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海蟾蜍中神经降压素的纯化、特性鉴定及致痉活性

Purification, characterization, and spasmogenic activity of neurotensin from the toad Bufo marinus.

作者信息

Warner F J, Burcher E, Carraway R, Conlon J M

机构信息

School of Physiology and Pharmacology, University of New South Wales, Sydney, Australia.

出版信息

Peptides. 1998;19(7):1255-61. doi: 10.1016/s0196-9781(98)00063-1.

Abstract

Neurotensin (NT) was isolated from an extract of the intestine of the cane toad, Bufo marinus and its primary structure established as: pGlu-Ala-Ile-Val-Ser-Lys-Ala-Arg-Arg-Pro-Tyr-Ile-Leu. This amino acid sequence shows five substitutions (Leu2 --> Ala, Tyr3 --> Ile, Glu4 --> Val, Asn5 --> Ser, and Pro7 --> Ala) compared with bovine NT. Synthetic Bufo NT (pD2 = 8.05 +/- 0.28) was equipotent and equally effective as bovine NT (pD2 = 8.24 +/- 0.38) in producing spasmogenic contraction of isolated segments of toad small intestine. However, the maximum response produced by Bufo NT was only 35 +/- 2% of that produced by substance P. The potencies, but not the maximum responses, to Bufo and bovine NT were significantly (p < 0.05) attenuated by pre-treatment with atropine but neither parameter was significantly diminished by tetrodotoxin and indomethacin. The data suggest that the action of NT involves interaction with receptors on toad intestinal smooth muscle that recognize the C-terminal region of NT (residues 8-13) that has been fully conserved during evolution of tetrapods. Contractile activity is mediated, at least in part, by release of acetylcholine.

摘要

神经降压素(NT)是从海蟾蜍(Bufo marinus)的肠道提取物中分离出来的,其一级结构确定为:pGlu-Ala-Ile-Val-Ser-Lys-Ala-Arg-Arg-Pro-Tyr-Ile-Leu。与牛NT相比,该氨基酸序列显示出五个取代(Leu2→Ala、Tyr3→Ile、Glu4→Val、Asn5→Ser和Pro7→Ala)。合成的蟾蜍NT(pD2 = 8.05±0.28)在引起蟾蜍小肠离体节段痉挛性收缩方面与牛NT(pD2 = 8.24±0.38)具有同等效力且效果相同。然而,蟾蜍NT产生的最大反应仅为P物质产生的最大反应的35±2%。阿托品预处理可显著(p<0.0)减弱对蟾蜍和牛NT的效力,但不减弱最大反应,而河豚毒素和吲哚美辛均未显著降低这两个参数。数据表明,NT的作用涉及与蟾蜍肠道平滑肌上识别NT C末端区域(第8 - 13位残基)的受体相互作用,该区域在四足动物进化过程中完全保守。收缩活性至少部分由乙酰胆碱的释放介导。

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