Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros

Base de dados
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
BMC Musculoskelet Disord ; 25(1): 451, 2024 Jun 06.
Artigo em Inglês | MEDLINE | ID: mdl-38844905

RESUMO

OBJECTIVE: Temporomandibular joint osteoarthritis (TMJOA) is a chronic degenerative joint disorder characterized by extracellular matrix degeneration and inflammatory response of condylar cartilage. ß-arrestin2 is an important regulator of inflammation response, while its role in TMJOA remains unknown. The objective of this study was to investigate the role of ß-arrestin2 in the development of TMJOA at the early stage and the underlying mechanism. METHODS: A unilateral anterior crossbite (UAC) model was established on eight-week-old wild-type (WT) and ß-arrestin2 deficiency mice to simulate the progression of TMJOA. Hematoxylin-eosin (HE) staining and microcomputed tomography (micro-CT) analysis were used for histological and radiographic assessment. Immunohistochemistry was performed to detect the expression of inflammatory and degradative cytokines, as well as autophagy related factors. Terminal-deoxynucleotidyl transferase mediated nick end labeling (TUNEL) assay was carried out to assess chondrocyte apoptosis. RESULTS: The loss of ß-arrestin2 aggravated cartilage degeneration and subchondral bone destruction in the model of TMJOA at the early stage. Furthermore, in UAC groups, the expressions of degradative (Col-X) and inflammatory (TNF-α and IL-1ß) factors in condylar cartilage were increased in ß-arrestin2 null mice compared with WT mice. Moreover, the loss of ß-arrestin2 promoted apoptosis and autophagic process of chondrocytes at the early stage of TMJOA. CONCLUSION: In conclusion, we demonstrated for the first time that ß-arrestin2 plays a protective role in the development of TMJOA at the early stage, probably by inhibiting apoptosis and autophagic process of chondrocytes. Therefore, ß-arrestin2 might be a potential therapeutic target for TMJOA, providing a new insight for the treatment of TMJOA at the early stage.


Assuntos
Cartilagem Articular , Modelos Animais de Doenças , Côndilo Mandibular , Camundongos Knockout , Osteoartrite , Transtornos da Articulação Temporomandibular , beta-Arrestina 2 , Animais , Osteoartrite/metabolismo , Osteoartrite/patologia , beta-Arrestina 2/metabolismo , beta-Arrestina 2/genética , Cartilagem Articular/patologia , Cartilagem Articular/metabolismo , Côndilo Mandibular/patologia , Côndilo Mandibular/metabolismo , Côndilo Mandibular/diagnóstico por imagem , Camundongos , Transtornos da Articulação Temporomandibular/metabolismo , Transtornos da Articulação Temporomandibular/patologia , Transtornos da Articulação Temporomandibular/diagnóstico por imagem , Transtornos da Articulação Temporomandibular/etiologia , Condrócitos/metabolismo , Condrócitos/patologia , Camundongos Endogâmicos C57BL , Apoptose , Articulação Temporomandibular/patologia , Articulação Temporomandibular/metabolismo , Articulação Temporomandibular/diagnóstico por imagem , Masculino , Microtomografia por Raio-X , Autofagia/fisiologia
2.
RSC Adv ; 11(25): 15010-15016, 2021 Apr 21.
Artigo em Inglês | MEDLINE | ID: mdl-35424050

RESUMO

Motility is significant in organisms. Studying the influence of motility on biological processes provides a new angle in understanding the essence of life. Biomineralization is a representative process for organisms in forming functional materials. In the present study, we investigated the biomineralization of iron oxides templated by Escherichia coli (E. coli) cells under oscillation. The formation of iron oxide minerals with acicular and banded morphology was observed. The surface charge of E. coli cells contributed to the biomineralization process. The surface components of E. coli cells including lipids, carbohydrates and proteins also have roles in regulating the formation and morphology of iron oxide minerals. As-prepared mineralized iron oxide nanomaterials showed activity in photocatalytic degradation of methylene blue as well as in electrocatalytic hydrogen evolution reaction. This study is helpful not only in understanding motility in biological processes, but also in developing techniques for fabricating functional nanomaterials.

