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Oral CBD-rich hemp extract modulates sterile inflammation in female and male rats
Introduction: Cannabidiol (CBD) extract from the cannabis plant has biomedical and nutraceutical potential. Unlike tetrahydrocannabinol (THC), CBD products produce few psychoactive effects and pose little risk for abuse. There is emerging preclinical and clinical evidence that CBD is stress modulato...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234154/ https://www.ncbi.nlm.nih.gov/pubmed/37275221 http://dx.doi.org/10.3389/fphys.2023.1112906 |
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author | Hopkins, Shelby Kelley, Tel Roller, Rachel Thompson, Robert S. Colagiovanni, Dorothy B. Chupka, Kris Fleshner, Monika |
author_facet | Hopkins, Shelby Kelley, Tel Roller, Rachel Thompson, Robert S. Colagiovanni, Dorothy B. Chupka, Kris Fleshner, Monika |
author_sort | Hopkins, Shelby |
collection | PubMed |
description | Introduction: Cannabidiol (CBD) extract from the cannabis plant has biomedical and nutraceutical potential. Unlike tetrahydrocannabinol (THC), CBD products produce few psychoactive effects and pose little risk for abuse. There is emerging preclinical and clinical evidence that CBD is stress modulatory and may have anti-inflammatory properties. People across the United States legally ingest CBD-rich hemp extracts to manage mental and physical health problems, including stress and inflammation. Preclinical studies have revealed potential mechanisms for these effects; however, the impact of this prior work is diminished because many studies: 1) tested synthetic CBD rather than CBD-rich hemp extracts containing terpenes and/or other cannabinoids thought to enhance therapeutic benefits; 2) administered CBD via injection into the peritoneal cavity or the brain instead of oral ingestion; and 3) failed to examine potential sex differences. To address these gaps in the literature, the following study tested the hypothesis that the voluntary oral ingestion of CBD-rich hemp extract will attenuate the impact of stressor exposure on plasma and tissue inflammatory and stress proteins in females and males. Methods: Adult male and female Sprague Dawley rats (10–15/group) were randomly assigned to be given cereal coated with either vehicle (coconut oil) or CBD-rich hemp extract (L-M0717, CBDrx/Functional Remedies, 20.0 mg/kg). After 7 days, rats were exposed to a well-established acute model of stress (100, 1.5 mA, 5-s, intermittent tail shocks, 90 min total duration) or remained in home cages as non-stressed controls. Results: Stressor exposure induced a robust stress response, i.e., increased plasma corticosterone and blood glucose, and decreased spleen weight (a surrogate measure of sympathetic nervous system activation). Overall, stress-induced increases in inflammatory and stress proteins were lower in females than males, and oral CBD-rich hemp extract constrained these responses in adipose tissue (AT) and mesenteric lymph nodes (MLN). Consistent with previous reports, females had higher levels of stress-evoked corticosterone compared to males, which may have contributed to the constrained inflammatory response measured in females. Discussion: Results from this study suggest that features of the acute stress response are impacted by oral ingestion of CBD-rich hemp extract in female and male rats, and the pattern of changes may be sex and tissue dependent. |
format | Online Article Text |
id | pubmed-10234154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102341542023-06-02 Oral CBD-rich hemp extract modulates sterile inflammation in female and male rats Hopkins, Shelby Kelley, Tel Roller, Rachel Thompson, Robert S. Colagiovanni, Dorothy B. Chupka, Kris Fleshner, Monika Front Physiol Physiology Introduction: Cannabidiol (CBD) extract from the cannabis plant has biomedical and nutraceutical potential. Unlike tetrahydrocannabinol (THC), CBD products produce few psychoactive effects and pose little risk for abuse. There is emerging preclinical and clinical evidence that CBD is stress modulatory and may have anti-inflammatory properties. People across the United States legally ingest CBD-rich hemp extracts to manage mental and physical health problems, including stress and inflammation. Preclinical studies have revealed potential mechanisms for these effects; however, the impact of this prior work is diminished because many studies: 1) tested synthetic CBD rather than CBD-rich hemp extracts containing terpenes and/or other cannabinoids thought to enhance therapeutic benefits; 2) administered CBD via injection into the peritoneal cavity or the brain instead of oral ingestion; and 3) failed to examine potential sex differences. To address these gaps in the literature, the following study tested the hypothesis that the voluntary oral ingestion of CBD-rich hemp extract will attenuate the impact of stressor exposure on plasma and tissue inflammatory and stress proteins in females and males. Methods: Adult male and female Sprague Dawley rats (10–15/group) were randomly assigned to be given cereal coated with either vehicle (coconut oil) or CBD-rich hemp extract (L-M0717, CBDrx/Functional Remedies, 20.0 mg/kg). After 7 days, rats were exposed to a well-established acute model of stress (100, 1.5 mA, 5-s, intermittent tail shocks, 90 min total duration) or remained in home cages as non-stressed controls. Results: Stressor exposure induced a robust stress response, i.e., increased plasma corticosterone and blood glucose, and decreased spleen weight (a surrogate measure of sympathetic nervous system activation). Overall, stress-induced increases in inflammatory and stress proteins were lower in females than males, and oral CBD-rich hemp extract constrained these responses in adipose tissue (AT) and mesenteric lymph nodes (MLN). Consistent with previous reports, females had higher levels of stress-evoked corticosterone compared to males, which may have contributed to the constrained inflammatory response measured in females. Discussion: Results from this study suggest that features of the acute stress response are impacted by oral ingestion of CBD-rich hemp extract in female and male rats, and the pattern of changes may be sex and tissue dependent. Frontiers Media S.A. 2023-05-18 /pmc/articles/PMC10234154/ /pubmed/37275221 http://dx.doi.org/10.3389/fphys.2023.1112906 Text en Copyright © 2023 Hopkins, Kelley, Roller, Thompson, Colagiovanni, Chupka and Fleshner. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Hopkins, Shelby Kelley, Tel Roller, Rachel Thompson, Robert S. Colagiovanni, Dorothy B. Chupka, Kris Fleshner, Monika Oral CBD-rich hemp extract modulates sterile inflammation in female and male rats |
title | Oral CBD-rich hemp extract modulates sterile inflammation in female and male rats |
title_full | Oral CBD-rich hemp extract modulates sterile inflammation in female and male rats |
title_fullStr | Oral CBD-rich hemp extract modulates sterile inflammation in female and male rats |
title_full_unstemmed | Oral CBD-rich hemp extract modulates sterile inflammation in female and male rats |
title_short | Oral CBD-rich hemp extract modulates sterile inflammation in female and male rats |
title_sort | oral cbd-rich hemp extract modulates sterile inflammation in female and male rats |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234154/ https://www.ncbi.nlm.nih.gov/pubmed/37275221 http://dx.doi.org/10.3389/fphys.2023.1112906 |
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