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1.
Altern Ther Health Med ; 29(6): 416-424, 2023 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-37384405

RESUMEN

Objective: This study is aimed to examine the correlation between the transitions in the muscular strength pre and post arthroscopic meniscus suture surgery. Methods: A total of 87 patients records were collected from the electronic medical records of the Second Affiliated Hospital of Soochow University from 2020 to 2021. Patients in the operative group underwent arthroscopic meniscus sutures. The isokinetic muscular strength test system (ISOMED2000) tool was utilized to examine the isokinetic intensity of the knee joins on both sides and the balance was marked and adjusted to the training methods before the test. The HSS score was used to assess the transitions in the knee activity. Results: There was a significant variation in the extensor muscle strength found on the affected portion where F value was observed at 3747.845 (P < .01). The extensor knee joint strength of the affected side was less than the healthy side when compared with pre-operation, one month, three months, and six months post-surgery where F values were found to be 5287.41, 5510.517, and 1947.91 respectively (P < .001). After six months of the surgery, there was an improvement in the isokinetic muscular strength of patients, where the measurement of the damaged side and the healthier side was observed as 89.11 ± 6.78 and 93.45 ± 5.59, respectively. Conclusion: Arthroscopic meniscus suture surgery is observed to have a superior influence on the treatments. After 6 months of surgery, the muscular force of the knee extensor on the affected joint portion enhanced remarkably in contrast to the other durations.


Asunto(s)
Articulación de la Rodilla , Menisco , Humanos , Articulación de la Rodilla/cirugía , Artroscopía , Músculo Esquelético , Fuerza Muscular/fisiología , Suturas
2.
Eur J Pharmacol ; 875: 172939, 2020 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-31978425

RESUMEN

The mechanisms driving the development and progression of Rheumatoid arthritis (RA) are complex, novel targeted therapies are gaining traction as potential methods to prevent or slow the progression of RA. Nobiletin is a derivative of citrus fruit that has been shown to attenuate the development of osteoarthritis and inhibit the expression of proinflammatory cytokines. However, the exact mechanisms by which nobiletin exerts these chondroprotective effects remain poorly understood. In the present study, we investigated the impact of nobiletin in mediating the effects of interleukin-21 (IL-21) in MH7A fibroblast-like synoviocytes (FLS), the main cell type found in the articular synovium. Firstly, we demonstrate that nobiletin (25 µM and 50 µM) reduced the expression of the IL-21 receptor by 29% and 51%, respectively, in FLS. Additionally, our findings demonstrate that nobiletin potently ameliorated IL-21-induced increased production of reactive oxygen species and 4-hydroxynonenal, increased expression of interleukin 6 (IL-6), tumor necrosis factor-α (TNF-α), and high-mobility group box 1 (HMGB1), and decreased mitochondrial membrane potential. We also demonstrate the ability of nobiletin to attenuate IL-21-induced expression of matrix metalloproteinases 3 and 13 (MMP-3, MMP-13), key degradative enzymes involved in RA-associated cartilage destruction. Finally, we show that the effects of nobiletin are mediated through the JAK1/STAT3 pathway, as nobiletin significantly reduced the phosphorylation of both JAK1 and STAT3. Taken together, our findings indicate that nobiletin may offer a safe and effective treatment against the development and progression of RA induced by the expression of IL-21 and its receptor.


