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血管平滑肌中细胞质糖酵解区室的NADH/NAD氧化还原状态

NADH/NAD redox state of cytoplasmic glycolytic compartments in vascular smooth muscle.

作者信息

Barron J T, Gu L, Parrillo J E

机构信息

Section of Cardiology, Department of Internal Medicine, Rush Medical College, Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612, USA.

出版信息

Am J Physiol Heart Circ Physiol. 2000 Dec;279(6):H2872-8. doi: 10.1152/ajpheart.2000.279.6.H2872.

Abstract

The cytoplasmic NADH/NAD redox potential affects energy metabolism and contractile reactivity of vascular smooth muscle. NADH/NAD redox state in the cytosol is predominately determined by glycolysis, which in smooth muscle is separated into two functionally independent cytoplasmic compartments, one of which fuels the activity of Na(+)-K(+)-ATPase. We examined the effect of varying the glycolytic compartments on cystosolic NADH/NAD redox state. Inhibition of Na(+)-K(+)-ATPase by 10 microM ouabain resulted in decreased glycolysis and lactate production. Despite this, intracellular concentrations of the glycolytic metabolite redox couples of lactate/pyruvate and glycerol-3-phosphate/dihydroxyacetone phosphate (thus NADH/NAD) and the cytoplasmic redox state were unchanged. The constant concentration of the metabolite redox couples and redox potential was attributed to 1) decreased efflux of lactate and pyruvate due to decreased activity of monocarboxylate B-H(+) transporter secondary to decreased availability of H(+) for cotransport and 2) increased uptake of lactate (and perhaps pyruvate) from the extracellular space, probably mediated by the monocarboxylate-H(+) transporter, which was specifically linked to reduced activity of Na(+)-K(+)-ATPase. We concluded that redox potentials of the two glycolytic compartments of the cytosol maintain equilibrium and that the cytoplasmic NADH/NAD redox potential remains constant in the steady state despite varying glycolytic flux in the cytosolic compartment for Na(+)-K(+)-ATPase.

摘要

细胞质中NADH/NAD的氧化还原电位影响血管平滑肌的能量代谢和收缩反应性。胞质溶胶中的NADH/NAD氧化还原状态主要由糖酵解决定,在平滑肌中糖酵解被分隔到两个功能独立的细胞质区室,其中一个为Na(+)-K(+)-ATP酶的活性提供能量。我们研究了改变糖酵解区室对胞质溶胶中NADH/NAD氧化还原状态的影响。用10微摩尔哇巴因抑制Na(+)-K(+)-ATP酶导致糖酵解和乳酸生成减少。尽管如此,糖酵解代谢物氧化还原对乳酸/丙酮酸和甘油-3-磷酸/磷酸二羟丙酮(从而NADH/NAD)的细胞内浓度以及细胞质氧化还原状态并未改变。代谢物氧化还原对和氧化还原电位的恒定浓度归因于:1)由于单羧酸B-H(+)转运体活性降低,继发于用于共转运的H(+)可用性降低,乳酸和丙酮酸的流出减少;2)细胞外空间中乳酸(可能还有丙酮酸)的摄取增加,可能由单羧酸-H(+)转运体介导,该转运体与Na(+)-K(+)-ATP酶活性降低特异性相关。我们得出结论,胞质溶胶中两个糖酵解区室的氧化还原电位保持平衡,并且尽管用于Na(+)-K(+)-ATP酶的胞质溶胶区室中的糖酵解通量变化,但细胞质NADH/NAD氧化还原电位在稳态下保持恒定。

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