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A protease inhibitor against acute stress-induced visceral hypersensitivity and paracellular permeability in rats.

机译:一种蛋白酶抑制剂,可抵抗大鼠急性应激引起的内脏超敏反应和细胞旁通透性。

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摘要

In the present study, we investigated the effects of camostat mesilate (CM), a synthetic protease inhibitor, on visceral sensitivity and paracellular permeability induced by the acute restraint stress. We also explored the possible mechanisms underlying these effects. The acute restraint stress was induced by wrapping the fore shoulders, upper forelimbs and thoracic trunk of Sprague-Dawley rats for 2h. Either CM (30, 100 and 300mg/kg) or saline was intragastrically administrated to the rats 30min before the acute restraint stress. Visceral perception was quantified as visceral motor response with an electromyography in a subset of rats. Paracellular permeability was determined in another subset of rats. We found that the visceral sensitivity and paracellular permeability were significantly reduced in the CM-treated rats. Moreover, the fecal protease activity was decreased in the CM-treated rats. The ZO-1 protein expression was markedly reduced by the stress treatment, but this decrease was suppressed by CM administration. Our data indicated that CM could efficiently inhibit visceral sensitivity and paracellular permeability induced by the acute restraint stress in rats. Therefore, CM might be an effective drug for the treatment of irritable bowel syndrome.
机译:在本研究中,我们研究了合成蛋白酶抑制剂camostat mesilate(CM)对急性束缚应激诱导的内脏敏感性和细胞旁通透性的影响。我们还探讨了这些影响的潜在机制。通过包裹Sprague-Dawley大鼠的前肩,上前肢和胸干2h诱导急性束缚应激。在急性束缚应激前30分钟,将CM(30、100和300mg / kg)或生理盐水灌胃给大鼠。用肌电图在一部分大鼠中将内脏知觉量化为内脏运动反应。在另一组大鼠中确定了细胞旁通透性。我们发现内脏敏感性和细胞旁通透性在经CM处理的大鼠中显着降低。此外,在经CM处理的大鼠中粪便蛋白酶活性降低。通过应力处理,ZO-1蛋白表达显着降低,但是通过CM给药可以抑制这种降低。我们的数据表明,CM可以有效抑制大鼠急性束缚应激诱导的内脏敏感性和细胞旁通透性。因此,CM可能是治疗肠易激综合症的有效药物。

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