Lecture 3

and John Dennison2



(1)
Department of Psychological Medicine, University of Otago School of Medicine, Wellington, New Zealand

(2)
Department of Anatomy, Otago Medical School, Dunedin, New Zealand

 







  • Nature of memory images


  • Retinal after-images and remembered visual images


  • The hypothesis of special sense cells and memory cells is insufficient as an explanation


  • Local signs in the retina


  • Visual representations


Lecture


Gentlemen!

Before we look more closely at symptoms of mental illnesses we must revisit the aforementioned Conceptualization Centre or, more precisely, those localized memory images. I hope that, on reflection, you conclude that this is not the alleged ‘Conceptualization Centre’ [Ed] said to have a definite localization, but probably the concepts themselves.

In introducing my first lecture, I presented as a statement of fact, confirmed in pathological cases, that central projection fields are localized to different areas of the cerebral cortex. We must recognize that such fields are also sites of remembered images; and it follows from this that these memory images also have definite locations. However, let us examine these memory images more closely.

First, I want to touch briefly on clinical facts which, in my opinion, totally validate the principle of localized memory images: These are clinical instances of sensory and motor aphasia, and cases of the so-called tactile anaesthesia of the hand. The former are probably well known by now, so I need not go into detail; but the importance of the latter is debated. Two related sets of facts provide support. On the one hand, cases have been seen where circumscribed cortical damage in the middle third of the two central gyri leads to permanent deficit, where the hand fails to recognize objects by touch, although disturbance of sensation itself can barely be detected. On the other hand, there are cases of spinal or peripheral disease where sensitivity, and—I stress—also muscle and position sense, is most severely disrupted, with only minor disturbance of tactile perception. The last-named cases demonstrate to some extent that even a very weak and patchy projection system can still conduct messages to the brain sufficient to support primary identification, provided the central projection fields and therefore the remembered images—tactile images, as we can call them here—are preserved. However, cases of the first [Ed] type can be based only on loss of primary identification itself, since disturbance of projection pathways themselves is clearly minimal. The principle that remembered images are localized to corresponding projection fields is established beyond all doubt by such facts, and thus this principle can be fairly applied to all projection fields.

If we return to our example of the organ of speech, we find that the process of recognition [W]—primary identification (see above)—requires solid ownership of memory images. The question then arises: How should one view such ownership? Evidently this concerns a special characteristic of the nervous system, that it undergoes lasting change in response to temporary stimuli, a property we call memory [W]. Such memory is seen, for example, in the fact that Faradic excitability of a nerve can be increased by frequent electrical stimulation [1]. The same stimulation then becomes more effective if it has often been administered previously; and therefore lasting change exists in the nerve as a result of the previous history of transient stimulation. All training is based on the same principle, for any form of learning: ‘Practice makes perfect’ [Ed]. Pathways that are initially hard to access become more firmly trodden in with each new training experience—you could say that they are ‘moulded by experience’ [W]. Thus when a memory of this sort reaches a person’s awareness via nerve pathways, it occurs specifically in nerve cell bodies. A reflex in the spinal cord mediated via its neuronal cell bodies takes place more easily the more frequently it has previously been elicited; and it has been demonstrated by studies of Ward [2], Jarisch and Schiff [3], and others that this is a special property of the neuronal perikarya. It would be reasonable to relate after-images of the retina mainly to their ganglion cells. Similarly, in the cerebral cortex you would ascribe changes persisting long after instantaneous stimulation, which we call memory images, primarily to neuronal cell bodies.

After this, it appears obvious that possession of such remembered images—contents of consciousness [W], we might say—depends directly on the projection system and sense organs by which those images were obtained. The consciousness of a person with poor eyesight, or one with generally deficient senses, is thus quite different from that of a normal person. An individual born blind will certainly have no remembered images of visual sensation. Were his sight to be surgically healed, this would provide a situation we otherwise see only when the pathology of visual agnosia occurs. Just as for an individual born blind, so too for one born deaf, the content of consciousness totally lacks an entire category of memory images originating from the sense of hearing. In partial cortical deficiencies, as observed from time to time in those who are mentally defective from birth and also have sensory deficits such as deafness, there is a similar lack of remembered images due to abnormal development of central projection fields. No less instructive in this connection is a comparison with animal brains. Humans have only a vestigial olfactory bulb, whereas many mammalian species have an olfactory bulb occupying a significant part of their cerebral hemispheres, with a separate ventricle and separate surface gyri. Everyday observation shows just how different is the consciousness of such animals, for example that of a dog from our own. It appears to be full of remembered olfactory images, and the animal, snuffling here and there, revels in all its joyful frame of mind, like the gourmet at table, or the eye of an artist beholding beautiful forms. The content of consciousness shown in this way depends on the state of the projection system and central projection fields, a relationship suggesting the following principle: Consciousness is a function of the central projection fields. If the assumption—that projection fields occupy the entire cortical mantle—is confirmed, then the corollary follows: Consciousness is a function of the cortical mantle.

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Nov 27, 2016 | Posted by in PSYCHOLOGY | Comments Off on Lecture 3

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