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他洛昔明,一种具有支气管扩张特性的新型呼吸兴奋剂。

Taloximine, a new respiratory stimulant with brochodilator properties.

作者信息

Daly M J, Lightowler J E, Pickering R W

出版信息

Br J Pharmacol. 1969 Feb;35(2):283-94. doi: 10.1111/j.1476-5381.1969.tb07987.x.

Abstract
  1. A novel phthalazine analogue taloximine (1-hydroxyimino-4(2-dimethyl-aminoethoxy)-1,2-dihydrophthalazine monohydrochloride monohydrate) stimulated respiration in conscious rabbits at doses of 7 mg/kg and above.2. Taloximine antagonized the depressant action of morphine on respiration in rabbits at doses of 10 mg/kg. At high doses it resuscitated rabbits after they had been given lethal doses of sodium pentobarbitone.3. In in vitro preparations of the trachea or bronchus taloximine was about equiactive with aminophylline. In the Konzett-Rössler preparation the intravenous ED50 for taloximine was about 18% of that of aminophylline, whereas after oral administration the two drugs were equiactive.4. Taloximine, unlike aminophylline, did not protect guinea-pigs against anaphylactic microshock to egg albumen.5. Taloximine shortened the duration of the loss of righting reflex in mice due to hexobarbitone more effectively than bemegride, nikethamide or vanillic acid diethylamide.6. In the dose required to stimulate respiration taloximine had only slight cardiovascular effects. Up to four times this dose produced no evidence of general excitation of the central nervous system.
摘要
  1. 一种新型酞嗪类似物他林洛明(1-羟基亚氨基-4-(2-二甲基氨基乙氧基)-1,2-二氢酞嗪盐酸盐一水合物)在剂量达到7毫克/千克及以上时可刺激清醒家兔的呼吸。

  2. 他林洛明在剂量为10毫克/千克时可拮抗吗啡对家兔呼吸的抑制作用。在高剂量时,它能使给予致死剂量戊巴比妥钠后的家兔复苏。

  3. 在气管或支气管的体外制剂中,他林洛明与氨茶碱的活性大致相当。在康泽特-罗斯勒制剂中,他林洛明的静脉注射半数有效量约为氨茶碱的18%,而口服给药后两种药物活性相当。

  4. 与氨茶碱不同,他林洛明不能保护豚鼠免受蛋清过敏性微休克的影响。

  5. 他林洛明比贝美格、尼可刹米或香草酸二乙酰胺更有效地缩短了小鼠因己巴比妥导致的翻正反射消失的持续时间。

  6. 在刺激呼吸所需的剂量下,他林洛明对心血管的影响很小。高达该剂量四倍时,未出现中枢神经系统普遍兴奋的迹象。

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