Acute and prolonged toxicity assessment of Cannabis sativa extract in rodents and lagomorphs
Cannabinoids offer a novel pharmacotherapeutic approach and can complement other medications to address unmet clinical needs in numerous patients, which has led to a global increase in the use of these products. No significant safety concerns have been identified in preclinical studies involving CBD...
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Elsevier
2025-06-01
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author | Alana C. Costa Arquimedes Gasparotto, Jr. Alana A.K. Garcia Cícero A.C. Pereira Emerson L.B. Lourenço Helena P.G. Joaquim |
author_facet | Alana C. Costa Arquimedes Gasparotto, Jr. Alana A.K. Garcia Cícero A.C. Pereira Emerson L.B. Lourenço Helena P.G. Joaquim |
author_sort | Alana C. Costa |
collection | DOAJ |
description | Cannabinoids offer a novel pharmacotherapeutic approach and can complement other medications to address unmet clinical needs in numerous patients, which has led to a global increase in the use of these products. No significant safety concerns have been identified in preclinical studies involving CBD and THC. However, the available data on the toxicity of combined CBD and THC are still inconclusive. Evaluating full-spectrum Cannabis sativa extracts is even more complex since whole extracts and isolated phytomolecules do not act in the same way. Given the growing interest in cannabinoid-containing products for human use and the fact that most cannabis treatments utilize entire inflorescence rather than isolated compounds, the current studies aim to evaluate the preclinical safety of a full-spectrum composition (THC, CBD, minor cannabinoids, terpenes, and flavonoids) Cannabis sativa extract (CSE). This research includes acute (single dose, with animals monitored for 14 days to assess potential effects) and long-term treatments (6 months for rodents and 9 months for rabbits) to assess safety and tolerance. This study demonstrates that a full-spectrum Cannabis sativa extract has a favorable safety profile in both acute and prolonged toxicity studies in rodents and rabbits. In acute toxicity tests, the extract did not show any significant behavioral or physiological changes after oral or intraperitoneal administration. Additionally, administering the extract acutely to rabbits had minimal impact on the central nervous, cardiovascular, and respiratory systems, with only a temporary reduction in motor activity at the highest dose. Prolonged administration of 6 months in rats and 9 months in rabbits did not lead to significant changes in organ histopathology, body weight, or behavior. Although liver enzymes were elevated at the highest doses, other biochemical and hematological parameters remained unchanged. CSE was well-tolerated, as no serious adverse effects were observed; however, a reduction in motor activity was noted in the highest dose group, highlighting the need for further investigation, which is proposed for future studies. |
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institution | Kabale University |
issn | 2214-7500 |
language | English |
publishDate | 2025-06-01 |
publisher | Elsevier |
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series | Toxicology Reports |
spelling | doaj-art-881c969b56e5472caa64490b4d941f4d2025-01-28T04:14:38ZengElsevierToxicology Reports2214-75002025-06-0114101918Acute and prolonged toxicity assessment of Cannabis sativa extract in rodents and lagomorphsAlana C. Costa0Arquimedes Gasparotto, Jr.1Alana A.K. Garcia2Cícero A.C. Pereira3Emerson L.B. Lourenço4Helena P.G. Joaquim5GreenCare Pharma, Vinhedo, SP, BrazilLaboratory of Electrophysiology and Cardiovascular Pharmacology, Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, MS, BrazilLaboratory of Pharmacology and Toxicology of Natural Products, Universidade Paranaense, Umuarama, PR, BrazilGreenCare Pharma, Vinhedo, SP, BrazilLaboratory of Pharmacology and Toxicology of Natural Products, Universidade Paranaense, Umuarama, PR, BrazilGreenCare Pharma, Vinhedo, SP, Brazil; Correspondence to: GreenCare Pharma, Division of Medical & Scientific Affairs, 255 Edgar Marchiori st, Vinhedo ZIP 13288-006, Brazil.Cannabinoids offer a novel pharmacotherapeutic approach and can complement other medications to address unmet clinical needs in numerous patients, which has led to a global increase in the use of these products. No significant safety concerns have been identified in preclinical studies involving CBD and THC. However, the available data on the toxicity of combined CBD and THC are still inconclusive. Evaluating full-spectrum Cannabis sativa extracts is even more complex since whole extracts and isolated phytomolecules do not act in the same way. Given the growing interest in cannabinoid-containing products for human use and the fact that most cannabis treatments utilize entire inflorescence rather than isolated compounds, the current studies aim to evaluate the preclinical safety of a full-spectrum composition (THC, CBD, minor cannabinoids, terpenes, and flavonoids) Cannabis sativa extract (CSE). This research includes acute (single dose, with animals monitored for 14 days to assess potential effects) and long-term treatments (6 months for rodents and 9 months for rabbits) to assess safety and tolerance. This study demonstrates that a full-spectrum Cannabis sativa extract has a favorable safety profile in both acute and prolonged toxicity studies in rodents and rabbits. In acute toxicity tests, the extract did not show any significant behavioral or physiological changes after oral or intraperitoneal administration. Additionally, administering the extract acutely to rabbits had minimal impact on the central nervous, cardiovascular, and respiratory systems, with only a temporary reduction in motor activity at the highest dose. Prolonged administration of 6 months in rats and 9 months in rabbits did not lead to significant changes in organ histopathology, body weight, or behavior. Although liver enzymes were elevated at the highest doses, other biochemical and hematological parameters remained unchanged. CSE was well-tolerated, as no serious adverse effects were observed; however, a reduction in motor activity was noted in the highest dose group, highlighting the need for further investigation, which is proposed for future studies.http://www.sciencedirect.com/science/article/pii/S2214750025000368CannabisCannabinoidsToxicitySafety |
spellingShingle | Alana C. Costa Arquimedes Gasparotto, Jr. Alana A.K. Garcia Cícero A.C. Pereira Emerson L.B. Lourenço Helena P.G. Joaquim Acute and prolonged toxicity assessment of Cannabis sativa extract in rodents and lagomorphs Toxicology Reports Cannabis Cannabinoids Toxicity Safety |
title | Acute and prolonged toxicity assessment of Cannabis sativa extract in rodents and lagomorphs |
title_full | Acute and prolonged toxicity assessment of Cannabis sativa extract in rodents and lagomorphs |
title_fullStr | Acute and prolonged toxicity assessment of Cannabis sativa extract in rodents and lagomorphs |
title_full_unstemmed | Acute and prolonged toxicity assessment of Cannabis sativa extract in rodents and lagomorphs |
title_short | Acute and prolonged toxicity assessment of Cannabis sativa extract in rodents and lagomorphs |
title_sort | acute and prolonged toxicity assessment of cannabis sativa extract in rodents and lagomorphs |
topic | Cannabis Cannabinoids Toxicity Safety |
url | http://www.sciencedirect.com/science/article/pii/S2214750025000368 |
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