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色甘酸钠、维拉帕米和尼卡地平对白三烯D4支气管收缩的拮抗作用。

Sodium cromoglycate, verapamil and nicardipine antagonism to leukotriene D4 bronchoconstriction.

作者信息

Advenier C, Cerrina J, Duroux P, Floch A, Pradel J, Renier A

出版信息

Br J Pharmacol. 1983 Feb;78(2):301-6. doi: 10.1111/j.1476-5381.1983.tb09395.x.

Abstract

1--The effects of nicardipine, verapamil and sodium cromoglycate (SCG) on the increase in pulmonary airway resistance(RAw) and decrease in pulmonary dynamic compliance (CDyn) induced by leukotriene D4 (LTD4) 0.5 micrograms kg-1 and acetylcholine (ACh) 3 micrograms kg-1 were investigated in anaesthetized guinea-pigs. The effects of these three agents on the contractile effects of LTD4 and ACh were tested on isolated tracheal preparations of the guinea-pig. 2--Nicardipine and verapamil (0.3 and 1 mg kg-1), as well as SCG (3 and 10 mg kg-1), partially but significantly inhibited the effects of LTD4 on RAw. Partial inhibition of the effect of LTD4 on CDyn was only observed with verapamil (0.3 and 1 mg kg-1). Nicardipine and verapamil had no effect on ACh-induced bronchoconstriction in vivo. 3--In concentrations higher than 10(-5) M, nicardipine and verapamil inhibited the contractile effects of LTD4 and ACh on guinea-pig isolated trachea. SCG had no effect on this preparation. 4--These results suggest that nicardipine, verapamil and SCG partially reduce the component of bronchoconstriction associated with stimulation of irritant receptors by LTD4. However, the site and mechanism of action of Ca2+-entry antagonists remain uncertain.

摘要
  1. 在麻醉的豚鼠中,研究了尼卡地平、维拉帕米和色甘酸钠(SCG)对由白三烯D4(LTD4)0.5微克/千克和乙酰胆碱(ACh)3微克/千克诱导的肺气道阻力(RAw)增加和肺动态顺应性(CDyn)降低的影响。在豚鼠离体气管制备物上测试了这三种药物对LTD4和ACh收缩作用的影响。2. 尼卡地平、维拉帕米(0.3和1毫克/千克)以及SCG(3和10毫克/千克)部分但显著地抑制了LTD4对RAw的作用。仅观察到维拉帕米(0.3和1毫克/千克)对LTD4对CDyn的作用有部分抑制。尼卡地平和维拉帕米对体内ACh诱导的支气管收缩无作用。3. 在浓度高于10^(-5) M时,尼卡地平和维拉帕米抑制了LTD4和ACh对豚鼠离体气管的收缩作用。SCG对该制备物无作用。4. 这些结果表明,尼卡地平、维拉帕米和SCG部分降低了与LTD4刺激刺激性受体相关的支气管收缩成分。然而,钙通道拮抗剂的作用部位和机制仍不确定。

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