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The effect of naloxone on vasopressin release from rat neurohypophysis incubated in vitro.

机译:纳洛酮对体外培养的大鼠神经垂体释放加压素的影响。

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摘要

Rat posterior pituitaries were superfused in vitro and stimulated electrically. The concentrations of vasopressin in the superfusion medium were determined by radioimmunoassay. When the pulses were applied in 10 sec trains with 10 sec intervals, vasopressin release per pulse increased progressively over the frequency range of 3-12 pulses/sec applied within the trains. The release was blocked by addition of tetrodotoxin or by removal of calcium ions from the superfusion medium. The opiate antagonist naloxone 1 or 10 microM was introduced into the superfusion medium before a second period of stimulation and enhanced vasopressin release from neurointermediate lobes after phasic stimulation at 9 pulses/sec within the trains, when compared to controls. However, naloxone 10 microM had not effect on vasopressin release from isolated neural lobes (intermediate lobes removed), although the addition of camel beta-endorphin 2 microM inhibited vasopressin release in a naloxone-reversible manner. After continuous stimulation at a frequency of 13 Hz naloxone 10 microM did not influence the release of vasopressin from neurointermediate lobes. We conclude that the evoked release of vasopressin from the neurointermediate lobe is reduced by an endogenous opiate of intermediate lobe origin, possibly beta-endorphin. Appropriate stimulation conditions are necessary for this mechanism to function.
机译:大鼠后垂体在体外被融合并被电刺激。通过放射免疫测定法测定灌注培养基中血管加压素的浓度。当以10秒的间隔在10秒的火车中施加脉冲时,每个脉冲的加压素释放在火车中施加的3-12个脉冲/秒的频率范围内逐渐增加。通过添加河豚毒素或通过从超融合培养基中去除钙离子来阻止释放。与训练组相比,在训练中以9脉冲/秒的速度进行第二次刺激和阶段性刺激后神经中间叶中加压素释放的增加,将鸦片拮抗剂纳洛酮1或10 microM引入超融合培养基中。但是,纳洛酮10 microM对从分离的神经叶释放的加压素没有影响(除去中间叶),尽管添加骆驼β-内啡肽2 microM以纳洛酮可逆的方式抑制了加压素的释放。在以13 Hz的频率连续刺激后,纳洛酮10 microM不会影响神经中间叶中加压素的释放。我们得出的结论是,从神经中间叶诱发的加压素释放由中间叶起源的内源性阿片(可能为β-内啡肽)降低。适当的刺激条件对于该机制起作用是必要的。

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