Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Molecules ; 28(13)2023 Jul 07.
Artículo en Inglés | MEDLINE | ID: mdl-37446928

RESUMEN

Formononetin (FNT) is a plant-derived isoflavone natural product with anti-inflammatory, antioxidant, and anti-allergic properties. We showed previously that FNT inhibits immunoglobulin E (IgE)-dependent mast cell (MC) activation, but the effect of FNT on IgE-independent MC activation is yet unknown. Our aim was to investigate the effects and possible mechanisms of action of FNT on IgE-independent MC activation and pseudoallergic inflammation. We studied the effects of FNT on MC degranulation in vitro with a cell culture model using compound C48/80 to stimulate either mouse bone marrow-derived mast cells (BMMCs) or RBL-2H3 cells. We subsequently measured ß-hexosaminase and histamine release, the expression of inflammatory factors, cell morphological changes, and changes in NF-κB signaling. We also studied the effects of FNT in several in vivo murine models of allergic reaction: C48/80-mediated passive cutaneous anaphylaxis (PCA), active systemic anaphylaxis (ASA), and 2,4-dinitrobenzene (DNCB)-induced atopic dermatitis (AD). The results showed that FNT inhibited IgE-independent degranulation of MCs, evaluated by a decrease in the release of ß-hexosaminase and histamine and a decreased expression of inflammatory factors. Additionally, FNT reduced cytomorphological elongation and F-actin reorganization and attenuated NF-κB p65 phosphorylation and NF-κB-dependent promoter activity. Moreover, the administration of FNT alleviated pseudoallergic responses in vivo in mouse models of C48/80-stimulated PCA and ASA, and DNCB-induced AD. In conclusion, we suggest that FNT may be a novel anti-allergic drug with great potential to alleviate pseudoallergic responses via the inhibition of IgE-independent MC degranulation and NF-κB signaling.


Asunto(s)
Anafilaxia , Antialérgicos , Isoflavonas , Ratones , Animales , Mastocitos , p-Metoxi-N-metilfenetilamina/farmacología , FN-kappa B/metabolismo , Degranulación de la Célula , Dinitroclorobenceno/metabolismo , Anafilaxia/tratamiento farmacológico , Isoflavonas/metabolismo , Inmunoglobulina E/metabolismo , Antialérgicos/uso terapéutico
2.
Zhongguo Zhong Yao Za Zhi ; 44(11): 2379-2389, 2019 Jun.
Artículo en Chino | MEDLINE | ID: mdl-31359667

RESUMEN

To evaluate the efficiency and safety between Wenxin Granule and antiarrhythmic drugs in the treatment of atrial fibrillation(AF). A total of 8 major electronic databases(CNKI, WanFang, VIP, CBM, Cochrane Library, Web of Science, PubMed, EMbase) were retrieved since the establishment of the database to January 10, 2019. Two reviewers extracted data, and assessed the methodological quality of the included studies. The Meta-analysis was made by RevMan 5.3 software. Finally, 42 studies involving 4 657 patients were included. The results of Meta-analysis showed that compared with antiarrhythmic drug, the combined administration with Wenxin Granule and antiarrhythmic drug had a better clinical efficiency(OR=3.37, 95%CI[2.69,4.22],I~2=0%,P<0.000 01)and efficacy on cardioversion(OR=2.32,95%CI[1.67,3.22],I~2=0%,P<0.000 01), with reduction in P_d(MD=-5.48,95%CI [-7.32,-3.64],I~2=0%,P<0.000 01)and P_(max)(MD=-9.91,95%CI[-12.86,-6.95],I~2=0%,P<0.000 01). The comparison between the combined application with Wenxin Granule and the single application of amiodarone showed a clinical efficiency(OR=2.89,95%CI[1.96,4.26],I~2=44%,P<0.000 01),and efficacy on sinus rhythm maintenance(OR=2.58,95%CI[1.82,3.66],I~2=3%,P<0.000 01). The comparison between the combined application with Wenxin Granule and the single application of amiodarone showed a clinical efficiency(OR=0.88,95%CI[0.53,1.46],I~2=0%,P=0.63). The combined treatment with Wenxin Granule has a better clinical efficiency in AF better than amiodarone, with no evidence for more benefits from the single administration with Wenxin Granules.


