Arsenic exposure accelerates type 1 diabetes mellitus progression via pyroptosis pathway in mice.

Lichao Lei, Mengling Chen, Chuan Qin, Linli Cai, Bing Liang
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Abstract

The relationship between arsenic exposure and the development of diabetes mellitus has garnered significant interest in recent years. However, current experimental studies have not definitively established the role of arsenic in the onset of diabetes mellitus. To investigate this relationship specifically concerning type 1 diabetes mellitus, Streptozocin (STZ) was utilized as an inducer to initiate the fundamental pathological changes associated with the disease. A high dose of STZ (50 mg/kg) served as the positive control, while a low dose of STZ (20 mg/kg) was administered in combination with arsenic at varying doses. The objective was to determine whether arsenic enhances the effects of STZ, thereby leading to an expedited onset and progression of type 1 diabetes mellitus. The preliminary investigation into the impact of arsenic exposure on experimental type 1 diabetic mice focused on the NLRP3/Caspase-1/GSDMD mediated pyroptosis pathway. The results showed that fasting blood glucose (FBG) was increased, glucose tolerance was impaired, insulin sensitivity was decreased, fasting serum insulin and the homeostatic model assessment-β (HOMA-β) were significantly reduced, hair arsenic content was increased, reactive oxygen species(ROS), interleukin (IL)-1β and IL-18 contents were increased, and the pathological morphology of pancreas was more serious in the combined group. Moreover, the expression levels of proteins associated with the NLRP3/Caspase-1/GSDMD-mediated pyroptosis pathway were elevated in the combined group. This study illustrates that exposure to arsenic, along with low-dose STZ, not only leads to pancreatic injury in mice, impacting insulin secretion and causing elevated blood glucose levels, thereby hastening the progression of type 1 diabetes, but also induces pyroptosis in pancreatic tissues by influencing the NLRP3/Caspase-1/GSDMD signaling pathway, further facilitating the development of type 1 diabetes.

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近年来,砷暴露与糖尿病发病之间的关系引起了人们的极大兴趣。然而,目前的实验研究尚未明确确定砷在糖尿病发病中的作用。为了具体研究 1 型糖尿病与砷的关系,研究人员利用链脲佐菌素(STZ)作为诱导剂,启动与该疾病相关的基本病理变化。高剂量 STZ(50 毫克/千克)作为阳性对照,而低剂量 STZ(20 毫克/千克)则与不同剂量的砷结合使用。目的是确定砷是否会增强 STZ 的作用,从而导致 1 型糖尿病的加速发生和发展。关于砷暴露对实验性 1 型糖尿病小鼠影响的初步调查侧重于 NLRP3/Caspase-1/GSDMD 介导的热蛋白沉积途径。结果表明,联合组小鼠空腹血糖(FBG)升高,糖耐量受损,胰岛素敏感性降低,空腹血清胰岛素和稳态模型评估-β(HOMA-β)显著降低,毛发砷含量升高,活性氧(ROS)、白细胞介素(IL)-1β和IL-18含量升高,胰腺病理形态更为严重。此外,NLRP3/Caspase-1/GSDMD 介导的热蛋白沉积途径相关蛋白的表达水平在联合组中也有所升高。本研究表明,小鼠在接触砷和低剂量 STZ 的同时,不仅会导致胰腺损伤,影响胰岛素分泌,引起血糖升高,从而加速 1 型糖尿病的发展,而且还会通过影响 NLRP3/Caspase-1/GSDMD 信号通路,诱导胰腺组织发生胰腺脓毒血症,进一步促进 1 型糖尿病的发展。
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