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      Camphene, a Plant-Derived Monoterpene, Reduces Plasma Cholesterol and Triglycerides in Hyperlipidemic Rats Independently of HMG-CoA Reductase Activity

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          Abstract

          Background

          Central to the pathology of coronary heart disease is the accumulation of lipids, cholesterol and triglycerides, within the intima of arterial blood vessels. The search for drugs to treat dislipidemia, remains a major pharmaceutical focus. In this study, we evaluated the hypolipidemic properties of the essential oil from Chios mastic gum (MGO).

          Methodology/Principal Findings

          The hypolipidemic effect of MGO was investigated in naïve as well as in rats susceptible to detergent-induced hyperlipidemia. Serum cholesterol and triglycerides were determined using commercial kits. HMG-CoA (3-hydroxy-3-methylglutaryl coenzyme A) reductase activity was measured in HepG2 cell extracts using a radioactive assay; cellular cholesterol and cholesterol esters were assessed using gas chromatography. MGO administration into naïve rats resulted in a dose-dependent reduction in the constitutive synthesis of serum cholesterol and triglycerides. In hyperlipidemic rats, MGO treatment had also a strong hypolipidemic effect. By testing various components of MGO, we show for the first time that the hypolipidemic action is associated with camphene. Administration of camphene at a dose of 30 µg/gr of body weight in hyperlipidemic rats resulted in a 54.5% reduction of total cholesterol ( p<0.001), 54% of Low Density Lipoprotein (LDL)-cholesterol ( p<0.001) and 34.5% of triglycerides ( p<0.001). Treatment of HepG2 cells with camphene led to a decrease in cellular cholesterol content to the same extend as mevinolin, a known HMG-CoA reductase inhibitor. The hypolipidemic action of camphene is independent of HMG-CoA reductase activity, suggesting that its hypocholesterolemic and hypotriglyceridemic effects are associated with a mechanism of action different than that of statins.

          Conclusions

          Given the critical role that the control of hyperlipidemia plays in cardiovascular disease, the results of our study provide insights into the use of camphene as an alternative lipid lowering agent and merits further evaluation.

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          Most cited references90

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          A rapid method of total lipid extraction and purification.

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            Lovastatin and beyond: the history of the HMG-CoA reductase inhibitors.

            In the 1950s and 1960s, it became apparent that elevated concentrations of plasma cholesterol were a major risk factor for the development of coronary heart disease, which led to the search for drugs that could reduce plasma cholesterol. One possibility was to reduce cholesterol biosynthesis, and the rate-limiting enzyme in the cholesterol biosynthetic pathway, 3-hydroxy-3-methyl-glutaryl-CoA (HMG-CoA) reductase, was a natural target. Here, I describe the discovery and development of lovastatin--the first approved inhibitor of HMG-CoA reductase--and the clinical trials that have provided the evidence for the ability of drugs in this class to reduce the morbidity and mortality associated with cardiovascular disease.
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              The discovery and development of HMG-CoA reductase inhibitors.

              A Endo (1992)
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2011
                3 November 2011
                : 6
                : 11
                : e20516
                Affiliations
                [1 ]Department of Genetics, Development and Molecular Biology, School of Biology, Aristotle University of Thessaloniki, Thessaloniki, Greece
                [2 ]ADNA Inc., Oklahoma City, Oklahoma, United States of America
                Griffith University, Australia
                Author notes

                Conceived and designed the experiments: IV PP MHC. Performed the experiments: IV NP. Analyzed the data: IV PP MHC. Contributed reagents/materials/analysis tools: PP MHC. Wrote the paper: IV PP MHC.

                Article
                PONE-D-11-06075
                10.1371/journal.pone.0020516
                3207810
                22073134
                f7a549d5-2e23-4a61-94a3-adadf394c2c4
                Vallianou et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 1 April 2011
                : 2 May 2011
                Page count
                Pages: 11
                Categories
                Research Article
                Biology
                Anatomy and Physiology
                Cardiovascular System
                Biochemistry
                Lipids
                Lipid Metabolism
                Metabolism
                Lipid Metabolism
                Proteins
                Lipoproteins
                Lipoprotein Metabolism
                Lipoprotein Secretion
                Plasma Proteins
                Drug Discovery
                Enzymes
                Chemistry
                Chromatography
                Gas Chromatography
                Thin Layer Chromatography
                Phytochemistry
                Phytochemicals
                Phytopharmacology
                Medicine
                Cardiovascular
                Atherosclerosis
                Cardiovascular Pharmacology
                Coronary Artery Disease
                Complementary and Alternative Medicine
                Drugs and Devices
                Cardiovascular Pharmacology
                Ethnopharmacology

                Uncategorized
                Uncategorized

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