GDNF, NGF and BDNF as Therapeutic Options for Neurodegeneration
Abstract
Glial cell-derived neurotrophic factor (GDNF), and the neurotrophin nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) are important for the survival, maintenance and regeneration of specific neuronal populations in the adult brain. Depletion of these neurotrophic factors has been linked with disease pathology and symptoms, and replacement strategies are considered as potential therapeutics for neurodegenerative diseases such as Parkinson's, Alzheimer's and Huntington's diseases. GDNF administration has recently been shown to be an effective treatment for Parkinson's disease, with clinical trials currently in progress. Trials with NGF for Alzheimer's disease are ongoing, with some degree of success. Preclinical results using BDNF also show much promise, although there are accompanying difficulties. Ultimately, the administration of a therapy involving proteins in the brain has inherent problems. Because of the blood-brain-barrier, the protein must be infused directly, produced by viral constructs, secreted from implanted protein-secreting cells or actively transported across the brain. An alternative to this is the use of a small molecule agonist, a modulator or enhancer targeting the associated receptors. We evaluate these neurotrophic factors as potential short or long-term treatments, weighing up preclinical and clinical results with the possible effects on the underlying neurodegenerative process.
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Neurotrophic factors BDNF and GDNF protect dopaminergic neurons in PD mice by preventing neuronal death.
“Neurotrophic factors, such as BDNF and GDNF, have been shown to protect dopaminergic neurons in PD mice by preventing neuronal death [31,32].”
From Neuroprotective Effects of Bifidobacterium breve CCFM1067 in MPTP-Induced Mouse Models of Parkinson’s Disease (2022) · cites this paper as [32]
Neurodegenerative and neuropsychiatric diseases may be partially caused by defects in synaptic plasticity associated with insufficient neuronal supply of BDNF and other neurotrophic factors.
“Furthermore, it was shown that neurodegenerative and neuropsychiatric diseases may be partially caused by defects in synaptic plasticity associated with the insufficient neuronal supply of BDNF and other neurotrophic factors [11,12,13].”
From BDNF as a Promising Therapeutic Agent in Parkinson’s Disease (2020) · cites this paper as [13]
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- Authors
- Allen, S. J., Watson, J. J., Shoemark, D. K., Barua, N. U., & Patel, N. K.
- Affiliations
- Frenchay Hospital (GB)
- Corresponding author
- Allen, Shelley J.
- Venue
- Pharmacology & Therapeutics
- Publisher
- Elsevier BV
- Published
- 2013-05
- Volume
- 138
- Issue
- 2
- Pages
- 155-175
- ISSN
- 0163-7258 (ISSN-L)
- OpenAlex
- W2006376003
- Cited by
- 820
- References
- 256
- Citations by year
- 2026: 42 · 2025: 68 · 2024: 80 · 2023: 74 · 2022: 64 · 2021: 68 · 2020: 49 · 2019: 56 · 2018: 66 · 2017: 53 · 2016: 71 · 2015: 48 · 2014: 63 · 2013: 17
- FWCI
- 6.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Pharmacology & Therapeutics (publishedVersion)
- PubMed (publishedVersion)
- Explore Bristol Research (submittedVersion)
- Bristol Research (University of Bristol) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Keywords
- glial cell line-derived neurotrophic factor, nerve growth factor, brain-derived neurotrophic factor, neurotrophic factors, neurodegenerative diseases, Parkinson's disease, Alzheimer's disease, Huntington's disease, blood-brain barrier, viral gene therapy, small molecule agonists, neurotrophin receptors
- MeSH terms
- Animals, Humans, Ligands, Models, Molecular, Nerve Growth Factors, Brain-Derived Neurotrophic Factor, Neurodegenerative Diseases, Glial Cell Line-Derived Neurotrophic Factor
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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