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超氧阴离子对培养的牛动脉平滑肌细胞内钙及收缩性的影响
引用本文:承伟,李智,小山澈野,大池正宏,伊东裕之.超氧阴离子对培养的牛动脉平滑肌细胞内钙及收缩性的影响[J].中国药理学通报,2001,17(2):190-193.
作者姓名:承伟  李智  小山澈野  大池正宏  伊东裕之
作者单位:1. 锦州医学院药学系,
2. 中国医科大学药理学教研室,
3. 九州大学医学院药理学教研室,
基金项目:国家留学基金和国家自然科学基金资助课题,No 39870891
摘    要:目的研究超氧阴离子对牛主动脉平滑肌细胞内钙及收缩性的影响。方法采用Fura-2测定牛肺动脉平滑肌细胞内钙及采用胶原凝胶实验方法分析平滑肌细胞的收缩性。结果超氧阴离子作用于平滑肌细胞后使ATP(10μmol·L-1)诱导的细胞内钙浓度的增加从(206± 10) nmol·L-1降到(147±15) nmol·L-1。 5 min内细胞内钙浓度增加的积分(∫ △[Ca2+]i·dt)从(12.2± 0.5)μmol· L-1·s-1降至(9.8± 0.8)μmol·L-1·s-1。thapsigargin在无钙溶液中诱导的细胞内钙浓度的增加不受超氧阴离子的影响,而在含钙的Kreba溶液中,超氧阴离子能使随后的钙释放激活的钙进入(△[Ca2+]iCRAC)从(27.3 ±1.0) nmol·L-1降到(13.5 ±1.0) nmol·L-1。ATP诱导的凝胶面积减少的百分比从24%±5%降到 7.4% ±0.2%;在无钙 Krebs溶液中,thapsigargin诱导的凝胶面积减少的百分比从 3.5%± 0.6%降到-0.5%±0.7%。结论超氧阴离子通过影响平滑肌细胞的内钙动员而降低它的收缩性。

关 键 词:  血管平滑肌  细胞培养  主动脉  黄嘌呤氧化酶  三磷酸腺苷

The effects of superoxide anion on intracellular Ca~(2 ) concentration and contractility in cultured bovine aortic smooth muscle cells
CHENG Wei,LI Zhi,Tetsuya Koyama,Masahiro Oike,Yushi Ito.The effects of superoxide anion on intracellular Ca~(2 ) concentration and contractility in cultured bovine aortic smooth muscle cells[J].Chinese Pharmacological Bulletin,2001,17(2):190-193.
Authors:CHENG Wei  LI Zhi  Tetsuya Koyama  Masahiro Oike  Yushi Ito
Abstract:AIM To study the effects of superoxide anion (O.2) on Ca2+ homeostasi and contractility in cultured bovine aortic smooth muscle cell. METHODS Using Fura-2 fluorescence technique to determine Ca2+ level and collagen gel contraction system to analyze muscle contractility. RESULTS ATP (10 μmol*L-1 )-induced Ca2+ transient was smaller in xanthine oxidase treated cells(X/XO) than control. The mean peak increment of [Ca2+]i(△[Ca2+]i peak) and the time integral of the elevated [Ca2+]i(∫△[Ca2+]i dt) for 5 min were decreased from (206.1±10.2) to (147.4±14.7) nmol·L-1,and from (12.2±0.5) to (9.8±0.8) μmol·L-1·s-1. Δ[Ca2+]i peak induced by thapsigargin(1 μmol·L-1 )in Ca2+-free solution was not affected by X/XO, but was decreased from (27.3±1.0) nmol·L-1 to (13.5±1.0) nmol·L-1 in Ca2+-containing solution because of the activation of CRAC(△[Ca2+]i CRAC). X/XO accelerated the velocity of thapsigargin-induced Ca2+ leak from (78.7±3.4) s to (64.8±4.40) s. Gel contraction area in X/XO-treated cells induced by ATP or thapsigargin (in Ca2+ free solution and in Krebs solution)was decreased from 23.6%±4.6% to 7.4%±0.2%, from 3.5%±0.6% to -1.0%±0.5%, and from 7.9%±1.4% to -0.5%±0.7%, respectively. CONCLUTION O.2 attenuats smooth muscle contraction by impairing some of Ca2+ mobilization pathways.
Keywords:calcium  vascular smooth muscle  cultured cells  aorta  xanthine oxidase  adenosine triphosphate
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