Cited by 25Genetic Neurodegenerative DiseasesRegulation of Appetite and ObesityAmyotrophic Lateral Sclerosis Research

Dual Therapy with Liraglutide and Ghrelin Promotes Brain and Peripheral Energy Metabolism in the R6/2 Mouse Model of Huntington’s Disease

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Duarte, Ana I., Sjögren, Marie, Santos, Maria S., Oliveira, Catarina R., Moreira, Paula I., Björkqvist, Maria·2018·Scientific Reports

Abstract

Neuronal loss alongside altered energy metabolism, are key features of Huntington’s disease (HD) pathology. The orexigenic gut-peptide hormone ghrelin is known to stimulate appetite and affect whole body energy metabolism. Liraglutide is an efficient anti-type 2 diabetes incretin drug, with neuroprotective effects alongside anorectic properties. Combining liraglutide with the orexigenic peptide ghrelin may potentially promote brain/cognitive function in HD. The R6/2 mouse model of HD exhibits progressive central pathology, weight loss, deranged glucose metabolism, skeletal muscle atrophy and altered body composition. In this study, we targeted energy metabolism in R6/2 mice using a co-administration of liraglutide and ghrelin. We investigated their effect on brain cortical hormone-mediated intracellular signalling pathways, metabolic and apoptotic markers, and the impact on motor function in HD. We here demonstrate that liraglutide, alone or together with ghrelin (subcutaneous daily injections of 150 µg/kg (ghrelin) and 0.2 mg/kg (liraglutide), for 2 weeks), normalized glucose homeostatic features in the R6/2 mouse, without substantially affecting body weight or body composition. Liraglutide alone decreased brain cortical active GLP-1 and IGF-1 levels in R6/2 mice, alongside higher ADP levels. Liraglutide plus ghrelin decreased brain insulin, lactate, AMP and cholesterol levels in R6/2 mice. Taken together, our findings encourage further studies targeting energy metabolism in HD.

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References 68 · Cited by 25

Authors
Duarte, A. I., Sjögren, M., Santos, M. S., Oliveira, C. R., Moreira, P. I., & Björkqvist, M.
Affiliations
  • Lund University (SE)
  • Centro de Neurociências e Biologia Celular (PT)
Corresponding author
Duarte, Ana I.
Venue
Scientific Reports
Published
2018-06-12
Volume
8
Issue
1
Pages
8961-8961
ISSN
2045-2322 (ISSN-L)
OpenAlex
W2805622227
Cited by
25
References
68
Citations by year
2026: 1 · 2025: 3 · 2024: 1 · 2023: 3 · 2022: 5 · 2021: 3 · 2020: 5 · 2019: 3 · 2018: 1
FWCI
1.37
Type
journal article
Language
en
Open access
Locations
  • Scientific Reports (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, other-oa)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
  • Lund University Publications (Lund University) (submittedVersion)
Funders
  • European Huntington's Disease Network
  • Vetenskapsrådet
  • Fundação para a Ciência e a Tecnologia (COMPETE, SFRH/BPD/84473/2012, PTDC/SAU-TOX/117481/2010, COMPETE_2020)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Genetic Neurodegenerative Diseases
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
  • Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
Keywords
Huntington's disease, liraglutide, ghrelin, dual therapy, brain energy metabolism, glucose homeostasis, R6/2 mouse model, glucagon-like peptide-1, insulin-like growth factor I, insulin, AMP, lactate, apoptosis, motor function, neuroprotection, skeletal muscle atrophy, body composition
MeSH terms
Liraglutide, Animals, Brain, Disease Models, Animal, Drug Therapy, Combination, Energy Metabolism, Humans, Huntington Disease, Male, Mice, Transgenic, Mice, Ghrelin

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