Literature DB >> 12573196

Cyclooxygenase-2 inhibitors: is there an association with coronary or renal events?

Richard J Bing1.   

Abstract

The article is concerned with the effects of specific cyclooxygenase-2 (COX-2) inhibitors and their relationship to thrombotic cardiovascular events and to renal disease. Clinical and experimental aspects of COX-2-specific inhibitors are cited. A COX-2 inhibitor, celecoxib, interferes with myocardial prostacyclin production and also produces hypertension. Data have shown that in animal experiments, celecoxib also lowers myocardial prostaglandin concentration but fails to inhibit thromboxane concentration to the same degree. In the kidney, celecoxib can result in glomerular and interstitial nephritis or papillary necrosis. As in infarcted heart muscle, the COX-2-specific inhibitor celecoxib causes a significant decline in prostaglandin in the renal medulla. It was concluded from both clinical and experimental findings that COX-2 inhibitors can cause thrombotic cardiovascular events as well as renal disease. For these reasons, care should be exercised in administering specific COX-2 inhibitors to patients with pre-existing cardiac or renal disease.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12573196     DOI: 10.1007/s11883-003-0082-2

Source DB:  PubMed          Journal:  Curr Atheroscler Rep        ISSN: 1523-3804            Impact factor:   5.113


  29 in total

1.  Cardiovascular events and COX-2 inhibitors.

Authors:  M Fleming
Journal:  JAMA       Date:  2001-12-12       Impact factor: 56.272

2.  Cyclooxygenase-2 inhibition and renal function.

Authors:  A Whelton
Journal:  Ann Intern Med       Date:  2001-06-05       Impact factor: 25.391

Review 3.  Cyclooxygenases: structural, cellular, and molecular biology.

Authors:  W L Smith; D L DeWitt; R M Garavito
Journal:  Annu Rev Biochem       Date:  2000       Impact factor: 23.643

4.  Localization of cyclooxygenase-1 and -2 in adult and fetal human kidney: implication for renal function.

Authors:  M Kömhoff; H J Grone; T Klein; H W Seyberth; R M Nüsing
Journal:  Am J Physiol       Date:  1997-04

Review 5.  Arachidonic acid metabolism.

Authors:  P Needleman; J Turk; B A Jakschik; A R Morrison; J B Lefkowith
Journal:  Annu Rev Biochem       Date:  1986       Impact factor: 23.643

6.  Regulation of cyclooxygenase-2 (COX-2) in rat renal cortex by adrenal glucocorticoids and mineralocorticoids.

Authors:  M Z Zhang; R C Harris; J A McKanna
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

Review 7.  Some aspects of biochemistry of myocardial infarction.

Authors:  R J Bing
Journal:  Cell Mol Life Sci       Date:  2001-03       Impact factor: 9.261

8.  Are selective COX-2 inhibitors nephrotoxic?

Authors:  M A Perazella; J Eras
Journal:  Am J Kidney Dis       Date:  2000-05       Impact factor: 8.860

9.  Nitric oxide, anti-inflammatory drugs on renal prostaglandins and cyclooxygenase-2.

Authors:  Masaru Miyataka; Kathryn A Rich; Marylou Ingram; Tadahiko Yamamoto; Richard J Bing
Journal:  Hypertension       Date:  2002-03-01       Impact factor: 10.190

10.  Gastrointestinal damage associated with the use of nonsteroidal antiinflammatory drugs.

Authors:  M C Allison; A G Howatson; C J Torrance; F D Lee; R I Russell
Journal:  N Engl J Med       Date:  1992-09-10       Impact factor: 91.245

View more
  2 in total

1.  Albumin microspheres as carriers for the antiarthritic drug celecoxib.

Authors:  Hetal Thakkar; Rakesh Kumar Sharma; Anil Kumar Mishra; Krishna Chuttani; Rayasa Ramchandra Murthy
Journal:  AAPS PharmSciTech       Date:  2005-09-20       Impact factor: 3.246

Review 2.  Reciprocal regulation of the nitric oxide and cyclooxygenase pathway in pathophysiology: relevance and clinical implications.

Authors:  Daniela Salvemini; Sangwon F Kim; Vincenzo Mollace
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2013-02-06       Impact factor: 3.619

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.