Literature DB >> 3328165

Lovastatin: a new cholesterol-lowering agent.

J J Krukemyer1, R L Talbert.   

Abstract

Lovastatin is a potent new drug for lowering serum cholesterol through inhibition of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, the rate-limiting enzyme for cholesterol biosynthesis. Metabolic studies with lovastatin in healthy volunteers and patients with hypercholesterolemia suggest reduced synthesis of low-density lipoprotein cholesterol (LDL-C) as well as enhanced catabolism LDL-C mediated through LDL receptors as the principal mechanisms for lipid-lowering effects. Total cholesterol and LDL-C are reduced by 30% or more on average when added to baseline therapy, with the effects being more pronounced in nonfamilial than in familial hypercholesterolemia. Optimal dosing appears to be 20 mg given twice a day. The most common adverse effects are gastrointestinal, while the most serious are elevated transaminase levels and the potential for lens opacities. Lovastatin is the first of a new class of lipid-lowering agents, and is effective when added to diet therapy or in combination with other drugs.

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Year:  1987        PMID: 3328165     DOI: 10.1002/j.1875-9114.1987.tb03524.x

Source DB:  PubMed          Journal:  Pharmacotherapy        ISSN: 0277-0008            Impact factor:   4.705


  12 in total

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Authors:  H Y Pan; J Triscari; A R DeVault; S A Smith; D Wang-Iverson; B N Swanson; D A Willard
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2.  Future of cholesteryl ester transfer protein (CETP) inhibitors: a pharmacological perspective.

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Journal:  Clin Pharmacokinet       Date:  2013-08       Impact factor: 6.447

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Journal:  Am J Cancer Res       Date:  2011-03-28       Impact factor: 6.166

Review 4.  Lipid-lowering drugs.

Authors:  K Pahan
Journal:  Cell Mol Life Sci       Date:  2006-05       Impact factor: 9.261

5.  Design, synthesis, and evaluation of prodrugs of ertapenem.

Authors:  Sheo B Singh; Diane Rindgen; Prudence Bradley; Lovji Cama; Wanying Sun; Michael J Hafey; Takao Suzuki; Nengxue Wang; Hao Wu; Basheng Zhang; Li Wang; Chongmin Ji; Hongshi Yu; Richard Soll; David B Olsen; Peter T Meinke; Deborah A Nicoll-Griffith
Journal:  ACS Med Chem Lett       Date:  2013-07-03       Impact factor: 4.345

6.  Applications of oxygen polarography to drug stability testing and formulation development: solution-phase oxidation of hydroxymethylglutaryl coenzyme A (HMG-CoA) reductase inhibitors.

Authors:  M J Kaufman
Journal:  Pharm Res       Date:  1990-03       Impact factor: 4.200

7.  Lovastatin inhibits gallstone formation in the cholesterol-fed prairie dog.

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8.  Enteroviruses harness the cellular endocytic machinery to remodel the host cell cholesterol landscape for effective viral replication.

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Journal:  Cell Host Microbe       Date:  2013-09-11       Impact factor: 21.023

9.  Lovastatin alters biliary lipid composition and dissolves gallstones: a long-term study in prairie dogs.

Authors:  Mohammad Z Abedin; Seth C Narins; Eun H Park; Peter R Smith; Kimberly S Kirkwood
Journal:  Dig Dis Sci       Date:  2002-10       Impact factor: 3.199

10.  Metabolomics approach reveals effects of antihypertensives and lipid-lowering drugs on the human metabolism.

Authors:  Elisabeth Altmaier; Gisela Fobo; Margit Heier; Barbara Thorand; Christine Meisinger; Werner Römisch-Margl; Melanie Waldenberger; Christian Gieger; Thomas Illig; Jerzy Adamski; Karsten Suhre; Gabi Kastenmüller
Journal:  Eur J Epidemiol       Date:  2014-05-10       Impact factor: 8.082

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