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1.
Nutrients ; 12(2)2020 Jan 26.
Artículo en Inglés | MEDLINE | ID: mdl-31991895

RESUMEN

Ginger (Zingiber officinale Roscoe) and its active compounds (gingerols, shogaols and paradols) have been reported as having beneficial functions for several diseases, including diabetes. In this study, we revealed that the steaming process could enhance the anti-diabetic potential of ginger. To confirm the anti-diabetic effect of steamed ginger extract (GG03), we assessed pancreatic islets impaired by alloxan in zebrafish and demonstrated anti-hyperglycemic efficacy in a mouse model. The EC50 values of ginger extract (GE) and GG03 showed that the efficacy of GG03 was greater than that of GE. In addition, LC50 values demonstrated that GG03 had lower toxicity than GE, and the comparison of the Therapeutic Index (TI) proved that GG03 is a safer functional food. Furthermore, our data showed that GG03 significantly lowered hyperglycemia in a diabetic mouse model. HPLC was performed to confirm the change in the composition of steamed ginger. Interestingly, GG03 showed a 375% increase in 1-dehydro-6-gingerdione (GD) compared with GE. GD has not yet been studied much pharmacologically. Thus, we identified the protective effects of GD in the damaged pancreatic islets of diabetic zebrafish. We further assessed whether the anti-diabetic mechanism of action of GG03 and GD involves insulin secretion. Our results suggest that GG03 and GD might stimulate insulin secretion by the closure of KATP channels in pancreatic ß-cells.


Asunto(s)
Diabetes Mellitus Experimental/tratamiento farmacológico , Alcoholes Grasos/farmacología , Guayacol/análogos & derivados , Hipoglucemiantes/farmacología , Células Secretoras de Insulina/efectos de los fármacos , Insulina/metabolismo , Canales KATP/antagonistas & inhibidores , Extractos Vegetales/farmacología , Zingiber officinale , Animales , Glucemia/efectos de los fármacos , Glucemia/metabolismo , Diabetes Mellitus Experimental/metabolismo , Diabetes Mellitus Experimental/patología , Alcoholes Grasos/aislamiento & purificación , Alcoholes Grasos/toxicidad , Zingiber officinale/química , Zingiber officinale/toxicidad , Guayacol/aislamiento & purificación , Guayacol/farmacología , Guayacol/toxicidad , Hipoglucemiantes/aislamiento & purificación , Hipoglucemiantes/toxicidad , Células Secretoras de Insulina/metabolismo , Células Secretoras de Insulina/patología , Canales KATP/metabolismo , Masculino , Ratones Endogámicos ICR , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/toxicidad , Raíces de Plantas , Bloqueadores de los Canales de Potasio/farmacología , Secretagogos/farmacología , Transducción de Señal , Vapor , Pez Cebra
2.
Nutrients ; 11(1)2019 Jan 08.
Artículo en Inglés | MEDLINE | ID: mdl-30626089

RESUMEN

Sensorineural hearing loss (SNHL) is one of the most common causes of disability, affecting over 466 million people worldwide. However, prevention or therapy of SNHL has not been widely studied. Avocado oil has shown many health benefits but it has not yet been studied in regards to SNHL. Therefore, we aimed to investigate the efficacy of avocado oil on SNHL in vitro and in vivo and elucidate its mode of action. For the present study, we used enhanced functional avocado oil extract (DKB122). DKB122 led to recovery of otic hair cells in zebrafish after neomycin-induced otic cell damage. Also, DKB122 improved auditory sensory transmission function in a mouse model of noise induced-hearing loss and protected sensory hair cells in the cochlea. In addition, RNA sequencing was performed to elucidate the mechanism involved. KEGG pathway enrichment analysis of differentially expressed genes showed that DKB122 protected House Ear Institute-Organ of Corti 1 (HEI-OC1) cells against neomycin-related alterations in gene expression due to oxidative stress, cytokine production and protein synthesis.


