Klinik für Anaesthesiologie, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Crit Care Med. 2010 Mar;38(3):922-7. doi: 10.1097/CCM.0b013e3181c31297.
To investigate the effects of continuous pyridostigmine infusion on immobilization-induced muscle weakness. Critical illness often results in immobilization of limb and respiratory muscles, leading to muscle atrophy and up-regulation of nicotinic acetylcholine receptors. Pyridostigmine reversibly blocks acetylcholinesterase and has the potential to improve neuromuscular transmission and decrease acetylcholine receptor number.
Prospective, randomized, controlled experimental study.
Animal laboratory, university hospital.
Male Sprague-Dawley rats.
A total of 40 rats were immobilized in one hind limb by pinning knee and ankle joints. Rats received either continuous pyridostigmine (15 mg.kg.day) or saline subcutaneously via implanted osmotic pumps.
After 7 days and 14 days of immobilization, neuromuscular function, atracurium pharmacodynamics, and expression of acetylcholine receptors were evaluated. At 7 days and 14 days after immobilization, muscle force decreased in all untreated groups, whereas effective doses for paralysis with atracurium and acetylcholine receptor number in the tibialis were significantly increased. Pyridostigmine-treated rats showed a significantly improved muscle force and muscle mass in the immobilized limb. This was associated with an attenuation of acetylcholine receptor up-regulation in the respective leg. At this time, the dose-response curve for atracurium on the immobilized side was shifted to the left in the pyridostigmine group. After 14 days, muscle tension was still less depressed with pyridostigmine infusion, and resistance to the effects of atracurium was still attenuated. However, there were no differences in acetylcholine receptor expression between the immobilized sides of both groups.
Continuous pyridostigmine infusion improves muscle weakness after 7 days and 14 days of immobilization. The up-regulation of acetylcholine receptors and the concomitant resistance to atracurium is attenuated in animals treated with pyridostigmine after 7 days of immobilization.
研究持续滴注吡啶斯的明对固定性肌肉无力的影响。危重病常导致肢体和呼吸肌固定,导致肌肉萎缩和烟碱型乙酰胆碱受体上调。吡啶斯的明可逆性地阻断乙酰胆碱酯酶,具有改善神经肌肉传递和减少乙酰胆碱受体数量的潜力。
前瞻性、随机、对照实验研究。
动物实验室,大学医院。
雄性 Sprague-Dawley 大鼠。
共 40 只大鼠通过固定膝关节和踝关节将一只后肢固定。大鼠通过植入的渗透泵皮下接受持续吡啶斯的明(15mg.kg.day)或生理盐水。
在固定 7 天和 14 天后,评估神经肌肉功能、阿曲库铵药效学和乙酰胆碱受体表达。在固定后 7 天和 14 天,所有未治疗组的肌肉力量均下降,而阿曲库铵致麻痹的有效剂量和胫骨乙酰胆碱受体数量显著增加。吡啶斯的明治疗组固定肢体的肌肉力量和肌肉质量明显改善。这与相应腿部乙酰胆碱受体上调的减弱有关。此时,吡啶斯的明组固定侧的阿曲库铵剂量-反应曲线向左移位。14 天后,仍持续输注吡啶斯的明,肌肉张力抑制程度较轻,对阿曲库铵的作用仍减弱。然而,两组固定侧的乙酰胆碱受体表达无差异。
连续输注吡啶斯的明可改善固定 7 天和 14 天后的肌肉无力。固定 7 天后,吡啶斯的明治疗的动物乙酰胆碱受体上调和对阿曲库铵的抵抗力减弱。