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1.
BMC Med Educ ; 22(1): 487, 2022 Jun 23.
Artigo em Inglês | MEDLINE | ID: mdl-35733187

RESUMO

BACKGROUND: Previous studies have primarily implemented problem-based learning (PBL) or flipped classroom (FC) teaching models in different majors; however, research on the combined PBL-FC teaching method in clinical medicine is scarce. Therefore, we investigated the combined PBL-FC teaching method in teaching ocular trauma on students' competencies. METHOD: About 75 ophthalmology postgraduates were randomly divided into PBL-FC and traditional teaching groups. Students completed pre-and post-class theoretical examinations, skills evaluation, learning ability scales, and feedback questionnaires. RESULTS: Both groups showed significantly higher theoretical scores and improved learning ability. Feedback questionnaire scores of the PBL-FC group's postgraduates without clinical experience were significantly higher than the traditional group's for some items; there was no difference between groups in postgraduates with clinical experience. PBL-FC group's pre-class preparation time was significantly longer than the traditional group's, but the post-class review time was significantly shorter. PBL-FC group's post-class theoretical performance was significantly higher than the traditional group's. There was no statistical difference between the groups regarding skill operation. Among postgraduates without clinical experience, the PBL-FC group's skill operation performance was significantly higher than the traditional group's; for postgraduates with clinical experience, the traditional group's skill operation performance was significantly higher than the PBL-FC group's. CONCLUSIONS: PBL-FC teaching is better for students without clinical experience or knowledge of ophthalmic diseases. Meanwhile, traditional teaching is a good choice for students with clinical experience who need more relevant knowledge.


Assuntos
Oftalmologia , Aprendizagem Baseada em Problemas , Competência Clínica , Humanos , Aprendizagem , Oftalmologia/educação , Aprendizagem Baseada em Problemas/métodos , Inquéritos e Questionários , Ensino
2.
Exp Cell Res ; 361(2): 210-216, 2017 12 15.
Artigo em Inglês | MEDLINE | ID: mdl-28988741

RESUMO

OBJECTIVE: The aim of this study was to demonstrate that altered gene expression of Smad7regulated NF-κB expression and ROS production on Ang II (Angiotensin II)-induced rat glomerular mesangial cell (GMC) proliferation. METHODS: pAdTrack-CMV-Smad7 was transduced into rat GMC by adeno-transduction using an ADV (adenovirus)-mediated vector in vivo. Diphenylene iodonium chloride (DPI) pre-treated GMC, and blocked ROS generation as determined by DCFH-DA method. Altered expressions of IκBα and p65 were monitored by Western blot analysis and immunofluorescence. GMC proliferation was tested by the Cell Counting Kit-8 assay. Apoptosis of GMC was detected by flow cytometric analysis. RESULTS: Over-expression of Smad7 dampened the ability of Ang II to promote ROS synthesis and inhibited the ability of Ang II to decrease functional expression of IκBα. Moreover, Smad7 increased nuclear IκBα expression. Smad7 did not significantly influence the capacity of Ang II to increase protein expression of NF-κB p65. However, immunofluorescence analysis showed that Smad7 reduced nuclear NF-κB p65 level. Further, over-expression of Smad7 promoted GMC apoptosis by inhibiting NF-κB activation, which alleviated the Ang II-promoted proliferation of GMC. CONCLUSIONS: Smad7 influenced NF-κB expression by regulating ROS generation, and induced GMC apoptosis to counter the Ang II-promoted proliferation.


Assuntos
Angiotensina II/farmacologia , Células Mesangiais/efeitos dos fármacos , Inibidor de NF-kappaB alfa/genética , Proteína Smad7/genética , Fator de Transcrição RelA/genética , Adenoviridae/genética , Adenoviridae/metabolismo , Animais , Apoptose/genética , Linhagem Celular , Proliferação de Células/efeitos dos fármacos , Fluoresceínas/metabolismo , Corantes Fluorescentes/metabolismo , Regulação da Expressão Gênica , Vetores Genéticos/química , Vetores Genéticos/metabolismo , Células Mesangiais/citologia , Células Mesangiais/metabolismo , Inibidor de NF-kappaB alfa/metabolismo , Oniocompostos/farmacologia , Ratos , Espécies Reativas de Oxigênio/metabolismo , Transdução de Sinais , Proteína Smad7/metabolismo , Fator de Transcrição RelA/metabolismo
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