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USP14 inhibitor IU1 prevents ventilator-induced lung injury in rats

机译:USP14抑制剂IU1预防大鼠呼吸机诱发的肺损伤

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The pathophysiology of ventilator-induced lung injury (VILI) involves multiple mechanisms including inflammation. USP14 removes the ubiquitin chain of I-kappa B, therefore inducing I-kappa B degradation and increasing cytokine release. The purpose of this study was to examine the protecting roles and mechanisms of USP14 inhibitor on I-kappa B expression and lung injury induced by high tidal volume ventilation in normal rat lung. Male Sprague-Dawley rats were divided into follows: Two ventilation modalities were used: rats in Groups LD (low volume + DMSO) and LI (low volume + IU1) received ventilation with a tidal volume of 8 ml/kg, while the rats in Groups HD (high volume + DMSO) and HI (high volume + IU1) were ventilated with a tidal volume of 40 ml/kg. The levels of lung wet-to-dry weight ratio were used as indicators of water metabolism in lung tissue; the detection of inflammatory cytokines in bronchoalveolar lavage (BAL) fluid was used to indicate inflammatory response, while lung injury was assessed by injury score and morphological changes under light microscope. The USP14 and I-kappa B protein level was measured in lung tissue by Western blot. Our results indicated that administration of IU1 alleviated ventilator-induced lung injury which was accompanied by reduced MPO activity, wet-to-dry weight ratio, lower TNF-alpha, IL-1 beta, IL-6 and IL-8 levels and increased I-kappa B expression in lung tissue. IU1 could significantly alleviate ventilator- induced rat lung injury by attenuate intrapulmonary inflammatory response.
机译:呼吸机诱发的肺损伤(VILI)的病理生理学涉及多种机制,包括炎症。 USP14去除了I-κB的泛素链,因此诱导I-κB降解并增加了细胞因子的释放。这项研究的目的是探讨USP14抑制剂对正常大鼠肺中高潮气量通气引起的I-κB表达和肺损伤的保护作用和机制。将雄性Sprague-Dawley大鼠分为以下两种:使用两种通气方式:LD组(低容量+ DMSO)和LI组(低容量+ IU1)的大鼠以8 ml / kg的潮气量进行通气,而在第3组的通气量为8 ml / kg。 HD组(高容量+ DMSO)和HI(高容量+ IU1)以40 ml / kg的潮气通气。肺干湿比的水平用作肺组织中水代谢的指标;支气管肺泡灌洗液(BAL)中炎性细胞因子的检测用于指示炎症反应,而在光学显微镜下通过损伤评分和形态变化来评估肺损伤。通过蛋白质印迹法测量肺组织中的USP14和I-κB蛋白水平。我们的结果表明,IU1的给药减轻了呼吸机诱发的肺损伤,并伴有MPO活性降低,干重比降低,TNF-alpha,IL-1 beta,IL-6和IL-8水平降低以及I增加-κB在肺组织中的表达。 IU1可通过减轻肺内炎症反应来显着减轻呼吸机诱发的大鼠肺损伤。

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