Cardio-protective and antioxidant properties of caffeic acid and chlorogenic acid: Mechanistic role of angiotensin converting enzyme, cholinesterase and arginase activities in cyclosporine induced hypertensive rats

[Display omitted] •Caffeic acid (CAA) and chlorogenic acid (CHA) possessed BP reducing effect in hypertensive rats (HTR).•CAA and CHA reduced ACE, cholinesterase and arginase activities in HTR.•CAA and CHA enhanced nitric oxide (NOx) level in HTR. Caffeic acid (CAA) and chlorogenic acid (CHA) are im...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2019-01, Vol.109, p.450-458
Hauptverfasser: Agunloye, Odunayo Michael, Oboh, Ganiyu, Ademiluyi, Adedayo Oluwaseun, Ademosun, Ayokunle Olubode, Akindahunsi, Akintunde Afolabi, Oyagbemi, Ademola Adetokunbo, Omobowale, Temidayo Olutayo, Ajibade, Temitayo Olabisi, Adedapo, Adeolu Alex
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Sprache:eng
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Zusammenfassung:[Display omitted] •Caffeic acid (CAA) and chlorogenic acid (CHA) possessed BP reducing effect in hypertensive rats (HTR).•CAA and CHA reduced ACE, cholinesterase and arginase activities in HTR.•CAA and CHA enhanced nitric oxide (NOx) level in HTR. Caffeic acid (CAA) and chlorogenic acid (CHA) are important members of hydroxycinnamic acid with natural antioxidant and cardio-protective properties. The present study aimed to determine the effect of CAA and CHA on systolic blood pressure, heart rates (HR) as well as on the activity of the angiotensin-1-converting enzyme (ACE), acetylcholinesterase (AChE), butrylcholinesterase (BChE) and arginase in cyclosporine-induced hypertensive rats. Experimental rats were distributed into 7 groups (n = 6): normotensive control rats; hypertensive rats (induced rats) as well as hypertensive- treated groups with captopril (10 mg/kg/day), CAA (10 and 15 mg/kg/day) and CHA (10 and 15 mg/kg/day), respectively. The experiment lasted for 7 days and the systolic blood pressure (SBP) and heart rates were recorded using tail-cuff method. Oral administration of captopril, caffeic acid and chlorogenic acid normalized hypertensive effect caused by cyclosporine administration. CAA and CHA significantly (P 
ISSN:0753-3322
1950-6007
DOI:10.1016/j.biopha.2018.10.044