Kobayashi H, Hasegawa Y, Ono H
Department of Pharmacy, Branch Hospital, Faculty of Medicine, University of Tokyo, Japan.
Eur J Pharmacol. 1996 Sep 5;311(1):29-35. doi: 10.1016/0014-2999(96)00402-5.
The centrally acting muscle relaxant cyclobenzaprine was thought to be an alpha 2-adrenoceptor agonist that reduced muscle tone by decreasing the activity of descending noradrenergic neurons. In the present study, we examined the effects of cyclobenzaprine on descending neurons by measuring the monosynaptic reflex in rats. Cyclobenzaprine reduced the monosynaptic reflex amplitude dose dependently and this effect was not inhibited by the alpha 2-adrenoceptor antagonists idazoxan and yohimbine. Cyclobenzaprine-induced monosynaptic reflex depression was not attenuated by noradrenergic neuronal lesions produced by 6-hydroxydopamine. However, cyclobenzaprine inhibited monosynaptic reflex facilitation induced by (+/-)-1-(4-iodo-2,5-dimethoxyphenyl)-2-aminopropane, a 5-HT2 receptor agonist, in spinalized rats markedly, and 5-HT depletion by DL-p-chlorophenylalanine inhibited the depressive effect of cyclobenzaprine on the monosynaptic reflex. These results suggest that cyclobenzaprine is a 5-HT2 receptor antagonist and that its muscle relaxant effect is due to inhibition of serotonergic, not noradrenergic, descending systems in the spinal cord.
中枢性肌肉松弛剂环苯扎林曾被认为是一种α2肾上腺素能受体激动剂,它通过降低下行去甲肾上腺素能神经元的活性来减轻肌张力。在本研究中,我们通过测量大鼠的单突触反射来研究环苯扎林对下行神经元的影响。环苯扎林剂量依赖性地降低单突触反射幅度,且这种作用不受α2肾上腺素能受体拮抗剂咪唑克生和育亨宾的抑制。6-羟基多巴胺造成的去甲肾上腺素能神经元损伤并未减弱环苯扎林引起的单突触反射抑制。然而,环苯扎林能显著抑制5-羟色胺2(5-HT2)受体激动剂(±)-1-(4-碘-2,5-二甲氧基苯基)-2-氨基丙烷在脊髓损伤大鼠中诱导的单突触反射易化,并且DL-对氯苯丙氨酸造成的5-羟色胺耗竭抑制了环苯扎林对单突触反射的抑制作用。这些结果表明,环苯扎林是一种5-HT2受体拮抗剂,其肌肉松弛作用是由于抑制了脊髓中5-羟色胺能而非去甲肾上腺素能下行系统。