Muhyaddin M S, Roberts P J, Woodruff G N
Eur J Pharmacol. 1983 Aug 19;92(1-2):9-14. doi: 10.1016/0014-2999(83)90102-4.
The release of preaccumulated [3H]noradrenaline from the isolated rat anococcygeus muscle, a tissue endowed with a rich noradrenergic innervation, was investigated. Field stimulation produced a marked, calcium-dependent enhancement in release, which could be substantially inhibited by the inclusion of low concentrations of GABA or (-)-baclofen (but not the (+)-isomer) in the bathing medium. Classical GABAA site agonists such as muscimol or 3-aminopropanesulphonic acid were inactive, or only weakly so. Picrotoxin and bicuculline were unable to antagonise the effects of GABA or baclofen on [3H]noradrenaline release, although 5-aminovalerate was effective. These data provide further evidence for the existence of GABAB receptors associated with presynaptic noradrenergic terminals in the rat anococcygeus muscle.
研究了从离体大鼠肛门尾骨肌释放预先积累的[3H]去甲肾上腺素的情况,该组织具有丰富的去甲肾上腺素能神经支配。场刺激使释放显著增强,且这种增强依赖于钙,在浴液中加入低浓度的GABA或(-)-巴氯芬(而非(+)-异构体)可显著抑制这种增强。经典的GABAA位点激动剂如蝇蕈醇或3-氨基丙烷磺酸无活性,或仅有微弱活性。印防己毒素和荷包牡丹碱无法拮抗GABA或巴氯芬对[3H]去甲肾上腺素释放的作用,尽管5-氨基戊酸有效。这些数据为大鼠肛门尾骨肌中与突触前去甲肾上腺素能终末相关的GABAB受体的存在提供了进一步证据。