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蛋白酶激活受体2:肠易激综合征治疗的新靶点。

Protease activated receptor 2: a new target for IBS treatment.

作者信息

Bueno L

机构信息

Neurogastroenterology Unit, INRA, Toulouse, France.

出版信息

Eur Rev Med Pharmacol Sci. 2008 Aug;12 Suppl 1:95-102.

Abstract

Proteinase-activated receptors (PARs) are G-protein-coupled receptors that are activated by the proteolytic cleavage of their N-terminal domain. The new N-terminal sequence that is exposed by proteolysis acts as a tethered ligand, which binds to and activates the receptor. PAR-2 is highly expressed in the gastrointestinal tract, where it is found in endothelial cells, colonic myocytes, enterocytes (both on basolateral and apical membranes), enteric neurons, terminals of mesenteric afferent nerves and immune cells. In the gastrointestinal tract, PAR-2 may be activated by tryptase from mast cells but also by luminal proteases such as trypsin and possibly bacterial proteases. In addition to effects on motility, ion and mucus secretion, activation of PAR-2 receptors from luminal affects visceral pain. In rats, the intracolonic infusion of PAR-2 agonists (SLIGRL, trypsin) initiates a delayed hypersensitivity to colonic distension. These effects are locally mediated since they are not observed for systemic administration. Interestingly, such pronociceptive effect of local activation of PAR-2 is associated with increased colonic paracellular permeability. Blockade of such increase in permeability, prevents the occurrence of hypersensitivity to rectal distension suggesting that activation of the local immune system by luminal toxins and antigens is responsible for the sensitization of primary afferent terminals to mechanical stimuli. Consequently, blockade of PAR-2 receptors at the periphery and/or inhibition of colonic luminal protease activity may be new interesting targets for the treatment of gut hypersensitivity and IBS. A recent study has evidenced that stool supernatants from diarrhea predominant IBS patients have a high level of serine-protease activity that increases permeability and colonic hypersensitivity when infused intra-colonically in mice, and these effects are linked to activation of PAR-2 receptors. These data support a possible role of luminal proteases in the pathogenesis of IBS and give a rationale to target PARs and more specifically PAR-2 as future treatment of IBS.

摘要

蛋白酶激活受体(PARs)是G蛋白偶联受体,通过其N端结构域的蛋白水解切割而被激活。蛋白水解后暴露的新N端序列作为拴系配体,与受体结合并激活受体。PAR-2在胃肠道中高度表达,在内皮细胞、结肠肌细胞、肠上皮细胞(基底外侧膜和顶端膜上均有)、肠神经元、肠系膜传入神经末梢和免疫细胞中均有发现。在胃肠道中,PAR-2可能被肥大细胞的类胰蛋白酶激活,但也可被腔内蛋白酶如胰蛋白酶以及可能的细菌蛋白酶激活。除了对运动、离子和黏液分泌有影响外,腔内PAR-2受体的激活还会影响内脏疼痛。在大鼠中,结肠内注入PAR-2激动剂(SLIGRL、胰蛋白酶)会引发对结肠扩张的迟发性超敏反应。这些效应是局部介导的,因为全身给药时未观察到。有趣的是,PAR-2局部激活的这种促痛觉效应与结肠旁细胞通透性增加有关。阻断这种通透性增加可防止对直肠扩张的超敏反应发生,这表明腔内毒素和抗原激活局部免疫系统是初级传入末梢对机械刺激敏感化的原因。因此,在外周阻断PAR-2受体和/或抑制结肠腔内蛋白酶活性可能是治疗肠道超敏反应和肠易激综合征的新的有趣靶点。最近的一项研究表明,腹泻型肠易激综合征患者的粪便上清液具有高水平的丝氨酸蛋白酶活性,当结肠内注入小鼠体内时会增加通透性和结肠超敏反应,这些效应与PAR-2受体的激活有关。这些数据支持腔内蛋白酶在肠易激综合征发病机制中可能起的作用,并为将PARs尤其是PAR-2作为肠易激综合征未来治疗靶点提供了理论依据。

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