Franklin M R, Finkle B S
J Interferon Res. 1985 Spring;5(2):265-72. doi: 10.1089/jir.1985.5.265.
Murine IFN(gamma) and human IFN(alpha)-AD:Bgl were compared over a limited dose range and after single and multiple dosing for their effect on male mouse liver oxidative and conjugative drug metabolizing enzymes. Both IFNs depressed the microsomal cytochrome P-450 concentration but did not alter cytosolic glutathione S-transferase nor microsomal UDP-glucuronosyltransferase activity. Both IFNs showed some slight hepatotoxicity (elevated serum ALT), alpha AD:Bgl more than gamma, especially after multiple dosing. While the IFNs did not produce significant increases in liver weight, they did increase the yield of microsomal protein. The increased endoplasmic reticulum may compensate for the decreased cytochrome P-450 concentration and so account for the lack of observed effect of the IFNs on hexobarbital sleep times in vivo. Overall, the minimal effects of murine gamma-IFN on the mouse liver were no different than those of human alpha AD:Bgl.
在有限的剂量范围内,对小鼠干扰素γ(Murine IFNγ)和人干扰素α-AD:Bgl(human IFNα-AD:Bgl)进行了单次和多次给药,比较它们对雄性小鼠肝脏氧化和结合型药物代谢酶的影响。两种干扰素均降低了微粒体细胞色素P-450浓度,但未改变胞质谷胱甘肽S-转移酶活性,也未改变微粒体UDP-葡萄糖醛酸基转移酶活性。两种干扰素均表现出一定程度的轻微肝毒性(血清谷丙转氨酶升高),α-AD:Bgl比γ更明显,尤其是在多次给药后。虽然干扰素未使肝脏重量显著增加,但确实提高了微粒体蛋白产量。内质网的增加可能补偿了细胞色素P-450浓度的降低,因此解释了在体内观察到的干扰素对己巴比妥睡眠时间缺乏影响的原因。总体而言,小鼠γ干扰素对小鼠肝脏的最小影响与人α-AD:Bgl的影响并无差异。