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1.
Eur Arch Otorhinolaryngol ; 278(8): 2745-2752, 2021 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32892305

RESUMEN

PURPOSE: To improve the efficacy of music therapy on tinnitus relief, specific music that was not repetitively played and satisfies individualized preference was developed. The aim of this study was to investigate effects of combination of the specific music and educational counseling on tinnitus relief in short term. METHODS: Sixty patients suffering from chronic tinnitus were included. The non-randomized controlled study was designed with two intervention groups: educational counseling (EC, which included a 1-h individualized instruction) and preferred music therapy [PMT, which included EC plus 15, 30-min preferred music sessions (PMS)]. Three assessments-the Chinese-Mandarin version of Tinnitus Handicap Inventory (THI-CM), Tinnitus Evaluation Questionnaire (TEQ), and Visual Analogue Scale (VAS) were administered before and 1, 2, 3 weeks after initiation of treatment to evaluate the efficacy. RESULTS: Twenty-six patients in PMT group attained a clinically meaningful improvement in THI compared to 15 in the EC group, though both groups achieved a statistically relevant reduction in the 3 assessments. CONCLUSION: The PMT had a positive impact on chronic tinnitus and related distress in a short term. It outperformed the separate EC, which is an appropriate treatment option in clinic. Therefore, it presents a possible complement to the therapeutic spectrum in chronic tinnitus. TRIAL REGISTRATION: Chinese Clinical Trial Registry, ChiCTR1900022624. Registered on 19 April 2019.


Asunto(s)
Musicoterapia , Música , Acúfeno , Consejo , Humanos , Encuestas y Cuestionarios , Acúfeno/terapia , Resultado del Tratamiento
2.
Nat Commun ; 11(1): 4457, 2020 09 08.
Artículo en Inglés | MEDLINE | ID: mdl-32901017

RESUMEN

Innate lymphoid cells (ILCs) and CD4+ T cells produce IL-22, which is critical for intestinal immunity. The microbiota is central to IL-22 production in the intestines; however, the factors that regulate IL-22 production by CD4+ T cells and ILCs are not clear. Here, we show that microbiota-derived short-chain fatty acids (SCFAs) promote IL-22 production by CD4+ T cells and ILCs through G-protein receptor 41 (GPR41) and inhibiting histone deacetylase (HDAC). SCFAs upregulate IL-22 production by promoting aryl hydrocarbon receptor (AhR) and hypoxia-inducible factor 1α (HIF1α) expression, which are differentially regulated by mTOR and Stat3. HIF1α binds directly to the Il22 promoter, and SCFAs increase HIF1α binding to the Il22 promoter through histone modification. SCFA supplementation enhances IL-22 production, which protects intestines from inflammation. SCFAs promote human CD4+ T cell IL-22 production. These findings establish the roles of SCFAs in inducing IL-22 production in CD4+ T cells and ILCs to maintain intestinal homeostasis.


Asunto(s)
Ácidos Grasos Volátiles/inmunología , Microbioma Gastrointestinal/inmunología , Inmunidad Innata , Interleucinas/biosíntesis , Animales , Butiratos/inmunología , Butiratos/metabolismo , Butiratos/farmacología , Linfocitos T CD4-Positivos/efectos de los fármacos , Linfocitos T CD4-Positivos/inmunología , Linfocitos T CD4-Positivos/microbiología , Citrobacter rodentium , Colitis/inmunología , Colitis/microbiología , Colitis/prevención & control , Infecciones por Enterobacteriaceae/inmunología , Infecciones por Enterobacteriaceae/microbiología , Infecciones por Enterobacteriaceae/prevención & control , Ácidos Grasos Volátiles/metabolismo , Ácidos Grasos Volátiles/farmacología , Microbioma Gastrointestinal/fisiología , Inhibidores de Histona Desacetilasas/farmacología , Humanos , Subunidad alfa del Factor 1 Inducible por Hipoxia/metabolismo , Técnicas In Vitro , Interleucinas/deficiencia , Interleucinas/genética , Linfocitos/efectos de los fármacos , Linfocitos/inmunología , Linfocitos/microbiología , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Ratones Transgénicos , Regiones Promotoras Genéticas , Receptores de Hidrocarburo de Aril/metabolismo , Receptores Acoplados a Proteínas G/metabolismo , Interleucina-22
3.
Chin J Integr Med ; 23(8): 617-624, 2017 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-25967608