Asunto(s)
Antiarrítmicos/farmacología , Fibrilación Atrial/tratamiento farmacológico , Medicamentos Herbarios Chinos/farmacología , Terapia Combinada , Cardioversión Eléctrica , Humanos
3.
J Nanosci Nanotechnol ; 19(2): 1130-1132, 2019 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-30360216

RESUMEN

The SrAl2B2O7:1%Eu3+ phosphors were obtained by solid-state reaction. Photoluminescence (PL) spectra are characterized the property of samples, and under the excitation of 394 nm, the sharp emission lines of SrAl2B2O7:1%Eu3+ can be assigned to Judd-Ofelt transitions (5D0-7FJ) of Eu3+, which are 5D0-7F1, 5D0-7F2, 5D0-7F3, and 5D0-7F4. The bond energy method is used to determine the site occupancy, and the occupancy of Eu3+ can be determined by comparing the deviation of its bond energy in different locations at Sr2+, Al3+ and B3+ sites. Theoretical calculation result indicates that Eu3+ would preferentially occupy the smaller energy variation sites Sr2+.

4.
J Nanosci Nanotechnol ; 19(2): 1145-1147, 2019 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-30360220

RESUMEN

The low concentration of Eu3+ doped Sr2CeO4 phosphors has been widely studied in recent years and in this paper, we researched the properties of high concentration Eu3+ doped in Sr2CeO4. The Sr2Ce(1-x)Eu4-x/2 (x = 0, 1%, 10%, 20%) phosphors were obtained by traditional solid-state reaction. Photoluminescence (PL) spectra are characterized the property of samples. PL spectra illustrate that the concentration of Eu3+ increased, the intensity of 5D0-7F1, 5D0-7F2 increased and intensity of Sr2CeO4 host emission intensity was decreased. The phenomenon can be ascribed to the energy transfer from Ce4+ to Eu3+. When the concentration of Eu3+ is 20%, the completely red emission can be obtained even if no other ions are doped under the excitation wavelength of 350 nm, it is proved that Eu3+ occupied Ce sites rather than Sr site in Sr2CeO4 samples. The conclusion we make is due to the value of |ΔEEuCe-O| and |ΔEEuSr-O| calculated by bond-energy method, the smaller the value, the easier it is for the doped ions Eu3+ to enter the site.

5.
Ying Yong Sheng Tai Xue Bao ; 27(2): 629-33, 2016 Feb.
Artículo en Chino | MEDLINE | ID: mdl-27396139

RESUMEN

In order to investigate the adaption of Locusta migratoria tibetensis to the. environment, this paper adopted the experiments with full light exposure (24L/OD), total. darkness (OL/24D), and low temperature (5 °C) to study the effects of low temperature and illumination stress on the cold-resistant substances of L. migratoria tibetensis. The results showed that the fat content of L. migratoria tibetensis reached 11.8%, which was the highest under the condition of full light exposure (24L/OD) without low temperature stress. The fat content of body in low temperature and darkness treatment (OL/24D) was 4.7%, which was the lowest. The trehalose, mannitol and sorbitol contents of locust after low temperature stress were significantly higher than that of locust without the same stress. Glycogen content of locust treated by full light exposure without low temperature 'stress was the highest (6.40 mg . g-1). Besides, low temperature and darkness treatment stimulated the accumulation of alanine, glutamic acid, lysine, and phenylalanine, benefiting the accumulation of multi-amino acids, glycerinum, micro-molecule carbohydrate, and the reduction of glycogen and fat content.


Asunto(s)
Frío , Locusta migratoria/química , Fotoperiodo , Estrés Fisiológico , Aclimatación , Aminoácidos/análisis , Animales , Carbohidratos/análisis , Glucógeno/análisis , Luz
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...