Baroreflex deficiency hampers angiogenesis after myocardial infarction via acetylcholine-7-nicotinic

来源 :中国药理学会第十一次全国学术会议 | 被引量 : 0次 | 上传用户:cxg2009
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  OBJECTIVE Angiogenesis is critical for re-establishing blood supply to ischaemic myocardium after myocardial infarction (MI).Human studies have associated arterial baroreflex (ABR) deficiency with higher rate of sudden death after MI.The present work was designed to examine whether ABR deficiency affects angiogenesis in MI rats.METHODS AND RESULTS Baroreflex sensitivity (BRS) was determined in conscious rats at 1 month after occlusion of the left anterior descending coronary artery.The survival time was significantly shorter in Sprague-Dawley rats with BRS < 0.60 ms/mmHg vs.those with BRS ≥0.60 ms/mmHg.Sinoaortic denervation destroyed ABR, and decreased capillary density, regional blood flow, and vascular endothelial growth factor (VEGF) concentration after MI.Ketanserin (0.6 mg·kg-1 ·d-1) enhanced BRS, and increased capillary density, regional blood flow and VEGF.Sinoaortic denervation also reduced the expression of vesicular acetylcholine (ACh) transporter and 7-nicotinic ACh receptor (7-nAChR).Angiogenesis after MI was significantly attenuated in 7-nAChR knockout mice.In contrast, increase in endogenous ACh with cholinesterase inhibitor pyridostigmine (30 mg·kg-1 · d-1) increased angiogenesis after MI.In cultured cardiac microvascular endothelial cells, ACh stimulated the expression of VEGF, pbesphorylation of VEGF receoptor-2, and tube formation in a manner dependent upon 7-nAChR.CONCLUSION Our results demonstrated that ABR deficiency could attenuate angiogenesis in ischaemic myocardium.These findings provide further mechanistic basis for enhancing baroreflex function in the treatment of MI.
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