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Title: Utilization and synthesis of glutamine in the lens

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:6180434

Previous studies with rat and calf lenses have shown that the primary source of lenticular glutamate for a wide variety of pathways is glutamine, which is more readily transported from the surrounding fluids than glutamate. In contrast, recent studies showed that monkey lenses utilize glutamate more rapidly than glutamine, although glutamine appears to enter monkey lenses more rapidly than glutamine. Further studies were initiated to elucidate the balance between transport, deamidation, and synthesis of glutamine in the lens. Glutamine synthesis in intact rat lenses was barely detectable; however, homogenates of adult rat lenses converted measurable amounts of (/sup 3/H)-glutamate to glutamine. The identity of the product was confirmed using glutaminase. Glutamine deamidation in intact rhesus monkey lenses incubated in TC-199 medium containing 2 mM glutamine was only 0.19 ..mu..mol g/sup -1/ hr/sup -1/, compared with 1.96 ..mu..mol g/sup -1/ hr/sup -1/ for rat lenses under identical conditions. However, under optimal assay conditions, glutaminase activity in monkey lens homogenates was similar to that of rat lens homogenates. Thus, the rate of synthesis and deamidation of glutamine by intact lenses is apparently limited factors other than total lenticular glutamine synthetase and glutaminase activity.

Research Organization:
Univ. of Tennessee, Memphis
OSTI ID:
6180434
Report Number(s):
CONF-870644-; TRN: 87-033965
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Vol. 46:6; Conference: 78. annual meeting of the American Society of Biological Chemists conference, Philadelphia, PA, USA, 7 Jun 1987
Country of Publication:
United States
Language:
English