Anaphylactoid reactions induced by Shuanghuanglian injection and Shenmai injection and metabolomics analysis
Introduction: Shuanghuanglian injection (lyophilized) (SHLI) is commonly used to treat respiratory tract infection. Shenmai injection (SMI) is mainly used to treat cardiovascular diseases. Despite their widespread clinical use, anaphylactoid reactions (ARs) induced by SHLI and SMI have been reported...
| Published in: | Frontiers in Pharmacology |
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| Main Authors: | , , , , , , , , , |
| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2023-07-01
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fphar.2023.1200199/full |
| _version_ | 1851845182215946240 |
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| author | Chi Zhang Chi Zhang Linqi Ouyang Xili Zhang Xili Zhang Wen Wen Wen Wen Yuqin Xu Shan Li Yingyu Li Yingyu Li Fuyuan He Fuyuan He Wenlong Liu Wenlong Liu Hongyu Liu |
| author_facet | Chi Zhang Chi Zhang Linqi Ouyang Xili Zhang Xili Zhang Wen Wen Wen Wen Yuqin Xu Shan Li Yingyu Li Yingyu Li Fuyuan He Fuyuan He Wenlong Liu Wenlong Liu Hongyu Liu |
| author_sort | Chi Zhang |
| collection | DOAJ |
| container_title | Frontiers in Pharmacology |
| description | Introduction: Shuanghuanglian injection (lyophilized) (SHLI) is commonly used to treat respiratory tract infection. Shenmai injection (SMI) is mainly used to treat cardiovascular diseases. Despite their widespread clinical use, anaphylactoid reactions (ARs) induced by SHLI and SMI have been reported, which have attracted broad attention. However, the impact of ARs on metabolic changes and the underlying mechanisms are still unclear.Methods: ICR mice were used as model animals and were treated with normal saline, C48/80, SHLI and SMI, respectively. The behavior of mice, auricle blue staining and Evans Blue exudation were used as indexes to evaluate the sensitization of SHLI and SMI and determine the optimal sensitization dose. Anaphylactoid mice model was established based on the optimal dose and enzyme-linked immunosorbent assay (ELISA) was used to model verification. Afterwards, plasma samples of administered mice were profiled by LC-MS metabolomics and analyzed to evaluate the changes in metabolites.Results: High doses of both SHLI and SMI can induce severe anaphylactoid reactions while the reaction induced by SMI was weaker. A Partial Least-Squares Discriminant Analysis (PLS-DA) score plot indicated that following administration, significant metabolic changes occurred in mice. 23 distinct metabolites, including deoxycholic acid, histamine, and 5-hydroxytryptophan, were identified in the SHLI groups. 11 distinct metabolites, including androsterone, 17α-hydroxypregnenolone, and 5-hydroxyindoleacetate, were identified in the SMI groups. Meanwhile, different metabolic pathways of SHLI and SMI were predicted by different metabolites. The associated metabolic pathways include steroid hormone biosynthesis, tryptophan metabolism, histidine metabolism, arachidonic acid metabolism, nicotinate and nicotinamide metabolism, and primary bile acid biosynthesis.Conclusion: Study showed that both SHLI and SMI can induce varying degrees of anaphylactoid reactions, a positive correlation between response intensity and dose was observed. Metabolomics showed that SHLI and SMI may promote the simultaneous release of hormones and inflammatory factors by disturbing relevant metabolic pathways, while SMI may also inhibit the release of inflammatory factors in arachidonic acid metabolic pathway, indicating both pro-inflammatory and anti-inflammatory effects. This study will serve as a reference for developing a new approach to evaluate the safety of SHLI and SMI from perspective of susceptible drug varieties. However, ARs mechanism requires further verification. |
| format | Article |
| id | doaj-art-9acfe51ec3d44dfaa802ea6d8b8a93b3 |
| institution | Directory of Open Access Journals |
| issn | 1663-9812 |
| language | English |
