Protective properties of GLP-1 and associated peptide hormones in neurodegenerative disorders.
Christian HolscherPublished in: British journal of pharmacology (2021)
Type 2 diabetes mellitus and the associated desensitisation of insulin signalling has been identified as a risk factor for progressive neurodegenerative disorders such as Alzheimer's disease, Parkinson's disease and others. Glucagon-like peptide 1 (GLP-1) is a hormone that has growth factor-like and neuroprotective properties. Several clinical trials have been conducted, testing GLP-1 receptor agonists in patients with Alzheimer's disease, Parkinson's disease or diabetes-induced memory impairments. The trials showed clear improvements in Alzheimer's disease, Parkinson's disease and diabetic patients. Glucose-dependent insulinotropic polypeptide/gastric inhibitory peptide (GIP) is the 'sister' incretin hormone of GLP-1. GIP analogues have shown neuroprotective effects in animal models of disease and can improve on the effects of GLP-1. Novel dual GLP-1/GIP receptor agonists have been developed that can enter the brain at an enhanced rate. The improved neuroprotective effects of these drugs suggest that they are superior to single GLP-1 receptor agonists and could provide disease-modifying care for Alzheimer's disease and Parkinson's disease patients.
Keyphrases
- clinical trial
- type diabetes
- growth factor
- healthcare
- multiple sclerosis
- cardiovascular disease
- adipose tissue
- ejection fraction
- glycemic control
- chronic kidney disease
- newly diagnosed
- end stage renal disease
- palliative care
- cognitive decline
- working memory
- brain injury
- insulin resistance
- patient reported outcomes
- molecular dynamics simulations
- prognostic factors
- subarachnoid hemorrhage
- stress induced