Sumaya Isabel C, Bailey Dee, Catlett Susan L
Department of Psychology, Behavioral Neuroscience Laboratory, California State University, Bakersfield, Bakersfield, CA 93311-1099, USA.
Department of Psychology, Behavioral Neuroscience Laboratory, California State University, Bakersfield, Bakersfield, CA 93311-1099, USA.
Pharmacol Biochem Behav. 2016 May;144:78-84. doi: 10.1016/j.pbb.2016.03.005. Epub 2016 Mar 12.
Investigation into the effects of a high-fat diet on depression in the context of 5-HT3 receptor function is important given 5-HT3 antagonism may represent a novel candidate for drug discovery. To more fully understand the relationship between the 5-HT3 receptor system, depression, and high-fat intake, our main interest was to study the short-term effects of a high-fat diet on the 5-HT3 receptor antagonist, ondansetron, and the 5-HT3 receptor agonist, 2-methyl-5-HT, as well as the SSRI, fluoxetine, in an animal model of depression. Male Sprague Dawley rats were fed either a standard diet (11% fat) or a high-fat diet (32.5% fat) for seven days then treated with either fluoxetine (10mg/kg, ip), ondansetron (1mg/kg, ip), 2-methyl-5-HT (3mg/kg, ip), fluoxetine+ondansetron or, 2-methyl-5-HT+ondansetron prior to the Forced Swim Test. In the standard diet group, treatment with the 5HT3 receptor agonist, 2-methyl-5-HT, served to significantly decrease time of immobility as compared to controls thus showing anti-depressive-like effects. Treatment with the 5-HT3 receptor antagonist, ondansetron, served to enhance the anti-depressive like effects of the SSRI, fluoxetine, as treatment with both the SSRI and 5-HT3 receptor antagonist dramatically decreased immobility. Importantly, in the high-fat diet groups, a week of high-fat intake served to: 1) counteract the anti-depressive-like effect of the SSRI, fluoxetine, 2) reverse the anti-depressive-like effect of the 5HT3 receptor agonist, 2-methyl-5-HT and 3) provide protection against the depressive-like effects induced by the Forced Swim Test as rats fed a high-fat diet displayed the lowest amounts of immobility. In the aggregate, these data suggest that both SSRIs and the 5HT3 receptor system are affected by short-term high-fat intake and that a short-term high-fat diet protects against depressive-like effects in an animal model of depression.
鉴于5-羟色胺3(5-HT3)受体拮抗作用可能是药物研发的新候选方向,研究高脂饮食在5-HT3受体功能背景下对抑郁症的影响具有重要意义。为了更全面地理解5-HT3受体系统、抑郁症和高脂摄入之间的关系,我们主要关注的是在抑郁症动物模型中研究高脂饮食对5-HT3受体拮抗剂昂丹司琼、5-HT3受体激动剂2-甲基-5-HT以及选择性5-羟色胺再摄取抑制剂(SSRI)氟西汀的短期影响。雄性斯普拉格-道利大鼠被喂食标准饮食(11%脂肪)或高脂饮食(32.5%脂肪)7天,然后在强迫游泳试验前用氟西汀(10mg/kg,腹腔注射)、昂丹司琼(1mg/kg,腹腔注射)、2-甲基-5-HT(3mg/kg,腹腔注射)、氟西汀+昂丹司琼或2-甲基-5-HT+昂丹司琼进行处理。在标准饮食组中,与对照组相比,用5-HT3受体激动剂2-甲基-5-HT治疗可显著减少不动时间,从而显示出抗抑郁样作用。用5-HT3受体拮抗剂昂丹司琼治疗可增强SSRI氟西汀的抗抑郁样作用,因为同时使用SSRI和5-HT3受体拮抗剂可显著减少不动时间。重要的是,在高脂饮食组中,一周的高脂摄入起到了以下作用:1)抵消SSRI氟西汀的抗抑郁样作用;2)逆转5-HT3受体激动剂2-甲基-5-HT的抗抑郁样作用;3)提供对强迫游泳试验诱导的抑郁样作用的保护,因为喂食高脂饮食的大鼠表现出最低的不动量。总体而言,这些数据表明,SSRI和5-HT3受体系统均受短期高脂摄入的影响,并且短期高脂饮食可在抑郁症动物模型中预防抑郁样作用。