首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >SEVERE INSTEAD OF MILD HYPERGLYCEMIA INHIBITS NEUROGENESIS IN THE SUBVENTRICULAR ZONE OF ADULT RATS AFTER TRANSIENT FOCAL CEREBRAL ISCHEMIA
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SEVERE INSTEAD OF MILD HYPERGLYCEMIA INHIBITS NEUROGENESIS IN THE SUBVENTRICULAR ZONE OF ADULT RATS AFTER TRANSIENT FOCAL CEREBRAL ISCHEMIA

机译:短暂性局灶性脑缺血后重度轻度高糖血症抑制成年大鼠心室下区神经发生

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Accumulated evidence suggests that enhanced neurogenesis stimulated by ischemic injury contributes to stroke outcome. However, it is unclear whether hyperglycemia, which is frequently tested positive in patients with acute ischemic stroke, influences stroke-induced neurogenesis. The aim of the present study is to examine the effect of hyperglycemia on stroke-induced neurogenesis in a rat model of transient focal cerebral ischemia. For this purpose, adult male Sprague-Dawley rats (220-250 g) were subjected to 90 min of middle cerebral artery occlusion (MCAO). Glucose was administered during ischemia to produce target blood levels ranging from 4.83 +/- 0.94 mM (normo-glycemia) to 20.76 +/- 1.56 mM. To label proliferating cells in ischemic ipsilateral subventricular zone (SVZ) of lateral ventricles, 5'-bromo-2'-deoxyuridine (BrdU) was injected 24 h after MCAO. Brains were harvested 2 h post-BrdU to evaluate the effects of hyperglycemia on infarct volume and SVZ cell proliferation. Rats that were severely hyperglycemic (19.26 +/- 1.48 mM to 20.76 +/- 1.56 mM) during ischemia had 24.26% increase in infarct volume (P < 0.05) and more serious neurological function deficits (P < 0.05). The severe hyperglycemic rats also showed dramatically decreased proliferation of neural stem/progenitor cells (NSPCs) (P < 0.05) and down-regulation of the phosphorylation of cyclic-AMP response element-binding protein (pCREB) (P < 0.05) and brain-derived neurotrophic factor (BDNF) (P < 0.05) in ipsilateral SVZ. But the abovementioned detrimental effects were not observed in rats that were rendered with mild hyperglycemia (9.43 +/- 1.39-10.13 +/- 1.24 mM). Our findings indicate that severe instead of mild hyperglycemia exacerbates ischemic injury and inhibits stroke-induced SVZ neurogenesis by a mechanism involving suppression of CREB and BDNF signaling. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:积累的证据表明,缺血性损伤刺激的神经发生增强可导致中风预后。然而,目前尚不清楚高血糖症是否会影响中风诱导的神经发生,高血糖症在急性缺血性中风患者中经常被检测为阳性。本研究的目的是在短暂性局灶性脑缺血大鼠模型中研究高血糖对中风诱导的神经发生的影响。为此,对成年雄性Sprague-Dawley大鼠(220-250 g)进行90分钟的大脑中动脉闭塞(MCAO)。在缺血期间给予葡萄糖以产生目标血液水平,范围从4.83 +/- 0.94 mM(正常血糖)到20.76 +/- 1.56 mM。为了标记侧脑室缺血性同侧脑室下区(SVZ)中的增殖细胞,在MCAO后24小时注射5'-溴-2'-脱氧尿苷(BrdU)。 BrdU后2小时收获大脑,以评估高血糖对梗塞体积和SVZ细胞增殖的影响。缺血期间严重高血糖(19.26 +/- 1.48 mM至20.76 +/- 1.56 mM)的大鼠梗塞体积增加24.26%(P <0.05),并且神经功能缺损更为严重(P <0.05)。严重的高血糖大鼠还显示出神经干/祖细胞(NSPCs)的增殖显着下降(P <0.05),并且环-AMP反应元件结合蛋白(pCREB)的磷酸化水平下调(P <0.05)和脑组织同侧SVZ中的神经源性神经营养因子(BDNF)(P <0.05)。但是,在患有轻度高血糖症(9.43 +/- 1.39-10.13 +/- 1.24 mM)的大鼠中未观察到上述有害作用。我们的发现表明,严重的而非轻度的高血糖会加剧缺血性损伤,并通过涉及抑制CREB和BDNF信号传导的机制抑制中风诱导的SVZ神经发生。 (C)2015年IBRO。由Elsevier Ltd.出版。保留所有权利。

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