Ghrelin Protects Lipopolysaccharide-Induced Acute Lung Injury Rats against Pulmonary Vascular Dysfunction by Inhibiting Inflammation

Objective. To determine the effect and mechanism of the anti-inflammatory agent ghrelin on pulmonary vascular dysfunction (PVD) in lipopolysaccharide- (LPS-) induced acute lung injury (ALI) rat models. Methods. Thirty-two adult male Sprague Dawley rats (n = 16/group) were randomly divided into ghrel...

Full description

Saved in:
Bibliographic Details
Main Authors: Guang Li, Chen-Liang Zhou, Wen-Fang Xia, Di Zhang, Hui-Qing Lin
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Canadian Respiratory Journal
Online Access:http://dx.doi.org/10.1155/2021/6643398
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832568487255474176
author Guang Li
Chen-Liang Zhou
Wen-Fang Xia
Di Zhang
Hui-Qing Lin
author_facet Guang Li
Chen-Liang Zhou
Wen-Fang Xia
Di Zhang
Hui-Qing Lin
author_sort Guang Li
collection DOAJ
description Objective. To determine the effect and mechanism of the anti-inflammatory agent ghrelin on pulmonary vascular dysfunction (PVD) in lipopolysaccharide- (LPS-) induced acute lung injury (ALI) rat models. Methods. Thirty-two adult male Sprague Dawley rats (n = 16/group) were randomly divided into ghrelin and saline groups, wherein ghrelin (10 nmol/kg) or saline was subcutaneously administered. After 30 min, eight rats from each group were randomly selected, and LPS (5 mg/kg) or saline was administered by intratracheal instillation to induce ALI. Four hours after establishing the ALI rat model, the mean pulmonary arterial pressure (mPAP), mean right ventricular systolic pressure (RVSP), levels of proinflammatory cytokines tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) in the bronchoalveolar lavage fluid (BALF), BALF cell count, wet-to-dry (W/D) lung weight ratios, and myeloperoxidase (MPO) activity in lung tissue for all four groups (ghrelin, ghrelin + ALI, saline, and saline + ALI) were measured. Immunohistochemical staining to detect alpha-smooth muscle actin (α-SMA) and proliferating cell nuclear antigen (PCNA) expression was performed to assess the intrapulmonary arterial wall thickness and the proliferation of smooth muscle cells, respectively. Results. The ghrelin-pretreated ALI rats showed lower mPAP, RVSP, PCNA expression, MPO activity, W/D lung weight ratio, TNF-α and IL-6 levels, and BALF cell count than the saline-pretreated ALI rats, but ghrelin had no effect on the intrapulmonary arterial wall thickness of ALI rats. Conclusion. Our results confirmed the association between inflammation and PVD in ALI and suggested that the suppression of inflammation by ghrelin pretreatment could protect LPS-induced ALI rats against PVD.
format Article
id doaj-art-34daa394da2040fab50b368c6d207a1e
institution Kabale University
issn 1198-2241
1916-7245
language English
publishDate 2021-01-01
publisher Wiley
record_format Article
series Canadian Respiratory Journal
spelling doaj-art-34daa394da2040fab50b368c6d207a1e2025-02-03T00:58:58ZengWileyCanadian Respiratory Journal1198-22411916-72452021-01-01202110.1155/2021/66433986643398Ghrelin Protects Lipopolysaccharide-Induced Acute Lung Injury Rats against Pulmonary Vascular Dysfunction by Inhibiting InflammationGuang Li0Chen-Liang Zhou1Wen-Fang Xia2Di Zhang3Hui-Qing Lin4Department of Critical Care Medicine, Renmin Hospital, Wuhan University, Wuhan, Hubei Province, ChinaDepartment of Critical Care Medicine, Renmin Hospital, Wuhan University, Wuhan, Hubei Province, ChinaDepartment of Critical Care Medicine, Renmin Hospital, Wuhan University, Wuhan, Hubei Province, ChinaDepartment of Critical Care Medicine, Renmin Hospital, Wuhan University, Wuhan, Hubei Province, ChinaDepartment