Sodium metavanadate induced cognitive decline, behavioral impairments, oxidative stress and down regulation of myelin basic protein in mice hippocampus: Ameliorative roles of β‐spinasterol, and stigmasterol

• Published in: Brain and behavior 2018-07, Vol.8 (7), p.e01014-n/a
• Main Authors: Adebiyi, Olamide Elizabeth, Olopade, James Olukayode, Olayemi, Funsho Olakitike
• Format: Article
• Language: English
• Subjects: Animals; antioxidant; Antioxidants; Antioxidants - metabolism; behavior; Behavior, Animal - drug effects; Cognitive Dysfunction - chemically induced; Cognitive Dysfunction - prevention & control; Down-Regulation - drug effects; Hippocampus - metabolism; Lipid Peroxidation - drug effects; Male; Memory; Memory Disorders - chemically induced; Memory Disorders - prevention & control; Mice; Mice, Inbred BALB C; Myelin Basic Protein - metabolism; Neurotoxicity; Neurotoxicity Syndromes - etiology; Original Research; Oxidative stress; Oxidative Stress - drug effects; Rodents; Sodium; stigmasterol; Stigmasterol - analogs & derivatives; Stigmasterol - pharmacology; Vanadates - toxicity; vanadium; β‐spinasterol
• ISSN: 2162-3279; 2162-3279
• DOI: 10.1002/brb3.1014

Introduction Exposures to toxic levels of vanadium and soluble vanadium compounds cause behavioral impairments and neurodegeneration via free radical production. Consequently, natural antioxidant sources have been explored for effective and cheap remedy following toxicity. Grewia carpinifolia has been shown to improve behavioral impairments in vanadium‐induced neurotoxicity, however, the active compounds implicated remains unknown. Therefore, this study was conducted to investigate ameliorative effects of bioactive compounds from G. carpinifolia on memory and behavioral impairments in vanadium‐induced neurotoxicity. Methods Sixty BALB/c mice were equally divided into five groups (A–E). A (control); administered distilled water, B (standard); administered α‐tocopherol (500 mg/kg) every 72 hr orally with daily dose of sodium metavanadate (3 mg/kg) intraperitoneally, test groups C, and D; received single oral dose of 100 μg β‐spinasterol or stigmasterol (bioactive compounds from G. carpinifolia), respectively, along with sodium metavanadate and the model group E, received sodium metavanadate only for seven consecutive days. Memory, locomotion and muscular strength were accessed using Morris water maze, Open field and hanging wire tests. In vivo antioxidant and neuroprotective activities were evaluated by measuring catalase, superoxide dismutase, MDA, H2O2, and myelin basic protein (MBP) expression in the hippocampus. Results In Morris water maze, stigmasterol significantly (p ≤ 0.05) decreased escape latency and increased swimming time in target quadrant (28.01 ± 0.02; 98.24 ± 17.38 s), respectively, better than α‐tocopherol (52.43 ± 13.25; 80.32 ± 15.21) and β‐spinasterol (42.09 ± 14.27; 70.91 ± 19.24) in sodium metavanadate‐induced memory loss (112.31 ± 9.35; 42.35 ± 11.05). β‐Spinasterol and stigmasterol significantly increased exploration and latency in open field and hanging wire tests respectively. Stigmasterol also increased activities of antioxidant enzymes, decreased oxidative stress markers and lipid peroxidation in mice hippocampal homogenates, and increased MBP expression. Conclusions The findings of this study indicate a potential for stigmasterol, a bioactive compound from G. carpinifolia in improving cognitive decline, motor coordination, and ameliorating oxidative stress in vanadium‐induced neurotoxicity. Sodium metavanadate toxicity resulted in demyelination, cognitive and behavioral impairment in mice. Stigmasterol. a bioactive compound from