المؤلفون: Samain, Emmanuel¹ elsamain@chu-besancon.fr, Pili-Floury, Sébastien¹, Bouillier, Hélène², Clichet, Adeline², Safar, Michel³, Dagher, Georges⁴, Marty, Jean, Renaud, Jean-François²

المصدر: Clinical & Experimental Pharmacology & Physiology. Mar2004, Vol. 31 Issue 3, p163-168. 6p.

مصطلحات موضوعية: *ALCOHOL, *CALCIUM, *ANGIOTENSINS, *AORTA, *HYPERTENSION, *LABORATORY rats

مستخلص: 1. Angiotensin (Ang) II is a potent vasopressor agent, involved in the short-term control of arterial blood pressure during anaesthesia. The aim of the present study was to test the hypothesis that propofol, a widely used intravenous anaesthetic agent, could alter the arterial response to AngII and to evaluate its effect in genetic hypertension. 2. We studied the effect of increasing concentrations of propofol (5.6 × 10−7 to 5.6 × 10−4 mol/L) on aortic ring maximal isometric tension elicited by AngII and on AngII-induced Ca2+ mobilization in aortic smooth muscle cells from Wistar-Kyoto (WKY) rats and spontaneously hypertensive rats (SHR). 3. Maximal tension developed by aortic rings from WKY rats was greater than that developed by rings from SHR. In both WKY rats and SHR, propofol at concentrations from 5.6 × 10−6 mol/L decreased maximal tension induced by AngII in a concentration-dependent manner. The magnitude of inhibition was higher in SHR than in WKY rats, whereas pD2 values were not different. In addition, Ca2+ mobilization induced by AngII was inhibited by propofol in a concentration-dependent manner, with the same magnitude and pD2 values. 4. These results suggest that the arterial response to AngII may be altered during propofol anaesthesia, particularly in hypertension. [ABSTRACT FROM AUTHOR]

المؤلفون: Samain, Emmanuel, Clichet, Adeline¹, Bouillier, Hélène¹, Chamiot-Clerc, Philippe¹, Safar, Michel, Marty, Jean, Renaud, Jean-François¹

المصدر: Clinical & Experimental Pharmacology & Physiology. Nov2002, Vol. 29 Issue 11, p1015-1017. 0p.

مصطلحات موضوعية: *AORTA, *HYPERTENSION, *NORADRENALINE

مستخلص: Summary 1. The effect of propofol on arterial tone in hypertension is poorly understood. We examined the effect of increasing concentrations of propofol (5.6 × 10-8 to 2.8 × 10-3 mol/L) on isometric tension developed by noradrenaline (10-7 mol/L)-contracted aortic rings from 12-week-old Wistar-Kyoto (WKY) rats and spontaneously hypertensive rats (SHR). 2. In both WKY rats and SHR, propofol induced a dose-dependent inhibition of contraction induced by noradrenaline, but the amplitude of relaxation was larger in the SHR than in WKY rats. 3. The effects of propofol was endothelium independent in WKY rats, whereas in SHR relaxation induced by propofol was greater in endothelium-intact than in endothelium-denuded rings. 4. In conclusion, we found significant differences in the effect of propofol in hypertensive rats, which may be related to differences in structural and functional properties of the arterial wall observed in hypertension. [ABSTRACT FROM AUTHOR]