Guevara-Ramírez Patricia, Tamayo-Trujillo Rafael, Ruiz-Pozo Viviana A, Cadena-Ullauri Santiago, Paz-Cruz Elius, Zambrano Ana Karina
Centro de Investigación Genética y Genómica, Facultad de Ciencias de la Salud Eugenio Espejo, Universidad UTE, Quito 170129, Ecuador.
Int J Mol Sci. 2025 Jul 7;26(13):6537. doi: 10.3390/ijms26136537.
Autism spectrum disorder (ASD) is a neurodevelopmental condition frequently associated with gastrointestinal symptoms, gut dysbiosis, and metabolic dysfunctions such as insulin resistance (IR). Recent evidence suggests that the gut microbiota may influence both metabolic and neurological processes through the gut-brain-metabolic axis. This review explores the molecular mechanisms linking dysbiosis, IR, and ASD, focusing on pathways such as TLR/NF-κB activation, PI3K/Akt/mTOR disruption, and the action of microbial metabolites, like short-chain fatty acids (SCFAs), lipopolysaccharide (LPS), and γ-aminobutyric acid (GABA). We discuss how dysbiosis may contribute to increased intestinal permeability, systemic inflammation, and neuroimmune activation, ultimately affecting brain development and behavior. Common microbial alterations in ASD and IR-including increased Clostridium, Desulfovibrio, and Alistipes, and reduced Bifidobacterium and butyrate-producing genera-suggest a shared pathophysiology. We also highlight potential therapeutic strategies, such as microbiota modulation, insulin-like growth factor 1 (IGF-1) treatment, and dietary interventions. Understanding these interconnected mechanisms may support the development of microbiota-targeted approaches for individuals with ASD metabolic comorbidities.
自闭症谱系障碍(ASD)是一种神经发育疾病,常伴有胃肠道症状、肠道菌群失调以及代谢功能障碍,如胰岛素抵抗(IR)。最近的证据表明,肠道微生物群可能通过肠-脑-代谢轴影响代谢和神经过程。本综述探讨了将菌群失调、IR和ASD联系起来的分子机制,重点关注Toll样受体/核因子κB(TLR/NF-κB)激活、磷脂酰肌醇-3激酶/蛋白激酶B/哺乳动物雷帕霉素靶蛋白(PI3K/Akt/mTOR)信号通路破坏以及微生物代谢产物(如短链脂肪酸(SCFAs)、脂多糖(LPS)和γ-氨基丁酸(GABA))的作用等途径。我们讨论了菌群失调如何导致肠道通透性增加、全身炎症和神经免疫激活,最终影响大脑发育和行为。ASD和IR中常见的微生物改变,包括梭菌属、脱硫弧菌属和艾氏菌属增加,以及双歧杆菌属和产丁酸菌属减少,提示存在共同的病理生理学机制。我们还强调了潜在的治疗策略,如微生物群调节、胰岛素样生长因子1(IGF-1)治疗和饮食干预。了解这些相互关联的机制可能有助于为患有ASD代谢合并症的个体开发针对微生物群的治疗方法。