Saengmearnuparp Thiraphat, Pintana Hiranya, Apaijai Nattayaporn, Chunchai Titikorn, Thonusin Chanisa, Kongkaew Aphisek, Lojanapiwat Bannakij, Chattipakorn Nipon, Chattipakorn Siriporn C
Neurophysiology unit, Cardiac Electrophysiology Research and Training Center, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand; Urology division, Department of Surgery, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand; Center of Excellence in Cardiac Electrophysiology Research, Chiang Mai University, Chiang Mai 50200, Thailand.
Neurophysiology unit, Cardiac Electrophysiology Research and Training Center, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand; Center of Excellence in Cardiac Electrophysiology Research, Chiang Mai University, Chiang Mai 50200, Thailand; Office of Research Administration, Chiang Mai University, Chiang Mai 50200, Thailand.
Behav Brain Res. 2024 Aug 24;472:115155. doi: 10.1016/j.bbr.2024.115155. Epub 2024 Jul 19.
Several studies have reported side effects of finasteride (FIN), such as anxiety/depression in young men. Obesity is also positively associated with anxiety/depression symptoms; however, the impacts of long-term FIN treatment and FIN withdrawal in young obese individuals are still elusive. The present study aimed to investigate the effect of long-term treatment and its withdrawal on anxiety/depression and brain pathologies in lean and obese adult male rats. Forty-eight male Wistar rats were equally divided into two groups and fed either a normal or high-fat diet. At age 13 weeks, rats in each dietary group were divided into three subgroups: 1) the control group receiving drinking water, 2) the long-term treatment group receiving FIN orally at 5 mg/kg/day for 6 weeks, and 3) the withdrawal group receiving FIN orally at 5 mg/kg/day for 2 weeks followed by a 4-week withdrawal period. Anxiety/depression-like behaviors, biochemical analysis, brain inflammation, oxidative stress, neuroactive steroids, brain metabolites, and microglial complexity were tested. The result showed that lean rats treated with long-term FIN and its withdrawal exhibited metabolic disturbances, depressive-like behavior, and both groups showed increased neurotoxic metabolites and reduced microglial complexity. Obesity itself led to metabolic disturbances and brain pathologies, including increased inflammation, oxidative stress, and quinolinic acid, as well as reduced microglial complexity, resulting in increased anxiety- and depression-like behaviors. Interestingly, the long-term FIN treatment group in obese rats showed attenuation of depressive-like behaviors, brain inflammation, and oxidative stress, along with increased brain antioxidants, suggesting the possible benefits of FIN in obese conditions.
多项研究报告了非那雄胺(FIN)的副作用,比如年轻男性出现焦虑/抑郁。肥胖也与焦虑/抑郁症状呈正相关;然而,长期服用FIN以及年轻肥胖个体停用FIN后的影响仍不明确。本研究旨在调查长期治疗及其停药对成年瘦型和肥胖雄性大鼠焦虑/抑郁及脑病理的影响。48只雄性Wistar大鼠平均分为两组,分别给予正常饮食或高脂饮食。13周龄时,每个饮食组的大鼠再分为三个亚组:1)对照组饮用自来水;2)长期治疗组,口服FIN,剂量为5mg/kg/天,持续6周;3)撤药组,口服FIN,剂量为5mg/kg/天,持续2周,随后停药4周。检测了焦虑/抑郁样行为、生化分析、脑炎症、氧化应激、神经活性类固醇、脑代谢物和小胶质细胞复杂性。结果显示,长期服用FIN及其撤药后的瘦型大鼠出现代谢紊乱、抑郁样行为,且两组均显示神经毒性代谢物增加,小胶质细胞复杂性降低。肥胖本身会导致代谢紊乱和脑病理变化,包括炎症、氧化应激和喹啉酸增加,以及小胶质细胞复杂性降低,从而导致焦虑和抑郁样行为增加。有趣的是,肥胖大鼠的长期FIN治疗组显示抑郁样行为、脑炎症和氧化应激减轻,同时脑抗氧化剂增加,这表明FIN在肥胖情况下可能具有益处。