Asunto(s)
Antioxidantes/farmacología , Artritis Reumatoide/tratamiento farmacológico , Flavonas/farmacología , Interleucinas/antagonistas & inhibidores , Transducción de Señal/efectos de los fármacos , Antioxidantes/uso terapéutico , Artritis Reumatoide/inmunología , Artritis Reumatoide/patología , Línea Celular , Evaluación Preclínica de Medicamentos , Flavonas/uso terapéutico , Humanos , Subunidad alfa del Receptor de Interleucina-21/metabolismo , Interleucinas/metabolismo , Janus Quinasa 1/metabolismo , Metaloproteinasa 13 de la Matriz/metabolismo , Metaloproteinasa 3 de la Matriz/metabolismo , Estrés Oxidativo/efectos de los fármacos , Estrés Oxidativo/inmunología , Factor de Transcripción STAT3/metabolismo , Transducción de Señal/inmunología , Membrana Sinovial/citología , Membrana Sinovial/inmunología , Membrana Sinovial/patología , Sinoviocitos
3.
Am J Phys Med Rehabil ; 98(10): 914-920, 2019 10.
Artículo en Inglés | MEDLINE | ID: mdl-31135464

RESUMEN

BACKGROUND: Inflammation and glial scar formation determine the recovery process after spinal cord injury. Hyperbaric oxygen is used as a rehabilitation therapy for various clinical diseases, including spinal cord injury. However, the relationship between hyperbaric oxygen therapy and inflammation or glial scar is not fully understood. OBJECTIVE: The aim of this study was to investigate the therapeutic effect and molecular mechanism of hyperbaric oxygen on spinal cord injury. METHODS: A total of 54 developing female Sprague-Dawley rats were randomly divided into sham group, spinal cord injury group, and hyperbaric oxygen group, with 18 rats in each group. The model of spinal cord injury was established using Allen's method. Hyperbaric oxygen therapy was administered once a day until the rats were killed. RESULTS: The results demonstrated inflammation and glial scar formation are involved in secondary spinal cord injury. After hyperbaric oxygen treatment, there was a notable improvement of the locomotor function in rats. Hyperbaric oxygen reduced the inflammatory reaction and glial scar formation by inhibiting inflammation-related factors iNOS and COX-2 and glial scar-related components GFAP and NG2. This process may be achieved by inhibiting AKT and NF-kB pathways. CONCLUSIONS: Hyperbaric oxygen effectively promotes the recovery of spinal cord injury by inhibiting inflammation and glial scar formation.


Asunto(s)
Cicatriz/prevención & control , Oxigenoterapia Hiperbárica , Neuroglía/patología , Traumatismos de la Médula Espinal/patología , Traumatismos de la Médula Espinal/terapia , Animales , Modelos Animales de Enfermedad , Femenino , Inflamación/prevención & control , Ratas , Ratas Sprague-Dawley , Recuperación de la Función , Traumatismos de la Médula Espinal/fisiopatología
4.
J Nat Med ; 72(1): 57-63, 2018 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-28856634

RESUMEN

Pachymic acid (PA) is a lanostane type triterpenoid isolated from Poria cocos, which possesses an anti-tumor effect in breast cancer, prostate cancer, lung cancer, and bladder cancer cells. In this study, we investigated the effect of PA on the growth and apoptosis of human immortalized cell line (HOS) and primary osteosarcoma cells by a Cell Counting Kit-8 (CCK-8) and Annexin V and propidium iodide (PI) staining, respectively. Western blot was used to measure the expression of cleaved Caspase 3, PTEN, and AKT, as well as the AKT phosphorylation. The Caspase 3 activity was determined using the Caspase-3 Colorimetric Assay Kit. From the results, PA significantly reduced cell proliferation in a concentration- and time-dependent manner. PA also induced cell apoptosis in a dose-dependent fashion. PA treatment led to increased Caspase 3 activation and PTEN expression, as well as reduced AKT phosphorylation. Moreover, Ac-DEVD-CHO (a Caspase 3/7 inhibitor) pre-treatment or PTEN knockdown partially blocked the effects of PA on cell proliferation and apoptosis. Caspase 3/7 inhibitor had an additive effect with PTEN knockdown. Collectively, our results suggested that induction of apoptosis by PA was mediated in part by PTEN/AKT signaling and Caspase 3/7 activity. This study provides evidence that PA might be useful in the treatment of human osteosarcoma.


