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影响大鼠色氨酸诱导低血糖的因素。

Factors affecting tryptophan-induced hypoglycaemia in rats.

作者信息

Lloyd P, Smith S A, Stribling D, Pogson C I

出版信息

Biochem Pharmacol. 1982 Nov 15;31(22):3563-9. doi: 10.1016/0006-2952(82)90576-7.

Abstract

The mechanisms whereby tryptophan administration leads to hypoglycaemia in some groups of rats but not others have been investigated. Animals insensitive to tryptophan are rendered responsive by adrenalectomy. This effect is reversed by steroid replacement. Turnover studies with [2-3H]glucose show that hypoglycaemia in sensitive animals is associated with a decrease in glucose synthesis. Tryptophan administration causes a marked and sustained increase in plasma glucagon concentrations in all animals. The locus of the inhibition of gluconeogenesis in tryptophan-sensitive animals is the reaction catalysed by phosphoenolpyruvate carboxykinase. The sensitivities to tryptophan of gluconeogenesis in isolated hepatocytes from normal and adrenalectomized animals were similar. Cells from chronically streptozotocin-diabetic animals required higher concentrations of the amino acid for the same effect. These results are discussed in relation to previous discrepancies in the literature, and a unifying hypothesis for tryptophan-induced hypoglycaemia is proposed.

摘要

已经对色氨酸给药在某些大鼠组中导致低血糖而在其他组中却不会导致低血糖的机制进行了研究。对色氨酸不敏感的动物在肾上腺切除术后会变得敏感。这种效应可通过类固醇替代而逆转。用[2-³H]葡萄糖进行的周转研究表明,敏感动物的低血糖与葡萄糖合成减少有关。在所有动物中,色氨酸给药都会导致血浆胰高血糖素浓度显著且持续升高。在色氨酸敏感的动物中,糖异生受抑制的位点是磷酸烯醇丙酮酸羧激酶催化的反应。来自正常动物和肾上腺切除动物的分离肝细胞中糖异生对色氨酸的敏感性相似。来自长期链脲佐菌素诱导糖尿病动物的细胞在产生相同效应时需要更高浓度的该氨基酸。结合文献中先前的差异对这些结果进行了讨论,并提出了一个关于色氨酸诱导低血糖的统一假说。

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