沙台合剂通过调节AQP5、NF-κB和p38 MAPK信号通路缓解Sjögren疾病性口干症。

IF 5.1 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-09-09 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S526278
Fangbin Liu, Jiyuan Chen, Chunai Gong, Minyan Chen, Gang Yang, Chun Chen, Ru Yao, Shengnan Li, Rong Wang, Yongfang Yuan
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引用次数: 0

摘要

简介:口干症通常由Sjögren疾病(SjD)或头颈部放疗引起,严重损害患者的生活质量,但有效的治疗方法仍然有限。中药由于其良好的疗效和低毒性,提供了很有前途的替代品。沙台合剂(STHJ)是一种旨在滋阴益气的复方中药配方,显示出治疗口干症的潜力。本研究旨在建立STHJ的质量控制标准,并评价其在口干症模型中的药效学、安全性和作用机制。方法:以黄芪和地黄的质量标记为重点,建立了中药三甲汤12种成分的定性鉴别方法,并对有效成分进行了定量分析。在Sprague-Dawley (SD)大鼠和BALB/c小鼠中使用毒蕈碱受体拮抗剂诱导口干。对大鼠主要脏器和唾液腺进行组织学检查,并通过免疫组织化学和免疫印迹法检测水通道蛋白-5 (AQP5)在颌下腺中的表达。通过唾液分泌、腺体重量和生化指标评估治疗效果。采用颌下腺免疫荧光法和ELISA法检测SjD小鼠的炎症因子(TNF-α、TNF-β、IFN-γ、IL-6)和自身抗体(抗ssa /Ro、抗ssb /La)。Western blotting检测NF-κB和MAPK p38通路的激活情况。对SD大鼠进行急性毒性评价。结果:STHJ可显著改善口干症状,增加唾液分泌量,上调AQP5,保留腺体形态。减少纤维化,抑制炎症细胞因子表达,抑制免疫细胞浸润。机制上,STHJ减弱NF-κB和MAPK p38通路的激活。未观察到急性毒性。结论:本研究首次建立了STHJ的质量控制标准,并在口干症模型中证实了其抗炎和免疫调节作用。研究结果表明,STHJ可能是一种安全有效的治疗SjD相关口干症和其他疾病的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Shatai Heji Mitigates Sjögren Disease-Induced Xerostomia by Regulating AQP5, NF-κB, and p38 MAPK Signaling Pathwaysaff.

Introduction: Xerostomia, commonly caused by Sjögren disease (SjD) or head and neck radiotherapy, significantly impairs patients' quality of life, yet effective treatments remain limited. Traditional Chinese Medicine (TCM) offers promising alternatives due to its favourable efficacy and low toxicity. Shatai Heji (STHJ), a compound TCM formulation designed to nourish yin and invigorate qi, shows therapeutic potential for xerostomia. This study aimed to establish quality control standards for STHJ and evaluate its pharmacodynamics, safety, and mechanisms of action in models of xerostomia.

Methods: A qualitative identification method was developed for the twelve herbal components of STHJ, with quantification of active constituents, focusing on quality markers for Astragalus and Rehmannia. Xerostomia was induced in Sprague-Dawley (SD) rats using a muscarinic receptor antagonist, and in BALB/c mice with SjD. Histological examination of major organs and salivary glands was performed, and aquaporin-5 (AQP5) expression in submandibular glands was assessed via Western blotting and immunohistochemistry. Therapeutic effects were evaluated through salivary secretion, glandular weight, and biochemical markers. In SjD mice, submandibular gland immunofluorescence and ELISA were used to assess inflammatory cytokines (TNF-α, TNF-β, IFN-γ, IL-6) and autoantibodies (anti-SSA/Ro, anti-SSB/La). Western blotting was used to analyse NF-κB and MAPK p38 pathway activation. Acute toxicity was assessed in SD rats.

Results: STHJ significantly improved xerostomia symptoms, increased salivary output, upregulated AQP5, and preserved glandular morphology. It reduced fibrosis, suppressed inflammatory cytokine expression, and inhibited immune cell infiltration. Mechanistically, STHJ attenuated activation of NF-κB and MAPK p38 pathways. No acute toxicity was observed.

Conclusion: This is the first study to establish quality control standards for STHJ and to demonstrate its anti-inflammatory and immunomodulatory effects in xerostomia models. The findings suggest that STHJ may serve as a safe and effective therapeutic option for xerostomia associated with SjD and other conditions.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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