Asunto(s)
Caspasa 3/metabolismo , Osteosarcoma/metabolismo , Fosfohidrolasa PTEN/metabolismo , Triterpenos/metabolismo , Apoptosis , Línea Celular Tumoral , Proliferación Celular , Humanos , Fosforilación , Proteínas Proto-Oncogénicas c-akt/metabolismo , Transducción de Señal
5.
Med Sci Monit ; 22: 3177-85, 2016 Sep 07.
Artículo en Inglés | MEDLINE | ID: mdl-27602557

RESUMEN

BACKGROUND This study aimed to compare the surgical outcomes between open pedicle screw fixation (OPSF) and percutaneous pedicle screw fixation (PPSF) for the treatment of thoracolumbar fractures, which has received scant research attention to date. MATERIAL AND METHODS Eight-four patients with acute and subacute thoracolumbar fractures who were treated with SSPSF from January 2013 to June 2014 at the Changzhou Hospital of Traditional Chinese Medicine (Changzhou, China) were retrospectively reviewed. The patients were divided into 4 groups: the OPSF with 4 basic screws (OPSF-4) group, the OPSF with 4 basic and 2 additional screws (OPSF-6) group, the PPSF with 4 basic screws (PPSF-4) group, and the PPSF with 4 basic and 2 additional screws (PPSF-6) group. The intraoperative, immediate postoperative, and over 1-year follow-up outcomes were evaluated and compared among these groups. RESULTS Blood loss in the PPSF-4 group and the PPSF-6 group was significantly less than in the OPSF-4 group and the OPSF-6 group (P<0.05). The OPSF-6 group exhibited significantly higher immediate postoperative correction percentage of anterior column height of fractured vertebra than the other 3 groups (P<0.05), and higher correction of sagittal regional Cobb angle and kyphotic angle of injured vertebra than in the PPSF-4 and -6 groups (P<0.05). In addition, there was no significant difference in the correction loss of percentage of anterior column height, and loss of sagittal Cobb angle and kyphotic angle of fractured vertebrae at final follow-up among the 4 groups (P>0.05). CONCLUSIONS OPSF with 6 screws had an advantage in the correction of injured vertebral height and kyphosis, and PPSF reduced the intraoperative blood loss of patients.


Asunto(s)
Fijación Interna de Fracturas/métodos , Vértebras Lumbares/cirugía , Tornillos Pediculares , Fracturas de la Columna Vertebral/cirugía , Vértebras Torácicas/cirugía , Adulto , Anciano , Femenino , Estudios de Seguimiento , Humanos , Vértebras Lumbares/diagnóstico por imagen , Masculino , Persona de Mediana Edad , Vértebras Torácicas/diagnóstico por imagen , Resultado del Tratamiento
6.
Water Sci Technol ; 72(8): 1446-54, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26465317

RESUMEN

This study assessed the characteristics of biosolids of a pilot-scale anaerobic membrane bioreactor (AnMBR) treating municipal wastewater. The production of total solids (TS) and volatile solids (VS) was comparable to that reported for the extended aeration system at solids residence time (SRT) longer than 40 days. The yields of TS and VS were reduced as SRT increased from 40 to 100 days and increased with the addition of 26 mg/L of FeCl3. The AnMBR destroyed 60-82% of the VS loading in feed wastewater and hence it was concluded the biosolids met the requirements for vector attraction reduction for land application. The concentrations of volatile suspended solids and total suspended solids in the sludge were less than those reported after anaerobic digestion of conventional primary and secondary sludge mixtures, and hence dewatering of the waste stream may be required for some applications. The nutrient content in terms of total Kjeldahl nitrogen and total phosphorus was similar to that of anaerobically digested municipal sludges. The dewaterability of the biosolids was poorer than that reported for sludges from aerobic treatment and anaerobically digested sludges. Dewaterability was improved by addition of FeCl3 and reduced SRT. The biosolids met standards for land application with regards to the concentration of heavy metals but would need further treatment to meet Class B pathogen indicator criteria.


