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Expression of NMDA Receptor and its Effect on Cell Proliferation in the Subventricular Zone of Neonatal Rat Brain

机译:新生大鼠脑室下区NMDA受体的表达及其对细胞增殖的影响

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We investigated the involvement of N-methyl d-aspartate receptor (NMDAR) in neurogenesis of rat's subventricular zone (SVZ). For this purpose, we determined expression of the NMDAR subunits NR1, NR2A, and NR2B in SVZ of the neonatal Sprague-Dawley rats using immunohistochemical techniques. All three NMDAR subunits were expressed during postnatal day (PND)-1 to PND-28 whereas each subunit showed a distinct expression pattern. We also examined the functional effect of this receptor on cell proliferation in this region and, in this regard, the animals received either intraperitoneal injection of NMDAR agonist NMDA (2 mg/kg/day) or selective non-competitive NMDAR antagonist MK-801 (10 mg/kg) or NR2B antagonist Ro25-6981 (40 mg/kg), respectively, at PND-3. A significant developmental increase of the total cell density was observed at PND-7 (P < 0.05) while proliferating cell nuclear antigen-positive cell density was significantly increased at PND-14 (P < 0.05) and at PND-28 (P < 0.05) in the SVZ after NMDA (2 mg/kg/day) injection. Our data show that the NMDAR activation promoted the cell proliferation in SVZ during the neonatal period. We, therefore, inferred that NMDAR is expressed in SVZ of the neonatal rat brain and can promote neurogenesis, as through cell proliferation process in that region, and can thus be used as a potential therapeutic target in neurodegenerative diseases.
机译:我们调查了N-甲基d-天冬氨酸受体(NMDAR)在大鼠脑室下区(SVZ)神经发生中的参与。为此,我们使用免疫组织化学技术确定了新生Sprague-Dawley大鼠的SVZ中NMDAR亚基NR1,NR2A和NR2B的表达。在出生后一天(PND)-1至PND-28期间,所有三个NMDAR亚基均表达,而每个亚基均表现出不同的表达模式。我们还检查了该受体对该区域细胞增殖的功能作用,就此而言,动物接受了腹膜内注射NMDAR激动剂NMDA(2 mg / kg /天)或选择性非竞争性NMDAR拮抗剂MK-801(在PND-3浓度分别为10 mg / kg或NR2B拮抗剂Ro25-6981(40 mg / kg)。在PND-7(P <0.05)观察到总细胞密度显着增长,而在PND-14(P <0.05)和PND-28(P <0.05)增殖细胞核抗原阳性细胞密度显着增加。 )注射NMDA(2 mg / kg /天)后在SVZ中)。我们的数据表明,NMDAR激活可促进新生儿时期SVZ中的细胞增殖。因此,我们推断,NMDAR在新生大鼠大脑的SVZ中表达并且可以促进神经发生,例如通过该区域的细胞增殖过程,因此可以用作神经退行性疾病的潜在治疗靶标。

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