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脂肪酸对灌注大鼠心脏葡萄糖磷酸化的抑制作用。

Inhibition of glucose phosphorylation by fatty acids in the perfused rat heart.

作者信息

Chatham J, Gilbert H F, Radda G K

机构信息

Department of Biochemistry, University of Oxford, England.

出版信息

FEBS Lett. 1988 Oct 10;238(2):445-9. doi: 10.1016/0014-5793(88)80529-5.

Abstract

The flux of glucose entering the glycolytic pathway under various metabolic conditions has been indirectly monitored in the Langendorff perfused rat heart using 31P-NMR spectroscopy. By totally inhibiting (greater than 95%) glyceraldehyde-3-phosphate dehydrogenase with low concentrations of iodoacetic acid (0.2 mM) in the perfusion medium, active glycolysis results in the accumulation of sugar phosphate species (fructose 1,6-bisphosphate, dihydroxyacetone phosphate, and glyceraldehyde 3-phosphate) which can be observed in the 31P-NMR spectrum. Using this technique, it has been shown that butyrate (10 mM) in the perfusion medium decreases the flux through the initial steps of the glycolytic pathway by at least 6-fold and that both glucose phosphorylation and glycogenolysis are inhibited. Upon total global ischemia in the presence of both glucose and butyrate, the glycolysis rate is stimulated approx. 100-fold.

摘要

利用31P-NMR光谱法,已在Langendorff灌注大鼠心脏中间接监测了在各种代谢条件下进入糖酵解途径的葡萄糖通量。通过在灌注介质中用低浓度的碘乙酸(0.2 mM)完全抑制(>95%)甘油醛-3-磷酸脱氢酶,活跃的糖酵解会导致磷酸糖物质(果糖1,6-二磷酸、磷酸二羟丙酮和甘油醛3-磷酸)积累,这可以在31P-NMR光谱中观察到。使用该技术已表明,灌注介质中的丁酸盐(10 mM)使通过糖酵解途径初始步骤的通量降低至少6倍,并且葡萄糖磷酸化和糖原分解均受到抑制。在同时存在葡萄糖和丁酸盐的情况下完全全脑缺血时,糖酵解速率被刺激约100倍。

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