Spatio-temporal expression of inducible nitric oxide synthase in and surrounding a region of rat fro

来源 :Neural Regeneration Research | 被引量 : 0次 | 上传用户:linjing912977
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
BACKGROUND:Inducible nitric oxide synthase(iNOS) cannot be detected in the neurons and glial cells of normal rats,but iNOS can be found in some neurons and glial cells of rats following ischemic,traumatic,neurotoxic or inflammatory damage. OBJECTIVE:To investigate iNOS expression and iNOS-positive cell types at various time points following damage to the rat frontal lobe using a sharp instrument. DESIGN:A nerve molecular biology,randomized,controlled study. TIME AND SETTING:This experiment was performed at the Department of Human Anatomy, Institute of Neurobiology,Medical School of Nantong University,between April 2006 and December 2007. MATERIALS:Rabbit anti-iNOS antibody(Santa Cruz,USA),biotin labeled goat anti-rabbit antibody(Sigma,USA),reverse transcription kit(Biouniquer,Hong Kong,China) and horseradish peroxidase labeled goat anti-rabbit antibody(Pierce,USA) were used for this study. METHODS:A total of 112 healthy rats aged 3 months were randomly assigned into a sham operation group(n=28) and a damage group(n=84).Rat models of frontal lobe damage were induced in the damage group using a sharp instrument to make an incision in the frontal lobe cortex. In the sham operation group,the rat bone window was opened but brain tissues were left intact. MAIN OUTCOME MEASURES:Parameters were measured at 3,6,12,24,72,120 and 168 hours following damage in both groups.Pathological changes were observed using Nissl staining and hematoxylin-eosin staining.Expression of iNOS mRNA,iNOS protein and iNOS-positive cells were examined by RT-PCR,Western blot analysis and immunohistochemistry,respectively. RESULTS:A large number of inflammatory cells infiltrated the damaged region 12 and 24 hours following damage.iNOS mRNA and iNOS protein expression increased in and around the damaged region 3 hours following damage,reached a peak at 24 hours,and then gradually decreased.The changes in iNOS-positive cell number reflected the changes in iNOS mRNA and iNOS protein expression after damage.iNOS was mainly found in neural cells at 3 and 6 hours,in macrophages at 12 and 24 hours,and in glial cells at 72 and 120 hours after damage. iNOS-positive cells were few in and surrounding the damaged region at 168 hours.There were a few iNOS-positive neural cells in the rat frontal lobe cortex in the sham operation group. CONCLUSION:Neurons,macrophages and glial cells can express iNOS following rat frontal lobe damage caused by a sharp instrument.The levels of iNOS expression,and the cell types expressing iNOS,change with time. BACKGROUND: Inducible nitric oxide synthase (iNOS) can not be detected in the neurons and glial cells of normal rats, but iNOS can be found in some neurons and glial cells of rats following ischemic, traumatic, neurotoxic or inflammatory damage. OBJECTIVE: To investigate iNOS expression and iNOS-positive cell types at various time points following damage to the rat frontal lobe using a sharp instrument. DESIGN: A nerve molecular biology, randomized, controlled study. TIME AND SETTING: This experiment was performed at the Department of Human Anatomy, Institute of Neurobiology, Medical School of Nantong University, between April 2006 and December 2007. MATERIALS: Rabbit anti-iNOS antibody (Santa Cruz, USA), biotin labeled goat anti-rabbit antibody (Sigma, USA) Hong Kong, China) and horseradish peroxidase labeled goat anti-rabbit antibody (Pierce, USA) were used for this study. METHODS: A total of 112 healthy rats aged 3 months were randomly assigned into a sham operation gr Rats models of frontal lobe damage were induced in the damage group using a sharp instrument to make an incision in the frontal lobe cortex. In the sham operation group, the rat (n = 28) The bone window was opened but the brain tissues were left intact. MAIN OUTCOME MEASURES: Parameters were measured at 3, 6, 12, 24, 72, 120 and 168 hours following damage in both groups. Pathological changes were observed using Nissl staining and hematoxylin-eosin staining. Expression of iNOS mRNA, iNOS protein and iNOS-positive cells were examined by RT-PCR, Western blot analysis and immunohistochemistry, respectively. RESULTS: A large number of inflammatory cells infiltrated the damaged region 12 and 24 hours following damage.iNOS mRNA and iNOS protein expression increased in and around the damaged region 3 hours following damage, reached a peak at 24 hours, and then gradually decreased. The changes in iNOS-positive cell number reflected the changes in iNOS mRNA and iNOS protein expression after dami.NOS was mainly found in neural cells at 3 and 6 hours, in macrophages at 12 and 24 hours, and in glial cells at 72 and 120 hours after damage. iNOS-positive cells were few in and surrounding the damaged region at 168 hours . There were a few iNOS-positive neural cells in the rat frontal lobe cortex in the sham operation group. CONCLUSION: Neurons, macrophages and glial cells can express iNOS the rat frontal lobe damage caused by a sharp instrument. The levels of iNOS expression, and the cell types expressing iNOS, change with time.
其他文献
醛 (酮 )氨法合成吡啶可用ZSM 5作催化剂 ,本文研究了ZSM 5催化剂的表面酸性与催化合成吡啶活性之间的关系 .合成了硅铝质量比为 12 0的ZSM 5 ,并用钴、铁对其进行改性 ,用吡
收藏有益吴北光大千世界无所不有,人们的兴趣五彩缤纷。作为一种文化,收藏热越来越广泛地进入我们的生活之中。收藏所以被称之为文化,是因为通过收集过程,以收藏品为媒介,人与人或
Adult stem cells from skeletal muscle cells were induced to differentiate into cardiocytes to see if stem cells from another different but histologically-compar
为民族化声乐教学的探索与提高,是我一生为之不懈追求,努力奋斗的神圣事业。 Exploration and improvement of national vocal music teaching are the sacred undertaking
目的:研究补阳还五汤抗全脑缺血后再灌注损伤的分子机制。方法 :将66只SD大鼠随机分为3组,即正常组、模型组和药物组(补阳还五汤预干预),模型组和药物组再分别设置2、24 h 2
目的:观察二母颗粒含药血清对肺腺癌A549及肝癌SMMC-7721细胞株增殖和凋亡的影响。方法:采用形态学及MTT法观察二母颗粒组(10g/kg)5%、10%、20%含药血清对A549及SMMC-7721细
请下载后查看,本文暂不支持在线获取查看简介。 Please download to view, this article does not support online access to view profile.
目的:研究芹菜素(Apigenin,APG)对大鼠肝脏局部缺血再灌注损伤的保护作用。方法:将动物随机分为假手术组、缺血再灌注组、芹菜素(5、10、20、40、80和120mg/kg)预处理组和金
研究了解和铬离子高、中能量重迭注入对50Mn18Cr4电机护环钢SCC性能的影响.SCC对比试验结果表明:(1)在QHJ-79标准硝酸盐介质中,离子注入试样的SCC出现时间(tf)比不经注入试样的延长了6倍以上,致钝和维钝电流密度下
一、概述 我厂曲拐传动多孔钻床中有一曲拐轴如图1所示,零件的两个回转中心的中心距和平行度要求都较高。该零件的加工路线是:车左端回转面钻中心孔→调头钻右端中心孔→磨d