3.
Oxid Med Cell Longev ; 2020: 8884320, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33224434

RESUMO

Valproate sodium (VPA) is a traditional antiepileptic drug with a neuroprotective role in cerebrovascular disease. After intracerebral hemorrhage (ICH), mechanical compression by hematoma, neuroinflammation, oxidative stress, and cytotoxicity of hematoma lysates caused the destruction of the blood brain barrier (BBB). Targeting BBB is a major therapeutic method for patients with ICH. The purpose of the present study was to explore the role of VPA in preserving BBB integrity in the ICH model and investigate the underlying molecular mechanisms. One hundred and thirty-six adult male CD1 mice were randomly divided into five groups in the study. Mice subjected to ICH were administered intraperitoneally with VPA at 3, 24, and 48 h post-ICH, respectively. Neurobehavioral assessments, BBB permeability, Evans blue fluorescence, hematoma volume, and protein expression were evaluated. The administration of VPA reduced BBB permeability and improved the neurobehavior significantly post-ICH. VPA administration significantly decreased the expression of phosphorylated nuclear factor-kappa B (p-NFκB), matrix metalloproteinases 9 (MMP9), tumor necrosis factorα (TNFα), and interleukin-6 (IL-6), while it enhanced the expression of claudin 5 and occludin in the brain. In conclusion, VPA administration maintained the integrity of BBB after experimental ICH, thus reducing brain edema and improving the neurological outcomes. Therefore, VPA administration might be a new therapeutic method to protect BBB integrity for patients with ICH.


Assuntos
Barreira Hematoencefálica , Hemorragia Cerebral , Ácido Valproico/farmacologia , Animais , Barreira Hematoencefálica/metabolismo , Barreira Hematoencefálica/patologia , Hemorragia Cerebral/tratamento farmacológico , Hemorragia Cerebral/metabolismo , Hemorragia Cerebral/patologia , Modelos Animais de Doenças , Regulação da Expressão Gênica/efeitos dos fármacos , Masculino , Camundongos
4.
PLoS One ; 9(5): e97753, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24840508

RESUMO

This study investigated the effect of cold plasma seed treatment on tomato bacterial wilt, caused by Ralstonia solanacearum (R. solanacearum), and the regulation of resistance mechanisms. The effect of cold plasma of 80W on seed germination, plant growth, nutrient uptake, disease severity, hydrogen peroxide (H2O2) concentration and activities of peroxidase (POD; EC 1.11.1.7), polyphenol oxidase (PPO; EC 1.10.3.2) and phenylalanine ammonia lyase (PAL; EC 4.3.1.5) were examined in tomato plants. Plasma treatment increased tomato resistance to R. solanacearum with an efficacy of 25.0%. Plasma treatment significantly increased both germination and plant growth in comparison with the control treatment, and plasma-treated plants absorbed more calcium and boron than the controls. In addition, H2O2 levels in treated plants rose faster and reached a higher peak, at 2.579 µM gFW-1, 140% greater than that of the control. Activities of POD (421.3 U gFW-1), PPO (508.8 U gFW-1) and PAL (707.3 U gFW-1) were also greater in the treated plants than in the controls (103.0 U gFW-1, 166.0 U gFW-1 and 309.4 U gFW-1, respectively). These results suggest that plasma treatment affects the regulation of plant growth, H2O2 concentration, and POD, PPO and PAL activity in tomato, resulting in an improved resistance to R. solanacearum. Consequently, cold plasma seed treatment has the potential to control tomato bacterial wilt caused by R. solanacearum.


Assuntos
Doenças das Plantas/microbiologia , Doenças das Plantas/prevenção & controle , Gases em Plasma/farmacologia , Ralstonia solanacearum/efeitos dos fármacos , Sementes/efeitos dos fármacos , Solanum lycopersicum/crescimento & desenvolvimento , Boro/metabolismo , Cálcio/metabolismo , Catecol Oxidase/metabolismo , Germinação/efeitos dos fármacos , Peróxido de Hidrogênio/metabolismo , Solanum lycopersicum/microbiologia , Peroxidase/metabolismo , Fenilalanina Amônia-Liase/metabolismo , Ralstonia solanacearum/fisiologia
SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa