Seihaito 是一种堪布药,可减少 IL-13 诱导的粘液分泌和上皮细胞增生

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of pharmacological sciences Pub Date : 2024-02-13 DOI:10.1016/j.jphs.2024.02.008
Tomoki Sekiya, Kazuhito Murakami, Yoichiro Isohama
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引用次数: 0

摘要

胃小管细胞增生和粘液分泌增多是包括哮喘在内的气道疾病的特征,过多的气道粘液往往会加重这些疾病。对于严重哮喘患者,即使是类固醇也不能完全有效地抑制粘液分泌,因此需要新的治疗方案。清白散是一种日本传统药物,临床上用作止咳和祛痰剂。在本研究中,我们考察了清白散对腺泡细胞分化和粘液分泌的影响。在体外研究中,利用豚鼠气管上皮细胞的气液界面培养,Seihaito抑制了IL-13诱导的鹅口疮细胞增殖和粘液产生的主要成分MUC5AC。Seihaito抑制了鹅口疮细胞特异性基因的表达,而没有改变睫状细胞特异性基因,这表明它抑制了鹅口疮细胞的分化。此外,Seihaito还抑制了转染有SPDEF(一种由IL-13激活的转录因子)的细胞中MUC5AC的表达。此外,Seihaito还能抑制体内经IL-13处理的小鼠肺部上皮细胞的增殖和MUC5AC mRNA的表达。总之,这些研究结果表明,Seihaito对腺泡细胞分化和粘液分泌具有抑制作用,而这至少部分是由于抑制了SPDEF。
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Seihaito, a Kampo medicine, attenuates IL-13-induced mucus production and goblet cell metaplasia

Goblet cell hyperplasia and increased mucus production are features of airway diseases, including asthma, and excess airway mucus often worsens these conditions. Even steroids are not uniformly effective in mucus production in severe asthma, and new therapeutic options are needed. Seihaito is a Japanese traditional medicine that is used clinically as an antitussive and expectorant. In the present study, we examined the effect of Seihaito on goblet cell differentiation and mucus production. In in vitro studies, using air–liquid interface culture of guinea-pig tracheal epithelial cells, Seihaito inhibited IL-13-induced proliferation of goblet cells and MUC5AC, a major component of mucus production. Seihaito suppressed goblet cell-specific gene expression, without changing ciliary cell-specific genes, suggesting that it inhibits goblet cell differentiation. In addition, Seihaito suppressed MUC5AC expression in cells transfected with SPDEF, a transcription factor activated by IL-13. Furthermore, Seihaito attenuated in vivo goblet cell proliferation and MUC5AC mRNA expression in IL-13-treated mouse lungs. Collectively, these findings demonstrated that Seihaito has an inhibitory effect on goblet cell differentiation and mucus production, which is at least partly due to the inhibition of SPDEF.

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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
104
审稿时长
31 days
期刊介绍: Journal of Pharmacological Sciences (JPS) is an international open access journal intended for the advancement of pharmacological sciences in the world. The Journal welcomes submissions in all fields of experimental and clinical pharmacology, including neuroscience, and biochemical, cellular, and molecular pharmacology for publication as Reviews, Full Papers or Short Communications. Short Communications are short research article intended to provide novel and exciting pharmacological findings. Manuscripts concerning descriptive case reports, pharmacokinetic and pharmacodynamic studies without pharmacological mechanism and dose-response determinations are not acceptable and will be rejected without peer review. The ethnopharmacological studies are also out of the scope of this journal. Furthermore, JPS does not publish work on the actions of biological extracts unknown chemical composition.
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