Chen Min, Zhang Fugui, Xiao Yifei, Jiang Xuejun, Yan Zhiqian, Wang Jinyi, Lv Xiting, Cui Jialu, Ha Linna, Chen Hui, Dang Yongkang, Qin Zifei, Yang Jing, Wu Baojian
Institute of Molecular Rhythm and Metabolism, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Department of Pharmacy, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.
Adv Sci (Weinh). 2025 Sep;12(34):e04526. doi: 10.1002/advs.202504526. Epub 2025 Jun 20.
Although the intestinal clock (the circadian timing system in the gastrointestinal tract) is known to direct a wide variety of diurnal nutrients and metabolites, its role in the functioning of extra-intestinal tissues such as the brain remains elusive. Here the role of the intestinal clock in shaping cognitive function is investigated. It is found that Bmal1-iKO mice (mice with Bmal1 [Brain and muscle Arnt-like protein 1] specifically knocked out in the intestine, a mouse line deficient in intestinal clock function) show a defect in cognitive memory irrespective of the time-of-day. Bmal1-iKO-associated cognitive decline is attributed to impaired adenosine signaling and compromised long-term potentiation (LTP) in the hippocampus. Adenosine signaling promotes LTP via enhancing BDNF expression and inhibiting synapse loss. Furthermore, the impairment in adenosine signaling is accounted for by the reductions in intestinal absorption of and hippocampal level of adenosine but not by a change in adenosine receptors. Consistently, adenosine supplementation rescues cognitive deficits associated with the malfunction of the intestinal clock. Moreover, BMAL1 regulates the expression of ADK (adenosine kinase, a primary enzyme for adenosine clearance) in the small intestine and thus promotes intestinal adenosine absorption through REV-ERBα which binds directly to Adk P2 promoter to inhibit its transcription. Together, an unsuspected role of the intestinal clock in controlling cognitive memory is identified, highlighting the intestinal clock as a promising target for the management of cognitive disorders.
尽管肠道时钟(胃肠道中的昼夜节律计时系统)已知可调控多种昼夜营养物质和代谢产物,但其在诸如大脑等肠外组织功能中的作用仍不明确。在此,研究了肠道时钟在塑造认知功能中的作用。研究发现,Bmal1-iKO小鼠(在肠道中特异性敲除Bmal1 [脑和肌肉芳香烃受体核转运蛋白样蛋白1]的小鼠,该小鼠品系肠道时钟功能缺陷)无论在一天中的何时都表现出认知记忆缺陷。与Bmal1-iKO相关的认知能力下降归因于海马体中腺苷信号受损和长时程增强(LTP)受损。腺苷信号通过增强脑源性神经营养因子(BDNF)表达和抑制突触丢失来促进LTP。此外,腺苷信号受损是由于腺苷的肠道吸收和海马体水平降低,而非腺苷受体的变化所致。一致地,补充腺苷可挽救与肠道时钟功能障碍相关的认知缺陷。此外,BMAL1调节小肠中腺苷激酶(ADK,一种用于腺苷清除的主要酶)的表达,从而通过与Adk P2启动子直接结合以抑制其转录的REV-ERBα促进肠道腺苷吸收。总之,确定了肠道时钟在控制认知记忆中一个未被怀疑的作用,突出了肠道时钟作为认知障碍管理的一个有前景的靶点。