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含巯基与不含巯基的血管紧张素转换酶抑制剂的自由基清除作用比较

Comparative free radical scavenging action of angiotensin-converting enzyme inhibitors with and without the sulfhydryl radical.

作者信息

Suzuki S, Sato H, Shimada H, Takashima N, Arakawa M

机构信息

Second Department of Medicine, Niigata University School of Medicine, Japan.

出版信息

Pharmacology. 1993 Jul;47(1):61-5. doi: 10.1159/000139079.

Abstract

The free radical scavenging effects of an angiotensin-converting enzyme (ACE) inhibitor containing sulfhydryl (SH; captopril) were compared with those of ACE inhibitors not containing SH (enalapril, enalaprilat, delapril and its de-esterified products). Electron spin resonance (ESR) using 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) as the spin trap showed that enalapril and delapril (0.6-4.8 mmol/l) inhibited hydroxyl radicals concentration-dependently. Captopril (2.4-10 mmol/l), enalaprilat and the de-esterified product of delapril (1.2-4.8 mmol/l) also inhibited hydroxyl radicals in a concentration-dependent manner. The effects of captopril and enalapril (2.4-4.8 mmol/l) on the scavenging of superoxide anion radical were also concentration-dependent. Delapril, its de-esterified product, and enalaprilat weakly inhibited superoxide anion radical. These results indicate that both SH- and non-SH-containing ACE inhibitors scavenge hydroxyl radical more strongly than the superoxide anion radical and that the free radical scavenging action of ACE inhibitors is probably not related only to the presence of the SH radical.

摘要

将含巯基(SH;卡托普利)的血管紧张素转换酶(ACE)抑制剂的自由基清除作用与不含SH的ACE抑制剂(依那普利、依那普利拉、地拉普利及其去酯产物)进行了比较。以5,5-二甲基-1-吡咯啉-N-氧化物(DMPO)作为自旋捕获剂的电子自旋共振(ESR)表明,依那普利和地拉普利(0.6 - 4.8 mmol/L)浓度依赖性地抑制羟自由基。卡托普利(2.4 - 10 mmol/L)、依那普利拉和地拉普利的去酯产物(1.2 - 4.8 mmol/L)也以浓度依赖性方式抑制羟自由基。卡托普利和依那普利(2.4 - 4.8 mmol/L)对超氧阴离子自由基的清除作用也呈浓度依赖性。地拉普利及其去酯产物以及依那普利拉对超氧阴离子自由基的抑制作用较弱。这些结果表明,含SH和不含SH的ACE抑制剂对羟自由基的清除作用均强于超氧阴离子自由基,且ACE抑制剂的自由基清除作用可能不仅仅与SH基团的存在有关。

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