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[1]张艺凡,王悦△,刘磊,等.青蒿琥酯对小鼠气道阻力及气道平滑肌牵张力的效应研究*[J].生物医学工程研究,2017,03:191-196.
 ZHANG Yifan,WANG Yue,LIU Lei,et al.The Effect of Artesunate on Murine Airway Resistance and Airway Smooth Muscle Cell Traction Force[J].Journal of Biomedical Engineering Research,2017,03:191-196.
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青蒿琥酯对小鼠气道阻力及气道平滑肌牵张力的效应研究*(PDF)

《生物医学工程研究》[ISSN:1006-6977/CN:61-1281/TN]

期数:
2017年03期
页码:
191-196
栏目:
出版日期:
2017-09-25

文章信息/Info

Title:
The Effect of Artesunate on Murine Airway Resistance and Airway Smooth Muscle Cell Traction Force
文章编号:
1672-6278 (2017)03-0191-06
作者:
张艺凡12王悦12△刘磊1李晶晶1邓林红12△
1.常州大学 生物医学工程与健康科学研究院暨常州市呼吸医学工程重点实验室,常州 213164;2.常州大学 制药与生命科学学院/护理学院,常州 213164
Author(s):
ZHANG Yifan12 WANG Yue12 LIU Lei1 LI Jingjing1 DENG Linhong12
1.Institute of Biomedical Engineering and Health Sciences, Changzhou Key Laboratory of Respiratory Medical Engineering, Changzhou University, Changzhou 213164, China;2.School of Pharmaceutical Engineering and Life Science, School of Nursing, Changzhou University, Changzhou 213164
关键词:
青蒿琥酯气道阻力气道平滑肌细胞牵张力哮喘
Keywords:
Artesunate Airway resistance Airway smooth muscle cell Traction forceAsthma
分类号:
R318
DOI:
10.19529/j.cnki.1672-6278.2017.03.01
文献标识码:
A
摘要:
青蒿琥酯是著名的抗疟药青蒿素的衍生物,可抑制哮喘动物的气道炎症,但其对气道阻力及平滑肌牵张力是否有影响未知。因此,首先建立了小鼠哮喘动物模型,通过肺功能仪检测青蒿琥酯对小鼠气道阻力的影响,并体外进行了小鼠气道平滑肌的分离培养,运用傅里叶变换牵张力显微术(FTTC)检测了青蒿琥酯对气道平滑肌牵张力的效应,并初步探讨了机制。结果显示,青蒿琥酯能有效降低哮喘小鼠的气道阻力,并呈现剂量依赖性,且120 μg青蒿琥酯对降低气道阻力的程度相当于3 μg沙丁胺醇(常规哮喘治疗)的效果;青蒿琥酯可降低气道平滑肌细胞的牵张力,并使胞内[Ca2+]i增加。表明青蒿琥酯是一种经济的、潜在的支气管舒张剂,为支气管哮喘的治疗提供新的前景。
Abstract:
Artesunate is a derivative of the well-known anti-malarial drug, artemisinin. It has been shown to inhibit airway inflammation in animal models of asthma, but is yet to be studied for its effect on airway resistance (Raw) and airway smooth muscle cell (ASMC) traction force. Since Raw and ASMC traction force are key elements in the pathogenesis and treatment of asthma, we thus evaluated the effect of artesunate on Raw and ASMC traction force with experimental mouse model of asthma. Mouse model of asthma was established by ovalbumin sensitization and challenge, and then tested for Raw w/o administration of artesunate at given dosage. On the other hand, ASMCs were harvested from the mouse lung and cultured in vitro. Subsequently, the in vitro cultured ASMCs were tested for traction force by using Fourier Transform Traction Force Cytometry (FTTC) in the absence or presence of artesunate. The results showed that artesunate dose dependently reduced Raw of the asthma mouse models, and 120μg artesunate was comparable to 3μg salbutamol (conventional asthma therapy) in effect of Raw reduction. Artesunate also attenuated traction force generated by in vitro ASMCs, together with increase of intracellular calcium concentration ([Ca2+]i). These results suggest that artesunate may be an inexpensive potential airway dilator, which provides new drug alternative choice for treating bronchial asthma.

参考文献/References

备注/Memo

备注/Memo:
(收稿日期:2017-03-13) 国家自然科学基金资助项目(11532003)△通信作者Email:wangyuebj2003@cczu.edu.cn; dlh@cczu.edu.cn
更新日期/Last Update: 2017-09-21