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Bioactive Peptide VHVV Upregulates the Long-Term Memory-Related Biomarkers in Adult Spontaneously Hypertensive Rats

Hypertension is one of the growing risk factors for the progression of long-term memory loss. Hypertension-mediated memory loss and treatment remain not thoroughly elucidated to date. Plant-based natural compounds are an alternative solution to treating human diseases without side effects associated...

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Autores principales: Ju, Da-Tong, K., Ashok Kumar, Kuo, Wei-Wen, Ho, Tsung-Jung, Chang, Ruey-Lin, Lin, Wan-Teng, Day, Cecilia Hsuan, Viswanadha, V. Vijaya Padma, Liao, Po-Hsiang, Huang, Chih-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627188/
https://www.ncbi.nlm.nih.gov/pubmed/31234585
http://dx.doi.org/10.3390/ijms20123069
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author Ju, Da-Tong
K., Ashok Kumar
Kuo, Wei-Wen
Ho, Tsung-Jung
Chang, Ruey-Lin
Lin, Wan-Teng
Day, Cecilia Hsuan
Viswanadha, V. Vijaya Padma
Liao, Po-Hsiang
Huang, Chih-Yang
author_facet Ju, Da-Tong
K., Ashok Kumar
Kuo, Wei-Wen
Ho, Tsung-Jung
Chang, Ruey-Lin
Lin, Wan-Teng
Day, Cecilia Hsuan
Viswanadha, V. Vijaya Padma
Liao, Po-Hsiang
Huang, Chih-Yang
author_sort Ju, Da-Tong
collection PubMed
description Hypertension is one of the growing risk factors for the progression of long-term memory loss. Hypertension-mediated memory loss and treatment remain not thoroughly elucidated to date. Plant-based natural compounds are an alternative solution to treating human diseases without side effects associated with commercial drugs. This study reveals that bioactive peptides extracted from soy hydrolysates mimic hypertension-mediated memory loss and neuronal degeneration and alters the memory molecular pathway in spontaneously hypertensive rats (SHR). The SHR animal model was treated with bioactive peptide VHVV (10 mg/kg/oral administration) and angiotensin-converting-enzyme (ACE) inhibitors (5 mg/kg/oral administration) for 24 weeks. We evaluated molecular level expression of brain-derived neurotrophic factor (BDNF), cAMP response element binding protein (CREB), and survival markers phospho-protein kinase B (P-AKT) and phosphoinositide 3-kinase (PI3K) after 24 weeks of treatment for SHR in this study. Western blotting, hematoxylin and eosin (H&E) staining, and immunohistochemistry showed long-term memory loss and neuronal degeneration in SHR animals. Bioactive peptide VHVV-treated animals upregulated the expression of long-term memory-relate proteins and neuronal survival. Spontaneously hypertensive rats treated with oral administration of bioactive peptide VHVV had activated CREB-mediated downstream proteins which may reduce hypertension-mediated long-term memory loss and maintain neuronal survival.
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spelling pubmed-66271882019-07-19 Bioactive Peptide VHVV Upregulates the Long-Term Memory-Related Biomarkers in Adult Spontaneously Hypertensive Rats Ju, Da-Tong K., Ashok Kumar Kuo, Wei-Wen Ho, Tsung-Jung Chang, Ruey-Lin Lin, Wan-Teng Day, Cecilia Hsuan Viswanadha, V. Vijaya Padma Liao, Po-Hsiang Huang, Chih-Yang Int J Mol Sci Article Hypertension is one of the growing risk factors for the progression of long-term memory loss. Hypertension-mediated memory loss and treatment remain not thoroughly elucidated to date. Plant-based natural compounds are an alternative solution to treating human diseases without side effects associated with commercial drugs. This study reveals that bioactive peptides extracted from soy hydrolysates mimic hypertension-mediated memory loss and neuronal degeneration and alters the memory molecular pathway in spontaneously hypertensive rats (SHR). The SHR animal model was treated with bioactive peptide VHVV (10 mg/kg/oral administration) and angiotensin-converting-enzyme (ACE) inhibitors (5 mg/kg/oral administration) for 24 weeks. We evaluated molecular level expression of brain-derived neurotrophic factor (BDNF), cAMP response element binding protein (CREB), and survival markers phospho-protein kinase B (P-AKT) and phosphoinositide 3-kinase (PI3K) after 24 weeks of treatment for SHR in this study. Western blotting, hematoxylin and eosin (H&E) staining, and immunohistochemistry showed long-term memory loss and neuronal degeneration in SHR animals. Bioactive peptide VHVV-treated animals upregulated the expression of long-term memory-relate proteins and neuronal survival. Spontaneously hypertensive rats treated with oral administration of bioactive peptide VHVV had activated CREB-mediated downstream proteins which may reduce hypertension-mediated long-term memory loss and maintain neuronal survival. MDPI 2019-06-23 /pmc/articles/PMC6627188/ /pubmed/31234585 http://dx.doi.org/10.3390/ijms20123069 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ju, Da-Tong
K., Ashok Kumar
Kuo, Wei-Wen
Ho, Tsung-Jung
Chang, Ruey-Lin
Lin, Wan-Teng
Day, Cecilia Hsuan
Viswanadha, V. Vijaya Padma
Liao, Po-Hsiang
Huang, Chih-Yang
Bioactive Peptide VHVV Upregulates the Long-Term Memory-Related Biomarkers in Adult Spontaneously Hypertensive Rats
title Bioactive Peptide VHVV Upregulates the Long-Term Memory-Related Biomarkers in Adult Spontaneously Hypertensive Rats
title_full Bioactive Peptide VHVV Upregulates the Long-Term Memory-Related Biomarkers in Adult Spontaneously Hypertensive Rats
title_fullStr Bioactive Peptide VHVV Upregulates the Long-Term Memory-Related Biomarkers in Adult Spontaneously Hypertensive Rats
title_full_unstemmed Bioactive Peptide VHVV Upregulates the Long-Term Memory-Related Biomarkers in Adult Spontaneously Hypertensive Rats
title_short Bioactive Peptide VHVV Upregulates the Long-Term Memory-Related Biomarkers in Adult Spontaneously Hypertensive Rats
title_sort bioactive peptide vhvv upregulates the long-term memory-related biomarkers in adult spontaneously hypertensive rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627188/
https://www.ncbi.nlm.nih.gov/pubmed/31234585
http://dx.doi.org/10.3390/ijms20123069
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