作者: E.H. Taniguti , Y.S. Ferreira , I.J.V. Stupp , E.B. Fraga-Junior , C.B. Mendonça
DOI: 10.1016/J.PHYSBEH.2018.02.034
关键词: Neuroprotection 、 Brain-derived neurotrophic factor 、 Internal medicine 、 Medicine 、 Oxidative stress 、 Melatonin 、 Pineal gland 、 Endocrinology 、 Open field 、 Lipid peroxidation 、 Neuroinflammation
摘要: Abstract Accumulating evidence indicates an interaction between inflammation and depression since increased levels of pro-inflammatory cytokines are associated with depression-related symptoms. Melatonin is a hormone synthesized secreted by the pineal gland antioxidant, anti-inflammatory antidepressant-like effects. In this way, it would be interesting to evaluate putative effect melatonin treatment in acute mice model depression. The present study aimed investigate on lipopolysaccharide (LPS) induced depressive-like behavior, neuroinflammation, oxidative stress alteration brain-derived neurotrophic fator (BDNF) levels. Mice were treated (10 mg/kg, i.p.) 30 min before LPS (0.5 mg/kg, injection. Twenty-four hours after infusion, submitted behavioral tests and, thereafter, biochemical determinations performed. prevented LPS-induced behavior forced swim tail suspension no alterations locomotor activity evaluated open field test. attenuated increase tumor necrosis factor-α (TNF-α) reduction BDNF hippocampus. Treatment also lipid peroxidation glutathione conclusion, suggests that exerted neuroprotective effects against which may related TNF-α release, modulation expression.