陈莹, 谢强敏, 沈文会, 杨秋火. 环孢素A气雾吸入对致敏大鼠气道高反应性的影响环孢素A气雾吸入对致敏大鼠气道高反应性的影响J. 药学学报, 2003, 38(7): 492-495.
引用本文: 陈莹, 谢强敏, 沈文会, 杨秋火. 环孢素A气雾吸入对致敏大鼠气道高反应性的影响环孢素A气雾吸入对致敏大鼠气道高反应性的影响J. 药学学报, 2003, 38(7): 492-495.
CHEN Ying, XIE Qiang-min, SHEN Wen-hui, YANG Qiu-huo. Effects of cyclosporin A aerosol on airway hyperresponsiveness in ratsJ. Acta Pharmaceutica Sinica, 2003, 38(7): 492-495.
Citation: CHEN Ying, XIE Qiang-min, SHEN Wen-hui, YANG Qiu-huo. Effects of cyclosporin A aerosol on airway hyperresponsiveness in ratsJ. Acta Pharmaceutica Sinica, 2003, 38(7): 492-495.

环孢素A气雾吸入对致敏大鼠气道高反应性的影响环孢素A气雾吸入对致敏大鼠气道高反应性的影响

Effects of cyclosporin A aerosol on airway hyperresponsiveness in rats

  • 摘要: 目的评价环孢素A气雾吸入给药对致敏大鼠气道高反应性的影响。方法用氯化乙酰甲胆碱(Mch)诱导抗原攻击后的致敏大鼠气道阻力(raw)、肺动态顺应性(Cdyn)、PC50和PC25变化,观察环孢素A气雾吸入给药后的抗气道高反应性作用。结果环孢素A 5,20 g·L-1气雾吸入给药,色甘酸钠20 g·L-1气雾吸入给药和地塞米松 (0.5 mg·kg-1, ip) 抑制Mch诱导的大鼠raw增高及Cdyn降低,增加raw PC50和 Cdyn PC25值。结论环孢素A气雾吸入给药能预防Mch引起的大鼠气道高反应性,是其治疗哮喘的一个有效途径。

     

    Abstract: AimTo study cyclosporin A (CsA) aerosol for anti-airway hyperresponsiveness (AHR) in sensitized rats. MethodsSensitized Sprague-Dawley rats were given cyclosporin A (5, 20 g·L-1) and sodium cromoglycate (SCG, 20 g·L-1) by aerosol (5 min per day), dexamethasone(DXM, 0.5 mg·kg-1) i p once per day for 7 d before antigen challenge. The respiratory resistance(raw)and lung dynamic compliance(Cdyn)of the rats induced by methacholine (Mch) were measured 24 h after ovalbumin(OA) challenge. The PC50 changes of raw and PC25 changes of Cdyn were also investigated. ResultsPretreatment with CsA, sodium cromoglycate and dexamethasone inhibited the increase of raw and decrease of Cdyn caused by inhaling Mch. The value of raw PC50 in the CsA(5 g·L-1) group 5.6 g·L-1, the CsA(20 g·L-1) group 6.4 g·L-1, the SCG group 8.3 g·L-1 and the DXM group 9.2 g·L-1, was significantly higher than that of the model group 1.9 g·L-1 (P<0.05). The value of Cdyn PC25 in the CsA(5 g·L-1) group 4.3 g·L-1, the CsA(20 g·L-1) group 5.4 g·L-1, the SCG group 6.4 g·L-1 and the DXM group 6.2 g·L-1, was significantly higher than that of the model group 1.1 g·L-1 (P<0.01). ConclusionAnti-AHR of CsA by aerosol in animal model offered an experimental evidence for topical inhalation of CsA in treatment of asthma.

     

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