosomal fraction of the cerebral cortex was ascertained. Tsuji et al. exposed mouse dams with their litters to D-allethrin by inhalation for 6 h from postnatal day 10 to 16. The inhalation administration method is the most relevant route of exposure for humans, including babies and infants, after indoor use of D-allethrin. The neonatal exposure to D-allethrin by inhalation did not induce effects either on the brain MAChR density or motor activity at 17 days and 4 months of age, or on performance in the leaming/memory test at 11 months of age [52]. Other unpublished studies with D-allethrin, S -bioallethrin, or deltamethrin were examined to confirm the results of Eriksson et al. and showed inconsistent results [53]. The reasons for discrepancy among these findings are unknown. 

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