- 영문명
- The Importance of Oxidative in the Inhibition of Vasorelaxation Induced by Quinolinedione Derivatives, OQ1 and OQ21
- 발행기관
- 대한약학회
- 저자명
- 김세련(Se Ryun Kim) 이주영(Joo Young Lee) 김화정(Hwa Jung Kim) 유충규(Chung Kyu Ryu) 정진호(Jin Ho Chung)
- 간행물 정보
- 『약학회지』제43권 제5호 (1999년), 652~658쪽, 전체 7쪽
- 주제분류
- 의약학 > 기타의약학
- 파일형태
- 발행일자
- 1999.10.28

국문 초록
영문 초록
To reveal the inhibitory mechanism of NO-dependent vasorelaxation by quinone derivatives (OQ1 and OQ21), we have compared the generation of free radicals by oxidative stress and the formation of cellular adducts by arylation. First, we measured oxygen consumption by quinone derivatives as a marker of oxidative stress in order to investigate whether these quinone compounds could generate reactive oxygen species. Both OQ1 and OQ21 generated free radicals and OQ21 was more potent. These results suggsted that free radicals be involved in the inhibition of vasorelaxation by quinones. Next, we measured the binding capacity of quinone derivatives with intracellular GSH and protein thiols (-SH) in order to investigate whether these quinones have arylation capacity. Compared to positive control groups (menadione), both OQ1 and OQ21 depleted intracellular GSH and protein thiols very slightly. These compounds have low toxicities in mammalian tissues. From these results, we concluded that the inhibition of vasorelaxation by quinone derivatives (OQ1, OQ21) may be caused by generation of free radicals.
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