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Pharmacological effects of active saponins from Panax ginseng Meyer

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dc.contributor.authorBae, Sin Ja-
dc.contributor.authorRho, Gyu Jin-
dc.contributor.authorKim, Kang Min-
dc.contributor.authorKang, Jae Seon-
dc.date.accessioned2022-12-26T15:04:29Z-
dc.date.available2022-12-26T15:04:29Z-
dc.date.issued2019-03-
dc.identifier.issn1596-5996-
dc.identifier.issn1596-9827-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/9384-
dc.description.abstractPurpose: To investigate the pharmacological effects of the active saponins isolated from Panax ginseng Meyer (P. ginseng) via extraction, heat treatment, and enzyme conversion. Methods: The effects of active saponins on rat blood were determined using a multichannel analyzer. The population doubling time (PDT) of mesenchymal stem cells (MSCs) and human-derived leukocyte cancer cells (A549) was determined by cell counting. beta-galactosidase was measured in human toothderived stem cells (HTS) using a beta-galactosidase ELISA kit. Results: Intraperitoneal administration of active saponins resulted in 30.09 % increase in red blood cell count and 55.55 % decrease in blood triglyceride concentrations. The stimulatory effect of active saponins (10 ng/mL) on cellular differentiation was determined based on PDT of MSCs, which decreased by 33.82 % compared to control. A 22.29 % increase in PDT of A549 cells demonstrated the suppressive effects of active saponins on cancer cell growth. Active saponins (10 ng/mL) also decreased intracellular beta-galactosidase concentration by 20.42 % in HTS cells. Conclusion: Administration of active saponins to rats extends the lifespan, promotes differentiation in MSCs, suppresses A549 cell differentiation, and reduces TG and beta-galactosidase associated with aging in HTS. Thus, active saponins have potentially beneficial effects in humans.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherPHARMACOTHERAPY GROUP-
dc.titlePharmacological effects of active saponins from Panax ginseng Meyer-
dc.typeArticle-
dc.publisher.location나이지리아-
dc.identifier.doi10.4314/tjpr.v18i3.16-
dc.identifier.scopusid2-s2.0-85065397364-
dc.identifier.wosid000462872300016-
dc.identifier.bibliographicCitationTROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH, v.18, no.3, pp 555 - 561-
dc.citation.titleTROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH-
dc.citation.volume18-
dc.citation.number3-
dc.citation.startPage555-
dc.citation.endPage561-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusCOMPOUND-K-
dc.subject.keywordPlusINTESTINAL BACTERIA-
dc.subject.keywordPlusRED GINSENG-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusGINSENOSIDES-
dc.subject.keywordPlusBIOMARKER-
dc.subject.keywordPlusCULTURE-
dc.subject.keywordPlusPLASMA-
dc.subject.keywordAuthorActive saponin-
dc.subject.keywordAuthorbeta-Galactosidase-
dc.subject.keywordAuthorDoubling time-
dc.subject.keywordAuthorMesenchymal stem cells-
dc.subject.keywordAuthorPanax ginseng-
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