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Brain: Broca's area
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Approximate location of Broca's area highlighted in gray
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Broca's area visible but not labeled.
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MeSH [1]

Broca's area is the section of the human brain (in the opercular and triangular sections of the inferior frontal gyrus of the frontal lobe of the cortex) that is involved in language processing, speech production and comprehension. Broca's and Wernicke's areas are found unilaterally in the brain.

It comprises of Brodmann's Area 44,[1] and some authorities also include Brodmann's Area 45[2][3][4]); Broca's Area is connected to Wernicke's area by a neural pathway called the arcuate fasciculus. The corresponding area in macaque monkeys is responsible for high-level control over orofacial actions.[5]

Etymology

Broca's area is named after Pierre Paul Broca, who first described it in 1861, after conducting a post mortem study on a speech-impaired patient.

Parts

There are two main parts of Broca's area, which express different roles during language comprehension and production:

  • Pars triangularis (anterior), which is thought to support the interpretation of various 'modes' of stimuli (plurimodal association) and the programming of verbal conducts
  • Pars opercularis (posterior), which is thought to support the management of only one kind of stimulus (unimodal association) and the coordination of the speech organs for the actual production of language, given its favorable position close to motor-related areas.

Aphasia

People suffering from damage to this area may show a condition called Broca's aphasia (sometimes known as expressive aphasia, motor aphasia, or nonfluent aphasia), which makes them unable to create grammatically-complex sentences: their speech is often described as telegraphic and contains little but content words. Patients usually are aware that they cannot speak properly. Comprehension in Broca's aphasia is relatively normal, although many studies have demonstrated that Broca's aphasics have trouble understanding certain kinds of syntactically complex sentences.[6]

This type of aphasia can be contrasted with Wernicke's aphasia, named for Karl Wernicke, which is characterized by damage to more posterior regions of the left hemisphere (in the superior temporal lobe). Wernicke's aphasia manifests as a more pronounced impairment in comprehension. Thus, while speech production remains normal grammatically, it is nonetheless often roundabout, vague or meaningless. It is therefore also known as receptive aphasia.

For example, in the following passage, a Broca's aphasic patient is trying to explain how he came to the hospital for dental surgery.

"Yes... ah... Monday... er... Dad and Peter H... (his own name), and Dad.... er... hospital... and ah... Wednesday... Wednesday, nine o'clock... and oh... Thursday... ten o'clock, ah doctors... two... an' doctors... and er... teeth... yah."[7]

PET and functional MRI have found decreases in activity in the Broca's area in stuttering.There is greater activation of the right hemisphere homologue of the Broca's area (area of Ross) which is believed to be a compensatory response to the hypoactivity in the Broca's area proper. Volumetric MRI has shown that the pars triangularis is smaller in people who stutter.

See also

References

  1. Mohr JP in Studies in Neurolinguistics (eds. Witaker H & Witaker NA) 201–235 (Academic, New York, 1976)
  2. Penfield W & Roberts L Speech and Brain Mechanisms (Princeton Univ Press, Princeton, 1959)
  3. Ojemann GA, Ojemann JG, Lettich E, Berger MS (1989). Cortical language localization in left, dominant hemisphere. An electical stimulation mapping investigation in 117 patients. J Neurosurg 71: 316–26.
  4. Duffau H et al. (2003). The role of dominant premotor cortex in language: a study uding intraoperative functional mapping in awake patients. Neuroimage 20: 1903–14.
  5. Petrides M, Cadoret G, Mackey S (2005). Orofacial somatomotor responses in the macaque monkey homologue of Broca's area. Nature 435: 1235–38.
  6. Caramazza A & Zurif E (1976). Dissociation of algorithmic and heuristic processes in language comprehension: evidence from aphasia. Brain and Language 3: 572–82.
  7. Goodglass H & Geschwind N. Language disorders. In E. Carterette and M.P. Friedman (eds.) Handbook of Perception: Language and Speech. Vol II (New York, Academic Press, 1976)
Telencephalon (cerebrum, cerebral cortex, cerebral hemispheres) - edit

primary sulci/fissures: medial longitudinal, lateral, central, parietoöccipital, calcarine, cingulate

frontal lobe: precentral gyrus (primary motor cortex, 4), precentral sulcus, superior frontal gyrus (6, 8), middle frontal gyrus (46), inferior frontal gyrus (Broca's area, 44-pars opercularis, 45-pars triangularis), prefrontal cortex (orbitofrontal cortex, 9, 10, 11, 12, 47)

parietal lobe: postcentral sulcus, postcentral gyrus (1, 2, 3, 43), superior parietal lobule (5), inferior parietal lobule (39-angular gyrus, 40), precuneus (7), intraparietal sulcus

occipital lobe: primary visual cortex (17), cuneus, lingual gyrus, 18, 19 (18 and 19 span whole lobe)

temporal lobe: transverse temporal gyrus (41-42-primary auditory cortex), superior temporal gyrus (38, 22-Wernicke's area), middle temporal gyrus (21), inferior temporal gyrus (20), fusiform gyrus (36, 37)

limbic lobe/fornicate gyrus: cingulate cortex/cingulate gyrus, anterior cingulate (24, 32, 33), posterior cingulate (23, 31),
isthmus (26, 29, 30), parahippocampal gyrus (piriform cortex, 25, 27, 35), entorhinal cortex (28, 34)

subcortical/insular cortex: rhinencephalon, olfactory bulb, corpus callosum, lateral ventricles, septum pellucidum, ependyma, internal capsule, corona radiata, external capsule

hippocampal formation: dentate gyrus, hippocampus, subiculum

basal ganglia: striatum (caudate nucleus, putamen), lentiform nucleus (putamen, globus pallidus), claustrum, extreme capsule, amygdala, nucleus accumbens

Some categorizations are approximations, and some Brodmann areas span gyri.

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