Ansari K S, Yu P H, Kruck T P, Tatton W G
Department of Physiology, University of Toronto, Ontario, Canada.
J Neurosci. 1993 Sep;13(9):4042-53. doi: 10.1523/JNEUROSCI.13-09-04042.1993.
The role of monoamine oxidase B (MAO-B) in R(-)-deprenyl-mediated rescue of rat facial motoneurons axotomized at postnatal day 14 (P14) was investigated using the (+)- and (-)-enantiomers of deprenyl [S(+)-deprenyl and R(-)-deprenyl]. Previously, doses of R(-)-deprenyl sufficient to inhibit MAO-B were shown to increase the survival of motoneurons following an apparent loss of target-derived trophic support caused by axotomy in P14 rats. In the present experiments, motoneuronal survival was measured 21 d after unilateral facial nerve transection at P14. The animals were treated with saline or doses of R(-)- or S(+)-deprenyl ranging from 0.001 to 10 mg/kg every 2 days (/2d). Frontal serial 10 microns sections were taken through the length of the facial nuclei ipsilaterally and contralaterally to the facial nerve transections. Every third section was immunoreacted for an antibody against ChAT to identify the motoneuron somata, while every adjacent third section was Nissl stained to assess motoneuronal survival. A second series of P14 rats was treated with similar doses of the two deprenyl enantiomers or saline and the brainstems removed for measurement of MAO-A and MAO-B activity at 4 hr after the treatments. Averages of 24% of the facial motoneurons survived axotomy with either saline treatment or 0.001 mg/kg/2d doses of R(-)-deprenyl. Doses of R(-)-deprenyl of 0.005, 0.01, and 10.0 mg/kg/2d increased the surviving facial motoneuron to 38%, 51%, and 48%, respectively, indicating an ED50 of about 0.005 mg/kg/2d. Doses of S(+)-deprenyl as high as 10 mg/kg/2d did not increase motoneuronal survival, revealing a stereospecificity for the increased survival of at least 2000-fold. The ED50 for MAO-B inhibition in the P14 brainstem was approximately 0.1 mg/kg for the (-)-enantiomer and 2.0 mg/kg for the (+)-enantiomer, revealing a 20-fold higher sensitivity of the enzyme toward the (-)-enantiomer in the P14 rat brainstem. A dose of 10 mg/kg of S(+)-deprenyl inhibited about 65% of brainstem MAO-B activity without increasing motoneuronal survival, whereas 0.005 and 0.01 mg/kg of R(-)-deprenyl increased motoneuronal survival without significant inhibition of brainstem MAO-B activity.(ABSTRACT TRUNCATED AT 400 WORDS)
使用去甲丙咪嗪的(+)-和(-)-对映体[S(+)-去甲丙咪嗪和R(-)-去甲丙咪嗪]研究了单胺氧化酶B(MAO-B)在R(-)-去甲丙咪嗪介导的对出生后第14天(P14)切断轴突的大鼠面部运动神经元的挽救中的作用。此前研究表明,足以抑制MAO-B的R(-)-去甲丙咪嗪剂量能够增加P14大鼠因轴突切断导致的靶源性营养支持明显丧失后运动神经元的存活率。在本实验中,于P14时单侧切断面神经,21天后测量运动神经元的存活率。动物每隔2天接受盐水或0.001至10 mg/kg剂量的R(-)-或S(+)-去甲丙咪嗪治疗。沿面神经横断同侧和对侧的面神经核全长制作连续的10微米额叶切片。每隔第三张切片用抗ChAT抗体进行免疫反应以识别运动神经元胞体,而每隔相邻的第三张切片进行尼氏染色以评估运动神经元的存活率。另一组P14大鼠用两种去甲丙咪嗪对映体或盐水的相似剂量进行治疗,治疗后4小时取出脑干测量MAO-A和MAO-B活性。盐水治疗或0.001 mg/kg/2d剂量的R(-)-去甲丙咪嗪治疗后,平均24%的面部运动神经元在轴突切断后存活。0.005、0.01和10.0 mg/kg/2d剂量的R(-)-去甲丙咪嗪分别将存活的面部运动神经元增加至38%、51%和48%,表明半数有效剂量(ED50)约为0.005 mg/kg/2d。高达10 mg/kg/2d剂量的S(+)-去甲丙咪嗪未增加运动神经元的存活率,显示出至少2000倍的存活增加的立体特异性。P14脑干中MAO-B抑制的ED50,(-)-对映体约为0.1 mg/kg,(+)-对映体为2.0 mg/kg,表明该酶在P14大鼠脑干中对(-)-对映体的敏感性高20倍。10 mg/kg剂量的S(+)-去甲丙咪嗪抑制约65%的脑干MAO-B活性但未增加运动神经元的存活率,而0.005和0.01 mg/kg的R(-)-去甲丙咪嗪增加运动神经元的存活率但未显著抑制脑干MAO-B活性。(摘要截取自400字)