槲皮素
神经炎症
脂多糖
促炎细胞因子
小胶质细胞
药理学
海马体
行为绝望测验
开阔地
内分泌学
内科学
化学
抗抑郁药
医学
炎症
生物化学
抗氧化剂
作者
Olusegun Adebayo Adeoluwa,Juliet N. Olayinka,Gladys Onyinye Adeoluwa,Elizabeth Toyin Akinluyi,Funmilayo Adeniyi,Adedamola Adediran Fafure,Kate Eberechukwu Nebo,Edem Ekpenyong Edem,Anthony T. Eduviere,Badamasi Abubakar
标识
DOI:10.1016/j.bbr.2023.114503
摘要
Major depressive disorder is a serious psychiatric illness having serious damaging effect on the quality of life of suffers. Quercetin is a plant flavonoid, mostly used as a constituent in dietary products. This study evaluated antidepressant effect of quercetin on lipopolysaccharide (LPS)-induced depression in rats.Twenty-one male rats were randomly assigned into three groups (n = 7): group 1 (vehicle only), group 2 (quercetin), group 3 (LPS). Rats were treated with vehicle (10 mL/kg, p.o.) or quercetin (50 mg/kg, p.o.) for seven days. Sixty minutes after treatment on day seven, all animals were injected with LPS (0.83 mg/kg, i.p.) except group 1 (vehicle only). Twenty-four hours after LPS injection, animals were assessed for depressive symptoms using forced swim, sucrose splash and open field tests. Animals were sacrificed; brain samples collected for bioassay of pro-inflammatory mediators, TNF-α, IL-6 and IL-17 were measured using enzyme-linked immunosorbent assay (ELISA) while expressions of NF-κB, inflammasomes, microglia and iNOS were quantified by immunohistochemistry.The LPS significantly (p < 0.05) decreased mobility of rats in FST and decreased sucrose preference, which is indicative of depressive-like behaviours. These behaviours were significantly (p < 0.05) attenuated by quercetin compared to control (vehicle only). Following LPS exposure, the expressions of inflammasomes, NF-κB, iNOS, proinflammatory cytokines and microglia positive cells in the hippocampus and prefrontal cortex were significantly (p < 0.05) elevated. All these were attenuated by pretreating animals with quercetin.Quercetin exhibit antidepressant-like property, which may be related to inhibition of neuroinflammatory signaling pathways.
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