Literature DB >> 6998514

Fetal metabolic response to phloridzin-induced hypoglycemia in pregnant rats.

N Freund, A Kervran, R Assan, J P Geloso, J Girard.   

Abstract

Phloridzin, an inhibitor of renal sugar transport, produces an important loss of glucose in urine of treated animals. In order to reduce severely the maternal glucose supply to the fetuses in short-term experiments, we have combined phloridzin administration to pregnant rats with 18 h starvation. Fetuses from starved phloridzin-treated mothers were compared with fetuses from starved mothers. Combined treatment markedly decreases fetal blood glucose concentration (-36%) and fetal liver glycogen stores (-76%). These changes are associated with a decrease in plasma insulin (-25%), a rise in plasma glucagon (+120%) and a marked increase of hepatic PEPCK activity (+400%). It appears from these results that phloridzin treatment for a short duration is able to induce glycogenolysis and the premature appearance of PEPCK in the liver of rat fetuses.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 6998514     DOI: 10.1159/000241382

Source DB:  PubMed          Journal:  Biol Neonate        ISSN: 0006-3126


  2 in total

1.  Chronic late-gestation hypoglycemia upregulates hepatic PEPCK associated with increased PGC1alpha mRNA and phosphorylated CREB in fetal sheep.

Authors:  Paul J Rozance; Sean W Limesand; James S Barry; Laura D Brown; Stephanie R Thorn; Dan LoTurco; Timothy R H Regnault; Jacob E Friedman; William W Hay
Journal:  Am J Physiol Endocrinol Metab       Date:  2007-12-04       Impact factor: 4.310

2.  Late gestation fetal hyperglucagonaemia impairs placental function and results in diminished fetal protein accretion and decreased fetal growth.

Authors:  Sarah N Cilvik; Stephanie R Wesolowski; Russ V Anthony; Laura D Brown; Paul J Rozance
Journal:  J Physiol       Date:  2021-05-10       Impact factor: 6.228

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.