Secretin receptors mediating rat forestomach relaxation.
Secretin receptors mediating rat forestomach relaxation.
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介导大鼠前胃松弛的促胰液素受体。
DOI:
10.1152/ajpgi.1993.264.5.g863
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发表时间:
1993
期刊:
影响因子:
--
通讯作者:
S. Vigna
中科院分区:
文献类型:
--
作者:
T. Steiner;A. Mangel;D. C. Mcvey;S. Vigna
Frozen sections of the rat stomach were incubated with 125I-labeled porcine secretin, and then secretin binding sites were localized by autoradiography. Saturable binding was observed only in the muscularis externa (circular and longitudinal smooth muscle layers) of the proximal nonglandular forestomach. Saturable binding was quantitated by densitometry. 125I-porcine secretin bound to a single class of high-affinity binding sites with a dissociation constant of 0.6 nM. Porcine and rat secretins were nearly equipotent in inhibiting saturable 125I-porcine secretin binding, and vasoactive intestinal polypeptide, peptide histidine-isoleucine, and glucagon were much weaker. Carbachol (100 microM) stimulated a sustained increase in tension in forestomach muscle in vitro, and porcine secretin caused relaxation of this stimulated contraction. We conclude that rat forestomach smooth muscle expresses a high-affinity specific secretin binding site that mediates relaxation. This putative secretin receptor may mediate some of the actions of secretin on gastric motility.