首页> 外文期刊>Journal of Neuropathology and Experimental Neurology: Official Journal of the American Association of Neuropathologists, Inc >NMDA receptor 1 expression in the brainstem of human infants and its relevance to the sudden infant death syndrome (SIDS).
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NMDA receptor 1 expression in the brainstem of human infants and its relevance to the sudden infant death syndrome (SIDS).

机译:NMDA受体1在人类婴儿脑干中的表达及其与婴儿猝死综合征(SIDS)的相关性。

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摘要

The N-methyl-D-aspartate (NMDA) glutamatergic receptor is widely expressed in the brain during the early postnatal period and, among other functions is involved in cardiorespiratory control and in cell death by excitotoxic mechanisms. This study examined NMDA receptor-1 (NR1) expression in the human infant brainstem and assessed whether expression differed between non-SIDS and SIDS infants. NRI mRNA was identified using non-radioactive in situ hybridization and quantified by optical density. NRI protein was identified by immunohistochemistry and quantified by cellular counting. Eight nuclei of the mid-medulla and 2 nuclei of the rostral pons were studied. NRI mRNA and protein were expressed in all nuclei studied, confirming that the NMDA receptor is widely distributed in the human infant brainstem. Compared to non-SIDS infants (n = 10). SIDS infants (n = 15) had increased mRNA in 6 nuclei of the mid-medulla (p < 0.05 for all) while protein was increased in the dorsal motor nucleus of the vagus (p = 0.04) and decreased in the nucleus of the spinal trigeminal tract (p = 0.03). No differences were observed in the rostral pons. This preliminary study suggests that abnormalities of the glutamatergic system are present in SIDS victims. Further studies will be required to delineate these abnormalities and to investigate potential underlying mechanisms and sequelae.
机译:N-甲基-D-天门冬氨酸(NMDA)谷氨酸能受体在产后早期在大脑中广泛表达,除其他功能外,还通过兴奋性毒性机制参与心肺控制和细胞死亡。这项研究检查了人类婴儿脑干中NMDA受体1(NR1)的表达,并评估了非SIDS和SIDS婴儿之间的表达是否不同。使用非放射性原位杂交鉴定NRI mRNA,并通过光密度定量。 NRI蛋白通过免疫组织化学鉴定,并通过细胞计数进行定量。研究了延髓中部的八个核和延髓桥的两个核。 NRI mRNA和蛋白均在所有研究的核中表达,证实NMDA受体广泛分布于人类婴儿脑干中。与非SIDS婴儿相比(n = 10)。 SIDS婴儿(n = 15)在延髓中部6个核中的mRNA增加(全部p <0.05),而迷走神经的背运动核中的蛋白增加(p = 0.04),在脊髓核中减少三叉神经束(p = 0.03)。延髓桥没有观察到差异。这项初步研究表明,SIDS受害者中存在谷氨酸能系统异常。需要进一步的研究来描述这些异常并调查潜在的潜在机制和后遗症。

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