The Role of α7-Nicotinic Acetylcholine Receptors in the Pathophysiology and Treatment of Parkinson's Disease

被引:0
作者
ElNebrisi, Eslam [1 ]
Lozon, Yosra [2 ]
Oz, Murat [3 ]
机构
[1] Dubai Med Univ, Dubai Med Coll Girls, Dept Biomed Sci, Dubai 20170, U Arab Emirates
[2] Dubai Med Univ, Dubai Pharm Coll Girls, Dept Pharmaceut Sci, Dubai 20170, U Arab Emirates
[3] Kuwait Univ, Coll Pharm, Dept Pharmacol & Therapeut, Safat 13110, Kuwait
关键词
alpha 7-nicotinic acetylcholine receptor; Parkinson's disease; neuroprotection; allosteric modulators; L-dopa-induced dyskinesia; neuroinflammation; dopamine release; cholinergic system; ALPHA-7 NICOTINIC RECEPTOR; DOPA-INDUCED DYSKINESIAS; POSITIVE ALLOSTERIC MODULATORS; LEVODOPA-INDUCED DYSKINESIAS; CHOLINERGIC STIMULATION; COGNITIVE IMPAIRMENT; DOPAMINERGIC-NEURONS; GLUTAMATE RECEPTORS; THERAPEUTIC TARGETS; RAT MODEL;
D O I
10.3390/ijms26073210
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The alpha 7 nicotinic acetylcholine receptor (alpha 7-nAChR) is a pivotal regulator of neurotransmission, neuroprotection, and immune modulation in the central nervous system. This review explores its structural and functional attributes, highlighting its therapeutic potential in neurodegenerative disorders, particularly Parkinson's disease (PD). alpha 7-nAChRs mediate synaptic plasticity, modulate inflammatory responses, and influence dopamine release, positioning them as a promising pharmacological target. Positive allosteric modulators (PAMs) enhance alpha 7-nAChR activity mainly by reducing desensitization, offering a superior therapeutic approach compared with direct agonists. Emerging preclinical studies suggest that alpha 7-nAChR activation mitigates dopaminergic neurodegeneration, improves L-dopa-induced dyskinesia, and reduces neuroinflammation. Despite promising findings, clinical trials have yielded mixed results, necessitating further research into optimizing alpha 7-targeted therapies. This review underscores the significance of alpha 7-nAChRs in PD pathophysiology and highlights future directions for their translational potential in neuroprotection and symptomatic relief.
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页数:19
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