| Brodmann area | |
|---|---|
3D representation of Brodmann areas
| |
| Details | |
| Part of | Cerebrum |
| Identifiers | |
| NeuroNames | 427 |
| FMA | 68596 |
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.
History
A number of important Brodmann areas have been marked out on this diagram.
Brodmann areas were originally defined and numbered by the German anatomist Korbinian Brodmann based on the cytoarchitectural organization of neurons he observed in the cerebral cortex using the Nissl method of cell staining. Brodmann published his maps of cortical areas in humans, monkeys, and other species in 1909, along with many other findings and observations regarding the general cell types and laminar organization of the mammalian cortex. The same Brodmann area number in different species does not necessarily indicate homologous areas. A similar, but more detailed cortical map was published by Constantin von Economo and Georg N. Koskinas in 1925.
Present importance
Brodmann
areas have been discussed, debated, refined, and renamed exhaustively
for nearly a century and remain the most widely known and frequently
cited cytoarchitectural organization of the human cortex.
Many of the areas Brodmann defined based solely on their neuronal
organization have since been correlated closely to diverse cortical
functions. For example, Brodmann areas 3, 1 and 2 are the primary somatosensory cortex; area 4 is the primary motor cortex; area 17 is the primary visual cortex; and areas 41 and 42 correspond closely to primary auditory cortex. Higher order functions of the association cortical areas are also consistently localized to the same Brodmann areas by neurophysiological, functional imaging, and other methods (e.g., the consistent localization of Broca's speech and language area to the left Brodmann areas 44 and 45).
However, functional imaging can only identify the approximate
localization of brain activations in terms of Brodmann areas since their
actual boundaries in any individual brain requires its histological examination.
Overview
Brodmann's classification of areas of the cortex
Different parts of the cerebral cortex are involved in different
cognitive and behavioral functions. The differences show up in a number
of ways: the effects of localized brain damage, regional activity
patterns exposed when the brain is examined using functional imaging
techniques, connectivity with subcortical areas, and regional
differences in the cellular architecture of the cortex. Neuroscientists describe most of the cortex—the part they call the neocortex—as
having six layers, but not all layers are apparent in all areas, and
even when a layer is present, its thickness and cellular organization
may vary. Scientists have constructed maps of cortical areas
on the basis of variations in the appearance of the layers as seen with
a microscope. One of the most widely used schemes came from Korbinian Brodmann, who split the cortex into 52 different areas and assigned each a number (many of these Brodmann areas
have since been subdivided). For example, Brodmann area 1 is the
primary somatosensory cortex, Brodmann area 17 is the primary visual
cortex, and Brodmann area 25 is the anterior cingulate cortex.
Topography of the primary motor cortex, showing which zone controls each body part
Many of those brain areas defined by Brodmann have their own complex
internal structures. In a number of cases, brain areas are organized
into topographic maps,
where adjoining bits of the cortex correspond to adjoining parts of the
body, or of some more abstract entity. A simple example of this type of
correspondence is the primary motor cortex, a strip of tissue running
along the anterior edge of the central sulcus. Motor areas innervating
each part of the body arise from a distinct zone, with neighboring body
parts represented by neighboring zones. Electrical stimulation of the
cortex at any point causes a muscle-contraction in the represented body
part. This "somatotopic" representation is not evenly distributed,
however. The head, for example, is represented by a region about three
times as large as the zone for the entire back and trunk. The size of
any zone correlates to the precision of motor control and sensory
discrimination possible. The areas for the lips, fingers, and tongue are
particularly large, considering the proportional size of their
represented body parts.
In visual areas, the maps are retinotopic; this means they reflect the topography of the retina, the layer of light-activated neurons lining the back of the eye. In this case too, the representation is uneven: the fovea—the
area at the center of the visual field—is greatly overrepresented
compared to the periphery. The visual circuitry in the human cerebral
cortex contains several dozen distinct retinotopic maps, each devoted to
analyzing the visual input stream in a particular way. The primary
visual cortex (Brodmann area 17), which is the main recipient of direct
input from the visual part of the thalamus, contains many neurons that
are most easily activated by edges with a particular orientation moving
across a particular point in the visual field. Visual areas farther
downstream extract features such as color, motion, and shape.
