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阿曲库铵分解产物及相关物质的药理作用。

Pharmacological action of breakdown products of atracurium and related substances.

作者信息

Chapple D J, Clark J S

出版信息

Br J Anaesth. 1983;55 Suppl 1:11S-15S.

PMID:6688001
Abstract

The neuromuscular and cardiovascular effects of the breakdown products of atracurium and related substances have been studied in cats anaesthetized with chloralose. Laudanosine, the quaternary acid and metholaudanosine had no neuromuscular blocking activity within the dose range 0.5-4 mg kg-1. However, the quaternary monoacrylate, the quaternary alcohol and the monoquaternary analogue produced a dose-dependent neuromuscular block within this dose range. At 4 mg kg-1 mean arterial pressure was significantly reduced by 30-70 mm Hg following the administration of the quaternary monoacrylate, laudanosine, the quaternary alcohol, metholaudanosine and the monoquaternary analogue. At this dose only the monoquaternary analogue caused significant sympathetic blockade after preganglionic nerve stimulation. Significant vagal blockade occurred after 4 mg kg-1 of the quaternary monoacrylate, the quaternary acid, the quaternary alcohol and the monoquaternary analogue. In view of the low potencies of these substances, it is likely that the quantities present either as an impurity or likely to be formed after administration of therapeutic doses of atracurium (0.3-0.6 mg kg-1 i.v.) are of no pharmacological importance.

摘要

在用氯醛糖麻醉的猫身上研究了阿曲库铵及其相关物质分解产物的神经肌肉和心血管效应。劳丹诺辛、季铵酸和甲基劳丹诺辛在0.5 - 4 mg kg⁻¹的剂量范围内没有神经肌肉阻滞活性。然而,季铵单丙烯酸酯、季铵醇和单季铵类似物在此剂量范围内产生了剂量依赖性的神经肌肉阻滞。给予季铵单丙烯酸酯、劳丹诺辛、季铵醇、甲基劳丹诺辛和单季铵类似物后,在4 mg kg⁻¹时平均动脉压显著降低30 - 70 mmHg。在此剂量下,只有单季铵类似物在节前神经刺激后引起显著的交感神经阻滞。给予4 mg kg⁻¹的季铵单丙烯酸酯、季铵酸、季铵醇和单季铵类似物后出现显著的迷走神经阻滞。鉴于这些物质的效力较低,作为杂质存在或在给予治疗剂量的阿曲库铵(0.3 - 0.6 mg kg⁻¹静脉注射)后可能形成的量可能没有药理学意义。

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