Medium-Dose Chronic Cannabidiol Treatment Reverses Object Recognition Memory Deficits of APPSwe /PS1ΔE9 Transgenic Female Mice

被引:34
作者
Coles, Madilyn [1 ]
Watt, Georgia [1 ]
Kreilaus, Fabian [1 ]
Karl, Tim [1 ,2 ]
机构
[1] Western Sydney Univ, Sch Med, Campbelltown, NSW, Australia
[2] Neurosci Res Australia, Randwick, NSW, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Alzheimer's disease; APP(Swe)/PS1 Delta E9; transgenic mouse model; cannabidiol; treatment; behavior; APPSWE/PS1DE9 MOUSE MODEL; AMYLOID PRECURSOR PROTEIN; NEUREGULIN-1 MUTANT MICE; ALZHEIMER-LIKE PATHOLOGY; BEHAVIORAL-CHARACTERISTICS; ENDOCANNABINOID SYSTEM; PREPULSE INHIBITION; MOTOR COORDINATION; OXIDATIVE STRESS; IN-VIVO;
D O I
10.3389/fphar.2020.587604
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative disease that causes behavioral and cognitive impairments. The phytocannabinoid cannabidiol (CBD) has anti-inflammatory, antioxidant, and neuroprotective properties, and in vitro and limited in vivo evidence suggests that CBD possesses therapeutic-like properties for the treatment of AD. Cannabinoids are known to have dose-dependent effects and the therapeutic potential of medium-dose CBD for AD transgenic mice has not been assessed in great detail yet. 12-month-old control and APP(Swe)/PS1 Delta E9 (APPxPS1) transgenic female mice were treated daily via intraperitoneal injection with 5 mg/kg bodyweight CBD (or vehicle) commencing three weeks prior to the assessment of behavioral domains including anxiety, exploration, locomotion, motor functions, cognition, and sensorimotor gating. APPxPS1 mice exhibited a hyperlocomotive and anxiogenic-like phenotype and had wild type-like motor and spatial learning abilities, although AD transgenic mice took generally longer to complete the cheeseboard training (due to a lower locomotion speed). Furthermore spatial learning and reversal learning was delayed by one day in APPxPS1 mice compared to control mice. All mice displayed intact spatial memory and retrieval memory, but APPxPS1 mice showed reduced levels of perseverance in the cheeseboard probe trial. Importantly, vehicle-treated APPxPS1 mice were characterized by object recognition deficits and delayed spatial learning, which were reversed by CBD treatment. Finally, impairments in sensorimotor gating of APPxPS1 mice were not affected by CBD. In conclusion, medium-dose CBD appears to have therapeutic value for the treatment of particular behavioral impairments present in AD patients. Future research should consider the molecular mechanisms behind CBD's beneficial properties for AD transgenic mice.
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页数:15
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