Walter R, Hadasová E, Scheuch E, Siegmund W
Department of Pharmacology, Ernst Moritz Arndt University, Greifswald, Germany.
Pharmazie. 1996 Jul;51(7):498-500.
There is evidence that immunostimulation depresses the function of various cytochrome P450 (CYP)-dependent monooxygenases but activates the arylamine N-acetyltransferase (NAT). Therefore, the effects of the synthetic immunostimulator polyriboinosinic-polyribocytidylic acid (plC, 8 mg/kg i.p.), of sublytic doses of the streptococcal toxin streptolysin O (SLO, 50 HU/kg i.v. for 5 d) and of the immunosuppressor cyclophosphamide (CP, 100 mg/kg i.p.) on NAT and some monooxygenases were studied in rat liver. It was also evaluated whether CP might antagonize the effects of plC and SLO on drug metabolism. SLO, plC and CP reduced CYP content and the activities of some monooxygenases. NAT was significantly inhibited by CP (given 5 d before sacrifice) but not by plC, SLO or CP when given 2 d before sacrifice. CP lacked any effect on NAT if it was administered prior to SLO. However, it deteriorated synergistically the inhibition of the monooxygenases caused by SLO and plC.
有证据表明免疫刺激会抑制各种细胞色素P450(CYP)依赖性单加氧酶的功能,但会激活芳基胺N - 乙酰转移酶(NAT)。因此,研究了合成免疫刺激剂聚肌苷酸 - 聚胞苷酸(聚肌胞苷酸,8mg/kg腹腔注射)、亚溶剂量的链球菌毒素链球菌溶血素O(链球菌溶血素O,50HU/kg静脉注射,持续5天)和免疫抑制剂环磷酰胺(环磷酰胺,100mg/kg腹腔注射)对大鼠肝脏中NAT和一些单加氧酶的影响。还评估了环磷酰胺是否可能拮抗聚肌胞苷酸和链球菌溶血素O对药物代谢的影响。链球菌溶血素O、聚肌胞苷酸和环磷酰胺降低了CYP含量和一些单加氧酶的活性。环磷酰胺(在处死前5天给予)显著抑制NAT,但在处死前2天给予时,聚肌胞苷酸、链球菌溶血素O或环磷酰胺对NAT没有抑制作用。如果在链球菌溶血素O之前给予环磷酰胺,则其对NAT没有任何影响。然而,它协同加剧了由链球菌溶血素O和聚肌胞苷酸引起的单加氧酶的抑制作用。