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   Anti-hypertensive effects of diminazene aceturate: An angiotensin-converting enzyme 2 activator in rats  
   
نویسنده de maria m.l.a. ,araújo l.d. ,fraga-silva r.a. ,pereira l.a.s. ,ribeiro h.j. ,menezes g.b. ,shenoy v. ,raizada m.k. ,ferreira a.j.
منبع protein and peptide letters - 2016 - دوره : 23 - شماره : 1 - صفحه:9 -16
چکیده    Previous studies have shown that activation of endogenous angiotensin-converting enzyme 2 (ace2) results in various beneficial effects in the cardiovascular system. recently,a new ace2 activator,named diminazene aceturate (dize),was described. here,we evaluated the actions of this compound in blood pressure (bp) and heart rate (hr) of conscious normotensive and hypertensive rats,as well as explored its mechanism of actions using isolated vessels. the renovascular model of hypertension was utilized. the participation of the angiotensin-(1-7) receptor mas and nitric oxide (no) in the effects of dize was evaluated using a-779 and l-name,respectively. it was observed that dize caused a marked decrease in bp with a compensatory increase in hr in nornotensive rats. accordingly,a significant reduction in the blood flow of the mesenteric bed was evidenced using intravital microscopy. moreover,in rats with renovascular hypertension,dize caused a decrease in bp similar to the hypotensive effect induced by captopril. importantly,this compound also prevented the development of cardiac hypertrophy induced by hypertension. the isolated vessels technique revealed that the vasodilator effects of dize were dependent on mas activation and no release. thus,our findings demonstrated that dize reduces the bp of normotensinve and hypertensive rats possibly by a mechanism involving mas and no. © 2015 bentham science publishers.
کلیدواژه Angiotensin-(1-7); Angiotensin-converting enzyme 2; Aortic vessels; Intravital microscopy; Mas receptor; Renin-angiotensin system; Renovascular hypertension
آدرس department of morphology,institute of biological sciences,federal university of minas gerais,av. antônio carlos,6627,belo horizonte,mg, Brazil, department of morphology,institute of biological sciences,federal university of minas gerais,av. antônio carlos,6627,belo horizonte,mg, Brazil, department of morphology,institute of biological sciences,federal university of minas gerais,av. antônio carlos,6627,belo horizonte,mg, Brazil, department of morphology,institute of biological sciences,federal university of minas gerais,av. antônio carlos,6627,belo horizonte,mg, Brazil, department of morphology,institute of biological sciences,federal university of minas gerais,av. antônio carlos,6627,belo horizonte,mg, Brazil, department of morphology,institute of biological sciences,federal university of minas gerais,av. antônio carlos,6627,belo horizonte,mg, Brazil, department of physiology and functional genomics,university of florida,gainesville,fl, United States, department of physiology and functional genomics,university of florida,gainesville,fl, United States, department of morphology,institute of biological sciences,federal university of minas gerais,av. antônio carlos,6627,belo horizonte,mg, Brazil
 
     
   
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