P-31 NMR-STUDIES OF ATP CONCENTRATIONS AND PI-ATP EXCHANGE IN THE RAT-KIDNEY INVIVO - EFFECTS OF INHIBITING AND STIMULATING RENAL METABOLISM

被引:6
作者
SHINE, N
XUAN, A
WEINER, MW
机构
[1] UNIV CALIF SAN FRANCISCO, VET ADM MED CTR, MAGNET RESONANCE UNIT, 4150 CLEMENT ST, SAN FRANCISCO, CA 94121 USA
[2] UNIV CALIF SAN FRANCISCO, VET ADM MED CTR, DEPT MED, SAN FRANCISCO, CA 94121 USA
[3] UNIV CALIF SAN FRANCISCO, VET ADM MED CTR, DEPT RADIOL, SAN FRANCISCO, CA 94121 USA
关键词
D O I
10.1002/mrm.1910140304
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Previous investigators found that cyanide (CN−) is a potent inhibitor of renal Na+ transport, while the uncoupling agent 2,4‐dinitrophenol (DNP) and fructose (both which lower ATP levels) are weak transport inhibitors. To examine the disparate effects of these substances measurements of ATP were performed, using 31P NMR, while simultaneously monitoring renal Na+ transport. Infusion of CN−, DNP, and fructose lowered whole kidney ATP levels by about the same extent (30%) while only CN− inhibited Na+ transport. This may be due to the fact that CN− has a potent action on the thick ascending limb of Henle, while fructose and DNP may have a more proximal action. Alternatively, ATP turnover may be a more important determinant of transport than ATP concentrations. Saturation transfer experiments were performed to measure Pi–ATP flux. Unilateral nephrectomy, high protein feeding, and methylprednisolone were used to stimulate metabolism and transport. The rate of Pi‐ATP flux was 20.1 μmol/min/g. However, because oxygen consumption was stimulated, the ATP/O ratio was 0.85, considerably less than the theoretical value of 3. Finally, atrial natriuretic factor, which increased Na+ transport, had no effect on Pi‐ATP flux. The results raise the possibility that the saturation transfer technique does not detect all Pi‐ATP flux, especially when renal metabolism is Stimulated. © 1990 Academic Press, Inc. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company
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页码:445 / 460
页数:16
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