نتایج جستجو برای: coa reductase inhibitors

تعداد نتایج: 246262  

Journal: :Stroke 1997
G J Blauw A M Lagaay A H Smelt R G Westendorp

BACKGROUND AND PURPOSE To estimate the effect of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors ("statins") on stroke ris, we combined the data of the randomized, placebo-controlled, double-blind trials with HMG-CoA reductase inhibitors published so far. METHODS The studies were identified using the Medline CD+ and Current Contents databases from January 1980 through May...

2012
Mahesh Kumar Teli Rajanikant G K

UNLABELLED BACKGROUND Coronary heart disease continues to be the leading cause of mortality and a significant cause of morbidity and account for nearly 30% of all deaths each year worldwide. High levels of cholesterol are an important risk factor for coronary heart disease. The blockage of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase activity by small molecule inhibitors has bee...

Journal: :The Journal of biological chemistry 1991
S Inoue S Bar-Nun J Roitelman R D Simoni

3-Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase is a key regulatory enzyme of cholesterol biosynthesis and is located in the endoplasmic reticulum (ER). A fusion protein, HMGal, consisting of the membrane domain of HMG-CoA reductase fused to Escherichia coli beta-galactosidase and expressed in Chinese hamster ovary (CHO) cells from the SV40 promoter, was previously constructed and was...

Journal: :Applied biochemistry and biotechnology 2011
Mohan-Kumari H Puttananjaiah Mohan Appasaheb Dhale Vaishali Gaonkar Shradha Keni

Atherosclerosis is a chronic inflammatory disease of multiple etiologies. It is associated with the accumulation of oxidized lipids in arterial lesions leading to coronary heart disease. 3-Hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (commonly known as statins) are widely used in cardiovascular disease prevention to lower the cholesterol. The antioxidant activity of HMG-Co...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2001
M Ishigami T Honda W Takasaki T Ikeda T Komai K Ito Y Sugiyama

HMG-CoA reductase inhibitors can be divided into two groups: those administered as the prodrug, i.e., the lactone form (e.g., simvastatin and lovastatin), and those administered in the active form, i.e., the acid form (e.g., pravastatin, fluvastatin, atorvastatin, and cerivastatin). In this study, the influence of the lactone and acid forms of various HMG-CoA reductase inhibitors on metabolism ...

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2004
J N Poynter G Rennert J D Bonner H S Rennert J K Greenson S B Gruber

1 Background: 3-hydroxy-2-methylglutaryl coenzyme A (HMG CoA) reductase inhibitors are effective lipid-lowering agents that also inhibit the growth of colon cancer cell lines and were noted to be associated with a reduced risk of colorectal cancer (CRC) in a randomized clinical trial of patients with myocardial infarction. We investigated the association between HMG CoA reductase inhibitors and...

2013
Ahmed Mohammed Kabel

3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase is the key enzyme in cholesterol synthesis. Statins are used in treatment of hypercholesterolemia as inhibitors of HMG-CoA reductase. Cancer cells overexpress HMG-CoA reductase enzyme. Recent studies have demonstrated that statins may inhibit the proliferation of human breast cancer cells. Statins have proangiogenic effects in low therapeutic c...

Journal: :novelty in biomedicine 0
ramin talaie department of internal medicine, modarres hospital, shahid beheshti university of medical sciences, tehran, iran mohammad bagher motevallian department of internal medicine, modarres hospital, shahid beheshti university of medical sciences, tehran, iran

background: although lipid lowering agents as statins are used frequently in hyperlipidemic patients as well as patients with cardiac disease, they could have major hepatic side effects, the aim of this study is to evaluate the safety of statins mainly atorvastatin on liver as estimated by liver aminotransferase assay. m aterials and methods: patients with indication of atorvastatin were includ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2002
Michi Ishigami Wataru Takasaki Toshihiko Ikeda Toru Komai Kiyomi Ito Yuichi Sugiyama

To identify an appropriate animal model for the study of drug interaction via CYP3A4 inhibition, the inhibition of in vitro mexazolam metabolism by various 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors [simvastatin (lactone), simvastatin acid, fluvastatin, atorvastatin, cerivastatin, pravastatin lactone, and pravastatin (acid)] in male and female rat liver microsomes was ...

2010
Robert Guthrie

Coronary heart disease treatment with HMG-CoA reductase inhibitors has been very successful. There is increasing interest in adding other lipid lowering therapy, primarily as additional therapy onto HMG-CoA reductase therapy. This paper will examine two of the more popular secondary agents, ezetimibe and niacin, and describe their research data and potential for usefulness in further reducing c...

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