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组胺H1受体参与糖尿病大鼠胚胎背侧端脑神经发生的增加。

The Histamine H1 Receptor Participates in the Increased Dorsal Telencephalic Neurogenesis in Embryos from Diabetic Rats.

作者信息

Solís Karina H, Méndez Laura I, García-López Guadalupe, Díaz Néstor F, Portillo Wendy, De Nova-Ocampo Mónica, Molina-Hernández Anayansi

机构信息

Departamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología "Isidro Espinosa de los Reyes", Mexico City, Mexico.

Programa Institucional de Biomedicina Molecular, Sección de Estudios de Posgrado e Investigación, Insituto Politécnico Nacional, Escuela Nacional de Medicina y Homeopatía, Mexico City, Mexico.

出版信息

Front Neurosci. 2017 Dec 14;11:676. doi: 10.3389/fnins.2017.00676. eCollection 2017.

Abstract

Increased neuron telencephalic differentiation during deep cortical layer formation has been reported in embryos from diabetic mice. Transitory histaminergic neurons within the mesencephalon/rhombencephalon are responsible for fetal histamine synthesis during development, fibers from this system arrives to the frontal and parietal cortex at embryo day (E) 15. Histamine is a neurogenic factor for cortical neural stem cells through H receptor (HR) which is highly expressed during corticogenesis in rats and mice. Furthermore, administration of an HR antagonist, chlorpheniramine, decreases the neuron markers microtubuline associated protein 2 (MAP2) and forkhead box protein 2. Interestingly, in the diabetic mouse model of diabetes induced with streptozotocin, an increase in fetal neurogenesis in terms of MAP2 expression in the telencephalon is reported at E11.5. Because of the reported effects on cortical neuron differentiation of maternal diabetes in one hand and of histamine in the other, here the participation of histamine and HR on the increased dorsal telencephalic neurogenesis was explored. First, the increased neurogenesis in the dorsal telencephalon at E14 in diabetic rats was corroborated by immunohistochemistry and Western blot. Then, changes during corticogenesis in the level of histamine was analyzed by ELISA and in HR expression by qRT-PCR and Western blot and, finally, we tested HR participation in the increased dorsal telencephalic neurogenesis by the systemic administration of chlorpheniramine. Our results showed a significant increase of histamine at E14 and in the expression of the receptor at E12. The administration of chlorpheniramine to diabetic rats at E12 prevented the increased expression of βIII-tubulin and MAP2 mRNAs (neuron markers) and partially reverted the increased level of MAP2 protein at E14, concluding that HR have an important role in the increased neurogenesis within the dorsal telencephalon of embryos from diabetic rats. This study opens new perspective on the participation of HA and HR receptor in early corticogenesis in health and disease.

摘要

据报道,糖尿病小鼠胚胎在深层皮质层形成过程中神经元端脑分化增加。中脑/后脑内的短暂性组胺能神经元在发育过程中负责胎儿组胺合成,该系统的纤维在胚胎第15天到达额叶和顶叶皮质。组胺是皮质神经干细胞的神经发生因子,通过在大鼠和小鼠皮质发生过程中高表达的H受体(HR)起作用。此外,给予HR拮抗剂氯苯那敏会降低神经元标志物微管相关蛋白2(MAP2)和叉头框蛋白2。有趣的是,在链脲佐菌素诱导的糖尿病小鼠模型中,据报道在胚胎第11.5天,端脑内MAP2表达方面的胎儿神经发生增加。鉴于一方面报道了母体糖尿病对皮质神经元分化的影响,另一方面报道了组胺的影响,在此探讨了组胺和HR对背侧端脑神经发生增加的参与情况。首先,通过免疫组织化学和蛋白质印迹证实了糖尿病大鼠在胚胎第14天背侧端脑神经发生增加。然后,通过酶联免疫吸附测定(ELISA)分析皮质发生过程中组胺水平的变化,通过定量逆转录聚合酶链反应(qRT-PCR)和蛋白质印迹分析HR表达,最后,通过全身给予氯苯那敏测试HR在背侧端脑神经发生增加中的参与情况。我们的结果显示,胚胎第14天组胺显著增加,胚胎第12天受体表达增加。在胚胎第12天给糖尿病大鼠施用氯苯那敏可防止βIII-微管蛋白和MAP2 mRNA(神经元标志物)表达增加,并部分逆转胚胎第14天MAP2蛋白水平的升高,得出结论:HR在糖尿病大鼠胚胎背侧端脑内神经发生增加中起重要作用。这项研究为组胺(HA)和HR受体在健康和疾病状态下早期皮质发生中的参与情况开辟了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5a7/5735119/4db6b665e904/fnins-11-00676-g0001.jpg

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