Universidade Federal Do Vale Do São Francisco (UNIVASF), Brazil; Rede Nordeste de Biotecnologia (RENORBIO), Brazil.
Universidade Federal Do Vale Do São Francisco (UNIVASF), Brazil.
J Ethnopharmacol. 2021 May 10;271:113868. doi: 10.1016/j.jep.2021.113868. Epub 2021 Jan 24.
There are many studies and therapeutic properties attributed to the flowers and leaves of the Cannabis species, but even with few pharmacological studies, Cannabis sativa L. (Cannabaceae) roots presents several therapeutic indications in folk medicine.
This study aimed to evaluate the anti-inflammatory and spasmolytic effects as well as the toxicological profile of the aqueous extract of Cannabis sativa roots (CsAqEx) in mice.
We assessed the anti-inflammatory effect with carrageenan-induced leukocyte migration assay, and carrageenan and histamine-induced paw edema methods; The spasmolytic effect was assessed through in vitro assays with isolated mice trachea. To assess motor coordination and mobility, mice went through the rotarod and open field tests, respectively. For the single-dose toxicity study, we administered CsAqEx at the dose of 1000 mg/kg by gavage. In a repeated dose toxicity study, animals received CsAqEx at doses of 25 mg or 100 mg/kg for 28 days.
The CsAqEx inhibited the migration of leukocytes at the doses of 25, 50, and 100 mg/kg. The CsAqEx showed anti-inflammatory activity after the intraplantar injection of carrageenan, presenting a reduction in edema formation at all tested doses (12.5, 25, 50 and 100 mg/kg). The dose of 12.5 mg/kg of CsAqEx prevented edema formation after intraplantar injection of histamine. In an organ bath, 729 μg/mL of CsAqEx did not promote spasmolytic effect on isolated mice tracheal rings contracted by carbachol (CCh) or potassium chloride (KCl). We did not observe clinical signs of toxicity in the animals after acute treatment with CsAqEx, which suggested that the median lethal dose (LD) is greater than 1000 mg/kg. Repeated dose exposure to the CsAqEx did not produce significant changes in hematological, biochemical, or organ histology parameters.
The results suggest that the anti-inflammatory effect of CsAqEx is related to the reduction of vascular extravasation and migration of inflammatory cells, without effects on the central nervous system. Moreover, there was no spasmolytic effect on airway smooth muscle and no toxicity was observed on mice.
许多研究和治疗特性归因于大麻属植物的花和叶,但即使有很少的药理学研究,大麻属大麻(大麻科)的根在民间医学中也有多种治疗适应症。
本研究旨在评估大麻根水提物(CsAqEx)在小鼠体内的抗炎和松弛作用以及毒理学特征。
我们通过角叉菜胶诱导白细胞迁移试验以及角叉菜胶和组胺诱导的爪肿胀试验评估抗炎作用;通过离体小鼠气管的体外试验评估松弛作用。为了评估运动协调和活动性,小鼠分别进行了转棒和旷场试验。对于单次剂量毒性研究,我们通过灌胃给予 CsAqEx 剂量为 1000mg/kg。在重复剂量毒性研究中,动物接受 CsAqEx 剂量为 25mg 或 100mg/kg,为期 28 天。
CsAqEx 在 25、50 和 100mg/kg 剂量下抑制白细胞迁移。CsAqEx 在角叉菜胶皮内注射后表现出抗炎活性,所有测试剂量(12.5、25、50 和 100mg/kg)均降低了肿胀形成。CsAqEx 剂量为 12.5mg/kg 可防止组胺皮内注射后肿胀形成。在器官浴中,729μg/mL 的 CsAqEx 对由卡巴胆碱(CCh)或氯化钾(KCl)收缩的离体小鼠气管环没有促进松弛作用。在急性 CsAqEx 治疗后,我们未观察到动物出现毒性的临床症状,这表明半数致死剂量(LD)大于 1000mg/kg。重复剂量暴露于 CsAqEx 不会导致血液学、生化或器官组织学参数发生显著变化。
结果表明,CsAqEx 的抗炎作用与减少血管外渗和炎症细胞迁移有关,而对中枢神经系统没有影响。此外,CsAqEx 对气道平滑肌没有松弛作用,对小鼠也没有毒性。