Hung Chi-Feng, Li Hsin-Ju, Chang Hsun-Hao, Lee Gon-Ann, Su Ming Jai
School of Medicine, Fu Jen Catholic University, No. 510 Zhongzheng Road, Xinzhuang District, New Taipei City 24205, Taiwan ; Big Data Research Centre, Fu Jen Catholic University, New Taipei City, Taiwan.
Department of Chemistry, Fu Jen Catholic University, New Taipei City, Taiwan.
Biomed Res Int. 2015;2015:906039. doi: 10.1155/2015/906039. Epub 2015 Mar 1.
The differential effects of a selective kappa- (κ-) opioid receptor agonist, U50488, were elucidated by monitoring the contraction of isolated guinea pig atrial and ventricular muscles. In electrically driven left atria, U50488 in nanomolar concentration range decreased the contractile force. Norbinaltorphimine (norBNI), a selective κ-receptor antagonist, and pertussis toxin (PTX) abolished the negative inotropic effect of U50488. In contrast, the inhibitory effect was not affected by the pretreatment of atropine or propranolol. Even though U50488 exerted a negative inotropic effect in the left atrium, it did not affect the contractile force of the right atrium and ventricles paced at 2 Hz. Similarly, the beating rate of the spontaneously beating right atrium was also unaffected by U50488. These results indicate that the activation of κ-opioid receptors can only produce negative inotropic effect in left atria via activation of PTX-sensitive G protein in guinea pigs. The absence of negative inotropic effects in right atria and ventricles suggests that there may be a greater distribution of functional κ-opioid receptors in guinea pig left atria than in right atria and ventricles, and the distribution of the receptors may be species-specific.
通过监测豚鼠离体心房和心室肌的收缩,阐明了选择性κ-阿片受体激动剂U50488的不同作用。在电驱动的左心房中,纳摩尔浓度范围的U50488降低了收缩力。选择性κ-受体拮抗剂norbinaltorphimine(norBNI)和百日咳毒素(PTX)消除了U50488的负性肌力作用。相反,阿托品或普萘洛尔预处理不影响这种抑制作用。尽管U50488在左心房产生负性肌力作用,但它不影响以2Hz起搏的右心房和心室的收缩力。同样,U50488也不影响自发搏动的右心房的搏动频率。这些结果表明,在豚鼠中,κ-阿片受体的激活仅通过激活PTX敏感的G蛋白在左心房产生负性肌力作用。右心房和心室中不存在负性肌力作用表明,豚鼠左心房中功能性κ-阿片受体的分布可能比右心房和心室中更多,并且受体的分布可能具有物种特异性。