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慢性吗啡治疗对小鼠输精管兴奋性接头电位的影响。

The effect of chronic morphine treatment of excitatory junction potentials in the mouse vas deferens.

作者信息

North R A, Vitek L V

出版信息

Br J Pharmacol. 1980 Mar;68(3):399-405. doi: 10.1111/j.1476-5381.1980.tb14553.x.

Abstract

1 Intracellular recordings were made from smooth muscle cells of vasa deferentia in vitro. Vasa from two groups of mice were studied; the first were naive and the second had been chronically pretreated with morphine for 3 days. The vasa from morphine-pretreated mice were maintained in Krebs solution containing normorphine (300 nM). 2 The resting membrane potentials of the smooth muscle cells were the same in both groups of mice. 3 The excitatory junction potentials (e.j.ps) evoked by stimulation of the intramural nerves were depressed by normorphine in both groups of mice. The EC50 for this action of normorphine was 560 nM for the naive group and 6.6 microM for the morphine-pretreated group. 4 The EC50 for adenosine in depressing e.j.p. amplitude was the same in the two groups. 5 Naloxone did not change the resting membrane potential in cells from either group of mice. In morphine-pretreated mice, naloxone caused a marked increase in the amplitude of the evoked e.j.p. 6 The EC50 for noradrenaline in causing a contractile response of the isolated vas deferens was the same in both groups of mice. 7 The results indicate that changes in postsynaptic sensitivity to transmitter do not occur following morphine pretreatment.

摘要
  1. 在体外对输精管平滑肌细胞进行细胞内记录。研究了两组小鼠的输精管;第一组是未处理的,第二组用吗啡进行了3天的慢性预处理。将经吗啡预处理小鼠的输精管置于含有去甲吗啡(300 nM)的 Krebs 溶液中。

  2. 两组小鼠平滑肌细胞的静息膜电位相同。

  3. 两组小鼠中,刺激壁内神经诱发的兴奋性突触后电位(e.j.ps)均被去甲吗啡抑制。去甲吗啡此作用的半数有效浓度(EC50)在未处理组为560 nM,在吗啡预处理组为6.6 μM。

  4. 腺苷抑制e.j.p.幅度的EC50在两组中相同。

  5. 纳洛酮未改变两组小鼠细胞的静息膜电位。在经吗啡预处理的小鼠中,纳洛酮使诱发的e.j.p.幅度显著增加。

  6. 去甲肾上腺素引起离体输精管收缩反应的EC50在两组小鼠中相同。

  7. 结果表明,吗啡预处理后突触后对递质的敏感性未发生变化。

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Supersensitivity to morphine of the transmurally stimulated vas deferens isolated from ethanol-pretreated mice.
Eur J Pharmacol. 1992 Jun 17;216(3):449-51. doi: 10.1016/0014-2999(92)90445-a.

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