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dc.contributor.authorNinsiima, Herbert Izo
dc.contributor.authorEze, Ejike Daniel
dc.contributor.authorSsekatawa, Kenneth
dc.contributor.authorNalugo, Halima
dc.contributor.authorAsekenye, Caroline
dc.contributor.authorOnanyang, David
dc.contributor.authorMunanura, Edson Ireeta
dc.contributor.authorAriong, Moses
dc.contributor.authorMatama, Kevin
dc.contributor.authorZirintunda, Gerald
dc.contributor.authorMbiydzenyuy, Ngala Elvis
dc.contributor.authorSsempijja, Fred
dc.contributor.authorAfodun, Adam Moyosore
dc.contributor.authorMujinya, Regan
dc.contributor.authorUsman, Ibe Michael
dc.contributor.authorAsiimwe, Oscar Hilary
dc.contributor.authorTibyangye, Julius
dc.contributor.authorKasozi, Keneth Iceland
dc.date.accessioned2023-03-02T19:54:25Z
dc.date.available2023-03-02T19:54:25Z
dc.date.issued2023-02-21
dc.identifier.citationNinsiima, H. I., Eze, E. D., Ssekatawa, K., Nalugo, H., Asekenye, C., Onanyang, D., ... & Kasozi, K. I. (2023). Green tea silver nanoparticles improve physiological motor and cognitive function in BALB/c mice during inflammation. Heliyon.en_US
dc.identifier.issn2405-8440
dc.identifier.urihttp://dir.muni.ac.ug/xmlui/handle/20.500.12260/499
dc.description.abstractInformation on the basic changes associated with green tea small molecules in acute inflammation is deficient. The purpose of the study was to characterize and establish the effects of green tea silver nanoparticles (AgNPs) following inflammation in BALB/c male mice. In this study, green tea silver nitrate nanoparticles were characterized and the extract were made up to constitute high (100%), medium (10%), and low (1%) concentrations for administration. Acute inflammation was induced in groups I–V of the experimental rodents by injecting 0.5 ml/kg of fresh egg albumin on the subplantar surface of the right hind paw and animals were monitored for 36 h. Group I–III were administered 100%, 10%, 1% green tea nanoparticles extract while group IV was given diclofenac. Group V was the positive control while group VI was the negative control that received the vehicle. Paw edema was measured at a 2 h interval for 3 days, while the pain was assessed by measuring the locomotion activity using the voluntary wheel running and the anxietylike behavior. Hypersensitivity was measured through the temperature sensation experiment and a non-linear regression analysis was done. Here, synthesized green tea AgNPs registered an absorbance band at 460 nm, phytochemicals due to presence of organic functional groups of O––C––O of oxycarbons, of C––C of a conjugate alkene, C––O of a stretching bond of a secondary alcohol. The silver green tea nanoparticles were spherical, covered by a slimy layer, capped and stable. Green tea AgNPs significantly decreased temperature hypersensitivity in BALB/c male mice and this demonstrated their protective effects. Low concentrations of green tea nanoparticles inhibited edema thus mimicking effects of diclofenac, however, the percentage of inhibition was highest in medium and high silver-tea nanoparticles concentrations demonstration the importance of concentration in therapeutics. Anxiety was lowest in BALB/c male mice treated with high concentrations of silver green tea nanoparticles, and this led to increased locomotory activity in mice. Green tea AgNPs have strong anti-inflammatory effects at high concentrations. Concentrations of green tea AgNPs modulated basic sensory and motor behaviors in BALB/c male mice demonstrating their importance in complementary and integrative medical practice.en_US
dc.description.sponsorshipAfrica Centre of Excellence in Materials, Product Development & Nanotechnology [P151847IDA].en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectSmall moleculesen_US
dc.subjectUganda teaen_US
dc.subjectThe safety of teaen_US
dc.subjectAgNPsen_US
dc.subjectPhysiology of nanoparticlesen_US
dc.subjectGreen tea synthesisen_US
dc.subjectSilver nanoparticlesen_US
dc.subjectAntibiotic resistanceen_US
dc.subjectCamellia sinensisen_US
dc.subjectprunus africanaen_US
dc.titleGreen tea silver nanoparticles improve physiological motor and cognitive function in BALB/c mice during inflammationen_US
dc.typeArticleen_US


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