Ketamine reduces amyloid β-protein degradation by suppressing neprilysin expression in primary cultured astrocytes

• Published in: Neuroscience letters Vol. 545; pp. 54 - 58
• Main Authors: Yamamoto, Naoki, Arima, Hajime, Naruse, Kaori, Kasahara, Rika, Taniura, Hideo, Hirate, Hiroyuki, Sugiura, Takeshi, Suzuki, Kenji, Sobue, Kazuya
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier Ireland Ltd 17.06.2013
• Subjects: Alzheimer's disease; Amyloid beta-Peptides - metabolism; Amyloid β-protein; Analgesics - administration & dosage; Animals; Astrocytes - drug effects; Astrocytes - metabolism; Cells, Cultured; Dose-Response Relationship, Drug; Down-Regulation - drug effects; Ketamine; Ketamine - administration & dosage; Neprilysin; Neprilysin - metabolism; Non-competitive N-methyl-d-aspartate receptor; Protein Denaturation; Rats; Rats, Sprague-Dawley; Non-competitive N-methyl-d-aspartate receptor; Aβ; AD; Ketamine; NEP; CNS; NMDAR; Neprilysin; IDE; Amyloid β-protein; Alzheimer's disease
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2013.04.016

•The brain expression of neprilysin may promote Aβ deposition in patients with AD.•The NMDAR antagonist ketamine and MK801 decreased the expression of NEP in astrocytes.•Ketamine reduced the expression of NEP by the suppression p38 MAPK activity in astrocytes.•NEP-reduced reagents suppressed the degradation of exogenous Aβ by astrocytes.•Ketamine suppresses Aβ degradation of NEP by reducing p38 MAPK-mediated pathway activity. Pathological accumulation of cortical amyloid β-protein (Aβ) is an early and consistent feature of Alzheimer's disease (AD). Aβ levels in the brain are determined by production and catabolism. Previous studies have suggested that deficits in the brain expression of neprilysin (NEP) and the insulin-degrading enzyme (IDE), which are both proteases involved in amyloid degradation, may promote Aβ deposition in patients with sporadic late-onset AD. Because the incidence of AD increases after surgical intervention, we examined whether ketamine, which is a general anaesthetic with neuroprotective properties for excitotoxic ischaemic damage, is associated with Aβ degradation by inducing NEP and IDE expression. The non-competitive N-methyl-d-aspartate receptor antagonist ketamine and MK801 significantly decreased the expression of NEP, but not IDE, in a concentration- and time-dependent manner through the dephosphorylation of p38 mitogen-activated protein kinase (MAPK) in cultured rat astrocytes. Furthermore, NEP-reduced reagents significantly suppressed the degradation of exogenous Aβ in cultured astrocytes. These results suggested that ketamine suppresses the Aβ degradation of NEP by reducing p38 MAPK-mediated pathway activity.