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dc.contributor.authorMohammed, Salman A. A.
dc.contributor.authorKhan, Riaz A.
dc.contributor.authorEl-Readi, Mahmoud Z.
dc.contributor.authorEmwas, Abdul-Hamid M.
dc.contributor.authorSioud, Salim
dc.contributor.authorPoulson, Benjamin Gabriel
dc.contributor.authorJaremko, Mariusz
dc.contributor.authorEldeeb, Hussein M.
dc.contributor.authorAl-Omar, Mohsen S.
dc.contributor.authorMohammed, Hamdoon A.
dc.date.accessioned2020-09-30T05:24:30Z
dc.date.available2020-09-30T05:24:30Z
dc.date.issued2020-09-29
dc.date.submitted2020-09-01
dc.identifier.citationMohammed, S. A. A., Khan, R. A., El-Readi, M. Z., Emwas, A.-H., Sioud, S., Poulson, B. G., … Mohammed, H. A. (2020). Suaeda vermiculata Aqueous-Ethanolic Extract-Based Mitigation of CCl4-Induced Hepatotoxicity in Rats, and HepG-2 and HepG-2/ADR Cell-Lines-Based Cytotoxicity Evaluations. Plants, 9(10), 1291. doi:10.3390/plants9101291
dc.identifier.issn2223-7747
dc.identifier.doi10.3390/plants9101291
dc.identifier.urihttp://hdl.handle.net/10754/665368
dc.description.abstractSuaeda vermiculata, an edible halophytic plant, used by desert nomads to treat jaundice, was investigated for its hepatoprotective bioactivity and safety profile on its mother liquor aqueous-ethanolic extract. Upon LC-MS (Liquid Chromatography-Mass Spectrometry) analysis, the presence of several constituents including three major flavonoids, namely quercetin, quercetin-3-O-rutinoside, and kaempferol-O-(acetyl)-hexoside-pentoside were confirmed. The aqueous-ethanolic extract, rich in antioxidants, quenched the DPPH (1,1-diphenyl-2-picrylhydrazyl) radicals, and also showed noticeable levels of radical scavenging capacity in ABTS (2,2'-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid) assay. For the hepatoprotective activity confirmation, the male rat groups were fed daily, for 7 days (n = 8/group, p.o.), either carboxyl methylcellulose (CMC) 0.5%, silymarin 200 mg/kg, the aqueous-ethanolic extract of the plant Suaeda vermiculata (100, 250, and 500 mg/kg extract), or quercetin (100 mg/kg) alone, and on day 7 of the administrations, all the animal groups, excluding a naïve (250 mg/kg aqueous-ethanolic extract-fed), and an intact animal group were induced hepatotoxicity by intraperitoneally administering carbon tetrachloride (CCl4). All the animals were sacrificed after 24 h, and aspartate transaminase and alanine transaminase serum levels were observed, which were noted to be significantly decreased for the aqueous-ethanolic extract, silymarin, and quercetin-fed groups in comparison to the CMC-fed group (p < 0.0001). No noticeable adverse effects were observed on the liver, kidney, or heart’s functions of the naïve (250 mg/kg) group. The aqueous-ethanolic extract was found to be safe in the acute toxicity (5 g/kg) test and showed hepatoprotection and safety at higher doses. Further upon, the cytotoxicity testings in HepG-2 and HepG-2/ADR (Adriamycin resistant) cell-lines were also investigated, and the IC50 values were recorded at 56.19±2.55 µg/mL, and 78.40±0.32 µg/mL (p < 0.001, Relative Resistance RR 1.39), respectively, while the doxorubicin (Adriamycin) IC50 values were found to be 1.3±0.064, and 4.77±1.05 µg/mL (p < 0.001, RR 3.67), respectively. The HepG-2/ADR cell-lines when tested in a combination of the aqueous-ethanolic extract with doxorubicin, a significant reversal in the doxorubicin’s IC50 value by 2.77 folds (p < 0.001, CI = 0.56) was noted as compared to the cytotoxicity test where the extract was absent. The mode of action for the reversal was determined to be synergistic in nature indicating the role of the aqueous-ethanolic extract.
dc.description.sponsorshipThe authors gratefully acknowledge Qassim University, represented by the Deanship of Scientific Research, on the financial support for this research under the number (pharmacy-2019-2-2-I-5606) during the academic year 1440AH/ 2019AD.
dc.description.sponsorshipThe authors disclose the receipt of the following financial support for the research and publication of this article. This work was supported by the Qassim University, represented by the Deanship of Scientific Research under the grant (pharmacy-2019-2-2-I-5606) during the academic year 1440AH / 2019AD.
dc.publisherMDPI AG
dc.relation.urlhttps://www.mdpi.com/2223-7747/9/10/1291
dc.rightsThis is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleSuaeda vermiculata Aqueous-Ethanolic Extract-Based Mitigation of CCl4-Induced Hepatotoxicity in Rats, and HepG-2 and HepG-2/ADR Cell-Lines-Based Cytotoxicity Evaluations
dc.typeArticle
dc.contributor.departmentNMR
dc.contributor.departmentOrganics
dc.contributor.departmentBioscience
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentBioscience Program
dc.identifier.journalPlants
dc.eprint.versionPublisher's Version/PDF
dc.contributor.institutionDepartment of Pharmacology and Toxicology, College of Pharmacy, Qassim University, Qassim 51452, Saudi Arabia.
dc.contributor.institutionDepartment of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Qassim 51452, Saudi Arabia.
dc.contributor.institutionDepartment of Clinical Biochemistry, Faculty of Medicine, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
dc.contributor.institutionDepartment of Biochemistry, Faculty of Pharmacy, Al-Azhar University, Assiut 71524, Egypt.
dc.contributor.institutionDepartment of Biochemistry, Faculty of Medicine, Al-Azhar University, Assiut, 71524, Egypt.
dc.contributor.institutionMedicinal Chemistry and Pharmacognosy Department, Faculty of Pharmacy, JUST, Irbid 22110, Jordan.
dc.contributor.institutionDepartment of Pharmacognosy, Faculty of Pharmacy, Al-Azhar University, Cairo, 11371, Egypt.
dc.identifier.volume9
dc.identifier.issue10
dc.identifier.pages1291
kaust.personEmwas, Abdul-Hamid M.
kaust.personSioud, Salim
kaust.personPoulson, Benjamin Gabriel
kaust.personJaremko, Mariusz
dc.date.accepted2020-09-22
refterms.dateFOA2020-09-30T05:27:57Z


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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.