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Medicinas Complementárias
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1.
Ecotoxicol Environ Saf ; 263: 115289, 2023 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-37499391

RESUMEN

BACKGROUND: Epidemiological studies about the effect of essential metal mixture on fasting plasma glucose (FPG) levels among elderly people are sparse. The object of this study was to examine the associations of single essential metals and essential metal mixture with FPG levels in Chinese community-dwelling elderly people. METHODS: The study recruited 2348 community-dwelling elderly people in total. Inductively coupled plasma-mass spectrometry was adopted to detect the levels of vanadium (V), selenium (Se), magnesium (Mg), cobalt (Co), calcium (Ca), and molybdenum (Mo) in urine. The relationships between single essential metals and essential metal mixture and FPG levels were evaluated by linear regression and Bayesian kernel machine regression (BKMR) models, respectively. RESULTS: In multiple-metal linear regression models, urine V and Mg were negatively related to the FPG levels (ß = - 0.016, 95 % CI: - 0.030 to - 0.003 for V; ß = - 0.021, 95 % CI: - 0.033 to - 0.009 for Mg), and urine Se was positively related to the FPG levels (ß = 0.024, 95 % CI: 0.014-0.034). In BKMR model, the significant relationships of Se and Mg with the FPG levels were also found. The essential metal mixture was negatively associated with FPG levels in a dose-response pattern, and Mg had the maximum posterior inclusion probability (PIP) value (PIP = 1.0000), followed by Se (PIP = 0.9968). Besides, Co showed a significant association with decreased FPG levels in older adults without hyperlipemia and in women. CONCLUSIONS: Both Mg and Se were associated with FPG levels, individually and as a mixture. The essential metal mixture displayed a linear dose-response relationship with reduced FPG levels, with Mg having the largest contribution to FPG levels, followed by Se. Further prospective investigations are necessary to validate these exploratory findings.


Asunto(s)
Glucemia , Ayuno , Metales , Selenio , Anciano , Femenino , Humanos , Teorema de Bayes , Glucemia/análisis , Cobalto/orina , Pueblos del Este de Asia , Ayuno/sangre , Ayuno/orina , Vida Independiente , Selenio/orina , Vanadio/orina , Espectrometría de Masas , Calcio/orina , Magnesio/orina , Molibdeno/orina , Metales/orina , Mezclas Complejas/orina
2.
PLoS One ; 9(6): e100129, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24941000

RESUMEN

Boswellic acid (BA)-containing extracts such as BSE have anti-inflammatory and immunomodulatory activity. In chronic schistosomiasis, the hepatic granuloma and fibrosis induced by egg deposition in the liver is the most serious pathological manifestations. However, little is known regarding the role of BAs in Schistosoma japonicum (S. japonicum) egg-induced liver granuloma and fibrosis. In order to investigate the effect of a water-soluble complex preparation of BSE, BSE-CD, on S. japonicum egg-induced liver pathology, liver granuloma and fibrosis were induced by infecting C57BL/6 mice with 18-22 cercariae of S. japonicum. S. japonicum cercariae infected mice were injected with BSE-CD at the onset of egg granuloma formation (early phase BSE-CD treatment after 4 weeks infection) or after the formation of liver fibrosis (late phase BSE-CD treatment after 7 weeks infection). Our data show that treatment of infected mice with BSE-CD significantly reduced both the extent of hepatic granuloma and fibrosis. Consistent with an inhibition of NF-κB signaling as evidenced by reduced IκB kinase (IKK) activation, the mRNA expression of VEGF (vascular endothelial growth factor, VEGF), TNF-α (tumor necrosis factor-alpha TNF-α) and MCP-1 (monocyte chemotactic protein 1, MCP-1) was decreased. Moreover, immunohistochemical analysis (IHC) revealed that the content of α-SMA in liver tissue of BSE-CD treated mice was dramatically decreased. Our findings suggest that BSE-CD treatment attenuates S. japonicum egg-induced hepatic granulomas and fibrosis, at least partly due to reduced NF-κB signaling and the subsequently decreased expression of VEGF, TNF-α, and MCP-1. Suppression of the activation of hepatic stellate cells (HSC) may also be involved in the therapeutic efficacy of BSE-CD.


Asunto(s)
Antihelmínticos/farmacología , Granuloma/tratamiento farmacológico , Cirrosis Hepática/tratamiento farmacológico , FN-kappa B/antagonistas & inhibidores , Extractos Vegetales/farmacología , Esquistosomiasis Japónica/tratamiento farmacológico , Triterpenos/farmacología , Actinas/genética , Actinas/metabolismo , Animales , Antihelmínticos/química , Cercarias/efectos de los fármacos , Cercarias/fisiología , Quimiocina CCL2/genética , Quimiocina CCL2/metabolismo , Regulación de la Expresión Génica , Granuloma/genética , Granuloma/parasitología , Granuloma/patología , Células Estrelladas Hepáticas/efectos de los fármacos , Células Estrelladas Hepáticas/metabolismo , Células Estrelladas Hepáticas/parasitología , Hígado/efectos de los fármacos , Hígado/metabolismo , Hígado/parasitología , Cirrosis Hepática/genética , Cirrosis Hepática/parasitología , Cirrosis Hepática/patología , Masculino , Ratones , Ratones Endogámicos C57BL , FN-kappa B/genética , FN-kappa B/metabolismo , Recuento de Huevos de Parásitos , Extractos Vegetales/química , Schistosoma japonicum/efectos de los fármacos , Schistosoma japonicum/fisiología , Esquistosomiasis Japónica/genética , Esquistosomiasis Japónica/parasitología , Esquistosomiasis Japónica/patología , Transducción de Señal , Factor de Necrosis Tumoral alfa/genética , Factor de Necrosis Tumoral alfa/metabolismo , Factor A de Crecimiento Endotelial Vascular/genética , Factor A de Crecimiento Endotelial Vascular/metabolismo
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