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多巴胺抑制大鼠皮质集合管中血管加压素依赖性环磷酸腺苷的生成。

Dopamine inhibits vasopressin-dependent cAMP production in the rat cortical collecting duct.

作者信息

Li L, Schafer J A

机构信息

Department of Physiology, Nephrology Research and Training Center, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.

出版信息

Am J Physiol. 1998 Jul;275(1):F62-7. doi: 10.1152/ajprenal.1998.275.1.F62.

Abstract

Dopamine inhibits Na+ and water reabsorption in the rat cortical collecting duct (CCD) in the presence of arginine vasopressin (AVP). This inhibition appears to involve the D4 dopamine receptor isoform, which inhibits cAMP production; however, the D1A receptor, which stimulates cAMP production, is also expressed in the CCD. To discriminate between these opposing effects, we measured cAMP production in intact CCD segments. The basal rate of cAMP production ranged from 6.5 to 10 fmol/mm of tubule length over a 7-min incubation period, and it was unaffected by either dopamine or the D1A-specific agonist fenoldopam. AVP increased cAMP production to the range of 85-153 fmol . mm-1 . 7 min-1. Whereas neither 0.1 nor 1.0 microM fenoldopam affected AVP-dependent cAMP production, dopamine reduced it in a dose-dependent manner, achieving a maximum inhibition of 50% at 10 microM. This effect was reversed by the D4 receptor antagonist clozapine but not by pimozide or spiperone (antagonists of D2 and D3 receptors) or by calphostin C or chelerythrine (inhibitors of protein kinase C). We conclude that dopamine inhibits transepithelial Na+ transport and osmotic water permeability in the presence of AVP by inhibition of cAMP production, which is mediated by the D4 receptor isoform linked via the inhibitory G protein Gi.

摘要

在存在精氨酸加压素(AVP)的情况下,多巴胺可抑制大鼠皮质集合管(CCD)对Na⁺和水的重吸收。这种抑制作用似乎涉及D4多巴胺受体亚型,该亚型可抑制环磷酸腺苷(cAMP)的产生;然而,能刺激cAMP产生的D1A受体在CCD中也有表达。为了区分这些相反的作用,我们测量了完整CCD节段中cAMP的产生。在7分钟的孵育期内,cAMP产生的基础速率在每毫米肾小管长度6.5至10飞摩尔之间,且不受多巴胺或D1A特异性激动剂非诺多泮的影响。AVP可使cAMP产生增加至85 - 153飞摩尔·毫米⁻¹·7分钟⁻¹的范围。虽然0.1微摩尔和1.0微摩尔的非诺多泮均不影响AVP依赖的cAMP产生,但多巴胺以剂量依赖的方式降低了它,在10微摩尔时达到最大抑制50%。D4受体拮抗剂氯氮平可逆转这种作用,但D2和D3受体拮抗剂匹莫齐特或螺哌隆,或蛋白激酶C抑制剂钙泊三醇或白屈菜红碱则不能。我们得出结论,在存在AVP的情况下,多巴胺通过抑制cAMP的产生来抑制跨上皮Na⁺转运和渗透水通透性,这是由通过抑制性G蛋白Gi连接的D4受体亚型介导的。

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