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7,8-Dihydroxyflavone alleviated the high-fat diet and alcohol-induced memory impairment: behavioral, biochemical and molecular evidence.

Authors :
Pandey, Surya Narayan
Kwatra, Mohit
Dwivedi, Durgesh Kumar
Choubey, Priyansha
Lahkar, Mangala
Jangra, Ashok
Source :
Psychopharmacology; Jun2020, Vol. 237 Issue 6, p1827-1840, 14p, 3 Diagrams, 1 Chart, 7 Graphs
Publication Year :
2020

Abstract

Rationale: Alcoholism and obesity impart a deleterious impact on human health and affects the quality of life. Chronic consumption of alcohol and western diet has been reported to cause memory deficits. 7,8-dihydroxyflavone (7,8-DHF), a TrkB agonist, comprises antioxidant and anti-inflammatory properties in treating various neurological disorders. Objectives: The current study was aimed to determine the protective effect and molecular mechanism of 7,8-DHF against alcohol and high-fat diet (HFD)-induced memory deficits in rats. Methods: The adult male Wistar rats were given alcohol (3–15%) and HFD ad libitum for 12 weeks in different experimental groups. 7,8-DHF (5 mg/kg) was intraperitoneally injected daily for the last 4 weeks (9th–12th week). Results: The alcohol and HFD administration caused cognitive impairment as evaluated through the Morris water maze (MWM) test in alcohol, HFD, and alcohol + HFD-fed animals. The last 4-week treatment of 7,8-DHF (5 mg/kg; i.p.) attenuated alcohol and HFD-induced memory loss. 7,8-DHF treatment also restored the glutathione (GSH) level along with attenuation of nitrite, malondialdehyde content (markers of oxidative and nitrosative stress), and reduction of the acetylcholinesterase activity in the hippocampus of alcohol and HFD-fed animals. Furthermore, the administration of 7,8-DHF caused downregulation of NF-κB, iNOS, and caspase-3 and upregulation of Nrf2, HO-1, and BDNF mRNA level in rat hippocampus. Conclusion: 7,8-DHF administration conferred beneficial effects against alcohol and HFD-induced memory deficit via its unique antioxidant, anti-inflammatory, anti-apoptotic potential, along with the activation of TrkB/BDNF signaling pathway in the hippocampus. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00333158
Volume :
237
Issue :
6
Database :
Complementary Index
Journal :
Psychopharmacology
Publication Type :
Academic Journal
Accession number :
143359083
Full Text :
https://doi.org/10.1007/s00213-020-05502-2