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雌激素对大鼠趋化因子受体CXCR2表达的影响:动脉粥样硬化的指征
引用本文:Lei ZB,Fu XJ,Lu ZT,Wang BC,Liu XL,You NZ. 雌激素对大鼠趋化因子受体CXCR2表达的影响:动脉粥样硬化的指征[J]. Acta pharmacologica Sinica, 2003, 24(7): 670-674,725
作者姓名:Lei ZB  Fu XJ  Lu ZT  Wang BC  Liu XL  You NZ
作者单位:济南军区总医院心内科,济南军区总医院心内科,济南军区总医院心内科,济南军区总医院心内科,济南军区总医院心内科,济南军区总医院心内科 济南 250031 中国,济南 250031 中国,济南 250031 中国,济南 250031 中国,济南 250031 中国,济南 250031 中国
基金项目:Project supported by the Medicinal Foundation of the Chinese People's Liberation Army (01Q015).
摘    要:目的:研究17β-雌二醇对体内单核细胞趋化因子受体CXCR2表达的影响.方法:流式细胞仪测定单核细胞趋化因子受体CXCR2的蛋白表达、逆转录PCR测定其mRNA水平.结果:在卵巢完整和切除卵巢的大鼠中,喂养富含胆固醇饮食6周增加单核细胞趋化因子受体CXCR2 mRNA和蛋白水平.在切除卵巢的大鼠,注射17β-雌二醇(5和20μg.kg^-1.d^-1)显著减少了胆固醇诱导的CXCR2 mRNA及蛋白表达的增加.正常饮食的大鼠,切除卵巢增加了趋化因子受体CXCR2 mRNA和蛋白水平的表达,但是注射17β-雌二醇可以防止它表达的增加.结论:生理性浓度的雌激素调节基础及胆固醇诱导的趋化因子受体CXCR2表达.

关 键 词:雌激素 大鼠 趋化因子受体 CXCR2 动脉粥样硬化 流式细胞仪 胆固醇

Effect of estradiol on chemokine receptor CXCR2 expression in rats: implications for atherosclerosis
Lei Zhu-Bin,Fu Xu-Jie,Lu Zhao-Tong,Wang Bao-Cheng,Liu Xian-Liang,You Nai-Zhen. Effect of estradiol on chemokine receptor CXCR2 expression in rats: implications for atherosclerosis[J]. Acta pharmacologica Sinica, 2003, 24(7): 670-674,725
Authors:Lei Zhu-Bin  Fu Xu-Jie  Lu Zhao-Tong  Wang Bao-Cheng  Liu Xian-Liang  You Nai-Zhen
Affiliation:Department of Cardiology, General Hospital of Ji'nan Military Area, Ji'nan 250031, China. leizhubin88@email.com.cn
Abstract:AIM: To study the effect of 17beta-estradiol on expression of chemokine receptor CXCR2 in monocytes in vivo. METHODS: Expressions of chemokine receptor CXCR2 mRNA and protein were measured by RT-PCR and flow cytometry, respectively. RESULTS: In both ovary-intact and ovariectomized (OVX) rats, CXCR2 protein and mRNA expression were significantly increased in rats fed with a high-cholesterol diet for 6 weeks. The cholesterol-induced increases in CXCR2 protein and mRNA expression were significantly attenuated in OVX rats injected with estradiol-17beta (17beta-E2) (5 and 20 microg x kg(-1) x d(-1)). In normal diet rats, CXCR2 protein and mRNA expression were increased in OVX rats compared with ovary-intact rats, and this increase was prevented by 17beta-E2. CONCLUSION: Both basal and hypercholesterolemia-induced increases in chemokine receptor CXCR2 are modulated by physiological concentrations of estradiol.
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