201. Hydroxysafflor yellow A increases BDNF and NMDARs in the hippocampus in a vascular dementia rat model
- Author
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Yan Cheng, Qingna Sun, Yiyi Wang, Mengya Xing, and Nan Zhang
- Subjects
Male ,0301 basic medicine ,medicine.medical_specialty ,Long-Term Potentiation ,Drug Evaluation, Preclinical ,Morris water navigation task ,Hippocampus ,Hippocampal formation ,Receptors, N-Methyl-D-Aspartate ,Rats, Sprague-Dawley ,Random Allocation ,03 medical and health sciences ,Chalcone ,0302 clinical medicine ,Neurotrophic factors ,Internal medicine ,Animals ,Medicine ,cardiovascular diseases ,Maze Learning ,Molecular Biology ,Nootropic Agents ,Spatial Memory ,Brain-derived neurotrophic factor ,business.industry ,Brain-Derived Neurotrophic Factor ,Dementia, Vascular ,General Neuroscience ,Quinones ,Long-term potentiation ,Up-Regulation ,Disease Models, Animal ,Neuroprotective Agents ,030104 developmental biology ,Endocrinology ,nervous system ,Synaptic plasticity ,NMDA receptor ,Angiogenesis Inducing Agents ,Neurology (clinical) ,biological phenomena, cell phenomena, and immunity ,business ,Neuroscience ,030217 neurology & neurosurgery ,Developmental Biology - Abstract
Hydroxysafflor yellow A (HSYA) is a drug that exerts angiogenesis regulatory and neuroprotective effects and has become an effective therapy for brain and heart ischemic disorders. There is no definite evidence supporting a therapeutic effect of HSYA in vascular dementia (VaD). We used HSYA in a rat model of chronic cerebral ischemia to determine its potential therapeutic effects in VaD. The Morris water maze (MWM) was used to evaluate spatial cognitive function, and long-term potentiation (LTP) was tested as a marker of synaptic plasticity. The expression levels of brain-derived neurotrophic factor (BDNF) and two subunits of N-methyl-d-aspartate receptor (NMDAR; GluN2A and GluN2B) in the hippocampus were measured via western blotting. The MWM results showed that the experimental VaD group had longer escape latencies than the sham group, whereas the HSYA group had a decreased escape latency compared with the VaD group (P
- Published
- 2016
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