Acetylcholinesterase (AChE) expression is pivotal during apoptosis. Indeed, AChE inhibitors partially protect cells from apoptosis. Insulin-dependent diabetes mellitus (IDDM) is characterized in part by pancreatic b-cell apoptosis. Here, we investigated the role of AChE in the development of IDDM and analyzed protective effects of AChE inhibitors. Multiple low-dose streptozotocin (MLD-STZ) administration resulted in IDDM in a mouse model. Western blot analysis, cytochemical staining, and immunofluorescence staining were used to detect AChE expression in MIN6 cells, primary b cells, and apoptotic pancreatic b cells of MLD-STZ-treated mice. AChE inhibitors were administered intraperitoneally to the MLD-STZ mice for 30 days. Blood glucose, plasma insulin, and creatine levels were measured, and glucose tolerance tests were performed. The effects of AChE inhibitors on MIN6 cells were also evaluated. AChE expression was induced in the apoptotic MIN6 cells and primary b cells in vitro and pancreatic islets in vivo when treated with STZ. Induction and progressive accumulation of AChE in the pancreatic islets were associated with apoptotic b cells during IDDM development. The administration of AChE inhibitors effectively decreased hyperglycemia and incidence of diabetes, and restored plasma insulin levels and plasma creatine clearance in the MLD-STZ mice. AChE inhibitors partially protected MIN6 cells from the damage caused by STZ treatment. Induction and accumulation of AChE in pancreatic islets and the protective effects of AChE inhibitors on the onset and development of IDDM indicate a close relationship between AChE and IDDM.
Background: Islet dysfunction is the main pathological process of type 2 diabetes mellitus (T2DM). Fibrosis causes islet dysfunction, but the current mechanism is still unclear. Here, bioinformatics analysis identified gene clusters closely related to T2DM and differentially expressed genes related to fibrosis, and animal models verified the roles of these genes.Methods: Human islet transcriptomic datasets were obtained from the Gene Expression Omnibus (GEO), and weighted gene coexpression network analysis (WGCNA) was applied to screen the key gene modules related to T2DM and analyze the correlations between the modules and clinical characteristics. Enrichment analysis was performed to identify the functions and pathways of the key module genes. WGCNA, protein-protein interaction (PPI) analysis and receiver operating characteristic (ROC) curve analysis were used to screen the hub genes. The hub genes were verified in another GEO dataset, the islets of high-fat diet (HFD)-fed Sprague-Dawley rats were observed by H&E and Masson’s trichrome staining, the fibrotic proteins were verified by immunofluorescence, and the hub genes were tested by immunohistochemistry.Results: The top 5,000 genes were selected according to the median absolute deviation, and 18 modules were analyzed. The yellow module was highly associated with T2DM, and its positive correlation with glycated hemoglobin (HbA1c) was significantly stronger than that with body mass index (BMI). Enrichment analysis revealed that extracellular matrix organization, the collagen-containing extracellular matrix and cytokine−cytokine receptor interaction might influence T2DM progression. The top three hub genes, interleukin 6 (IL6), IL11 and prostaglandin-endoperoxide synthase 2 (PTGS2), showed upregulated expression in T2DM. In the validation dataset, IL6, IL11, and PTGS2 levels were upregulated in T2DM, and IL6 and PTGS2 expression was positively correlated with HbA1c and BMI; however, IL11 was positively correlated only with HbA1c. In HFD-fed Sprague-Dawley rats, the positive of IL6 and IL11 in islets was stronger, but PTGS2 expression was not significantly altered. The extent of fibrosis, irregular cellular arrangement and positive actin alpha 2 (ACTA2) staining in islets was significantly greater in HFD-fed rats than in normal diet-fed rats.Conclusion: Glucotoxicity is a major factor leading to increased IL6 and IL11 expression, and IL6-and IL11-induced fibrosis might be involved in islet dysfunction.
Rule-based energy management strategies not only make little use of the efficient area of engines and generators but also need to perform better planning in the time domain. This paper proposed a multi-signal vehicle speed prediction model based on the long short-term memory (LSTM) network, improving the accuracy of vehicle speed prediction by considering multiple signals. First, various signals were collected by simulating the vehicle model, and a Pearson correlation analysis was performed on the collected multiple signals in order to improve the model’s prediction accurate, and the appropriate signal was selected as the input to the prediction model. The experimental results indicate that the prediction method greatly improves the predictive effect compared with the support vector machine (SVM) vehicle speed prediction method. Secondly, the method was combined with the model predictive control-equivalent consumption strategy (MPC-ECMS) to form a control strategy suitable for power maintenance conditions enabling the equivalent factor to be adjusted adaptively in real-time and the target state of charge (SoC) value to be set. Pontryagin minimum principle (PMP) enables the battery to calculate the range extender output power at each moment. PMP, as the core algorithm of ECMS, is a common real-time optimal control algorithm. Then, taking into account the engine’s operating characteristics, the calculated range extender power was filtered to make the engine run smoothly. Finally, hardware-in-the-loop simulation (HIL) was used to verify the model. The simulation results demonstrate that this method uses less fuel than the equivalent fuel consumption minimum strategy (ECMS) by 1.32%, 9.47% when compared to the power-following control strategy, 15.66% when compared to the SVM-MPC-ECMS, and only 3.58% different from the fuel consumption of the dynamic programming (DP) control algorithm. This shows that this energy management approach can significantly improve the overall vehicle fuel economy.
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