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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >THE POTENTIAL IMPACTS OF THE ANTI-EPILEPTIC DRUG (OXCARBAZEPINE) ON ALBINO RAT’S NEONATES DURING LACTATION
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THE POTENTIAL IMPACTS OF THE ANTI-EPILEPTIC DRUG (OXCARBAZEPINE) ON ALBINO RAT’S NEONATES DURING LACTATION

机译:哺乳期抗癫痫药物(氧卡巴西汀)对白化病大鼠新生代的潜在影响

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Objective: This study was undertaken to evaluate the potential risks of the anti-epileptic drug (oxcarbazepine [OXC]) administration on neonates. Methods: The nursing rats orally administered from 7 th day of gestation until the 28 day of lactation with 108 mg/kg OXC (human equivalent dose) daily. The neonates at day 7, 14, 21, and 28 of lactation were sacrificed and the postnatal developmental signs and skeletal malformation and the histopathology of liver, kidney, and brain of the pups were examined. th Results: Our results showed that OXC induced a significant reduction in the neonatal weight and length, delayed, weak and incomplete ossification, wavy ribs and the neonatal liver revealed histopathological changes, pyknotic hepatocytes, cytoplasmic vacuolization, dilated sinusoid, and necrotic area. Kidney revealed alternation changes, enlargement of the glomerulus, renal tubules degeneration, and lymphatic infiltration. Brain (cerebral cortex and cerebellum) showed neurodegenerative changes, vacuolization of neuropil, congested and dilated blood vessel and dark stain neurons. Biochemical studies showed that OXC induced a reduction in the level glutathione reduced an important intracellular antioxidant, and catalase (enzymatic antioxidant) compared to control group. Conclusions: We support and proof the potential risks of the OXC administration on neonates.
机译:目的:本研究旨在评估抗癫痫药(奥卡西平[OXC])对新生儿的潜在风险。方法:从妊娠第7天到哺乳期28天,每天口服108 mg / kg OXC(人当量)的哺乳期大鼠。处死哺乳期第7、14、21和28天的新生儿,检查幼崽的产后发育体征和骨骼畸形以及肝,肾和脑的组织病理学。结果:我们的结果表明OXC引起新生儿体重和身长的显着减少,延迟,软弱和不完全的骨化,肋骨波浪和新生儿肝脏显示出组织病理学变化,黏结性肝细胞,细胞质空泡化,正弦窦扩张和坏死区域。肾脏显示交替变化,肾小球增大,肾小管变性和淋巴浸润。脑(大脑皮层和小脑)显示神经退行性改变,神经纤维的空泡化,血管充血和扩张以及深色神经元。生化研究表明,与对照组相比,OXC诱导的谷胱甘肽水平降低降低了重要的细胞内抗氧化剂和过氧化氢酶(酶促抗氧化剂)。结论:我们支持并证明OXC给药对新生儿的潜在风险。

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