Detailed Information

Cited 1 time in webofscience Cited 5 time in scopus
Metadata Downloads

Korean Red Pine ( Pinus densiflora ) Bark Extract Attenuates Aβ-Induced Cognitive Impairment by Regulating Cholinergic Dysfunction and NeuroinflammationKorean Red Pine (Pinus densiflora) Bark Extract Attenuates Aβ-Induced Cognitive Impairment by Regulating Cholinergic Dysfunction and Neuroinflammation

Other Titles
Korean Red Pine (Pinus densiflora) Bark Extract Attenuates Aβ-Induced Cognitive Impairment by Regulating Cholinergic Dysfunction and Neuroinflammation
Authors
Go Min JiKim Jong MinKang Jin YongPark Seon KyeongLee Chang JunKim Min JiLee Hyo RimKim Tae YoonJoo Seung Gyum김대옥허호진
Issue Date
Sep-2022
Publisher
한국미생물·생명공학회
Keywords
Korean red pine bark extract; amyloid beta; cognitive dysfunction; neuroprotective effect; cholinergic system; mitochondrial dysfunction
Citation
Journal of Microbiology and Biotechnology, v.32, no.9, pp.1154 - 1167
Indexed
SCIE
SCOPUS
KCI
Journal Title
Journal of Microbiology and Biotechnology
Volume
32
Number
9
Start Page
1154
End Page
1167
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/893
DOI
10.4014/jmb.2207.07015
ISSN
1017-7825
Abstract
In this study, we investigated the anti-amnesic effect of Korean red pine (Pinus densiflora) bark extract (KRPBE) against amyloid beta1-42 (Aβ1-42)-induced neurotoxicity. We found that treatment with KRPBE improved the behavioral function in Aβ-induced mice, and also boosted the antioxidant system in mice by decreasing malondialdehyde (MDA) content, increasing superoxide dismutase (SOD) activities, and reducing glutathione (GSH) levels. In addition, KRPBE improved the cholinergic system by suppressing reduced acetylcholine (ACh) content while also activating acetylcholinesterase (AChE), regulating the expression of choline acetyltransferase (ChAT), postsynaptic density protein-95 (PSD-95), and synaptophysin. KRPBE also showed an ameliorating effect on cerebral mitochondrial deficit by regulating reactive oxygen species (ROS), mitochondrial membrane potential (MMP) and ATP levels. Moreover, KRPBE modulated the expression levels of neurotoxicity indicators Aβ and phosphorylated tau (p-tau) and inflammatory cytokines TNF-α, p- IκB-α, and IL-1β. Furthermore, we found that KRPBE improved the expression levels of neuronal apoptosis-related markers BAX and BCl-2 and increased the expression levels of BDNF and p-CREB. Therefore, this study suggests that KRPBE treatment has an anti-amnestic effect by modulating cholinergic system dysfunction and neuroinflammation in Aβ1-42-induced cognitive impairment in mice.
Files in This Item
There are no files associated with this item.
Appears in
Collections
ETC > Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Altmetrics

Total Views & Downloads

BROWSE