Morphology Department, Biosciences Institute, UNESP - Univ Estadual Paulista, Botucatu/SP, Brazil.
Chem Biol Interact. 2013 Nov 25;206(2):272-8. doi: 10.1016/j.cbi.2013.10.003. Epub 2013 Oct 9.
Based on ethnopharmacological indications that Mentha species may be used in the treatment of gastrointestinal diseases, this study aimed to characterize the gastroprotective mechanisms of menthol (ME), the major compound of the essential oil from species of the genus Mentha. The gastroprotective action of ME was analyzed in gastric ulcers that were induced by ethanol or indomethacin in Wistar male rats. The mechanisms responsible for the gastroprotective effect were assessed by analyzing the amount of mucus secreted, involvement of non-protein sulfhydryl (NP-SH) compounds, involvement of calcium ion channels and NO/cGMP/K(+)ATP pathway, gastric antisecretory activity and the prostaglandin E2 (PGE2) production. The anti-diarrheal activity and acute toxicity of ME were also evaluated. Oral treatment with ME (50mg/kg) offered 88.62% and 72.62% of gastroprotection against ethanol and indomethacin, respectively. There was an increased amount of mucus and PGE2 production. The gastroprotective activity of ME involved NP-SH compounds and the stimulation of K(+)ATP channels, but not the activation of calcium ion channels or the production of NO. The oral administration of ME induced an antisecretory effect as it decreased the H(+) concentration in gastric juice. ME displayed anti-diarrheal and antiperistaltic activity. There were no signs of toxicity in the biochemical analyses performed in the rats' serum. These results demonstrated that ME provides gastroprotective and anti-diarrheal activities with no toxicity in rats.
基于民族药理学的指示,薄荷属植物的某些种可能被用于治疗胃肠道疾病,本研究旨在描述薄荷醇(ME)的胃保护机制,ME 是薄荷属植物精油的主要化合物。通过分析乙醇或吲哚美辛诱导的 Wistar 雄性大鼠胃溃疡,分析 ME 的胃保护作用。通过分析分泌的粘液量、非蛋白巯基(NP-SH)化合物的参与、钙离子通道和 NO/cGMP/K(+)ATP 途径的参与、胃分泌活性和前列腺素 E2(PGE2)的产生来评估胃保护作用的机制。还评估了 ME 的抗腹泻活性和急性毒性。ME(50mg/kg)的口服治疗对乙醇和吲哚美辛分别提供了 88.62%和 72.62%的胃保护作用。粘液和 PGE2 的产生增加。ME 的胃保护活性涉及 NP-SH 化合物和 K(+)ATP 通道的刺激,但不涉及钙离子通道的激活或 NO 的产生。ME 的口服给药可诱导抗分泌作用,因为它降低了胃液中的 H(+)浓度。ME 具有抗腹泻和抗蠕动活性。在大鼠血清中进行的生化分析中没有毒性迹象。这些结果表明,ME 为大鼠提供了胃保护和抗腹泻作用,且无毒性。
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