Opioid System and Alzheimer's Disease

被引:66
作者
Cai, Zhiyou [2 ]
Ratka, Anna [1 ]
机构
[1] Texas A&M Hlth Sci Ctr, Irma Lerma Rangel Coll Pharm, Dept Pharmaceut Sci, Kingsville, TX 78363 USA
[2] Anhui Med Univ, Luan Affiliated Hosp, Luan Peoples Hosp, Dept Neurol, Luan 237005, Anhui, Peoples R China
关键词
Opioid system; Beta-amyloid; Neurotransmitter; Hyperphosphorylated tau; Alzheimer's disease; GROWTH-FACTOR RECEPTOR; AMYLOID PRECURSOR PROTEIN; METHYL-D-ASPARTATE; NOCICEPTIN/ORPHANIN FQ RECEPTOR; SUPPRESSES SPINAL NEUROINFLAMMATION; PRODYNORPHIN-DERIVED PEPTIDE; TRANSGENIC MOUSE MODEL; CENTRAL NERVOUS-SYSTEM; IN-VITRO; NOREPINEPHRINE RELEASE;
D O I
10.1007/s12017-012-8180-3
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The opioid system may be involved in the pathogenesis of AD, including cognitive impairment, hyperphosphorylated tau, A beta production, and neuroinflammation. Opioid receptors influence the regulation of neurotransmitters such as acetylcholine, norepinephrine, GABA, glutamate, and serotonin which have been implicated in the pathogenesis of AD. Opioid system has a close relation with A beta generation since dysfunction of opioid receptors retards the endocytosis and degradation of BACE1 and gamma-secretase and upregulates BACE1 and gamma-secretase, and subsequently, the production of A beta. Conversely, activation of opioid receptors increases the endocytosis of BACE1 and gamma-secretase and downregulates BACE1 and gamma-secretase, limiting the production of A beta. The dysfunction of opioid system (opioid receptors and opioid peptides) may contribute to hyperphosphorylation of tau and neuroinflammation, and accounts for the degeneration of cholinergic neurons and cognitive impairment. Thus, the opioid system is potentially related to AD pathology and may be a very attractive drug target for novel pharmacotherapies of AD.
引用
收藏
页码:91 / 111
页数:21
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