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Cannabidiol ameliorates lipopolysaccharide-induced cardiovascular toxicity by its antioxidant and anti-inflammatory activity via regulating IL-6, Hif1α, STAT3, eNOS pathway

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dc.creator Özmen, Özlem
dc.creator Taner, Rümeysa
dc.creator TEPEBAŞI, Muhammet Yusuf
dc.creator Temel, Esra Nurlu
dc.creator AŞCI, Halil
dc.creator Garlı, Simge
dc.date 2024-12-01T00:00:00Z
dc.date.accessioned 2025-02-25T10:39:35Z
dc.date.available 2025-02-25T10:39:35Z
dc.identifier dbfd096b-7817-43c8-a252-903f550f6b9b
dc.identifier 10.1007/s11033-024-09772-3
dc.identifier https://avesis.sdu.edu.tr/publication/details/dbfd096b-7817-43c8-a252-903f550f6b9b/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/101589
dc.description Background: Systemic inflammation causes several organ damage by activating the intracellular signaling mechanisms. Heart and aorta tissues are the structures mostly affected by this situation. By examining underlying processes, this study sought to determine whether cannabidiol (CBD) may have protective effects against the cardiovascular damage brought on by lipopolysaccharide (LPS). Materials and methods: A total of 32 female rats were randomly allocated to one of four groups: control, lipopolysaccharide (LPS) (5 mg/kg, i.p., single dose), LPS + CBD (5 mg/kg, i.p., single dose), and CBD groups. The rats were killed six hours after receiving LPS, and tissues from the heart and aorta were taken. Histopathological and immunohistochemical analyzes were performed. Oxidative stress was evaluated biochemically by spectrophotometric method. Expression levels of genes were studied by RT-qPCR method. Results: Histopathological analysis of the LPS group showed moderate hyperemia, hemorrhages, edema, inflammation, and myocardial cell damage. There was a slight to moderate increase in Cox-1, G-CSF, and IL-3 immunoexpressions, along with enhanced expressions of IL-6, Hif1α, and STAT3 genes, and decreased expressions of eNOS genes. Additionally, there were increased levels of TOS and decreased TAS levels observed biochemically. CBD treatment effectively reversed and improved all of these observed changes. Conclusions: CBD protects the heart and aorta against systemic inflammation through its antioxidant and anti-inflammatory activity via regulating IL-6, Hif1α, STAT3, and eNOS intracellular pathways.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Cannabidiol ameliorates lipopolysaccharide-induced cardiovascular toxicity by its antioxidant and anti-inflammatory activity via regulating IL-6, Hif1α, STAT3, eNOS pathway
dc.type info:eu-repo/semantics/article


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