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[自发性高血压大鼠在动脉高血压发生前及发生过程中非典型β-肾上腺素能介导的舒张功能受损]

[Impairment of atypical beta-adrenergic-mediated relaxation in spontaneously hypertensive rats before and during the development of arterial hypertension].

作者信息

Mallem Y, Gogny M, Gautier F, Bucas V, Desfontis J Cl

机构信息

Unité de pharmacologie fonctionnelle UPSP 5304 Ecole nationale vétérinaire de Nantes.

出版信息

Arch Mal Coeur Vaiss. 2003 Jul-Aug;96(7-8):804-7.

Abstract

The aims of this study was to characterize the functional response of atypical beta-adrenoceptors (beta-AR) in rat aorta and to investigate whether this relaxation was altered before and during the development of hypertension. Aortic rings from 4 or 12 weeks old Wistar Kyoto (WKY) rats or spontaneously hypertensive rats (SHR) were placed in organ baths and constricted with phenylephrine. Then, cumulative concentration-relaxation curves to the beta-AR agonists were constructed. In intact aortic rings from 12 weeks old WKY rats, CGP 12,177 (CGP) and cyanopindolol (partial beta 3-AR agonists and atypical beta-AR agonists with beta 1/beta 2-AR antagonist properties) produced concentration-dependent relaxation (pD2 = 5.09 +/- 0.03; Emax = 60.4 +/- 2.5%; n = 9; pD2 = 6.17 +/- 0.05; Emax = 95.9 +/- 1%; n = 5 respectively). The endothelium removal did not modify this relaxation. In 12 weeks old WKY rats, the endothelium-independent relaxation to CGP was not modified in the presence of nadolol (beta 1/beta 2-AR antagonist) or L-748 337 (beta 3-AR antagonist) excluding the participation of beta 1, beta 2 et beta 3-AR in this effect. By contrast, this relaxation was significantly inhibited by CGP 20712A or bupranolol, atypical beta-AR antagonists at high concentrations. In 12 weeks old SHR, endothelium-independent relaxation to CGP or cyanopindolol was greatly inhibited. In order to sought out whether impairment of atypical beta-AR-mediated relaxation was due to hypertension, experiments were performed in 4 weeks old SHR. At this age, CGP-induced relaxation was greatly inhibited compared to that obtained in age-matched WKY rats. In 12 weeks old SHR pretreated with pertussis toxin (10 micrograms/kg i.p./3 days), the relaxant effect to CGP was partly restored. We conclude that the atypical beta-AR were functionally expressed in aortic vascular smooth muscle cells of rat aorta. In 4 or 12 weeks old SHR rats, atypical beta-AR-mediated relaxation was impaired, suggesting that this dysfunction occurs before the establishment of hypertension. Gi proteins may be one of the factors that contributes to this impairment.

摘要

本研究的目的是表征大鼠主动脉中非典型β-肾上腺素能受体(β-AR)的功能反应,并研究在高血压发生之前和期间这种舒张作用是否发生改变。将4周或12周龄的Wistar Kyoto(WKY)大鼠或自发性高血压大鼠(SHR)的主动脉环置于器官浴槽中,并用去氧肾上腺素使其收缩。然后,构建β-AR激动剂的累积浓度-舒张曲线。在12周龄WKY大鼠的完整主动脉环中,CGP 12,177(CGP)和氰吲哚洛尔(部分β3-AR激动剂以及具有β1/β2-AR拮抗剂特性的非典型β-AR激动剂)产生浓度依赖性舒张(pD2 = 5.09±0.03;Emax = 60.4±2.5%;n = 9;pD2 = 6.17±0.05;Emax = 95.9±1%;n = 5)。去除内皮并未改变这种舒张作用。在12周龄WKY大鼠中,在存在纳多洛尔(β1/β2-AR拮抗剂)或L-748 337(β3-AR拮抗剂)的情况下,对CGP的非内皮依赖性舒张作用未改变,排除了β1、β2和β3-AR参与此效应。相比之下,这种舒张作用在高浓度时被非典型β-AR拮抗剂CGP 20712A或布普诺洛尔显著抑制。在12周龄SHR中,对CGP或氰吲哚洛尔的非内皮依赖性舒张作用被极大抑制。为了探究非典型β-AR介导的舒张作用受损是否归因于高血压,在4周龄SHR中进行了实验。在这个年龄,与年龄匹配的WKY大鼠相比,CGP诱导的舒张作用被极大抑制。在12周龄经百日咳毒素预处理(10微克/千克腹腔注射/3天)的SHR中,对CGP的舒张作用部分恢复。我们得出结论,非典型β-AR在大鼠主动脉的血管平滑肌细胞中功能性表达。在4周或12周龄的SHR大鼠中,非典型β-AR介导的舒张作用受损,表明这种功能障碍在高血压确立之前就已发生。Gi蛋白可能是导致这种功能障碍的因素之一。

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