Schwartz-Giblin S, McCarthy M M, Robbins A
Laboratory of Neurobiology and Behavior, Rockefeller University, New York, NY, USA.
Brain Res. 1996 Feb 26;710(1-2):178-88. doi: 10.1016/0006-8993(95)01304-0.
We tested the hypothesis that the effect of systemic injections of diazepam (DZ, 125 mg/kg) to reduce the quality of the reproductive behavior, lordosis, and to reduce the EMG of lumbar back muscles involved in lordosis (Schwartz-Giblin et al., 1984) is exerted through a reticulospinal pathway with cells of origin in the nucleus gigantocellularis that excites lumbar motoneurons indirectly (Robbins et al., 1990, Robbins et al., 1992). In contrast, DZ facilitates lordosis behavior when infused into the midbrain central gray (McCarthy et al., 1995). Direct deposits of crystalline mixtures of DZ (20-80 ng) in dextrose were delivered to the medullary reticular formation (MRF) by diffusion from a cannula inserted through a guide to which a bipolar stimulating electrode was attached. The multiunit EMG response evoked by 20 (300 ms long) stimulus trains was recorded in back and neck muscles, lateral longissimus and splenius before and 5, 15, 30 and 60 min after local DZ deposits. There was a significant reduction in EMG response over this time period when stimulus intensities were within the range of 1.2-1.5 times threshold (Friedman two-way non-parametric test, P < 0.002). Large amplitude motor units that provide large tensions were the most sensitive to DZ-induced inhibition. Control deposits of dextrose had no significant effect. Systemic injections of progesterone (1 mg, i.p.) 60 min after DZ deposits, but not after dextrose deposits, further reduced the MRF-evoked EMG responses over the course of 1 h. As predicted, DZ infusions into the midbrain central gray did not reduce the reticulospinal-evoked axial muscle response, consistent with the facilitatory effect of midbrain central gray infusions of DZ on the lordosis quotient. The results suggest that benzodiazepine agonists (if endogenous) acting at sites in the MRF would be effective muscle relaxants during pregnancy, prior to the fall in progesterone that precedes labor.
全身注射地西泮(DZ,125毫克/千克)会降低生殖行为(脊柱前凸)的质量,并降低参与脊柱前凸的腰背部肌肉的肌电图(Schwartz - Giblin等人,1984年),其作用是通过一条网状脊髓通路实现的,该通路起源于巨细胞网状核的细胞,间接兴奋腰运动神经元(Robbins等人,1990年,Robbins等人,1992年)。相比之下,当将DZ注入中脑中央灰质时,它会促进脊柱前凸行为(McCarthy等人,1995年)。将DZ(20 - 80纳克)与葡萄糖的结晶混合物通过一根插入带有双极刺激电极的引导管的套管扩散,直接注入延髓网状结构(MRF)。在局部注入DZ之前以及之后5、15、30和60分钟,记录在背部和颈部肌肉、外侧最长肌和夹肌中由20次(每次300毫秒长)刺激序列诱发的多单位肌电图反应。当刺激强度在阈值的1.2 - 1.5倍范围内时,在此时间段内肌电图反应有显著降低(Friedman双向非参数检验,P < 0.002)。提供大张力的大振幅运动单位对DZ诱导的抑制最为敏感。葡萄糖的对照注入没有显著影响。在注入DZ 60分钟后而非葡萄糖注入后,腹腔注射孕酮(1毫克)在1小时内进一步降低了MRF诱发的肌电图反应。正如所预测的,将DZ注入中脑中央灰质并没有降低网状脊髓诱发的轴向肌肉反应,这与中脑中央灰质注入DZ对脊柱前凸商数的促进作用一致。结果表明,在分娩前孕酮下降之前,作用于MRF部位的苯二氮䓬激动剂(如果是内源性的)在怀孕期间将是有效的肌肉松弛剂。