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大鼠脓毒症时肾糖异生的代谢调节

Metabolic regulation of renal gluconeogenesis in response to sepsis in the rat.

作者信息

Ardawi M S, Khoja S M, Newsholme E A

机构信息

Department of Clinical Biochemistry, College of Medicine and Allied Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.

出版信息

Clin Sci (Lond). 1990 Nov;79(5):483-90. doi: 10.1042/cs0790483.

Abstract
  1. The regulation of renal gluconeogenesis was studied in rats made septic by a caecal ligation and puncture technique. 2. Blood glucose concentrations were not markedly different in septic rats, but lactate, pyruvate and alanine concentrations were markedly increased, compared with sham-operated rats. Conversely, blood ketone body concentrations were significantly decreased in septic rats. Both plasma insulin and glucagon concentrations were markedly elevated in response to sepsis. 3. The maximal activities of glucose-6-phosphatase (EC 3.1.3.9), fructose-1,6-bisphosphatase (EC 3.1.3.11), pyruvate carboxylase (EC 6.4.1.1) and phosphoenolpyruvate carboxykinase (EC 4.1.1.49) were markedly decreased in kidneys obtained from septic rats, suggesting diminished renal gluconeogenesis. 4. Renal concentrations of lactate, pyruvate and other gluconeogenetic intermediates were markedly elevated in septic rats, whereas those of acetyl-CoA and fructose 2,6-bisphosphate were decreased and unchanged, respectively. 5. The rate of gluconeogenesis from added lactate, pyruvate and glycerol was decreased in isolated incubated renal tubules from septic rats. 6. Sepsis decreased the arteriovenous concentration difference for glucose, lactate, and alanine. Septic rats showed decreased net rates of glucose production and net rates of removal of lactate and alanine as compared with sham-operated controls. 7. It is concluded that the diminished capacity for renal gluconeogenesis in septic rats could be the result of changes in the maximal activities or regulation of key non-equilibrium gluconeogenic enzymes or both, but the effect of other factors (e.g. toxins) has not been excluded.
摘要
  1. 采用盲肠结扎和穿刺技术使大鼠发生脓毒症,以此研究肾糖异生的调节机制。2. 脓毒症大鼠的血糖浓度与假手术大鼠相比无显著差异,但乳酸、丙酮酸和丙氨酸浓度显著升高。相反,脓毒症大鼠的血酮体浓度显著降低。脓毒症发生后,血浆胰岛素和胰高血糖素浓度均显著升高。3. 从脓毒症大鼠获取的肾脏中,葡萄糖-6-磷酸酶(EC 3.1.3.9)、果糖-1,6-二磷酸酶(EC 3.1.3.11)、丙酮酸羧化酶(EC 6.4.1.1)和磷酸烯醇式丙酮酸羧激酶(EC 4.1.1.49)的最大活性显著降低,提示肾糖异生减少。4. 脓毒症大鼠肾脏中乳酸、丙酮酸和其他糖异生中间产物的浓度显著升高,而乙酰辅酶A和果糖2,6-二磷酸的浓度分别降低和未改变。5. 脓毒症大鼠离体培养的肾小管中,由添加的乳酸、丙酮酸和甘油生成葡萄糖的速率降低。6. 脓毒症降低了葡萄糖、乳酸和丙氨酸的动静脉浓度差。与假手术对照组相比,脓毒症大鼠的葡萄糖净生成率以及乳酸和丙氨酸的净清除率均降低。7. 得出结论:脓毒症大鼠肾糖异生能力降低可能是关键非平衡糖异生酶的最大活性或调节发生变化,或两者皆有改变的结果,但其他因素(如毒素)的影响尚未排除。

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