Department of Gastroenterology, State Key Laboratory of Organ Failure Research, Nanfang Hospital, Southern Medical University, 510515 Guangzhou, Guangdong, China.
Department of Pediatrics, The Sixth Affiliated Hospital, Sun Yat-sen University, 510655 Guangzhou, China.
Behav Neurol. 2022 Feb 17;2022:6711160. doi: 10.1155/2022/6711160. eCollection 2022.
The biological mechanisms linking diet-related obesity and autistic behaviors remain unclear. Metformin has proven to be beneficial in the treatment of many syndromes, including autism spectrum disorder. Therefore, the aim of this study was to assess whether metformin treatment could ameliorate metabolic and behavioral alterations in C57BL/6 mice kept on a high-fat diet (HFD), and whether these changes were related to modifications in the gut microbiota and 5-HT levels. As expected, ten weeks of HFD ingestion increased body weight, adiposity, and glucose levels. HFD-fed mice showed a marked aggravation of repetitive behaviors (marble burying and self-grooming), and this was prevented by metformin administration. In addition, HFD-fed mice increased the total distance travelled in the open field test. This hyperactivity was counteracted by metformin cotreatment. In the elevated plus maze test, HFD-fed mice showed a reduced number of entries into the open arms. Interestingly, both HFD and metformin cotreatment increased social interactions in the three-chamber test. HFD increased the levels of intestinal tryptophan and 5-hydroxyindoleacetic acid. Metformin stimulated gut tryptophan and promoted the synthesis of 5-HT in the HFD group. , , , and were enriched in HFD-fed mice, whereas the HFD group cotreated with metformin was enriched in and . was positively correlated with sociability and 5-HT pathway components in mice that received metformin. In summary, HFD consumption elicited a complex phenotype comprising higher levels of anxiety-like and repetitive behaviors but also increased sociability. Metformin could potentially improve HFD-induced disorders in the autistic spectrum through a mechanism involving positive modulation of 5-HT levels in the gut and its microbiota composition.
饮食相关肥胖与自闭症行为之间的生物学机制尚不清楚。二甲双胍已被证明对多种综合征(包括自闭症谱系障碍)的治疗有益。因此,本研究旨在评估二甲双胍治疗是否可以改善高脂肪饮食(HFD)喂养的 C57BL/6 小鼠的代谢和行为改变,以及这些变化是否与肠道微生物群和 5-HT 水平的改变有关。正如预期的那样,十周的 HFD 摄入增加了体重、肥胖和血糖水平。HFD 喂养的小鼠表现出明显的重复行为(埋丸和自我梳理)加重,而二甲双胍给药可预防这种情况。此外,HFD 喂养的小鼠增加了旷场试验中的总行进距离。二甲双胍共同治疗可逆转这种多动行为。在高架十字迷宫试验中,HFD 喂养的小鼠进入开放臂的次数减少。有趣的是,HFD 和二甲双胍共同治疗均可增加三箱测试中的社交互动。HFD 增加了肠道色氨酸和 5-羟吲哚乙酸的水平。二甲双胍刺激肠道色氨酸并促进 HFD 组中 5-HT 的合成。 , , , 和 在 HFD 喂养的小鼠中富集,而用二甲双胍共同治疗的 HFD 组在 和 中富集。 与接受二甲双胍治疗的小鼠的社交能力和 5-HT 途径成分呈正相关。总之,HFD 摄入引起了一种复杂的表型,包括更高水平的焦虑样和重复行为,但也增加了社交能力。二甲双胍可能通过积极调节肠道和其微生物群组成中的 5-HT 水平来改善 HFD 引起的自闭症谱系障碍。