Literature DB >> 16018787

Nicotinic acid: the broad-spectrum lipid drug. A 50th anniversary review.

L A Carlson1.   

Abstract

Nicotinic acid has, like the Roman God Janus, two faces. One is the vitamin. The other is the broad-spectrum lipid drug. The Canadian pathologist Rudolf Altschul discovered 50 years ago that nicotinic acid in gram doses lowered plasma levels of cholesterol. From the point of view of treatment of the dyslipidaemias that are risk factors for clinical atherosclerosis nicotinic acid is a miracle drug. It lowers the levels of all atherogenic lipoproteins--VLDL and LDL with subclasses as well as Lp(a)--and in addition it raises more than any other drug the levels of the protective HDL lipoproteins. Trials have shown that treatment with nicotinic acid reduces progression of atherosclerosis, and clinical events and mortality from coronary heart disease. The new combination treatment with statin-lowering LDL and nicotinic acid-raising HDL is reviewed. A basic effect of nicotinic acid is the inhibition of fat-mobilizing lipolysis in adipose tissue leading to a lowering of plasma free fatty acids, which has many metabolic implications which are reviewed. The very recent discovery of a nicotinic acid receptor and the finding that the drug stimulates the expression of the ABCA 1 membrane cholesterol transporter have paved the way for exciting and promising new 50 years in the history of nicotinic acid.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16018787     DOI: 10.1111/j.1365-2796.2005.01528.x

Source DB:  PubMed          Journal:  J Intern Med        ISSN: 0954-6820            Impact factor:   8.989


  125 in total

Review 1.  Cardiovascular disease risk reduction by raising HDL cholesterol--current therapies and future opportunities.

Authors:  K Mahdy Ali; A Wonnerth; K Huber; J Wojta
Journal:  Br J Pharmacol       Date:  2012-11       Impact factor: 8.739

2.  How much do we really know about our favorite cosmeceutical ingredients?

Authors:  Jacquelyn Levin; Saira B Momin
Journal:  J Clin Aesthet Dermatol       Date:  2010-02

Review 3.  Functional selectivity of GPCR signaling in animals.

Authors:  Lei Zhou; Laura M Bohn
Journal:  Curr Opin Cell Biol       Date:  2013-12-22       Impact factor: 8.382

Review 4.  Molecular regulation of HDL metabolism and function: implications for novel therapies.

Authors:  Daniel J Rader
Journal:  J Clin Invest       Date:  2006-12       Impact factor: 14.808

5.  Liver fat reduction with niacin is influenced by DGAT-2 polymorphisms in hypertriglyceridemic patients.

Authors:  Miao Hu; Winnie Chiu Wing Chu; Shizuya Yamashita; David Ka Wai Yeung; Lin Shi; Defeng Wang; Daisaku Masuda; Yaling Yang; Brian Tomlinson
Journal:  J Lipid Res       Date:  2012-02-07       Impact factor: 5.922

6.  Flushing out the role of GPR109A (HM74A) in the clinical efficacy of nicotinic acid.

Authors:  Nicholas B Pike
Journal:  J Clin Invest       Date:  2005-12       Impact factor: 14.808

Review 7.  Drug repositioning: playing dirty to kill pain.

Authors:  Leandro Francisco Silva Bastos; Márcio Matos Coelho
Journal:  CNS Drugs       Date:  2014-01       Impact factor: 5.749

8.  A randomized, double-blind, placebo-controlled trial of niacinamide for reduction of phosphorus in hemodialysis patients.

Authors:  Steven C Cheng; Daniel O Young; Yihung Huang; James A Delmez; Daniel W Coyne
Journal:  Clin J Am Soc Nephrol       Date:  2008-04-02       Impact factor: 8.237

9.  Extended-release niacin acutely suppresses postprandial triglyceridemia.

Authors:  M Haris U Usman; Arman Qamar; Ramprasad Gadi; Scott Lilly; Harsh Goel; Jaison Hampson; Megan L Mucksavage; Grace A Nathanson; Daniel J Rader; Richard L Dunbar
Journal:  Am J Med       Date:  2012-07-25       Impact factor: 4.965

10.  Anatomical profiling of G protein-coupled receptor expression.

Authors:  Jean B Regard; Isaac T Sato; Shaun R Coughlin
Journal:  Cell       Date:  2008-10-31       Impact factor: 41.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.