| Literature DB >> 27785616 |
Jana Semakova1, Petra Hyroššová1, Andrés Méndez-Lucas1, Ernest Cutz2, Jordi Bermudez1, Shawn Burgess3, Soledad Alcántara4, José C Perales5,6.
Abstract
Whole body cytosolic phosphoenolpyruvate carboxykinase knockout (PEPCK-C KO) mice die early after birth with profound hypoglycemia therefore masking the role of PEPCK-C in adult, non-gluconeogenic tissues where it is expressed. To investigate whether PEPCK-C deletion in the liver was critically responsible for the hypoglycemic phenotype, we reexpress this enzyme in the liver of PEPCK-C KO pups by early postnatal administration of PEPCK-C-expressing adenovirus. This maneuver was sufficient to partially rescue hypoglycemia and allow the pups to survive and identifies the liver as a critical organ, and hypoglycemia as the critical pathomechanism, leading to early postnatal death in the whole-body PEPCK-C knockout mice. Pathology assessment of survivors also suggest a possible role for PEPCK-C in lung maturation and muscle metabolism.Entities:
Keywords: Gluconeogenesis; Hepatic lipidosis; KO; Liver; Neonatal hypoglycemia; PEPCK
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Year: 2016 PMID: 27785616 DOI: 10.1007/s13105-016-0528-y
Source DB: PubMed Journal: J Physiol Biochem ISSN: 1138-7548 Impact factor: 4.158