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氨氯地平对兔降结肠顶端膜钠通透性影响的动力学

Kinetics of the effect of amiloride on the permeability of the apical membrane of rabbit descending colon to sodium.

作者信息

Moran W M, Hudson R L, Schultz S G

出版信息

J Membr Biol. 1985;87(1):55-65. doi: 10.1007/BF01870699.

Abstract

The effects of the addition of graded concentrations of amiloride, (A)m, to the mucosal bathing solution on the permeability of the apical membrane of rabbit descending colon to Na (PmNa) were determined when the Na activity in the mucosal bathing solution, (Na)m, was 18, 32 or 100 mM. PmNa was obtained from current-voltage relations determined on tissues bathed with a high-K serosal solution before and after the addition of a maximally inhibitory concentration of amiloride to the mucosal solution as described by Turnheim et al. (Turnheim, K., Thompson, S.M., Schultz, S.G. 1983. J. Membrane Biol. 76:299-309). The results indicate that: (1) As demonstrated previously (Turnheim et al., 1983), PmNa decreases with increasing (Na)m. (2) PmNa also decreases hyperbolically with increasing (A)m. Kinetic analyses of the effect of amiloride on PmNa are consistent with the conclusions that: (i) the stoichiometry between the interaction of amiloride with apical membrane receptors that results in a decrease in PmNa is one-for-one; (ii) there is no evidence for cooperativity between amiloride and these binding sites; (iii) the value of (A)m needed to halve PmNa at a fixed (Na)m is 0.6-1.0 microM; and, (iv) this value is independent of (Na)m over the fivefold range studied. These findings are consistent with the notion that the sites with which amiloride interacts to bring about closure of the channels through which Na crosses the apical membrane are kinetically distinct from the sites with which (Na)m interacts to bring about closure (i.e., "self-inhibition"). In short, the effects of (Na)m and (A)m on PmNa in this tissue appear to be independent and additive.

摘要

当黏膜浴液中的钠活性([Na]m)为18、32或100 mM时,测定了向黏膜浴液中添加不同浓度的氨氯吡咪([A]m)对兔降结肠顶端膜对钠的通透性(PmNa)的影响。如Turnheim等人(Turnheim, K., Thompson, S.M., Schultz, S.G. 1983. J. Membrane Biol. 76:299 - 309)所述,PmNa是根据在向黏膜溶液中添加最大抑制浓度的氨氯吡咪之前和之后,用高钾浆膜溶液灌注的组织所测定的电流 - 电压关系获得的。结果表明:(1)如先前所示(Turnheim等人,1983),PmNa随[Na]m的增加而降低。(2)PmNa也随[A]m的增加呈双曲线下降。对氨氯吡咪对PmNa影响的动力学分析与以下结论一致:(i)氨氯吡咪与顶端膜受体相互作用导致PmNa降低的化学计量比为一对一;(ii)没有证据表明氨氯吡咪与这些结合位点之间存在协同作用;(iii)在固定的[Na]m下,使PmNa减半所需的[A]m值为0.6 - 1.0 microM;并且,(iv)在所研究的五倍范围内,该值与[Na]m无关。这些发现与以下观点一致,即氨氯吡咪与之相互作用以导致钠穿过顶端膜的通道关闭的位点在动力学上与[Na]m与之相互作用以导致关闭的位点(即“自我抑制”)不同。简而言之,[Na]m和[A]m对该组织中PmNa的影响似乎是独立且可加的。

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