
pmid: 37606719
pmc: PMC10791998
AbstractParkinson’s disease (PD) is a neurodegenerative disease due to the degeneration of dopaminergic neurons (DNs) in the substantia nigra (SN). The liver X receptor (LXR) is involved in different neurodegenerative diseases. Therefore, the objective of the present review was to clarify the possible role of LXR in PD neuropathology. LXRs are the most common nuclear receptors of transcription factors that regulate cholesterol metabolism and have pleiotropic effects, including anti-inflammatory effects and reducing intracellular cholesterol accumulation. LXRs are highly expressed in the adult brain and act as endogenous sensors for intracellular cholesterol. LXRs have neuroprotective effects against the development of neuroinflammation in different neurodegenerative diseases by inhibiting the expression of pro-inflammatory cytokines. LXRs play an essential role in mitigating PD neuropathology by reducing the expression of inflammatory signaling pathways, neuroinflammation, oxidative stress, mitochondrial dysfunction, and enhancement of BDNF signaling.In conclusion, LXRs, through regulating brain cholesterol homeostasis, may be effectual in PD. Also, inhibition of node-like receptor pyrin 3 (NLRP3) inflammasome and nuclear factor kappa B (NF-κB) by LXRs could effectively prevent neuroinflammation in PD. Taken together, LXRs play a crucial role in PD neuropathology by inhibiting neuroinflammation and associated degeneration of DNs.
Physiology, Dopaminergic, Dopamine, Peroxisome Proliferator-Activated Receptors, Nuclear Receptors, Immunology, Biochemistry, Gene, Article, Inflammasome, Neuroinflammation, lipid, Biochemistry, Genetics and Molecular Biology, Health Sciences, Substantia nigra, Liver X receptor ; Article ; Dopaminergic Neurons/metabolism [MeSH] ; Brain/metabolism [MeSH] ; Liver X Receptors/metabolism [MeSH] ; Humans [MeSH] ; Neurodegenerative Diseases/metabolism [MeSH] ; Neurodegenerative diseases ; Cholesterol/metabolism [MeSH] ; Parkinson Disease/pathology [MeSH] ; Neuroinflammatory Diseases [MeSH] ; Parkinson’s disease, Humans, Disease, Liver X receptor, Molecular Biology, Biology, Internal medicine, Neuropathology, Liver X Receptors, Inflammation, Molecular Physiology of Purinergic Signalling, Dopaminergic Neurons, FOS: Clinical medicine, Brain, Life Sciences, Parkinson Disease, Neurodegenerative Diseases, Neuroprotection, Cholesterol, Cholesterol Metabolism and Atherosclerosis, FOS: Biological sciences, Nuclear receptor, Neuroinflammatory Diseases, Medicine, Surgery, LXR, Transcription factor, Neuroscience, Receptor
Physiology, Dopaminergic, Dopamine, Peroxisome Proliferator-Activated Receptors, Nuclear Receptors, Immunology, Biochemistry, Gene, Article, Inflammasome, Neuroinflammation, lipid, Biochemistry, Genetics and Molecular Biology, Health Sciences, Substantia nigra, Liver X receptor ; Article ; Dopaminergic Neurons/metabolism [MeSH] ; Brain/metabolism [MeSH] ; Liver X Receptors/metabolism [MeSH] ; Humans [MeSH] ; Neurodegenerative Diseases/metabolism [MeSH] ; Neurodegenerative diseases ; Cholesterol/metabolism [MeSH] ; Parkinson Disease/pathology [MeSH] ; Neuroinflammatory Diseases [MeSH] ; Parkinson’s disease, Humans, Disease, Liver X receptor, Molecular Biology, Biology, Internal medicine, Neuropathology, Liver X Receptors, Inflammation, Molecular Physiology of Purinergic Signalling, Dopaminergic Neurons, FOS: Clinical medicine, Brain, Life Sciences, Parkinson Disease, Neurodegenerative Diseases, Neuroprotection, Cholesterol, Cholesterol Metabolism and Atherosclerosis, FOS: Biological sciences, Nuclear receptor, Neuroinflammatory Diseases, Medicine, Surgery, LXR, Transcription factor, Neuroscience, Receptor
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