Diabetic Neuropathy Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Front Endocrinol (Lausanne). 2023 Nov 28;14:1208441. doi: 10.3389/fendo.2023.1208441. eCollection 2023.
Various animal and cell culture models of diabetes mellitus (DM) have been established and utilized to study diabetic peripheral neuropathy (DPN). The divergence of metabolic abnormalities among these models makes their etiology complicated despite some similarities regarding the pathological and neurological features of DPN. Thus, this study aimed to review the omics approaches toward DPN, especially on the metabolic states in diabetic rats and mice induced by chemicals (streptozotocin and alloxan) as type 1 DM models and by genetic mutations (MKR, db/db and ob/ob) and high-fat diet as type 2 DM models. Omics approaches revealed that the pathways associated with lipid metabolism and inflammation in dorsal root ganglia and sciatic nerves were enriched and controlled in the levels of gene expression among these animal models. Additionally, these pathways were conserved in human DPN, indicating the pivotal pathogeneses of DPN. Omics approaches are beneficial tools to better understand the association of metabolic changes with morphological and functional abnormalities in DPN.
已建立并利用各种糖尿病(DM)动物和细胞培养模型来研究糖尿病周围神经病变(DPN)。尽管这些模型的 DPN 病理和神经特征存在某些相似之处,但代谢异常的差异使得其病因变得复杂。因此,本研究旨在综述 DPN 的组学方法,特别是化学物质(链脲佐菌素和四氧嘧啶)诱导的 1 型 DM 模型和遗传突变(MKR、db/db 和 ob/ob)以及高脂肪饮食诱导的 2 型 DM 模型中糖尿病大鼠和小鼠的代谢状态。组学方法表明,与背根神经节和坐骨神经中脂质代谢和炎症相关的途径在这些动物模型中的基因表达水平上是丰富和受调控的。此外,这些途径在人类 DPN 中也得到了保守,表明 DPN 的关键发病机制。组学方法是更好地理解代谢变化与 DPN 形态和功能异常之间关联的有益工具。