Li L, Zhou J, Xing S
Department of Pharmacology, Beijing Geriatric Clinical and Research Center, P.R. China.
Adv Neuroimmunol. 1996;6(3):289-93. doi: 10.1016/s0960-5428(96)00024-1.
The aim of the review is to summarize our recent studies on the influence of the thymus on liver functions and its intermediary pathway in rats. Young adult thymectomized rats were used as a model in the experiments, and either thymic peptides or sex hormones were supplemented to these animals. Liver microsomal cytochrome P-450 and aminopyrine-N-demethylase (ADM) activities were decreased in thymectomized rats, and the change in the male was more significant than that in female rats. An increase of liver malondialdehyde (MDA) and a decrease of liver glutathione (GSH) and superoxide dismutase activity were observed in the female thymectomized rats, but not in the males. Accompanied by the increase of MDA, a decline of membrane fluidity of liver microsomes and mitochondria and a decrease of Ca2+ uptake by liver microsomes were exhibited in the female thymectomized rats. Subcutaneous injection of thymic peptides decreased MDA level, and increased GSH content, membrane fluidity and Ca2+ uptake by microsomes in the liver of thymectomized rats. On the other hand, male thymectomized rats showed a decrease of hypothalamic luteinizing hormone-releasing hormone (LHRH), plasma luteinizing hormone (LH) and testosterone levels. Subcutaneous injection of testosterone propionate to these animals restored their liver P-450 and ADM activities to normal levels. Female thymectomized rats exhibited a decline of hypothalamic LHRH and plasma estradiol levels. Supplementation of estradiol benzoate reversed the increase of liver MDA in these animals. The data suggest that the thymus may influence liver functions through the hypothalamus-pituitary-gonad axis. Thus, a new "thymus-neuroendocrine-liver pathway' is proposed, which may account for the significance of the thymus in maintaining homeostasis and integrative functions in the body.
本综述的目的是总结我们最近关于胸腺对大鼠肝功能的影响及其中间途径的研究。实验中使用年轻成年去胸腺大鼠作为模型,并对这些动物补充胸腺肽或性激素。去胸腺大鼠肝脏微粒体细胞色素P - 450和氨基比林 - N - 脱甲基酶(ADM)活性降低,雄性大鼠的变化比雌性大鼠更显著。在雌性去胸腺大鼠中观察到肝脏丙二醛(MDA)增加,肝脏谷胱甘肽(GSH)和超氧化物歧化酶活性降低,但在雄性大鼠中未观察到。伴随着MDA的增加,雌性去胸腺大鼠肝脏微粒体和线粒体的膜流动性下降,肝脏微粒体对Ca2+的摄取减少。皮下注射胸腺肽可降低去胸腺大鼠肝脏的MDA水平,并增加GSH含量、膜流动性和微粒体对Ca2+的摄取。另一方面,雄性去胸腺大鼠下丘脑促黄体生成素释放激素(LHRH)、血浆促黄体生成素(LH)和睾酮水平降低。对这些动物皮下注射丙酸睾酮可使其肝脏P - 450和ADM活性恢复到正常水平。雌性去胸腺大鼠下丘脑LHRH和血浆雌二醇水平下降。补充苯甲酸雌二醇可逆转这些动物肝脏MDA的增加。数据表明,胸腺可能通过下丘脑 - 垂体 - 性腺轴影响肝功能。因此,提出了一条新的“胸腺 - 神经内分泌 - 肝脏途径”,这可能解释了胸腺在维持机体稳态和整合功能中的重要性。