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Anti-inflammatory potential of cannabidiol (CBD) on combination of caecal slurry, LPS, and E. coli-induced systemic inflammatory response syndrome (SIRS) in Sprague Dawley Rats

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Inflammopharmacology Aims and scope Submit manuscript

Abstract

Objective

The study objective was to evaluate the therapeutic effect of cannabidiol (CBD) on a combination of caecal slurry, lipopolysaccharide (LPS), and Escherichia coli (E. coli)-induced systemic inflammatory response syndrome (SIRS) in male Sprague Dawley rats.

Methods

The therapeutic activity was monitored in behavioral tests and inflammatory biomarkers by the enzyme-linked immune sorbent assay (ELISA) method.

Results

Behavioral tasks were significantly increased like a tail flick response by 73.84% (p ≤ 0.001), grip strength by 33.56% (p ≤ 0.028), locomotor activity by 20.71% (p = 0.034) in the CBD (60 mg/kg) group compared to disease control (DC) group. Levels of inflammatory serum biomarkers like interleukin-1β (IL-1β), matrix metallopeptidase-9 (MMP-9), IL-6, and tumor necrosis factor-alpha (TNF-α) were significantly decreased by 29.56 (p = 0.041), 71.20 (p ≤ 0.001), 35.05 (p ≤ 0.001), and 75.56% (p = 0.002), respectively, in the CBD-60 compared with DC. Inflammatory cytokines levels, viz. IL-1β, MMP-9, IL-6, and TNF-α, in the liver were significantly (p ≤ 0.001) decreased by 81.01, 40.41, 22.84, and 69.46%, respectively, in CBD-60 to DC. Similarly, levels of inflammatory cytokines such as IL-1β and MMP-9 in the kidney were significantly (p ≤ 0.001) decreased by 80.90 and 43.93%, respectively, in CBD-60 compared to DC.

Conclusion

Taken together, results suggest that CBD treatment significantly improved behavioral tasks and decreased the level of inflammatory cytokines under SIRS conditions that might provide an opportunity to manage acute and chronic inflammatory disorders.

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Data availability

The datasets generated during and/or analyzed during the current study will be available from the corresponding author on reasonable request.

Abbreviations

CBD:

Cannabidiol

E. coli :

Escherichia coli

SIRS:

Systemic inflammatory response syndrome

ELISA:

Enzyme-linked immune sorbent assay

DC:

Disease control

IL-1β:

Interleukin-1β

MMP-9:

Matrix metallopeptidase-9

TNF-α:

Tumor necrosis factor-alpha

CPCSEA:

Committee for the Purpose of Control and Supervision of Experiment on Animals

IAEC:

Institutional Animal Ethical Committee

CMC:

Carboxymethylcellulose

ANOVA:

One-way analysis of variance

NC:

Normal control

DEX:

Dexamethasone

CI:

Confidence interval

GPR55:

G protein-coupled receptor 55

CB1 :

Cannabinoid 1

α3 GlyRs:

Alpha 3 glycine receptors

TRPV1:

Transient receptor potential cation channel subfamily V member 1

5-HT1A :

5-Hydroxy tryptamine 1A

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Acknowledgements

The authors extend their sincere thanks and gratitude to Dabur Research Foundation, India, for providing the facilities and support that enabled the successful completion of the work.

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Authors

Contributions

MKT: contributes to the concept and design of the work. SCM: analysis and interpretation of data with manuscript preparation. MG: analysis and interpretation of data with drafting the work. SJ: revised manuscript critically for important intellectual content; and final approval of the version to be published.

Corresponding author

Correspondence to Snehasis Jana.

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Conflict of interest

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors. The authors declare that they have no competing interests related to this work.

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Trivedi, M.K., Mondal, S., Gangwar, M. et al. Anti-inflammatory potential of cannabidiol (CBD) on combination of caecal slurry, LPS, and E. coli-induced systemic inflammatory response syndrome (SIRS) in Sprague Dawley Rats. Inflammopharmacol 30, 225–232 (2022). https://doi.org/10.1007/s10787-021-00901-z

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  • DOI: https://doi.org/10.1007/s10787-021-00901-z

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