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[腹膜炎所致脓毒症休克时肝脏糖酵解中间产物及葡萄糖调节酶:大鼠实验研究]

[Hepatic glycolytic intermediates and glucoregulatory enzymes in septic shock due to peritonitis: experimental study in rats].

作者信息

Ebata T, Hirata K, Denno R, Gotoh Y, Azuma K, Ishida K, Hasegawa I, Hayasaka H

出版信息

Nihon Geka Gakkai Zasshi. 1984 Jan;85(1):1-5.

PMID:6234452
Abstract

The hypoglycemia in septic shock due to peritonitis indicates deranged carbohydrate metabolism. To determine if this metabolic failure could be attributed to changes of glucoregulatory enzymes and glycolytic intermediates, activities and changes of these substances in septic shock have been studied in rats. Liver tissue was sampled 5 hours after induction of peritonitis by cecal incision in fasted male rats. Hepatic glycolytic intermediates were assayed by UV-spectrophotometry. Peritonitis caused 33% decrease in glucose-6-phosphate (G6P), a 2.5 fold increase in fructose-1,6-diphosphate (FDP) and a 3.5 fold increase in lactate. Phosphoenolpyruvate (PEP) levels did not show a significant increase in peritonitis. We investigated activities of glucose-6-phosphatase (G6Pase), fructose-1,6-diphosphatase (FDPase), phosphofructokinase ( PFKase ) and pyruvate kinase ( PKase ) in mitochondria-free supernatants from rat liver homogenates. Tissue was sampled 5 hours after induction of peritonitis by cecal incision. Assays were conducted at optimal substrate levels at pH 7.4; NADH charges produced by coupled reactions were determined by UV-spectrophotometry. A significant increase of PFKase and PKase specific activity was observed. These changes were consistent with stimulated glycolysis. For gluconeogenesis to achieve maximum efficiency it would be necessary to inhibit PFKase and PKase completely.

摘要

腹膜炎所致脓毒性休克中的低血糖表明碳水化合物代谢紊乱。为了确定这种代谢衰竭是否可归因于葡萄糖调节酶和糖酵解中间产物的变化,我们在大鼠中研究了脓毒性休克时这些物质的活性和变化。在禁食的雄性大鼠中,通过盲肠切开诱导腹膜炎5小时后采集肝脏组织。用紫外分光光度法测定肝脏糖酵解中间产物。腹膜炎导致6-磷酸葡萄糖(G6P)降低33%,1,6-二磷酸果糖(FDP)增加2.5倍,乳酸增加3.5倍。腹膜炎时磷酸烯醇丙酮酸(PEP)水平未显示显著升高。我们研究了大鼠肝脏匀浆无线粒体上清液中葡萄糖-6-磷酸酶(G6Pase)、1,6-二磷酸果糖酶(FDPase)、磷酸果糖激酶(PFKase)和丙酮酸激酶(PKase)的活性。通过盲肠切开诱导腹膜炎5小时后采集组织样本。在pH 7.4的最佳底物水平下进行测定;通过紫外分光光度法测定偶联反应产生的NADH电荷。观察到PFKase和PKase比活性显著增加。这些变化与糖酵解受刺激一致。为了使糖异生达到最大效率,有必要完全抑制PFKase和PKase。

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