Chand N
Res Commun Chem Pathol Pharmacol. 1979 Aug;25(2):215-26.
Isolated rat lung parenchymal strips responded to carbachol, 5-HT and phenylephrine (PE) with contractions. Bradykinin (BK), histamine, PGF2 alpha, PGE1, PGE2 and dimaprit were either inactive or produced weak relaxations. Isoproterenol, noradrenaline (NA) and epinephrine (E) relaxed lung strips. The further increase in their concentrations produced contractions of varying magnitudes. The lung strips contracted to 5-HT or carbachol, responded to isoproterenol and E and NA with relaxations. Metiamide and cimetidine (selective histamine H2-receptor antagonists) did not alter responses to histamine and carbachol. Propranolol (a beta-adrenoceptor blocker) antagnoized or reversed relaxations to E and isoproterenol, and markedly enhanced contractions to NA, PE and E. Atropine and phentolamine or dibenzyline antagonized contractions to carbachol and sympathomimetic agents, respectively. From study it may be concluded that there are alpha- and beta-adrenergic receptors mediating contractions and relaxations in the peripheral airways of rat.
分离的大鼠肺实质条对卡巴胆碱、5-羟色胺和去氧肾上腺素(PE)产生收缩反应。缓激肽(BK)、组胺、前列腺素F2α、前列腺素E1、前列腺素E2和二甲双胍要么无活性,要么产生微弱的舒张反应。异丙肾上腺素、去甲肾上腺素(NA)和肾上腺素(E)使肺条舒张。它们浓度的进一步增加会产生不同程度的收缩。肺条对5-羟色胺或卡巴胆碱收缩,对异丙肾上腺素、E和NA产生舒张反应。甲硫咪胺和西咪替丁(选择性组胺H2受体拮抗剂)不改变对组胺和卡巴胆碱的反应。普萘洛尔(一种β-肾上腺素能受体阻滞剂)拮抗或逆转对E和异丙肾上腺素的舒张反应,并显著增强对NA、PE和E的收缩反应。阿托品和酚妥拉明或苄基乙胺分别拮抗对卡巴胆碱和拟交感神经药的收缩反应。从研究中可以得出结论,在大鼠外周气道中存在介导收缩和舒张的α-和β-肾上腺素能受体。