普瑞巴林对白化大鼠出生后小脑皮质发育的可能影响(组织学和超微结构研究)。

S. Ouies, Z. Ismail, Mostafa Atya
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引用次数: 0

摘要

背景:普瑞巴林是一种用于治疗神经性疼痛、广泛性焦虑障碍和癫痫的口服药物;作为局部癫痫的治疗方法。只有在怀孕期间,小脑的发育才不完全;但在出生后持续到小脑成熟(出生后发育)。研究普瑞巴林对白化病大鼠出生后小脑皮质发育的可能影响。材料与方法:将60只妊娠白化大鼠分为3组;A组:20只对照母鼠的20只子代;B组:20只母鼠的20只子代,口服普瑞巴林剂量为150mg/kg; C组:20只母鼠的25只子代,口服普瑞巴林剂量为600mg/kg。三组大鼠分别在出生后(1、2、3周)和成年后(2.5个月)处死。打开颅骨,取出小脑,进行光镜和透射电镜观察。结果:妊娠和哺乳期给药普瑞巴林在产后早期就有明显的作用,这种作用一直延续到成年期;表现为外颗粒层增加(主要在第2周和第3周);各处理组分子层厚度均减小;浦肯野细胞萎缩、形态异常,出现细胞膜不清、细胞核破坏;主要是高剂量。内颗粒层分化延迟,颗粒细胞出现细胞质膜和细胞器明显破坏。结论:产前和产后低剂量和高剂量普瑞巴林均可引起小脑皮质细胞成分的丧失和变形,并呈剂量依赖性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Possible Effect of pregabalin on the postnatal development of the cerebellar cortex in albino rats (Histological &Ultrastrucural study).
Background: Pregabalin is an oral medication that is used to treat neuropathic pain, generalized anxiety disorder and epilepsy; as a therapy for partial seizures. Cerebellar development is not complete during gestation only; but continues after birth to maturation of the cerebellum (postnatal development).Aim of the Work: To study the possible effect of Pregabalin on the postnatal development of the cerebellar cortex of albino rat.Materialandmethods:60 pregnant albino rats were allocated into three groups; Group A: Included 20offspring of 20 control mothers, Group B: Included 20 offspring of 20 mothers treated orally with pregabalin at a dose of 150mg/kg, and Group C:included 25 offspring of 20 mothers treated orally with pregabalin at a dose of 600mg/kg. In the three groups rats were sacrificed at postnatal (age 1, 2, 3 weeks), in addition to adult age (2.5 months).The skulls were opened and the cerebella were removed and processed for light and transmission electron microscope. Results: Pregabalin administration during pregnancy and lactation caused its marked effect during early postnatal life and this effect extended till the adult stage; in the form of increase in the external granular layer (mainly in the 2nd and 3rd weeks); less thickness of the molecular layer in all treated groups; shrunken and abnormal shaped Purkinje cells which appeared with ill-defined cell membranes and destructed nuclei; mainly at higher dose. There were also delayed differentiation of the internal granular layer and granule cells appeared with destructed cytoplasmic membrane and organelles which appeared prominent at higher doses. Conclusion: Pre and postnatal administration of pregabalin in both low and high doses caused loss of cellular components, distortions of cerebellar cortical cells in a dose dependent manner.
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