In auditory areas, the primary map is tonotopic.
Sounds are parsed according to frequency (i.e., high pitch vs. low
pitch) by subcortical auditory areas, and this parsing is reflected by
the primary auditory zone of the cortex. As with the visual system,
there are a number of tonotopic cortical maps, each devoted to analyzing
sound in a particular way.
Within a topographic map there can sometimes be finer levels of
spatial structure. In the primary visual cortex, for example, where the
main organization is retinotopic and the main responses are to moving
edges, cells that respond to different edge-orientations are spatially
segregated from one another.
For humans and other primates
- Areas 3, 1 and 2 – Primary somatosensory cortex in the postcentral gyrus (frequently referred to as Areas 3, 1, 2 by convention)
- Area 4– Primary motor cortex
- Area 5 – Superior parietal lobule
- Area 6 – Premotor cortex and Supplementary Motor Cortex (Secondary Motor Cortex) (Supplementary motor area)
- Area 7 – Visuo-Motor Coordination
- Area 8 – Includes Frontal eye fields
- Area 9 – Dorsolateral prefrontal cortex
- Area 10 – Anterior prefrontal cortex (most rostral part of superior and middle frontal gyri)
- Area 11 – Orbitofrontal area (orbital and rectus gyri, plus part of the rostral part of the superior frontal gyrus)
- Area 12 – Orbitofrontal area (used to be part of BA11, refers to the area between the superior frontal gyrus and the inferior rostral sulcus)
- Area 13 and Area 14* – Insular cortex
- Area 15* – Anterior Temporal lobe
- Area 16 – Insular cortex
- Area 17 – Primary visual cortex (V1)
- Area 18 – Secondary visual cortex (V2)
- Area 19 – Associative visual cortex (V3, V4, V5)
- Area 20 – Inferior temporal gyrus
- Area 21 – Middle temporal gyrus
- Area 22 – Part of the superior temporal gyrus, included in Wernicke's area
- Area 23 – Ventral posterior cingulate cortex
- Area 24 – Ventral anterior cingulate cortex.
- Area 25 – Subgenual area (part of the Ventromedial prefrontal cortex)[5]
- Area 26 – Ectosplenial portion of the retrosplenial region of the cerebral cortex
- Area 27 – Piriform cortex
- Area 28 – Ventral entorhinal cortex
- Area 29 – Retrosplenial cortex
- Area 30 – Subdivision of retrosplenial cortex
- Area 31 – Dorsal Posterior cingulate cortex
- Area 32 – Dorsal anterior cingulate cortex
- Area 33 – Part of anterior cingulate cortex
- Area 34 – Dorsal entorhinal cortex (on the Parahippocampal gyrus)
- Area 35 – Part of the perirhinal cortex (in the rhinal sulcus)
- Area 36 – Part of the perirhinal cortex (in the rhinal sulcus)
- Area 37 – Fusiform gyrus
- Area 38 – Temporopolar area (most rostral part of the superior and middle temporal gyri)
- Area 39 – Angular gyrus, considered by some to be part of Wernicke's area
- Area 40 – Supramarginal gyrus considered by some to be part of Wernicke's area
- Areas 41 and 42 – Auditory cortex
- Area 43 – Primary gustatory cortex
- Areas 44 and 45 – Broca's area, includes the opercular part and triangular part of the inferior frontal gyrus
- Area 46 – Dorsolateral prefrontal cortex
- Area 47 – Orbital part of inferior frontal gyrus
- Area 48 – Retrosubicular area (a small part of the medial surface of the temporal lobe)
- Area 49 – Parasubicular area in a rodent
- Area 52 – Parainsular area (at the junction of the temporal lobe and the insula)
(*) Area only found in non-human primates.
Some of the original Brodmann areas have been subdivided further, e.g., "23a" and "23b".
Criticism
When von Bonin and Bailey constructed a brain map for the macaque
monkey they found the description of Brodmann inadequate and wrote:
"Brodmann (1907), it is true, prepared a map of the human brain which
has been widely reproduced, but, unfortunately, the data on which it was
based was never published" They instead used the cytoarchitechtonic scheme of Constantin von Economo and Georg N. Koskinas published in 1925 which had the "only acceptable detailed description of the human cortex".
