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Qualitative analysis of chemical components in Berberis kaschgarica Rupr. and study on the in vitro anti-inflammatory effects of its alkaloids
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  • Published: 02 March 2026

Qualitative analysis of chemical components in Berberis kaschgarica Rupr. and study on the in vitro anti-inflammatory effects of its alkaloids

  • Saimire Ainiwaer1,2,3,4 na1,
  • Dilihuma Dilimulati1,2,3,4 na1,
  • Ainiwaer Wumaier1,2,3,4 &
  • …
  • Wenting Zhou1,2,3,4 

Scientific Reports , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biochemistry
  • Cardiology
  • Diseases
  • Drug discovery
  • Plant sciences

Abstract

Berberis kaschgarica Rupr. fruits (BKF) can reduce blood pressure, regulate blood lipid levels, and exert anti-inflammatory and anti-oxidative effects. Additionally, alkaloids are among the active components in BKF. Sensitive and selective high-performance liquid chromatography with mass spectrometry, network pharmacology, and bioinformatic analysis was conducted. We identified 544 metabolites and 105 secondary metabolites from BFK. Among the secondary metabolites, 24 were alkaloids. Moreover, there were 583 potential drug targets and 4,481 human anti-atherosclerosis targets. Finally, 366 intersecting targets of BFK against atherosclerosis were identified. These targets were enriched in 546 terms in biological processes, 48 terms in cell components, 121 terms in molecular functions, and 36 signaling pathways. Notably, 18 of the 24 alkaloids were fat-soluble alkaloids (FSA), and the remaining 6 were water-soluble alkaloids (WSA). Because oxyberberine (OBB) was predicted to have an ideal anti-atherosclerosis effect and was further studied. We established four intervention groups: FSA, WSA, total alkaloids (TA), and OBB. The effects of these alkaloids on caspase-11-induced pyroptosis and TLR4-induced inflammation in LPS-stimulated mouse macrophages in vitro were explored. The anti-pyroptosis results demonstrated significant evaluation in caspase-11, caspase-1, IL-1β, IL-18, and, GSDMD. Additionally, there were significant decreases in MMP3 and MMP9 in the supernatant, as well as the expression of TLR4 and pSTAT3. Conclusively, BKF contains numerous effective components, making it a valuable natural medicinal material with substantial developmental and utilitarian potential. In in vitro experiments, the alkaloids from BKF can reduce the LPS-induced expression of caspase-11 and GSDMD. Compared with previous studies on BKF, which had gaps in systematic identification of bioactive subtypes via basic colorimetry and unclear anti-AS mechanisms. our study advances research by using UPLC-MS/MS for the first time to identify 544 metabolitesin BKF, establishing a comprehensive metabolite profile and integrating network pharmacology and in vitro assays to first link BKF alkaloids to regulating caspase-11-mediated pyroptosis and TLR4-induced inflammation. Moreover, our findings contribute to compositional innovation, mechanistic breakthroughs, and translational value.

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Data availability

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

BKF:

Berberis kaschgarica Rupr. fruits

FSA:

Fat-soluble alkaloids

OBB:

Oxyberberine

TA:

Total alkaloids

WSA:

Water-soluble alkaloids

BKF:

Berberis kaschgarica Rupr. fruits

FSA:

Fat-soluble alkaloids

OBB:

Oxyberberine

TA:

Total alkaloids

WSA:

Water-soluble alkaloids

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Funding

The authors appreciate financial support from the funding of the Natural Science Foundation for Distinguished Young Scholars of Xinjiang Autonomous Region (2025D01E32); Tianshan Talents-Youth Science and Technology Innovation Talents Training Program of Xinjiang Autonomous Region (2022TSYCCX0035); ; Xinjiang Key Laboratory of Natural Medicines Active Components and Drug Release Technology (XJDX1713); Xinjiang Key Laboratory of Biopharmaceuticals and Medical Devices (2023); Engineering Research Center of Xinjiang and Central Asian Medicine Resources, Ministry of Education (2023).

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  1. These authors contributed equally to this work: Saimire Ainiwaer and Dilihuma Dilimulati.

Authors and Affiliations

  1. Department of Pharmacology, School of Pharmacy, Xinjiang Medical University, Urumqi, Xinjiang, P.R. China

    Saimire Ainiwaer, Dilihuma Dilimulati, Ainiwaer Wumaier & Wenting Zhou

  2. Xinjiang Key Laboratory of Active Components and Drug Release Technology of Natural Medicines, Urumqi, 830017, Xinjiang, China

    Saimire Ainiwaer, Dilihuma Dilimulati, Ainiwaer Wumaier & Wenting Zhou

  3. Xinjiang Key Laboratory of Biopharmaceuticals and Medical Devices, Urumqi, 830017, China

    Saimire Ainiwaer, Dilihuma Dilimulati, Ainiwaer Wumaier & Wenting Zhou

  4. Engineering Research Center of Xinjiang and Central Asian Medicine Resources, Ministry of Education, Urumqi, 830017, China

    Saimire Ainiwaer, Dilihuma Dilimulati, Ainiwaer Wumaier & Wenting Zhou

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Contributions

Conceptualization, S.A. and D.D.; methodology, S.A.; software, D.D; validation, S.A.; formal analysis, S.A. and D.D.; investigation, W.Z. and A.W.; data curation, S.A.; writing—original draft preparation, S.A.; writing—review and editing, W.Z. and A.W.; visualization, W.Z.; supervision, W.Z. and A.W.; project administration, W.Z.; funding acquisition, W.Z. All authors have read and agreed to the published version of the manuscript. Figure 12 in the manuscript was drawn in Figdraw.

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Correspondence to Ainiwaer Wumaier or Wenting Zhou.

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Ainiwaer, S., Dilimulati, D., Wumaier, A. et al. Qualitative analysis of chemical components in Berberis kaschgarica Rupr. and study on the in vitro anti-inflammatory effects of its alkaloids. Sci Rep (2026). https://doi.org/10.1038/s41598-026-41856-x

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  • Received: 06 September 2025

  • Accepted: 23 February 2026

  • Published: 02 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-41856-x

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Keywords

  • Berberis Kaschgarica Rupr.
  • Alkaloids
  • Inflammation
  • Pyroptosis
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