Antihypertensive and endothelium-dependent vasodilator effects of aqueous extract of Cistus ladaniferus

• Published in: Biochemical and biophysical research communications Vol. 389; no. 1; pp. 145 - 149
• Main Authors: Belmokhtar, Mounia, Bouanani, Nour Elhouda, Ziyyat, Abderrahim, Mekhfi, Hassane, Bnouham, Mohamed, Aziz, Mohamed, Matéo, Philippe, Fischmeister, Rodolphe, Legssyer, Abdelkhaleq
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 06-11-2009; Elsevier
• Subjects: 2K-1C renovascular hypertension; Animals; Antihypertensive Agents - pharmacology; Blood Pressure - drug effects; Cardiology and cardiovascular system; Cistus - chemistry; Cistus ladaniferus; Endothelium, Vascular - drug effects; Heart; Heart - drug effects; Human health and pathology; Hypertension - physiopathology; l-NAME; Life Sciences; NG-Nitroarginine Methyl Ester - pharmacology; Plant Extracts - pharmacology; Rat; Rats; Rats, Wistar; Thoracic aorta; Vasodilator Agents - pharmacology; Water - chemistry; Thoracic aorta; Heart; 2K-1C renovascular hypertension; Rat; l-NAME; Cistus ladaniferus
• DOI: 10.1016/j.bbrc.2009.08.113
• EISSN: 1090-2104
• ISSN: 0006-291X

Cistus ladaniferus L. (Cistaceae) is a medicinal plant originated from the Mediterranean region which exerts different pharmacological effects. In the present study, our goal was to examine whether the plant possessed antihypertensive properties. Aqueous extract of Cistus leaves (AEC, 500mg/kg/day) reduced systemic blood pressure (SBP) in two animal models of hypertension, the l-NAME and renovascular two kidney-one clip (2K-1C) hypertensive rats. In the former, AEC prevented the increase in SBP when co-administered with l-NAME during four weeks (164±3mm Hg in l-NAME vs. 146±1mm Hg in l-NAME+AEC, p<0.001). In the latter, AEC reversed the increase in SBP when administered during four weeks after installation of the hypertension (146±5mm Hg with AEC vs. 179±6mm Hg without, p<0.05). AEC treatment also reversed the endothelial dysfunction observed in both animal models of hypertension. A direct effect on cardiac and vascular tissue was also tested by examining the contractile effects of AEC in rat isolated aortic rings and Langendorff perfused hearts. AEC (10mg/L) had no effect on left ventricular developed pressure and heart rate in isolated perfused heart. However, AEC produced a strong relaxation of pre-contracted rat aortic rings (80±2% relaxation, n=25). When the rings were denuded from endothelium or were incubated with 1mM Nω-nitro-l-arginine (l-NNA), the relaxant effect of AEC was lost. We conclude that C. ladaniferus possesses antihypertensive properties which are mainly due to an endothelium-dependent vasodilatory action.