Schiønning J D
Department of Neurobiology, University of Aarhus, Denmark.
Toxicol Appl Pharmacol. 1993 Jul;121(1):43-9. doi: 10.1006/taap.1993.1127.
Mercuric chloride was injected into the triceps surae muscle of adult male Wistar rats. Following a survival period of 1, 2, 3, 6, or 100 days, the rats were euthanized by transcardial perfusion. Sections of lumbar spinal cord segments (L4-L6) with corresponding dorsal root ganglia were subjected to the autometallographical silver-enhancement technique in order to localize mercury at both light and electron microscopical levels. Intramuscular injections of mercury resulted in ipsilateral accumulations of mercury in ventral horn motoneurons and dorsal root ganglion cells after a survival period of 2 days. Mercury deposits were still present when animals were allowed to survive 100 days. The mercury staining was suppressed ipsilateral to the intramuscular mercury injection by a microinjection of colchicine into the sciatic nerve or by ligation of the sciatic nerve. At the ultrastructural level, mercury was detected within lysosomes of target cells. The findings indicate that mercury is transported retrogradely in axons of ventral horn motoneurons and dorsal root ganglion cells.
将氯化汞注射到成年雄性Wistar大鼠的腓肠肌中。在1、2、3、6或100天的存活期后,通过心脏灌注使大鼠安乐死。对带有相应背根神经节的腰脊髓节段(L4-L6)切片进行自动金属显影银增强技术处理,以便在光学和电子显微镜水平上定位汞。肌肉内注射汞后,在2天的存活期后,同侧腹角运动神经元和背根神经节细胞中出现汞的积累。当动物存活100天时,汞沉积物仍然存在。通过向坐骨神经微量注射秋水仙碱或结扎坐骨神经,可抑制肌肉内汞注射同侧的汞染色。在超微结构水平上,在靶细胞的溶酶体内检测到汞。这些发现表明,汞在腹角运动神经元和背根神经节细胞的轴突中逆行运输。