Suppr超能文献

使用Sprague-Dawley大鼠进行遗传毒性和口服重复剂量毒性研究对大麻提取物的安全性评估

Safety Assessment of a Hemp Extract using Genotoxicity and Oral Repeat-Dose Toxicity Studies in Sprague-Dawley Rats.

作者信息

Dziwenka Margitta, Coppock Robert, Alexander McCorkle, Palumbo Eddie, Ramirez Carlos, Lermer Stephen

机构信息

Toxalta Consulting Ltd, Box 8, Vegreville, AB, T9C 1R1 Canada.

RW Coppock, DVM, Toxicologist and Associates Ltd, PO Box 2031, Vegreville, AB T9C 1T2 Canada.

出版信息

Toxicol Rep. 2020 Feb 20;7:376-385. doi: 10.1016/j.toxrep.2020.02.014. eCollection 2020.

Abstract

Cannabinoids are extracted from L. and are used for a variety of medicinal purposes. Recently, there has been a focus on the cannabinoid Cannabidiol (CBD) and its potential benefits. This study investigated the safety of a proprietary extract of consisting of 9% hemp extract (of which 6.27% is CBD) and 91% olive oil. The mutagenic potential of the hemp extract was evaluated with the AMES assay inclusive of a hepatic drug metabolizing mix (S9) rich in CYP enzymes. The test article did not elicit evidence of bacterial mutagenicity. GLP compliant 14-day and a 90-day toxicity study were conducted. Olive oil was used as a control. The 90-day study had a 28-day recovery period. Treatments for the 14-day non-recovery range-finding study were 0, 1000, 2000 and 4000 mg test article/kg body weight (bw)/day for 14 days. There was a non-statistically significant ( > 0.05) decrease in body weights for the male and female rats receiving the test article. Hypoactivity, hyperactivity, reduced food consumption and piloerection were observed in the rats receiving 4000 mg test article/kg bw. Histopathology showed an increase in the size of liver cells (hypertrophy) around the central vein (centrilobular) in Groups 3 (3/10) and 4 (5/10) that correlated with increased liver weights. In the 90-day study, 8 groups of rats were dosed with 0, 200, 400 and 800 mg test article/kg bw/day. Groups 5 to 8 had a 28-day recovery. There were no test article-linked changes in clinical observations, physical examinations, Functional Observation Battery, ophthalmology, Motor Activity Assessment, hematology, clinical chemistries and macropathology (all groups). With the exception of the liver and adrenal gland, no test article-linked pathology was observed. For all rats receiving the test article, histopathology showed hypertrophy of liver cells around the central vein. The increase of liver weight is most likely caused by hypertrophy due to up-regulation of the hepatic drug metabolizing enzymes. The hepatocellular hypertrophy was completely reversed in 28 days and was not considered to be an adverse effect. Vacuolization of the adrenal zona fasciculata was observed in the control and 800 mg test article/kg bw groups. The vacuolization of the zona fasciculata was of the same incidence and severity in treatment and control male rats and correlated with an increased in the weights of the adrenal glands. In addition, a statistically significant increase (p<0.05) in adrenal-to-body weight ratios was observed for females receiving 800 mg test article/kg bw. This increase in adrenal-to-body weight ratio did not correlate with any of the pathology findings. The NOAEL for the test article is 800 mg/kg bw/day for female and 400 mg/kg bw/day for male Sprague Dawley rats.

摘要

大麻素从大麻中提取,用于多种医疗目的。最近,人们关注大麻素大麻二酚(CBD)及其潜在益处。本研究调查了一种专利提取物的安全性,该提取物由9%的大麻提取物(其中6.27%是CBD)和91%的橄榄油组成。采用包含富含细胞色素P450酶的肝脏药物代谢混合物(S9)的AMES试验评估大麻提取物的致突变潜力。受试物未引发细菌致突变性的证据。进行了符合GLP规范的14天和90天毒性研究。橄榄油用作对照。90天研究有28天的恢复期。14天非恢复期剂量探索研究的处理为0、1000、2000和4000毫克受试物/千克体重(bw)/天,持续14天。接受受试物的雄性和雌性大鼠体重有非统计学显著(>0.05)下降。在接受4000毫克受试物/千克bw的大鼠中观察到活动减少、活动亢进、食物消耗减少和竖毛。组织病理学显示,第3组(3/10)和第4组(5/10)中央静脉周围(小叶中心)的肝细胞大小增加(肥大),这与肝脏重量增加相关。在90天研究中,8组大鼠分别给予0、200、400和800毫克受试物/千克bw/天。第5至8组有28天的恢复期。在临床观察、体格检查、功能观察组合、眼科、运动活动评估、血液学、临床化学和大体病理学(所有组)方面,未观察到与受试物相关的变化。除肝脏和肾上腺外,未观察到与受试物相关的病理学变化。对于所有接受受试物的大鼠,组织病理学显示中央静脉周围的肝细胞肥大。肝脏重量增加很可能是由于肝脏药物代谢酶上调导致的肥大。肝细胞肥大在28天内完全逆转,不被认为是不良反应。在对照组和800毫克受试物/千克bw组中观察到肾上腺束状带空泡化。束状带空泡化在受试组和对照雄性大鼠中的发生率和严重程度相同,且与肾上腺重量增加相关。此外,接受800毫克受试物/千克bw的雌性大鼠肾上腺与体重之比有统计学显著增加(p<0.05)。肾上腺与体重之比的这种增加与任何病理学发现均无关联。受试物对雌性Sprague Dawley大鼠的无观察到有害作用水平(NOAEL)为800毫克/千克bw/天,对雄性为400毫克/千克bw/天。

