Umeda E, Satoh T, Nagashima H, Potter P E, Tarkovács G, Vizi E S
Department of Anesthesiology, SDF Yokosuka Naval Hospital, Kanagawa, Japan.
Brain Res Bull. 1997;42(2):129-32. doi: 10.1016/s0361-9230(96)00223-7.
The modulation of noradrenaline (NA) release from rat spinal cord slices was investigated and the subtype of presynaptic alpha 2-adrenoceptors involved in the negative feedback modulation was characterized using in vitro perfusion experiments. Rat spinal cord slices were loaded with [3H]NA and the release of radioactivity at rest and in response to field stimulation was determined. The alpha 2-adrenoceptor agonists, clonidine and dexmedetomidine inhibited the stimulation-evoked release of NA from spinal cord slices, whereas alpha 2-adrenoceptor antagonists yohimbine and CH-38083 (7,8-(methylenedioxy)-14-alpha-hydroxyalloberbane HCI), enhanced it. ARC 239, a selective alpha 2B-antagonist, had no effect on the release. In contrast, BRL 44408 a selective alpha 2A-antagonist increased the release of NA. Our results indicate that the negative feedback modulation of NA release from noradrenergic fibres in the spinal cord is mediated via alpha 2A subtype of alpha 2-adrenoceptors.
研究了大鼠脊髓切片中去甲肾上腺素(NA)释放的调节,并通过体外灌注实验确定了参与负反馈调节的突触前α2肾上腺素能受体亚型。将大鼠脊髓切片用[3H]NA标记,并测定静息时和电场刺激时放射性的释放。α2肾上腺素能受体激动剂可乐定和右美托咪定抑制脊髓切片中刺激诱发的NA释放,而α2肾上腺素能受体拮抗剂育亨宾和CH-38083(7,8-(亚甲二氧基)-14-α-羟基别罗勒烷盐酸盐)则增强其释放。选择性α2B拮抗剂ARC 239对释放无影响。相反,选择性α2A拮抗剂BRL 44408增加了NA的释放。我们的结果表明,脊髓中去甲肾上腺素能纤维释放NA的负反馈调节是通过α2肾上腺素能受体的α2A亚型介导的。