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人离体支气管对大内皮素-1、大内皮素-2和大内皮素-3的收缩反应以及内皮素转换酶抑制作用

Contraction to big endothelin-1, big endothelin-2 and big endothelin-3, and endothelin-converting enzyme inhibition in human isolated bronchi.

作者信息

Yap E Y, Battistini B, McKay K O

机构信息

Department of Pharmacology, The University of Sydney, New South Wales, Australia.

出版信息

Br J Pharmacol. 2000 Jan;129(1):170-6. doi: 10.1038/sj.bjp.0703006.

Abstract

All three endothelin precursor peptides, i.e. big endothelin-1 (big ET-1), big endothelin-2 (big ET-2) and big endothelin-3 (big ET-3), produced contractile responses in human isolated bronchi, demonstrating the presence of functional endothelin-converting enzyme (ECE) in this tissue. The maximal contractile responses were equal to 108.4+/-8.0% (0.1 microM big ET-1; n=4), 85.2+/-11.8% (0.1 microM big ET-2; n=7) and 43.0+/-7.2% (0.1 microM big ET-3; n=5) of the reference response to acetylcholine (1 mM). The response to big ET-1 (0.1 microM), but not endothelin-1 (ET-1, 0.1 microM), was diminished after overnight storage of the tissue at 4 degrees C, demonstrating instability of the enzyme. The responses to all three big-endothelins were significantly inhibited, by the ECE inhibitors CGS 26393 and CGS 26303, in a concentration-related manner. The responses to the mature peptides ET-1, endothelin-2 (ET-2), and endothelin-3 (ET-3) were unaffected by CGS 26393 and CGS 26303. Phosphoramidon (10 microM) also produced an inhibition of the response to big ET-1 that was equivalent to that produced by CGS 26393 (10 microM). Combination of CGS 26393 (10 microM) and phosphoramidon (10 microM) did not produce an additive inhibition. These results demonstrate the presence of functional ECE for all three big endothelins in human bronchus and inhibition of the enzyme by newly developed orally active ECE inhibitors, as well as phosphoramidon. British Journal of Pharmacology (2000) 129, 170 - 176

摘要

所有三种内皮素前体肽,即大内皮素-1(big ET-1)、大内皮素-2(big ET-2)和大内皮素-3(big ET-3),均可使离体人支气管产生收缩反应,表明该组织中存在功能性内皮素转换酶(ECE)。最大收缩反应分别相当于乙酰胆碱(1 mM)参考反应的108.4±8.0%(0.1 μM big ET-1;n = 4)、85.2±11.8%(0.1 μM big ET-2;n = 7)和43.0±7.2%(0.1 μM big ET-3;n = 5)。在4℃下将组织过夜保存后,对big ET-1(0.1 μM)的反应减弱,但对内皮素-1(ET-1,0.1 μM)的反应未减弱,表明该酶不稳定。ECE抑制剂CGS 26393和CGS 26303以浓度相关的方式显著抑制了对所有三种大内皮素的反应。对成熟肽ET-1、内皮素-2(ET-2)和内皮素-3(ET-3)的反应不受CGS 26393和CGS 26303的影响。磷酰胺素(10 μM)也对big ET-1的反应产生了与CGS 26393(10 μM)相当的抑制作用。CGS 26393(10 μM)和磷酰胺素(10 μM)联合使用未产生相加抑制作用。这些结果表明,人支气管中存在针对所有三种大内皮素的功能性ECE,新开发的口服活性ECE抑制剂以及磷酰胺素可抑制该酶。《英国药理学杂志》(2000年)129卷,170 - 176页

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