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Cellular Signaling and Anti-Apoptotic Effects of Prolactin-Releasing Peptide and Its Analog on SH-SY5Y Cells

机译:催乳素释放肽的细胞信号和抗凋亡效应及其在SH-SY5Y细胞上的模拟

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摘要

Prolactin-releasing peptide (PrRP), a natural ligand for the GPR10 receptor, is a neuropeptide with anorexigenic and antidiabetic properties. Due to its role in the regulation of food intake, PrRP is a potential drug for obesity treatment and associated type 2 diabetes mellitus (T2DM). Recently, the neuroprotective effects of lipidized PrRP analogs have been proven. In this study, we focused on the molecular mechanisms of action of natural PrRP31 and its lipidized analog palm11-PrRP31 in the human neuroblastoma cell line SH-SY5Y to describe their cellular signaling and possible anti-apoptotic properties. PrRP31 significantly upregulated the phosphoinositide-3 kinase-protein kinase B/Akt (PI3K-PKB/Akt) and extracellular signal-regulated kinase/cAMP response element-binding protein (ERK-CREB) signaling pathways that promote metabolic cell survival and growth. In addition, we proved via protein kinase inhibitors that activation of signaling pathways is mediated specifically by PrRP31 and its palmitoylated analog. Furthermore, the potential neuroprotective properties were studied through activation of anti-apoptotic pathways of PrRP31 and palm11-PrRP31 using the SH-SY5Y cell line and rat primary neuronal culture stressed with toxic methylglyoxal (MG). The results indicate increased viability of the cells treated with PrRP and palm11-PrRP31 and a reduced degree of apoptosis induced by MG, suggesting their potential use in the treatment of neurological disorders.
机译:延髓酸释放肽(PRRP),GPR10受体的天然配体,是具有厌氧和抗糖尿病性质的神经肽。由于其在食物摄入量调节中的作用,PRRP是肥胖治疗和相关2型糖尿病(T2DM)的潜在药物。最近,已经证明了脂质化PRRP类似物的神经保护作用。在本研究中,我们专注于天然PRRP31及其脂质化的模拟Palm11-PRRP31在人神经母细胞瘤细胞系SH-SY5Y中的作用的分子机制,以描述它们的细胞信号传导和可能的抗凋亡性质。 PRRP31显着上调了磷酸阳性-3激酶 - 蛋白激酶B / AKT(PI3K-PKB / AKT)和细胞外信号调节的激酶/营响应元件结合蛋白(ERK-CREB)信号传导途径,其促进代谢细胞存活和生长。此外,通过蛋白激酶抑制剂证明,通过PRRP31及其棕榈酰化的类似物介导信号通路的激活。此外,通过使用SH-SY5Y细胞系和大鼠原发性神经元培养物,通过激活PRRP31和Palm11-PRRP31的抗凋亡途径来研究潜在的神经保护性能。抑制毒性甲基乙二醛(Mg)。结果表明,用PRRP和Palm11-PRRP31处理的细胞的可生存率增加,并且MG诱导的细胞凋亡程度降低,表明它们在治疗神经系统疾病的潜在用途。

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