Hypotensive activity of Campomanesia xanthocarpa leaf extract: beyond angiotensin II type 1 receptor blockage

Abstract The ability of Campomanesia xanthocarpa leaf extract (CXLE) to alter blood pressure and heart rate was evaluated in anesthetized rats. The CXLE-induced hypotension was evaluated before and after losartan, methylatropine, L-N(ω)-nitro-L-arginine methyl ester (L-NAME), hexamethonium, indomethacin, glibenclamide, or nifedipine administration. The constituents of CXLE were identified by LC-DAD-MS. CXLE decreased blood pressure in a dose-dependent manner; only the highest dose decreased heart rate. The hypotension induced by CXLE was sensitive only to losartan, nifedipine, and glibenclamide. L-NAME decreased the time to recover 50% of the hypotensive effect of CXLE without altering its magnitude. Flavan-3-ols, proanthocyanidins (dimers and trimers), and glycosylated flavonols were identified from CXLE. The chemical constituents of CXLE seem to induce not only angiotensin II type 1 receptor blockage, but also ATP-sensitive potassium channels activation and L-type voltage-dependent Ca2+ channels inactivation. Nitric oxide is involved in the maintenance of the hypotensive effect of CXLE.

[1]  A. Novaković,et al.  (−)‐Epicatechin‐induced relaxation of isolated human saphenous vein: Roles of K+ and Ca2+ channels , 2018, Phytotherapy research : PTR.

[2]  A. Mendez,et al.  Chemical Composition and Hypotensive Effect of Campomanesia xanthocarpa , 2017, Evidence-based complementary and alternative medicine : eCAM.

[3]  C. Nakamura,et al.  Antiviral Activity of Crude Hydroethanolic Extract from Schinus terebinthifolia against Herpes simplex Virus Type 1 , 2016, Planta Medica.

[4]  N. Lopes,et al.  Flavanone glycosides from Bidens gardneri Bak. (Asteraceae). , 2013, Phytochemistry.

[5]  L. Moreno,et al.  Lack of synergistic interaction between quercetin and catechin in systemic and pulmonary vascular smooth muscle. , 2011, The British journal of nutrition.

[6]  M. Dos Santos,et al.  Hypotensive effect of aqueous extract of Averrhoa carambola L. (Oxalidaceae) in rats: an in vivo and in vitro approach. , 2011, Journal of ethnopharmacology.

[7]  H. Katus,et al.  Cardiovascular ion channels as a molecular target of flavonoids. , 2010, Cardiovascular therapeutics.

[8]  F. Villarreal,et al.  (−)-Epicatechin Activation of Endothelial Cell Endothelial Nitric Oxide Synthase, Nitric Oxide, and Related Signaling Pathways , 2010, Hypertension.

[9]  T. Kanda,et al.  Apple Procyanidins Induced Vascular Relaxation in Isolated Rat Aorta through NO/cGMP Pathway in Combination with Hyperpolarization by Multiple K+ Channel Activations , 2009, Bioscience, biotechnology, and biochemistry.

[10]  G. Beecher,et al.  Liquid chromatographic/electrospray ionization mass spectrometric studies of proanthocyanidins in foods. , 2003, Journal of mass spectrometry : JMS.

[11]  X. Yao,et al.  Involvement of endothelium/nitric oxide in vasorelaxation induced by purified green tea (-)epicatechin. , 1999, Biochimica et biophysica acta.

[12]  N. Yanaihara,et al.  Glibenclamide-sensitive hypotension produced by helodermin assessed in the rat. , 1998, Biological & pharmaceutical bulletin.

[13]  Y. Huang,et al.  Vasorelaxant effects of purified green tea epicatechin derivatives in rat mesenteric artery. , 1998, Life sciences.

[14]  M. Claeys,et al.  Characterization of flavone and flavonol aglycones by collision‐induced dissociation tandem mass spectrometry , 1997 .

[15]  P. Vanhoutte,et al.  Endothelium‐derived relaxing and contracting factors , 1989, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[16]  P. Timmermans,et al.  Nonpeptide angiotensin II receptor antagonists. IX. Antihypertensive activity in rats of DuP 753, an orally active antihypertensive agent. , 1990, The Journal of pharmacology and experimental therapeutics.