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Ischemia-induced cognitive impairment is improved via remyelination and restoration of synaptic density in the hippocampus after treatment with cog-up® in a gerbil model of ischemic stroke

Authors
Lee, T.-K.Hong, J.Lee, J.-W.Kim, S.-S.Sim, H.Lee, J.-C.Kim, D.W.Lim, S.S.Kang, I.J.Won, M.-H.
Issue Date
Dec-2021
Publisher
MDPI
Keywords
Cornu Ammonis 1; Glutaminergic synapse; Ischemia-reperfusion injury; Memory func-tion; Oligodendrocyte; Pyramidal cells
Citation
Veterinary Sciences, v.8, no.12
Journal Title
Veterinary Sciences
Volume
8
Number
12
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/61990
DOI
10.3390/vetsci8120321
ISSN
2306-7381
2306-7381
Abstract
Cerebrovascular disease such as ischemic stroke develops cognitive impairment due to brain tissue damage including neural loss, demyelination and decrease in synaptic density. In the present study, we developed transient ischemia in the forebrain of the gerbil and found cognitive impairment using the Barnes maze test and passive avoidance test for spatial memory and learning memory, respectively. In addition, neuronal loss/death was detected in the Cornu Ammonis 1 (CA1) region of the gerbil hippocampus after the ischemia by cresyl violet histochemistry, immuno-histochemistry for neuronal nuclei and histofluorescence with Fluoro-Jade B. Furthermore, in the CA1 region following ischemia, myelin and vesicular synaptic density were significantly decreased using immunohistochemistry for myelin basic protein and vesicular glutamate transporter 1. In the gerbils, treatment with COG-up® (a combined extract of Erigeron annuus (L.) Pers. and Brassica oleracea Var.), which was rich in scutellarin and sinapic acid, after the ischemia, significantly improved ischemia-induced decline in memory function when compared with that shown in gerbils treated with vehicle after the ischemia. In the CA1 region of these gerbils, COG-up® treatment significantly promoted the remyelination visualized using immunohistochemistry myelin basic protein, increased oligodendrocytes visualized using a receptor-interacting protein, and restored the density of gluta-matergic synapses visualized using double immunofluorescence for vesicular glutamate transporter 1 and microtubule-associated protein, although COG-up® treatment did not protect pyramidal cells (principal neurons) located in the CA1 region form the ischemic insult. Considering the current findings, a gerbil model of ischemic stroke apparently showed cognitive impairment accompanied by ischemic injury in the hippocampus; also, COG-up® can be employed for improving cognitive decline following ischemia-reperfusion injury in brains. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
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