Lujie Lin, Zhuqian Tang, Huijuan Xie, Lixin Yang, Bin Yang, Hua Li
{"title":"基于多技术数据融合的五味子和五味子化学特征和抗氧化活性差异表征","authors":"Lujie Lin, Zhuqian Tang, Huijuan Xie, Lixin Yang, Bin Yang, Hua Li","doi":"10.3390/molecules29204865","DOIUrl":null,"url":null,"abstract":"<p><p><i>Schisandra chinensis</i> (Turcz.) Baill. (<i>S. chinensis</i>) and <i>Schisandra sphenanthera</i> Rehd. et Wils (<i>S. sphenanthera</i>) are called \"Wuweizi\" in traditional Chinese medicine, and they have distinct clinical applications. To systematically compare the differential characteristics of <i>S. chinensis</i> and <i>S. sphenanthera</i>, this study employed ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS) and gas chromatography-mass spectrometry (GC-MS) to construct chemical profiles of these two species from different regions. In total, 31 non-volatiles and 37 volatiles were identified in <i>S. chinensis</i>, whereas 40 non-volatiles and 34 volatiles were detected in <i>S. sphenanthera</i>. A multivariate statistical analysis showed that the non-volatiles tigloygomisin P, schisandrol A, schisantherin C, and 6-O-benzoylgomisin O and the volatiles ylangene, γ-muurolene, and β-pinene distinguish these species. Additionally, the metabolism of oxygen free radicals can contribute to the development of various diseases, including cardiovascular and neurodegenerative diseases. Therefore, antioxidant activities were evaluated using 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2'-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS) scavenging assays. The results showed that <i>S. sphenanthera</i> exhibited significantly higher antioxidant potential. A gray relational analysis indicated that the key contributors to the antioxidant activity of <i>S. chinensis</i> were schisandrol A, gomisin G, schisantherin C, pregomisin, gomisin J, and schisantherin B. For <i>S. sphenanthera</i>, the key contributors included gomisin K2, schisantherin B, gomisin J, pregomisin, schisantherin C, schisandrin, gomisin G, schisantherin A, schisanhenol, and α-pinene. The identification of the differential chemical markers and the evaluation of the antioxidant activities provide a foundation for further research into the therapeutic applications of these species. This innovative study provides a robust framework for the quality control and therapeutic application of <i>S. chinensis</i> and <i>S. sphenanthera</i>, offering new insights into their medicinal potential.</p>","PeriodicalId":19041,"journal":{"name":"Molecules","volume":null,"pages":null},"PeriodicalIF":4.2000,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11510710/pdf/","citationCount":"0","resultStr":"{\"title\":\"Characterization of Differences in Chemical Profiles and Antioxidant Activities of <i>Schisandra chinensis</i> and <i>Schisandra sphenanthera</i> Based on Multi-Technique Data Fusion.\",\"authors\":\"Lujie Lin, Zhuqian Tang, Huijuan Xie, Lixin Yang, Bin Yang, Hua Li\",\"doi\":\"10.3390/molecules29204865\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Schisandra chinensis</i> (Turcz.) Baill. (<i>S. chinensis</i>) and <i>Schisandra sphenanthera</i> Rehd. et Wils (<i>S. sphenanthera</i>) are called \\\"Wuweizi\\\" in traditional Chinese medicine, and they have distinct clinical applications. To systematically compare the differential characteristics of <i>S. chinensis</i> and <i>S. sphenanthera</i>, this study employed ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS) and gas chromatography-mass spectrometry (GC-MS) to construct chemical profiles of these two species from different regions. In total, 31 non-volatiles and 37 volatiles were identified in <i>S. chinensis</i>, whereas 40 non-volatiles and 34 volatiles were detected in <i>S. sphenanthera</i>. A multivariate statistical analysis showed that the non-volatiles tigloygomisin P, schisandrol A, schisantherin C, and 6-O-benzoylgomisin O and the volatiles ylangene, γ-muurolene, and β-pinene distinguish these species. Additionally, the metabolism of oxygen free radicals can contribute to the development of various diseases, including cardiovascular and neurodegenerative diseases. Therefore, antioxidant activities were evaluated using 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2'-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS) scavenging assays. The results showed that <i>S. sphenanthera</i> exhibited significantly higher antioxidant potential. A gray relational analysis indicated that the key contributors to the antioxidant activity of <i>S. chinensis</i> were schisandrol A, gomisin G, schisantherin C, pregomisin, gomisin J, and schisantherin B. For <i>S. sphenanthera</i>, the key contributors included gomisin K2, schisantherin B, gomisin J, pregomisin, schisantherin C, schisandrin, gomisin G, schisantherin A, schisanhenol, and α-pinene. The identification of the differential chemical markers and the evaluation of the antioxidant activities provide a foundation for further research into the therapeutic applications of these species. 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Characterization of Differences in Chemical Profiles and Antioxidant Activities of Schisandra chinensis and Schisandra sphenanthera Based on Multi-Technique Data Fusion.
Schisandra chinensis (Turcz.) Baill. (S. chinensis) and Schisandra sphenanthera Rehd. et Wils (S. sphenanthera) are called "Wuweizi" in traditional Chinese medicine, and they have distinct clinical applications. To systematically compare the differential characteristics of S. chinensis and S. sphenanthera, this study employed ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS) and gas chromatography-mass spectrometry (GC-MS) to construct chemical profiles of these two species from different regions. In total, 31 non-volatiles and 37 volatiles were identified in S. chinensis, whereas 40 non-volatiles and 34 volatiles were detected in S. sphenanthera. A multivariate statistical analysis showed that the non-volatiles tigloygomisin P, schisandrol A, schisantherin C, and 6-O-benzoylgomisin O and the volatiles ylangene, γ-muurolene, and β-pinene distinguish these species. Additionally, the metabolism of oxygen free radicals can contribute to the development of various diseases, including cardiovascular and neurodegenerative diseases. Therefore, antioxidant activities were evaluated using 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2'-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS) scavenging assays. The results showed that S. sphenanthera exhibited significantly higher antioxidant potential. A gray relational analysis indicated that the key contributors to the antioxidant activity of S. chinensis were schisandrol A, gomisin G, schisantherin C, pregomisin, gomisin J, and schisantherin B. For S. sphenanthera, the key contributors included gomisin K2, schisantherin B, gomisin J, pregomisin, schisantherin C, schisandrin, gomisin G, schisantherin A, schisanhenol, and α-pinene. The identification of the differential chemical markers and the evaluation of the antioxidant activities provide a foundation for further research into the therapeutic applications of these species. This innovative study provides a robust framework for the quality control and therapeutic application of S. chinensis and S. sphenanthera, offering new insights into their medicinal potential.
期刊介绍：
Molecules (ISSN 1420-3049, CODEN: MOLEFW) is an open access journal of synthetic organic chemistry and natural product chemistry. All articles are peer-reviewed and published continously upon acceptance. Molecules is published by MDPI, Basel, Switzerland. Our aim is to encourage chemists to publish as much as possible their experimental detail, particularly synthetic procedures and characterization information. There is no restriction on the length of the experimental section. In addition, availability of compound samples is published and considered as important information. Authors are encouraged to register or deposit their chemical samples through the non-profit international organization Molecular Diversity Preservation International (MDPI). Molecules has been launched in 1996 to preserve and exploit molecular diversity of both, chemical information and chemical substances.
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