Microbial Ecology, Nutrition and Health Research Unit, Institute of Agrochemistry and Food Technology, National Research Council (IATA-CSIC), C/ Catedratico Agustin Escardino 7, 46980, Paterna-Valencia, Spain.
Centro de Investigación Biomédica en Red en Enfermedades Neurodegenerativas (CIBERNED), Cell Biology Department, University of Valencia, Valencia, Spain.
Mol Neurobiol. 2018 Jun;55(6):5337-5352. doi: 10.1007/s12035-017-0768-z. Epub 2017 Sep 18.
Obesity, besides being a problem of metabolic dysfunction, constitutes a risk factor for psychological disorders. Experimental models of diet-induced obesity have revealed that obese animals are prone to anxious and depressive-like behaviors. The present study aimed to evaluate whether Bifidobacterium pseudocatenulatum CECT 7765 could reverse the neurobehavioral consequences of obesity in a high-fat diet (HFD) fed mouse model via regulation of the gut-brain axis. Adult male wild-type C57BL-6 mice were fed a standard diet or HFD, supplemented with either placebo or the bifidobacterial strain for 13 weeks. Behavioral tests were performed, and immune and neuroendocrine parameters were analyzed including leptin and corticosterone and their receptors, Toll-like receptor 2 (TLR2) and neurotransmitters. We found that obese mice showed anhedonia (p < 0.050) indicative of a depressive-like behavior and an exaggerated hypothalamic-pituitary axis (HPA)-mediated stress response to acute physical (p < 0.001) and social stress (p < 0.050), but these alterations were ameliorated by B. pseudocatenulatum CECT 7765 (p < 0.050). These behavioral effects were parallel to reductions of the obesity-associated hyperleptinemia (p < 0.001) and restoration of leptin signaling (p < 0.050), along with fat mass loss (p < 0.010). B. pseudocatenulatum CECT 7765 administration also led to restoration of the obesity-induced reductions in adrenaline in the hypothalamus (p < 0.010), involved in the hypothalamic control of energy balance. Furthermore, the bifidobacterial strain reduced the obesity-induced upregulation of TLR2 protein or gene expression in the intestine (p < 0.010) and the hippocampus (p < 0.050) and restored the alterations of 5-HT levels in the hippocampus (p < 0.050), which could contribute to attenuating the obesity-associated depressive-like behavior (p < 0.050). In summary, the results indicate that B. pseudocatenulatum CECT 7765 could play a role in depressive behavior comorbid with obesity via regulation of endocrine and immune mediators of the gut-brain axis.
肥胖不仅是代谢功能紊乱的问题,也是心理障碍的一个风险因素。饮食诱导肥胖的实验模型表明,肥胖动物容易出现焦虑和抑郁样行为。本研究旨在评估双歧杆菌假长双歧杆菌 CECT7765 是否可以通过调节肠道-大脑轴来逆转高脂肪饮食(HFD)喂养小鼠模型中肥胖的神经行为后果。成年雄性野生型 C57BL-6 小鼠喂食标准饮食或 HFD,并补充安慰剂或双歧杆菌菌株 13 周。进行行为测试,并分析免疫和神经内分泌参数,包括瘦素和皮质酮及其受体、Toll 样受体 2(TLR2)和神经递质。我们发现肥胖小鼠表现出快感缺失(p<0.050),表明存在抑郁样行为,以及对急性身体(p<0.001)和社会压力(p<0.050)的下丘脑-垂体轴(HPA)介导的应激反应过度,而这些改变可以通过双歧杆菌假长双歧杆菌 CECT7765 得到改善(p<0.050)。这些行为效应与肥胖相关的高瘦素血症的降低(p<0.001)和瘦素信号的恢复(p<0.050)平行,同时还伴随着脂肪质量的减少(p<0.010)。双歧杆菌假长双歧杆菌 CECT7765 的给药还导致了肥胖诱导的下丘脑肾上腺素减少的恢复(p<0.010),这与下丘脑对能量平衡的控制有关。此外,该双歧杆菌菌株还降低了肥胖引起的肠道(p<0.010)和海马(p<0.050)中 TLR2 蛋白或基因表达的上调,并恢复了海马 5-HT 水平的改变(p<0.050),这可能有助于减轻肥胖相关的抑郁样行为(p<0.050)。总之,这些结果表明,双歧杆菌假长双歧杆菌 CECT7765 通过调节肠道-大脑轴的内分泌和免疫介质,可能在肥胖伴发的抑郁行为中发挥作用。