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Steamed Ginger May Enhance Insulin Secretion through K(ATP) Channel Closure in Pancreatic β-Cells Potentially by Increasing 1-Dehydro-6-Gingerdione Content

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 con...

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Detalles Bibliográficos
Autores principales: Nam, Youn Hee, Hong, Bin Na, Rodriguez, Isabel, Park, Min Seon, Jeong, Seo Yule, Lee, Yeong-Geun, Shim, Ji Heon, Yasmin, Tamanna, Kim, Na Woo, Koo, Young Tae, Lee, Sang Hun, Paik, Dong-Hyun, Jeong, Yong Joon, Jeon, Hyelin, Kang, Se Chan, Baek, Nam-In, Kang, Tong Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7071297/
https://www.ncbi.nlm.nih.gov/pubmed/31991895
http://dx.doi.org/10.3390/nu12020324
Descripción
Sumario: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 EC(50) values of ginger extract (GE) and GG03 showed that the efficacy of GG03 was greater than that of GE. In addition, LC(50) 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 K(ATP) channels in pancreatic β-cells.