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Neuroprotective effects of Withania somnifera on ischemic stroke are mediated via anti-inflammatory response and modulation of neurotransmitter levels
被引:1
作者:
Sood, Abhilasha
[1
,3
]
Mehrotra, Arpit
[1
,3
]
Dhawan, Devinder K.
[2
]
Sandhir, Rajat
[1
]
机构:
[1] Panjab Univ, Dept Biochem, Hargobind Khorana Block,Sect 25, Chandigarh 160014, India
[2] Panjab Univ, Dept Biophys, Hargobind Khorana Block,Sect 25, Chandigarh 160014, India
[3] Chitkara Univ, Chitkara Sch Hlth Sci, Dept Allied Hlth Sci, Rajpura 140401, Punjab, India
关键词:
Brain;
Inflammation;
Neurotransmitters;
Phytochemicals;
Stroke;
Withania somnifera;
FACTOR-KAPPA-B;
EXPERIMENTAL-MODEL;
ASHWAGANDHA;
ACTIVATION;
AMINES;
RATS;
D O I:
10.1016/j.neuint.2024.105867
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:
The present study was designed to evaluate the beneficial effects of hydroalcoholic root extract of Withania somnifera (WS) on ischemia-reperfusion injury (IRI) induced by Middle Cerebral Artery Occlusion (MCAO). MCAO animals showed increase in IL-6, TNF-alpha and MCP-1 levels in terms of mRNA and protein levels. Concomitantly, mRNA and protein levels for astrocyte and microglial activation markers; GFAP and IBA-1, were increased in MCAO animals. COX-2 and NF-k beta protein beta protein levels were also increased in the brains of MCAO animals. The levels of neurotransmitters; glutamate and GABA were increased in the MCAO animals. On the contrary, levels of catecholamines; dopamine, norepinephrine and serotonin were reduced in the MCAO animals. Additionally, MCAO animals showed reduced locomotor activity. However, pre-supplementation with WS hydro- alcoholic root extract at a dose of 300 mg/kg, body weight to MCAO animals reduced the expression of IL-6, TNF-alpha and MCP-1. In addition, WS also reduced the number of GFAP and Iba-1 positive cells in comparison to MCAO animals. WS pre-supplementation was also observed to inhibit MCAO induced increase in COX-2; NF-k beta beta proteins and reduce the glutamate levels. The levels of GABA, dopamine, norepinephrine and serotonin were increased in WS pre-supplemented MCAO animals. WS pre-supplementation also prevented motor deficits in the MCAO animals. Taken together, these findings suggest that WS is effective in attenuating IRI induced neuroinflammation, neurochemical alterations and motor deficits in MCAO model of ischemic stroke thereby suggesting its ameliorative role in ischemia-reperfusion injury.
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