The vertebrate cerebrum (brain) is formed by two cerebral hemispheres that are separated by a groove, the longitudinal fissure. The brain can thus be described as being divided into left and right cerebral hemispheres. Each of these hemispheres has an outer layer of grey matter, the cerebral cortex, that is supported by an inner layer of white matter. In eutherian (placental) mammals, the hemispheres are linked by the corpus callosum, a very large bundle of nerve fibers. Smaller commissures, including the anterior commissure, the posterior commissure and the fornix, also join the hemispheres and these are also present in other vertebrates. These commissures transfer information between the two hemispheres to coordinate localized functions.
Human brain seen from front.
|Anatomical terms of neuroanatomy|
Macroscopically the hemispheres are roughly mirror images of each other, with only subtle differences, such as the Yakovlevian torque seen in the human brain, which is a slight warping of the right side, bringing it just forward of the left side. On a microscopic level, the cytoarchitecture of the cerebral cortex, shows the functions of cells, quantities of neurotransmitter levels and receptor subtypes to be markedly asymmetrical between the hemispheres. However, while some of these hemispheric distribution differences are consistent across human beings, or even across some species, many observable distribution differences vary from individual to individual within a given species.
Each cerebral hemisphere has an outer layer of cerebral cortex which is of grey matter and in the interior of the cerebral hemispheres is an inner layer or core of white matter known as the centrum semiovale. The interior portion of the hemispheres of the cerebrum includes the lateral ventricles, the basal nuclei, and the white matter.
If the upper part of either hemisphere be removed, at a level about 1.25 cm above the corpus callosum, the central white matter will be exposed as an oval-shaped area, the centrum ovale minus, surrounded by a narrow convoluted margin of gray substance, and studded with numerous minute red dots (puncta vasculosa), produced by the escape of blood from divided bloodvessels.
If the remaining portions of the hemispheres be slightly drawn apart a broad band of white substance, the corpus callosum, will be observed, connecting them at the bottom of the longitudinal fissure; the margins of the hemispheres which overlap the corpus callosum are called the labia cerebri.
Each labium is part of the cingulate gyrus already described; and the slit-like interval between it and the upper surface of the corpus callosum is termed the callosal sulcus.
If the hemispheres be sliced off to a level with the upper surface of the corpus callosum, the white substance of that structure will be seen connecting the two hemispheres.
The large expanse of medullary matter now exposed, surrounded by the convoluted margin of gray substance, is called the centrum ovale majus. The blood supply to the centrum ovale is from the superficial middle cerebral artery. The cortical branches of this artery descend to provide blood to the centrum ovale.
The cerebral hemispheres are derived from the telencephalon. They arise five weeks after conception as bilateral invaginations of the walls. The hemispheres grow round in a C-shape and then back again, pulling all structures internal to the hemispheres (such as the ventricles) with them. The intraventricular foramina (also called the foramina of Monro) allows communication with the lateral ventricles. The choroid plexus is formed from ependymal cells and vascular mesenchyme.
Broad generalizations are often made in popular psychology about certain functions (e.g. logic, creativity) being lateralized, that is, located in the right or left side of the brain. These claims are often inaccurate, as most brain functions are actually distributed across both hemispheres. Most scientific evidence for asymmetry relates to low-level perceptual functions rather than the higher-level functions popularly discussed (e.g. subconscious processing of grammar, not "logical thinking" in general). In addition to this lateralization of some functions, the low-level representations also tend to represent the contralateral side of the body.
The best example of an established lateralization is that of Broca's and Wernicke's Areas (language) where both are often found exclusively on the left hemisphere. These areas frequently correspond to handedness however, meaning the localization of these areas is regularly found on the hemisphere opposite to the dominant hand. Function lateralization such as semantics, prosodic, intonation, accentuation, prosody, etc. has since been called into question and largely been found to have a neuronal basis in both hemispheres.
Perceptual information is processed in both hemispheres, but is laterally partitioned: information from each side of the body is sent to the opposite hemisphere (visual information is partitioned somewhat differently, but still lateralized). Similarly, motor control signals sent out to the body also come from the hemisphere on the opposite side. Thus, hand preference (which hand someone prefers to use) is also related to hemisphere lateralization.
In some aspects, the hemispheres are asymmetrical; the right side is slightly bigger. There are higher levels of the neurotransmitter norepinephrine on the right and higher levels of dopamine on the left. There is more white matter (longer axons) on the right and more grey matter (cell bodies) on the left.
Linear reasoning functions of language such as grammar and word production are often lateralized to the left hemisphere of the brain. In contrast, holistic reasoning functions of language such as intonation and emphasis are often lateralized to the right hemisphere of the brain. Other integrative functions such as intuitive or heuristic arithmetic, binaural sound localization, etc. seem to be more bilaterally controlled.
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