Asunto(s)
Reactores Biológicos , Aguas del Alcantarillado/química , Administración de Residuos , Anaerobiosis , Membranas Artificiales , Metales Pesados , Nitrógeno/análisis , Fósforo/análisis , Proyectos Piloto , Aguas del Alcantarillado/análisis , Aguas Residuales
7.
Acupunct Med ; 33(5): 400-5, 2015 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-26104377

RESUMEN

OBJECTIVE: To investigate the analgesic and anti-inflammatory effects of transcutaneous electrical nerve stimulation (TENS) at local or distant acupuncture points in a rat model of the third lumbar vertebrae transverse process syndrome. METHODS: Forty Sprague-Dawley rats were randomly divided into control, model, model plus local acupuncture point stimulation at BL23 (model+LAS) and model plus distant acupuncture point stimulation at ST36 (model+DAS) groups. All rats except controls underwent surgical third lumbar vertebrae transverse process syndrome modelling on day 2. Thereafter, rats in the model+LAS and model+DAS groups were treated daily with TENS for a total of six treatments (2/100 Hz, 30 min/day) from day 16 to day 29. Thermal pain thresholds were measured once a week during treatment and were continued until day 57, when local muscle tissue was sampled for RT-PCR and histopathological examination after haematoxylin and eosin staining. mRNA expression of interleukin-1 ß (IL-1ß), tumour necrosis factor-α (TNF-α) and inducible nitric oxide synthase (iNOS) was determined. RESULTS: Thermal pain thresholds of all model rats decreased relative to the control group. Both LAS and DAS significantly increased the thermal pain threshold at all but one point during the treatment period. Histopathological assessment revealed that the local muscle tissues around the third lumbar vertebrae transverse process recovered to some degree in both the model+LAS and model+DAS groups; however, LAS appeared to have a greater effect. mRNA expression of IL-1ß, TNF-α and iNOS in the local muscle tissues was increased after modelling and attenuated in both model+LAS and model+DAS groups. The beneficial effect was greater after LAS than after DAS. CONCLUSIONS: TENS at both local (BL23) and distant (ST36) acupuncture points had a pain-relieving effect in rats with the third lumbar vertebrae transverse process syndrome, and LAS appeared to have greater anti-inflammatory and analgesic effects than DAS. TRIAL REGISTRATION NUMBER: 09073.


Asunto(s)
Dolor de la Región Lumbar/terapia , Vértebras Lumbares/lesiones , Fracturas de la Columna Vertebral/terapia , Estimulación Eléctrica Transcutánea del Nervio , Animales , Modelos Animales de Enfermedad , Masculino , Umbral del Dolor , Ratas , Ratas Sprague-Dawley , Fracturas de la Columna Vertebral/patología
8.
PLoS One ; 9(8): e104016, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25089831

RESUMEN

Great controversy exists regarding the biologic responses of osteoblasts to X-ray irradiation, and the mechanisms are poorly understood. In this study, the biological effects of low-dose radiation on stimulating osteoblast proliferation, differentiation and fracture healing were identified using in vitro cell culture and in vivo animal studies. First, low-dose (0.5 Gy) X-ray irradiation induced the cell viability and proliferation of MC3T3-E1 cells. However, high-dose (5 Gy) X-ray irradiation inhibited the viability and proliferation of osteoblasts. In addition, dynamic variations in osteoblast differentiation markers, including type I collagen, alkaline phosphatase, Runx2, Osterix and osteocalcin, were observed after both low-dose and high-dose irradiation by Western blot analysis. Second, fracture healing was evaluated via histology and gene expression after single-dose X-ray irradiation, and low-dose X-ray irradiation accelerates fracture healing of closed femoral fractures in rats. In low-dose X-ray irradiated fractures, an increase in proliferating cell nuclear antigen (PCNA)-positive cells, cartilage formation and fracture calluses was observed. In addition, we observed more rapid completion of endochondral and intramembranous ossification, which was accompanied by altered expression of genes involved in bone remodeling and fracture callus mineralization. Although the expression level of several osteoblast differentiation genes was increased in the fracture calluses of high-dose irradiated rats, the callus formation and fracture union were delayed compared with the control and low-dose irradiated fractures. These results reveal beneficial effects of low-dose irradiation, including the stimulation of osteoblast proliferation, differentiation and fracture healing, and highlight its potential translational application in novel therapies against bone-related diseases.


