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类固醇结构对小鼠内毒素致死过程中肝脏代谢的影响。

Influence of steroid structure in relation to liver metabolism during endotoxin lethality in mice.

作者信息

Lazar G, Sekiya S, Agarwal M K

出版信息

Exp Cell Biol. 1977;45(3-4):176-83. doi: 10.1159/000162869.

Abstract

The influence of a number of steroid molecules on hepatic metabolism was determined in relationship to their ability to alter endotoxin lethality in intact mice. Progesterone, testosterone, estradiol, pregnenolone-16-alpha-carbonitrile and spironolactone did not alter endotoxin lethality, liver glycogen or tryptophan pyrrolase (TP) levels; all these materials increased liver tyrosine transaminase (TT) levels most probably due to mediation by endogenously liberated glucocorticoid hormones. Aldosterone and deoxycorticosterone induced liver TP, TT and glycogen but did not protect against lethality. Cortisone, hydrocortisone, triamcinolone, dexamethasone and 9-alpha-fluorohydrocortisone protected against lethality, increased liver glycogen and TT, but only triamcinolone induced liver TP. Collectively, there was no clear relationship between the protective effect and the increase or decrease of a given liver process. These further emphasize the need to reconsider molecular mechanisms of endotoxic reactions.

摘要

研究了多种甾体分子对肝脏代谢的影响,并将其与它们改变完整小鼠内毒素致死率的能力联系起来。孕酮、睾酮、雌二醇、孕烯醇酮-16-α-腈和螺内酯不会改变内毒素致死率、肝糖原或色氨酸吡咯酶(TP)水平;所有这些物质都会升高肝脏酪氨酸转氨酶(TT)水平,这很可能是由于内源性释放的糖皮质激素介导的。醛固酮和脱氧皮质酮可诱导肝脏TP、TT和糖原,但不能预防致死率。可的松、氢化可的松、曲安西龙、地塞米松和9-α-氟氢化可的松可预防致死率,增加肝糖原和TT,但只有曲安西龙可诱导肝脏TP。总体而言,保护作用与特定肝脏过程的增加或减少之间没有明确的关系。这些进一步强调了重新考虑内毒素反应分子机制的必要性。

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