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β-氨基丙腈诱导大鼠产生的先天性脊柱侧凸和脊髓损伤。

Congenital kyphoscoliosis and spinal cord lesion produced in the rat by beta-aminopropionitrile.

作者信息

Nogami H, Terashima Y, Tamaki K, Oohira A

出版信息

Teratology. 1977 Dec;16(3):351-7. doi: 10.1002/tera.1420160316.

Abstract

Pregnant rats received the lathyrogen beta-aminopropionitrile (1,500 mg/kg) intraperitoneally on day 16 (plug day = 0 day). Kyphoscoliosis was produced in a high incidence in the fetuses at the level of the upper thoracic spine as early as 24 hours after treatment. Although most of the affected newborns died within two weeks, survivors were studied until 20 weeks after birth. Survivors developed paraplegia in consequence of kyphoscoliosis. Both spinal deformity and motor disturbance were progressive. Biochemical and electron microscopic observations suggested that beta-aminopropionitrile treatment resulted in an inhibition of collagen formation in the spinal column and surrounding longitudinal ligaments of the fetuses six hours after the treatment. In addition, electron micrographs of vertebral bodies showed a decrease of proteoglycan granules in the extracellular matrix. Therefore, rupture and collapse of weakened ligaments and vertebral bodies might result in severe spinal deformity and spinal cord lesion.

摘要

怀孕大鼠在第16天(合笼日=第0天)腹腔注射致脊柱侧凸剂β-氨基丙腈(1500毫克/千克)。早在治疗后24小时,胎儿上胸椎水平就出现了高发病率的脊柱侧凸。虽然大多数受影响的新生儿在两周内死亡,但对存活者进行了研究,直至出生后20周。存活者因脊柱侧凸而发展为截瘫。脊柱畸形和运动障碍都是进行性的。生化和电子显微镜观察表明,β-氨基丙腈治疗导致治疗后6小时胎儿脊柱和周围纵向韧带中的胶原蛋白形成受到抑制。此外,椎体的电子显微照片显示细胞外基质中的蛋白聚糖颗粒减少。因此,薄弱韧带和椎体的破裂和塌陷可能导致严重的脊柱畸形和脊髓损伤。

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