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作 者:洪华山[1] 陈凤荣[2] 朱应葆[2] 王一波[1] 林岚[1] 江琼[1]
机构地区:[1]福建医科大学附属协和医院心内科,福州350001 [2]北京大学第三医院心内科,北京100083
出 处:《中国药理学通报》2001年第2期151-154,共4页Chinese Pharmacological Bulletin
基 金:福建省教委(No 99A063);教育部博士点资金(No 9724)资助课题
摘 要:目的研究3β,5α,6β-胆甾烷二醇(Triol)诱导血管平滑肌细胞(VSMCs)凋亡及其与25-羟胆固醇(25-OH)比较的特点。方法体外培养VSMCs、光镜、透射电镜及TUNEL技术。结果VSMCs经Triol处理后,贴壁层细胞呈现核染色质浓集,核碎裂和凋亡小体形成等凋亡的超微结构变化;TUNEL显示VSMCs凋亡细胞数随Triol浓度的增加而增多;剂量为 30 μmol·L-1的 Triol和 25-OH诱导 VSMCs的凋亡作用,前者不能而后者能被 50 μmol·L-1的胆固醇所抑制。结论Triol能诱导VSMCs凋亡,不同氧化甾醇可能有不同的作用通道和机制;氧化甾醇诱导VSMCs凋亡可能是引起动脉粥样硬化斑块破溃,导致急性心血管事件发生的机制之一。AIM To study the apoptosis and characterization of cultured vascular smooth muscle coils (VSMCs) induced by cholestan-3β, 5α, 6β-triol (Triol) and compared with 25-hydryoxycholestrol (25-OH). METHODS The culture of vascular mus- cle smooth cells (VSMCs), light and electron transmission microscopy and TdT-mediated dUPT nickend labeling (TUNEL) technique. RESULTS After being treated with oxyterols, VSMCs showed apoptosis of ultrastracture change including shrinkage, condensation of nuclear chromatin, fragmentation nuclei and formation of apoptotic body. TUNEL revealed that Triol-induced apoptosis in VSMCs was in a concentration-dependent manner. The effect of Triol and 25-OH at a 30 μmol· L-1 concentration in culture medium induced apoptosis of VSMCs, the former was not but the latter was inhibited by cholesterol at a 50 μmol·L-1 concentration. CONCLUSION Triol can induce VSMCs apoptosis in vitro and oxysterol-in- duced apoptosis in VSMCs may be mediated through various pathway and different mechanism. Oxysterol induced apoptosis in VSMCs may play an important role in triggering atherosclerosis plaque rupture and result to the onset of the acute coronary syndromes.
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