The type 2 diabetes drug liraglutide reduces chronic inflammation induced by irradiation in the mouse brain
Abstract
Chronic inflammation in the brain is found in a range of neurodegenerative diseases such as Parkinson's or Alzheimer's disease. We have recently shown that analogues of the glucagon-like polypeptide 1 (GLP-1) such as liraglutide have potent neuroprotective properties in a mouse model of Alzheimer's disease. We also found a reduction of activated microglia in the brain. This finding suggests that GLP-1 analogues such as liraglutide have anti-inflammatory properties. To further characterise this property, we tested the effects of liraglutide on the chronic inflammation response induced by exposure of the brain to 6 Gy (X-ray). Animals were injected i.p. with 25 nmol/kg once daily for 30 days. Brains were analysed for cytokine levels, activated microglia and astrocyte levels, and nitrite levels as a measure for nitric oxide production and protein expression of iNOS. Exposure of the brain to 6 Gy induced a pronounced chronic inflammation response in the brain. The activated microglia load in the cortex and dentate gyrus region of hippocampus (P<0.001), and the activated astrocyte load in the cortex (P<0.01) was reduced by liraglutide. Furthermore, the pro-inflammatory cytokine levels of IL-6 (P<0.01), IL-12p70 (P<0.01), IL-1β (P<0.05), and total nitrite concentration were reduced in the brains of animals treated with liraglutide. The results demonstrate that liraglutide is effective in reducing a number of parameters linked to the chronic inflammation response. Liraglutide or similar GLP-1 analogues may be a suitable treatment for reducing the chronic inflammatory response in the brain found in several neurodegenerative conditions.
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GLP-1-based therapies show anti-inflammatory effects on the liver, vascular system including aorta and vein endothelial cells, brain, kidney, lung, testis, and skin by reducing the production of inflammatory cytokines and infiltration of immune cells in the tissues.
“emerging data suggest that GLP-1-based therapies also showed anti-inflammatory effects on the liver, vascular system including aorta and vein endothelial cells, brain, kidney, lung, testis, and skin by reducing the production of inflammatory cytokines and infiltration of immune cells in the tissues [17, 21–25].”
From Anti-Inflammatory Effects of GLP-1-Based Therapies beyond Glucose Control (2016) · cites this paper as [24]
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References 56 · Cited by 119
- Authors
- Parthsarathy, V., & Hölscher, C.
- Affiliations
- University of Ulster (GB)
- Corresponding author
- Hölscher, Christian
- Venue
- European Journal of Pharmacology
- Publisher
- Elsevier BV
- Published
- 2013-01
- Volume
- 700
- Issue
- 1-3
- Pages
- 42-50
- ISSN
- 0014-2999 (ISSN-L)
- OpenAlex
- W2026462831
- Cited by
- 119
- References
- 56
- Citations by year
- 2026: 3 · 2025: 11 · 2024: 10 · 2023: 9 · 2022: 12 · 2021: 6 · 2020: 7 · 2019: 9 · 2018: 10 · 2017: 11 · 2016: 9 · 2015: 9 · 2014: 7 · 2013: 6
- FWCI
- 3.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Pharmacology (publishedVersion)
- PubMed (publishedVersion)
- University of Derby Online Research Archive. (University of Derby) (submittedVersion)
- Lancaster EPrints (Lancaster University) (submittedVersion)
- Funders
- Alzheimer Research UK charity Trust
- Vice Chancellor Research Studentship
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- liraglutide, GLP-1 analogues, neuroinflammation, brain irradiation, microglial activation, astrocyte activation, inflammatory cytokines, nitric oxide, inducible nitric oxide synthase, neuroprotection, neurodegenerative diseases, Alzheimer's disease
- MeSH terms
- Liraglutide, Animals, Anti-Inflammatory Agents, Astrocytes, Body Weight, Brain, Diabetes Mellitus, Type 2, Eating, Inflammation, Male, Mice, Inbred C57BL, Nitrites, Radiation Injuries, Experimental, Cytokines, Microglia, Mice, Glucagon-Like Peptide 1, Nitric Oxide Synthase Type II
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