王斌, 张孝清, 王金唏, 杨思军, 肖继皋. 钙拮抗剂TMB-8抑制BHQ,NE和KCl引起的培养乳牛基底动脉单个平滑肌细胞内游离钙的升高J. 药学学报, 1997, 32(11): 819-823.
引用本文: 王斌, 张孝清, 王金唏, 杨思军, 肖继皋. 钙拮抗剂TMB-8抑制BHQ,NE和KCl引起的培养乳牛基底动脉单个平滑肌细胞内游离钙的升高J. 药学学报, 1997, 32(11): 819-823.
B Wang, XQ Zhang, JX Wang SJ Yang , JG Xiao, . 8-(N,N-DIETHYLAMINO)-n-OCTYL-3,4,5-TRIMETHOXYBENZOATE(TMB-8) REDUCED THE ELEVATION OF Ca2+i INDUCED BY BHQ, NE AND KCl IN CULTURED SINGLE SMOOTH MUSCLE CELLS OF THE CALF BASILAR ARTERYJ. Acta Pharmaceutica Sinica, 1997, 32(11): 819-823.
Citation: B Wang, XQ Zhang, JX Wang SJ Yang , JG Xiao, . 8-(N,N-DIETHYLAMINO)-n-OCTYL-3,4,5-TRIMETHOXYBENZOATE(TMB-8) REDUCED THE ELEVATION OF Ca2+i INDUCED BY BHQ, NE AND KCl IN CULTURED SINGLE SMOOTH MUSCLE CELLS OF THE CALF BASILAR ARTERYJ. Acta Pharmaceutica Sinica, 1997, 32(11): 819-823.

钙拮抗剂TMB-8抑制BHQ,NE和KCl引起的培养乳牛基底动脉单个平滑肌细胞内游离钙的升高

8-(N,N-DIETHYLAMINO)-n-OCTYL-3,4,5-TRIMETHOXYBENZOATE(TMB-8) REDUCED THE ELEVATION OF Ca2+i INDUCED BY BHQ, NE AND KCl IN CULTURED SINGLE SMOOTH MUSCLE CELLS OF THE CALF BASILAR ARTERY

  • 摘要: 用ARCMMIC阳离子测定系统,测量单个细胞内游离钙浓度(Ca2+i),研究8-(N,N-二乙胺)-n-辛基3,4,5-三甲氧基苯甲酸酯(TMB-8)对培养乳牛基底动脉平滑肌Ca2+i的作用。在细胞外钙浓度为1.3mmol·L-1时,TMB-8(30μmol·L-1)可明显抑制BHQ,NE及KCl引起Ca2+i的升高。在细胞外钙为零+EGTA 0.1mmol·L-1时,TMB-8(10,30及100μmol·L-1)可浓度依赖性地降低静息Ca2+i,TMB-8(30μmol·L-1)可几乎完全阻断BHQ及NE引起Ca2+i的增加。研究表明TMB-8降低培养乳牛基底动脉平滑肌Ca2+i的机制,主要是抑制肌浆网Ca2+的释放,或增加肌浆网对Ca2+的摄入,并由此间接地抑制细胞外钙的内流。

     

    Abstract: The effect of 8-(N,N-diethylamino)-n-octyl-3,4,5-trimethoxybenzoate (TMB-8) on the elevation of Ca2+i induced by 2,5-di(tert-butyl)-1,4-benzohydroquinone (BHQ), norepinephrine (NE), KCl in cultured single smooth muscle cells of the calf basilar artery was studied by a system of measurement of AR-CM-MIC, using Fura-2/AM as a fluoresent indicator. In the presence of extracellular Ca2+ 1.3 mmol·L-1, the resting Ca2+i was not changed by TMB-8 (10, 30 and 100 μmol·L-1), but the elevation of Ca2+i induced by BHQ, NE and KCl were reduced by TMB-8 (30 μmol·L-1) significantly. In Ca2+ free Hank′s solution containing EGTA 0.1 mmol·L-1, the resting Ca2+i was markedly reduced by TMB-8 (10,30 and 100 μmol·L-1), and the increase of Ca2+i evoked by BHQ and NE was blocked completely by TMB-8 (30 μmol·L-1). The result suggested that TMB-8 inhibited the Ca2+ release from intracellular stores or increased the up-take of Ca2+ into sarcoplasmic reticulum and the inhibition of Ca2+-influx from extracellular site may be an indirect machanism.

     

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