School of Health Sciences, Federal University of Grande Dourados - Dourados, Mato Grosso do Sul State, Brazil.
Postgraduate Program in Chemistry, Federal University of Grande Dourados - Dourados, Mato Grosso do Sul State, Brazil.
J Ethnopharmacol. 2021 Feb 10;266:113440. doi: 10.1016/j.jep.2020.113440. Epub 2020 Oct 3.
In the State of Mato Grosso do Sul, the watery sap of Doliocarpus dentatus is used to alleviate thirst, and the leaves of this species are used to relieve pain and swelling associated with inflammatory processes.
This study aimed to analyze the compounds of the leaves from the aqueous extract of D. dentatus (EADd) and evaluate its toxicogenetic and pain relief effects in animal models.
Compounds were identified in EADd by UHPLC-HRMS (Ultra high-performance liquid chromatography coupled to high resolution mass spectrometry). The oral dose of 17 mg/kg EADd, calculated according to ethnopharmacological uses, and doses between 30 and 300 mg/kg were used to test Swiss mice in formalin- and acetic acid-induced models of pain and behavior. EADd (100-2000 mg/kg) was assayed in mice by comet, micronucleus, and phagocytosis tests and by peripheral leukocyte counts.
Phenolic compounds and flavonoids as well as trigonelline and isoquercetin were identified in EADd. All oral doses of EADd exhibited antinociceptive activity, as indicated by a decrease in pain in both phases, a decrease in cold hypersensitivity induced by formalin, and a decrease in abdominal contortions induced by acetic acid. EADd did not alter the exploratory, motor or motivational activities of the animals. The comet and micronucleus tests indicated that EADd was not genotoxic and did not change the phagocytic activity or peripheral leukocyte count.
These results demonstrate that EADd could act as an antinociceptive agent that does not present genotoxicity. This study should contribute to justifying, in part, the popular use of D. dentatus in pain management, ensuring its safe use.
在马托格罗索州,多利卡帕鲁斯齿状的水状汁液被用于解渴,而该物种的叶子则被用于缓解与炎症过程相关的疼痛和肿胀。
本研究旨在分析多利卡帕鲁斯齿状叶的水提物(EADd)中的化合物,并在动物模型中评估其毒遗传和缓解疼痛的作用。
通过 UHPLC-HRMS(超高效液相色谱与高分辨率质谱联用)对 EADd 中的化合物进行鉴定。根据民族药理学用途计算出 17mg/kg 的 EADd 口服剂量,以及 30 至 300mg/kg 的剂量,用于在福尔马林和醋酸诱导的疼痛和行为模型中测试瑞士小鼠。用彗星、微核和吞噬作用试验以及外周白细胞计数来检测 EADd(100-2000mg/kg)在小鼠中的作用。
EADd 中鉴定出了酚类化合物和类黄酮,以及三叶草碱和异槲皮苷。EADd 的所有口服剂量均表现出镇痛活性,表现为两个阶段的疼痛减轻、福尔马林诱导的冷敏感减轻以及醋酸诱导的腹部扭曲减轻。EADd 不改变动物的探索性、运动性或动机性活动。彗星和微核试验表明,EADd 没有遗传毒性,也不改变吞噬活性或外周白细胞计数。
这些结果表明,EADd 可能作为一种镇痛剂,不具有遗传毒性。本研究应部分证明多利卡帕鲁斯齿状在疼痛管理中的广泛应用是合理的,确保其安全使用。