Xu Hanyuan, Chen Haishu, Li Yihao, Luo Tiancheng, Zhao Danrui, Chen Xiaoxiao, Zhang Haozhan, Hu Xinyun, Xu Hui, Wang Yiquan, Shentu Yangping, Tong Zhiqian
Beijing Geriatric Hospital, Beijing, China.
Alberta Institute, Wenzhou Medical University, Wenzhou, China.
Nutr Diabetes. 2025 Aug 19;15(1):35. doi: 10.1038/s41387-025-00390-x.
Diabetes mellitus (DM) is a chronic metabolic disorder associated with a range of serious complications, including insulin resistance (IR) and cognitive impairments. IR is recognized as a high-risk factor for the development of cognitive decline. However, it remains unclear which endogenous or exogenous factors induce these two pathological features. Recent studies indicate that certain diets, environmental pollutants, and genetic deficiencies or polymorphisms influence the metabolism of endogenous formaldehyde. Formaldehyde has been implicated in the onset of DM. Notably, elevated levels of formaldehyde have been detected in the blood, peripheral organs (such as the spleen and liver), and brains of both DM patients and animal models of diabetes. Formaldehyde-induced hyperglycemia and high glucose levels generate formaldehyde, creating a vicious cycle that speeds up diabetic complications. Further, excessive formaldehyde induces IR through three distinct mechanisms: alteration of the biologically active conformation of insulin, reduction in insulin receptor expression, and modification of insulin receptor structure. In addition, excessive formaldehyde can impair cognitive functions by inhibiting N-methyl-D-aspartate (NMDA) receptors and exacerbating brain IR. In this review, we discuss the pivotal role of diet-derived formaldehyde in diabetes and propose that reduction of formaldehyde by the formaldehyde scavengers may be a new strategy for treating DM patients.
糖尿病(DM)是一种慢性代谢紊乱疾病,与一系列严重并发症相关,包括胰岛素抵抗(IR)和认知障碍。IR被认为是认知功能下降发展的高危因素。然而,尚不清楚哪些内源性或外源性因素会诱发这两种病理特征。最近的研究表明,某些饮食、环境污染物以及遗传缺陷或多态性会影响内源性甲醛的代谢。甲醛与DM的发病有关。值得注意的是,在DM患者和糖尿病动物模型的血液、外周器官(如脾脏和肝脏)以及大脑中都检测到甲醛水平升高。甲醛诱导的高血糖和高血糖水平又会产生甲醛,从而形成一个加速糖尿病并发症的恶性循环。此外,过量的甲醛通过三种不同机制诱导IR:胰岛素生物活性构象的改变、胰岛素受体表达的降低以及胰岛素受体结构的修饰。此外,过量的甲醛可通过抑制N-甲基-D-天冬氨酸(NMDA)受体和加剧脑IR来损害认知功能。在本综述中,我们讨论了饮食来源的甲醛在糖尿病中的关键作用,并提出用甲醛清除剂降低甲醛含量可能是治疗DM患者的一种新策略。