中国药理学通报
中國藥理學通報
중국약이학통보
CHINESE PHARMACOLOGICAL BULLETIN
2001年
1期
89-91
,共3页
郝胜利%张孙曦%唐朝枢%何其华%凤志慧%安丽芝
郝勝利%張孫晞%唐朝樞%何其華%鳳誌慧%安麗芝
학성리%장손희%당조추%하기화%봉지혜%안려지
牛磺酸%H2O2%平滑肌细胞%核%共聚焦显微成像术%Fluo-3%Ca2+
牛磺痠%H2O2%平滑肌細胞%覈%共聚焦顯微成像術%Fluo-3%Ca2+
우광산%H2O2%평활기세포%핵%공취초현미성상술%Fluo-3%Ca2+
目的毒性剂量H2O2可引起细胞坏死或凋亡, 此过程是否与H2O2引起的核[Ca2+]([Ca2+]n)变化有关未见报导。本文研究牛磺酸对H2O2引起的血管平滑肌细胞(VSMC)[Ca2+]n与胞浆[Ca2+]([Ca2+]c)的变化影响。方法应用激光共聚焦显微镜对负载Fluo-3的培养大鼠VSMC的[Ca2+]n及[Ca2+]c变化进行研究。结果在0.5% H2O2作用下,[Ca2+]n与[Ca2+]c持续升高,用抗氧化细胞保护剂-牛磺酸20 mmol*L-1预处理细胞,可降低H2O2引起的[Ca2+]n 升幅 (P<0.05),但不影响[Ca2+]c升幅(P>0.05),表明[Ca2+]n变化与[Ca2+]c变化对牛磺酸反应性存在差异。结论 VSMC的核Ca2+调控与胞浆Ca2+调控各自具有一定的独立性。牛磺酸对H2O2引起的大鼠VSMC核Ca2+的变化具有保护作用。
目的毒性劑量H2O2可引起細胞壞死或凋亡, 此過程是否與H2O2引起的覈[Ca2+]([Ca2+]n)變化有關未見報導。本文研究牛磺痠對H2O2引起的血管平滑肌細胞(VSMC)[Ca2+]n與胞漿[Ca2+]([Ca2+]c)的變化影響。方法應用激光共聚焦顯微鏡對負載Fluo-3的培養大鼠VSMC的[Ca2+]n及[Ca2+]c變化進行研究。結果在0.5% H2O2作用下,[Ca2+]n與[Ca2+]c持續升高,用抗氧化細胞保護劑-牛磺痠20 mmol*L-1預處理細胞,可降低H2O2引起的[Ca2+]n 升幅 (P<0.05),但不影響[Ca2+]c升幅(P>0.05),錶明[Ca2+]n變化與[Ca2+]c變化對牛磺痠反應性存在差異。結論 VSMC的覈Ca2+調控與胞漿Ca2+調控各自具有一定的獨立性。牛磺痠對H2O2引起的大鼠VSMC覈Ca2+的變化具有保護作用。
목적독성제량H2O2가인기세포배사혹조망, 차과정시부여H2O2인기적핵[Ca2+]([Ca2+]n)변화유관미견보도。본문연구우광산대H2O2인기적혈관평활기세포(VSMC)[Ca2+]n여포장[Ca2+]([Ca2+]c)적변화영향。방법응용격광공취초현미경대부재Fluo-3적배양대서VSMC적[Ca2+]n급[Ca2+]c변화진행연구。결과재0.5% H2O2작용하,[Ca2+]n여[Ca2+]c지속승고,용항양화세포보호제-우광산20 mmol*L-1예처리세포,가강저H2O2인기적[Ca2+]n 승폭 (P<0.05),단불영향[Ca2+]c승폭(P>0.05),표명[Ca2+]n변화여[Ca2+]c변화대우광산반응성존재차이。결론 VSMC적핵Ca2+조공여포장Ca2+조공각자구유일정적독립성。우광산대H2O2인기적대서VSMC핵Ca2+적변화구유보호작용。
AIM As one of the reactive oxygen species, toxic dose of H2O2 leads to the necrosis or apoptosis of many kinds of cells. It is nuclear whether these processes are related with the changes of nuclear Ca2+ elicited by H2O2. This study on the effect of taurine on changes of nuclear and cytosolic (Ca2+) elicited by H2O2 in rat vascular smooth muscle cells. METHODS The techniques of Fluo-3 and laser scanning confocal microscopy were used. RESULTS Rapid and sustaining rise of nuclear [Ca2+] ([Ca2+]n) and cytosolic [Ca2+]([Ca2+]c) were found in cultured rat vascular smooth muscle cells upon adding of 0.5% H2O2. Pretreatment of the cells with 20 mmol*L-1 taurine, a regulator of cellular Ca2+ homestasis, significantly decreased the rise amplitude of [Ca2+]n (P<0.05), but failed to affect that of [Ca2+]c (P>0.05) elicited by H2O2. It was suggested that the changes of [Ca2+]n and [Ca2+]c have different respond to taurine. CONCLUSION It was concluded that there exist the independent regulating mechanisms of Ca2+ in the nucleus from differences between the nucleus and cytosol Ca2+ in sensitivity to action of H2O2 and taurine.