Butterfly Pea Flower (Clitoria ternatea Linn.) Extract Ameliorates Cardiovascular Dysfunction and Oxidative Stress in Nitric Oxide-Deficient Hypertensive Rats

被引:19
|
作者
Maneesai, Putcharawipa [1 ]
Iampanichakul, Metee [1 ]
Chaihongsa, Nisita [1 ]
Poasakate, Anuson [1 ]
Potue, Prapassorn [1 ]
Rattanakanokchai, Siwayu [2 ]
Bunbupha, Sarawoot [3 ]
Chiangsaen, Petcharat [4 ]
Pakdeechote, Poungrat [1 ,5 ]
机构
[1] Khon Kaen Univ, Dept Physiol, Fac Med, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Fac Vet Med, Khon Kaen 40002, Thailand
[3] Mahasarakham Univ, Fac Med, Maha Sarakham 44000, Thailand
[4] Bangkokthonburi Univ, Fac Med, Bangkok 10170, Thailand
[5] Khon Kaen Univ, Res Inst Human High Performance & Hlth Promot, Khon Kaen 40002, Thailand
关键词
Clitoria ternatea Linn; left ventricular and vascular dysfunction; oxidative stress; renin– angiotensin system; inflammation;
D O I
10.3390/antiox10040523
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we examine whether Clitoria ternatea Linn. (CT) can prevent N omega-nitro-L-arginine methyl ester hydrochloride (L-NAME)-induced cardiac and vascular dysfunction in rats. Male Sprague Dawley rats were given L-NAME (40 mg/kg, drinking water) and orally administered with CT extract (300 mg/kg/day) or lisinopril (2.5 mg/kg/day) for 5 weeks. The main phytochemical components of the CT extract were found to be flavonoids. The CT extract alleviated the high blood pressure in rats receiving L-NAME. Decreased vasorelaxation responses to acetylcholine and enhanced contractile responses to sympathetic nerve stimulation in aortic rings and mesenteric vascular beds of L-NAME treated rats were ameliorated by CT extract supplementation. Left ventricular hypertrophy and dysfunction were developed in L-NAME rats, which were partially prevented by CT extract treatment. The CT extract alleviated upregulated endothelial nitric oxide synthase expression, decreased plasma nitrate/nitrite levels, and increased oxidative stress in L-NAME rats. It suppressed high levels of serum angiotensin-converting enzyme activity, plasma angiotensin II, and cardiac angiotensin II type 1 receptor, NADPH oxidases 2, nuclear factor-kappa B, and tumor necrosis factor-alpha expression. The CT extract, therefore, partially prevented L-NAME-induced hypertension and cardiovascular alterations in rats. These effects might be related to a reduction in the oxidative stress and renin-angiotensin system activation due to L-NAME in rats.
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页数:16
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