Rao M R, Hutcheson A E, Markov A K
Department of Medicine, University of Mississippi Medical Center, Jackson, USA.
Drug Chem Toxicol. 1998 Feb;21(1):27-34. doi: 10.3109/01480549809017848.
Cyclosporin A (CsA), an immunosuppressive agent is known to induce cellular toxic effects by alerting calcium homeostasis. Nitric oxide (NO) has been implicated in a number of physiologic roles in the mammalian cardiovascular system (CVS). The aim of our present study is to investigate the effects of CsA on the rat CV NO pathway. We measured iNOS and cNOS activities in the 100,000 g soluble fraction of ventricles and serum nitrite (NO2-) and nitrite (NO3-) levels in rats treated with 25 mg/kg or 50 mg/kg body weight of CsA/24 hr in olive oil. CsA inhibited cNOS activity of rat ventricles and failed to bring about changes in their iNOS activity. Serum NO2-/NO3- levels were elevated in CsA treated tars. Most of these changes were found to be statistically significant (P < 0.01) at 50 mg/kg body wt of CsA. It is likely that elevation of serum NO2-/NO3- levels may cause myocardial toxicity by alerting rat CV NO pathway.
环孢素A(CsA)是一种免疫抑制剂,已知它会通过改变钙稳态来诱导细胞毒性作用。一氧化氮(NO)在哺乳动物心血管系统(CVS)的许多生理作用中都有涉及。我们当前研究的目的是调查CsA对大鼠心血管NO途径的影响。我们测量了用25毫克/千克或50毫克/千克体重的CsA/24小时橄榄油处理的大鼠心室100,000克可溶部分中的诱导型一氧化氮合酶(iNOS)和内皮型一氧化氮合酶(cNOS)活性以及血清亚硝酸盐(NO2-)和硝酸盐(NO3-)水平。CsA抑制了大鼠心室的cNOS活性,但未能引起其iNOS活性的变化。在接受CsA处理的大鼠中血清NO2-/NO3-水平升高。在50毫克/千克体重的CsA时,发现这些变化大多具有统计学意义(P < 0.01)。血清NO2-/NO3-水平升高可能通过改变大鼠心血管NO途径而导致心肌毒性。