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Inhibition of Janus kinase signaling during controlled mechanical ventilation prevents ventilation-induced diaphragm dysfunction

机译:在受控的机械通气过程中抑制Janus激酶信号传导可防止通气引起的diaphragm肌功能障碍

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摘要

Controlled mechanical ventilation (CMV) is associated with the development of diaphragm atrophy and contractile dysfunction, and respiratory muscle weakness is thought to contribute significantly to delayed weaning of patients. Therefore, therapeutic strategies for preventing these processes may have clinical benefit. The aim of the current study was to investigate the role of the Janus kinase (JAK)/signal transducer and activator of transcription 3 (STAT3) signaling pathway in CMV-mediated diaphragm wasting and weakness in rats. CMV-induced diaphragm atrophy and contractile dysfunction coincided with marked increases in STAT3 phosphorylation on both tyrosine 705 (Tyr705) and serine 727 (Ser727). STAT3 activation was accompanied by its translocation into mitochondria within diaphragm muscle and mitochondrial dysfunction. Inhibition of JAK signaling during CMV prevented phosphorylation of both target sites on STAT3, eliminated the accumulation of phosphorylated STAT3 within the mitochondria, and reversed the pathologic alterations in mitochondrial function, reduced oxidative stress in the diaphragm, and maintained normal diaphragm contractility. In addition, JAK inhibition during CMV blunted the activation of key proteolytic pathways in the diaphragm, as well as diaphragm atrophy. These findings implicate JAK/STAT3 signaling in the development of diaphragm muscle atrophy and dysfunction during CMV and suggest that the delayed extubation times associated with CMV can be prevented by inhibition of Janus kinase signaling.—Smith, I. J., Godinez, G. L., Singh, B. K., McCaughey, K. M., Alcantara, R. R., Gururaja, T., Ho, M. S., Nguyen, H. N., Friera, A. M., White, K. A., McLaughlin, J. R., Hansen, D., Romero, J. M., Baltgalvis, K. A., Claypool, M. D., Li, W., Lang, W., Yam, G. C., Gelman, M. S., Ding, R., Yung, S. L., Creger, D. P., Chen, Y., Singh, R., Smuder, A. J., Wiggs, M. P., Kwon, O.-S., Sollanek, K. J., Powers, S. K., Masuda, E. S., Taylor, V. C., Payan, D. G., Kinoshita, T., Kinsella, T. M. Inhibition of Janus kinase signaling during controlled mechanical ventilation prevents ventilation-induced diaphragm dysfunction.
机译:受控机械通气(CMV)与diaphragm肌萎缩和收缩功能障碍的发展相关,并且呼吸肌无力被认为是导致患者断奶延迟的重要原因。因此,预防这些过程的治疗策略可能具有临床益处。本研究的目的是研究Janus激酶(JAK)/信号转导子和转录激活因子3(STAT3)信号通路在CMV介导的diaphragm肌消瘦和虚弱中的作用。 CMV引起的diaphragm肌萎缩和收缩功能障碍与酪氨酸705(Tyr705)和丝氨酸727(Ser727)上的STAT3磷酸化显着增加同时发生。 STAT3激活伴随着其向隔膜肌内线粒体的转运和线粒体功能障碍。在CMV中抑制JAK信号传导可防止STAT3上两个靶位的磷酸化,消除了线粒体内磷酸化STAT3的积累,并逆转了线粒体功能的病理变化,降低了隔膜的氧化应激,并维持了正常的隔膜收缩性。另外,在CMV期间JAK抑制抑制了b肌中关键蛋白水解途径的激活以及diaphragm肌萎缩。这些发现暗示JAK / STAT3信号参与CMV期间diaphragm肌萎缩和功能障碍的发展,并提示通过抑制Janus激酶信号传导可以预防与CMV相关的拔管时间延迟。—史密斯,IJ,戈迪尼斯,GL,辛格,BK ,麦考伊(McCaughey),KM,阿尔坎塔拉(Alcantara),RR,古鲁拉贾(Gururaja),T。,何,MS,阮,汉尼(HN),弗里拉(Friera),上午,怀特(KA),麦克劳林(McLaughlin),小李,汉森(Hansen),D。 ,Li,W.,Lang,W.,Yam,GC,Gelman,MS,Ding,R.,Yung,SL,Creger,DP,Chen,Y.,Singh,R.,Smuder,AJ,Wiggs,MP, Kwon,O.-S.,K.Sollanek,KJ,Powers,SK,Masuda,ES,Taylor,VC,Payan,DG,Kinoshita,T.,Kinsella,TM在受控的机械通气过程中抑制Janus激酶信号可防止通气引起的隔膜功能障碍。

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