Literature DB >> 16187690

Taking the 20-HETE out of the cardiovascular system: the potential of 20-HETE synthesis inhibitors.

Sheila A Doggrell1.   

Abstract

In addition to being metabolized by cyclooxygenase and lipooxygenase to prostaglandins and leukotrienes, arachidonic acid can be metabolized to 20-hydroxyeicosatetraenoic acid (20-HETE) by cytochrome P450 enzymes omega-hydroxylases. As 20-HETE has both pro-hypertensive and antihypertensive actions, inhibitors of 20-HETE synthase may not be useful as antihypertensives in all forms of hypertension. However, 20-HETE synthase inhibitors can have cardioprotective and cerebroprotective effects in animal models, and can inhibit angiogenesis; therefore they may have clinical potential in these areas.

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Year:  2005        PMID: 16187690

Source DB:  PubMed          Journal:  Curr Opin Investig Drugs        ISSN: 1472-4472


  1 in total

1.  Inhibition of 20-HETE synthesis and action protects the kidney from ischemia/reperfusion injury.

Authors:  Uwe Hoff; Ivo Lukitsch; Lyubov Chaykovska; Mechthild Ladwig; Cosima Arnold; Vijay L Manthati; T Florian Fuller; Wolfgang Schneider; Maik Gollasch; Dominik N Muller; Bert Flemming; Erdmann Seeliger; Friedrich C Luft; John R Falck; Duska Dragun; Wolf-Hagen Schunck
Journal:  Kidney Int       Date:  2010-10-20       Impact factor: 10.612

  1 in total

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