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Purinoceptors in inflammation: potential as anti-inflammatory therapeutic targets.

机译:炎症中的嘌呤受体:潜在的抗炎治疗靶点。

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摘要

Purinergic receptors or purinoceptors are expressed in many mammalian cells and are activated by extracellular purines (adenine, purine nucleotides and nucleosides). Both adenosine (P1) and nucleotideucleoside (P2, grouped in P2X and P2Y subtypes) receptors exert important role in the inflammatory processes. The significative up-regulation of many purinoceptors located on the immune cells (neutrophils, eosinophils, monocytes, macrophages, mast cells and lymphocytes) in the course of inflammatory diseases supports the interpretation of their functions. New insights into the involvement of purinoceptors also in the neuro-inflammatory diseases (e.g. conditions of chronic inflammation associated with neurodegenerative diseases) are proposed. The identification of antagonists of purinergic receptors potentially useful to control inflammatory pathways represents the object of many studies reported in the recent literature. Aim of this review is to recapitulate the most recent data and experimental findings that highlight the critical, double edge, effect of these receptors in inflammation, making consistent the possibility to target them to control and regulate inflammation.
机译:嘌呤能受体或嘌呤受体在许多哺乳动物细胞中表达,并被胞外嘌呤(腺嘌呤,嘌呤核苷酸和核苷)激活。腺苷(P1)和核苷酸/核苷(P2,分为P2X和P2Y亚型)受体均在炎症过程中发挥重要作用。在炎症性疾病过程中,位于免疫细胞(嗜中性粒细胞,嗜酸性粒细胞,单核细胞,巨噬细胞,肥大细胞和淋巴细胞)上的许多嘌呤受体的显着上调支持了其功能的解释。提出了嘌呤受体也参与神经炎性疾病(例如与神经退行性疾病有关的慢性炎症的状况)的新见解。嘌呤能受体拮抗剂的潜在识别可用于控制炎症途径,这代表了最近文献报道的许多研究的目的。这篇综述的目的是概括最近的数据和实验结果,这些数据和实验结果突出了这些受体在炎症中的关键,双重作用,从而使靶向它们控制和调节炎症的可能性一致。

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