Langer J, Seeber U, Kuschinsky K, Sontag K H
Naunyn Schmiedebergs Arch Pharmacol. 1979 Aug;308(2):149-54. doi: 10.1007/BF00499057.
Effects of haloperidol on rat flexor and extensor alpha-motoneurones were studied in ventral roots of laminectomized rats under halothane anesthesia. The alpha-motoneurones were activated by tetanic stimulation of low-threshold afferents (group I and II), either of the ipsilateral peroneal nerve ("flexor alpha-motoneurones") or gastrocnemius-soleus nerve ("extensor alpha-motoneurones"). Haloperidol, given in the doses of 0.075, 0.15 and 0.30 mg/kg i.p. inhibited the reflex activation of flexor alpha-motoneurones; higher doses seemed to be more effective than lower ones. Apomorphine (2 mg/kg s.c.) partially antagonized the inhibitory action of haloperidol with some latency. Higher doses of haloperidol (0.15-0.60 mg/kg i.p.) also inhibited the reflex activation of extensor alpha-motoneurones; this inhibitory effect was, at least for a short time, antagonized by apomorphine (2 mg/kg s.c.). The threshold for reflex activation both of flexor and extensor alpha-motoneurones was raised by haloperidol and lowered by a subsequent administration of apomorphine. Our results suggest that akinesia and catalepsy, induced in rats by haloperidol might be, at least in part, due to a decrease in sensitivity of alpha-motoneurones to proprioceptive stimuli.
在氟烷麻醉下,对行椎板切除术大鼠的腹侧神经根进行研究,观察氟哌啶醇对大鼠屈肌和伸肌α运动神经元的影响。通过对低阈值传入神经(I组和II组)进行强直刺激来激活α运动神经元,这些传入神经来自同侧腓总神经(“屈肌α运动神经元”)或比目鱼肌-腓肠肌神经(“伸肌α运动神经元”)。腹腔注射剂量为0.075、0.15和0.30mg/kg的氟哌啶醇可抑制屈肌α运动神经元的反射激活;高剂量似乎比低剂量更有效。皮下注射阿扑吗啡(2mg/kg)会有一定延迟地部分拮抗氟哌啶醇的抑制作用。更高剂量的氟哌啶醇(0.15 - 0.60mg/kg腹腔注射)也会抑制伸肌α运动神经元的反射激活;这种抑制作用至少在短时间内会被皮下注射阿扑吗啡(2mg/kg)所拮抗。氟哌啶醇会提高屈肌和伸肌α运动神经元的反射激活阈值,而随后注射阿扑吗啡则会降低该阈值。我们的结果表明,氟哌啶醇在大鼠中诱导的运动不能和僵住症可能至少部分是由于α运动神经元对本体感受刺激的敏感性降低所致。