Hino M, Ono H, Fukuda H
Gen Pharmacol. 1986;17(4):379-83. doi: 10.1016/0306-3623(86)90178-3.
The brain stem areas involved in the inhibitory effect of chlorpromazine (CPZ) on the monosynaptic reflex (MSR) in the lumbar spinal cord of rats were investigated following brain stem transection and focal thermo-lesioning. Transection of the medulla oblongata markedly reduced the effect of CPZ, while transection in the mid-brain or more anterior level did not alter the effect of CPZ. With regard to focal lesions at various sites of the brain stem, lesioning of the medial portion of the medulla oblongata most effectively attenuated the MSR inhibition by CPZ and also attenuated the MSR inhibition induced by phenoxybenzamine. Bilateral lesioning of the locus coeruleus did not attenuate the MSR inhibition by CPZ. These results suggest that the pathway involved in the inhibitory effect of CPZ on the MSR originates in the pons and passes through the medial portion of the medulla oblongata, and that the coerulo-spinal pathway is not the major pathway involved in the effect of CPZ.
在大鼠脑干横断和局灶性热损伤后,研究了参与氯丙嗪(CPZ)对大鼠腰髓单突触反射(MSR)抑制作用的脑干区域。延髓横断显著降低了CPZ的作用,而中脑或更靠前水平的横断并未改变CPZ的作用。关于脑干不同部位的局灶性损伤,延髓内侧部分的损伤最有效地减弱了CPZ对MSR的抑制作用,也减弱了苯氧苄胺诱导的MSR抑制作用。蓝斑双侧损伤并未减弱CPZ对MSR的抑制作用。这些结果表明,CPZ对MSR抑制作用所涉及的通路起源于脑桥并经过延髓内侧部分,并且蓝斑-脊髓通路不是CPZ作用所涉及的主要通路。