Englebach I M, Lappe R W, Hand J M
Wyeth-Ayerst Research, Princeton, NJ 08540.
Pulm Pharmacol. 1988;1(3):119-23. doi: 10.1016/s0952-0600(88)80009-7.
The present study examined the bronchoprotective and bronchodilator efficacy of infused human atrial natriuretic factor [102-126] (Anaritide) in the guinea pig. Anesthetized and paralyzed male guinea pigs, ventilated via a tracheal cannula, were placed in a plethysmograph for measurement of agonist-induced changes in pulmonary mechanics. Reductions in dynamic compliance of the lung and airway conductance were produced either by 3 to 7 tidal volume breaths of leukotriene D4 (0.125 micrograms/ml) delivered through an ultrasonic nebulizer or by intravenous histamine (2.8 +/- 0.2 micrograms/kg). Infusion of Anaritide (1 microgram/kg/min), before evoking bronchoconstriction with either LTD4 or histamine, produced a significant protection against bronchoconstriction produced by aerosol LTD4, but not against histamine-induced bronchoconstriction of similar magnitude. In other experiments, Anaritide infusion (0.5-2 micrograms/kg/min) also rapidly reversed a stable LTD4-induced decrease in airway conductance, but did not produce a similar reversal of the decrease in dynamic compliance. The data provide evidence that intravenous Anaritide exerts both bronchoprotective and bronchodilator effects against LTD4-induced bronchospasm.
本研究检测了输注人心房利钠因子[102 - 126](阿那立肽)对豚鼠的支气管保护和支气管扩张作用。将经气管插管通气的麻醉且麻痹的雄性豚鼠置于体积描记器中,以测量激动剂引起的肺力学变化。通过超声雾化器给予3至7次潮气量的白三烯D4(0.125微克/毫升)或静脉注射组胺(2.8±0.2微克/千克),可导致肺动态顺应性和气道传导率降低。在使用白三烯D4或组胺诱发支气管收缩之前,输注阿那立肽(1微克/千克/分钟)可显著保护豚鼠免受雾化白三烯D4引起的支气管收缩,但对组胺诱导的同等程度支气管收缩无保护作用。在其他实验中,输注阿那立肽(0.5 - 2微克/千克/分钟)也能迅速逆转白三烯D4诱导的气道传导率稳定下降,但对动态顺应性下降无类似的逆转作用。这些数据表明,静脉注射阿那立肽对白三烯D4诱导的支气管痉挛具有支气管保护和支气管扩张作用。