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温度降低对豚鼠盲肠带对拟胆碱药反应性的影响。

Effect of temperature reduction on responsiveness to cholinomimetics in the taenia caeci of the guinea-pig.

作者信息

Darroch S A, Gardner A, Vong Y M, Choo L K, Mitchelson F

机构信息

School of Pharmacology, Victorian College of Pharmacy, Parkville, Australia.

出版信息

J Auton Pharmacol. 1991 Apr;11(2):109-19. doi: 10.1111/j.1474-8673.1991.tb00250.x.

Abstract
  1. The effect of temperature reduction on the interaction of carbachol (CCh) and McN-A-343 (McN) with muscarinic receptors in the guinea-pig taenia caeci was investigated. 2. McN, a partial agonist, acted on the smooth muscle to produce contraction. The response was unaffected by tetrodotoxin and the pKB for inhibition by pirenzepine was 6.8, indicating that ganglionic M1 receptors were not involved in the response. 3. Reduction in temperature from 37 degrees C to 18 degrees C for 3 h led to a marked reduction in the contractile response to McN (2-200 microM) but no reduction in the response to CCh (0.1-3 microM). 4. The reduction in temperature was not accompanied by any change in the affinity of McN or CCh for muscarine receptors in binding experiments with [3H]-QNB. 5. The KA value for CCh determined after irreversible receptor inactivation with propylbenzilylcholine mustard followed by ca 60-min wash-out was 7.6 microM, a value similar to that obtained in binding experiments. 6. The EC50 for McN in producing contraction at 37 degrees C (2.1 microM) was similar to the KA value for the partial agonist obtained in experiments with the irreversible antagonist phenoxybenzamine (2.5 microM). It was also similar to the KB value determined at 18 degrees C (3.4 microM) when McN could be used as an antagonist of contractions to CCh. 7. At 18 degrees C, phosphatidylinositol (PI) hydrolysis by CCh was reduced to 23% of that at 37 degrees C. 8. It is concluded that reduction of muscarinic receptor activation of the PI pathway by cholinomimetics with lowering of the temperature could account for the findings with McN on contractility.
摘要
  1. 研究了温度降低对豚鼠盲肠带中卡巴胆碱(CCh)和 McN - A - 343(McN)与毒蕈碱受体相互作用的影响。2. McN 作为部分激动剂,作用于平滑肌产生收缩。该反应不受河豚毒素影响,哌仑西平抑制反应的 pKB 为 6.8,表明神经节 M1 受体不参与该反应。3. 温度从 37℃降至 18℃持续 3 小时导致对 McN(2 - 200μM)的收缩反应显著降低,但对 CCh(0.1 - 3μM)的反应未降低。4. 在与[3H] - QNB 的结合实验中,温度降低并未伴随 McN 或 CCh 对毒蕈碱受体亲和力的任何变化。5. 用丙基苯甲酰胆碱氮芥不可逆地使受体失活并冲洗约 60 分钟后测定的 CCh 的 KA 值为 7.6μM,该值与结合实验中获得的值相似。6. McN 在 37℃产生收缩的 EC50(2.1μM)与在用不可逆拮抗剂苯氧苄胺的实验中获得的部分激动剂的 KA 值(2.5μM)相似。当 McN 用作 CCh 收缩的拮抗剂时,它也与在 18℃测定的 KB 值(3.4μM)相似。7. 在 18℃时,CCh 引起的磷脂酰肌醇(PI)水解降至 37℃时的 23%。8. 得出结论,随着温度降低,拟胆碱药对 PI 途径的毒蕈碱受体激活的减少可以解释 McN 对收缩性的研究结果。

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