of Thoracic Surgery, Renmin Hospital, Wuhan University, Wuhan, Hubei Province, ChinaObjective. To determine the effect and mechanism of the anti-inflammatory agent ghrelin on pulmonary vascular dysfunction (PVD) in lipopolysaccharide- (LPS-) induced acute lung injury (ALI) rat models. Methods. Thirty-two adult male Sprague Dawley rats (n = 16/group) were randomly divided into ghrelin and saline groups, wherein ghrelin (10 nmol/kg) or saline was subcutaneously administered. After 30 min, eight rats from each group were randomly selected, and LPS (5 mg/kg) or saline was administered by intratracheal instillation to induce ALI. Four hours after establishing the ALI rat model, the mean pulmonary arterial pressure (mPAP), mean right ventricular systolic pressure (RVSP), levels of proinflammatory cytokines tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) in the bronchoalveolar lavage fluid (BALF), BALF cell count, wet-to-dry (W/D) lung weight ratios, and myeloperoxidase (MPO) activity in lung tissue for all four groups (ghrelin, ghrelin + ALI, saline, and saline + ALI) were measured. Immunohistochemical staining to detect alpha-smooth muscle actin (α-SMA) and proliferating cell nuclear antigen (PCNA) expression was performed to assess the intrapulmonary arterial wall thickness and the proliferation of smooth muscle cells, respectively. Results. The ghrelin-pretreated ALI rats showed lower mPAP, RVSP, PCNA expression, MPO activity, W/D lung weight ratio, TNF-α and IL-6 levels, and BALF cell count than the saline-pretreated ALI rats, but ghrelin had no effect on the intrapulmonary arterial wall thickness of ALI rats. Conclusion. Our results confirmed the association between inflammation and PVD in ALI and suggested that the suppression of inflammation by ghrelin pretreatment could protect LPS-induced ALI rats against PVD.http://dx.doi.org/10.1155/2021/6643398
spellingShingle Guang Li
Chen-Liang Zhou
Wen-Fang Xia
Di Zhang
Hui-Qing Lin
Ghrelin Protects Lipopolysaccharide-Induced Acute Lung Injury Rats against Pulmonary Vascular Dysfunction by Inhibiting Inflammation
Canadian Respiratory Journal
title Ghrelin Protects Lipopolysaccharide-Induced Acute Lung Injury Rats against Pulmonary Vascular Dysfunction by Inhibiting Inflammation
title_full Ghrelin Protects Lipopolysaccharide-Induced Acute Lung Injury Rats against Pulmonary Vascular Dysfunction by Inhibiting Inflammation
title_fullStr Ghrelin Protects Lipopolysaccharide-Induced Acute Lung Injury Rats against Pulmonary Vascular Dysfunction by Inhibiting Inflammation
title_full_unstemmed Ghrelin Protects Lipopolysaccharide-Induced Acute Lung Injury Rats against Pulmonary Vascular Dysfunction by Inhibiting Inflammation
title_short Ghrelin Protects Lipopolysaccharide-Induced Acute Lung Injury Rats against Pulmonary Vascular Dysfunction by Inhibiting Inflammation
title_sort ghrelin protects lipopolysaccharide induced acute lung injury rats against pulmonary vascular dysfunction by inhibiting inflammation
url http://dx.doi.org/10.1155/2021/6643398
work_keys_str_mv AT guangli ghrelinprotectslipopolysaccharideinducedacutelunginjuryratsagainstpulmonaryvasculardysfunctionbyinhibitinginflammation
AT chenliangzhou ghrelinprotectslipopolysaccharideinducedacutelunginjuryratsagainstpulmonaryvasculardysfunctionbyinhibitinginflammation
AT wenfangxia ghrelinprotectslipopolysaccharideinducedacutelunginjuryratsagainstpulmonaryvasculardysfunctionbyinhibitinginflammation
AT dizhang ghrelinprotectslipopolysaccharideinducedacutelunginjuryratsagainstpulmonaryvasculardysfunctionbyinhibitinginflammation
AT huiqinglin ghrelinprotectslipopolysaccharideinducedacutelunginjuryratsagainstpulmonaryvasculardysfunctionbyinhibitinginflammation