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去-精氨酸9-缓激肽诱导单个牛气管平滑肌细胞内钙离子浓度升高。

Des-Arg9-bradykinin-induced increases in intracellular calcium ion concentration in single bovine tracheal smooth muscle cells.

作者信息

Marsh K A, Hill S J

机构信息

Department of Physiology and Pharmacology, University of Nottingham Medical School, Queen's Medical Centre.

出版信息

Br J Pharmacol. 1994 Jul;112(3):934-8. doi: 10.1111/j.1476-5381.1994.tb13170.x.

Abstract
  1. Dynamic video imaging was used to measure the des-Arg9-bradykinin-induced changes in the intracellular free calcium ion concentration ([Ca2+]i) of single bovine tracheal smooth muscle (BTSM) cells. 2. In the presence of extracellular calcium ions, des-Arg9-bradykinin (1 nM-10 microM) produced a concentration-dependent increase in the [Ca2+]i over basal levels yielding an EC50 value of 316 nM. The percentage of cells responding to each concentration of des-Arg9-bradykinin also increased in a concentration-dependent manner (from 9% to 100%). 3. The bradykinin B2 receptor antagonist, D-Arg[Hyp3,Thi5,8,D-Phe7]-bradykinin (10 microM), was without effect on the calcium response of the cells when added 2 min prior to des-Arg9-bradykinin (100 nM). However, the B1 receptor antagonist, des-Arg9Leu8-bradykinin (10 microM), completely abolished the des-Arg9-bradykinin-induced response. 4. Under calcium-free conditions, des-Arg9-bradykinin induced an increase in [Ca2+]i at concentrations of 1 microM and 10 microM. The response to 10 microM des-Arg9-bradykinin was reduced by preincubation of either D-Arg[Hyp3, Thi5,8,D-Phe7]-bradykinin (10 microM) or des-Arg9Leu8-bradykinin (10 microM). 5. We conclude that bradykinin B1 receptors are expressed by cultured BTSM cells and mediate the des-Arg9-bradykinin-induced influx of calcium ions at low agonist concentrations (< 1 microM). At higher concentrations, des-Arg9-bradykinin (1 microM and 10 microM) can stimulate both B1 and B2 receptors to effect intracellular calcium release under calcium-free conditions.
摘要
  1. 采用动态视频成像技术测量去-精氨酸9-缓激肽诱导的单个牛气管平滑肌(BTSM)细胞内游离钙离子浓度([Ca2+]i)的变化。2. 在细胞外存在钙离子的情况下,去-精氨酸9-缓激肽(1 nM - 10 microM)使[Ca2+]i浓度依赖地高于基础水平增加,产生的半数有效浓度(EC50)值为316 nM。对每种浓度去-精氨酸9-缓激肽作出反应的细胞百分比也呈浓度依赖性增加(从9%增至100%)。3. 缓激肽B2受体拮抗剂D-Arg[Hyp3,Thi5,8,D-Phe7]-缓激肽(10 microM),在去-精氨酸9-缓激肽(100 nM)加入前2分钟添加时,对细胞的钙反应无影响。然而,B1受体拮抗剂去-精氨酸9-亮氨酸8-缓激肽(10 microM)完全消除了去-精氨酸9-缓激肽诱导的反应。4. 在无钙条件下,去-精氨酸9-缓激肽在1 microM和10 microM浓度时诱导[Ca2+]i增加。对10 microM去-精氨酸9-缓激肽的反应,可被预先孵育D-Arg[Hyp3,Thi5,8,D-Phe7]-缓激肽(10 microM)或去-精氨酸9-亮氨酸8-缓激肽(10 microM)降低。5. 我们得出结论,培养的BTSM细胞表达缓激肽B1受体,并在低激动剂浓度(<1 microM)下介导去-精氨酸9-缓激肽诱导的钙离子内流。在较高浓度下,去-精氨酸9-缓激肽(1 microM和10 microM)在无钙条件下可刺激B1和B2受体以影响细胞内钙释放。

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