Dual Therapy with Liraglutide and Ghrelin Promotes Brain and Peripheral Energy Metabolism in the R6/2 Mouse Model of Huntington’s Disease
Open accessAbstract
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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The neuroprotective effect of GLP-1 is effective in AD and PD, and also in other NDD such as HD, ALS, and MS.
“The neuroprotective effect of GLP-1 is not only effective in AD and PD, but also in other NDD such as HD (Duarte et al. 2018), ALS (Li et al. 2012), and MS (DellaValle et al. 2016).”
From Therapeutic effect of GLP-1 engineered strain on mice model of Alzheimer’s disease and Parkinson’s disease (2020) · cites this paper as Duarte et al. 2018
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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.
- ORCID
- Venue
- Scientific Reports
- Published
- 2018-06-12
- Volume
- 8
- Issue
- 1
- Pages
- 8961-8961
- ISSN
- 2045-2322 (ISSN-L)
- PMC
- PMC5997749
- 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
- gold
- doi.org
- 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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