Underlying anti-hypertensive mechanism of the Mizuhopecten yessoensis derived peptide NCW in spontaneously hypertensive rats via widely targeted kidney metabolomics

The angiotensin-converting enzyme (ACE) inhibitory peptide NCW derived from Mizuhopecten yessoensis has been demonstrated to have significant in vivo anti-hypertensive effects, however, its anti-hypertensive mechanism is still not fully clarified. This study established a UPLC-Q-TRAP-MS/MS-based wid...

Full description

Saved in:
Bibliographic Details
Main Authors: Wenjun Xue, Wenzhu Zhao, Sijia Wu, Zhipeng Yu
Format: Article
Language:English
Published: Tsinghua University Press 2024-01-01
Series:Food Science and Human Wellness
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213453023001556
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832557581580632064
author Wenjun Xue
Wenzhu Zhao
Sijia Wu
Zhipeng Yu
author_facet Wenjun Xue
Wenzhu Zhao
Sijia Wu
Zhipeng Yu
author_sort Wenjun Xue
collection DOAJ
description The angiotensin-converting enzyme (ACE) inhibitory peptide NCW derived from Mizuhopecten yessoensis has been demonstrated to have significant in vivo anti-hypertensive effects, however, its anti-hypertensive mechanism is still not fully clarified. This study established a UPLC-Q-TRAP-MS/MS-based widely targeted kidney metabolomics approach to explore the changes of kidney metabolic profiles and to clarify the anti-hypertensive mechanism of peptide NCW in spontaneously hypertensive rats (SHRs). Multivariate statistical analysis indicated that the kidney metabolic profiles were clearly separated between the SHR-NCW and SHR-Untreated groups. A total of 85 metabolites were differentially regulated, and 16 metabolites were identified as potential kidney biomarkers, e.g., 3-hydroxybutyrate, malonic acid, deoxycytidine, and L-aspartic acid. The peptide NCW might regulate kidney metabolic disorder of SHRs to alleviate hypertension by suppressing inflammation and improving nitric oxide production under the regulation of linoleic acid metabolism, folate related pathways, synthesis and degradation of ketone bodies, pyrimidine metabolism, β-alanine metabolism, and retinal metabolism.
format Article
id doaj-art-71a2c512739640cd8fb551be7413f2ab
institution Kabale University
issn 2213-4530
language English
publishDate 2024-01-01
publisher Tsinghua University Press
record_format Article
series Food Science and Human Wellness
spelling doaj-art-71a2c512739640cd8fb551be7413f2ab2025-02-03T04:09:17ZengTsinghua University PressFood Science and Human Wellness2213-45302024-01-01131472481Underlying anti-hypertensive mechanism of the Mizuhopecten yessoensis derived peptide NCW in spontaneously hypertensive rats via widely targeted kidney metabolomicsWenjun Xue0Wenzhu Zhao1Sijia Wu2Zhipeng Yu3School of Food Science and Engineering, Hainan University, Haikou 570228, China; College of Food Science and Engineering, Bohai University, Jinzhou 121013, ChinaSchool of Food Science and Engineering, Hainan University, Haikou 570228, ChinaLab of Nutrition and Functional Food, Jilin University, Changchun 130062, ChinaSchool of Food Science and Engineering, Hainan University, Haikou 570228, China; Corresponding author at: School of Food Science and Engineering, Hainan University, Haikou 570228, China.The angiotensin-converting enzyme (ACE) inhibitory peptide NCW derived from Mizuhopecten yessoensis has been demonstrated to have significant in vivo anti-hypertensive effects, however, its anti-hypertensive mechanism is still not fully clarified. This study established a UPLC-Q-TRAP-MS/MS-based widely targeted kidney metabolomics approach to explore the changes of kidney metabolic profiles and to clarify the anti-hypertensive mechanism of peptide NCW in spontaneously hypertensive rats (SHRs). Multivariate statistical analysis indicated that the kidney metabolic profiles were clearly separated between the SHR-NCW and SHR-Untreated groups. A total of 85 metabolites were differentially regulated, and 16 metabolites were identified as potential kidney biomarkers, e.g., 3-hydroxybutyrate, malonic acid, deoxycytidine, and L-aspartic acid. The peptide NCW might regulate kidney metabolic disorder of SHRs to alleviate hypertension by suppressing inflammation and improving nitric oxide production under the regulation of linoleic acid metabolism, folate related pathways, synthesis and degradation of ketone bodies, pyrimidine metabolism, β-alanine metabolism, and retinal metabolism.http://www.sciencedirect.com/science/article/pii/S2213453023001556ACE inhibitory peptideKidneyMechanismMetabolomicsSpontaneously hypertensive rats
spellingShingle Wenjun Xue
Wenzhu Zhao
Sijia Wu
Zhipeng Yu
Underlying anti-hypertensive mechanism of the Mizuhopecten yessoensis derived peptide NCW in spontaneously hypertensive rats via widely targeted kidney metabolomics
Food Science and Human Wellness
ACE inhibitory peptide
Kidney
Mechanism
Metabolomics
Spontaneously hypertensive rats
title Underlying anti-hypertensive mechanism of the Mizuhopecten yessoensis derived peptide NCW in spontaneously hypertensive rats via widely targeted kidney metabolomics
title_full Underlying anti-hypertensive mechanism of the Mizuhopecten yessoensis derived peptide NCW in spontaneously hypertensive rats via widely targeted kidney metabolomics
title_fullStr Underlying anti-hypertensive mechanism of the Mizuhopecten yessoensis derived peptide NCW in spontaneously hypertensive rats via widely targeted kidney metabolomics
title_full_unstemmed Underlying anti-hypertensive mechanism of the Mizuhopecten yessoensis derived peptide NCW in spontaneously hypertensive rats via widely targeted kidney metabolomics
title_short Underlying anti-hypertensive mechanism of the Mizuhopecten yessoensis derived peptide NCW in spontaneously hypertensive rats via widely targeted kidney metabolomics
title_sort underlying anti hypertensive mechanism of the mizuhopecten yessoensis derived peptide ncw in spontaneously hypertensive rats via widely targeted kidney metabolomics
topic ACE inhibitory peptide
Kidney
Mechanism
Metabolomics
Spontaneously hypertensive rats
url http://www.sciencedirect.com/science/article/pii/S2213453023001556
work_keys_str_mv AT wenjunxue underlyingantihypertensivemechanismofthemizuhopectenyessoensisderivedpeptidencwinspontaneouslyhypertensiveratsviawidelytargetedkidneymetabolomics
AT wenzhuzhao underlyingantihypertensivemechanismofthemizuhopectenyessoensisderivedpeptidencwinspontaneouslyhypertensiveratsviawidelytargetedkidneymetabolomics
AT sijiawu underlyingantihypertensivemechanismofthemizuhopectenyessoensisderivedpeptidencwinspontaneouslyhypertensiveratsviawidelytargetedkidneymetabolomics
AT zhipengyu underlyingantihypertensivemechanismofthemizuhopectenyessoensisderivedpeptidencwinspontaneouslyhypertensiveratsviawidelytargetedkidneymetabolomics