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胰岛素刺激蟾蜍膀胱中的钠转运。

Insulin-stimulated sodium transport in toad urinary bladder.

作者信息

Cobb M H, Yang C P, Brown J A, Scott W N

出版信息

Biochim Biophys Acta. 1986 Mar 27;856(1):123-9. doi: 10.1016/0005-2736(86)90018-0.

Abstract

Mammalian and teleost insulins increase active sodium transport by the toad urinary bladder at subnanomolar concentrations. This stimulation is evident within 15 min and persists for hours. Porcine proinsulin and a cross-linked derivative of bovine insulin are less effective than porcine insulin in stimulating the short-circuit current (SCC), indicating the specificity appropriate for activation of sodium transport through an insulin receptor. The initial stimulation by insulin of the SCC is not blocked by pretreatment with actinomycin D, puromycin, cycloheximide, or tunicamycin. However, in the presence of any one of these inhibitors the sustained increase in SCC is blocked and the rise is short-lived, lasting only 45 to 90 min. In amphotericin-treated bladders, the addition of insulin did not further stimulate SCC.

摘要

哺乳动物和硬骨鱼的胰岛素在亚纳摩尔浓度下可增加蟾蜍膀胱的活性钠转运。这种刺激在15分钟内即可显现,并持续数小时。猪胰岛素原和牛胰岛素的交联衍生物在刺激短路电流(SCC)方面不如猪胰岛素有效,这表明通过胰岛素受体激活钠转运具有特异性。胰岛素对SCC的初始刺激不会被放线菌素D、嘌呤霉素、环己酰亚胺或衣霉素预处理所阻断。然而,在存在这些抑制剂中的任何一种的情况下,SCC的持续增加会被阻断,且升高是短暂的,仅持续45至90分钟。在两性霉素处理的膀胱中,添加胰岛素不会进一步刺激SCC。

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