NPFFR2-deficient mice fed a high-fat diet develop strong intolerance to glucose

0573381 - ÚOCHB 2024 RIV GB eng J - Journal Article
Karnošová, Alena - Strnadová, Veronika - Železná, Blanka - Kuneš, Jaroslav - Kašpárek, Petr - Maletínská, Lenka
NPFFR2-deficient mice fed a high-fat diet develop strong intolerance to glucose.
Clinical science. Roč. 137, č. 10 (2023), s. 847-862. ISSN 0143-5221. E-ISSN 1470-8736
R&D Projects: GA ČR(CZ) GA21-03691S; GA MŠMT(CZ) LX22NPO5104; GA MŠMT ED2.1.00/19.0395; GA MŠMT(CZ) ED1.1.00/02.0109; GA MŠMT(CZ) LM2018126
Institutional support: RVO:61388963 ; RVO:68378050
Keywords : glucose intolerance * high-fat diet * insulin resistance * knockout mice * neuropeptide FF
OECD category: Physiology (including cytology); Biochemistry and molecular biology (UMG-J)
Impact factor: 6, year: 2022
Method of publishing: Open access
https://doi.org/10.1042/CS20220880

A previous study on neuropeptide FF receptor 2 (NPFFR2)-deficient mice has demonstrated that NPFFR2 is involved in the control of energy balance and thermogenesis. Here, we report on the metabolic impact of NPFFR2 deficiency in male and female mice that were fed either a standard diet (STD) or a high-fat diet (HFD) and each experimental group consisted of ten individuals. Both male and female NPFFR2 knockout (KO) mice exhibited severe glucose intolerance that was exacerbated by a HFD diet. In addition, reduced insulin pathway signaling proteins in NPFFR2 KO mice fed a HFD resulted in the development of hypothalamic insulin resistance. HFD feeding did not cause liver steatosis in NPFFR2 KO mice of either sex, but NPFFR2 KO male mice fed a HFD had lower body weights, white adipose tissues, and liver and lower plasma leptin levels compared with their wild-type (WT) controls. Lower liver weight in NPFFR2 KO male mice compensated for HFD-induced metabolic stress by increased liver PPARα and plasma FGF21 hepatokine, which supported fatty acid β-oxidation in the liver and white adipose tissue. Conversely, NPFFR2 deletion in female mice attenuated the expression of Adra3β and Pparγ, which inhibited lipolysis in adipose tissue.
Permanent Link: https://hdl.handle.net/11104/0343845