Vitamin D3 attenuates cognitive deficits and neuroinflammatory responses in ICV-STZ induced sporadic Alzheimer's disease

被引:65
|
作者
Yamini, P. [1 ]
Ray, R. S. [1 ]
Chopra, Kanwaljit [1 ]
机构
[1] Panjab Univ, Pharmacol Res Lab, UIPS, UGC Ctr Adv Study, Chandigarh 160014, India
关键词
Alzheimer's disease; Vitamin D-3; Neuroprotection; Memory; Acetylcholine; Neuroinflammation; OXIDATIVE STRESS; INTRACEREBROVENTRICULAR STREPTOZOTOCIN; AMYLOID-BETA; MITOCHONDRIAL DYSFUNCTION; CHOLINERGIC TRANSMISSION; MEMORY IMPAIRMENT; PROTECTIVE ROLE; NITRIC-OXIDE; MOUSE-BRAIN; RAT-BRAIN;
D O I
10.1007/s10787-017-0372-x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by intracellular neurofibrillary tangles and extracellular Ab deposition. Growing experimental evidence indicate diverse biological effects of vitamin D-3 including antioxidant, neuroprotective, anti-inflammatory and cardiovascular benefits. However, the underlying neuroprotective mechanism of vitamin D-3 is still largely elusive. Therefore, the present study was aimed to investigate the neuroprotective effects of vitamin D-3 on ICV-STZ induced sporadic AD. Our study demonstrated that vitamin D-3 pretreatment significantly improved spatial learning and memory functions and effectively mitigated ICV-STZ mediated neuronal oxidative stress, mitochondrial aberrations and improved cholinergic functions. Moreover, vitamin D-3 attenuated hippocampal neuroinflammatory response and reduced neuronal death in cortex and hippocampus. Our findings indicated that prophylactic vitamin D-3 supplementation ameliorated ICV-STZ mediated neurobehavioral alterations, oxidative stress and neuroinflammation thereby improving cholinergic functions and reversed degenerative changes in brain. Thus, our study further provides evidence for its therapeutic supplementation for various neurodegenerative disorders including AD. [GRAPHICS] .
引用
收藏
页码:39 / 55
页数:17
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