P75 neurotrophin receptor as a therapeutic target for drug development to treat neurological diseases.
Liu-Lin XiongLi ChenIsaac Bul DengXin-Fu ZhouTing-Hua WangPublished in: The European journal of neuroscience (2022)
The interaction of neurotrophins with their receptors is involved in the pathogenesis and progression of various neurological diseases, including Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, spinal cord injury and acute and chronic cerebral damage. The p75 neurotrophin receptor (p75NTR) plays a pivotal role in the development of neurological dysfunctions as a result of its high expression, abnormal processing and signalling. Therefore, p75NTR represents as a vital therapeutic target for the treatment of neurodegeneration, neuropsychiatric disorders and cerebrovascular insufficiency. This review summarizes the current research progress on the p75NTR signalling in neurological deficits. We also summarize the present therapeutic approaches by genetically and pharmacologically targeting p75NTR for the attenuation of pathological changes. Based on the evolving knowledge, the role of p75NTR in the regulation of tau hyperphosphorylation, Aβ metabolism, the degeneration of motor neurons and dopaminergic neurons has been discussed. Its position as a biomarker to evaluate the severity of diseases and as a druggable target for drug development has also been elucidated. Several prototype small molecule compounds were introduced to be crucial in neuronal survival and functional recovery via targeting p75NTR. These small molecule compounds represent desirable agents in attenuating neurodegeneration and cell death as they abolish activation-induced neurotoxicity of neurotrophins via modulating p75NTR signalling. More comprehensive and in-depth investigations on p75NTR-based drug development are required to shed light on effective treatment of numerous neurological disorders.
Keyphrases
- small molecule
- cell death
- spinal cord injury
- cerebral ischemia
- amyotrophic lateral sclerosis
- spinal cord
- poor prognosis
- drug induced
- traumatic brain injury
- subarachnoid hemorrhage
- liver failure
- cognitive decline
- protein protein
- brain injury
- high glucose
- respiratory failure
- drug delivery
- diabetic rats
- acute respiratory distress syndrome
- mechanical ventilation