Bułdak Łukasz, Machnik Grzegorz, Skudrzyk Estera, Bołdys Aleksandra, Okopień Bogusław
Department of Internal Medicine and Clinical Pharmacology, School of Medicine in Katowice, Medical University of Silesia, 40-752 Katowice, Poland.
Exp Ther Med. 2019 Apr;17(4):2861-2869. doi: 10.3892/etm.2019.7245. Epub 2019 Feb 6.
GLP-1 agonists such as exenatide and liraglutide are novel drugs for the treatment of diabetes and obesity. While improvements in glycemic control can rely on an incretin effect, the mechanisms behind the loss of weight following therapy have yet to be completely elucidated, and seem to be associated with alterations in eating habits, resulting from changes in cytokines e.g. interleukin 1β (IL-1β) and oxidative signaling in the central nervous system (CNS). Increased levels of IL-1β and reactive oxygen species have been demonstrated to exert anorexigenic properties, and astrocytes appear to actively participate in maintaining the integrity of the CNS, which includes the paracrine secretion of inflammatory cytokines and involvement in the redox status. Therefore, the present study decided to explore the influence of exenatide [a glucagon-like peptide 1 (GLP-1 agonist)] on inflammatory and oxidative stress markers in cultured human astrocytes as a potential target for weight reduction therapies. In an experimental setting, normal human astrocytes were subjected to various glycemic conditions, including 40 mg/dl-hypoglycemic, 100 mg/dl-normoglycemic and 400 mg/dl-hyperglycemic, and exenatide, which is a GLP-1 agonist. The involvement of intracellular signaling by a protein kinase A (PKA) in the action of exenatide was estimated using a specific PKA inhibitor-PKI (14-22). The expression levels of IL-1β, nuclear factor kappa κB (NFκB), glial-fibrillary acidic protein (GFAP), p22 NADPH oxidase, glutathione peroxidase, catalase, superoxide dismutase 1, and reactive oxidative species were measured. The present study demonstrated that varying glucose concentrations in the culture media did not affect the protein expression or the level of reactive oxygen species. Conversely, exenatide led to an increase in IL-1β in normoglycemic culture conditions, which was accompanied by the increased expression of p22, glutathione peroxidase and the reduced expression of GFAP. Changes in the expression of IL-1β and p22 were dependent on the activation of PKA. The present study concluded that exenatide predominantly affected astrocytes in normoglycemic conditions, and hypothesize that this impact demonstrated one of novel mechanisms associated with astrocyte signaling that may contribute to weight loss.
艾塞那肽和利拉鲁肽等胰高血糖素样肽-1(GLP-1)激动剂是治疗糖尿病和肥胖症的新型药物。虽然血糖控制的改善可能依赖于肠促胰岛素效应,但治疗后体重减轻背后的机制尚未完全阐明,似乎与饮食习惯的改变有关,这种改变是由细胞因子如白细胞介素1β(IL-1β)的变化和中枢神经系统(CNS)中的氧化信号传导引起的。已证明IL-1β水平升高和活性氧具有厌食特性,星形胶质细胞似乎积极参与维持CNS的完整性,这包括炎性细胞因子的旁分泌分泌和参与氧化还原状态。因此,本研究决定探讨艾塞那肽[一种胰高血糖素样肽1(GLP-1激动剂)]对培养的人星形胶质细胞中炎症和氧化应激标志物的影响,作为减肥疗法的潜在靶点。在实验环境中,将正常人星形胶质细胞置于各种血糖条件下,包括40mg/dl低血糖、100mg/dl正常血糖和400mg/dl高血糖,以及GLP-1激动剂艾塞那肽。使用特异性蛋白激酶A(PKA)抑制剂-PKI(14-22)评估PKA在艾塞那肽作用中的细胞内信号传导参与情况。测量了IL-1β、核因子κB(NFκB)、胶质纤维酸性蛋白(GFAP)、p22烟酰胺腺嘌呤二核苷酸磷酸氧化酶、谷胱甘肽过氧化物酶、过氧化氢酶、超氧化物歧化酶1和活性氧的表达水平。本研究表明,培养基中不同的葡萄糖浓度不影响蛋白质表达或活性氧水平。相反,在正常血糖培养条件下,艾塞那肽导致IL-1β增加,同时p22、谷胱甘肽过氧化物酶表达增加,GFAP表达降低。IL-1β和p22表达的变化依赖于PKA的激活。本研究得出结论,艾塞那肽在正常血糖条件下主要影响星形胶质细胞,并推测这种影响证明了与星形胶质细胞信号传导相关的新机制之一,这可能有助于体重减轻。