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Supportive or detrimental roles of P2Y receptors in brain pathology?-The two faces of P2Y receptors in stroke and neurodegeneration detected in neural cell and in animal model studies

机译:P2Y受体在脑病理中的支持作用或有害作用?-在神经细胞和动物模型研究中检测到P2Y受体在中风和神经退行性变中的两个面

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This review describing the role of P2Y receptors in neuropathological conditions focuses on obvious differences between results demonstrating either a role in neuroprotection or in neurodegeneration, depending on in vitro and in vivo models. Such critical juxtaposition puts special emphasis on discussions of beneficial and detrimental effects of P2Y receptor agonists and antagonists in these models. The mechanisms reported to underlie the protection in vitro include increased expression of oxidoreductase genes, like carbonyl reductase and thioredoxin reductase; increased expression of inhibitor of apoptosis protein-2; extracellular signal-regulated kinase- and Akt-mediated antiapoptotic signaling; increased expression of Bcl-2 proteins, neurotrophins, neuropeptides, and growth factors; decreased Bax expression; non-amyloidogenic APP shedding; and increased neurite outgrowth in neuronal cells. Animal studies investigating the influence of P2Y receptors in middle cerebral artery occlusion (MCAO) models for stroke prove beneficial effects of P2Y receptor antagonists. In MCAO mice and rats, the application of broad-range P2 receptor antagonists decreased the infarct volume and improved neurological outcome. Moreover, antagonists of the P2Y(1) receptor, one of the most abundant P2Y receptor subtypes in brain tissue, decreased neuronal loss and improved spatial memory in rats after traumatic brain injury (TBI). Currently available data show a discrepancy between in vitro and in vivo models concerning the benefits of P2Y receptor activation in pathological conditions. In vitro models demonstrate protection by P2Y receptor agonists, but in vivo P2Y receptor activation deteriorates the outcome after MCAO and controlled cortical impact brain injury, a TBI model. To broaden the scope of the review, we additionally discuss publications that demonstrate detrimental effects of P2Y receptor agonists in vitro and publications showing protective effects of agonists in vivo. All these studies help to better understand the significant role of P2Y receptors especially in stroke models and to develop pharmacological strategies for the treatment of stroke.
机译:这篇关于P2Y受体在神经病理学疾病中的作用的综述着重于结果之间的明显差异,这些结果证明了在神经保护作用或神经变性中的作用,具体取决于体外和体内模型。这种关键的并置特别强调了在这些模型中P2Y受体激动剂和拮抗剂的有益和有害作用的讨论。据报道,在体外进行保护的机制包括增加氧化还原酶基因的表达,例如羰基还原酶和硫氧还蛋白还原酶。增加凋亡蛋白2抑制剂的表达;细胞外信号调节激酶和Akt介导的抗凋亡信号; Bcl-2蛋白,神经营养蛋白,神经肽和生长因子的表达增加; Bax表达降低;非淀粉样蛋白脱落并增加神经元细胞中神经突的生长。动物研究调查了P2Y受体在中风的大脑中动脉闭塞(MCAO)模型中的影响,证明了P2Y受体拮抗剂的有益作用。在MCAO小鼠和大鼠中,广谱P2受体拮抗剂的应用减少了梗塞体积并改善了神经功能。此外,P2Y(1)受体的拮抗剂是脑组织中最丰富的P2Y受体亚型之一,在大鼠颅脑外伤(TBI)后减少了神经元丢失并改善了空间记忆。当前可获得的数据显示,在病理条件下,关于P2Y受体激活的益处,体外模型和体内模型之间存在差异。体外模型显示了P2Y受体激动剂的保护作用,但体内P2Y受体的激活会恶化MCAO和可控的皮质撞击性脑损伤(TBI模型)后的结果。为了扩大本综述的范围,我们另外讨论了证明P2Y受体激动剂在体外具有有害作用的出版物和表明激动剂在体内具有保护作用的出版物。所有这些研究有助于更好地理解P2Y受体的重要作用,尤其是在中风模型中,并开发出治疗中风的药理策略。

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