Effect of furosemide on parathyroid hormone stimulated guinea pig renal adenylate cyclase and thyrotrophin and fluoride stimulated human thyroid adenylate cyclase.

J Thode, T Børresen, K Beck, S N Madsen
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引用次数: 5

Abstract

The effect of furosemide 8 X 10(-4) mol/l an 8 X 10(-5) mol/l on parathyroid hormone stimulated adenylate cyclase was studied in renal tissue slices from guinea pigs. Furosemide caused a dose-dependent inhibition of the effect of parathyroid hormone on production of cyclic AMP, without having any significant effect on the basal cyclic AMP production. Furosemide in similar concentrations did not inhibit the stimulatory effect of thyrotrophin and fluoride in human thyroid homogenates suggesting that furosemide is not an universal inhibitor of adenylate cyclase and that the inhibition is not caused by a direct action of furosemide on the adenylate cyclase enzyme. Furosemide did not interfere with binding of cyclic AMP to cyclic AMP binding protein kinase from rabbit muscle. The results indicate that furosemide exerts an inhibitory influence either upon binding of parathyroid hormone to renal receptors or upon transmission of impulse from receptor to adenylate cyclase. The inhibitory influence of furosemide on parathyroid hormone action in kidney could explain the value of furosemide in the acute treatment of hypercalcaemia, but also suggest that chronic treatment with furosemide might interfere with normal calcium metabolism.

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速尿对甲状旁腺激素刺激豚鼠肾腺苷酸环化酶及促甲状腺素和氟化物刺激人甲状腺腺苷酸环化酶的影响。
研究了速尿8 × 10(-4) mol/l和8 × 10(-5) mol/l对豚鼠肾组织切片甲状旁腺激素刺激的腺苷酸环化酶的影响。速尿对甲状旁腺激素对环AMP产生的抑制作用呈剂量依赖性,对基础环AMP产生无显著影响。相似浓度的呋塞米没有抑制人甲状腺匀浆中促甲状腺素和氟化物的刺激作用,这表明呋塞米不是腺苷酸环化酶的普遍抑制剂,而且这种抑制不是由呋塞米对腺苷酸环化酶的直接作用引起的。速尿不干扰兔肌环AMP与环AMP结合蛋白激酶的结合。结果表明,呋塞米对甲状旁腺激素与肾受体的结合或对从受体到腺苷酸环化酶的脉冲传递具有抑制作用。呋塞米对肾脏甲状旁腺激素作用的抑制作用可以解释呋塞米在急性高钙血症治疗中的价值,但也提示长期使用呋塞米可能会干扰正常的钙代谢。
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