Touyz R M, Tolloczko B, Schiffrin E L
Clinical Research Institute of Montréal, University of Montréal, Québec, Canada.
Am J Hypertens. 1995 Feb;8(2):104-12. doi: 10.1016/0895-7061(94)00173-9.
Insulin attenuates vasoconstrictor-stimulated intracellular calcium ([Ca2+]i) responses in cells from normotensive rats. To determine whether these effects may be altered in hypertension, this study assesses the effects of physiologic concentrations of insulin on angiotensin II-stimulated [Ca2+]i in primary unpassaged cultured vascular smooth muscle cells (VSMC) from mesenteric arteries from spontaneously hypertensive rats (SHR), Wistar Kyoto (WKY), and Wistar rats. [Ca2+]i was measured microphotometrically in cells from 3-, 9-, and 17-week-old rats by the Fura 2 methodology. Basal, angiotensin II-stimulated (1 nmol/L), and insulin-attenuated (70 microU/mL) angiotensin II-induced [Ca2+]i did not differ in VSMC obtained from 3-week-old WKY, Wistar, and SHR. Basal and angiotensin II-stimulated [Ca2+]i in VSMC from 9- and 17-week-old SHR was significantly greater (P < .01) than that in cells from age-matched WKY and Wistar rats. Insulin decreased angiotensin II-stimulated [Ca2+]i responses in all groups, but the effect was significantly blunted in cells from 9- and 17-week-old SHR. The magnitude of inhibition of angiotensin II-stimulated [Ca2+]i responses induced by insulin was 63 +/- 12 nmol/l (WKY), 60 +/- 10 nmol/L (Wistar), and 28 +/- 8 nmol/L (SHR), (P < .01 v normotensive) in cells from 9-week-old rats and 70 +/- 15 nmol/L (WKY), 67 +/- 12 nmol/L (Wistar), and 25 +/- 10 nmol/L (SHR) (P < .01 v normotensive) in cells from 17-week-old rats. Insulin increased angiotensin II-stimulated [Ca2+]i recovery rate to basal values in cells from WKY rats, but had no effect on the rate of recovery in VSMC from SHR. (ABSTRACT TRUNCATED AT 250 WORDS)
胰岛素可减弱正常血压大鼠细胞中血管收缩剂刺激的细胞内钙([Ca2+]i)反应。为确定高血压时这些效应是否会改变,本研究评估了生理浓度胰岛素对来自自发性高血压大鼠(SHR)、Wistar Kyoto(WKY)大鼠和Wistar大鼠肠系膜动脉的原代未传代培养血管平滑肌细胞(VSMC)中血管紧张素II刺激的[Ca2+]i的影响。采用Fura 2方法通过显微光度法测量3周龄、9周龄和17周龄大鼠细胞中的[Ca2+]i。从3周龄WKY、Wistar和SHR获取的VSMC中,基础、血管紧张素II刺激(1 nmol/L)和胰岛素减弱(70 μU/mL)的血管紧张素II诱导的[Ca2+]i无差异。9周龄和17周龄SHR的VSMC中基础和血管紧张素II刺激的[Ca2+]i显著高于(P <.01)年龄匹配的WKY和Wistar大鼠细胞中的[Ca2+]i。胰岛素降低了所有组中血管紧张素II刺激的[Ca2+]i反应,但在9周龄和17周龄SHR的细胞中该效应明显减弱。在9周龄大鼠的细胞中,胰岛素诱导的血管紧张素II刺激的[Ca2+]i反应抑制幅度为63±12 nmol/L(WKY)、60±10 nmol/L(Wistar)和28±8 nmol/L(SHR)(与正常血压组相比P <.01),在17周龄大鼠的细胞中为70±15 nmol/L(WKY)、67±12 nmol/L(Wistar)和25±10 nmol/L(SHR)(与正常血压组相比P <.01)。胰岛素提高了WKY大鼠细胞中血管紧张素II刺激的[Ca2+]i恢复到基础值的速率,但对SHR的VSMC恢复速率无影响。(摘要截断于250字)