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Abstract Heme oxygenase (HO) is the rate-limiting enzyme in the metabolism of heme-releasing bioactive molecules carbon monoxide (CO), biliverdin, and iron, each with beneficial cardiovascular actions. Biliverdin is rapidly reduced to bilirubin, a potent antioxidant, by the enzyme biliverdin reductase, and iron is rapidly sequestered by ferritin in the cell. Several studies have demonstrated that HO-1 induction can attenuate the development of hypertension as well as lower blood pressure in established hypertension in both genetic and experimental models. HO-1 induction can also reduce target organ injury and can be beneficial in cardiovascular diseases, such as heart attack and stroke. Recent studies have also identified a beneficial role for HO-1 in the regulation of body weight and metabolism in diabetes and obesity. Chronic HO-1 induction lowers body weight and corrects hyperglycemia and hyperinsulinemia. Chronic HO-1 induction also modifies the phenotype of adipocytes in obesity from one of large, cytokine producing to smaller, adiponectin producing. Finally, chronic induction of HO-1 increases oxygen consumption, CO 2 , and heat production and activity in obese mice. This review will discuss the current understanding of the actions of the HO system to lower blood pressure and body weight and how HO or its metabolites may be ideal candidates for the development of drugs that can both reduce blood pressure and lower body weight. carbon monoxide bilirubin biliverdin adiponectin kidney inflammation Copyright © 2012 the American Physiological Society « Previous | Next Article » Table of Contents This Article Published online before print November 2011 , doi: 10.​1152/​ajpregu.​00517.​2011 AJP - Regu Physiol January 2012 vol. 302 no. 2 R207-R214 » Abstract Free Full Text Free to you Full Text (PDF) Free to you All Versions of this Article: ajpregu.00517.2011v1 302/2/R207 most recent Classifications Review Services Email this article to a friend Alert me when this article is cited Alert me if a correction is posted Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Download to citation manager Citing Articles Load citing article information Citing articles via Web of Science Google Scholar Articles by Hosick, P. A. Articles by Stec, D. E. PubMed PubMed citation Articles by Hosick, P. A. Articles by Stec, D. E. Related Content Load related web page information Current Issue January 2012, 302 (2) Alert me to new issues of AJP - Regu Physiol About the Journal Information for Authors Submit a Manuscript Ethical Policies AuthorChoice PubMed Central Policy Reprints and Permissions Advertising Press Copyright © 2012 the American Physiological Society Print ISSN: 0363-6119 Online ISSN: 1522-1490 var gaJsHost = (("https:" == document.location.protocol) ? "https://ssl." : "http://www."); document.write(unescape("%3Cscript src='" + gaJsHost + "google-analytics.com/ga.js' type='text/javascript'%3E%3C/script%3E")); var pageTracker = _gat._getTracker("UA-2924550-1"); pageTracker._trackPageview();

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Heme oxygenase, a novel target for the treatment of hypertension and obesity?

Hosick, Peter A.; Stec, David E.
AJP - Regulatory, Integrative and Comparative Physiology , Volume 302 (2): R207
The American Physiological SocietyJan 1, 2012

More Info

  • Publisher American Physiological Society
  • Copyright Copyright © 2012 the American Physiological Society
  • ISSN 0363-6119
  • eISSN 1522-1490
  • D.O.I. 10.1152/ajpregu.00517.2011
  • Publisher site Get PDF  

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