首页> 外文期刊>Archives of Insect Biochemistry and Physiology >Adenosine modulates the (Na++K+)ATPase activity in Malpighian tubules isolated from Rhodnius prolixus.
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Adenosine modulates the (Na++K+)ATPase activity in Malpighian tubules isolated from Rhodnius prolixus.

机译:腺苷调节从Rhodnius prolixus分离的Malpighian小管中的(Na ++ K +)ATPase活性。

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The role of adenosine on regulation of the (Na++K+)ATPase activity present in the Malpighian tubules isolated from Rhodnius prolixus was investigated. Adenosine decreases the (Na++K+) ATPase specific activity by 88%, in a dose-dependent manner, withmaximal effect at a concentration of 10-9 M. This effect was mimicked by N6-cyclohexyladenosine (CHA) at 10-8 M, an agonist for A1 adenosine receptor, and was reversed by 10-9 M 8-cyclopentyl-1,3-dipropylxanthine (DPCPX), an antagonist for A1 adenosinereceptor. On the other hand, 5'-N-ethyl-carboxamide adenosine (NECA), an agonist for A2 adenosine receptor, used in the range of 10-9-10-5 M, did not change the (Na++K+)ATPase specific activity. In the same way, 10-8 M 3,7-dimethyl-1-propargylxanthine (DMPX), an antagonist for A2 adenosine receptor, did not modify the inhibitory effect of adenosine. These data suggest that the inhibitory effect of adenosine on the (Na++K+)ATPase specific activity present in Malpighian tubules from R. prolixus is mediated by A1 adenosine receptor activation.
机译:研究了腺苷对从罗得氏红球菌分离出的马氏管中(Na ++ K +)ATPase活性的调节作用。腺苷以剂量依赖性方式使(Na ++ K +)ATPase比活性降低88%,在10-9 M的浓度下具有最大作用。在10-8 M的N6-环己基腺苷(CHA)可以模仿这种作用,是A1腺苷受体的激动剂,被10-9 M 8-环戊基-1,3-二丙基黄嘌呤(DPCPX)(A1腺苷受体的拮抗剂)逆转。另一方面,在10-9-10-5 M范围内使用的A2腺苷受体激动剂5'-N-乙基羧酰胺腺苷(NECA)不会改变(Na ++ K +)ATPase具体活动。同样,A2腺苷受体的拮抗剂10-8 M 3,7-二甲基-1-炔丙基黄嘌呤(DMPX)不会改变腺苷的抑制作用。这些数据表明腺苷对来自螺旋体的马氏小管中存在的(Na ++ K +)ATPase比活性的抑制作用是由A1腺苷受体激活介导的。

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