RESUMEN

OBJECTIVE: To elucidate the mechanism of Chinese tuina in treating sciatic nerve crush injury, and to detect the levels of tissue plasminogen activator (tPA) and plasminogen activator inhibitor-1 (PAI-1), which is thought to play an important role in nerve regeneration. METHODS: Thirty-two adult male Sprague-Dawley rats were subjected to sciatic nerve crush injury and 16 rats (sham-operated group) went through a sham operation. Control group was given no treatment while tuina group received tuina therapy since day 7 post-surgery. Tuina treatment was performed once a day and lasted for 20 days. The sciatic functional index was examined every 5 days during the treatment session. The rats' gastrocnemius muscles were evaluated for changes in mass and immunohistochemistry techniques were performed to detect the levels of tPA and PAI-1. RESULTS: Tuina therapy improved the motor function of sciatic nerve injured rats (P<0.05), however, it did not increase muscle volume (P<0.05). Tuina downregulated the levels of tPA and PAI-1 (P<0.05). CONCLUSIONS: The present study implies that tuina treatment could accelerate rehabilitation of peripheral nerve injury.


Asunto(s)
Regulación hacia Abajo , Medicina Tradicional China , Nervio Ciático/lesiones , Nervio Ciático/patología , Activador de Tejido Plasminógeno/metabolismo , Animales , Masculino , Músculos/patología , Compresión Nerviosa , Tamaño de los Órganos , Inhibidor 1 de Activador Plasminogénico/metabolismo , Ratas Sprague-Dawley
4.
Chin J Integr Med ; 23(12): 908-915, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-27145942

RESUMEN

OBJECTIVE: To explore the protective effects of Tibetan medicine Zuo-Mu-A Decoction (, ZMAD) on the blood parameters and myocardium of high altitude polycythemia (HAPC) model rats. METHODS: Forty male Wistar rats were randomly divided into 4 groups by a random number table, including the normal, model, Rhodiola rosea L. (RRL) and ZMAD groups (10 in each group). Every group was raised in Lhasa to create a HAPC model except the normal group. After modeling, rats in the RRL and the ZMAD groups were administered intragastrically with RRL (20 mL/kg) and ZMAD (7.5 mL/kg) once a day for 2 months, respectively; for the normal and the model groups, 5 mL of distilled water was administered intragastrically instead of decoction. Then routine blood and hematologic rheology parameters were taken, levels of erythropoietin and 8-hydroxy-2'-deoxyguanosine (8-OHdG) were tested, and ultrastructural change in the left ventricular myocardium was observed using transmission electron microscopy. RESULTS: Compared with the model group, ZMAD significantly reduced the red blood cell count, hemoglobin levels, whole blood viscosity at low/middle shear rates, plasma viscosity, erythrocyte electrophoretic time, erythropoietin and 8-OHdG levels, and also increased the erythrocyte deformation index (P<0.05). There was no difference in all results between the RRL and the ZMAD groups. The cardiac muscle fibers were well-protected, mitochondrial matrix swelled mildly and ultrastructure changes were less prominent in the ZMAD group compared with the model group. CONCLUSION: ZMAD has significant protective effects on the blood parameters against HAPC, and also has the beneficial effect in protecting against myocardial injury.


Asunto(s)
Mal de Altura/sangre , Mal de Altura/tratamiento farmacológico , Medicina Tradicional Tibetana , Miocardio/patología , Policitemia/sangre , Policitemia/tratamiento farmacológico , Sustancias Protectoras/uso terapéutico , 8-Hidroxi-2'-Desoxicoguanosina , Mal de Altura/complicaciones , Animales , Desoxiguanosina/análogos & derivados , Desoxiguanosina/sangre , Modelos Animales de Enfermedad , Eritropoyetina/sangre , Miocardio/ultraestructura , Policitemia/complicaciones , Sustancias Protectoras/farmacología , Reología/efectos de los fármacos
5.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi ; 31(4): 888-93, 2014 Aug.
Artículo en Chino | MEDLINE | ID: mdl-25464808