Asunto(s)
Aminoácidos/biosíntesis , Regulación de la Expresión Génica/efectos de los fármacos , Células Ciliadas Auditivas/efectos de los fármacos , Pérdida Auditiva Sensorineural , Persea/química , Fitoterapia , Aceites de Plantas/farmacología , Animales , Percepción Auditiva/efectos de los fármacos , Cóclea/citología , Cóclea/efectos de los fármacos , Cóclea/metabolismo , Células Ciliadas Auditivas/metabolismo , Células Ciliadas Auditivas/fisiología , Pérdida Auditiva Provocada por Ruido/tratamiento farmacológico , Pérdida Auditiva Provocada por Ruido/genética , Pérdida Auditiva Provocada por Ruido/metabolismo , Pérdida Auditiva Provocada por Ruido/fisiopatología , Pérdida Auditiva Sensorineural/tratamiento farmacológico , Pérdida Auditiva Sensorineural/genética , Pérdida Auditiva Sensorineural/metabolismo , Pérdida Auditiva Sensorineural/fisiopatología , Redes y Vías Metabólicas/efectos de los fármacos , Redes y Vías Metabólicas/genética , Ratones , Extractos Vegetales/farmacología , Extractos Vegetales/uso terapéutico , Aceites de Plantas/uso terapéutico , Análisis de Secuencia de ARN , Pez Cebra
3.
Eur J Nutr ; 55(3): 1011-20, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25939797

RESUMEN

PURPOSE: There is limited evidence whether environmental exposure to perfluorinated compounds (PFCs) affects insulin resistance (IR) and whether vitamin C intake protects against the adverse effect of PFCs. This study was carried out to investigate the effect of PFCs on IR through oxidative stress, and the effects of a 4-week consumption of vitamin C supplement compared placebo on development of IR by PFCs. METHODS: For a double-blind, community-based, randomized, placebo-controlled crossover intervention of vitamin C, we assigned 141 elderly subjects to both vitamin C and placebo treatments for 4 weeks. We measured serum levels of PFCs to estimate PFC exposures and urinary levels of malondialdehyde (MDA) and 8-hydroxy-2'-deoxyguanosine (8-OHdG) for oxidative stress. We also measured levels of fasting glucose and insulin and derived the homeostatic model assessment (HOMA) index to assess IR. RESULTS: Perfluorooctane sulfonate (PFOS) and perfluorododecanoic acid (PFDoDA) levels were found to be positively associated with HOMA index at the baseline and after placebo treatment. Risks of IR for the top decile of PFOS and PFDoDA exposures were significantly elevated compared with those with lower PFOS and PFDoDA exposures (both, P < 0.0001). However, the effects of PFOS and PFDoDA on HOMA disappeared after vitamin C supplementation (both, P > 0.30). Furthermore, PFOS and PFDoDA levels were also significantly associated with MDA and 8-OHdG levels, and MDA levels were positively associated with HOMA index. CONCLUSION: PFOS and PFDoDA exposures were positively associated with IR and oxidative stress, and vitamin C supplementation protected against the adverse effects of PFOS and PFDoDA on IR.


Asunto(s)
Ácido Ascórbico/administración & dosificación , Caprilatos/toxicidad , Fluorocarburos/toxicidad , Resistencia a la Insulina , 8-Hidroxi-2'-Desoxicoguanosina , Anciano , Anciano de 80 o más Años , Pueblo Asiatico , Biomarcadores/orina , Glucemia/metabolismo , Cotinina/orina , Creatinina/orina , Estudios Cruzados , Desoxiguanosina/análogos & derivados , Desoxiguanosina/orina , Suplementos Dietéticos , Método Doble Ciego , Humanos , Insulina/sangre , Malondialdehído/orina , Persona de Mediana Edad , Estrés Oxidativo/efectos de los fármacos , República de Corea
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