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青蛙骨骼肌中静息状态与胰岛素刺激下氨基酸转运的差异。

Differences between resting and insulin-stimulated amino acid transport in frog skeletal muscle.

作者信息

Grinstein S, Erlij D

出版信息

J Membr Biol. 1977 Jun 24;35(1):9-28. doi: 10.1007/BF01869937.

Abstract

We have compared some features of the resting and the insulin-stimulated uptake of alpha-aminoisobutyrate (AIB) in frog skeletal muscle. We found a substantial difference between the two processes, namely, that resting AIB uptake is Na-independent while the insulin-stimulated fraction of the AIB uptake is Na-dependent. Since the amino acid transport systems in frog skeletal muscle are poorly characterized, we have also surveyed some of their properties. One of the most interesting findings of this survey is that both the uptake and efflux of AIB are inhibited by low concentrations of PCMBS (parachloro-mercury-benzene sulfonic acid 5 X 10(-5) M). In contrast, the carrier mediated transport of basic amino acids is neither inhibited by this mercurial agent nor accelerated by insulin. The action of PCMBS strongly suggests the presence of a critical sulfhydryl group in the amino acid carrier system utilized by AIB. This group is exposed to the outside solution since PCMBS penetrates cell membranes poorly, and in addition its inhibitory actions were reverted by agents that do not penetrate the cell membrane like albumin or glutathione.

摘要

我们比较了青蛙骨骼肌中α-氨基异丁酸(AIB)静息摄取和胰岛素刺激摄取的一些特征。我们发现这两个过程之间存在显著差异,即静息状态下AIB的摄取不依赖于钠,而胰岛素刺激的AIB摄取部分则依赖于钠。由于青蛙骨骼肌中的氨基酸转运系统特性了解甚少,我们还研究了它们的一些特性。这项研究最有趣的发现之一是,低浓度的对氯汞苯磺酸盐(PCMBS,5×10⁻⁵ M)会抑制AIB的摄取和流出。相比之下,碱性氨基酸的载体介导转运既不受这种汞剂抑制,也不会被胰岛素加速。PCMBS的作用强烈表明,AIB所利用的氨基酸载体系统中存在一个关键的巯基。由于PCMBS穿透细胞膜的能力较差,这个基团暴露于外部溶液中,此外,其抑制作用可被像白蛋白或谷胱甘肽这样不能穿透细胞膜的试剂逆转。

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