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沙泰合剂通过调节水通道蛋白5、核因子κB和p38丝裂原活化蛋白激酶信号通路减轻干燥综合征诱导的口干症

Shatai Heji Mitigates Sjögren Disease-Induced Xerostomia by Regulating AQP5, NF-κB, and p38 MAPK Signaling Pathwaysaff.

作者信息

Liu Fangbin, Chen Jiyuan, Gong Chunai, Chen Minyan, Yang Gang, Chen Chun, Yao Ru, Li Shengnan, Wang Rong, Yuan Yongfang

机构信息

Department of Pharmacy, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.

出版信息

Drug Des Devel Ther. 2025 Sep 9;19:7979-7998. doi: 10.2147/DDDT.S526278. eCollection 2025.

Abstract

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.

摘要

引言

口干症通常由干燥综合征(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。由于疗效良好且毒性低,传统中药(TCM)提供了有前景的替代方案。沙太合剂(STHJ)是一种旨在滋阴补气的复方中药制剂,对口干症具有治疗潜力。本研究旨在建立STHJ的质量控制标准,并评估其在口干症模型中的药效学、安全性及作用机制。

方法

建立了STHJ十二味草药成分的定性鉴定方法,并对活性成分进行定量,重点关注黄芪和熟地黄的质量标志物。使用毒蕈碱受体拮抗剂诱导Sprague-Dawley(SD)大鼠出现口干症,并诱导BALB/c小鼠患上SjD。对主要器官和唾液腺进行组织学检查,并通过蛋白质免疫印迹法和免疫组织化学法评估下颌下腺中水通道蛋白5(AQP5)的表达。通过唾液分泌、腺体重量和生化标志物评估治疗效果。在SjD小鼠中,使用下颌下腺免疫荧光和酶联免疫吸附测定法评估炎性细胞因子(TNF-α、TNF-β、IFN-γ、IL-6)和自身抗体(抗SSA/Ro、抗SSB/La)。采用蛋白质免疫印迹法分析NF-κB和丝裂原活化蛋白激酶p38(MAPK p38)信号通路的激活情况。在SD大鼠中评估急性毒性。

结果

STHJ显著改善了口干症症状,增加了唾液分泌量,上调了AQP5表达,并保持了腺体形态。它减少了纤维化,抑制了炎性细胞因子表达,并抑制了免疫细胞浸润。机制上,STHJ减弱了NF-κB和MAPK p38信号通路的激活。未观察到急性毒性。

结论

这是第一项建立STHJ质量控制标准并证明其在口干症模型中具有抗炎和免疫调节作用的研究。研究结果表明,STHJ可能是与SjD及其他病症相关的口干症的一种安全有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/12433209/00ce93f585c6/DDDT-19-7979-g0001.jpg

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