Nagele R G, Bush K T, Hunter E T, Kosciuk M C, Lee H
Department of Pediatrics, University of Medicine and Dentistry of New Jersey, School of Osteopathic Medicine, Camden 08103.
Teratology. 1989 Jul;40(1):29-36. doi: 10.1002/tera.1420400105.
The biomechanical basis of diazepam (Valium/Roche)-induced neural tube defects in the chick was investigated using a combination of electron microscopy and morphometry. Embryos at stage 8 (four-somite stage) of development were explanted and grown for 6 hr in nutrient medium containing 400 micrograms/ml diazepam. Nearly 80% of these embryos exhibited neural tube defects that were most pronounced in the forming midbrain region and typified by a "relaxation" or "collapse" of neural folds. The hindbrain and spinal cord regions were less affected. Electron microscopy revealed that neuroepithelial cells in diazepam-treated embryos had smoother apical surfaces and broader apical widths than did controls. Morphometric measurements supported this observation and further showed that these effects were focused at sites within the wall of the forming neural tube that typically exhibit the greatest degree of bending and apical constriction (i.e., the floor and midlateral walls). Overall results indicate that neural tube defects associated with exposure to diazepam are due largely to a general inhibition of the contractile activity of apical microfilament bundles in neuroepithelial cells. These findings 1) emphasize the important contribution of microfilament-mediated apical constriction of neuroepithelial cells in providing the driving forces for bending of the neuroepithelium during neural tube formation and 2) suggest that agents or conditions that impair their contractile activity could play a role in the pathogenesis of certain types of neural tube defects.
运用电子显微镜和形态测量学相结合的方法,研究了地西泮(安定/罗氏)诱导鸡神经管缺陷的生物力学基础。处于发育第8阶段(四体节期)的胚胎被移出,并在含有400微克/毫升地西泮的营养培养基中培养6小时。近80%的这些胚胎表现出神经管缺陷,在形成中的中脑区域最为明显,其特征为神经褶的“松弛”或“塌陷”。后脑和脊髓区域受影响较小。电子显微镜显示,与对照组相比,用地西泮处理的胚胎中的神经上皮细胞具有更光滑的顶端表面和更宽的顶端宽度。形态测量学测量结果支持了这一观察,并进一步表明这些影响集中在形成中的神经管壁内通常表现出最大程度弯曲和顶端收缩的部位(即底部和中外侧壁)。总体结果表明,与接触地西泮相关的神经管缺陷主要是由于神经上皮细胞顶端微丝束收缩活性的普遍抑制。这些发现1)强调了微丝介导的神经上皮细胞顶端收缩在神经管形成过程中为神经上皮弯曲提供驱动力方面的重要贡献,2)表明损害其收缩活性的药物或条件可能在某些类型神经管缺陷的发病机制中起作用。