The study of relation between behavior abnormalities and biomolecular abnormalities in intrauterine growth retardation rats
宫内生长迟缓大鼠行为异常与生物分子异常关系的研究
基本信息
- 批准号:17591139
- 负责人:
- 金额:$ 2.11万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:2005
- 资助国家:日本
- 起止时间:2005 至 2006
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Background : To elucidate the mechanism of brain insults in intrauterine growth retardation (IUGR) infant, we conducted the bio-molecular studies in the brain of fetal/neonatal rats.Materials and Methods : IUGR model rats were induced by synthetic thromboxane A2 (STA2) administration to maternal rats. We evaluated apoptosis in the rat brain histologically and quantitatively by using TUNEL and western blotting, respectively. The expressions of chondroitin sulfate proteoglycan (CSPG), such as Neurocan, Phosphacan and Neuroglycan, were evaluated by immuno-histochemical methods and western blotting methodsResults : The mean birth weight in IUGR and control was 4.73 +/- 0.33g and 5.95 +/- 0.35g, respectively. There were more apoptotic cell numbers in the IUGR compared to in control. However, there was not difference in the expression of BCL-2, BAX and β-actin between two groups. In the immuno-histological study, the expression of Neurocan, Phosphacan and Neuroglycan were elevated in IUGR rats. Also, in the western blotting analysis, the expression of Neurocan, Phosphacan were elevated in IUGR rats. The localization of CSPG was not different between two groups.Conclusions : The results in this study suggested that CSPG might be associated with the brain insult in IUGR infants. These findings provide the key of the elucidation of brain insults in IUGR.
背景资料:为探讨宫内发育迟缓(IUGR)新生儿脑损伤的机制,本研究对胎/新生大鼠脑组织进行了生物分子学研究。材料与方法:采用合成血栓素A_2(STA_2)诱发IUGR模型。采用TUNEL法和Western blotting法分别从组织学和定量两个方面对大鼠脑组织中的细胞凋亡进行了研究。结果:IUGR组和对照组的平均出生体重分别为4.73 ± 0.33g和5.95 ± 0.35g; IUGR组凋亡细胞数明显多于对照组。而BCL-2、BAX和β-actin的表达在两组间差异无统计学意义。免疫组化结果显示,IUGR大鼠脑组织中Neurocan、Phosphacan和Neuroglycan的表达明显升高。Western blotting分析显示,IUGR大鼠脑组织中Neurocan、Phosphacan表达增强。结论:CSPG可能与IUGR患儿的脑损伤有关。这些发现为阐明IUGR脑损伤的机制提供了关键。
项目成果
期刊论文数量(13)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Delirious behavior in children with influenza : its clinical features and EEG findings.
流感儿童的谵妄行为:临床特征和脑电图结果。
- DOI:
- 发表时间:2005
- 期刊:
- 影响因子:0
- 作者:Okumura A;Nakano T;et al.
- 通讯作者:et al.
A New Method of Blood Sampling Reduces Pain for Newborn Infants : a prospective, randomized controlled clinical trial.
一种减少新生儿疼痛的新血液采样方法:一项前瞻性、随机对照临床试验。
- DOI:
- 发表时间:2007
- 期刊:
- 影响因子:0
- 作者:Sato Y;Fukasawa T;Hayakawa M;Yatsuya H;Hatakeyama M;Ogawa A;Kuno K
- 通讯作者:Kuno K
Possible antenatal and perinatal related factors in development of cystic periventricular leukomalacia
- DOI:10.1016/j.braindev.2004.02.011
- 发表时间:2005-01-01
- 期刊:
- 影响因子:1.7
- 作者:Murata, Y;Itakura, A;Mizutani, S
- 通讯作者:Mizutani, S
The MRI findings of the right-sided fetal lung can be used to predict postnatal mortality and the requirement for extracorporeal membrane oxygenation in isolated left-sided congenital diaphragmatic hernia
- DOI:10.1203/pdr.0b013e3180676cdb
- 发表时间:2007-07-01
- 期刊:
- 影响因子:3.6
- 作者:Hayakawa, Masahiro;Seo, Takahiko;Kojima, Seiji
- 通讯作者:Kojima, Seiji
Amplitude spectral analysis of theta/alpha/beta waves in preterm infants
早产儿 θ/α/β 波的幅度谱分析
- DOI:
- 发表时间:2006
- 期刊:
- 影响因子:0
- 作者:Okumura;A. et al.
- 通讯作者:A. et al.
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HAYAKAWA Masahiro其他文献
HAYAKAWA Masahiro的其他文献
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{{ truncateString('HAYAKAWA Masahiro', 18)}}的其他基金
The study of the neurological effects of GH therapy for SGA rats
GH治疗对SGA大鼠神经功能影响的研究
- 批准号:
23591594 - 财政年份:2011
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
A research of nutritional strategies to prevent metabolic syndrome in patients with fetal growth restriction
胎儿生长受限患者预防代谢综合征的营养策略研究
- 批准号:
20591296 - 财政年份:2008
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
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