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醫(yī)學(xué)論文范文:17β_雌二醇對(duì)新生牛血清誘導(dǎo)的血管平滑肌細(xì)胞增殖反應(yīng)的影響及其機(jī)制

來(lái)源:本站原創(chuàng) 更新:2013-9-5 論文投稿平臺(tái)

醫(yī)學(xué)論文范文:17β_雌二醇對(duì)新生牛血清誘導(dǎo)的血管平滑肌細(xì)胞增殖反應(yīng)的影響及其機(jī)制

【摘要】 目的:探討雌甾_1,3,5(10)_三烯_3,17β_二醇(17β_雌二醇)對(duì)新生牛血清誘導(dǎo)血管平滑肌細(xì)胞(VSMCs)增殖反應(yīng)的影響及其機(jī)制。方法:用新生牛血清刺激培養(yǎng)的VSMCs增殖,MTT法檢測(cè)17β_雌二醇對(duì)新生牛血清誘導(dǎo)的VSMCs增殖的影響,并用Western blot檢測(cè)caveolin_1蛋白,誘導(dǎo)型一氧化氮合酶(iNOS)及NO在此過(guò)程中的變化。結(jié)果:與對(duì)照組比,新生牛血清可促進(jìn)VSMCs增殖(P<0.05),17β_雌二醇作用24h后能明顯抑制上述作用(P<0.05);17β_雌二醇預(yù)處理可抑制新生牛血清誘導(dǎo)的VSMCs中caveolin_1,iNOS蛋白表達(dá)下降及NO釋放(P<0.05);17β_雌二醇受體阻斷劑1_{4_[2_(n,n_二甲氨基)乙氧基]苯}_1,2_二苯_1_丁烯(他莫昔芬)預(yù)處理可部分逆轉(zhuǎn)17β_雌二醇的抑制作用(P<0.05)。結(jié)論:17β_雌二醇通過(guò)其受體可抑制新生牛血清誘導(dǎo)的VSMCs增殖,此過(guò)程與上調(diào)caveolin_1蛋白表達(dá),激活iNOS,增加NO釋放有關(guān)。

【關(guān)鍵詞】 17β_雌二醇;caveolin_1;誘導(dǎo)型一氧化氮合酶;血管平滑肌細(xì)胞

Influence of 17β_estradiol on Vascular Smooth Muscle Cells Proliferation Induced

by Fetal Calf Serum and Its MechanismLIU Hai_mei1,ZHAO Xiao_feng2,XU Jin_wen3,LIN Gui_ping3,WANG Ting_huai3

(1 Department of Physiology,Guangzhou University of Chinese Medicine,Guangzhou 510006,China,2 Department of Physiology,Me_dical College of Shaoguan University,Shaoguan 512026,China,3 Department of Physiology,Zhongshan Medical College,Sun_Yat Sen University,Guangzhou 510080,China)

[Abstract]Objective: To investigate the influence of 17β_estradiol on vascular smooth muscle cells(VSMCs)proliferation induced by fetal calf serum and the related mechanism. Methods: The fetal calf serum was used to stimulate cultured VSMCs proliferation(P<0.05),and the effects of estrogen on VSMCs proliferation were determined by MTT,and the expressions of caveolin_1 and inducible nitric oxide synthase(iNOS)were also detected by Western blot. Results: Compared with the normal control group, the fetal calf serum could increase the VSMCs proliferation(P<0.05), and inhibit proliferation effect of fetal calf serum,pretreated with estradiol for 24 hours(P<0.05). Western bolt results further proved that 17β_estradiol inhibited the downregulation of caveolin_1, iNOS and NO induced by fetal calf serum, which was prevented by pretreatment with estrogen antagonist, Tamoxifen(P<0.05). Conclusion: 17β_estradiol can inhibit VSMCs proliferation induced by fetal calf serum, and this effect is mediated by estrogen receptor. 17β_estradiol increases caveolin_1 and iNOS protein expression, and NO release,leading to the inhibition of VSMCs proliferation induced by fetal calf serum醫(yī).學(xué)全.在.線網(wǎng)站gydjdsj.org.cn.

[Key Words]17β_estradiol,caveolin_1,inducible nitric oxide synthase,vascular smooth muscle cell

血管損傷后,刺激因子誘導(dǎo)的血管平滑肌細(xì)胞(VSMCs)的過(guò)度增殖和遷移是再狹窄發(fā)生的關(guān)鍵[1_2],臨床及流行病學(xué)資料顯示,雌甾_1,3,5(10)_三烯_3,17β_二醇(17β_雌二醇)具有心血管保護(hù)作用,我室前期的實(shí)驗(yàn)研究也證實(shí)這點(diǎn)[3],在離體培養(yǎng)的VSMCs中17β_雌二醇可抑制ET_1誘導(dǎo)的VSMCs增殖,此過(guò)程與抑制細(xì)胞外信號(hào)通路1/2(ERK1/2)有關(guān)。17β_雌二醇的血管保護(hù)作用與誘導(dǎo)NO生成有關(guān),但在VSMCs中,17β_雌二醇通過(guò)何種途徑誘導(dǎo)NO合成,目前尚未明了。因此,本研究利用離體培養(yǎng)的胸主動(dòng)脈VSMCs,觀察caveolin_1及誘導(dǎo)型一氧化氮合酶(iNOS)在17β_雌二醇誘導(dǎo)NO合成及抑制VSMCs增殖中的作用和機(jī)制。


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