Katchborian-Neto Albert, Santos Mário Ferreira Conceição, Vilas-Boas Diego Fernandes, Dos Santos Elda Gonçalves, Veloso Márcia Paranho, Bueno Paula Carolina Pires, Caldas Ivo Santana, Soares Marisi Gomes, Dias Danielle Ferreira, Chagas-Paula Daniela Aparecida
Institute of Chemistry, Federal University of Alfenas, Rua Gabriel Monteiro da Silva 700, 37130-001, Alfenas, Minas Gerais, Brazil.
Department of Chemistry and Physics, Center of Exact, Natural and Health Sciences, Federal University of Espírito Santo, Alto Universitário, 29500-000, Alegre, Espírito Santo, Brazil.
Chem Biodivers. 2022 Oct;19(10):e202200409. doi: 10.1002/cbdv.202200409. Epub 2022 Sep 26.
Ayahuasca is a psychoactive and psychedelic decoct composed mainly of Banisteriopsis caapi and Psychotria viridis plant species. The beverage is rich in alkaloids and it is ritualistically used by several indigenous communities of South America as a natural medicine. There are also reports in the literature indicating the prophylaxis potential of Ayahuasca alkaloids against internal parasites. In the present study, Ayahuasca exhibited moderate in vitro activity against Trypanosoma cruzi trypomastigotes (IC 95.78 μg/mL) compared to the reference drug benznidazole (IC 2.03 μg/mL). The β-carboline alkaloid harmine (HRE), isolated from B. caapi, was considered active against the trypomastigotes forms (IC 6.37), and the tryptamine N, N-dimethyltryptamine (DMT), isolated from P. viridis was also moderately active with IC of 21.02 μg/mL. Regarding the in vivo evaluations, no collateral effects were observed. The HRE alone demonstrated the highest trypanocidal activity in a dose-responsive manner (10 and 100 mg/kg). The Ayahuasca and the association between HRE and DMT worsened the parasitaemia, suggesting a modulation of the immunological response during the T. cruzi infection, especially by increasing total Immunoglobulin (IgG) and IgG1 antibody levels. The in silico molecular docking revealed HRE binding with low energy at two sites of the Trypanothione reductase enzyme (TR), which are absent in humans, and thus considered a promissory target for drug discovery. In conclusion, Ayahuasca compounds seem to not be toxic at the concentrations of the in vivo evaluations and can promote trypanocidal effect in multi targets, including control of parasitaemia, immunological modulation and TR enzymatic inhibition, which might benefit the treatments of patients with Chagas' disease. Moreover, the present study also provides scientific information to support the prophylactic potential of Ayahuasca against internal parasites.
阿亚瓦斯卡是一种主要由卡皮藤和绿心籽植物物种组成的具有精神活性和致幻作用的煎剂。这种饮料富含生物碱,南美洲的几个土著社区将其作为天然药物用于仪式。文献中也有报道表明阿亚瓦斯卡生物碱对体内寄生虫有预防潜力。在本研究中,与参考药物苯硝唑(IC50为2.03μg/mL)相比,阿亚瓦斯卡在体外对克氏锥虫锥鞭毛体表现出中等活性(IC50为95.78μg/mL)。从卡皮藤中分离出的β-咔啉生物碱哈尔明(HRE)被认为对锥鞭毛体形式有活性(IC50为6.37),从绿心籽中分离出的色胺N,N-二甲基色胺(DMT)也有中等活性,IC50为21.02μg/mL。关于体内评估,未观察到副作用。单独的HRE以剂量反应方式表现出最高的杀锥虫活性(10和100mg/kg)。阿亚瓦斯卡以及HRE和DMT的组合使寄生虫血症恶化,表明在克氏锥虫感染期间免疫反应受到调节,特别是通过增加总免疫球蛋白(IgG)和IgG1抗体水平。计算机模拟分子对接显示HRE在锥虫硫醇还原酶(TR)的两个位点以低能量结合,而这两个位点在人类中不存在,因此被认为是药物发现的一个有前景的靶点。总之,阿亚瓦斯卡化合物在体内评估的浓度下似乎无毒,并且可以在多个靶点上促进杀锥虫作用,包括控制寄生虫血症、免疫调节和TR酶抑制,这可能有利于恰加斯病患者的治疗。此外,本研究还提供了科学信息来支持阿亚瓦斯卡对体内寄生虫的预防潜力。