Cruz-Salomón Kelly Del Carmen, Cruz-Rodríguez Rosa Isela, Espinosa-Juárez Josué Vidal, Cruz-Salomón Abumalé, Briones-Aranda Alfredo, Ruiz-Lau Nancy, Ruíz-Valdiviezo Víctor Manuel
Tecnológico Nacional de México, Campus Tuxtla Gutiérrez, Tuxtla Gutierrez 29050, Mexico.
Escuela de Ciencias Químicas, Universidad Autónoma de Chiapas, Ocozocoautla de Espinosa 29140, Mexico.
Pharmaceuticals (Basel). 2022 Jul 29;15(8):943. doi: 10.3390/ph15080943.
L. is an herb used in traditional medicine in Mexico and its roots have been studied to treat pain. However, until now, the antinociceptive properties of the leaves have not been investigated, being the main section used empirically for the treatment of diseases. For this reason, this study aimed to evaluate the antinociceptive and toxoicological activity of various extracts (aqueous, hexanic, and methanolic) from L. leaves in NIH mice and to perform an in silico analysis of the phytochemical compounds. Firstly, the antinociceptive effect was analyzed using the formalin model and the different doses of each of the extracts that were administered orally to obtain the dose-response curves. In addition, acute toxicity was determined by the up and down method and serum biochemical analysis. Later, the phytochemical study of extracts was carried out by thin layer chromatography (TLC) and visible light spectroscopy, and the volatile chemical components were analyzed by gas chromatography-mass spectrometry (GC/MS). Moreover, the most abundant compounds identified in the phytochemical study were analyzed in silico to predict their biological activity (PASSonline) and toxicology (OSIRIS Property Explorer). As a result, it was known that all extracts at doses from 10 to 316 mg/kg significantly reduced the pain response in both phases of the formalin model, with values of 50-60% for the inflammatory response. The toxicological studies (DL50) exhibited that all extracts did not cause any mortality up to the 2000 mg/kg dose level. This was corroborated by the values in the normal range of the biochemical parameters in the serum. Finally, the phytochemical screening of the presence of phenolic structures (coumarins, flavonoids) and terpenes (saponins and terpenes) was verified, and the highest content was of a lipid nature, 1.65 ± 0.54 meq diosgenin/mL in the methanolic extract. A total of 54 components were identified, 11 were the most abundant, and only four (Eicosane, Methyl oleate, 4-bis(1-phenylethyl) phenol, and Ethyl linolenate) of them showed a probability towards active antinociceptive activity in silico greater than 0.5. These results showed that the L. leaf extract possesses molecules with antinociceptive activity.
L. 是一种在墨西哥传统医学中使用的草药,其根部已被研究用于治疗疼痛。然而,直到现在,其叶子的抗伤害感受特性尚未得到研究,而叶子是经验性用于治疗疾病的主要部位。因此,本研究旨在评估L. 叶的各种提取物(水提取物、己烷提取物和甲醇提取物)对NIH小鼠的抗伤害感受和毒理学活性,并对植物化学化合物进行计算机模拟分析。首先,使用福尔马林模型分析抗伤害感受作用,并口服给予每种提取物的不同剂量以获得剂量反应曲线。此外,通过上下法和血清生化分析确定急性毒性。随后,通过薄层色谱法(TLC)和可见光光谱法对提取物进行植物化学研究,并通过气相色谱 - 质谱联用(GC/MS)分析挥发性化学成分。此外,对植物化学研究中鉴定出的最丰富的化合物进行计算机模拟分析,以预测其生物活性(PASSonline)和毒理学(OSIRIS属性浏览器)。结果表明,所有剂量为10至316 mg/kg的提取物在福尔马林模型的两个阶段均显著降低疼痛反应,炎症反应的值为50 - 60%。毒理学研究(LD50)表明,所有提取物在2000 mg/kg剂量水平以下均未导致任何死亡。血清生化参数在正常范围内的值证实了这一点。最后,验证了酚类结构(香豆素、黄酮类)和萜类(皂苷和萜类)的植物化学筛选结果,甲醇提取物中脂质性质的含量最高,为1.65±0.54 meq薯蓣皂苷元/mL。共鉴定出54种成分,其中11种最为丰富,其中只有四种(二十烷、油酸甲酯、4 - 双(1 - 苯乙基)苯酚和亚麻酸乙酯)在计算机模拟中显示出具有活性抗伤害感受活性的概率大于0.5。这些结果表明,L. 叶提取物具有具有抗伤害感受活性的分子。