An increase in alveolar fluid clearance induced by hyperinsulinemia in obese rats with LPS-induced acute lung injury.

Autor: Deng J; Department of Respiratory Medicine, Traditional Chinese Medical Hospital of Jiangbei District, Chongqing, China. Electronic address: 375131161@qq.com., Wang DX; Department of Respiratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China., Tang J; Department of Respiratory Medicine, Traditional Chinese Medical Hospital of Jiangbei District, Chongqing, China., Liang AL; Department of Respiratory Medicine, Traditional Chinese Medical Hospital of Jiangbei District, Chongqing, China., He ZL; Department of Respiratory Medicine, Traditional Chinese Medical Hospital of Jiangbei District, Chongqing, China., Xiang DK; Department of Respiratory Medicine, Traditional Chinese Medical Hospital of Jiangbei District, Chongqing, China., Yan TG; Department of Respiratory Medicine, Traditional Chinese Medical Hospital of Jiangbei District, Chongqing, China.
Jazyk: angličtina
Zdroj: Respiratory physiology & neurobiology [Respir Physiol Neurobiol] 2020 Aug; Vol. 279, pp. 103470. Date of Electronic Publication: 2020 May 28.
DOI: 10.1016/j.resp.2020.103470
Abstrakt: A lower mortality rate is observed in obese patients with acute lung injury (ALI), which is referred to as the obesity paradox, in several studies and recent meta-analyses. Hyperinsulinemia is characterized as the primary effect of obesity, and exogenous insulin attenuates LPS-induced pulmonary edema. The detailed mechanism responsible for the effect of hyperinsulinemia on pulmonary edema and alveolar filling needs to be elucidated. SD rats were fed with a high-fat diet (HFD) for a total of 14 weeks. SD rats were anesthetized and intraperitoneally injected with 10 mg/kg lipopolysaccharide (LPS), while control rats received only saline vehicle. Insulin receptor antagonist S961 (20 nmol/kg) was given by the tail vein and serum, and glucocorticoid-induced protein kinase-1 (SGK-1) inhibitor EMD638683 (20 mg/kg) was administrated intragastrically prior to LPS exposure. The lungs were isolated for the measurement of alveolar fluid clearance. The protein expression of epithelial sodium channel (ENaC) was detected by Western blot. Insulin level in serum was significantly higher in HFD rats compared with normal diet rats in the presence or absence of LPS pretreatment. Hyperinsulinemia induced by high fat feeding increased alveolar fluid clearance and the abundance of α-ENaC, β-ENaC, and γ-ENaC in both normal rats and ALI rats. Moreover, these effects were reversed in response to S961. EMD638683 prevented the simulation of alveolar fluid clearance and protein expression of ENaC in HFD rats with ALI. These findings suggest that hyperinsulinemia induced by obesity results in the stimulation of alveolar fluid clearance via the upregulation of the abundance of ENaC in clinical acute lung injury, whereas theses effects are prevented by an SGK-1 inhibitor.
Competing Interests: Declaration of Competing Interest None.
(Copyright © 2020 Elsevier B.V. All rights reserved.)
Databáze: MEDLINE
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