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自发性高血压大鼠和WKY大鼠的血管平滑肌细胞增殖:生长抑制调节机制存在特异性差异的证据。

Vascular smooth muscle cell proliferation in SHR and WKY rats: evidence for specific differences in growth inhibitory regulatory mechanisms.

作者信息

Agrotis A, Bray P J, Saltis J, Bobik A

机构信息

Baker Medical Research Institute, Alfred Hospital, Prahran, Victoria, Australia.

出版信息

Clin Exp Pharmacol Physiol. 1993 May;20(5):327-30. doi: 10.1111/j.1440-1681.1993.tb01696.x.

Abstract
  1. This study examined and compared the actions of transforming growth factor-beta 1 (TGF-beta 1), heparin, dexamethasone and interferon-gamma on platelet-derived growth factor-BB (PDGF-BB)-stimulated proliferation of vascular smooth muscle cells (VSMC) from normotensive, Wistar-Kyoto (WKY) rats and spontaneously hypertensive rats (SHR). 2. Heparin, dexamethasone and interferon-gamma all inhibited VSMC proliferation stimulated by PDGF-BB in both SHR and WKY rats. There was no difference (P > 0.05) in their inhibitory effects, which varied between 40 and 85% for the different agents. 3. Similarly, TGF-beta 1 inhibited PDGF-BB-stimulated VSMC proliferation in WKY rats by approximately 50%. In contrast, TGF-beta 1 potentiated growth factor action on cell proliferation in the SHR by approximately 40%. 4. Specific TGF-beta 1-stimulated regulatory mechanisms involved in the inhibition of proliferation are absent in SHR and this defect may contribute to the vascular hypertrophy which is apparent in genetic hypertension.
摘要
  1. 本研究检测并比较了转化生长因子-β1(TGF-β1)、肝素、地塞米松和干扰素-γ对来自正常血压的Wistar-Kyoto(WKY)大鼠和自发性高血压大鼠(SHR)的血小板衍生生长因子-BB(PDGF-BB)刺激的血管平滑肌细胞(VSMC)增殖的作用。2. 肝素、地塞米松和干扰素-γ均抑制了SHR和WKY大鼠中由PDGF-BB刺激的VSMC增殖。它们的抑制作用没有差异(P>0.05),不同药物的抑制作用在40%至85%之间。3. 同样,TGF-β1在WKY大鼠中抑制了约50%的由PDGF-BB刺激的VSMC增殖。相比之下,TGF-β1在SHR中使生长因子对细胞增殖的作用增强了约40%。4. SHR中不存在参与增殖抑制的特定TGF-β1刺激的调节机制,这种缺陷可能导致在遗传性高血压中明显的血管肥大。

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