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比较依那西普和地塞米松对哮喘模型气道上皮和重塑的 TNF 拮抗作用。

Comparison of TNF antagonism by etanercept and dexamethasone on airway epithelium and remodeling in an experimental model of asthma.

机构信息

MD, Celal Bayar University Medical Faculty, Dept. of Pediatric Allergy and Pulmonology, Manisa, Turkey.

出版信息

Int Immunopharmacol. 2013 Nov;17(3):768-73. doi: 10.1016/j.intimp.2013.08.021. Epub 2013 Sep 22.

Abstract

BACKGROUND

The aim of the study was to compare the influence of TNF antagonism and corticosteroid treatment on epithelial, smooth muscle and basement membrane component of airway remodeling in an experimental murine model of chronic asthma.

METHODS

We used 30 BALB/c mice. Group 1 not exposed to ovalbumin or any medication was designated as control group. Chronic asthma model was achieved in the other three groups with intraperitoneal (IP) and inhaled ovalbumin. Then, Group 2 received IP saline, Group 3 received IP dexamethasone and Group 4 received IP etanercept. Epithelial, subepithelial smooth muscle and basement membrane thickness as well as goblet cells and mast cells were examined on samples isolated from left lung.

RESULTS

Etanercept treatment led to thinner epithelial and basement membrane layer and lower goblet and mast cell number than untreated asthmatic mice (p<0.001, p=0.001, p=0.005 and p=0.03 respectively). Neither epithelial and basement membrane thickness nor mast cell number was different among mice treated with etanercept and dexamethasone (p=0.38, p=0.79 and p=0.51 respectively). However, etanercept group was associated with thicker subepithelial muscle layer but lower goblet cell number (p<0.001 and p=0.04 respectively) than dexamethasone group.

CONCLUSIONS

Corticosteroids are more effective in decreasing smooth muscle mass while TNF antagonists in reducing goblet cell number in animal model of asthma. Therefore, further research is needed to assess the synergistic use of TNF antagonism and dexamethasone for more rational remodeling control.

摘要

背景

本研究旨在比较 TNF 拮抗剂和皮质类固醇治疗对慢性哮喘实验性小鼠模型中气道重塑的上皮、平滑肌和基底膜成分的影响。

方法

我们使用了 30 只 BALB/c 小鼠。未暴露于卵清蛋白或任何药物的第 1 组被指定为对照组。另外三组通过腹腔内(IP)和吸入卵清蛋白建立慢性哮喘模型。然后,第 2 组接受 IP 生理盐水,第 3 组接受 IP 地塞米松,第 4 组接受 IP 依那西普。从左肺分离的样本中检查上皮、上皮下平滑肌和基底膜厚度以及杯状细胞和肥大细胞。

结果

与未经治疗的哮喘小鼠相比,依那西普治疗导致上皮和基底膜层更薄,杯状细胞和肥大细胞数量更少(p<0.001,p=0.001,p=0.005 和 p=0.03)。依那西普和地塞米松治疗的小鼠上皮和基底膜厚度或肥大细胞数量无差异(p=0.38,p=0.79 和 p=0.51)。然而,依那西普组与地塞米松组相比,上皮下肌肉层更厚,但杯状细胞数量更少(p<0.001 和 p=0.04)。

结论

皮质类固醇在减少平滑肌质量方面更有效,而 TNF 拮抗剂在减少哮喘动物模型中的杯状细胞数量方面更有效。因此,需要进一步研究来评估 TNF 拮抗剂和地塞米松的协同使用,以实现更合理的重塑控制。

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