Literature DB >> 21697637

Rapid rehydration and moderate plasma glucose elevation by fluid containing enzymatically synthesized glycogen.

Kei Inagaki1, Kengo Ishihara, Mariko Ishida, Ai Watanabe, Mika Fujiwara, Yuko Komatsu, Mika Shirai, Yoshiho Kato, Ami Takanezawa, Takashi Furuyashiki, Hiroki Takata, Yousuke Seyama.   

Abstract

Enzymatically synthesized glycogen (ESG) has high solubility and its solution has low osmotic pressure. Therefore ESG solution could be rapidly absorbed and could be adequate for water rehydration and carbohydrate supplementation during exercise. The object of this study was to evaluate the gastric emptying time and plasma glucose elevation after an administration of ESG solution in comparison with another carbohydrate solution by using a laboratory animal. Male BALB/c mice were administered 10% w/v solution of glucose, maltodextrin, starch, naturally synthesized glycogen (NSG) and ESG at a dose of 20 µL/g body weight for the measurement of gastric emptying rate (Experiment 1) and 10 µL/g body weight for the measurement of plasma glucose elevation (Experiment 2). The osmolarity of gastric content was lower in the ESG and maltodextrin group than the other carbohydrate group. Weight of gastric fluid was significantly lower in the ESG and water group than the glucose group (p<0.01). Plasma glucose level was significantly lower in the ESG group than the glucose group from 0 to 60 min after administration (p<0.01), whereas plasma glucose level was same from 60 to 120 min for the ESG and glucose group (p=0.948). In Experiment 3, BALB/c mice ran on a treadmill for 2 h and were administered 8% of ESG or glucose solution (1.75, 3.5 or 7.0 µL/g body weight) every 20 min during running. There was no difference in post-exercise muscle glycogen level. These data suggest that 1) ESG beverage does not disturb water absorption because of its short gastric emptying time and 2) ESG slowly elevates plasma glucose level and maintains it for a prolonged time compared to the glucose solution.

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Year:  2011        PMID: 21697637     DOI: 10.3177/jnsv.57.170

Source DB:  PubMed          Journal:  J Nutr Sci Vitaminol (Tokyo)        ISSN: 0301-4800            Impact factor:   2.000


  1 in total

1.  Cannabidiol and Cannabidiol Metabolites: Pharmacokinetics, Interaction with Food, and Influence on Liver Function.

Authors:  Kieran Shay Struebin Abbotts; Taylor Russell Ewell; Hannah Michelle Butterklee; Matthew Charles Bomar; Natalie Akagi; Gregory P Dooley; Christopher Bell
Journal:  Nutrients       Date:  2022-05-21       Impact factor: 6.706

  1 in total

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