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Exploring the hepatoprotective properties of citronellol: In vitro and in silico studies on ethanol-induced damage in HepG2 cells.
Malik, Muhammad Nasir Hayat; Abid, Iqra; Ismail, Sana; Anjum, Irfan; Qadir, Halima; Maqbool, Tahir; Najam, Komal; Ibenmoussa, Samir; Bourhia, Mohammed; Salamatullah, Ahmad Mohammad; Wondmie, Gezahign Fentahun.
Affiliation
  • Malik MNH; Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
  • Abid I; Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
  • Ismail S; Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
  • Anjum I; Department of Basic Medical Sciences, Shifa College of Pharmaceutical Sciences, Shifa Tameer-e-Millat University, Islamabad, Pakistan.
  • Qadir H; Department of Basic Medical Sciences, Shifa College of Pharmaceutical Sciences, Shifa Tameer-e-Millat University, Islamabad, Pakistan.
  • Maqbool T; Institute of Molecular Biology and Biotechnology, The University of Lahore, Lahore, Pakistan.
  • Najam K; Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
  • Ibenmoussa S; Laboratory of Therapeutic and Organic Chemistry, Faculty of Pharmacy, University of Montpellier, Montpellier, 34000, France.
  • Bourhia M; Laboratory of Biotechnology and Natural Resources Valorization, Faculty of Sciences, Ibn Zohr University, 80060, Agadir, Morocco.
  • Salamatullah AM; Department of Food Science & Nutrition, College of Food and Agricultural Sciences, King Saud University, 11 P.O. Box 2460, Riyadh, 11451, Saudi Arabia.
  • Wondmie GF; Department of Biology, Bahir Dar University, P.O.Box 79, Bahir Dar, Ethiopia.
Open Life Sci ; 19(1): 20220950, 2024.
Article in En | MEDLINE | ID: mdl-39290493
ABSTRACT
Citronellol (CT) is a monoterpene alcohol present in the essential oil of plants of the genus Cymbopogon and exhibits diverse pharmacological activities. The aim of the current study was to investigate the hepatoprotective potential of CT against ethanol-induced toxicity in HepG2 cell lines. Silymarin (SIL) was used as a standard drug. MTT, crystal violet assay, DAPI, and PI staining were carried out to assess the effect of ethanol and CT on cell viability. RT-PCR determined the molecular mechanisms of hepatoprotective action of CT. CT ameliorated cell viability and restricted ethanol-induced cell death. DAPI and PI staining showed distinct differences in cell number and morphology. Less cell viability was observed in the diseased group obviously from strong PI staining when compared to the CT- and SIL-treated group. Moreover, CT showed downregulation of interleukin (IL-6), transforming growth factor-beta 1 (TGF-ß1), collagen type 1 A 1 (COL1A1), matrix metalloproteinase-1 (MMP-1), tissue inhibitor of metalloproteinase-1 (TIMP-1) and glutathione peroxidase-7 (GPX-7) levels. Molecular docking studies supported the biochemical findings. It is concluded that the cytoprotective activity of CT against ethanol-induced toxicity might be explained by its anti-inflammatory, immunomodulatory, and collagen-regulating effects.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Open Life Sci Year: 2024 Document type: Article Affiliation country: Pakistán Country of publication: Polonia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Open Life Sci Year: 2024 Document type: Article Affiliation country: Pakistán Country of publication: Polonia