斑马鱼
乳酸脱氢酶A
乳酸
碳水化合物代谢
糖酵解
丙酮酸脱氢酶复合物
乳酸脱氢酶
生物化学
果糖
化学
生物
药理学
新陈代谢
酶
基因
细菌
遗传学
作者
Hyo Hee Kim,Bipin Vaidya,Se‐Young Cho,Joseph Sang‐Il Kwon,Duwoon Kim
标识
DOI:10.1016/j.jff.2022.105098
摘要
The anti-hyperglycemic activity of alginate oligosaccharide (AOS) and its mechanism were elucidated in a hyperglycemic zebrafish model. The model was prepared by inducing high glucose in zebrafish for the study. AOS treatment significantly reduced blood glucose level and delayed mortality in hyperglycemic zebrafish. To explain the anti-hyperglycemic mechanism of AOS, a comparative proteomic analysis was performed in three groups (control, hyperglycemic, AOS-treated hyperglycemic) of zebrafish. Among 639 identified proteins, 72 proteins modulated by AOS treatment were classified into key biofunctional categories, including energy metabolism and survival. Ingenuity pathway analysis predicted that AOS treatment inhibits lactic acid production by suppressing hypoxia inducible factor 1 subunit a (HIF1A) via modulating insulin receptor (INSR), sirtuin 1 (SIRT1) and lactate dehydrogenase A (LDHA); and induces glucose oxidation by enhancing pyruvate dehydrogenase 1 (PDHA1) via decreasing pyruvate dehydrogenase kinase isoform 2 (PDK2). Subsequently, RT-qPCR analysis verified the reduction of hif1a, pdk2 and ldha gene expression, and the elevation of insr and sirt1 expression by AOS treatment in hyperglycemic zebrafish. In conclusion, AOS could be an alternative therapeutic agent to ameliorate hyperglycemia by stimulating glucose oxidation and suppressing lactic acid pathway.
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