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低渗介质中肾近端小管的等容调节

Isovolumetric regulation of renal proximal tubules in hypotonic medium.

作者信息

Lohr J W

机构信息

Department of Medicine, State University of New York, Buffalo.

出版信息

Ren Physiol Biochem. 1990 Sep-Oct;13(5):233-40. doi: 10.1159/000173364.

Abstract

Isolated nonperfused proximal tubules maintained their cell volume at a constant level (isovolumetric regulation, IVR), when osmolality of the bathing medium was gradually decreased from 290 to 190 mosm at 1.5 and 5.0 mosm/min. Hypotonic IVR was blocked by inhibiting the Na(+)-K+ pump with ouabain (10(-4) M) when osmolality was decreased at 1.5 or 5 mosm/min. Concentration-dependent inhibition of cell volume maintenance was observed in the presence of the K+ channel blocker barium (10(-3)-10(-2) M) when osmolality decreased at 5 mosm/min. Quinine (10(-3) M), another K+ channel blocker, also inhibited IVR at osmolality decreases of 1.5 and 5 mosm/min. These results suggest that the maintenance of constant cell volume during gradual hypoosmotic exposure involves mechanisms that depend on intact Na-K-ATPase and the controlled loss of intracellular K+.

摘要

当灌流介质的渗透压以1.5和5.0 mosm/分钟的速度从290 mosm逐渐降至190 mosm时,分离出的无灌注近端小管将其细胞体积维持在恒定水平(等容调节,IVR)。当渗透压以1.5或5 mosm/分钟的速度降低时,用哇巴因(10⁻⁴ M)抑制Na⁺-K⁺泵可阻断低渗IVR。当渗透压以5 mosm/分钟的速度降低时,在存在K⁺通道阻滞剂钡(10⁻³ - 10⁻² M)的情况下,观察到细胞体积维持的浓度依赖性抑制。另一种K⁺通道阻滞剂奎宁(10⁻³ M)在渗透压降低1.5和5 mosm/分钟时也抑制IVR。这些结果表明,在逐渐低渗暴露期间维持恒定细胞体积涉及依赖完整钠钾ATP酶和细胞内K⁺受控丢失的机制。

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