Departamento de Fisiología y Farmacología, Centro de Ciencias Básicas, Universidad Autónoma de Aguascalientes, Aguascalientes, Ags, México.
Escuela Superior de Huejutla, Universidad Autónoma del Estado de Hidalgo, Huejutla de Reyes, Hidalgo, México.
Purinergic Signal. 2024 Dec;20(6):629-643. doi: 10.1007/s11302-024-10006-1. Epub 2024 Apr 8.
Intestinal low-grade inflammation induced by a high-fat diet has been found to detonate chronic systemic inflammation, which is a hallmark of obesity, and precede the apparition of insulin resistance, a key factor for developing type 2 diabetes (T2D). Aberrant purinergic signaling pathways have been implicated in the pathogenesis of inflammatory bowel disease and other gastrointestinal diseases. However, their role in the gut inflammation associated with obesity and T2D remains unexplored. C57BL/6 J mice were fed a cafeteria diet for 21 weeks and received one injection of streptozotocin in their sixth week into the diet. The gene expression profile of purinergic signaling components in colon tissue was assessed by RT-qPCR. Compared to control mice, the treated group had a significant reduction in colonic length and mucosal and muscular layer thickness accompanied by increased NF-κB and IL-1β mRNA expression. Furthermore, colonic P2X2, P2X7, and A3R gene expression levels were lower, while the P2Y2, NT5E, and ADA expression levels increased. In conclusion, these data suggest that these purinergic signaling components possibly play a role in intestinal low-grade inflammation associated with obesity and T2D and thus could represent a novel therapeutic target for the treatment of the metabolic complications related to these diseases.
高脂肪饮食引起的肠道低度炎症已被发现会引发慢性全身炎症,这是肥胖的标志,并先于胰岛素抵抗的出现,而胰岛素抵抗是 2 型糖尿病(T2D)发生的关键因素。嘌呤能信号通路异常与炎症性肠病和其他胃肠道疾病的发病机制有关。然而,它们在与肥胖和 T2D 相关的肠道炎症中的作用仍未得到探索。C57BL/6J 小鼠喂食 cafeteria 饮食 21 周,并在第六周接受一次链脲佐菌素注射。通过 RT-qPCR 评估嘌呤能信号转导成分在结肠组织中的基因表达谱。与对照组相比,治疗组的结肠长度、黏膜和肌层厚度明显减少,同时 NF-κB 和 IL-1β mRNA 的表达增加。此外,结肠 P2X2、P2X7 和 A3R 基因的表达水平降低,而 P2Y2、NT5E 和 ADA 的表达水平增加。总之,这些数据表明,这些嘌呤能信号转导成分可能在与肥胖和 T2D 相关的肠道低度炎症中发挥作用,因此可能成为治疗与这些疾病相关的代谢并发症的新的治疗靶点。