Abstract
Aquatic animals often exhibit glucose intolerance following a glucose load, and understanding the mechanisms of glucose uptake is crucial for elucidating the underlying processes. Sodium-dependent glucose transporter 1 (SGLT1) plays a crucial role in the process of intestinal glucose absorption and transport in vertebrates, but there is limited information about its function in crustaceans. This study identified the SGLT1 gene (named MrSGLT1) from Macrobrachium rosenbergii. The full cDNA sequence is 3764bp, encoding 903 amino acids. Unlike SGLT1 in most teleost fish, which have 14 transmembrane domains, MrSGLT1 protein has only 12. MrSGLT1 was predominantly expressed in the intestine, with its expression increasing after feeding. This was accompanied by elevated levels of glucose and trehalose in the hemolymph, and increased glycogen levels in the hepatopancreas. Silencing MrSGLT1 in vivo resulted in decreased glucose and trehalose levels in the hemolymph and reduced glycogen levels in the hepatopancreas, although muscle glycogen levels were unaffected. Moreover, knockdown of MrSGLT1 led to increased expression of genes involved in glycogenolysis and decreased expression of genes associated with glycogenesis, inhibiting postprandial glycogen accumulation in the hepatopancreas. Feeding-induced glycolysis was also inhibited following MrSGLT1 silencing, while no significant changes were observed in gluconeogenesis-related genes. These findings highlight the critical role of MrSGLT1 in regulating postprandial glucose homeostasis in crustaceans.
Published Version
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