TY - JOUR
T1 - Antihypertensive, antioxidant, antidyslipidemic and endothelial modulating activities of a polyherbal formulation (POL-10)
AU - Aziz, Nauman
AU - Mehmood, Malik Hassan
AU - Mandukhal, Safur Rehman
AU - Bashir, Samra
AU - Raoof, Sidra
AU - Gilani, Anwarul Hassan
N1 - Funding Information:
The present study was supported by the Pakistan Science Foundation through research grant PSF/R&D/S-AKU/Bio (377).
PY - 2009/1
Y1 - 2009/1
N2 - The present investigation was aimed at providing the pharmacological basis for the medicinal use of a polyherbal formulation (POL-10) in hypertension and dyslipidemia. In spontaneously hypertensive rats, POL-10 significantly (p < 0.05) reduced blood pressure to 183.2 ± 2.97 vs 198.1 ± 5.2 mmHg (Mean ± S.E.M; n = 7-10), improved endothelial dysfunction (p < 0.01) by increasing acetylcholine-induced relaxation up to 46.0 ± 6.7% vs 24.6 ± 3.8% (n = 5-10) and decreased serum triglycerides (TG) to 54.5 ± 3.3 vs. 93.84 ± 5.7 mg/dl (p < 0.001). In high fat diet-induced hypercholesterolemia, POL-10 caused reduction in total cholesterol (TC), low density lipoproteins (LDL) levels and the atherogic index (TC-HDL/HDL). It decreased TG levels in tyloxapol-induced hyperlipidemia and increased high-density lipoprotein cholesterol (HDL-C) and reduced atherogenic index in normotensive rats. It exhibited strong antioxidant activity in different in vitro assays. In isolated smooth muscle preparation, POL-10 exhibited calcium channel blocking (CCB) activity by inhibition of high K+- induced contractions and rightward shift of Ca++ concentration-response curves similar to that of verapamil. In conclusion, these findings rationalize the medicinal use of POL-10 in cardiovascular disorders which are mediated through multiple pathways such as, antioxidant, CCB, inhibition of lipid biosynthesis and absorption.
AB - The present investigation was aimed at providing the pharmacological basis for the medicinal use of a polyherbal formulation (POL-10) in hypertension and dyslipidemia. In spontaneously hypertensive rats, POL-10 significantly (p < 0.05) reduced blood pressure to 183.2 ± 2.97 vs 198.1 ± 5.2 mmHg (Mean ± S.E.M; n = 7-10), improved endothelial dysfunction (p < 0.01) by increasing acetylcholine-induced relaxation up to 46.0 ± 6.7% vs 24.6 ± 3.8% (n = 5-10) and decreased serum triglycerides (TG) to 54.5 ± 3.3 vs. 93.84 ± 5.7 mg/dl (p < 0.001). In high fat diet-induced hypercholesterolemia, POL-10 caused reduction in total cholesterol (TC), low density lipoproteins (LDL) levels and the atherogic index (TC-HDL/HDL). It decreased TG levels in tyloxapol-induced hyperlipidemia and increased high-density lipoprotein cholesterol (HDL-C) and reduced atherogenic index in normotensive rats. It exhibited strong antioxidant activity in different in vitro assays. In isolated smooth muscle preparation, POL-10 exhibited calcium channel blocking (CCB) activity by inhibition of high K+- induced contractions and rightward shift of Ca++ concentration-response curves similar to that of verapamil. In conclusion, these findings rationalize the medicinal use of POL-10 in cardiovascular disorders which are mediated through multiple pathways such as, antioxidant, CCB, inhibition of lipid biosynthesis and absorption.
KW - Antidyslipidemic
KW - Antihypertensive
KW - Antioxidant
KW - Endothelial dysfunction
KW - Polyherbal
UR - http://www.scopus.com/inward/record.url?scp=57149087849&partnerID=8YFLogxK
U2 - 10.1016/j.vph.2008.09.003
DO - 10.1016/j.vph.2008.09.003
M3 - Article
C2 - 18940267
AN - SCOPUS:57149087849
SN - 1537-1891
VL - 50
SP - 57
EP - 64
JO - Vascular Pharmacology
JF - Vascular Pharmacology
IS - 1-2
ER -