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[采用“靶点垂钓”策略鉴定寿辉通便胶囊的肠道直接靶点]

[Identification of intestine direct targets of Shouhui Tongbian Capsules using "target fishing" strategy].

作者信息

Guo Qiang, Yao Lu, Liu Zhong, Yao Jing-Chun, Tu Peng-Fei, Zeng Ke-Wu

机构信息

State Key Laboratory of Natural and Biomimetic Drugs,School of Pharmaceutical Sciences,Peking University Beijing 100191,China.

State Key Laboratory of Generic Manufacture Technology of Chinese Traditional Medicine,Lunan Pharmaceutical Group Co.,Ltd. Linyi 276006,China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2021 Feb;46(3):505-510. doi: 10.19540/j.cnki.cjcmm.20201125.403.


DOI:10.19540/j.cnki.cjcmm.20201125.403
PMID:33645013
Abstract

"Target fishing" strategy was used to investigate the direct targets and mechanism of Shouhui Tongbian Capsules on relaxing bowel. Magnetic beads cross-linked with the chemical constituents from Shouhui Tongbian Capsules were prepared. The potential target proteins were captured from the total protein lysates of rat intestine using the beads. The captured proteins were further identified by LC-MS/MS, and the associated pathways were analyzed by Cytoscape. RESULTS:: showed that 138 potential target proteins were identified, which were involved in eight signaling pathways, including tricarboxylic acid cycle, pyrimidine metabolism, sulfur metabolism, fatty acid degradation, alanine/aspartate/glutamate metabolism, arginine/proline metabolism, valine/leucine/isoleucine degradation, and β-alanine metabolism. Taken together, Shouhui Tongbian Capsules may exert relaxing bowel effect by acting on multiple signaling pathways to promote intestinal gurgling, inhibit inflammation, as well as improve intestinal barrier function, intestinal water secretion, and intestinal flora.

摘要

采用“靶向垂钓”策略研究首荟通便胶囊润肠通便的直接靶点及作用机制。制备与首荟通便胶囊化学成分交联的磁珠,利用磁珠从大鼠肠组织总蛋白裂解物中捕获潜在的靶蛋白。通过液相色谱-串联质谱法(LC-MS/MS)进一步鉴定捕获的蛋白,并利用Cytoscape软件分析相关通路。结果显示,共鉴定出138个潜在靶蛋白,涉及三羧酸循环、嘧啶代谢、硫代谢、脂肪酸降解、丙氨酸/天冬氨酸/谷氨酸代谢、精氨酸/脯氨酸代谢、缬氨酸/亮氨酸/异亮氨酸降解和β-丙氨酸代谢8条信号通路。综上所述,首荟通便胶囊可能通过作用于多条信号通路,促进肠道蠕动、抑制炎症以及改善肠道屏障功能、肠道水分泌和肠道菌群,从而发挥润肠通便作用。

相似文献

[1]
[Identification of intestine direct targets of Shouhui Tongbian Capsules using "target fishing" strategy].

Zhongguo Zhong Yao Za Zhi. 2021-2

[2]
[Mechanism of Shouhui Tongbian Capsules in treating constipation based on network pharmacology and molecular docking].

Zhongguo Zhong Yao Za Zhi. 2021-2

[3]
[Therapeutic effect and mechanism of Shouhui Tongbian Capsules on slow transit constipation model mice].

Zhongguo Zhong Yao Za Zhi. 2021-2

[4]
[Metabonomics study of Shouhui Tongbian Capsules in slow transit constipation based on UPLC-ESI-QE-Orbitrap-MS].

Zhongguo Zhong Yao Za Zhi. 2021-2

[5]
[Molecular mechanism study of Shouhui Tongbian Capsules on promoting energy metabolism of gastrointestinal stromal cells].

Zhongguo Zhong Yao Za Zhi. 2021-2

[6]
Shouhui Tongbian Capsules induce regression of inflammation to improve intestinal barrier in mice with constipation by targeted binding to Prkaa1: With no obvious toxicity.

Biomed Pharmacother. 2023-5

[7]
Integrative microbiomics, proteomics and lipidomics studies unraveled the preventive mechanism of Shouhui Tongbian Capsules on cerebral ischemic stroke injury.

J Ethnopharmacol. 2025-1-30

[8]
Observation on the Efficacy of Shouhui Tongbian Capsule in the Treatment of Functional Constipation and Study on Its Regulatory Effect on Intestinal Flora.

J Healthc Eng. 2021

[9]
Integration of UPLC-MS/MS-based metabolomics and desorption electrospray ionization-mass spectrometry imaging reveals that Shouhui Tongbian Capsule alleviates slow transit constipation by regulating bile acid metabolism.

J Chromatogr B Analyt Technol Biomed Life Sci. 2024-10-15

[10]
Shouhui Tongbian Capsule ameliorates constipation via gut microbiota-5-HT-intestinal motility axis.

Biomed Pharmacother. 2022-10

引用本文的文献

[1]
Molecular Target Identification of Gossypol Against Cervical Cancer Based on Target Fishing Technology.

Pharmaceutics. 2025-6-30

[2]
Global Identification of Anti-Melanoma Cellular Targets by Photochemically Induced Coupling of Reactions on the Surface of Magnetic Particles.

Pharmaceutics. 2024-12-2

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