| publishDate | 2023-07-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| spelling | doaj-art-9acfe51ec3d44dfaa802ea6d8b8a93b32025-08-19T22:26:35ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122023-07-011410.3389/fphar.2023.12001991200199Anaphylactoid reactions induced by Shuanghuanglian injection and Shenmai injection and metabolomics analysisChi Zhang0Chi Zhang1Linqi Ouyang2Xili Zhang3Xili Zhang4Wen Wen5Wen Wen6Yuqin Xu7Shan Li8Yingyu Li9Yingyu Li10Fuyuan He11Fuyuan He12Wenlong Liu13Wenlong Liu14Hongyu Liu15The First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaThe First Hospital of Hunan University of Chinese Medicine, Changsha, ChinaIntroduction: Shuanghuanglian injection (lyophilized) (SHLI) is commonly used to treat respiratory tract infection. Shenmai injection (SMI) is mainly used to treat cardiovascular diseases. Despite their widespread clinical use, anaphylactoid reactions (ARs) induced by SHLI and SMI have been reported, which have attracted broad attention. However, the impact of ARs on metabolic changes and the underlying mechanisms are still unclear.Methods: ICR mice were used as model animals and were treated with normal saline, C48/80, SHLI and SMI, respectively. The behavior of mice, auricle blue staining and Evans Blue exudation were used as indexes to evaluate the sensitization of SHLI and SMI and determine the optimal sensitization dose. Anaphylactoid mice model was established based on the optimal dose and enzyme-linked immunosorbent assay (ELISA) was used to model verification. Afterwards, plasma samples of administered mice were profiled by LC-MS metabolomics and analyzed to evaluate the changes in metabolites.Results: High doses of both SHLI and SMI can induce severe anaphylactoid reactions while the reaction induced by SMI was weaker. A Partial Least-Squares Discriminant Analysis (PLS-DA) score plot indicated that following administration, significant metabolic changes occurred in mice. 23 distinct metabolites, including deoxycholic acid, histamine, and 5-hydroxytryptophan, were identified in the SHLI groups. 11 distinct metabolites, including androsterone, 17α-hydroxypregnenolone, and 5-hydroxyindoleacetate, were identified in the SMI groups. Meanwhile, different metabolic pathways of SHLI and SMI were predicted by different metabolites. The associated metabolic pathways include steroid hormone biosynthesis, tryptophan metabolism, histidine metabolism, arachidonic acid metabolism, nicotinate and nicotinamide metabolism, and primary bile acid biosynthesis.Conclusion: Study showed that both SHLI and SMI can induce varying degrees of anaphylactoid reactions, a positive correlation between response intensity and dose was observed. Metabolomics showed that SHLI and SMI may promote the simultaneous release of hormones and inflammatory factors by disturbing relevant metabolic pathways, while SMI may also inhibit the release of inflammatory factors in arachidonic acid metabolic pathway, indicating both pro-inflammatory and anti-inflammatory effects. This study will serve as a reference for developing a new approach to evaluate the safety of SHLI and SMI from perspective of susceptible drug varieties. However, ARs mechanism requires further verification.https://www.frontiersin.org/articles/10.3389/fphar.2023.1200199/fullshuanghuanglian injectionshenmai injectionanaphylactoid reactionsLC-MS metabolomicsmetabolic pathways |
| spellingShingle | Chi Zhang Chi Zhang Linqi Ouyang Xili Zhang Xili Zhang Wen Wen Wen Wen Yuqin Xu Shan Li Yingyu Li Yingyu Li Fuyuan He Fuyuan He Wenlong Liu Wenlong Liu Hongyu Liu Anaphylactoid reactions induced by Shuanghuanglian injection and Shenmai injection and metabolomics analysis shuanghuanglian injection shenmai injection anaphylactoid reactions LC-MS metabolomics metabolic pathways |
| title | Anaphylactoid reactions induced by Shuanghuanglian injection and Shenmai injection and metabolomics analysis |
| title_full | Anaphylactoid reactions induced by Shuanghuanglian injection and Shenmai injection and metabolomics analysis |
| title_fullStr | Anaphylactoid reactions induced by Shuanghuanglian injection and Shenmai injection and metabolomics analysis |
| title_full_unstemmed | Anaphylactoid reactions induced by Shuanghuanglian injection and Shenmai injection and metabolomics analysis |
| title_short | Anaphylactoid reactions induced by Shuanghuanglian injection and Shenmai injection and metabolomics analysis |
| title_sort | anaphylactoid reactions induced by shuanghuanglian injection and shenmai injection and metabolomics analysis |
| topic | shuanghuanglian injection shenmai injection anaphylactoid reactions LC-MS metabolomics metabolic pathways |
| url | https://www.frontiersin.org/articles/10.3389/fphar.2023.1200199/full |
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