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首页> 外文期刊>American Journal of Physiology >Functional characterization of basolateral and luminal dopamine receptors in rabbit CCD.
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Functional characterization of basolateral and luminal dopamine receptors in rabbit CCD.

机译:兔CCD的基底外侧和腔多巴胺受体的功能表征。

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Previous studies reported the existence of both D1- and D2-like receptors in the cortical collecting duct (CCD). However, especially with regard to natriuresis, it remains controversial. In the present study, rabbit CCD was perfused to characterize the receptor subtypes responsible for the tubular actions. Basolateral dopamine (DA) induced a dose-dependent depolarization of transepithelial voltage. Basolateral domperidone, a D2-like receptor antagonist, abolished depolarization, whereas SKF-81297, a D1-like receptor agonist, showed no significant change. In addition, bromocriptine, a D2-like receptor agonist, also caused depolarization, whereas SKF-81297, a D1-like receptor agonist, did not depolarize significantly. Moreover, RBI-257, a D4-specific antagonist, reversed the basolateral DA-induced depolarization. In contrast to the basolateral side, luminal DA caused depolarization via a D1-like receptor; however the change was less than that for basolateral DA. For further evaluation, 22Na+ flux (J(Na))was measured to confirm the effect of DA on Na+ transport. Basolateral DA also caused a suppression of J(Na), and this reaction was abolished by domperidone. These results suggested that the basolateral D2-like receptor is mainly responsible for the natriuretic action of DA in rabbit CCD.
机译:先前的研究报道了皮质收集管(CCD)中同时存在D1和D2样受体。但是,特别是在利尿方面,它仍然存在争议。在本研究中,兔CCD被灌注以表征负责肾小管动作的受体亚型。基底外侧多巴胺(DA)引起跨上皮电压的剂量依赖性去极化。 D2样受体拮抗剂基底外侧多潘立酮取消了去极化作用,而D1样受体激动剂SKF-81297则没有明显变化。另外,溴隐亭(一种D2样受体激动剂)也引起去极化,而SKF-81297(一种D1样受体激动剂)并未显着去极化。此外,D4特异性拮抗剂RBI-257逆转了基底外侧DA诱导的去极化。与基底外侧相反,管腔DA通过类D1受体引起去极化。然而,这种改变小于基底外侧DA的改变。为了进一步评估,测量了22Na +通量(J(Na)),以确认DA对Na +转运的影响。基底外侧DA也引起J(Na)的抑制,并且该反应被多潘立酮消除。这些结果表明,基底外侧D2样受体主要负责DA在兔CCD中的利钠作用。

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