Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, Jazan University, PO Box 114, Jazan, Saudi Arabia.
Substance Abuse and Toxicology Research Center, Jazan University, PO Box 114, Jazan, Saudi Arabia; School of Health Sciences, University of Petroleum and Energy Studies, Dehradun, Uttarakhand, 248007, India.
J Ethnopharmacol. 2022 May 10;289:115055. doi: 10.1016/j.jep.2022.115055. Epub 2022 Jan 29.
Syzygium aromaticum L. volatile oil (clove oil) has been traditionally used for various stomach disorders including inflammatory conditions. Eugenol is the major constituent present in the volatile oil, and it has been established as a gastroprotective agent through many published studies, but the exact and complete mechanism of ulcer protection is not delineated yet. Moreover, it plays precisely the opposite effect in higher dose in antiulcer properties with worsening the ulcer at a higher dose.
This study aims to carry out the prophylactic cytoprotective effect of eugenol with single low doses and explore the probable interrelated underlying transcriptional and translational level mechanism of cytoprotection such as antioxidative, anti-inflammatory, mucous generation in rats using ethanol-induced ulcer model.
Rats were administered with different doses of eugenol before ethanol intragastrically. The effects of the eugenol on mucous production, Nitric oxide generation, PGE2 synthesis, lipid peroxidation were recorded together with cytokines measurement in the blood. TNF-α and IL-6, two key cytokines, were also studied in specific. In addition, studies on the immunohistochemical and gene expression of HSP70 and iNOS indicators have been conducted.
According to our findings, Eugenol substantially reduced the ulcer index and completely protected the mucosa from lesions. By restoring the lowered GSH and NP-SH levels, the protective effect of the eugenol was found to be augmented at both doses. This finding has corresponded to an increase in MDA, which was lowered by ethanol administration. Pre-treatment with eugenol on the ethanol-induced ulcer reduced the plasma NO levels and increased PGE2 along with a decreased TNF-α and IL-6 concentration. Additionally, significant transcriptional and translational upregulation of HSP70 and downregulation of iNOS were detected in the eugenol-treated rat stomach tissue.
Our findings demonstrated that eugenol had a considerable gastroprotective impact at low doses, which could be attributed to its ability to regulate inflammatory reactions and antioxidant capacity.
丁香挥发油(丁香油)传统上用于治疗各种胃部疾病,包括炎症性疾病。丁香油中的主要成分是丁香酚,通过许多已发表的研究已经确定它是一种胃保护剂,但溃疡保护的确切和完整机制尚未阐明。此外,它在更高剂量下具有相反的抗溃疡作用,更高剂量会使溃疡恶化。
本研究旨在通过乙醇诱导的溃疡模型,用单低剂量进行丁香酚的预防性细胞保护作用,并探索其在大鼠中的抗氧化、抗炎、粘液生成等细胞保护相关的潜在转录和翻译水平机制。
大鼠给予不同剂量的丁香酚后,再给予乙醇灌胃。记录丁香酚对粘液生成、一氧化氮生成、PGE2 合成、脂质过氧化的影响,并检测血液中的细胞因子。还研究了两个关键细胞因子 TNF-α 和 IL-6。此外,还进行了 HSP70 和 iNOS 指标的免疫组织化学和基因表达研究。
根据我们的发现,丁香酚可显著降低溃疡指数,并完全保护粘膜免受损伤。通过恢复降低的 GSH 和 NP-SH 水平,发现丁香酚在两个剂量下都增强了保护作用。这一发现与 MDA 的降低相对应,MDA 是由乙醇给药引起的。在乙醇诱导的溃疡前用丁香酚预处理可降低血浆 NO 水平,增加 PGE2,并降低 TNF-α 和 IL-6 浓度。此外,在丁香酚处理的大鼠胃组织中检测到 HSP70 的转录和翻译显著上调和 iNOS 的下调。
我们的研究结果表明,丁香酚在低剂量时具有显著的胃保护作用,这可能归因于其调节炎症反应和抗氧化能力。