Cardiovascular Research Center, Shantou University Medical College, Shantou, China.
Bio-analytical Laboratory, Shantou University Medical College, Shantou, China.
Eur J Pharmacol. 2021 Feb 15;893:173828. doi: 10.1016/j.ejphar.2020.173828. Epub 2020 Dec 23.
This study was to determine how endothelium-dependent contractions (EDCs) change in iliac arteries of Wistar-Kyoto (WKYs) and spontaneously hypertensive rats (SHRs) during the transition from adolescence to adulthood and the underlying mechanism(s). We also aimed to elucidate effects of L-798106, an EP3 receptor antagonist, on EDCs and the blood pressure increase in adolescent SHRs. Blood vessels were isolated for functional and biochemical analyses. EDCs were comparable in adolescent iliac arteries of both strains, and contractions to ACh, prostacyclin (PGI), the EP3 receptor agonist sulprostone and the TP receptor agonist U46619 in adult vessels were less prominent compared with those in the adolescents, while the attenuation of vasoconstrictions to ACh, PGI or U46619 with age was to a lesser extent in SHRs. PGI production was decreased to a similar level in adult arteries. TP and EP3 expressions were downregulated in adult vessels, whereas the extent of TP downregulation was less in SHRs. L-798106 partially suppressed the vasoconstrictions to U46619 and attenuated EDCs to a greater extent than SQ29548, and administration of L-798106 blunted the blood pressure increase with age in prehypertensive SHRs. These results demonstrate the comparable EDCs in iliac arteries of the adolescents are decreased in the adults, but relatively larger EDCs in adult SHRs can be a reflection of differential downregulation of TP and EP3 receptors during the transition from adolescence to adulthood. Also, our data suggest that blockade of both TP and EP3 receptors starting from the prehypertensive stage suppresses EDCs and the development of hypertension in SHRs.
这项研究旨在确定从青春期到成年过渡期间,Wistar-Kyoto(WKY)和自发性高血压大鼠(SHR)的髂动脉中内皮依赖性收缩(EDC)如何变化,以及潜在的机制。我们还旨在阐明 EP3 受体拮抗剂 L-798106 对青春期 SHR 的 EDC 和血压升高的影响。分离血管用于功能和生化分析。在两种品系的青春期髂动脉中,EDC 是可比的,而成年血管中对 ACh、前列环素(PGI)、EP3 受体激动剂 sulprostone 和 TP 受体激动剂 U46619 的收缩作用与青春期相比不太明显,而随着年龄的增长,ACh、PGI 或 U46619 的血管收缩减弱程度在 SHR 中较小。PGI 的产生在成年动脉中降低到相似的水平。TP 和 EP3 的表达在成年血管中下调,而 SHR 中的下调程度较小。L-798106 部分抑制 U46619 的血管收缩,并比 SQ29548 更能减弱 EDC,并且在预高血压 SHR 中,L-798106 的给药使年龄相关的血压升高减弱。这些结果表明,青春期髂动脉中可比的 EDC 在成年期降低,但成年 SHR 中相对较大的 EDC 可能反映了从青春期到成年过渡期间 TP 和 EP3 受体的差异下调。此外,我们的数据表明,从预高血压阶段开始阻断 TP 和 EP3 受体可以抑制 SHR 的 EDC 和高血压的发展。