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Selective CB 2 Receptor Agonist, HU-308, Reduces Systemic Inflammation in Endotoxin Model of Pneumonia-Induced Acute Lung Injury

Title: Selective CB 2 Receptor Agonist, HU-308, Reduces Systemic Inflammation in Endotoxin Model of Pneumonia-Induced Acute Lung Injury
Authors: Stefan Hall; Sufyan Faridi; Purvi Trivedi; Saki Sultana; Bithika Ray; Tanya Myers; Irene Euodia; David Vlatten; Mathieu Castonguay; Juan Zhou; Melanie Kelly; Christian Lehmann
Source: International Journal of Molecular Sciences, Vol 23, Iss 15857, p 15857 (2022)
Publisher Information: MDPI AG
Publication Year: 2022
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: acute lung injury; ARDS; inflammation; cytokines; cannabinoid type II receptor (CB 2 ); intravital microscopy; Biology (General); QH301-705.5; Chemistry; QD1-999
Description: Acute respiratory distress syndrome (ARDS) and sepsis are risk factors contributing to mortality in patients with pneumonia. In ARDS, also termed acute lung injury (ALI), pulmonary immune responses lead to excessive pro-inflammatory cytokine release and aberrant alveolar neutrophil infiltration. Systemic spread of cytokines is associated with systemic complications including sepsis, multi-organ failure, and death. Thus, dampening pro-inflammatory cytokine release is a viable strategy to improve outcome. Activation of cannabinoid type II receptor (CB 2 ) has been shown to reduce cytokine release in various in vivo and in vitro studies. Herein, we investigated the effect of HU-308, a specific CB 2 agonist, on systemic and pulmonary inflammation in a model of pneumonia-induced ALI. C57Bl/6 mice received intranasal endotoxin or saline, followed by intravenous HU-308, dexamethasone, or vehicle. ALI was scored by histology and plasma levels of select inflammatory mediators were assessed by Luminex assay. Intravital microscopy (IVM) was performed to assess leukocyte adhesion and capillary perfusion in intestinal and pulmonary microcirculation. HU-308 and dexamethasone attenuated LPS-induced cytokine release and intestinal microcirculatory impairment. HU-308 modestly reduced ALI score, while dexamethasone abolished it. These results suggest administration of HU-308 can reduce systemic inflammation without suppressing pulmonary immune response in pneumonia-induced ALI and systemic inflammation.
Document Type: article in journal/newspaper
Language: English
Relation: https://www.mdpi.com/1422-0067/23/24/15857; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067; https://doaj.org/article/18af6fde32aa48a9bed08d96d9c94095
DOI: 10.3390/ijms232415857
Availability: https://doi.org/10.3390/ijms232415857; https://doaj.org/article/18af6fde32aa48a9bed08d96d9c94095
Accession Number: edsbas.F5F36690
Database: BASE