4.7 Article

Autophagy suppression plays a role in parenteral nutrition-associated lung injury

期刊

CLINICAL NUTRITION
卷 40, 期 2, 页码 560-570

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.clnu.2020.06.002

关键词

Parenteral nutrition-associated lung injury; Autophagy; Parenteral nutrition; Intestinal failure; Hospital-acquired pneumonia; Lung barrier impairment

资金

  1. National Natural Science Foundation of China [81470797, 81770531]
  2. Science Foundation of Outstanding Youth in Jiangsu Province [BK20170009]
  3. Military Medical Innovation Project [18CXZ031]
  4. National Science and Technology Research Funding for Public Welfare Medical Projects [201502022]
  5. 13th Five-Year Plan Foundation of Jiangsu Province for Medical Key Talents [ZDRCA2016091]

向作者/读者索取更多资源

Long-term parenteral nutrition (PN) usage is associated with increased incidence of pneumonia. PN impairs lung barrier, disrupts pulmonary microbiota homeostasis, and induces bacterial translocation. Autophagy suppression may play a crucial role in inducing PN-associated lung injury.
Background & aims: The long-term usage of parenteral nutrition (PN) is associated with the increased incidence of pneumonia. Few studies have focused on the pathogenesis of PN-associated lung injury (PNLI). Previous studies have found that autophagy suppression may be an important mechanism for PNassociated complications. The present study aimed to investigate the effect of PN on lung barrier impairment and its association with autophagy. Methods: We retrospectively identified intestinal failure patients admitted to a clinical nutrition service center to determine the morbidity of hospital-acquired pneumonia (HAP) and its association with PN. In animal studies, we established the PNLI mouse model to measure severity of lung injury, lung barrier, pulmonary microbiota in bronchoalveolar fluid (BALF), levels of autophagy and apoptosis, and the inflammatory signaling pathway. Result: Among the 259 patients, 37 (14.3%) patients developed HAP. Multivariate analysis revealed that prolonged PN was an independent predictor for HAP. In animal studies, we found that PN impaired the lung barrier and disturbed pulmonary microbiota homeostasis. The abundance of Actinomycetes and Firmicutes phyla in BALF were significantly increased, while the Bacteroidetes phylum decreased. Bacterial translocations in the lung were observed by fluorescence in situ hybridization. PN caused autophagy suppression and activated the apoptosis level and inflammatory HMGB1/RAGE/NF-kB signaling pathway. The intervention of exogenous rapamycin can attenuate the impairment of the lung barrier, reduce apoptosis and inhibit inflammatory signaling by upregulation of autophagy. Conclusion: PN had a damaging effect on the lung barrier, disturbed pulmonary microbiota homeostasis, and induced bacterial translocation. Autophagy suppression might be a crucial mechanism in inducing PNLI. (c) 2020 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.

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