Donnerer J
Institut für Experimentelle und Klinische Pharmakologie, Universität Graz, Austria.
Naunyn Schmiedebergs Arch Pharmacol. 1989 Sep;340(3):352-4. doi: 10.1007/BF00168522.
(1) The stimulation of adrenocorticotrophic hormone (ACTH) release by FG 7142 was found to be 50% inhibited in capsaicin-desensitized rats indicating that the excitatory effect of this inverse benzodiazepine agonist is partly mediated through capsaicin-sensitive afferents. (2) The in vitro release of substance P from spinal cord slices was stimulated in a tetrodotoxin-resistant manner by FG 7142. No stimulation of the substance R release by FG 7142 was observed when spinal cord slices were taken from capsaicin-pretreated rats which lack afferent C-fibres. (3) Ro 15-1788 antagonized the in vivo as well as the in vitro stimulatory effects of FG 7142 indicating that they were brought about by interaction with benzodiazepine receptors. (4) It is concluded that FG 7142 has a direct excitatory effect on central terminals of capsaicin-sensitive afferents and that neurotransmitters released from primary afferents are involved in inducing ACTH release following administration of FG 7142 in vivo.
(1) 研究发现,在辣椒素脱敏大鼠中,FG 7142对促肾上腺皮质激素(ACTH)释放的刺激作用被抑制了50%,这表明这种反向苯二氮䓬激动剂的兴奋作用部分是通过辣椒素敏感传入神经介导的。(2) FG 7142以河豚毒素抗性方式刺激脊髓切片中P物质的体外释放。当从缺乏传入C纤维的辣椒素预处理大鼠获取脊髓切片时,未观察到FG 7142对物质R释放的刺激作用。(3) Ro 15 - 1788拮抗FG 7142的体内和体外刺激作用,表明这些作用是通过与苯二氮䓬受体相互作用产生的。(4) 得出的结论是,FG 7142对辣椒素敏感传入神经的中枢终末具有直接兴奋作用,并且在体内给予FG 7142后,初级传入神经释放的神经递质参与诱导ACTH释放。