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心房颤动时心房肌细胞L型Ca2+通道与肌浆网间Ca2+信号转导的探讨
引用本文:刘元生,郭继鸿,许原,张海澄,李学斌,张幼怡,袁兰.心房颤动时心房肌细胞L型Ca2+通道与肌浆网间Ca2+信号转导的探讨[J].中国病理生理杂志,2005,21(10):1927-1929.
作者姓名:刘元生  郭继鸿  许原  张海澄  李学斌  张幼怡  袁兰
作者单位:1北京大学人民医院心内科, 北京 100044;北京大学2第三医院血管研究所,
3医学部激光共聚焦显微镜室, 北京 100083
基金项目:国家自然科学基金资助项目(No.30271431),北京大学985项目,北京市自然科学基金资助项目(No.7032030),首都医学发展科研基金资助项目(No.20023036)
摘    要:目的:探讨房颤时心房肌细胞膜上L型Ca2+通道与肌浆网之间的Ca2+信号转导。 方法: 杂种犬10条,随机分为正常对照组和单纯房颤组。房颤组用起搏器行右心房快速起搏(500±20)次/分,术后观测24周。正常对照组不植入起搏器。胶原酶Ⅱ型分离心房肌细胞,用激光共聚焦显微镜检测L型Ca2+ 通道对细胞内Ca2+浓度变化的影响;L型Ca2+通道与肌浆网三磷酸肌醇受体(IP3R)和兰尼碱受体(RyR)之间的Ca2+信号转导。 结果: (1)L型Ca2+通道与肌浆网IP3R之间的Ca2+信号转导:正常对照组、单纯房颤组的心房肌细胞在用mibefradil和丁卡因分别阻滞T型Ca2+通道和RyR后给予细胞膜激动剂时,细胞内Ca2+浓度均升高(分别为1.4000±0.0776和1.5169±0.4414),组间比较无显著差异(P>0.05);(2)L型Ca2+通道与肌浆网RyR之间的Ca2+信号转导:正常对照组的心房肌细胞在用mibefradil和肝素分别阻滞T型Ca2+通道和IP3R后给予细胞膜激动剂时,细胞内Ca2+浓度升高(1.5576±0.1989),单纯房颤组的细胞内Ca2+浓度也升高(1.5372±0.2952),两组间比较无显著差异(P>0.05)。 结论: 房颤时L型Ca2+通道与RyR和IP3R之间可能存在信号转导,但其可能在房颤时的细胞内Ca2+超载及异常Ca2+信号转导方面不起重要作用。

关 键 词:心房颤动  钙通道  信号转导  受体  兰尼碱  受体  肌醇1  4  5-三磷酸  
文章编号:1000-4718(2005)10-1927-03
收稿时间:2004-02-17
修稿时间:2004-02-172004-05-12

An approach to calcium signal transmission between L-type calcium channel and sarcoplasmic reticulum of atrial myocytes during atrial fibrillation
LIU Yuan-sheng,GUO Ji-hong,XU Yuan,ZHANG Hai-cheng,LI Xue-bin,ZHANG You-yi,YUAN Lan.An approach to calcium signal transmission between L-type calcium channel and sarcoplasmic reticulum of atrial myocytes during atrial fibrillation[J].Chinese Journal of Pathophysiology,2005,21(10):1927-1929.
Authors:LIU Yuan-sheng  GUO Ji-hong  XU Yuan  ZHANG Hai-cheng  LI Xue-bin  ZHANG You-yi  YUAN Lan
Institution:1Department of Cardiology, Peking University People's Hospital, Beijing 100044, China;2Vessel Institute of the Third Hospital,3Laser Confocal Imaging Unit, Peking University, Beijing 100083, China
Abstract:AIM: To inquire into the Ca2+ signal transmission from L-type calcium channel to the sarcoplasma reticulum in atrial fibrillation. METHODS: Ten adult cross-bred dogs were used in the experiment. Five dogs underwent continuous rapid atrial pacing (500±20 beats/min) for twenty-four weeks to create persistent atrial fibrillation. Another group of size-matched dogs (n=5) without pacemaker implantation was used as a control group. Canine atrial myocytes were isolated by enzymatic dissociation. The Ca2+ cytosolic transient in atrial myocytes was analyzed by confocal imaging after loading myocytes with the acetoxymethyl ester of fluo-3 (Fluo-3/AM). Ca2+ signal transmission from L-type Ca2+ channels in the plasma membrane to the sarcoplasma reticular IP3R and RyR in atrial myocytes during atria fibrillation were measured. RESULTS: (1) Ca2+ signal transmission from L-type calcium channel to IP3R in the sarcoplasma reticulum:intracellular Ca2+concentration was slightly increased in two groups after blocking T-type calcium channel and RyR, but showed no statistic significance (P>0.05) between them. (2) Ca2+ signal transmission from L-type calcium channel to RyR in the sarcoplasma reticulum: intracellular Ca2+concentration was risen (1.5576±0.1989) in control groups after blocking T-type calcium channel and IP3R, and no significance was observed (P>0.05) compared with that in atrial fibrillation group (1.5372±0.2952). CONCLUSIONS: Ca2+ signal transmission possibly exists from L-type calcium channel to RyR and IP3R in the sarcoplasma reticulum, but it does not play an important role in intracellular Ca2+-overload and abnormal Ca2+ signal transmission during atrial fibrillation.
Keywords:Atrial fibrillation  Calcium channels  Signal transduction  Receptors  ryanodine  Receptors  inositol 1  4  5- triphosphate
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