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[几种激素对大鼠肾脏中环3',5'-核苷酸磷酸二酯酶的影响]

[Effect of several hormones on cyclic 3',5'-nucleotide phosphodiesterase in rat kidneys].

作者信息

Iwase K

出版信息

Nihon Naibunpi Gakkai Zasshi. 1983 Oct 20;59(10):1678-91. doi: 10.1507/endocrine1927.59.10_1678.

Abstract

Kidney function is regulated by several hormones which act through adenylate cyclase-cyclic AMP system. The present study was undertaken to investigate cyclic AMP- and cyclic GMP-phosphodiesterase (cAMP-PDE and cGMP-PDE respectively) activities in the rat kidney, and also the effect of several hormones affecting the kidney function on these enzyme activities in vitro. Rat kidneys were separated into cortex and medulla. These were homogenized in 50 mM Tris-HCl buffer, pH 7.5, containing 0.32 M sucrose and fractionated by centrifugation. PDE activity was measured in all fractions, using the two-step assay system. A low substrate concentration (0.5 microM) was used, unless otherwise stated. Substantial activity was present in all of the fractions and most of the activity existed in the soluble fraction (105000 X g supernatant). Cyclic GMP-PDE activity was dominant in both cortex and medulla. The rat kidney contained two forms of cAMP-PDE, one of which had a Km of 2.0 X 10(-4) M and another which had a low Km of 2.5 X 10(-5) M, and one form of cGMP-PDE with a Km of 2.5 X 10(-5) M. These cAMP-PDE and cGMP-PDE were purified by Sepharose-6B column chromatography. Cyclic AMP-PDE activity was found in a broad area associated with two peaks and cGMP-PDE activity had one peak corresponding to the same peak as the high molecular weight cAMP-PDE. Calmodulin was eluted after the peak of cGMP-PDE activity. Both cAMP-PDE and cGMP-PDE activities were inhibited by calcium ion at a concentration of more than 5.0 X 10(-4) M. Cyclic GMP-PDE activity was not activated by calmodulin in the presence of enough calcium ion. The effect of 1 alpha, 25(OH)2 Vit D3, parathyroid hormone (PTH), antidiuretic hormone (ADH), calcitonin (CT), angiotensin II, and trichlormethiazide on the partially purified cAMP-PDE and cGMP-PDE activities were examined. 1 alpha, 25(OH)2 Vit D3 activated cAMP-PDE activity and did not affect cGMP-PDE activity. The concentrations of 1 alpha, 25(OH)2 Vit D3 producing 50% activation of cAMP-PDE activity were 5.0 X 10(-11) M (cortex) and 6.7 X 10(-10) M (medulla). CT and ADH inhibited both cAMP-PDE activities. The concentrations of CT producing 50% inhibition of cAMP-PDE activity were 4.0 X 10(-5) M (cortex) and 3.3 X 10(-7) M (medulla), and those of cGMP-PDE activity were 1.0 X 10(-5) M (cortex) and 1.0 X 10(-4) M (medulla). Concerning ADH, the concentrations required for 50% inhibition of cAMP-PDE activity were 5.3 X 10(-6) M (cortex) and about 1.0 X 10(-3) M (medulla), and those of cGMP-PDE activity were 5.3 X 10(-3) M (cortex) and 5.3 X 10(-8) M (medulla).(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

肾功能受多种通过腺苷酸环化酶 - 环磷酸腺苷系统起作用的激素调节。本研究旨在调查大鼠肾脏中环磷酸腺苷磷酸二酯酶(cAMP - PDE)和环磷酸鸟苷磷酸二酯酶(cGMP - PDE)的活性,以及几种影响肾功能的激素在体外对这些酶活性的作用。将大鼠肾脏分为皮质和髓质。将其在含有0.32M蔗糖的50mM Tris - HCl缓冲液(pH 7.5)中匀浆,然后通过离心分级分离。使用两步测定系统测量所有组分中的磷酸二酯酶活性。除非另有说明,使用低底物浓度(0.5 microM)。所有组分中均存在大量活性,且大部分活性存在于可溶性组分(105000×g上清液)中。环磷酸鸟苷磷酸二酯酶活性在皮质和髓质中均占主导。大鼠肾脏含有两种形式的cAMP - PDE,其中一种的Km为2.0×10(-4)M,另一种的低Km为2.5×10(-5)M,以及一种Km为2.5×10(-5)M的cGMP - PDE形式。这些cAMP - PDE和cGMP - PDE通过琼脂糖 - 6B柱色谱法纯化。发现cAMP - PDE活性在与两个峰相关的宽区域中,cGMP - PDE活性有一个与高分子量cAMP - PDE相同峰对应的峰。钙调蛋白在cGMP - PDE活性峰之后洗脱。当钙离子浓度超过5.0×10(-4)M时,cAMP - PDE和cGMP - PDE活性均受到抑制。在有足够钙离子存在的情况下,钙调蛋白不会激活cGMP - PDE活性。检测了1α,25(OH)2维生素D3、甲状旁腺激素(PTH)、抗利尿激素(ADH)、降钙素(CT)、血管紧张素II和三氯噻嗪对部分纯化的cAMP - PDE和cGMP - PDE活性的影响。1α,25(OH)2维生素D3激活cAMP - PDE活性,不影响cGMP - PDE活性。产生50% cAMP - PDE活性激活的1α,25(OH)2维生素D3浓度在皮质中为5.0×10(-11)M,在髓质中为6.7×10(-10)M。CT和ADH均抑制两种cAMP - PDE活性。产生50% cAMP - PDE活性抑制的CT浓度在皮质中为4.0×10(-5)M,在髓质中为3.3×10(-7)M,而cGMP - PDE活性的浓度在皮质中为1.0×10(-5)M,在髓质中为1.0×10(-4)M。关于ADH,产生50% cAMP - PDE活性抑制所需的浓度在皮质中为5.3×10(-6)M,在髓质中约为1.0×10(-3)M,而cGMP - PDE活性的浓度在皮质中为5.3×10(-3)M,在髓质中为5.3×10(-8)M。(摘要截于400字)

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