Article (Scientific journals)
Neprilysin deficiency reduces hepatic gluconeogenesis in high fat-fed mice.
Esser, Nathalie; Mongovin, Stephen M; Mundinger, Thomas O et al.
2023In Peptides, 168, p. 171076
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Keywords :
Cholecystokinin; Glucagon-like peptide-1; Gluconeogenesis; Glycogenolysis; Liver; Neprilysin; Cellular and Molecular Neuroscience; Endocrinology; Physiology; Biochemistry
Abstract :
[en] Neprilysin is a peptidase that cleaves glucoregulatory peptides, including glucagon-like peptide-1 (GLP-1) and cholecystokinin (CCK). Some studies suggest that its inhibition in diabetes and/or obesity improves glycemia, and that this is associated with enhanced insulin secretion, glucose tolerance and insulin sensitivity. Whether reduced neprilysin activity also improves hepatic glucose metabolism has not been explored. We sought to determine whether genetic deletion of neprilysin suppresses hepatic glucose production (HGP) in high fat-fed mice. Nep+/+ and Nep-/- mice were fed high fat diet for 16 weeks, and then underwent a pyruvate tolerance test (PTT) to assess hepatic gluconeogenesis. Since glycogen breakdown in liver can also yield glucose, we assessed liver glycogen content in fasted and fed mice. In Nep-/- mice, glucose excursion during the PTT was reduced when compared to Nep+/+ mice. Further, liver glycogen levels were significantly greater in fasted but not fed Nep-/- versus Nep+/+ mice. Since gut-derived factors modulate HGP, we tested whether gut-selective inhibition of neprilysin could recapitulate the suppression of hepatic gluconeogenesis observed with whole-body inhibition, and this was indeed the case. Finally, the gut-derived neprilysin substrates, GLP-1 and CCK, are well-known to suppress HGP. Having previously demonstrated elevated plasma GLP-1 levels in Nep-/- mice, we now measured plasma CCK bioactivity and reveal an increase in Nep-/- versus Nep+/+ mice, suggesting GLP-1 and/or CCK may play a role in reducing HGP under conditions of neprilysin deficiency. In sum, neprilysin modulates hepatic gluconeogenesis and strategies to inhibit its activity may reduce HGP in type 2 diabetes and obesity.
Disciplines :
Endocrinology, metabolism & nutrition
Author, co-author :
Esser, Nathalie  ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques ; Centre Hospitalier Universitaire de Liège - CHU > > Service de diabétologie, nutrition, maladies métaboliques ; Veterans Affairs Puget Sound Health Care System, Seattle, WA, United States, Division of Metabolism, Endocrinology and Nutrition, Department of Medicine, University of Washington, Seattle, WA, United States
Mongovin, Stephen M;  Veterans Affairs Puget Sound Health Care System, Seattle, WA, United States
Mundinger, Thomas O;  Division of Metabolism, Endocrinology and Nutrition, Department of Medicine, University of Washington, Seattle, WA, United States
Barrow, Breanne M;  Veterans Affairs Puget Sound Health Care System, Seattle, WA, United States
Zraika, Sakeneh ;  Veterans Affairs Puget Sound Health Care System, Seattle, WA, United States, Division of Metabolism, Endocrinology and Nutrition, Department of Medicine, University of Washington, Seattle, WA, United States
Language :
English
Title :
Neprilysin deficiency reduces hepatic gluconeogenesis in high fat-fed mice.
Publication date :
10 August 2023
Journal title :
Peptides
ISSN :
0196-9781
eISSN :
1873-5169
Publisher :
Elsevier BV, United States
Volume :
168
Pages :
171076
Peer reviewed :
Peer Reviewed verified by ORBi
Funders :
NIH - National Institutes of Health
Available on ORBi :
since 29 August 2023

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