Proteomics analysis reveals the mechanism of anemoside B4 in treating clinical mastitis in dairy cows

(1) Background: The therapeutic efficacy of AB4 in cows with CM is well-established, but the specific mechanism remains to be explored. This study was based on Label free relative quantitative proteomics technology to reveal the internal mechanism of AB4 treatment of CM; (2) Methods: Twelve healthy...

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Main Authors: Zeru Zhang, Yuquan Zhao, Zhetong Su, Ke Dong, Zhicai Zuo, Yixin Huang, Shumin Yu, Suizhong Cao, Liuhong Shen
Format: Article
Language:English
Published: Taylor & Francis Group 2025-12-01
Series:Italian Journal of Animal Science
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Online Access:http://dx.doi.org/10.1080/1828051X.2024.2441345
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author Zeru Zhang
Yuquan Zhao
Zhetong Su
Ke Dong
Zhicai Zuo
Yixin Huang
Shumin Yu
Suizhong Cao
Liuhong Shen
author_facet Zeru Zhang
Yuquan Zhao
Zhetong Su
Ke Dong
Zhicai Zuo
Yixin Huang
Shumin Yu
Suizhong Cao
Liuhong Shen
author_sort Zeru Zhang
collection DOAJ
description (1) Background: The therapeutic efficacy of AB4 in cows with CM is well-established, but the specific mechanism remains to be explored. This study was based on Label free relative quantitative proteomics technology to reveal the internal mechanism of AB4 treatment of CM; (2) Methods: Twelve healthy Chinese Holstein cows (group C) and twelve Chinese Holstein cows (group T) with CM were selected. Administer 30 mL of AB4 via intramuscular injection to cows with CM once per day, for 7 consecutive days. The tail venous blood of group C on any day and group T before medication on day 1 (designated as T1) and after medication on day 7 (designated as T2) were collected. Randomly divide the samples from each of the three groups into three subgroups (three biological replicates, with each replicate consisting of an equal mixture of four plasma samples). They are labelled C1, C2, C3 and T1-1, T1-2, T1-3, T2-1, T2-2, T2-3. The differential proteins of AB4 in the treatment of CM were screened and bioinformatic analysis was performed; (3) Results: AB4 could regulate the levels of HSPs and other proteins, participate in chemokine signal transduction, leukocyte migration across endothelial cells, MAPKs pathway and other pathways to improve the inflammatory response of the body. In addition, the cured cows showed significantly higher complement lev-els, b-defensin 12 levels, and the ability to regulate lipid metabolism compared to diseased and healthy cows, suggesting that AB4 can directly activate C2, triggering downstream responses to activate the complement system, while stimulating defensins secretion and regulating lipid metabolism.
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publishDate 2025-12-01
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series Italian Journal of Animal Science
spelling doaj-art-90b362b22e874cd1bce8d3ffef61b29e2025-01-02T11:34:22ZengTaylor & Francis GroupItalian Journal of Animal Science1594-40771828-051X2025-12-01241788810.1080/1828051X.2024.24413452441345Proteomics analysis reveals the mechanism of anemoside B4 in treating clinical mastitis in dairy cowsZeru Zhang0Yuquan Zhao1Zhetong Su2Ke Dong3Zhicai Zuo4Yixin Huang5Shumin Yu6Suizhong Cao7Liuhong Shen8The Key Laboratory of Animal Disease and Human Health of Sichuan Province, The Medical Research Center for Cow Disease, College of Veterinary Medicine, Sichuan Agricultural UniversityThe Key Laboratory of Animal Disease and Human Health of Sichuan Province, The Medical Research Center for Cow Disease, College of Veterinary Medicine, Sichuan Agricultural UniversityResearch and Development Center, Guangxi Innovates Medical Technology Co., LtdResearch and Development Center, Sichuan Yuqiang Materia Medica Biotechnology Co., LtdThe Key Laboratory of Animal Disease and Human Health of Sichuan Province, The Medical Research Center for Cow Disease, College of Veterinary Medicine, Sichuan Agricultural UniversityThe Key Laboratory of Animal Disease and Human Health of Sichuan Province, The Medical Research Center for Cow Disease, College of Veterinary Medicine, Sichuan Agricultural UniversityThe Key Laboratory of Animal Disease and Human Health of Sichuan Province, The Medical Research Center for Cow Disease, College of Veterinary Medicine, Sichuan Agricultural UniversityThe Key Laboratory of Animal Disease and Human Health of Sichuan Province, The Medical Research Center for Cow Disease, College of Veterinary Medicine, Sichuan Agricultural UniversityThe Key Laboratory of Animal Disease and Human Health of Sichuan Province, The Medical Research Center for Cow Disease, College of Veterinary Medicine, Sichuan Agricultural University(1) Background: The therapeutic efficacy of AB4 in cows with CM is well-established, but the specific mechanism remains to be explored. This study was based on Label free relative quantitative proteomics technology to reveal the internal mechanism of AB4 treatment of CM; (2) Methods: Twelve healthy Chinese Holstein cows (group C) and twelve Chinese Holstein cows (group T) with CM were selected. Administer 30 mL of AB4 via intramuscular injection to cows with CM once per day, for 7 consecutive days. The tail venous blood of group C on any day and group T before medication on day 1 (designated as T1) and after medication on day 7 (designated as T2) were collected. Randomly divide the samples from each of the three groups into three subgroups (three biological replicates, with each replicate consisting of an equal mixture of four plasma samples). They are labelled C1, C2, C3 and T1-1, T1-2, T1-3, T2-1, T2-2, T2-3. The differential proteins of AB4 in the treatment of CM were screened and bioinformatic analysis was performed; (3) Results: AB4 could regulate the levels of HSPs and other proteins, participate in chemokine signal transduction, leukocyte migration across endothelial cells, MAPKs pathway and other pathways to improve the inflammatory response of the body. In addition, the cured cows showed significantly higher complement lev-els, b-defensin 12 levels, and the ability to regulate lipid metabolism compared to diseased and healthy cows, suggesting that AB4 can directly activate C2, triggering downstream responses to activate the complement system, while stimulating defensins secretion and regulating lipid metabolism.http://dx.doi.org/10.1080/1828051X.2024.2441345anemoside b4clinical mastitiscowsproteomics
spellingShingle Zeru Zhang
Yuquan Zhao
Zhetong Su
Ke Dong
Zhicai Zuo
Yixin Huang
Shumin Yu
Suizhong Cao
Liuhong Shen
Proteomics analysis reveals the mechanism of anemoside B4 in treating clinical mastitis in dairy cows
Italian Journal of Animal Science
anemoside b4
clinical mastitis
cows
proteomics
title Proteomics analysis reveals the mechanism of anemoside B4 in treating clinical mastitis in dairy cows
title_full Proteomics analysis reveals the mechanism of anemoside B4 in treating clinical mastitis in dairy cows
title_fullStr Proteomics analysis reveals the mechanism of anemoside B4 in treating clinical mastitis in dairy cows
title_full_unstemmed Proteomics analysis reveals the mechanism of anemoside B4 in treating clinical mastitis in dairy cows
title_short Proteomics analysis reveals the mechanism of anemoside B4 in treating clinical mastitis in dairy cows
title_sort proteomics analysis reveals the mechanism of anemoside b4 in treating clinical mastitis in dairy cows
topic anemoside b4
clinical mastitis
cows
proteomics
url http://dx.doi.org/10.1080/1828051X.2024.2441345
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