Periarchicortex is one of two subtypes of periallocortex, [1] [2] the other being peripaleocortex. [3] It is formed at borders between archicortex (a subtype of allocortex) and isocortex and shows slow histological transition from the four-layered structure typical for archicortex to the six-layered structure typical for isocortex. [1]
Cortical areas that are generally considered to belong to periarchicortex, include presubiculum, parasubiculum, entorhinal cortex, perirhinal cortex, retrosplenial cortex, periarchicortical part of cingulate cortex, posterior part of subcallosal area, and subgenual area. [1]
Periarchicortex does not contact immediately at borders with the true isocortex and does not transit directly into it. Instead, another transitional area from the isocortex side, called proisocortex, is formed at such borders. [4] So, at borders between "true" archicortex and true isocortex, there are two transitional areas. One such area, which is anatomically located closer to the archicortex side and histologically more resembling it, is called periarchicortex. [1] Another transitional area, which is anatomically located closer to the true isocortex and histologically more resembling it, is called proisocortex. [4]
The cerebral cortex, also known as the cerebral mantle, is the outer layer of neural tissue of the cerebrum of the brain, in humans and other mammals. It is separated into two cortices, by the longitudinal fissure that divides the cerebrum into the left and right cerebral hemispheres. The two hemispheres are joined beneath the cortex by the corpus callosum. The cerebral cortex is the largest site of neural integration in the central nervous system. It plays a key role in memory, attention, perception, awareness, thought, language, and consciousness.
A Brodmann area is a region of the cerebral cortex, in the human or other primate brain, defined by its cytoarchitecture, or histological structure and organization of cells.
The neocortex, also called the neopallium and isocortex, is the part of the mammalian brain involved in higher-order brain functions such as sensory perception, cognition, generation of motor commands, spatial reasoning and language.
Brodmann Area 14 is one of Brodmann's subdivisions of the cerebral cortex in the brain. It was defined by Brodmann in the guenon monkey . While Brodmann, writing in 1909, argued that no equivalent structure existed in humans, later work demonstrated that area 14 has a clear homologue in the human ventromedial prefrontal cortex.
The allocortex is one of the two types of cerebral cortex, the other being the neocortex. It is characterized by having just three or four cell layers, in contrast with the six layers of the neocortex, and takes up a much smaller area than the neocortex. There are three subtypes of allocortex: the paleocortex, the archicortex, and the periallocortex – a transitional zone between the neocortex and the allocortex.
Brodmann area 13 is a subdivision of the cerebral cortex as defined on the guenon monkey and on the basis of cytoarchitecture. Brodmann area 13 is found in humans as part of the insula. This structure lies between the lateral and medial layers of the brain. Thus it is sometimes misidentified as not being a Brodmann area.
Brodmann Area 15 is one of Brodmann's subdivisions of the cerebral cortex in the brain.
Cytoarchitecture, also known as cytoarchitectonics, is the study of the cellular composition of the central nervous system's tissues under the microscope. Cytoarchitectonics is one of the ways to parse the brain, by obtaining sections of the brain using a microtome and staining them with chemical agents which reveal where different neurons are located.
In anatomy of animals, the paleocortex, or paleopallium is a region within the telencephalon in the brain which is older in an evolutionary sense than the archicortex and the neocortex.
The paralimbic cortex is an area of three-layered cortex that includes the following regions: the piriform cortex, entorhinal cortex, the parahippocampal cortex on the medial surface of the temporal lobe, and the cingulate cortex just above the corpus callosum.
Percival Sylvester Bailey was an American neuropathologist, neurosurgeon and psychiatrist who was a native of rural southern Illinois.
In neuroanatomy, pallium refers to the layers of grey and white matter that cover the upper surface of the cerebrum in vertebrates. The non-pallial part of the telencephalon builds the subpallium. In basal vertebrates the pallium is a relatively simple three-layered structure, encompassing 3-4 histogenetically distinct domains, plus the olfactory bulb. It used to be thought that pallium equals cortex and subpallium equals telencephalic nuclei, but it has turned out, according to comparative evidence provided by molecular markers, that the pallium develops both cortical structures and pallial nuclei, whereas the subpallium develops striatal, pallidal, diagonal-innominate and preoptic nuclei, plus the corticoid structure of the olfactory tuberculum. In mammals, the cortical part of the pallium registers a definite evolutionary step-up in complexity, forming the cerebral cortex, most of which consists of a progressively expanded six-layered portion isocortex, with simpler three-layered cortical regions allocortex at the margins. The allocortex subdivides into hippocampal allocortex, medially, and olfactory allocortex, laterally.
The line of Gennari is a band of myelinated axons that run parallel to the surface of the cerebral cortex on the banks of the calcarine fissure in the occipital lobe. This formation is visible to the naked eye as a white strip running through the cortical grey matter, and is the reason the primate V1 is also referred to as "striate cortex." The line of Gennari is due to dense axonal input from the thalamus to layer IV of visual cortex. The structure is named for its discoverer, Francesco Gennari, who first observed it in 1776 as a medical student at the University of Parma. He described it in a book which he published six years later. Although non-primate species have areas that are designated primary visual cortex, some lack a stria of Gennari.
Agranular insula is a portion of the cerebral cortex defined on the basis of internal structure in the human, the macaque, the rat, and the mouse. Classified as allocortex (periallocortex), it is in primates distinguished from adjacent neocortex (proisocortex) by absence of the external granular layer (II) and of the internal granular layer (IV). It occupies the anterior part of the insula, the posterior portion of the orbital gyri and the medial part of the temporal pole. In rodents it is located on the ventrolateral surface of the cortex rostrally, between the piriform area ventrally and the gustatory area or the visceral area dorsally.
Granular insular cortex refers to a portion of the cerebral cortex defined on the basis of internal structure in the human and macaque, the rat, and the mouse. Classified as neocortex, it is in primates distinguished from adjacent allocortex (periallocortex) by the presence of granular layers – external granular layer (II) and internal granular layer (IV) – and by differentiation of the external pyramidal layer (III) into sublayers. In primates it occupies the posterior part of the insula. In rodents it is located on the lateral surface of the cortex rostrally, dorsal to the gustatory area or, more caudally, dorsal to the agranular insula.
Mesocortex is the transitional areas of the cerebral cortex, formed at borders between true isocortex and true allocortex. Parts of mesocortex that lie closer to the true isocortex and have more resemblance to the isocortex in their cytoarchitectonics and histology, are called proisocortex. Parts of mesocortex that lie closer to the true allocortex and have more resemblance to the allocortex in their cytoarchitectonics and histology, are called periallocortex.
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