首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Adenosine Promotes Wound Healing and Mediates Angiogenesis in Response to Tissue Injury Via Occupancy of A2A Receptors
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Adenosine Promotes Wound Healing and Mediates Angiogenesis in Response to Tissue Injury Via Occupancy of A2A Receptors

机译:腺苷促进伤口愈合并通过A2A受体的占用介导组织损伤反应中的血管生成。

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摘要

Recent evidence indicates that topical application of adenosine A2A receptor agonists, unlike growth factors, increases the rate at which wounds close in normal animals and promotes wound healing in diabetic animals as well as growth factors, yet neither the specific adenosine receptor involved nor the mechanism(s) by which adenosine receptor occupancy promotes wound healing have been fully established. To determine which adenosine receptor is involved and whether adenosine receptor-mediated stimulation of angiogenesis plays a role in promotion of wound closure we compared the effect of topical application of the adenosine receptor agonist CGS-21680 (2->p-[2-carboxyethyl]phenethyl-amino-5′->N-ethylcarboxamido-adenosine) on wound closure and angiogenesis in adenosine A2A receptor knockout mice and their wild-type littermates. There was no change in the rate of wound closure in the A2A receptor knockout mice compared to their wild-type littermates although granulation tissue formation was nonhomogeneous and there seemed to be greater inflammation at the base of the wound. Topical application of CGS-21680 increased the rate of wound closure and increased the number of microvessels in the wounds of wild-type mice but did not affect the rate of wound closure in A2A receptor knockout mice. Similarly, in a model of internal trauma and repair (murine air pouch model), endogenously produced adenosine released into areas of internal tissue injury stimulates angiogenesis because there was a marked reduction in blood vessels in the walls of healing air pouches of A2A receptor knockout mice compared to their wild-type controls. Inflammatory vascular leakage and leukocyte accumulation in the inflamed air pouch were similarly reduced in the A2A receptor knockout mice reflecting the reduced vascularity. Thus, targeting the adenosine A2A receptor is a novel approach to promoting wound healing and angiogenesis in normal individuals and those suffering from chronic wounds.
机译:最近的证据表明,与生长因子不同,局部应用腺苷A2A受体激动剂可以增加正常动物伤口的闭合速度,并促进糖尿病动物以及生长因子的伤口愈合,但既没有特定的腺苷受体也没有机制( s)腺苷受体占据促进伤口愈合的作用已经完全确立。为了确定涉及哪个腺苷受体以及腺苷受体介导的血管生成刺激是否在促进伤口闭合中起作用,我们比较了局部应用腺苷受体激动剂CGS-21680(2- > p -[2-羧乙基]苯乙基-氨基-5'-> N -乙基羧酰胺基-腺苷)对腺苷A2A受体敲除小鼠及其野生型同窝仔的伤口闭合和血管新生的作用。与A2A受体敲除小鼠相比,野生型同窝仔小鼠的伤口闭合速率没有变化,尽管肉芽组织形成不均匀,并且在伤口底部的炎症似乎更大。 CGS-21680的局部应用增加了野生型小鼠伤口的闭合速率,并增加了微血管的数量,但并未影响A2A受体敲除小鼠的伤口闭合速率。同样,在内部创伤和修复模型(鼠气袋模型)中,内源产生的腺苷释放到内部组织损伤区域中会刺激血管生成,因为A2A受体敲除小鼠的气袋壁上的血管明显减少与其野生型对照相比。在A2A受体敲除小鼠中,发炎的气囊中的炎性血管渗漏和白细胞积聚同样减少,反映出血管减少。因此,靶向腺苷A2A受体是在正常个体和患有慢性伤口的那些人中促进伤口愈合和血管生成的新方法。

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