Asunto(s)
Regeneración Ósea/efectos de la radiación , Fracturas del Fémur/radioterapia , Fémur/efectos de la radiación , Curación de Fractura/efectos de la radiación , Fosfatasa Alcalina/genética , Fosfatasa Alcalina/metabolismo , Animales , Biomarcadores/metabolismo , Regeneración Ósea/fisiología , Diferenciación Celular/efectos de la radiación , Línea Celular , Proliferación Celular/efectos de la radiación , Supervivencia Celular/efectos de la radiación , Colágeno Tipo I/genética , Colágeno Tipo I/metabolismo , Subunidad alfa 1 del Factor de Unión al Sitio Principal/genética , Subunidad alfa 1 del Factor de Unión al Sitio Principal/metabolismo , Relación Dosis-Respuesta en la Radiación , Fracturas del Fémur/genética , Fracturas del Fémur/metabolismo , Fracturas del Fémur/patología , Fémur/lesiones , Fémur/metabolismo , Curación de Fractura/fisiología , Expresión Génica , Masculino , Ratones , Osteoblastos/citología , Osteoblastos/fisiología , Osteoblastos/efectos de la radiación , Osteocalcina/genética , Osteocalcina/metabolismo , Antígeno Nuclear de Célula en Proliferación/genética , Antígeno Nuclear de Célula en Proliferación/metabolismo , Ratas , Ratas Sprague-Dawley , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Rayos X
9.
J Asian Nat Prod Res ; 12(4): 265-72, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20419536

RESUMEN

Transplantation of olfactory ensheathing cells (OECs) is currently considered to be one of the most promising repair strategies for human spinal cord injury. However, the factors that regulate OECs are still poorly understood. Ginsenoside Rg1 (Rg1), the phytosterol from Panax ginseng, is a potent neuroprotective agent that promotes axonal regeneration. The aim of this study is to determine whether Rg1 would influence the biological activity of OECs. Primary cultured OECs from the olfactory bulb of neonatal rats were treated with Rg1 of various concentrations and durations. Using MTT and bromodeoxyuridine assays, we found that Rg1 significantly promoted cell proliferation, with an optimal concentration of 40 mug/ml of Rg1 at 72 h. In addition, RT-PCR and ELISA assays showed that Rg1 could upregulate the mRNA expression and secretion of glial cell-derived neurotrophic factor, brain-derived neurotrophic factor, and nerve growth factor. These results suggest that Rg1 may have a great potential in OEC therapy.


Asunto(s)
Ginsenósidos/farmacología , Factores de Crecimiento Nervioso/efectos de los fármacos , Regeneración Nerviosa/efectos de los fármacos , Fármacos Neuroprotectores/farmacología , Vías Olfatorias/citología , Vías Olfatorias/efectos de los fármacos , Panax/química , Traumatismos de la Médula Espinal/terapia , Animales , Secuencia de Bases , Factor Neurotrófico Derivado del Encéfalo/efectos de los fármacos , Factor Neurotrófico Derivado del Encéfalo/metabolismo , Ginsenósidos/química , Ginsenósidos/aislamiento & purificación , Estructura Molecular , Factores de Crecimiento Nervioso/metabolismo , Fármacos Neuroprotectores/química , Fármacos Neuroprotectores/aislamiento & purificación , Ratas
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