Thurman C L, Higgins J T
Department of Medicine, Medical College of Ohio, Toledo.
Biochim Biophys Acta. 1988 Nov 3;945(1):81-91. doi: 10.1016/0005-2736(88)90365-3.
We have observed that serosal catecholamines increase the amplitude of the short-circuit current (Isc) in the toad urinary bladder by as much as 450%. Chemical sympathectomy with 10(-6) M 6-hydroxydopamine and the sympathomimetic effects of 10(-5) M tyramine indicate a reservoir of amines in the serosal stroma of the tissue. The urinary epithelium from the toad responds to six adrenoceptor agonists: (-)-epinephrine, (-)-norepinephrine, (-)-phenylephrine, clonidine, methoxamine and oxymetazoline. The alpha 2-adrenoceptor agonist clonidine is most potent for stimulating Isc. Some agonists were found to diminish Isc. Apparently this is related to a simultaneous increase in the transepithelial flux of both chloride and sodium. The Isc response to the catecholamines is also inhibited by several adrenoceptor antagonists. The alpha 2-adrenoceptor antagonist yohimbine is more effective than the alpha 1-antagonist prazosin for blocking the stimulation of epithelial transport. As a result of these studies, we have tentatively classified the serosal adrenoceptor of the toad urinary bladder as alpha 2.
我们观察到,浆膜儿茶酚胺可使蟾蜍膀胱的短路电流(Isc)幅度增加多达450%。用10⁻⁶ M 6-羟基多巴胺进行化学交感神经切除术以及10⁻⁵ M酪胺的拟交感神经效应表明,该组织的浆膜基质中存在胺类储存库。蟾蜍的尿上皮对六种肾上腺素能受体激动剂有反应:(-)-肾上腺素、(-)-去甲肾上腺素、(-)-去氧肾上腺素、可乐定、甲氧明和羟甲唑啉。α₂-肾上腺素能受体激动剂可乐定对刺激Isc最有效。发现一些激动剂会降低Isc。显然,这与氯化物和钠的跨上皮通量同时增加有关。儿茶酚胺引起的Isc反应也受到几种肾上腺素能受体拮抗剂的抑制。α₂-肾上腺素能受体拮抗剂育亨宾在阻断上皮运输刺激方面比α₁-拮抗剂哌唑嗪更有效。这些研究的结果使我们初步将蟾蜍膀胱的浆膜肾上腺素能受体归类为α₂。