Cannabis sativa L. Leaf Oil Displays Cardiovascular Protective Effects in Hypertensive Rats

被引:0
|
作者
Khamseekaew, Juthamas [1 ]
Duangjinda, Monchai [2 ]
Maneesai, Putcharawipa [1 ]
Labjit, Chanon [3 ]
Rattanakanokchai, Siwayu [4 ]
Rongpan, Sudarat [1 ,5 ]
Pakdeechote, Poungrat [1 ]
Potue, Prapassorn [1 ]
机构
[1] Khon Kaen Univ, Fac Med, Dept Physiol, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Fac Agr, Dept Anim Sci, Khon Kaen 40002, Thailand
[3] Khon Kaen Univ, Fac Agr, Dept Hort, Khon Kaen 40002, Thailand
[4] Khon Kaen Univ, Fac Vet Med, Khon Kaen 40002, Thailand
[5] Princess Naradhiwas Univ, Fac Med, Dept Physiol, Narathiwat 96000, Thailand
关键词
Cannabis sativa L. leaf oil; hemp leaf oil; cardiovascular function; L-NAME-induced hypertensive rats; ARGININE METHYL-ESTER; NITRIC-OXIDE; L-NAME; OXIDATIVE STRESS; BLOOD-PRESSURE; NAD(P)H OXIDASE; INHIBITION; RESPONSES; ENOS; HYPERTROPHY;
D O I
10.3390/ijms26051897
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
Hemp (Cannabis sativa L.) leaf oil (HLO) contains several bioactive compounds such as phenolics, flavonoids, and quercetin. However, the effects of HLO on hypertensive conditions have not yet been investigated. This study investigated the cardiovascular protective effects of HLO in a nitric oxide (NO) synthase inhibitor-induced hypertensive rat model. Five weeks of HLO administration significantly prevented blood pressure elevation, improved cardiac function, and mitigated cardiac hypertrophy. Furthermore, HLO ameliorated vascular dysfunction by reducing sympathetic nerve stimulation-induced vasoconstriction, increasing endothelium-dependent vasorelaxation, as well as decreasing vascular wall thickness and vascular smooth muscle cell proliferation. HLO inhibited renin-angiotensin system (RAS) activation and downregulated angiotensin II type 1 (AT1) receptor and NADPH oxidase expression. Additionally, HLO normalized the circulating NO metabolites, decreased oxidative stress, and enhanced antioxidant status. These findings suggest that HLO protects against cardiovascular dysfunction and preserves its morphology. The mechanism of action might involve the suppression of RAS overactivity and oxidative stress through the Ang II/AT1 receptor/NOX2 pathway in NO-deficient hypertension.
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页数:17
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