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Embryonic skeleton development and neonatal learning and memory ability of rats anesthetized with pentobarbital sodium: Differences of administration occasion and time
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作者 Changling Peng Yuhua Zhu Ankang Hu Xiaorong Zhu 《Neural Regeneration Research》 SCIE CAS CSCD 2006年第9期844-846,共3页
BACKGROUND: Generally speaking, anesthesia is often used in gravid body and it has been already proved that many kind of medicine can result in malformation. OBJECTIVE: To explore embryonic skeleton development and ne... BACKGROUND: Generally speaking, anesthesia is often used in gravid body and it has been already proved that many kind of medicine can result in malformation. OBJECTIVE: To explore embryonic skeleton development and neonatal learning and memory of rats anesthetized with pentobarbital sodium in gravid rats. DESIGN: A randomized control trial. SETTING: Laboratory Animal Center of Xuzhou Medical College. MATERIALS: A total of 80 adult female SD rats, of clean grade and weighing 220-240 g, were selected in this study. The main reagents were detailed as follows: pentobarbital sodium (Shanghai Xingzhi Chemical Plant, batch number: 921019); MG-2 maze test apparatus (Zhangjiagang Biomedical Instrument Factory); somatotype microscope (Beijing Taike Instrument Co., Ltd.). METHODS: ① A total of 160 SD rats of half males and females were selected in this study. All rats were copulated. The day that the plug was checked out in the vagina next day was looked as the first day of pregnancy. Gravid rats were divided randomly into four groups, including early anesthesia group, second anesthesia group, late anesthesia group and control group with 20 in each group. Rats in the early anesthesia group were injected with 25 mg/kg soluble pentobarbitone on the 7th day of pregnancy for once; rats in the second anesthesia group were anesthetized with 25 mg/kg soluble pentobarbitone on the 7th and the 14th days of pregnancy for once; rats in the late anesthesia group were anesthetized with 25 mg/kg soluble pentobarbitone on the 14th day of pregnancy for once; rats in the control group did not treat with anything. The time of anesthetizing was controlled in 3 to 4 hours and ether was absorbed while the time was not enough. ② Half of each group was sacrificed on day 20th of pregnancy and the fetus was taken out to be stained with alizarin red S. After stained, the fetal skeleton was examined. The learning and memorizing of one-month rats that were given birth by the rest gravid rats were tested through electric mare method. Determine their study ability according to their correct rate of 90% or above of arrival at the safe area in 20 s. After they finally learned to arrive at the safe area correctly, test them once more in 24 hours and record the correct rate of 15 times. MAIN OUTCOME MEASURES: The rate of malformation in fetus and ability of learning and memory in one-month rats. RESULTS: A total of 80 female rats were anesthetized in this experiment. Totally 490 immature rats were tested with maze testing machine and 196 fetuses were stained with alizarin red S to observe the development of their skeleton. However, one of the 80 female rats was led to death because of overdose. ① Malformation