Effects of Liraglutide and Fenretinide treatments on the diabetic phenotype of neuronal human BACE1 knock-in mice

Dekeryte Dekeryte, Claire Hull, Kaja Plucińska, Shakil Khan, Sarah Kamli-Salino, Nimesh Mody, Nicola Morrice, Christopher McLaughlin, Victor A Gault, Bettina Platt, Mirela Delibegovic

Research output: Contribution to journalArticle

Abstract

We recently reported that brain-specific human β-secretase 1 (BACE1) knock-in (PLB4), a mouse model of sporadic Alzheimer's disease (AD), also develops a severe diabetic phenotype characterised by impaired glucose homeostasis, decreased insulin sensitivity and a fatty liver phenotype. Hence, we here aimed to assess if targeted anti-diabetic therapies (Liraglutide and Fenretinide) would attenuate the diabetic and behavioural phenotype of these mice. PLB4 mice and wild-type (WT) controls were administered Liraglutide or Fenretinide for ten consecutive weeks alongside vehicle-treated mice. Physiological (body weight and mass composition, glucose tolerance, serum hormone concentration), behavioural (locomotor activity) and molecular assessments were performed in mice pre- and post-treatment. Liraglutide and Fenretinide treatments inhibited adiposity gain and decreased circulating serum triglyceride (with Liraglutide) and leptin (with Fenretinide) levels in PLB4 mice. We also found that PLB4 mice exhibited increased levels of serum dipeptidyl peptidase 4 (DPP4), together with up-regulated hepatic expression of Dpp4, retinol binding protein 4 (Rbp4) and sterol regulatory element-binding 1c (Srebp1c), which was normalised by both treatments. Interestingly, Liraglutide treatment slowed down habituation to a novel environment and increased secondary night activity peak in WT mice, suggesting an impact on circadian activity regulation. However, neither treatment improved glucose homeostasis in PLB4 mice, implying that impaired glucose metabolism in this genotype may not be associated with glucagon like peptide 1 (GLP-1) and/or RBP4-mediated pathways. In summary, this study provides new insights into molecular mechanisms underlying neuronal BACE1-mediated metabolic regulation and implicates BACE1 as a putative regulator of systemic DPP4 levels.

LanguageEnglish
Pages222-230
Number of pages9
JournalBIiochemical Pharmacology
Volume166
Early online date16 May 2019
DOIs
Publication statusPublished - 1 Aug 2019

Fingerprint

Fenretinide
Phenotype
Dipeptidyl Peptidase 4
Glucose
Retinol-Binding Proteins
Amyloid Precursor Protein Secretases
Glucagon-Like Peptide 1
Sterols
Leptin
Metabolism
Liver
Homeostasis
Brain
Serum
Triglycerides
Liraglutide
Hormones
Insulin
Adiposity
Fatty Liver

Keywords

  • BACE1
  • Type 2 diabetes
  • DPP-4
  • liraglutide
  • insulin resistance
  • DPP4
  • Insulin resistance
  • Liraglutide

Cite this

Dekeryte, D., Hull, C., Plucińska, K., Khan, S., Kamli-Salino, S., Mody, N., ... Delibegovic, M. (2019). Effects of Liraglutide and Fenretinide treatments on the diabetic phenotype of neuronal human BACE1 knock-in mice. 166, 222-230. https://doi.org/10.1016/j.bcp.2019.05.020
Dekeryte, Dekeryte ; Hull, Claire ; Plucińska, Kaja ; Khan, Shakil ; Kamli-Salino, Sarah ; Mody, Nimesh ; Morrice, Nicola ; McLaughlin, Christopher ; Gault, Victor A ; Platt, Bettina ; Delibegovic, Mirela . / Effects of Liraglutide and Fenretinide treatments on the diabetic phenotype of neuronal human BACE1 knock-in mice. 2019 ; Vol. 166. pp. 222-230.
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Dekeryte, D, Hull, C, Plucińska, K, Khan, S, Kamli-Salino, S, Mody, N, Morrice, N, McLaughlin, C, Gault, VA, Platt, B & Delibegovic, M 2019, 'Effects of Liraglutide and Fenretinide treatments on the diabetic phenotype of neuronal human BACE1 knock-in mice', vol. 166, pp. 222-230. https://doi.org/10.1016/j.bcp.2019.05.020

Effects of Liraglutide and Fenretinide treatments on the diabetic phenotype of neuronal human BACE1 knock-in mice. / Dekeryte, Dekeryte; Hull, Claire; Plucińska, Kaja; Khan, Shakil; Kamli-Salino, Sarah; Mody, Nimesh; Morrice, Nicola; McLaughlin, Christopher; Gault, Victor A; Platt, Bettina; Delibegovic, Mirela .

Vol. 166, 01.08.2019, p. 222-230.

Research output: Contribution to journalArticle

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AU - Dekeryte, Dekeryte

AU - Hull, Claire

AU - Plucińska, Kaja

AU - Khan, Shakil

AU - Kamli-Salino, Sarah

AU - Mody, Nimesh

AU - Morrice, Nicola

AU - McLaughlin, Christopher

AU - Gault, Victor A

AU - Platt, Bettina

AU - Delibegovic, Mirela

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