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Antigout Effects of Plantago asiatica: Xanthine Oxidase Inhibitory Activities Assessed by Electrochemical Biosensing Method
The XOD inhibitory effects of Plantaginis Semen, that is, the seeds of P. asiatisca, and its representative four single compounds, acteoside, 1H-indolo-3-carbaldehyde, isoacteoside, and myristic acid, were evaluated by electron transfer signal blocking activities (ETSBA), which is based on the elect...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842727/ https://www.ncbi.nlm.nih.gov/pubmed/29681967 http://dx.doi.org/10.1155/2018/1364617 |
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author | Zeng, Jin-Xiang Wang, Juan Zhang, Shou-Wen Zhu, Ji-Xiao Li, Min Huang, Wei-Hua Wan, Jin-Yi Yao, Hai-Qiang Wang, Chong-Zhi Yuan, Chun-Su |
author_facet | Zeng, Jin-Xiang Wang, Juan Zhang, Shou-Wen Zhu, Ji-Xiao Li, Min Huang, Wei-Hua Wan, Jin-Yi Yao, Hai-Qiang Wang, Chong-Zhi Yuan, Chun-Su |
author_sort | Zeng, Jin-Xiang |
collection | PubMed |
description | The XOD inhibitory effects of Plantaginis Semen, that is, the seeds of P. asiatisca, and its representative four single compounds, acteoside, 1H-indolo-3-carbaldehyde, isoacteoside, and myristic acid, were evaluated by electron transfer signal blocking activities (ETSBA), which is based on the electron transfer signal of XOD enzymatic reaction. The blocking activities were detected using an electrochemical biosensing method. Compared with control, significant effects were observed after the addition of P. asiatica extract, acteoside, and 1H-indolo-3-carbaldehyde (all p < 0.05). The IC50 values of the extract and acteoside are 89.14 and 7.55 μg·mL(−1), respectively. The IC20 values of the extract, acteoside, and 1H-indolo-3-carbaldehyde are 24.28, 3.88, and 16.16 μg·mL(−1), respectively. Due to the relatively lower inhibitory potential of 1H-indolo-3-carbaldehyde, its IC50 was not obtained. In addition, isoacteoside and myristic acid did not show any XOD inhibitory effects. Our data demonstrated that the XOD inhibitory effects of the extract, acteoside, and 1H-indolo-3-carbaldehyde can be accurately evaluated by the ETSBA method. The results from this study indicated that Plantaginis Semen significantly inhibited XOD activities to reduce hyperuricemia and treat gout. The study also proves that measuring the electron transfer signal blocking activities is a simple, sensitive, and accurate method to evaluate the XOD inhibitory effects. |
format | Online Article Text |
id | pubmed-5842727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-58427272018-04-21 Antigout Effects of Plantago asiatica: Xanthine Oxidase Inhibitory Activities Assessed by Electrochemical Biosensing Method Zeng, Jin-Xiang Wang, Juan Zhang, Shou-Wen Zhu, Ji-Xiao Li, Min Huang, Wei-Hua Wan, Jin-Yi Yao, Hai-Qiang Wang, Chong-Zhi Yuan, Chun-Su Evid Based Complement Alternat Med Research Article The XOD inhibitory effects of Plantaginis Semen, that is, the seeds of P. asiatisca, and its representative four single compounds, acteoside, 1H-indolo-3-carbaldehyde, isoacteoside, and myristic acid, were evaluated by electron transfer signal blocking activities (ETSBA), which is based on the electron transfer signal of XOD enzymatic reaction. The blocking activities were detected using an electrochemical biosensing method. Compared with control, significant effects were observed after the addition of P. asiatica extract, acteoside, and 1H-indolo-3-carbaldehyde (all p < 0.05). The IC50 values of the extract and acteoside are 89.14 and 7.55 μg·mL(−1), respectively. The IC20 values of the extract, acteoside, and 1H-indolo-3-carbaldehyde are 24.28, 3.88, and 16.16 μg·mL(−1), respectively. Due to the relatively lower inhibitory potential of 1H-indolo-3-carbaldehyde, its IC50 was not obtained. In addition, isoacteoside and myristic acid did not show any XOD inhibitory effects. Our data demonstrated that the XOD inhibitory effects of the extract, acteoside, and 1H-indolo-3-carbaldehyde can be accurately evaluated by the ETSBA method. The results from this study indicated that Plantaginis Semen significantly inhibited XOD activities to reduce hyperuricemia and treat gout. The study also proves that measuring the electron transfer signal blocking activities is a simple, sensitive, and accurate method to evaluate the XOD inhibitory effects. Hindawi 2018-02-22 /pmc/articles/PMC5842727/ /pubmed/29681967 http://dx.doi.org/10.1155/2018/1364617 Text en Copyright © 2018 Jin-Xiang Zeng et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zeng, Jin-Xiang Wang, Juan Zhang, Shou-Wen Zhu, Ji-Xiao Li, Min Huang, Wei-Hua Wan, Jin-Yi Yao, Hai-Qiang Wang, Chong-Zhi Yuan, Chun-Su Antigout Effects of Plantago asiatica: Xanthine Oxidase Inhibitory Activities Assessed by Electrochemical Biosensing Method |
title | Antigout Effects of Plantago asiatica: Xanthine Oxidase Inhibitory Activities Assessed by Electrochemical Biosensing Method |
title_full | Antigout Effects of Plantago asiatica: Xanthine Oxidase Inhibitory Activities Assessed by Electrochemical Biosensing Method |
title_fullStr | Antigout Effects of Plantago asiatica: Xanthine Oxidase Inhibitory Activities Assessed by Electrochemical Biosensing Method |
title_full_unstemmed | Antigout Effects of Plantago asiatica: Xanthine Oxidase Inhibitory Activities Assessed by Electrochemical Biosensing Method |
title_short | Antigout Effects of Plantago asiatica: Xanthine Oxidase Inhibitory Activities Assessed by Electrochemical Biosensing Method |
title_sort | antigout effects of plantago asiatica: xanthine oxidase inhibitory activities assessed by electrochemical biosensing method |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842727/ https://www.ncbi.nlm.nih.gov/pubmed/29681967 http://dx.doi.org/10.1155/2018/1364617 |
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