Department of Metabolism and Endocrinology, National Clinical Research Center for Metabolic Disease, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, People's Republic of China.
Department of Radiology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, People's Republic of China.
Int J Nanomedicine. 2024 Oct 2;19:10077-10095. doi: 10.2147/IJN.S441847. eCollection 2024.
Anecdotal reports have praised the benefits of cold exposure, exemplified by activities like winter swimming and cold water immersion. Cold exposure has garnered acclaim for its potential to confer benefits and potentially alleviate diabetes. We posited that systemic cold temperature (CT, 4-8°C) likely influences the organism's blood components through ambient temperature, prompting our investigation into the effects of chronic cold exposure on type 2 diabetic (T2DM) mice and our initial exploration of how cold exposure mitigates the incidence of T2DM.
The effects of CT (4-8°C) or room temperature (RT, 22-25°C) on T2DM mice were investigated. Mice blood and organ specimens were collected for fully automated biochemical testing, ELISA, HE staining, immunohistochemistry, and immunofluorescence. Glucose uptake was assessed using flow cytometry with 2-NBDG. Changes in potential signaling pathways such as protein kinase B (AKT), phosphorylated AKT (p-AKT), insulin receptor substrates 1 (IRS1), and phosphorylated IRS1 (p-IRS1) were evaluated by Western blot.
CT or CT mice plasma-derived extracellular vesicles (CT-EVs) remarkably reduced blood glucose levels and improved insulin sensitivity in T2DM mice. This treatment enhanced glucose metabolism, systemic insulin sensitivity, and insulin secretion function while promoting glycogen accumulation in the liver and muscle. Additionally, CT-EVs treatment protected against the streptozocin (STZ)-induced destruction of islets in T2DM mice by inhibiting β-cell apoptosis. CT-EVs also shielded islets from destruction and increased the expression of p-IRS1 and p-AKT in adipocytes and hepatocytes. In vitro experiments further confirmed its pro-insulin sensitivity effect.
Our data indicate that cold exposure may have a potentially beneficial effect on the development of T2DM, mainly through the anti-diabetic effect of plasma-derived EVs released during cold stimulation. This phenomenon could significantly contribute to understanding the lower prevalence of diabetes in colder regions.
有传闻称,冷水浸泡等冷暴露活动有益,冷暴露对糖尿病的潜在缓解作用也受到赞誉。我们推测,全身冷温度(CT,4-8°C)可能会通过环境温度影响机体的血液成分,这促使我们研究慢性冷暴露对 2 型糖尿病(T2DM)小鼠的影响,并初步探索冷暴露如何减轻 T2DM 的发病率。
研究了 CT(4-8°C)或室温(RT,22-25°C)对 T2DM 小鼠的影响。收集小鼠血液和器官标本进行全自动生化检测、ELISA、HE 染色、免疫组织化学和免疫荧光检测。使用 2-NBDG 通过流式细胞术评估葡萄糖摄取。通过 Western blot 评估潜在信号通路的变化,如蛋白激酶 B(AKT)、磷酸化 AKT(p-AKT)、胰岛素受体底物 1(IRS1)和磷酸化 IRS1(p-IRS1)。
CT 或 CT 小鼠血浆衍生的细胞外囊泡(CT-EVs)显著降低 T2DM 小鼠的血糖水平并提高胰岛素敏感性。这种治疗方法增强了葡萄糖代谢、全身胰岛素敏感性和胰岛素分泌功能,同时促进了肝和肌肉中的糖原积累。此外,CT-EVs 治疗通过抑制β细胞凋亡来保护 T2DM 小鼠的胰岛免受 STZ 诱导的破坏。CT-EVs 还保护胰岛免受破坏,并增加了脂肪细胞和肝细胞中 p-IRS1 和 p-AKT 的表达。体外实验进一步证实了其促进胰岛素敏感性的作用。
我们的数据表明,冷暴露可能对 T2DM 的发展具有潜在的有益影响,主要是通过冷刺激期间释放的血浆衍生 EVs 的抗糖尿病作用。这一现象可能对理解较冷地区糖尿病患病率较低有重要意义。