Schiønning J, Møller-Madsen B
Department of Neurobiology, University of Aarhus, Denmark.
Acta Neuropathol. 1991;81(4):434-42. doi: 10.1007/BF00293465.
The autometallographic method has been used in conjunction light and electron microscopy to determine the exact localization of mercury in the rat spinal cord. Adult male Wistar rats were treated intraperitoneally with accumulative doses of mercuric chloride (100-200 micrograms HgCl2 daily). Transverse sections of the first cervical segment (C1), fifth cervical segment (C5), sixth thoracic segment (T6), and first lumbar segment (L1) of the spinal cord were examined. The distribution pattern of mercury was dose dependent. In ventral horn motoneurons and neurons of nucleus dorso-medialis (C1) pronounced staining was found after a total dosage of 1200 micrograms HgCl2. In nucleus intermedio-lateralis (T6, L1) and nucleus cervicalis centralis (C1) stained neurons were first seen after 2600 micrograms HgCl2. Ultrastructurally, mercury deposits were exclusively located in lysosomes of neurons, astrocytes, endothelial cells, and ependymal cells.
运用自动金相法结合光学显微镜和电子显微镜来确定汞在大鼠脊髓中的精确位置。成年雄性Wistar大鼠腹腔注射累积剂量的氯化汞(每日100 - 200微克HgCl₂)。对脊髓的第一颈段(C1)、第五颈段(C5)、第六胸段(T6)和第一腰段(L1)进行横切检查。汞的分布模式呈剂量依赖性。在腹角运动神经元和背内侧核(C1)的神经元中,总剂量达到1200微克HgCl₂后发现明显染色。在中间外侧核(T6、L1)和颈中央核(C1)中,在2600微克HgCl₂后首次见到染色神经元。在超微结构上,汞沉积物仅位于神经元、星形胶质细胞、内皮细胞和室管膜细胞的溶酶体中。