Hatta S, Suzuki Y, Miyamoto A, Takemura H, Ohshika H
Jpn J Pharmacol. 1986 Apr;40(4):561-7. doi: 10.1254/jjp.40.561.
The effects of 8-(2-dimethylaminoethyl)-3-oxo-4-phenyl-1-thia-4,8-diazaspiro [4, 5] decane dihydrochloride monohydrate (Y-8845) on carbon tetrachloride (CCl4)-induced liver injury were investigated in rats. CCl4-induced attenuation of the plasma cyclic AMP (cAMP) response to glucagon stimulation was significantly prevented by pretreatment with Y-8845. Y-8845 also effectively suppressed the increases in the activities of serum transaminases as well as the decreases in microsomal glucose-6-phosphatase activity and microsomal cytochrome P-450 concentrations induced by CCl4. In rats at 72 hr after CCl4 administration, the plasma cAMP response to glucagon, microsomal glucose-6-phosphatase activity and P-450 concentration were all below the control level. Y-8845 treatment after CCl4 administration rectified these reductions to nearly normal levels. Furthermore, Y-8845 stimulated DNA synthesis during liver regeneration after CCl4 intoxication. These results demonstrate that Y-8845 has a protective effect against CCl4-induced injury in the liver and a stimulating effect on the recovery of the damaged liver.
研究了8-(2-二甲基氨基乙基)-3-氧代-4-苯基-1-硫杂-4,8-二氮杂螺[4,5]癸烷二盐酸盐一水合物(Y-8845)对四氯化碳(CCl4)诱导的大鼠肝损伤的影响。Y-8845预处理可显著预防CCl4诱导的血浆环磷酸腺苷(cAMP)对胰高血糖素刺激反应的减弱。Y-8845还有效抑制了CCl4诱导的血清转氨酶活性升高以及微粒体葡萄糖-6-磷酸酶活性和微粒体细胞色素P-450浓度降低。在给予CCl4后72小时的大鼠中,血浆cAMP对胰高血糖素的反应、微粒体葡萄糖-6-磷酸酶活性和P-450浓度均低于对照水平。给予CCl4后进行Y-8845治疗可将这些降低恢复至接近正常水平。此外,Y-8845在CCl4中毒后的肝再生过程中刺激DNA合成。这些结果表明,Y-8845对CCl4诱导的肝损伤具有保护作用,并对受损肝脏的恢复具有刺激作用。