Martin J E, Sosa-Melgarejo J A, Swash M, Mather K, Leigh P N, Berry C L
Department of Morbid Anatomy, Royal London Hospital, Whitechapel, U.K.
Virchows Arch A Pathol Anat Histopathol. 1991;419(5):403-8. doi: 10.1007/BF01605074.
Compounds causing neurolathyrism are putative aetiological agents in neurodegenerative disorders including amyotrophic lateral sclerosis. beta-Aminopropionitrile (BAPN) is one such compound. We have administered this lathyrogenic agent at a dose of 1 g/kg by the intraperitoneal route in experiments in adult Sprague-Dawley rats during a period of 10 weeks. The rats developed marked kyphoscoliosis, ataxia with paralysis and muscle wasting of the hind limbs. Vacuolation and loss of Purkinje cells developed, but no anterior horn cell degeneration was noted. Immunohistochemical studies of phosphorylated neurofilaments and the 72 kDa heat shock protein were normal and no intraneuronal ubiquitinated inclusions were seen. High-dose intraperitoneal BAPN in the rat causes Purkinje cell changes, but no other central nervous system abnormalities.
导致骨软化症的化合物被认为是包括肌萎缩侧索硬化症在内的神经退行性疾病的病因。β-氨基丙腈(BAPN)就是这样一种化合物。在成年Sprague-Dawley大鼠的实验中,我们以1 g/kg的剂量通过腹腔注射途径给予这种致畸形剂,持续10周。大鼠出现了明显的脊柱后凸侧弯、共济失调伴瘫痪以及后肢肌肉萎缩。浦肯野细胞出现空泡化和丢失,但未观察到前角细胞变性。磷酸化神经丝和72 kDa热休克蛋白的免疫组织化学研究结果正常,未发现神经元内泛素化包涵体。大鼠腹腔注射高剂量BAPN会导致浦肯野细胞改变,但不会引起其他中枢神经系统异常。