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卡巴胆碱诱发的豚鼠回肠平滑肌在接近冰点时收缩的机制。

Mechanism of carbachol-evoked contractions of guinea-pig ileal smooth muscle close to freezing point.

作者信息

Blackwood A M, Bolton T B

机构信息

Department of Pharmacology and Clinical Pharmacology, St George's Hospital Medical School, London.

出版信息

Br J Pharmacol. 1993 Aug;109(4):1029-37. doi: 10.1111/j.1476-5381.1993.tb13725.x.

Abstract
  1. The effect of lowering the temperature to near freezing-point upon the contractions and [3H]-inositol phosphate responses to carbachol were investigated in longitudinal smooth muscle from the guinea-pig ileum. 2. The peak amplitude of the contraction to a single application of 100 microM carbachol was the same at 37 degrees C and temperatures near freezing-point. However, the sensitivity to carbachol was reduced upon lowering the temperature and the time to peak contraction was increased from 5-10 s to 2-10 min. Even when the temperature was maintained near freezing-point, washing off carbachol produced a relaxation and eventual return of tension to basal levels. 3. Incubating the tissue in 140 mM K+, calcium-free solution or in calcium channel antagonists significantly reduced the carbachol-induced contraction to 10-30% of the control at 37 degrees C and also at 3 degrees C. Thus the majority of the activator calcium required for contraction entered the tissue via voltage-dependent calcium channels (VDCs) at both 37 degrees C and 3 degrees C. 4. The contractions produced by high potassium solutions were less at temperatures close to freezing-point than those at 37 degrees C suggesting that voltage-dependent calcium entry was inhibited as the temperature was lowered. 5. A small part of the contractile response to 100 microM carbachol was resistant to the removal of extracellular calcium at both 37 degrees C and 3 degrees C and this component was increased under depolarizing conditions. This suggests that the release of stored calcium contributes to a minor degree to contraction at both 37 degrees C and 3 degrees C.6. Although 100 microM carbachol produced a statistically significant rise in several [3H]-inositol phosphate isomers at both 37 degrees C and 3 degrees C, the production of [3H]-inositol phosphates was less at 3 degrees C than at 37 degrees C and the increase in their production caused by carbachol was much slower.7. These results suggest that the carbachol-induced contraction at 3 degrees C utilizes both calcium entry through VDCs and calcium release from intracellular stores, as at 37 degrees C. The components of the responses dependent upon intracellular calcium release at 37 degrees C and at temperatures near freezing-point were similar. However, the production of [3H]-inositol phosphates, including the calcium-mobilizing second messenger inositol (1,4,5) trisphosphate (Ins(1,4,5)P3), is reduced at such low temperatures.
摘要
  1. 研究了将温度降至接近冰点对豚鼠回肠纵行平滑肌收缩及对卡巴胆碱的[3H]-肌醇磷酸反应的影响。2. 单次应用100微摩尔卡巴胆碱引起的收缩峰值幅度在37℃和接近冰点的温度下相同。然而,降低温度时对卡巴胆碱的敏感性降低,收缩达到峰值的时间从5 - 10秒增加到2 - 10分钟。即使温度维持在接近冰点,洗去卡巴胆碱也会引起松弛,张力最终恢复到基础水平。3. 将组织置于140毫摩尔钾离子、无钙溶液或钙通道拮抗剂中孵育,在37℃和3℃时,均能显著将卡巴胆碱诱导的收缩降低至对照的10% - 30%。因此,收缩所需的大部分激活钙在37℃和3℃时均通过电压依赖性钙通道(VDCs)进入组织。4. 高钾溶液引起的收缩在接近冰点的温度下比在37℃时小,这表明随着温度降低,电压依赖性钙内流受到抑制。5. 对100微摩尔卡巴胆碱的收缩反应的一小部分在37℃和3℃时均对细胞外钙的去除有抗性,并且在去极化条件下该成分增加。这表明在37℃和3℃时,储存钙的释放对收缩有较小程度的贡献。6. 虽然100微摩尔卡巴胆碱在37℃和3℃时均使几种[3H]-肌醇磷酸异构体在统计学上有显著升高,但在3℃时[3H]-肌醇磷酸的产生比在37℃时少,且卡巴胆碱引起的其产生增加要慢得多。7. 这些结果表明,在3℃时卡巴胆碱诱导的收缩与在37℃时一样,利用了通过VDCs的钙内流和细胞内储存钙的释放。在37℃和接近冰点的温度下,依赖于细胞内钙释放的反应成分相似。然而,在如此低的温度下,包括钙动员第二信使肌醇(1,4,5)三磷酸(Ins(1,4,5)P3)在内的[3H]-肌醇磷酸的产生减少。

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