Padilla J, López R M, López P, Castillo M C, Querejeta E, Ruiz A, Castillo E F
Sección de Estudios de Posgrado e Investigación, Escuela Superior de Medicina, Instituto Politécnico Nacional, México, DF, México.
Braz J Med Biol Res. 2014 Sep;47(9):789-98. doi: 10.1590/1414-431x20143073. Epub 2014 Aug 1.
We examined the contractile responsiveness of rat thoracic aortas under pressure overload after long-term suprarenal abdominal aortic coarctation (lt-Srac). Endothelium-dependent angiotensin II (ANG II) type 2 receptor (AT2R)-mediated depression of contractions to ANG II has been reported in short-term (1 week) pressure-overloaded rat aortas. Contractility was evaluated in the aortic rings of rats subjected to lt-Srac or sham surgery (Sham) for 8 weeks. ANG I and II levels and AT2R protein expression in the aortas of lt-Srac and Sham rats were also evaluated. lt-Srac attenuated the contractions of ANG II and phenylephrine in the aortas in an endothelium-independent manner. However, lt-Srac did not influence the transient contractions induced in endothelium-denuded aortic rings by ANG II, phenylephrine, or caffeine in Ca2+-free medium or the subsequent tonic constrictions induced by the addition of Ca2+ in the absence of agonists. Thus, the contractions induced by Ca2+ release from intracellular stores and Ca2+ influx through stored-operated channels were not inhibited in the aortas of lt-Srac rats. Potassium-elicited contractions in endothelium-denuded aortic rings of lt-Srac rats remained unaltered compared with control tissues. Consequently, the contractile depression observed in aortic tissues of lt-Srac rats cannot be explained by direct inhibition of voltage-operated Ca2+ channels. Interestingly, 12-O-tetradecanoylphorbol-13-acetate-induced contractions in endothelium-denuded aortic rings of lt-Srac rats were depressed in the presence but not in the absence of extracellular Ca2+. Neither levels of angiotensins nor of AT2R were modified in the aortas after lt-Srac. The results suggest that, in rat thoracic aortas, lt-Srac selectively inhibited protein kinase C-mediated activation of contraction that is dependent on extracellular Ca2+ entry.
我们研究了长期肾上腺上腹部主动脉缩窄(lt-Srac)后压力过载情况下大鼠胸主动脉的收缩反应性。在短期(1周)压力过载的大鼠主动脉中,已报道存在内皮依赖性血管紧张素II(ANG II)2型受体(AT2R)介导的对ANG II收缩反应的抑制作用。对接受lt-Srac或假手术(Sham)8周的大鼠主动脉环的收缩性进行了评估。还评估了lt-Srac大鼠和假手术大鼠主动脉中ANG I和II的水平以及AT2R蛋白表达。lt-Srac以不依赖内皮的方式减弱了主动脉中ANG II和去氧肾上腺素的收缩作用。然而,lt-Srac并不影响无钙培养基中ANG II、去氧肾上腺素或咖啡因在内皮剥脱的主动脉环中诱导的瞬时收缩,也不影响在无激动剂情况下添加Ca2+后随后的强直收缩。因此,lt-Srac大鼠主动脉中由细胞内钙库释放Ca2+和通过储存-操纵性通道内流Ca2+所诱导的收缩未受抑制。与对照组织相比,lt-Srac大鼠内皮剥脱的主动脉环中钾离子诱导的收缩保持不变。因此,lt-Srac大鼠主动脉组织中观察到的收缩抑制不能用对电压门控Ca2+通道的直接抑制来解释。有趣的是,在有细胞外Ca2+存在但无细胞外Ca2+时不存在的情况下,lt-Srac大鼠内皮剥脱的主动脉环中12-O-十四烷酰佛波醇-13-乙酸酯诱导的收缩受到抑制。lt-Srac后主动脉中血管紧张素和AT2R的水平均未改变。结果表明,在大鼠胸主动脉中,lt-Srac选择性抑制了依赖细胞外Ca2+内流的蛋白激酶C介导的收缩激活。