Yang Cui, Yang Jinyan, Xu Xiangting, Yan Sanmei, Pan Shitian, Pan Xiaoxia, Zhang Changhong, Leung George Pakheng
Ethnic Drug Screening & Pharmacology Center, Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650500, China; Department of Pharmacology & Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Ethnic Drug Screening & Pharmacology Center, Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650500, China.
Prostaglandins Other Lipid Mediat. 2014 Aug;112:1-8. doi: 10.1016/j.prostaglandins.2014.05.001. Epub 2014 May 28.
The objective of this study was to investigate the 14,15-epoxyeicosatrienoic acid (14,15-EET)-induced vasodilatations as well as the underlying signaling pathways in rat mesenteric arteries from young, adult and old normotensive (WKY) and hypertensive rats. Protein expressions for prostaglandin EP(1-4) receptors, large conductance Ca(2+)-activated K(+) (BK(Ca)) channels, and adenylate cyclase (AC) were determined together with 14,15-EET-induced vasodilatations in primary- versus secondary-branches of the mesenteric artery. Responses to 14,15-EET were greater in the smaller secondary- versus primary-branches (and also more sensitive with lower EC50) and were reduced in vessels from old (80 weeks) rats as well as from vessels from the spontaneous hypertensive rats (SHR). Regardless of age or hypertension responses to 14,15-EET were inhibited by the EP2 antagonist AH6809, BK(Ca) channel inhibitor iberiotoxin, or 3',5'-cyclic monophosphate (cAMP)-protein kinase A (PKA) pathway antagonists. These data indicate 14,15-EET-induced vasodilatation is mediated via the activation of EP2 receptors and opening of BK(Ca) channels. The expressions of the EP2 receptor and AC were markedly reduced in vessels from SHR as well as old rats, whereas BK(Ca) expression was reduced in old WKY and SHR, but not adult SHR. Furthermore, expression of the p53 protein, an indicator of cell senescence and apoptosis, was elevated in adult and old SHR as well as in old WKY. In summary, attenuated 14,15-EET-induced vasodilatation in mesenteric arteries from old normotensive WKY as well as adult and old SHR is associated with reduced expression of EP2 receptors and AC.
本研究的目的是调查14,15-环氧二十碳三烯酸(14,15-EET)诱导的大鼠肠系膜动脉血管舒张以及年轻、成年和老年正常血压(WKY)大鼠和高血压大鼠中潜在的信号通路。测定前列腺素EP(1-4)受体、大电导钙激活钾(BK(Ca))通道和腺苷酸环化酶(AC)的蛋白表达,并结合肠系膜动脉一级分支与二级分支中14,15-EET诱导的血管舒张情况进行分析。14,15-EET对较小的二级分支血管的舒张作用大于一级分支血管(且对较低EC50更敏感),而老年(80周)大鼠以及自发性高血压大鼠(SHR)的血管对其反应减弱。无论年龄或高血压情况如何,EP2拮抗剂AH6809、BK(Ca)通道抑制剂iberiotoxin或3',5'-环磷酸腺苷(cAMP)-蛋白激酶A(PKA)途径拮抗剂均可抑制对14,15-EET的反应。这些数据表明,14,15-EET诱导的血管舒张是通过EP2受体的激活和BK(Ca)通道的开放介导的。SHR以及老年大鼠血管中EP2受体和AC的表达明显降低,而老年WKY和SHR中BK(Ca)的表达降低,但成年SHR中未降低。此外,细胞衰老和凋亡指标p53蛋白在成年和老年SHR以及老年WKY中的表达均升高。总之,老年正常血压WKY以及成年和老年SHR的肠系膜动脉中14,15-EET诱导的血管舒张减弱与EP2受体和AC表达降低有关。