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dc.contributor.authorAkhtar, Nabilah Mohammad Yaqoob-
dc.contributor.authorJantan, Ibrahim-
dc.contributor.authorArshad, Laiba-
dc.contributor.authorHaque, Md. Areeful-
dc.date.accessioned2021-04-26T05:05:52Z-
dc.date.available2021-04-26T05:05:52Z-
dc.date.issued2019-11-21-
dc.identifier.citationAkhtar, N.M.Y., Jantan, I., Arshad, L. et al. Standardized ethanol extract, essential oil and zerumbone of Zingiber zerumbet rhizome suppress phagocytic activity of human neutrophils. BMC Complement Altern Med 19, 331 (2019). https://doi.org/10.1186/s12906-019-2748-5en_US
dc.identifier.otherhttps://doi.org/10.1186/s12906-019-2748-5-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1262-
dc.descriptionhttps://bmccomplementmedtherapies.biomedcentral.com/articles/10.1186/s12906-019-2748-5#citeasen_US
dc.description.abstractBackground: Zingiber zerumbet rhizome and its bioactive metabolites have previously been reported to exhibit innumerable pharmacological properties particularly anti-inflammatory activities. In the present study, the 80% ethanol extract, essential oil and zerumbone of Z. zerumbet rhizomes were explored for their in vitro immunosuppressive properties on chemotaxis, CD11b/CD18 expression, phagocytosis and chemiluminescence of isolated human polymorphonuclear neutrophils (PMNs). Methods: The extract was analyzed quantitatively by performing a validated reversed phase high performance liquid chromatography (RP-HPLC). Zerumbone was isolated by chromatographic technique while the essential oil was acquired through hydro-distillation of the rhizomes and further analyzed by gas chromatography (GC) and GC MS. Chemotaxis assay was assessed by using a 24-well cell migration assay kit, while CD18 integrin expression and phagocytic engulfment were measured using flow cytometry. The reactive oxygen species (ROS) production was evaluated by applying lucigenin- and luminol-enhanced chemiluminescence assays. Results: Zerumbone was found to be the most abundant compound in the extract (242.73 mg/g) and the oil (58.44%). Among the samples tested, the oil revealed the highest inhibition on cell migration with an IC50 value of 3.24 μg/mL. The extract, oil and zerumbone showed moderate inhibition of CD18 integrin expression in a dose dependent trend. Z. zerumbet extract showed the highest inhibitory effect on phagocytic engulfment with percentage of phagocytizing cells of 55.43% for PMN. Zerumbone exhibited strong inhibitory activity on oxidative burst of zymosan- and PMA-stimulated neutrophils. Zerumbone remarkably inhibited extracellular ROS production in PMNs with an IC50 value of 17.36 μM which was comparable to that of aspirin. Conclusion: The strong inhibition on the phagocytosis of neutrophils by Z. zerumbet extract and its essential oil might be due the presence of its chemical components particularly zerumbone which was capable of impeding phagocytosis at different stages.en_US
dc.language.isoenen_US
dc.publisherBMC Complementary and Alternative Medicineen_US
dc.relation.ispartofseriesBMC Complement Altern Med 19, 331 (2019).;-
dc.subjectHuman neutrophilsen_US
dc.subjectZingiber zerumbeten_US
dc.subject, Zerumbone,en_US
dc.subjectEssential oil,en_US
dc.subjectImmunosuppressive effects,en_US
dc.subjectPhagocytic activityen_US
dc.titleStandardized ethanol extract, essential oil and zerumbone of Zingiber zerumbet rhizome suppress phagocytic activity of human neutrophilsen_US
dc.typeArticleen_US
Appears in Collections:Pharmacy Department

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