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Cannabis Extract CT-921 Has a High Efficacy–Adverse Effect Profile in a Neuropathic Pain Model

BACKGROUND: Legalization of cannabis encourages the development of specific cultivars to treat disease such as neuropathic pain. Because of the large number of cultivars, it is necessary to prioritize extracts before proceeding to clinical trials. PURPOSE: To compare extracts of two unique cannabis...

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Autores principales: Rouhollahi, Elham, MacLeod, Bernard A, Barr, Alasdair M, Puil, Ernest
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443010/
https://www.ncbi.nlm.nih.gov/pubmed/32884239
http://dx.doi.org/10.2147/DDDT.S247584
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author Rouhollahi, Elham
MacLeod, Bernard A
Barr, Alasdair M
Puil, Ernest
author_facet Rouhollahi, Elham
MacLeod, Bernard A
Barr, Alasdair M
Puil, Ernest
author_sort Rouhollahi, Elham
collection PubMed
description BACKGROUND: Legalization of cannabis encourages the development of specific cultivars to treat disease such as neuropathic pain. Because of the large number of cultivars, it is necessary to prioritize extracts before proceeding to clinical trials. PURPOSE: To compare extracts of two unique cannabis cultivars (CT-921, CT-928) for treatment of neuropathic pain induced by constriction of sciatic nerve in mice and to illustrate the use of this animal model to set priority for future trials. METHODS: Pain severity was measured by threshold force causing paw withdrawal. Dose–response relationships and time course were determined for intravenously injected extracts of cultivars and vehicle. The doses for allodynia relief were correlated with decreased respiratory rate, temperature and behavioral changes. RESULTS: Effective analgesic dose for 50 and 95% (ED(50An) and ED(95An)) was 15, and 29 mg/kg for CT-921 and 0.9 and 4.7 for CT-928. At ED(50An), for both extracts, the duration was 120 min. At ED(95An), administration of CT-928 significantly decreased respiratory rate while CT-921 did not. CT-928 decreased temperature more than CT-921. CT-928 produced frantic hyperactivity not seen with CT-921. At equivalent analgesic doses, THC was much less in CT-921 than in CT-928 suggesting interactions with components other than THC influenced the analgesia. At equivalent analgesic doses, efficacy-to-adverse effect profile for CT-928 was worse than for CT-921. CONCLUSION: Both extracts relieved neuropathic pain; however, CT-921 had a better efficacy-to-adverse effect profile, a rational basis for prioritizing cultivars for future clinical evaluation.
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spelling pubmed-74430102020-09-02 Cannabis Extract CT-921 Has a High Efficacy–Adverse Effect Profile in a Neuropathic Pain Model Rouhollahi, Elham MacLeod, Bernard A Barr, Alasdair M Puil, Ernest Drug Des Devel Ther Original Research BACKGROUND: Legalization of cannabis encourages the development of specific cultivars to treat disease such as neuropathic pain. Because of the large number of cultivars, it is necessary to prioritize extracts before proceeding to clinical trials. PURPOSE: To compare extracts of two unique cannabis cultivars (CT-921, CT-928) for treatment of neuropathic pain induced by constriction of sciatic nerve in mice and to illustrate the use of this animal model to set priority for future trials. METHODS: Pain severity was measured by threshold force causing paw withdrawal. Dose–response relationships and time course were determined for intravenously injected extracts of cultivars and vehicle. The doses for allodynia relief were correlated with decreased respiratory rate, temperature and behavioral changes. RESULTS: Effective analgesic dose for 50 and 95% (ED(50An) and ED(95An)) was 15, and 29 mg/kg for CT-921 and 0.9 and 4.7 for CT-928. At ED(50An), for both extracts, the duration was 120 min. At ED(95An), administration of CT-928 significantly decreased respiratory rate while CT-921 did not. CT-928 decreased temperature more than CT-921. CT-928 produced frantic hyperactivity not seen with CT-921. At equivalent analgesic doses, THC was much less in CT-921 than in CT-928 suggesting interactions with components other than THC influenced the analgesia. At equivalent analgesic doses, efficacy-to-adverse effect profile for CT-928 was worse than for CT-921. CONCLUSION: Both extracts relieved neuropathic pain; however, CT-921 had a better efficacy-to-adverse effect profile, a rational basis for prioritizing cultivars for future clinical evaluation. Dove 2020-08-17 /pmc/articles/PMC7443010/ /pubmed/32884239 http://dx.doi.org/10.2147/DDDT.S247584 Text en © 2020 Rouhollahi et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Rouhollahi, Elham
MacLeod, Bernard A
Barr, Alasdair M
Puil, Ernest
Cannabis Extract CT-921 Has a High Efficacy–Adverse Effect Profile in a Neuropathic Pain Model
title Cannabis Extract CT-921 Has a High Efficacy–Adverse Effect Profile in a Neuropathic Pain Model
title_full Cannabis Extract CT-921 Has a High Efficacy–Adverse Effect Profile in a Neuropathic Pain Model
title_fullStr Cannabis Extract CT-921 Has a High Efficacy–Adverse Effect Profile in a Neuropathic Pain Model
title_full_unstemmed Cannabis Extract CT-921 Has a High Efficacy–Adverse Effect Profile in a Neuropathic Pain Model
title_short Cannabis Extract CT-921 Has a High Efficacy–Adverse Effect Profile in a Neuropathic Pain Model
title_sort cannabis extract ct-921 has a high efficacy–adverse effect profile in a neuropathic pain model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443010/
https://www.ncbi.nlm.nih.gov/pubmed/32884239
http://dx.doi.org/10.2147/DDDT.S247584
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