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环孢素A、硫唑嘌呤和泼尼松龙对大鼠肝细胞碳水化合物代谢的影响。

Effect of cyclosporin A, azathioprine, and prednisolone on carbohydrate metabolism of rat hepatocytes.

作者信息

Riegel W, Stephan E, Ballé C, Heidland A, Hörl W H

机构信息

Department of Medicine, University of Freiburg, Federal Republic of Germany.

出版信息

Transpl Int. 1990 May;3(1):2-7. doi: 10.1007/BF00333193.

Abstract

The effect of different immunosuppressive drugs (prednisolone, azathioprine, cyclosporin A) on liver carbohydrate metabolism in the rat was investigated. Daily administration of prednisolone (3 mg/kg body weight) and azathioprine (2 mg/kg body weight) intraperitoneally for 2 weeks caused significantly lower liver glycogen content than that in NaCl-treated controls. Liver glucose and lactate content, as well as plasma glucose, glucagon, and serum insulin concentration of these animals, remained unchanged. There were no differences in any of these parameters between cyclosporin A (15 mg/kg body weight)-treated and vehicle (olive oil/ethanol)-treated animals. Prednisolone caused significantly lower glucose production in isolated rat hepatocytes using Na-pyruvate as the substrate, whereas glucose production was unchanged in hepatocytes of azathioprine-treated rats using pyruvate or L-serine as substrates. Glucose production from pyruvate or serine was significantly inhibited by cyclosporin A compared to the vehicle, but did not differ from the effects of azathioprine and prednisolone. Lactate production was significantly lower in cyclosporin-treated animals than in those given either the vehicle or azathioprine. Cyclosporin A completely reversed the inhibition of hepatocyte glycogen consumption caused by the vehicle. However, glycogen production in the presence of cyclosporin A was comparable to the effects of prednisolone and azathioprine. Finally, hepatocyte ketone body production using pyruvate as the substrate was higher in the presence of all immunosuppressive drugs. In the presence of serine, acetoacetate production increased in rats treated with 50 mg/kg body weight cyclosporin A, and beta-hydroxybutyrate production in animals receiving 15 and 50 mg/kg body weight cyclosporin A.

摘要

研究了不同免疫抑制药物(泼尼松龙、硫唑嘌呤、环孢素A)对大鼠肝脏碳水化合物代谢的影响。连续2周每天腹腔注射泼尼松龙(3毫克/千克体重)和硫唑嘌呤(2毫克/千克体重),导致肝脏糖原含量显著低于用氯化钠处理的对照组。这些动物的肝脏葡萄糖和乳酸含量以及血浆葡萄糖、胰高血糖素和血清胰岛素浓度均保持不变。环孢素A(15毫克/千克体重)处理组和赋形剂(橄榄油/乙醇)处理组动物在这些参数上均无差异。以丙酮酸钠为底物时,泼尼松龙使分离的大鼠肝细胞中的葡萄糖生成显著降低,而以丙酮酸盐或L-丝氨酸为底物时,硫唑嘌呤处理的大鼠肝细胞中的葡萄糖生成未发生变化。与赋形剂相比,环孢素A显著抑制了丙酮酸盐或丝氨酸生成葡萄糖,但与硫唑嘌呤和泼尼松龙的作用无差异。环孢素处理的动物中乳酸生成显著低于给予赋形剂或硫唑嘌呤的动物。环孢素A完全逆转了赋形剂对肝细胞糖原消耗的抑制作用。然而,环孢素A存在时的糖原生成与泼尼松龙和硫唑嘌呤的作用相当。最后,以丙酮酸盐为底物时,所有免疫抑制药物存在下肝细胞酮体生成均增加。在丝氨酸存在的情况下,用50毫克/千克体重环孢素A处理的大鼠中乙酰乙酸生成增加,接受15和50毫克/千克体重环孢素A的动物中β-羟基丁酸生成增加。

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