精油通过 Nrf2/HO-1 通路减轻大鼠胃溃疡。

Essential Oil Mitigates Peptic Ulcer in Rats through Nrf2/HO-1 Pathway.

机构信息

Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, Saudi Arabia.

出版信息

Molecules. 2022 Nov 15;27(22):7908. doi: 10.3390/molecules27227908.

Abstract

Extreme ethanol ingestion is associated with developing gastric ulcers. (yarrow) is one of the most commonly used herbs with numerous proven pharmacological actions. The goal of the hereby investigation is to explore the gastroprotective action of yarrow essential oil against ethanol-induced gastric ulcers and to reveal the unexplored mechanisms. Rats were distributed into five groups (); the control group administered 10% Tween 20, orally, for two weeks; the ethanol group administered absolute ethanol (5 mL/kg) to prompt gastric ulcer on the last day of the experiment. Yarrow essential oil 100 or 200 mg/kg + ethanol groups pretreated with yarrow oil (100 or 200 mg/kg, respectively), orally, for two weeks prior to gastric ulcer induction by absolute ethanol. Lanso + ethanol group administered 20 mg/kg lansoprazole, orally, for two weeks prior to gastric ulcer induction by ethanol. Results of the current study showed that ethanol caused several macroscopic and microscopic alterations, amplified lipid peroxidation, pro-inflammatory cytokines, and apoptotic markers, as well as diminished PGE, NO, and antioxidant enzyme activities. On the other hand, animals pretreated with yarrow essential oil exhibited fewer macroscopic and microscopic modifications, reduced ulcer surface, and increased Alcian blue binding capacity, pH, and pepsin activity. In addition, yarrow essential oil groups exhibited reduced pro-inflammatory cytokines, apoptotic markers, and MDA, restored the PGE and NO levels, and recovered the antioxidant enzyme activities. Ethanol escalated Nrf2 and HO-1 expressions, whereas pretreatment of yarrow essential oil caused further intensification in Nrf2 and HO-1. To conclude, the current study suggested yarrow essential oil as a gastroprotective agent against ethanol-induced gastric lesions. This gastroprotective effect could be related to the antioxidant, anti-inflammatory, and anti-apoptotic actions of the essential oil through the instigation of the Nrf2/HO-1 pathway.

摘要

极度乙醇摄入与胃溃病的形成有关。 (艾菊)是一种最常用的草药,具有众多已证实的药理学作用。本研究的目的是探讨艾菊精油对乙醇诱导的胃溃疡的胃保护作用,并揭示其未被探索的机制。将大鼠分为五组();对照组给予 10%吐温 20,口服,两周;乙醇组给予绝对乙醇(5 mL/kg),在实验的最后一天诱发胃溃病。艾菊精油 100 或 200 mg/kg+乙醇组分别用艾菊油(100 或 200 mg/kg)预处理,口服,在绝对乙醇诱导胃溃病前两周。 Lanso+乙醇组给予 20 mg/kg 兰索拉唑,口服,在乙醇诱导胃溃病前两周。本研究结果表明,乙醇引起了几种宏观和微观的改变,放大了脂质过氧化、促炎细胞因子和凋亡标志物的作用,同时降低了 PGE、NO 和抗氧化酶的活性。另一方面,用艾菊精油预处理的动物表现出较少的宏观和微观改变,溃疡表面减少,增加了粘蛋白结合能力、pH 值和胃蛋白酶活性。此外,艾菊精油组显示出减少的促炎细胞因子、凋亡标志物和 MDA,恢复了 PGE 和 NO 水平,并恢复了抗氧化酶的活性。乙醇上调了 Nrf2 和 HO-1 的表达,而用艾菊精油预处理则进一步强化了 Nrf2 和 HO-1。总之,本研究表明艾菊精油是一种对抗乙醇诱导胃损伤的胃保护剂。这种胃保护作用可能与精油的抗氧化、抗炎和抗凋亡作用有关,通过诱导 Nrf2/HO-1 途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f03/9692697/fac94cd45499/molecules-27-07908-g001.jpg

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