Cargando…

Alteration of Amino Acid Profiling Influenced by the Active Ingredients of DanHong Injection After Prescription Optimization

INTRODUCTION: The aim of this work was to optimize the formulation composition of DanHong injection and to study the disturbance of microscopic components of cerebral ischemia in amino acid metabolites and metabolic pathways. The subtle relationship among these three substances and the influence of...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Zhili, Zhu, Yan, Xu, Wenjuan, Luo, Kaitao, Xiao, Hongbin, Wang, Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876559/
https://www.ncbi.nlm.nih.gov/pubmed/31819368
http://dx.doi.org/10.2147/DDDT.S220314
_version_ 1783473230776893440
author Guo, Zhili
Zhu, Yan
Xu, Wenjuan
Luo, Kaitao
Xiao, Hongbin
Wang, Zhong
author_facet Guo, Zhili
Zhu, Yan
Xu, Wenjuan
Luo, Kaitao
Xiao, Hongbin
Wang, Zhong
author_sort Guo, Zhili
collection PubMed
description INTRODUCTION: The aim of this work was to optimize the formulation composition of DanHong injection and to study the disturbance of microscopic components of cerebral ischemia in amino acid metabolites and metabolic pathways. The subtle relationship among these three substances and the influence of metabolic pathways were also studied. METHODS: In this study, the central composite design (CCD) matrix and response surface methodology (RSM) were used to design the experiments and to evaluate the interactive effects of three substances. Targeted metabolomics was used to detect the amino acid variation in CCD sets. RESULTS: Response surfaces were generated, and the formulation was optimized by superimposing the contour plots. It was found that the optimum values of the responses could be obtained at an SAB concentration (x1) of 8–9 mg/kg, a TSN concentration (x2) of 14–16 mg/kg, and an HSYA yellow A concentration (x3) of 6 mg/kg. Statistical analysis showed that the three independent variables had significant effects (p < 0.05) on the responses. A total of 22 experimental runs were performed, and the kinetic data were analyzed using a second-order polynomial. Model algorithm calculation indicated that glutamic acid, serine, leucine, glycine, and valine had a very close correlation with the active ingredients. Methionine, aspartic acid, asparagine, glutamic acid, and valine were important for distinguishing different groups, and they were identified as potential biomarkers. Cluster analysis and pathway analysis indicated that the valine, leucine, and isoleucine degradation (VLI degradation) pathway was the major metabolic pathway. Arginine and proline metabolites were most frequently detected, and they were closely associated with other networks according to the network analysis results. VLI degradation pathway and arginine and proline metabolism pathway had a significant influence on cerebral ischemia. DISCUSSION: The integration of CCD and metabolomics may be an effective strategy for optimizing the formulation composition and identifying the mechanism of action of traditional chinese medicine.
format Online
Article
Text
id pubmed-6876559
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-68765592019-12-09 Alteration of Amino Acid Profiling Influenced by the Active Ingredients of DanHong Injection After Prescription Optimization Guo, Zhili Zhu, Yan Xu, Wenjuan Luo, Kaitao Xiao, Hongbin Wang, Zhong Drug Des Devel Ther Original Research INTRODUCTION: The aim of this work was to optimize the formulation composition of DanHong injection and to study the disturbance of microscopic components of cerebral ischemia in amino acid metabolites and metabolic pathways. The subtle relationship among these three substances and the influence of metabolic pathways were also studied. METHODS: In this study, the central composite design (CCD) matrix and response surface methodology (RSM) were used to design the experiments and to evaluate the interactive effects of three substances. Targeted metabolomics was used to detect the amino acid variation in CCD sets. RESULTS: Response surfaces were generated, and the formulation was optimized by superimposing the contour plots. It was found that the optimum values of the responses could be obtained at an SAB concentration (x1) of 8–9 mg/kg, a TSN concentration (x2) of 14–16 mg/kg, and an HSYA yellow A concentration (x3) of 6 mg/kg. Statistical analysis showed that the three independent variables had significant effects (p < 0.05) on the responses. A total of 22 experimental runs were performed, and the kinetic data were analyzed using a second-order polynomial. Model algorithm calculation indicated that glutamic acid, serine, leucine, glycine, and valine had a very close correlation with the active ingredients. Methionine, aspartic acid, asparagine, glutamic acid, and valine were important for distinguishing different groups, and they were identified as potential biomarkers. Cluster analysis and pathway analysis indicated that the valine, leucine, and isoleucine degradation (VLI degradation) pathway was the major metabolic pathway. Arginine and proline metabolites were most frequently detected, and they were closely associated with other networks according to the network analysis results. VLI degradation pathway and arginine and proline metabolism pathway had a significant influence on cerebral ischemia. DISCUSSION: The integration of CCD and metabolomics may be an effective strategy for optimizing the formulation composition and identifying the mechanism of action of traditional chinese medicine. Dove 2019-11-21 /pmc/articles/PMC6876559/ /pubmed/31819368 http://dx.doi.org/10.2147/DDDT.S220314 Text en © 2019 Guo et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Guo, Zhili
Zhu, Yan
Xu, Wenjuan
Luo, Kaitao
Xiao, Hongbin
Wang, Zhong
Alteration of Amino Acid Profiling Influenced by the Active Ingredients of DanHong Injection After Prescription Optimization
title Alteration of Amino Acid Profiling Influenced by the Active Ingredients of DanHong Injection After Prescription Optimization
title_full Alteration of Amino Acid Profiling Influenced by the Active Ingredients of DanHong Injection After Prescription Optimization
title_fullStr Alteration of Amino Acid Profiling Influenced by the Active Ingredients of DanHong Injection After Prescription Optimization
title_full_unstemmed Alteration of Amino Acid Profiling Influenced by the Active Ingredients of DanHong Injection After Prescription Optimization
title_short Alteration of Amino Acid Profiling Influenced by the Active Ingredients of DanHong Injection After Prescription Optimization
title_sort alteration of amino acid profiling influenced by the active ingredients of danhong injection after prescription optimization
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876559/
https://www.ncbi.nlm.nih.gov/pubmed/31819368
http://dx.doi.org/10.2147/DDDT.S220314
work_keys_str_mv AT guozhili alterationofaminoacidprofilinginfluencedbytheactiveingredientsofdanhonginjectionafterprescriptionoptimization
AT zhuyan alterationofaminoacidprofilinginfluencedbytheactiveingredientsofdanhonginjectionafterprescriptionoptimization
AT xuwenjuan alterationofaminoacidprofilinginfluencedbytheactiveingredientsofdanhonginjectionafterprescriptionoptimization
AT luokaitao alterationofaminoacidprofilinginfluencedbytheactiveingredientsofdanhonginjectionafterprescriptionoptimization
AT xiaohongbin alterationofaminoacidprofilinginfluencedbytheactiveingredientsofdanhonginjectionafterprescriptionoptimization
AT wangzhong alterationofaminoacidprofilinginfluencedbytheactiveingredientsofdanhonginjectionafterprescriptionoptimization