Cinnamaldehyde reduces inflammatory responses in chronic rhinosinusitis by inhibiting TRPM8 expression.

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL American journal of translational research Pub Date : 2024-12-15 eCollection Date: 2024-01-01 DOI:10.62347/CPZN1117
Yi Cai, Mingjian Xie, Zhoumu Fang, Yanfei Bai, Jiang Bian
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Abstract

Objective: This study aimed to investigate the effects of cinnamaldehyde (CA) intervention on transient receptor potential melastatin 8 (TRPM8) expression in human nasal epithelial cells (HNECs) and mouse models of chronic rhinosinusitis (CRS) and determine the alleviating effects of CA on CRS.

Methods: HNECs were treated with CA, and the protein levels and mRNA expression of pro-inflammatory cytokines, namely, interleukin-25 (IL-25), IL-33, and thymic stromal lymphopoietin (TSLP), were measured by enzyme-linked immunosorbent assay and real-time reverse-transcription polymerase chain reaction (RT-PCR). TRPM8 expression levels were examined by RT-PCR and western blot. The C57BL/6 mice were randomly divided into three groups (control group, model group, CA group). The model and CA groups were induced by intranasal drip intervention of ovalbumin (OVA) three times a week for 9 weeks. Each mouse was individually observed in a single cage to record the frequency of nose scratching and sneezing within 10 minutes. Histologic examination of nasal mucosa in mice was done using hematoxylin-eosin staining to compare the degree of inflammation. Pro-inflammatory cytokine levels and TRPM8 expression levels were measured in mouse nasal lavage fluid.

Results: In vitro experiments demonstrated that CA intervention in HNECs significantly reduced the protein and mRNA of IL-25, IL-33, TSLP, and TRPM8. In vivo analysis showed that the CA group exhibited fewer nose scratching and sneezing symptoms and reduced nasal mucosal inflammation as well as lower levels of IL-25, IL-33, and TSLP in nasal lavage fluid and tissues than the model group.

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肉桂醛通过抑制TRPM8表达减少慢性鼻窦炎的炎症反应。
目的:本研究旨在探讨肉桂醛(CA)干预对人鼻上皮细胞(HNECs)和慢性鼻窦炎(CRS)小鼠模型中美拉他汀8 (TRPM8)瞬时受体电位表达的影响,并确定CA对CRS的缓解作用。方法:CA处理HNECs,采用酶联免疫吸附法和实时反转录聚合酶链反应(RT-PCR)检测促炎细胞因子白介素-25 (IL-25)、IL-33和胸腺基质淋巴生成素(TSLP)的蛋白水平和mRNA表达。RT-PCR和western blot检测TRPM8的表达水平。将C57BL/6小鼠随机分为3组(对照组、模型组、CA组)。模型组和CA组均采用卵清蛋白(OVA)滴注干预,每周3次,连续9周。在一个单独的笼子里观察每只老鼠,记录10分钟内抓鼻子和打喷嚏的频率。采用苏木精-伊红染色对小鼠鼻黏膜进行组织学检查,比较炎症程度。测定小鼠鼻灌洗液中促炎细胞因子水平和TRPM8表达水平。结果:体外实验表明CA干预HNECs可显著降低IL-25、IL-33、TSLP、TRPM8的蛋白表达和mRNA表达。体内分析显示,CA组大鼠抓鼻、打喷嚏症状减少,鼻黏膜炎症减轻,鼻腔灌洗液和组织中IL-25、IL-33、TSLP水平低于模型组。
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American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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