首页> 美国卫生研究院文献>American Journal of Physiology - Regulatory Integrative and Comparative Physiology >D1-like dopamine receptors downregulate Na+-K+-ATPase activity and increase cAMP production in the posterior gills of the blue crab Callinectes sapidus
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D1-like dopamine receptors downregulate Na+-K+-ATPase activity and increase cAMP production in the posterior gills of the blue crab Callinectes sapidus

机译:D1样多巴胺受体下调蓝蟹Callinectes sapidus后g的Na + -K + -ATPase活性并增加cAMP的产生

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摘要

Dopamine-mediated regulation of Na+-K+-ATPase activity in the posterior gills of some crustaceans has been reported to be involved in osmoregulation. The dopamine receptors of invertebrates are classified into three groups based on their structure and pharmacology: D1- and D2-like receptors and a distinct invertebrate receptor subtype (INDR). We tested the hypothesis that a D1-like receptor is expressed in the blue crab Callinectes sapidus and regulates Na+-K+-ATPase activity. RT-PCR, using degenerate primers, showed the presence of D1βR mRNA in the posterior gill. The blue crab posterior gills showed positive immunostaining for a dopamine D5 receptor (D5R or D1βR) antibody in the basolateral membrane and cytoplasm. Confocal microscopy showed colocalization of Na+-K+-ATPase and D1βR in the basolateral membrane. To determine the effect of D1-like receptor stimulation on Na+-K+-ATPase activity, intact crabs acclimated to low salinity for 6 days were given an intracardiac infusion of the D1-like receptor agonist fenoldopam, with or without the D1-like receptor antagonist . Fenoldopam increased cAMP production twofold and decreased Na+-K+-ATPase activity by 50% in the posterior gills. This effect was blocked by coinfusion with , which had no effect on Na+-K+-ATPase activity by itself. Fenoldopam minimally decreased D1βR protein expression (10%) but did not affect Na+-K+-ATPase α-subunit protein expression. This study shows the presence of functional D1βR in the posterior gills of euryhaline crabs chronically exposed to low salinity and highlights the evolutionarily conserved function of the dopamine receptors on sodium homeostasis.
机译:据报道,多巴胺介导的一些甲壳类动物后g中Na + -K + +-sup--ATPase活性的调节与渗透调节有关。无脊椎动物的多巴胺受体根据其结构和药理作用分为三类:D1和D2样受体和独特的无脊椎动物受体亚型(INDR)。我们检验了一种假设,即在蓝蟹inCallinectes sapidus中表达D1样受体并调节Na + -K + -ATPase活性。使用简并引物的RT-PCR显示后g中存在D1βRmRNA。蓝蟹后g在基底外侧膜和细胞质中对多巴胺D5受体(D5R或D1βR)抗体表现出阳性免疫染色。共聚焦显微镜检查显示,Na + -K + -ATPase和D1βR在基底外侧膜中共定位。为了确定D1样受体刺激对Na + -K + -ATPase活性的影响,对适应性低盐度达6天的完整螃蟹进行心内输注。 D1样受体激动剂非诺多巴,有或没有D1样受体拮抗剂。非诺多m使后g的cAMP产量增加两倍,并使Na + -K + -ATPase活性降低50%。与的共融合可阻止这种作用,而Na本身对Na + -K + -ATPase活性没有影响。非诺多m使D1βR蛋白表达降低最小(10%),但不影响Na + -K + -ATPaseα-亚基蛋白表达。这项研究表明,在长期暴露于低盐度的鱼腥蟹后g中存在功能性D1βR,并强调了多巴胺受体对钠稳态的进化保守功能。

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