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作 者:周永巧[1,2] 王震[2] 刘莉[1,2] 王微[1,2] 韩愈[2] 陈彩宇[2] 任红梅[2] 何多芬[2] 杨剑[2] 曾春雨[2]
机构地区:[1]汕头大学医学院第一附属医院心血管内科,广东汕头515041 [2]第三军医大学大坪医院野战外科研究所心血管内科,重庆市心血管病研究所,重庆400016
出 处:《第三军医大学学报》2012年第7期581-584,共4页Journal of Third Military Medical University
基 金:国家重点基础研究发展计划(973计划,2012CB517801);国家自然科学基金(31130029);国家杰出青年科学基金(30925018);重庆市杰出青年科学基金(CSTC2009BA5044)~~
摘 要:目的探讨多巴胺D1类受体对神经肽Y(neuropeptide Y,NPY)受体介导的Sprague-Dawley(SD)大鼠原代血管平滑肌细胞(vascular smooth muscle cells,VSMCs)增殖的影响。方法以NPY(10-8~10-11mol/L)刺激SD大鼠胸主动脉培养的VSMCs,观察在D1类多巴胺受体激动剂Fenoldopam(10-8mol/L)存在的情况下,神经肽Y促VSMCs增殖作用的变化。细胞增殖的检测采用[3H]胸腺嘧啶核苷([3H]-TdR)掺入率的变化表示及MTT方法。结果 NPY呈浓度依赖性促进SD大鼠VSMCs的异常增殖,最高增殖幅度达(77±9)%(P<0.05),该增殖作用由NPY Y1受体亚型介导。多巴胺D1类受体激动剂Fenoldopam对VSMCs无增殖影响,但Fenoldopam可抑制NPY Y1亚型受体介导VSMCs的增殖作用,该作用通过PKA途径发挥作用。结论多巴胺D1类受体激活抑制NPY受体介导的促VSMCs增殖作用,可能参与心血管疾病的发生、发展过程。Objective To determine the effect of D1-like dopamine receptor on neuropeptide Y(NPY)-mediated proliferation in primary cultured vascular smooth muscle cells(VSMCs) derived from thoracic aorta of Sprague-Dawley(SD) rats.Methods After VSMCs were isolated from SD rat thoracic aorta and identified by morphology and immunocytocchemistry,the cells at passage 4 to 8 were treated by 10-8 to 10-11 mol/L NPY in presence or absence of D1-like receptor agonist fenoldopam(10-8 mol/L),blocker BIBP3226(10-6 mol/L),or antagonist SCH23390(10-8 mol/L)to observe NPY-mediated proliferation in VSMCs.The proliferation of VSMCs was investigated by -TdR incorporation and MTT assay.Results NPY resulted in an increased proliferation of VSMCs in a concentration-dependent manner,with a maximal proliferative amplitude of(77±9)%(P0.05).D1-like receptor agonist,fenoldopam,completely blocked the NPY Y1-mediated proliferation in VSMCs,although the agonist had no effect on the proliferation of VSMCs by itself,which might be through protein kinase A pathway.Conclusion Activation of D1-like receptor inhibits NPY Y1-mediated proliferation in VSMCs,which might be involved in the pathogenesis of cardiovascular diseases.
关 键 词:多巴胺受体 神经肽YY1受体 细胞增殖 血管平滑肌细胞
分 类 号:R322.12[医药卫生—人体解剖和组织胚胎学] R329.28[医药卫生—基础医学]
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