Developmental changes in binding sites and reactivity for CGRP and VIP in porcine pulmonary arteries

被引:9
|
作者
Hislop, AA
Boels, PJ
Deutsch, J
Polak, JM
Haworth, SG
机构
[1] Inst Child Hlth, Vasc Biol & Pharmacol Unit, London WC1N 1EH, England
[2] Royal Postgrad Med Sch, Dept Histochem, London W12 0NN, England
关键词
CGRP; VIP; ligand binding; pulmonary artery; development;
D O I
10.1016/S0196-9781(97)00480-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During postnatal adaptation pulmonary arteries dilate. CGRP and VIP are pulmonary vasodilators. In this report, porcine lungs from newborn to adult were studied. Radiolabeled ligand binding and autoradiography showed CGRP binding sites on the endothelium of pulmonary arteries and veins, which increased postnatally, and VIP binding sites on smooth muscle, which decreased. Isolated conduit arteries relaxed normally (initially endothelium dependent) in response to CGRP from birth. VIP first caused relaxation at 10 days and was endothelium dependent. Age-related changes in receptor binding density were not always reflected in an appropriate alteration in pharmacological response. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:703 / 714
页数:12
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