首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effects of muscarinic M2 and M3 receptor stimulation and antagonism on responses to isoprenaline of guinea-pig trachea in vitro.
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Effects of muscarinic M2 and M3 receptor stimulation and antagonism on responses to isoprenaline of guinea-pig trachea in vitro.

机译:毒蕈碱M2和M3受体的刺激和拮抗作用对豚鼠气管对异丙肾上腺素反应的影响。

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摘要

1. In guinea-pig and canine airway smooth muscle, there is reduced beta-adrenoceptor agonist sensitivity in tissues pre-contracted with muscarinic agonists when compared to tissues pre-contracted with other spasmogens, such as histamine or leukotriene D4. This reduced sensitivity may be the result of an interaction between muscarinic receptors and beta-adrenoceptors. In this study the effects of M2 receptor antagonism and stimulation have been investigated on the relaxant potency of isoprenaline in guinea-pig isolated tracheal smooth muscle. 2. (+)-cis-Dioxolane contracted isolated tracheal strips in a concentration-dependent manner (EC50 = 11.5 +/- 0.9 nM). The rank order of antagonist apparent affinities (with pA2 values in parentheses) was atropine (9.4 +/- 0.1) > zamifenacin (8.2 +/- 0.1) > para-fluoro-hexahydro-siladiphenidol (p-F-HHSiD, 7.2 +/- 0.1) > pirenzepine (6.5 +/- 0.1) > methoctramine (5.5 +/- 0.1). Schild slopes were not significantly different from unity. This was consistent with a role of muscarinic M3 receptors in mediating contraction. 3. In tissues pre-contracted to 3 g isometric tension using (+)-cis-dioxolane (0.2 microM, approximately EC80), the relaxant potency of isoprenaline was significantly (P < 0.05) increased by 0.3 microM methoctramine (control EC50 = 32.2 +/- 4.3 nM, plus methoctramine EC50 = 19.1 +/- 4.5 nM). This concentration of methoctramine had no effect on contractile responses to (+)-cis-dioxolane (control, EC50 = 17.6 +/- 3.2 nM, plus methoctramine, EC50 = 21.0 +/- 4.4 nM).(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在豚鼠和犬气道平滑肌中,与使用其他痉挛源(例如组胺或白三烯D4)预先收缩的组织相比,经毒蕈碱激动剂预先收缩的组织的β-肾上腺素受体激动剂敏感性降低。这种降低的敏感性可能是毒蕈碱受体与β-肾上腺素受体之间相互作用的结果。在这项研究中,已研究了M2受体拮抗作用和刺激作用对豚鼠离体气管平滑肌中异丙肾上腺素的松弛作用。 2.(+)-顺-二氧戊环以浓度依赖的方式收缩分离的气管带(EC50 = 11.5 +/- 0.9 nM)。拮抗剂表观亲和力的等级顺序(括号中为pA2值)为阿托品(9.4 +/- 0.1)>扎米非那汀(8.2 +/- 0.1)>对氟-六氢-硅二氮杂酚(pF-HHSiD,7.2 +/- 0.1 )>哌仑西平(6.5 +/- 0.1)>甲基辛巴明(5.5 +/- 0.1)。希尔德坡度与统一没有显着差异。这与毒蕈碱M3受体在介导收缩中的作用一致。 3.在使用(+)-顺-二氧戊环(0.2 microM,约EC80)预收缩至3 g等轴测张力的组织中,异丙肾上腺素的松弛力显着提高(P <0.05),增加0.3 microM methoctramine(对照EC50 = 32.2) +/- 4.3 nM,再加上甲基辛胺EC50 = 19.1 +/- 4.5 nM。甲基辛巴胺的这一浓度对(+)-顺-二氧戊环的收缩反应没有影响(对照,EC50 = 17.6 +/- 3.2 nM,加上甲基辛巴胺,EC50 = 21.0 +/- 4.4 nM)(摘要截断为250字)。

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