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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.

作者信息

Tepebaşı Muhammet Yusuf, Aşcı Halil, Özmen Özlem, Taner Rümeysa, Temel Esra Nurlu, Garlı Simge

机构信息

Department of Medical Genetics, Suleyman Demirel University, Isparta, 32300, Turkey.

Department of Medical Pharmacology, Faculty of Medical, Suleyman Demirel University, Isparta, Turkey.

出版信息

Mol Biol Rep. 2024 Jul 18;51(1):825. doi: 10.1007/s11033-024-09772-3.


DOI:10.1007/s11033-024-09772-3
PMID:39023749
Abstract

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.

摘要

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Protective effect and mechanism of cannabidiol on myocardial injury in exhaustive exercise training mice.

Chem Biol Interact. 2022-9-25

[2]
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Signal Transduct Target Ther. 2022-6-24

[3]
Clotting Dysfunction in Sepsis: A Role for ROS and Potential for Therapeutic Intervention.

Antioxidants (Basel). 2021-12-30

[4]
Cannabidiol modulation of oxidative stress and signalling.

Neuronal Signal. 2021-8-24

[5]
Endothelial Dysfunction Driven by Hypoxia-The Influence of Oxygen Deficiency on NO Bioavailability.

Biomolecules. 2021-7-3

[6]
Metabolism pathways of arachidonic acids: mechanisms and potential therapeutic targets.

Signal Transduct Target Ther. 2021-2-26

[7]
The Roles of Matrix Metalloproteinases and Their Inhibitors in Human Diseases.

Int J Mol Sci. 2020-12-20

[8]
The Role of HIF in Immunity and Inflammation.

Cell Metab. 2020-10-6

[9]
The effects of sepsis on endothelium and clinical implications.

Cardiovasc Res. 2021-1-1

[10]
Hypoxic-inflammatory responses under acute hypoxia: In Vitro experiments and prospective observational expedition trial.

Int J Mol Sci. 2020-2-4

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