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in partial fulfil]ment of the - MSpace - University of Manitoba

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Dur<strong>in</strong>g dark adaptation, a large amount <strong>of</strong> Vitam<strong>in</strong> A (ret<strong>in</strong>ol) is<br />

converted <strong>in</strong>to rhodops<strong>in</strong> and reconversion <strong>of</strong> ret<strong>in</strong>ene and ops<strong>in</strong> <strong>in</strong>to<br />

rhodops<strong>in</strong> also takes place. Because <strong>of</strong> <strong>the</strong>se reconversions, <strong>the</strong> visual<br />

receptors (rods) become so sensitive that even a m<strong>in</strong>ute amount <strong>of</strong> light<br />

causes excitation. The regeneration <strong>of</strong> rhodops<strong>in</strong> <strong>in</strong> <strong>the</strong> ret<strong>in</strong>a is<br />

dependent on Vitam<strong>in</strong> A (figure 5). In night bl<strong>in</strong>dness, <strong>the</strong> ret<strong>in</strong>a conta<strong>in</strong>s<br />

less rhodops<strong>in</strong> than a normal ret<strong>in</strong>a and <strong>the</strong> rate <strong>of</strong> regeneration<br />

<strong>of</strong> rhodops<strong>in</strong> is much slower, and this condiLion could be reflected on<br />

dark adaptation ability <strong>of</strong> <strong>in</strong>dividuals (Guyton, 1976), "<br />

62<br />

The relationship between <strong>the</strong> ability to see <strong>in</strong> <strong>the</strong> dark and Vitam<strong>in</strong> A<br />

status was demonstrated by Dowl<strong>in</strong>g and I.iald (1958). Rats were ma<strong>in</strong>ta<strong>in</strong>ed<br />

on Vitam<strong>in</strong> À Ceficient diet. The liver Vitam<strong>in</strong> À level began to<br />

fall steadily with<strong>in</strong> <strong>the</strong> first week <strong>of</strong> <strong>the</strong> start <strong>of</strong> <strong>the</strong> Vitam<strong>in</strong> À deficient<br />

diet, with<strong>in</strong> three weeks reached about 5% <strong>of</strong> <strong>the</strong> normal value.<br />

Then Lhe blood Vitam<strong>in</strong> À level was depleted and reached 0% which was<br />

followed by a depletion <strong>in</strong> <strong>the</strong> rhodops<strong>in</strong> concentration <strong>of</strong> <strong>the</strong> ret<strong>in</strong>a.<br />

These conditions, f<strong>in</strong>a1ly, resulted <strong>in</strong> an <strong>in</strong>crease <strong>in</strong> <strong>the</strong> visual threshold<br />

(f<strong>in</strong>al dark adapted threshold), mark<strong>in</strong>g <strong>the</strong> onset <strong>of</strong> night bl<strong>in</strong>dness.<br />

F<strong>in</strong>al dark adapted threshold is <strong>the</strong> m<strong>in</strong>imum amount <strong>of</strong> light which<br />

illum<strong>in</strong>ates a given surface <strong>in</strong> order to render it visible (Hecht and<br />

Mandelbaum, 1939). F<strong>in</strong>al dark adaptaLion threshoLd was def<strong>in</strong>ed as <strong>the</strong><br />

average <strong>of</strong> three ascend<strong>in</strong>g and lhree descend<strong>in</strong>g thresholds obta<strong>in</strong>ed<br />

after 35-40 m<strong>in</strong>utes <strong>in</strong> <strong>the</strong> dark (Russel1 et aI., 1973).

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