相似文献

1
Safety Assessment of a Hemp Extract using Genotoxicity and Oral Repeat-Dose Toxicity Studies in Sprague-Dawley Rats.
Toxicol Rep. 2020 Feb 20;7:376-385. doi: 10.1016/j.toxrep.2020.02.014. eCollection 2020.
5
Safety of Elixinol Hemp Extract: Genetic Toxicity and Subchronic Toxicity in Rats.
J Toxicol. 2023 Dec 11;2023:5982883. doi: 10.1155/2023/5982883. eCollection 2023.

引用本文的文献

2
Genotoxic assessment of a L. extract.
Pharm Biol. 2025 Apr 29;63(1):357-363. doi: 10.1080/13880209.2025.2499075. Epub 2025 May 6.
3
Discovering the Potential of Cannabidiol for Cosmeceutical Development at the Cellular Level.
Pharmaceuticals (Basel). 2025 Feb 2;18(2):202. doi: 10.3390/ph18020202.
4
Genotoxicity of selected cannabinoids in human lymphoblastoid TK6 cells.
Arch Toxicol. 2024 Oct;98(10):3439-3451. doi: 10.1007/s00204-024-03826-y. Epub 2024 Aug 22.
5
Safety study of cannabidiol products in healthy dogs.
Front Vet Sci. 2024 Mar 1;11:1349590. doi: 10.3389/fvets.2024.1349590. eCollection 2024.
6
Safety of Elixinol Hemp Extract: Genetic Toxicity and Subchronic Toxicity in Rats.
J Toxicol. 2023 Dec 11;2023:5982883. doi: 10.1155/2023/5982883. eCollection 2023.
10
Toxicological safety evaluation of Qin-Zhi-Zhu-Dan formula in rats during the treatment and recovery periods.
Front Pharmacol. 2022 Aug 25;13:987997. doi: 10.3389/fphar.2022.987997. eCollection 2022.

本文引用的文献

1
Beyond THC and Endocannabinoids.
Annu Rev Pharmacol Toxicol. 2020 Jan 6;60:637-659. doi: 10.1146/annurev-pharmtox-010818-021441. Epub 2019 Oct 3.
2
A Mechanistic and Pathophysiological Approach for Stroke Associated with Drugs of Abuse.
J Clin Med. 2019 Aug 23;8(9):1295. doi: 10.3390/jcm8091295.
3
Therapeutic Prospects of Cannabidiol for Alcohol Use Disorder and Alcohol-Related Damages on the Liver and the Brain.
Front Pharmacol. 2019 May 31;10:627. doi: 10.3389/fphar.2019.00627. eCollection 2019.
4
Hepatotoxicity of a Cannabidiol-Rich Cannabis Extract in the Mouse Model.
Molecules. 2019 Apr 30;24(9):1694. doi: 10.3390/molecules24091694.
5
The endocannabinoid system and stroke: A focused review.
Brain Circ. 2019 Jan-Mar;5(1):1-7. doi: 10.4103/bc.bc_29_18. Epub 2019 Mar 27.
6
The Endocannabinoid System and Cannabidiol's Promise for the Treatment of Substance Use Disorder.
Front Psychiatry. 2019 Feb 19;10:63. doi: 10.3389/fpsyt.2019.00063. eCollection 2019.
8
An Assessment of the Genotoxicity and Subchronic Toxicity of a Supercritical Fluid Extract of the Aerial Parts of Hemp.
J Toxicol. 2018 Jun 7;2018:8143582. doi: 10.1155/2018/8143582. eCollection 2018.
9
Evaluation of genotoxicity of Forssk. extract on mice bone marrow cells .
Toxicol Rep. 2018 May 18;5:625-631. doi: 10.1016/j.toxrep.2018.05.007. eCollection 2018.
10
Mutagenicity and genotoxicity of ClearTaste.
Toxicol Rep. 2018 Jan 12;5:196-206. doi: 10.1016/j.toxrep.2017.12.015. eCollection 2018.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验