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Roles of the µ-opioid receptor and its related signaling pathways in the pathogenesis of premenstrual syndrome liver-qi stagnation

机译:μ阿片受体及其相关信号通路在经前期综合征肝气郁结发病机制中的作用

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摘要

The present study aimed to investigate the roles of the µ-opioid receptor (MOR) and its related signaling pathways in the pathogenesis of premenstrual syndrome (PMS) liver-qi stagnation, along with the therapeutic effects of the Shu-Yu capsule in treating the condition. A PMS liver-qi stagnation rat model was established using a chronic restraint stress method. The protein expression level of MOR within rat hippocampal tissue was detected via western blot analysis and cyclic adenosine monophosphate (cAMP) levels within the supernatant of a rat hippocampal cell culture were determined by ELISA. The western blot analysis indicated that the hippocampal expression level of MOR was significantly elevated in the PMS liver-qi stagnation model group. However, subsequent treatment with a Shu-Yu capsule was found to significantly decrease the level of MOR expression. In addition, in vitro experiments were performed, whereby primary hippocampal neurons were treated with model rat serum. It was observed that the level of MOR expression was significantly elevated, while brain-derived neurotrophic factor (BDNF) and cAMP levels in the culture supernatant were significantly decreased. These effects were reversed by treatment with serum from the Shu-Yu capsule-treated rats. Furthermore, when treated with the MOR activator DAMGO, the following were significantly decreased in the primary neurons: Phosphorylation levels of cAMP response element binding protein and extracellular signal-regulated protein kinases (ERK); BDNF expression; and cAMP content in the culture supernatant. These effects were reversed in primary neurons treated with DAMGO and Shu-Yu-containing rat serum. Collectively, the data suggest that increased MOR expression and activation of the cAMP/ERK signaling pathway in the hippocampus may be involved in the pathogenesis of PMS liver-qi stagnation. Furthermore, the efficacy of the Shu-Yu capsule in treating the condition may be via its regulation of MOR receptor signaling.
机译:本研究旨在探讨μ阿片受体(MOR)及其相关信号通路在经前期综合征(PMS)肝气郁结的发病机制中的作用,以及舒俞胶囊在治疗A型肝癌中的治疗作用。健康)状况。采用慢性束缚应激法建立了PMS肝气郁结大鼠模型。通过蛋白质印迹分析检测大鼠海马组织中MOR的蛋白表达水平,并通过ELISA测定大鼠海马细胞培养物上清液中的环磷酸腺苷(cAMP)水平。 Western印迹分析表明,在PMS肝气郁结模型组中,MOR的海马表达水平显着升高。然而,随后用舒豫胶囊进行的治疗显着降低了MOR表达水平。另外,进行了体外实验,用模型大鼠血清处理了原代海马神经元。观察到,MOR表达水平显着升高,而培养上清液中脑源性神经营养因子(BDNF)和cAMP水平显着降低。这些作用通过用舒俞胶囊治疗的大鼠的血清治疗而逆转。此外,当用MOR激活剂DAMGO治疗时,初级神经元的下列物质明显减少:cAMP反应元件结合蛋白和细胞外信号调节蛋白激酶(ERK)的磷酸化水平; BDNF表达;培养上清液中的cAMP含量。在用DAMGO和含Shu-Yu的大鼠血清处理的原代神经元中,这些作用被逆转。总体而言,数据表明,海马中MOR表达的增加和cAMP / ERK信号通路的激活可能与PMS肝气郁结的发病机制有关。此外,舒豫胶囊治疗病症的功效可能是通过其对MOR受体信号传导的调节。

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