Essential oils of marrubium peregrinum resisted ethanol-induced

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Khaled Abdul-Aziz Ahmed
Khalid M. Alqaisi
Noralhuda Ayad Ibrahim
Ahmed A.J. Jabbar
Qosay A. Al-Balas
Muneera S.M. Al-Saleem
Rawaz Rizgar Hassan
Goran Noori Salih
Muzhda Haydar Saber
Hanan Ibrahim Althagbi
Jehan Y. Al-Humaidi
Mohammed M. Rahman
Ahmed Hameed Al-Dabhawi
Talal Salem Al-Qaisi

Keywords

Abstract

Marrubium peregrinum has been acknowledged as a traditional therapeutic plant that relieves stomach aches and gastrointestinal disorders. The present investigation evaluates the acute toxicity and gastroprotective potential of the essential oil of Marrubium peregrinum (EOMP) in absolute ethanol-mediated ulceration. It identifies the molecular pathways that underlie its bioactivities. The anti-ulcer potentials of EOMP (100 and 200 mg/kg) were evaluated macroscopically and microscopically. Moreover, toxicological evaluation included behavioral, biochemical, and histological alterations that could occur because of EOMP ingestion.


Pre-treatment with EOMP (100 and 200 mg/kg) noticeably reduced the severity of gastric injury mediated by absolute ethanol and lowered hemorrhagic and gastric tissue disruptions. OEMP ingestion (100 and 200 mg/kg) one hour before ethanol delivery significantly inhibited lesion incidence by 73.72 % and 77.65 %, respectively. EOMP supplementation resisted ethanol-induced histological alterations and restored gastric defensive factors (increasing mucin secretion and pH). Moreover, EOMP-treated rats exhibited higher HSP 70 and lower Bax proteins, parallel with increased prostaglandin E2, catalase, and superoxide dismutase contents. The ethanol-mediated oxidative stress (MDA) and gastric inflammation (TNF-α, interleukin-6) were significantly mimicked as a result of EOMP pre-treatments.


The Toxicity evaluation evidenced the safety ingestion of up to 2 g/kg EOMP in rats without any noticeable morbidity throughout the two-week toxicity trial.


These outcomes present the prophylactic effect of EOMP against ethanol-mediated stomach toxicity by strengthening gastric defense factors, increasing endogenous antioxidants, lowering inflammatory mediators, and reducing apoptotic actions. Altogether, they contributed to faster gastric tissue recovery as a result of EOMP pretreatments, without any toxicity incidence.

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