Literature DB >> 11735122

HMG-CoA reductase inhibitors reduce adhesion of human monocytes to endothelial cells.

D Teupser1, M Bruegel, O Stein, Y Stein, J Thiery.   

Abstract

HMG-CoA reductase inhibitors (statins) are believed to reduce coronary heart disease by mechanisms in addition to their well-known cholesterol-lowering effect. We studied the effect of these drugs on monocyte cell adhesion to endothelium. Pretreatment of monocytic cells (U937, THP-1, human CD14(+) monocytes) with 0.01-10 microM concentrations of atorvastatin, cerivastatin, or simvastatin significantly reduced cell adhesion to endothelium. In contrast, pretreatment of endothelium with statins did not affect adhesion of monocytes. Adhesion of monocytes to vascular cell adhesion molecule-1-coated dishes was reduced by these drugs. Cerivastatin also reduced PMA induction of NF-kappaB. Since monocyte adhesion to endothelium is an early event in atherogenesis, treatment with statins in prevention of coronary heart disease may have additional salutary effects to lowering of plasma LDL cholesterol. Our results indicate that the reduction of monocyte adhesion by HMG-CoA reductase inhibitors may be considered as a class effect. (c)2001 Elsevier Science.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11735122     DOI: 10.1006/bbrc.2001.6066

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  8 in total

1.  Losartan and simvastatin inhibit platelet activation in hypertensive patients.

Authors:  Shosaku Nomura; Akira Shouzu; Seitarou Omoto; Mitsushige Nishikawa; Shirou Fukuhara; Toshiji Iwasaka
Journal:  J Thromb Thrombolysis       Date:  2004-12       Impact factor: 2.300

2.  Simvastatin reduces VCAM-1 expression in human umbilical vein endothelial cells exposed to lipopolysaccharide.

Authors:  Johnson Chia-Shen Yang; Faye Huang; Chia-Jung Wu; Yi-Chun Chen; Tsu-Hsiang Lu; Ching-Hua Hsieh
Journal:  Inflamm Res       Date:  2012-01-15       Impact factor: 4.575

3.  Oxidative stress and inflammation are differentially affected by atorvastatin, pravastatin, rosuvastatin, and simvastatin on lungs from mice exposed to cigarette smoke.

Authors:  Thiago Santos Ferreira; Manuella Lanzetti; Marina Valente Barroso; Carlos Romualdo Rueff-Barroso; Cláudia Farias Benjamim; Lycia de Brito-Gitirana; Luís Cristóvão Porto; Samuel Santos Valença
Journal:  Inflammation       Date:  2014-10       Impact factor: 4.092

4.  Atherosclerosis induced by chronic inhibition of the synthesis of nitric oxide in moderately hypercholesterolaemic rabbits is suppressed by pitavastatin.

Authors:  Masaki Kitahara; Tatsuro Kanaki; Itsuko Ishii; Yasushi Saito
Journal:  Br J Pharmacol       Date:  2010-03-03       Impact factor: 8.739

5.  Simvastatin inhibits leukocyte accumulation and vascular permeability in the retinas of rats with streptozotocin-induced diabetes.

Authors:  Shinsuke Miyahara; Junichi Kiryu; Kenji Yamashiro; Kazuaki Miyamoto; Fumitaka Hirose; Hiroshi Tamura; Hideto Katsuta; Kazuaki Nishijima; Akitaka Tsujikawa; Yoshihito Honda
Journal:  Am J Pathol       Date:  2004-05       Impact factor: 4.307

Review 6.  Management of hyperlipidaemia associated with heart transplantation.

Authors:  Klaus Wenke
Journal:  Drugs       Date:  2004       Impact factor: 9.546

Review 7.  Coronary microvasculopathy in heart transplantation: Consequences and therapeutic implications.

Authors:  Alessandra Vecchiati; Sara Tellatin; Annalisa Angelini; Sabino Iliceto; Francesco Tona
Journal:  World J Transplant       Date:  2014-06-24

8.  Atorvastatin at reperfusion reduces myocardial infarct size in mice by activating eNOS in bone marrow-derived cells.

Authors:  Yikui Tian; Joel Linden; Brent A French; Zequan Yang
Journal:  PLoS One       Date:  2014-12-03       Impact factor: 3.240

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.