Pawar Ganesh R, Agrawal Yogeeta O, Nakhate Kartik T, Patil Chandragouda R, Sharma Charu, Ojha Shreesh, Mahajan Umesh B, Goyal Sameer N
Department of Pharmacology, R. C. Patel Institute of Pharmaceutical Education and Research Shirpur 425405, Maharashtra, India.
Shri Vile Parle Kelavani Mandal's Institute of Pharmacy Dhule 424001, Maharashtra, India.
Am J Transl Res. 2022 Oct 15;14(10):7098-7108. eCollection 2022.
In the era of globalization, a sedentary lifestyle is highly linked with obesity and neurobehavioral complications such as depression. While depression is associated with dopamine dysfunction in the ventral tegmental area (VTA), ghrelin enhances the dopaminergic activity in the VTA. Therefore, the present study aimed to assess the effect of ghrelin on depression-like behaviour in rats subjected to a high-fat diet (HFD) and disturbed diurnal rhythm (DDR) for 45 days.
The neurobehavioral deficits resulting from HFD and DDR in rats, and the behaviour modulation by intra-VTA administration of ghrelin, alone or in combination with ghrelin receptor antagonist were confirmed by evaluation of behavioural parameters in the elevated plus-maze, forced swim test, open field test, and rotarod assessment. Further, the levels of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β) and IL-6, oxidative stress marker malondialdehyde (MDA), and antioxidants enzymes like superoxide dismutase (SOD), reduced glutathione (GSH), and catalase (CAT) were measured.
The levels of TNF-α, IL-1β, IL-6, and MDA were increased in the brain of HFD and DDR exposed rats, while that of SOD, GSH, and CAT were reduced. Intra-VTA ghrelin administration from day 41-45 to the HFD and DDR exposed rats improved cognitive behaviour and physical activity confirming the antidepressant effect. Moreover, ghrelin restored the levels of SOD, GSH and CAT efficiently, and reduced that of MDA, TNF-α, IL-1β and IL-6, which signifies its protective effect.
Overall, this study confirmed the ameliorative effect of ghrelin in HFD- and DDR-induced depression-like behaviour.
在全球化时代,久坐不动的生活方式与肥胖以及诸如抑郁症等神经行为并发症高度相关。虽然抑郁症与腹侧被盖区(VTA)的多巴胺功能障碍有关,但胃饥饿素可增强VTA中的多巴胺能活性。因此,本研究旨在评估胃饥饿素对高脂饮食(HFD)和昼夜节律紊乱(DDR)45天的大鼠抑郁样行为的影响。
通过在高架十字迷宫、强迫游泳试验、旷场试验和转棒试验中评估行为参数,证实了HFD和DDR导致的大鼠神经行为缺陷,以及单独或与胃饥饿素受体拮抗剂联合使用时,VTA内注射胃饥饿素对行为的调节作用。此外,还测量了促炎细胞因子如肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和IL-6的水平、氧化应激标志物丙二醛(MDA)以及抗氧化酶如超氧化物歧化酶(SOD)、还原型谷胱甘肽(GSH)和过氧化氢酶(CAT)的水平。
暴露于HFD和DDR的大鼠大脑中,TNF-α、IL-1β、IL-6和MDA的水平升高,而SOD、GSH和CAT的水平降低。从第41至45天对暴露于HFD和DDR的大鼠进行VTA内注射胃饥饿素,改善了认知行为和身体活动,证实了其抗抑郁作用。此外,胃饥饿素有效地恢复了SOD、GSH和CAT的水平,并降低了MDA、TNF-α、IL-1β和IL-6的水平,这表明了其保护作用。
总体而言,本研究证实了胃饥饿素对HFD和DDR诱导的抑郁样行为具有改善作用。