Tsukamoto I, Kojo S
Department of Food Science and Nutrition, Nara Women's University, Japan.
Biochim Biophys Acta. 1990 Mar 26;1033(3):287-90. doi: 10.1016/0304-4165(90)90135-j.
The increases in the activity of hepatic thymidylate synthetase and thymidine kinase, which catalyzes the formation of thymidylate via the de novo and salvage pathways, respectively, were significantly suppressed 24 h after 70% partial hepatectomy in female rats administered either alpha- or beta-adrenoreceptor antagonists. The injection of beta-antagonist to male or ovariectomized female rats had no effect on the activities of these enzymes. Only alpha-adrenoceptor antagonist depressed these enzymatic activities of 24-h-regenerating liver in male and ovariectomized female rats. The decrease of the activities of thymidylate synthetase and thymidine kinase was accompanied by a concomitant reduction of DNA content in 24-h-regenerating liver. It is concluded that catecholamine regulates the female rat liver regeneration through both alpha- and beta-adrenergic pathways by the inductions of thymidylate synthase and thymidine kinase, while in adult male and ovariectomized female rats, only the alpha-mediated pathway is involved.
在分别给予α-或β-肾上腺素能拮抗剂的雌性大鼠中,70%部分肝切除术后24小时,催化通过从头合成途径和补救途径形成胸苷酸的肝胸苷酸合成酶和胸苷激酶的活性增加被显著抑制。给雄性或去卵巢雌性大鼠注射β-拮抗剂对这些酶的活性没有影响。只有α-肾上腺素能拮抗剂会降低雄性和去卵巢雌性大鼠24小时再生肝脏中这些酶的活性。胸苷酸合成酶和胸苷激酶活性的降低伴随着24小时再生肝脏中DNA含量的相应减少。结论是,儿茶酚胺通过诱导胸苷酸合成酶和胸苷激酶,通过α-和β-肾上腺素能途径调节雌性大鼠肝脏再生,而在成年雄性和去卵巢雌性大鼠中,仅涉及α介导的途径。