Woodruff J L, Bykalo M K, Loyo-Rosado F Z, Maissy E S, Sadek A T, Hersey M, Erichsen J M, Maxwell N D, Wilson M A, Wood S K, Hashemi P, Grillo C A, Reagan L P
University of South Carolina School of Medicine, Department of Pharmacology, Physiology, and Neuroscience, Columbia, SC, USA; Columbia VA Health Care System, Columbia, SC, USA.
University of South Carolina School of Medicine, Department of Pharmacology, Physiology, and Neuroscience, Columbia, SC, USA.
Appetite. 2024 Aug 1;199:107389. doi: 10.1016/j.appet.2024.107389. Epub 2024 Apr 30.
The complications of obesity extend beyond the periphery to the central nervous system (CNS) and include an increased risk of developing neuropsychiatric co-morbidities like depressive illness. Preclinical studies support this concept, including studies that have examined the effects of a high-fat diet (HFD) on depressive-like behaviors. Although women are approximately two-fold more likely to develop depressive illness compared to men, most preclinical studies have focused on the effects of HFD in male rodents. Accordingly, the goal of this study was to examine depressive-like behaviors in male and female rats provided access to a HFD. In agreement with prior studies, male and female rats provided a HFD segregate into an obesity phenotype (i.e., diet-induced obesity; DIO) or a diet resistant (DR) phenotype. Upon confirmation of the DR and DIO phenotypes, behavioral assays were performed in control chow, DR, and DIO rats. In the sucrose preference test, male DIO rats exhibited significant decreases in sucrose consumption (i.e., anhedonia) compared to male DR and male control rats. In the forced swim test (FST), male DIO rats exhibited increases in immobility and decreases in climbing behaviors in the pre-test sessions. Interestingly, male DR rats exhibited these same changes in both the pre-test and test sessions of the FST, suggesting that consumption of a HFD, even in the absence of the development of an obesity phenotype, has behavioral consequences. Female rats did not exhibit differences in sucrose preference, but female DIO rats exhibited increases in immobility exclusively in the test session of the FST, behavioral changes that were not affected by the stage of the estrous cycle. Collectively, these studies demonstrate that access to a HFD elicits different behavioral outcomes in male and female rats.
肥胖的并发症不仅影响外周,还会波及中枢神经系统(CNS),包括罹患神经精神共病(如抑郁症)风险的增加。临床前研究支持这一观点,其中包括研究高脂饮食(HFD)对类似抑郁行为的影响。尽管女性患抑郁症的可能性约为男性的两倍,但大多数临床前研究都集中在HFD对雄性啮齿动物的影响上。因此,本研究的目的是检查给予HFD的雄性和雌性大鼠的类似抑郁行为。与先前的研究一致,给予HFD的雄性和雌性大鼠会分为肥胖表型(即饮食诱导肥胖;DIO)或饮食抵抗(DR)表型。在确认DR和DIO表型后,对对照组、DR组和DIO组大鼠进行行为分析。在蔗糖偏好试验中,与雄性DR组和雄性对照组大鼠相比,雄性DIO组大鼠的蔗糖消耗量显著降低(即快感缺失)。在强迫游泳试验(FST)中,雄性DIO组大鼠在预试验阶段的不动时间增加,攀爬行为减少。有趣的是,雄性DR组大鼠在FST的预试验和试验阶段均出现了相同的变化,这表明即使没有肥胖表型的发展,食用HFD也会产生行为后果。雌性大鼠在蔗糖偏好方面没有表现出差异,但雌性DIO组大鼠仅在FST的试验阶段出现不动时间增加,这些行为变化不受发情周期阶段的影响。总的来说,这些研究表明,给予HFD会在雄性和雌性大鼠中引发不同的行为结果。