Harper B, Hughes I E
Br J Pharmacol. 1979 Dec;67(4):511-7. doi: 10.1111/j.1476-5381.1979.tb08696.x.
1 The effect of various antidepressants (5 x 10(-8) to 2 x 10(-5) M) on the resting overflow of tritium, on the evoked overflow and the contractile response to electrical stimulation (2.5 Hz, 2.0 ms) has been determined in mouse vas deferens previously incubated with [(3)H]-(-)-noradrenaline.2 Mianserin and ORG GC 94 produced a concentration-dependent increase of more than two fold in the electrically evoked overflow and the contractile response and, at the highest concentration, slightly increased resting release. These effects were largely unchanged in the presence of a concentration of cocaine effective in blocking noradrenaline uptake (1.1 x 10(-5) M).3 The ability of phentolamine (1 x 10(-5) M) to increase both the evoked overflow of tritium and the contractile response was greatly reduced when these parameters were already elevated by the presence of mianserin or ORG GC 94.4 The inhibitory effect of exogenous (-)-noradrenaline on evoked overflow was greatly reduced in the presence of mianserin or ORG GC 94 (4 x 10(-6) M).5 The inhibitory effect of clonidine on the twitch response of the mouse vas deferens was antagonized by mianserin and ORG GC 94 in a competitive manner (pA(2) values 7.3 and 7.1 respectively).6 Maprotiline, desipramine and nortriptyline (> 3 x 10(-6) M) produced a parallel fall in both evoked tritium overflow and in the contractile response and increased the resting overflow at higher concentrations. These effects were largely unchanged in the presence of cocaine (1.1 x 10(-5) M).7 Doxepin, imipramine and iprindole all increased resting overflow at high concentrations (2 x 10(-5) M) but produced only small changes in evoked overflow and in the contractile response at lower concentrations.8 It is concluded that mianserin and ORG GC 94 produce a blockade of presynaptic alpha-adrenoceptors which could contribute to an antidepressant effect but that this type of action is not common to all antidepressants.
在预先用[³H]-(-)-去甲肾上腺素孵育的小鼠输精管中,已测定了各种抗抑郁药(5×10⁻⁸至2×10⁻⁵M)对氚的静息释放、诱发释放以及对电刺激(2.5Hz,2.0ms)的收缩反应的影响。
米安色林和ORG GC 94使电诱发释放和收缩反应呈浓度依赖性增加两倍以上,在最高浓度时,静息释放略有增加。在存在有效阻断去甲肾上腺素摄取的可卡因浓度(1.1×10⁻⁵M)时,这些作用基本未变。
当这些参数已因米安色林或ORG GC 94的存在而升高时,酚妥拉明(1×10⁻⁵M)增加氚诱发释放和收缩反应的能力大大降低。
在存在米安色林或ORG GC 94(4×10⁻⁶M)时,外源性(-)-去甲肾上腺素对诱发释放的抑制作用大大降低。
可乐定对小鼠输精管抽搐反应的抑制作用被米安色林和ORG GC 94以竞争性方式拮抗(pA₂值分别为7.3和7.1)。
马普替林、地昔帕明和去甲替林(>3×10⁻⁶M)使诱发的氚释放和收缩反应同时平行下降,并在较高浓度时增加静息释放。在存在可卡因(1.1×10⁻⁵M)时,这些作用基本未变。
多塞平、丙咪嗪和茚满二氮卓在高浓度(2×10⁻⁵M)时均增加静息释放,但在较低浓度时对诱发释放和收缩反应仅产生微小变化。
得出结论:米安色林和ORG GC 94产生突触前α-肾上腺素能受体的阻断作用,这可能有助于产生抗抑郁作用,但这种作用类型并非所有抗抑郁药所共有。