RESUMEN

Tinnitus is a subjective sensation of sound without external stimulation. It has become ubiquitous and has therefore aroused much attention in recent years. According to the survey, ameliorating tinnitus based on special music and reducing pressure have good effects on the treatment of it. Meantime, vicious cycle chains between tinnitus and bad feelings have been broken. However, tinnitus therapy has been restricted by using looping music. Therefore, a method of generating fractal tones based on musical instrument digital interface (MIDI) technology and pink noise has been proposed in this paper. The experimental results showed that the fractal fragments were self-similar, incompletely reduplicate, and no sudden changes in pitches and would have a referential significance for tinnitus therapy.


Asunto(s)
Estimulación Acústica , Fractales , Acúfeno/rehabilitación , Humanos , Música , Ruido
6.
Sci Signal ; 4(165): mr4, 2011 Mar 22.
Artículo en Inglés | MEDLINE | ID: mdl-21427407

RESUMEN

Substantial advances in our understanding of the developmental and functional relationship between regulatory T cells (T(regs)) and T helper 17 (T(H)17) cells and their potential clinical applications have been made. In response to these breakthroughs, the second international conference entitled "China Tregs/Th17 2010 Shanghai Conference," held in Shanghai, China, was dedicated to this topic. Various types of T(regs) and T(H)17 cells, as well as their relevant cytokines, were discussed. Here, we summarize some of the findings shared at the conference, specifically focusing on the biology of T(H)17 cells, including interleukin-17 (IL-17)-producing innate cells, T(regs), and the factors that control the critical balance between T(regs) and cells of the T(H)17 lineage.


Asunto(s)
Transducción de Señal/inmunología , Linfocitos T Reguladores/inmunología , Células Th17/inmunología , Diferenciación Celular/inmunología , Humanos , Interleucina-17/inmunología , Interleucina-17/metabolismo , Modelos Inmunológicos , Linfocitos T Reguladores/metabolismo , Células Th17/metabolismo , Yin-Yang
7.
PLoS One ; 3(12): e4009, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-19104661

RESUMEN

The Kv1.3 potassium channel plays an essential role in effector memory T cells and has been implicated in several important autoimmune diseases including multiple sclerosis, psoriasis and type 1 diabetes. A number of potent small molecule inhibitors of Kv1.3 channel have been reported, some of which were found to be effective in various animal models of autoimmune diseases. We report herein the identification of clofazimine, a known anti-mycobacterial drug, as a novel inhibitor of human Kv1.3. Clofazimine was initially identified as an inhibitor of intracellular T cell receptor-mediated signaling leading to the transcriptional activation of human interleukin-2 gene in T cells from a screen of the Johns Hopkins Drug Library. A systematic mechanistic deconvolution revealed that clofazimine selectively blocked the Kv1.3 channel activity, perturbing the oscillation frequency of the calcium-release activated calcium channel, which in turn led to the inhibition of the calcineurin-NFAT signaling pathway. These effects of clofazimine provide the first line of experimental evidence in support of a causal relationship between Kv1.3 and calcium oscillation in human T cells. Furthermore, clofazimine was found to be effective in blocking human T cell-mediated skin graft rejection in an animal model in vivo. Together, these results suggest that clofazimine is a promising immunomodulatory drug candidate for treating a variety of autoimmune disorders.


Asunto(s)
Señalización del Calcio/efectos de los fármacos , Clofazimina/farmacología , Canal de Potasio Kv1.3/antagonistas & inhibidores , Linfocitos T/efectos de los fármacos , Animales , Antibacterianos/metabolismo , Antibacterianos/farmacología , Señalización del Calcio/inmunología , Células Cultivadas , Clofazimina/metabolismo , Evaluación Preclínica de Medicamentos , Humanos , Factores Inmunológicos/metabolismo , Factores Inmunológicos/farmacología , Interleucina-2/metabolismo , Células Jurkat , Canal de Potasio Kv1.3/genética , Canal de Potasio Kv1.3/metabolismo , Ratones , Modelos Biológicos , Factores de Transcripción NFATC/metabolismo , Unión Proteica , Multimerización de Proteína/efectos de los fármacos , Trasplante de Piel/inmunología , Linfocitos T/metabolismo , Transfección
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