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Supplementation with D-serine prevents the onset of cognitive deficits in adult offspring after maternal immune activation

机译:用D-丝氨酸补充防止成人后代在母体免疫激活后的认知缺陷发作

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Prenatal maternal infection contributes to the etiology of schizophrenia, with D-serine, an endogenous co-agonist of the N-methyl-D-aspartate (NMDA) receptor, playing a role in the pathophysiology of this disease. We examined whether supplementation with D-serine during juvenile and adolescent stages could prevent the onset of cognitive deficits, prodromal and the core symptoms of schizophrenia in adult offspring after maternal immune activation (MIA). Juvenile offspring exposed prenatally to poly(I:C) showed reduced expression of NMDA receptor subunits in the hippocampus. Supplementing drinking water with D-serine (600?mg/L from P28 to P56) prevented the onset of cognitive deficits in adult offspring after MIA, in a significant manner. This study shows that supplementing offspring with D-serine during juvenile and adolescent stages could prevent the onset of psychosis in adulthood, after MIA. Therefore, early intervention with D-serine may prevent the occurrence of psychosis in high-risk subjects.
机译:产前的母体感染有助于精神分裂症的病因,用D-丝氨酸,N-甲基-D-天冬氨酸(NMDA)受体的内源共激剂,在该疾病的病理生理学中发挥作用。我们检查了在幼年和青少年阶段期间对D-丝氨酸进行补充,可以防止认知缺陷,产物和精神分裂症的核心症状在母体免疫激活后成人后代(MIA)。少年后代暴露于聚(i:c)的预先暴露(I:c)表明,在海马中的NMDA受体亚基表达减少。用D-丝氨酸(P28至P56的600×mg / L补充饮用水)在MIA之后,在MIA之后的成人后代在成人后代的认知缺陷发生了饮用水。本研究表明,在幼儿期间,补充在青少年和青少年阶段的D-丝氨酸的后代可以防止在MIA之后的成年人心理学发生。因此,与D-丝氨酸的早期干预可能会阻止高风险受试者的精神病发生。

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