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Effects of Scrophularia buergeriana Extract (Brainon(®)) on Aging-Induced Memory Impairment in SAMP8 Mice

Alzheimer’s disease (AD) is a worldwide problem. Currently, there are no effective drugs for AD treatment. Scrophularia buergeriana Miquel (SB) is a traditional herbal medicine used in Korea to treat various diseases. Our previous studies have shown that ethanol extract of SB roots (SBE, Brainon(®))...

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Autores principales: Kim, Hae Lim, Lee, Sung Kwon, Min, Da Eun, Bastola, Tonking, Chang, Bo Yoon, Bae, Jin Hye, Lee, Dong Ryung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9955813/
https://www.ncbi.nlm.nih.gov/pubmed/36826029
http://dx.doi.org/10.3390/cimb45020084
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author Kim, Hae Lim
Lee, Sung Kwon
Min, Da Eun
Bastola, Tonking
Chang, Bo Yoon
Bae, Jin Hye
Lee, Dong Ryung
author_facet Kim, Hae Lim
Lee, Sung Kwon
Min, Da Eun
Bastola, Tonking
Chang, Bo Yoon
Bae, Jin Hye
Lee, Dong Ryung
author_sort Kim, Hae Lim
collection PubMed
description Alzheimer’s disease (AD) is a worldwide problem. Currently, there are no effective drugs for AD treatment. Scrophularia buergeriana Miquel (SB) is a traditional herbal medicine used in Korea to treat various diseases. Our previous studies have shown that ethanol extract of SB roots (SBE, Brainon(®)) exhibits potent anti-amnesic effects in Aβ(1–42)- or scopolamine-treated memory impairment mice model and neuroprotective effects in a glutamate-induced SH-SY5Y cell model. In this study, we evaluated the therapeutic effects of Brainon(®) and its mechanism of action in senescence-accelerated mouse prone 8 (SAMP8) mice. Brainon(®) (30 or 100 mg/kg/day) was orally treated to six-month-old SAMP8 mice for 12 weeks. Results revealed that Brainon(®) administration effectually ameliorated cognitive deficits in Y-maze and passive avoidance tests. Following the completion of behavioral testing, western blotting was performed using the cerebral cortex. Results revealed that Brainon(®) suppressed Aβ(1–42) accumulation, Tau hyperphosphorylation, oxidative stress, and inflammation and alleviated apoptosis in SAMP8 mice. Brainon(®) also promoted synaptic function by downregulating the expression of AChE and upregulating the expression of p-CREB/CREB and BDNF. Furthermore, Brainon(®) restored SAMP8-reduced expression of ChAT and -dephosphorylated of ERK and also decreased AChE expression in the hippocampus. Furthermore, Brainon(®) alleviated AD progression by promoting mitophagy/autophagy to maintain normal cellular function as a novel finding of this study. Our data suggest that Brainon(®) can remarkably improve cognitive deficiency with the potential to be utilized in functional food for improving brain health.
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spelling pubmed-99558132023-02-25 Effects of Scrophularia buergeriana Extract (Brainon(®)) on Aging-Induced Memory Impairment in SAMP8 Mice Kim, Hae Lim Lee, Sung Kwon Min, Da Eun Bastola, Tonking Chang, Bo Yoon Bae, Jin Hye Lee, Dong Ryung Curr Issues Mol Biol Article Alzheimer’s disease (AD) is a worldwide problem. Currently, there are no effective drugs for AD treatment. Scrophularia buergeriana Miquel (SB) is a traditional herbal medicine used in Korea to treat various diseases. Our previous studies have shown that ethanol extract of SB roots (SBE, Brainon(®)) exhibits potent anti-amnesic effects in Aβ(1–42)- or scopolamine-treated memory impairment mice model and neuroprotective effects in a glutamate-induced SH-SY5Y cell model. In this study, we evaluated the therapeutic effects of Brainon(®) and its mechanism of action in senescence-accelerated mouse prone 8 (SAMP8) mice. Brainon(®) (30 or 100 mg/kg/day) was orally treated to six-month-old SAMP8 mice for 12 weeks. Results revealed that Brainon(®) administration effectually ameliorated cognitive deficits in Y-maze and passive avoidance tests. Following the completion of behavioral testing, western blotting was performed using the cerebral cortex. Results revealed that Brainon(®) suppressed Aβ(1–42) accumulation, Tau hyperphosphorylation, oxidative stress, and inflammation and alleviated apoptosis in SAMP8 mice. Brainon(®) also promoted synaptic function by downregulating the expression of AChE and upregulating the expression of p-CREB/CREB and BDNF. Furthermore, Brainon(®) restored SAMP8-reduced expression of ChAT and -dephosphorylated of ERK and also decreased AChE expression in the hippocampus. Furthermore, Brainon(®) alleviated AD progression by promoting mitophagy/autophagy to maintain normal cellular function as a novel finding of this study. Our data suggest that Brainon(®) can remarkably improve cognitive deficiency with the potential to be utilized in functional food for improving brain health. MDPI 2023-02-03 /pmc/articles/PMC9955813/ /pubmed/36826029 http://dx.doi.org/10.3390/cimb45020084 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Hae Lim
Lee, Sung Kwon
Min, Da Eun
Bastola, Tonking
Chang, Bo Yoon
Bae, Jin Hye
Lee, Dong Ryung
Effects of Scrophularia buergeriana Extract (Brainon(®)) on Aging-Induced Memory Impairment in SAMP8 Mice
title Effects of Scrophularia buergeriana Extract (Brainon(®)) on Aging-Induced Memory Impairment in SAMP8 Mice
title_full Effects of Scrophularia buergeriana Extract (Brainon(®)) on Aging-Induced Memory Impairment in SAMP8 Mice
title_fullStr Effects of Scrophularia buergeriana Extract (Brainon(®)) on Aging-Induced Memory Impairment in SAMP8 Mice
title_full_unstemmed Effects of Scrophularia buergeriana Extract (Brainon(®)) on Aging-Induced Memory Impairment in SAMP8 Mice
title_short Effects of Scrophularia buergeriana Extract (Brainon(®)) on Aging-Induced Memory Impairment in SAMP8 Mice
title_sort effects of scrophularia buergeriana extract (brainon(®)) on aging-induced memory impairment in samp8 mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9955813/
https://www.ncbi.nlm.nih.gov/pubmed/36826029
http://dx.doi.org/10.3390/cimb45020084
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