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In vitro and in vivo exploitation of cell stress pathways using methanolic extracts of Phlomis stewartii in diabetic rat's model

dc.contributor.authorRasheed, Mamoon Ur
dc.contributor.authorNaqvi, Syed Ali Raza
dc.contributor.authorHassan, Sadaf Ul
dc.contributor.authorHaq, Atta Ul
dc.contributor.authorJanjua, Muhammad Ramazan Saeed Ashraf
dc.contributor.authorMahmoud, Mohamed H.
dc.contributor.authorBatiha, Gaber El-Saber
dc.contributor.authorRashid, Haroon
dc.contributor.authorRahim, Muhammad Abdul
dc.contributor.authorRocha, João Miguel
dc.date.accessioned2024-06-12T15:20:08Z
dc.date.available2024-06-12T15:20:08Z
dc.date.issued2024-10-01
dc.description.abstractVarious bioactive constituents present in plants are used to treat metabolic disorders linked to oxidative stress and obesity. Low-grade to chronic inflammation and IR are considered as main causes of obesity, which is strongly correlated with the prevalence and incidence of Type-2 Diabetes Mellitus (T2DM). In this study, the biological influence of Phlomis stewartii extracts was evaluated in vitro and in vivo using rat diabetic models. The biological effects included anti-inflammatory, anti-proliferative, anti-apoptotic, metabolic hormonal via molecular signaling pathways, and antioxidant potential. The extracts from P. stewartii exhibited the strongest DPPH and FRAP potential for LM (38.92 µg/mL) and (45.28 µg/mL) respectively. Moreover, the high absorbance for reducing power was observed in leaves methanol (LM) 1.36 which is greater than flower methanol (FM) 1.12, and whole plant methanol (WPM) 1.21 at a concentration of 500 µg/mL when comparing treated groups to the negative control (NC), and positive control (PC) groups. The results of an Enzyme-linked Immunosorbent Assay (ELISA) study measuring a metabolic hormonal profile that includes Triiodothyronine (T3), Thyroxine (T4), Thyroid Stimulating Hormone (TSH), insulin, leptin, and glucokinase showed that LM has been greatly recovered. The study examined the gene expression analysis of cell stress pathways, and it found that the PC groups had higher levels of Janus kinase (JAK), Signal Transducer and Activator of Transcription (STATS) pathways through JAK (JAK-2 and STAT-1), G protein-Coupled Receptor Kinase 2 (GRK-2), Calmodulin 2 (CALM-2), Proteins Inhibitor of Activated STAT 1 (PIAS-1), Forkhead Box 01, 03, 04, (FOXO-1, FOXO-3, FOXO-4), Bcl-2 Associated X-protein (BAX), B-cell Lymphoma 2 (BCL-2), Interleukins (IL-6, IL-1β), and Tumour Necrosis Factor-α (TNF-α). On the other hand, downregulation was observed in NC groups and P. stewartii extract-treated groups. The outcome of this study suggests a strong relationship towards ameliorative effects.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.indcrop.2024.118861pt_PT
dc.identifier.eid85194902905
dc.identifier.issn0926-6690
dc.identifier.urihttp://hdl.handle.net/10400.14/45482
dc.identifier.wos001263729200001
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectAntioxidantspt_PT
dc.subjectBiological activitiespt_PT
dc.subjectDiabetespt_PT
dc.subjectPhenolic acidspt_PT
dc.subjectPhlomis stewartiipt_PT
dc.subjectPhytochemicalspt_PT
dc.titleIn vitro and in vivo exploitation of cell stress pathways using methanolic extracts of Phlomis stewartii in diabetic rat's modelpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleIndustrial Crops and Productspt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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