experiment: Learning ability of second anesthesia group was evidently different from the control group while the other two groups were not in the electric mare method. The fetal skeleton malformation rate of three experimental groups was 87.0%, 60.9% and 17.9%, respectively, while it was 5.6% in the control group. ② Electric mare method: Times of rats which arrived at the safe regions were respectively 49.0±31.0, 68.0±35.0, 47.0±31.0 and 44.0±21.0 in early anesthesia group, second anesthesia group, late anesthesia group and control group; and then, there was significant difference between the second anesthesia group and the control group (P < 0.05). Exact rates of memory of rats were respectively (64.36±14.35)%, (62.15±18.33)%, (54.19±12.28)% and (68.24±15.91)% in early anesthesia group, second anesthesia group, late anesthesia group and control group; and then, there were no significant differences as compared with the control group (P > 0.05). CONCLUSION: The influence of anesthesia with pentobarbital sodium is obvious in fetal skeleton development and learning and memory ability. 展开更多
关键词 Embryonic skeleton development and neonatal learning and memory ability of rats anesthetized with pentobarbital sodium Differences of administration occasion and time
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半滑舌鳎Dorsalin-1-like基因的克隆与表达
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作者 马骞 庄志猛 +1 位作者 柳淑芳 唐启升 《中国水产科学》 CAS CSCD 北大核心 2013年第6期1123-1131,共9页
Dorsalin-1是骨形态发生蛋白(bone morphogenetic proteins,BMPs)家族成员,在调控脊椎动物神经系统的发育中具有重要作用。目前,国内外有关脊椎动物Dorsalin-1的研究报道十分有限。本研究克隆了半滑舌鳎(Cynoglossus semilaevis)Dorsali... Dorsalin-1是骨形态发生蛋白(bone morphogenetic proteins,BMPs)家族成员,在调控脊椎动物神经系统的发育中具有重要作用。目前,国内外有关脊椎动物Dorsalin-1的研究报道十分有限。本研究克隆了半滑舌鳎(Cynoglossus semilaevis)Dorsalin-1-like基因的cDNA序列,并分析了Dorsalin-1-like mRNA在半滑舌鳎成鱼的组织表达差异及其在早期发育阶段的表达水平变化。研究结果表明,半滑舌鳎Dorsalin-1-like基因cDNA全长为1 961 bp,包括了153 bp的5′非翻译区(5′UTR)、编码419个氨基酸的1 260 bp的开放读码框(ORF),以及548 bp的3′非翻译区(3′UTR)。同源性分析和分子进化聚类分析结果显示,半滑舌鳎Dorsalin-1-like鲀与红鳍东方(Taleifugu rubripes)、尼罗罗非鱼(Oreochromis niloticus)等的同源性最高,并与之共同聚为鱼类Dorsalin-1分支。此外,Dorsalin-1-like mRNA在半滑舌鳎成鱼的13个组织中具有广泛的分布,并在心脏组织中表达量最高,在肝、脊髓等组织中次之。在半滑舌鳎早期发育阶段(卵期、仔鱼、稚鱼、幼鱼)中,Dorsalin-1-like在卵期中的胚胎期表达量最高,其次为前期仔鱼期。上述实验结果表明,Dorsalin-1在调控卵期和仔鱼期的早期发育中具有重要作用,并可能通过调节神经系统的发育进而参与心脏、骨骼等组织的发育调控。本研究旨在揭示Dorsalin-1-like基因在调控半滑舌鳎早期神经系统发育的重要作用,并为筛选半滑舌鳎骨骼发育的调控因子奠定理论基础。 展开更多
关键词 半滑舌鳎 Dorsalin-1 1ike MRNA表达 早期发育 骨骼发育 神经系统
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中西声乐发展脉络与存在形态之比较
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作者 李猛 张旭东 《商丘师范学院学报》 CAS 2005年第6期174-176,共3页
中西声乐艺术具有相似的声乐起源观与初始形态,在发展过程中,又呈现出不同的脉络与形质状态。
关键词 中国声乐艺术 西方声乐艺术 发展脉络 存在形态 比较
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儿童矮小262例病因分析 被引量:2
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作者 王晓宁 《中国基层医药》 CAS 2005年第12期1720-1721,共2页
目的探讨本地区儿童矮小的病因及干预。方法回顾性分析262例身高儿童矮小的身高、骨龄、生长激素水平、甲状腺功能及微量元素等指标。结果262例儿童矮小中,内分泌异常所致的矮小占首位(38.55%,101/262),其中生长激素缺乏性矮小(GHD)38例... 目的探讨本地区儿童矮小的病因及干预。方法回顾性分析262例身高儿童矮小的身高、骨龄、生长激素水平、甲状腺功能及微量元素等指标。结果262例儿童矮小中,内分泌异常所致的矮小占首位(38.55%,101/262),其中生长激素缺乏性矮小(GHD)38例,性早熟22例;体质延迟性矮小67例,男女发病比例为2.75;遗传性矮小35例;特发性矮小33例。67例体质延迟性矮小患儿的病因:食欲不振41例,睡眠不足29例,活动过多23例,微量元素缺乏36例。结论内分泌异常仍然是矮小的主要原因。 展开更多
关键词 发育障碍 儿童 人生长激素 年龄测定 骨骼 病因
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