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突触前毒蕈碱和腺苷受体参与烟碱型乙酰胆碱受体拮抗剂引起的大鼠 2 Hz 诱发的四成串肌松衰减。

Presynaptic muscarinic and adenosine receptors are involved in 2 Hz-induced train-of-four fade caused by antinicotinic neuromuscular relaxants in the rat.

机构信息

Department of Pharmacology and Therapeutics, State University of Maringá, Paraná, Brazil.

出版信息

Clin Exp Pharmacol Physiol. 2011 Nov;38(11):764-70. doi: 10.1111/j.1440-1681.2011.05588.x.

Abstract
  1. Train-of-four fade (TOF(fade) ) is a clinically useful parameter to monitor the degree of block of neuromuscular transmission in curarized patients. Experimentally, TOF(fade) has been attributed to the blockade of facilitatory nicotinic receptors on motor nerve terminals. There is less information regarding the involvement of coexistent presynaptic receptors (e.g. muscarinic M(1) and M(2) , adenosine A(1) and A(2A) ) in the TOF(fade) produced by antinicotinic agents. 2. In the present study, we evaluated the TOF(fade) caused by antinicotinic neuromuscular relaxants (hexamethonium, d-tubocurarine, vecuronium and rocuronium) as the ratio of the muscle tension produced in the rat diaphragm by the fourth to the first stimulus (T(4) /T(1) ) of a train-of-four stimuli delivered to the phrenic nerve trunk at a frequency of 2 Hz. 3. All antinicotinic agents, except hexamethonium, decreased the amplitude of muscle tension during the first stimulus. Hexamethonium, (5.47 mmol/L), d-tubocurarine- (1.1 μmol/L), vecuronium (4.7 μmol/L)- and rocuronium (9.8 μmol/L)-induced TOF(fade) was attenuated by 10 nmol/L pirenzepine (an M(1) receptor antagonist), 1 μmol/L methoctramine (an M(2) receptor antagonist) and 2.5 nmol/L 1,3-dipropyl-8-cyclopentylxanthine (an A(1) receptor antagonist). Blockade of the A(2A) receptor with 10 nmol/L ZM241385 partially reversed the TOF(fade) induced by d-tubocurarine, vecuronium and rocuronium, but not that caused by the 'pure' neuronal nicotinic receptor antagonist hexamethonium, unless one increased the concentration of ZM241385 to 50 nmol/L. 4. The data indicate that presynaptic M(1) , M(2) , A(1) and A(2A) receptors play a role in neuromuscular TOF(fade) caused by antinicotinic neuromuscular relaxants. Such interplay depends on adenosine tonus and on the affinity of neuromuscular blocking agents for neuronal versus muscular nicotinic receptors.
摘要
  1. 肌搐衰减(TOF(fade))是监测肌松患者神经肌肉阻滞程度的一个临床有用的参数。在实验中,TOF(fade)归因于运动神经末梢上促进型烟碱受体的阻滞。关于共存的突触前受体(例如毒蕈碱 M(1)和 M(2)、腺苷 A(1)和 A(2A))在烟碱拮抗剂引起的 TOF(fade)中的参与,信息较少。

  2. 在本研究中,我们评估了烟碱拮抗剂(六烃季铵、去极化肌松药、维库溴铵和罗库溴铵)引起的 TOF(fade),其为在频率为 2 Hz 时递送至膈神经干的四脉冲刺激的第四刺激与第一刺激(T(4)/T(1))产生的大鼠膈神经张力的比值。

  3. 除六烃季铵外,所有烟碱拮抗剂均降低了第一刺激期间的肌肉张力幅度。10 nmol/L 哌仑西平(M(1)受体拮抗剂)、1 μmol/L 美加明(M(2)受体拮抗剂)和 2.5 nmol/L 1,3-二丙基-8-环戊基黄嘌呤(A(1)受体拮抗剂)减弱了六烃季铵(5.47 mmol/L)、去极化肌松药(1.1 μmol/L)、维库溴铵(4.7 μmol/L)和罗库溴铵(9.8 μmol/L)诱导的 TOF(fade)。

  4. 用 10 nmol/L ZM241385 阻断 A(2A)受体部分逆转了去极化肌松药、维库溴铵和罗库溴铵引起的 TOF(fade),但不逆转“纯”神经元烟碱受体拮抗剂六烃季铵引起的 TOF(fade),除非将 ZM241385 的浓度增加至 50 nmol/L。

  5. 数据表明,突触前 M(1)、M(2)、A(1)和 A(2A)受体在烟碱拮抗剂引起的神经肌肉 TOF(fade)中发挥作用。这种相互作用取决于腺苷张力和神经肌肉阻滞剂对神经元与肌肉烟碱受体的亲和力。

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