自发性高血压大鼠主动脉平滑肌细胞异常增殖和局部肾素—血管？…

目的：探讨ＳＨＲ大鼠主动脉平滑肌细胞（ＡＳＭＣ）异常增殖和肾素－血管紧张素系统９ＲＡＳ）的关系。方法：测定血管紧张素Ⅱ（Ａｎｇ）、卡托普利（Ｃａｐ）、沙拉新（Ｓａｒ）对培养的ＳＨＲ、ＷＫＹ ＡＳＭＣ增殖的Ａｎｇ、血管紧张素转化酶（ＡＣＥ）的影响，结果：Ａｎｇ在２％血清培养基中可刺激ＳＨＲ ＡＳＭＣ增生，ＳＨＲ ＡＳＭＣ分裂增殖能力比ＷＫＹ强，ＳＨＲ ＡＳＭＣ ＲＡＳ处于高功能状态。Ｃａｐ长期（４周

Proliferation of aortic smooth muscle cells and renin-angiotensin system in SHR rats.

AIM: To study the relationship between the enhanced proliferation and renin-angiotensin system (RAS) of aortic smooth muscle cells (ASMC) from SHR rats. METHODS: To measure the effects of angiotensin II (Ang), captopril (Cap), saralasin (Sar) on proliferation, Ang and angiotensin converting enzyme (ACE) levels in cultured ASMC from WKY and SHR rats. RESULTS: Ang was a bifunctional growth factor, which induced SHR ASMC hyperplasia in 2% FCS-RPMI 1640 medium, but not in serum free (SF)-medium. SHR ASMC had stronger proliferative ability compared with WKY while SHR ASMC RAS was activated. Enhanced proliferation of SHR ASMC and ACE activity were obviously inhibited by long-term treatment (4-wk) of both Cap and Sar, while Ang content decreased in Cap treatment group and increased in Sar treatment group. The antiproliferative effect of Cap and Sar on SHR ASMC was stronger than that on WKY. SHR, WKY ASMC RAS were not influenced by short-term (24 h) treatment of Cap. CONCLUSION: Long-term treatment of Cap and Sar suppressed SHR ASMC growth through inhibition of Ang generation or blockade of Ang binding to its receptor.