Ximenia americana L.: Chemical Characterization and Gastroprotective Effect

Analytica Pub Date : 2023-04-30 DOI:10.3390/analytica4020012
R. T. Pessoa, I. S. Alcântara, Lucas Yure Santos da Silva, R. S. Costa, Tarcísio Mendes Silva, C. D. M. Oliveira-Tintino, A. G. B. Ramos, M. R. C. Oliveira, A. O. Martins, B. C. G. V. D. Lacerda, Edlane Martins de Andrade, J. Ribeiro-Filho, C. M. Lima, H. Coutinho, I. A. Menezes
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Abstract

Ximenia americana L., popularly known in Brazil as “ameixa do-mato, ameixa-brava, and ameixa-do-sertão,” is widely used in folk medicine to treat several intestinal disorders. The present study assessed the potential mechanisms of action underlying the gastroprotective activity of the hydroethanolic extract of Ximenia americana L. (EHXA) stem bark. The acute toxicity of EHXA was estimated, and later, the gastroprotective effect in mice was assessed through acute models of gastric lesions induced by acidified or absolute ethanol and indomethacin, where the following mechanisms were pharmacologically analyzed: the involvement of prostaglandins (PG), histamine (H2) receptors, ATP-dependent potassium channels, sulfhydryl groups (SH), α2 adrenergic receptors, nitric oxide (NO), myeloperoxidase (MPO), gastric mucus production, and acetylcholine-mediated intestinal motility. Regarding toxicity, EHXA did not cause deaths or signs of toxicity (LD50 greater than or equal to 2000 mg/kg/p.o.). When the gastroprotective effect was assessed, EHXA (50, 100, and 200 mg/kg/p.o.) reduced the rate of lesions induced by acidified ethanol by 65.63; 53.66, and 58.02% in absolute ethanol at 88.91, 78.82, and 74.68%, respectively, when compared to the negative control group. In the indomethacin-induced gastric injury model, the reductions were 84.69, 55.99, 55.99, and 42.50%, respectively. The study revealed that EHXA might stimulate mucus production and reduce intestinal motility through SH groups, NO production, and activation of α2 adrenergic receptors. The results indicated that EHXA had significant gastroprotective activity in the evaluated models. However, further investigation is required to elucidate the cellular and molecular events underlying the action of EHXA components and to correlate them with the modulation of the signaling pathways, as demonstrated by the current pharmacological approach. Therefore, the results demonstrated in the present study, as well as previously reported findings, support the recommendation of using this species in traditional communities in Brazil.
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美洲西米尼亚:化学特性及胃保护作用
美洲西米尼亚,在巴西被称为“美洲西米尼亚-马托、美洲西米尼亚-布拉瓦和美洲西米尼亚- sert”,在民间医学中被广泛用于治疗几种肠道疾病。本研究评估了西menia americana L. (EHXA)茎皮氢乙醇提取物胃保护活性的潜在作用机制。评估EHXA的急性毒性,然后通过酸化或无水乙醇和吲哚美辛致小鼠急性胃损伤模型,评估其胃保护作用,药理学分析其机制如下:前列腺素(PG)、组胺(H2)受体、atp依赖性钾通道、巯基(SH)、α2肾上腺素能受体、一氧化氮(NO)、髓过氧化物酶(MPO)、胃粘液生成和乙酰胆碱介导的肠道运动的参与。关于毒性,EHXA没有造成死亡或毒性迹象(LD50大于或等于2000 mg/kg/p.o)。当评估胃保护作用时,EHXA(50、100和200 mg/kg/p.o)使酸化乙醇引起的病变率降低了65.63%;与阴性对照组相比,无水乙醇含量分别为88.91、78.82、74.68%,分别为53.66、58.02%。在吲哚美辛致胃损伤模型中,分别减少84.69%、55.99%、55.99%和42.50%。研究发现EHXA可能通过SH组、NO的产生和α2肾上腺素能受体的激活来刺激黏液的产生,降低肠道蠕动。结果表明,EHXA在评价模型中具有显著的胃保护作用。然而,需要进一步的研究来阐明EHXA成分作用背后的细胞和分子事件,并将它们与信号通路的调节联系起来,正如目前的药理学方法所证明的那样。因此,本研究的结果以及先前报道的结果支持在巴西传统社区使用该物种的建议。
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