Saturday, November 10, 2007

The Functions of Various Nerve Centers

In order to understand the functions of the cerebrum, it is necessary, however, to have a clear knowledge of the general nature of the lower nerve centers. The spinal cord, as the lowest of these centers, contains the essential junction points for a large number of bodily reflexes which can occur quite perfectly without any participation by higher regulative centers, although they may be subject to interference or reinforcement through the action of the latter. The cord also acts as a conduit through which impulses are conducted from the body surface and internal organs to the brain. The functions of the medulla oblongata, which connects the spinal cord to the brain, are similar to those of the cord, but involve reflexes of the head-end of the body and the regulation of the more vital processes, such as those of circulation and respiration. The cerebellum, which is a portion of the brain adjacent to the medulla, receives afferent nerve impulses primarily from sense-organs located in the motor apparatus (muscles, tendons and joint-surfaces) and from the equilibrium sense mechanism of the inner ears. The efferent impulses which leave the cerebellum pass to all portions of the voluntary musculature, and are concerned in the automatic maintenance of tension and coördination between the various muscular units. The cerebellum appears to be a device for adjusting the details of motor innervation, usually under the guidance of the cerebral cortex. It is possible that it is endowed by heredity with a stock of "records," which enable it to produce and reproduce specific types of motor reaction when circumstances demand them, although these reaction forms are not linked with any definite stimuli. As examples of such reaction forms, we may consider some of the items on James' list of simple instincts: "sucking, biting, chew ing, licking, grimacing, etc." However, the prime duty of the cerebellum seems to consist in the maintenance of tonus and balance throughout the voluntary musculature.

In the mid-brain, which is enveloped by the mass of the cerebrum, we find further regions of reflex transfer, which, however, are usually more complex and variable in their action than is the case with the centers of the spinal cord or medulla. The thalamus, which is an important portion of the fore-brain, forms a kind of vestibule to the cerebral cortex, since practically all of the sensory nerve currents which are destined for the cortex, pass through the thalamus. Here, also, is found a synaptic center for all of the pain nerves of the body, and many of the mimetic expressions of instinct or emotion are probably controlled directly from centers in this general region of the brain. There is a very definite interaction between the thalamus and the cerebral cortex in regard to pain impulses, and possibly also with reference to impulses which give rise to pleasure. Concerning this relationship we shall have a great deal more to say in later chapters.

The cerebrum is by far the largest portion of the brain in the human being although it is practically absent in many lower vertebrates. It consists of a very intricate network of conducting fibres, which have myriads of junction points, located for the most part in the surface of the organ, a large part of which is adjacent to the bony case of the skull. The convolutions and fissures in this surface appear to have the function of increasing its area to a maximum. The cerebrum is divided, right and left, into two halves known as the cerebral hemispheres. The right hemisphere is connected almost exclusively with the left side of the body, while the left hemisphere deals with the affairs of the right side.

The cerebral cortex receives a very large number of nerve fibres from all of the sensory surfaces of the body and also gives rise to fibres which pass to all of the skeletal, or so-called voluntary muscles. These fibres are segregated and distributed to special zones, known as projection areas. Thus, we have surfaces in the cortex which are exclusively for visual, for auditory, for olfactory, for tactual, for motor impulses, and so on. The motor area is devoted to the transmission of impulses along the pyramidal neurones. These sensory and motor projection areas by no means exhaust the entire surface of the cortex, and it is natural to suppose that the remaining and intervening parts will be employed for purposes of association between the sensory and motor zones. This supposition has already been corroborated to a convincing extent by empirical observation. It is evidently in the association areas of the cortex that we should look for the principal basis of specificity in voluntary behavior.

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