Effect of diabetes mellitus on total amount of bone resorption in denture supporting tissue under continuous pressure

糖尿病对持续压力下义齿支持组织骨吸收总量的影响

基本信息

  • 批准号:
    09671987
  • 负责人:
  • 金额:
    $ 0.13万
  • 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:
    1997
  • 资助国家:
    日本
  • 起止时间:
    1997 至 1998
  • 项目状态:
    已结题

项目摘要

Effect of diabetes mellitus on bone dynamics in denture supporting tissue has not been investigated enough. The purpose of this study was to investigate the effect of diabetes mellitus on bone resorption in the tissues under denture base caused by continuous pressure exerted through denture base by using bone histomorphometry.Two-hundreds and fifty streptozotocin-induced diabetic male rats (n=50 X 5 groups) of Wistar strain were used in this study. Denture base was applied to the molar region of the hard palate at 22 weeks of age. In 3 loaded groups, the denture bases were designed to load a continuous pressure of 1.0, 10.0 or 20.0 kPa to the palate, respectively. In covering groups, the denture base was designed to contact with the palate without any mechanical pressure. The non-denture-wearing group received no intentional treatment. The cleansing of the palate and removable denture base was carried out at 3 or 4 days intervals. Palatal tissue block was excised from 5 rats of each experimental group after the denture insertion at one week interval. The specimens were stained with Villanueva bone stain, embedded in methyl-methacrylate, and ground to 50mum thickness. Eroded surface and osteoclast surface were calculated by using two dimensional graphic analysis system. Amount of bone resorption was calculated as (A) - (B) ; (A) Formed bone tissue during 12 weeks prior to the denture insertion in covering group, (B) Remained bone tissue after the end of bone resorption in each bone resorbed group at each experimental period.Bone resorption was observed in 10.0 and 20.0 kPa groups until 3 and 4 weeks after the denture insertion, respectively. Total amount of bone resorption was 60*16mum in 10.0 kPa group and 87*17mum in 20.0 kPa group. Comparing these results with results in normal rats in same condition as this study, it was showed that diabetes mellitus prolongs the term of bone resorption and increases total amount of bone resorption.
糖尿病对义齿支持组织中骨动力学的影响尚未得到足够的研究。为探讨糖尿病对义齿基托持续压力引起的基托下组织骨吸收的影响,选用Wistar系糖尿病雄性大鼠250只(n=50 × 5组)。22周时,将义齿基托应用于硬腭的磨牙区域。在3个加载组中,义齿基托分别被设计成向腭部施加1.0、10.0和20.0 kPa的持续压力。在覆盖组中,义齿基托被设计成与腭接触而没有任何机械压力。不戴义齿组不接受任何治疗。每隔3或4天进行腭和可摘义齿基托的清洁。实验组和对照组各取5只大鼠,每隔1周,于义齿戴入后切取腭部组织块。标本用Villanueva骨染色剂染色,包埋在甲基丙烯酸甲酯中,并研磨至50 μ m厚。用二维图形分析系统计算侵蚀面和破骨细胞面。骨吸收量按(A)-(B)计算:(A)覆盖组戴入义齿前12周内形成的骨组织,(B)各实验阶段各骨吸收组骨吸收结束后的剩余骨组织,10.0和20.0 kPa组分别观察到戴入义齿后3周和4周的骨吸收。10.0kPa组骨吸收总量为60 × 16 μ m,20.0kPa组为87 × 17 μ m。与正常大鼠在相同条件下的实验结果比较,表明糖尿病延长了骨吸收的时间,增加了骨吸收的总量。

项目成果

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SATO Takashi其他文献

Proposal and Trial of Vocational Training for Industrial Robot Technician Compatible with the Smart Factory
与智能工厂相适应的工业机器人技术人员职业培训的建议与尝试
  • DOI:
    10.4307/jsee.68.1_75
  • 发表时间:
    2020
  • 期刊:
  • 影响因子:
    0
  • 作者:
    SATO Takashi;KIKUCHI Takuo;TAKAHASHI Koji
  • 通讯作者:
    TAKAHASHI Koji
ものづくりアスリートのためのスキルテックを活用した訓練法の動向調査
使用技能技术培养运动员的训练方法趋势调查
  • DOI:
  • 发表时间:
    2023
  • 期刊:
  • 影响因子:
    0
  • 作者:
    SATO Takashi;KIKUCHI Takuo;TAKAHASHI Koji;島田貴仁・高木大資・讃井知・春田悠佳;菊池拓男
  • 通讯作者:
    菊池拓男
Covid-19 による高齢者の対人相互作用および日常活動の変化 パンデミック前後のパネル調査による個人要因・地区要因の検討
Covid-19导致老年人人际交往和日常活动的变化通过疫情前后的小组调查考察个人和地区因素
  • DOI:
  • 发表时间:
    2022
  • 期刊:
  • 影响因子:
    0
  • 作者:
    SATO Takashi;KIKUCHI Takuo;TAKAHASHI Koji;島田貴仁・高木大資・讃井知・春田悠佳
  • 通讯作者:
    島田貴仁・高木大資・讃井知・春田悠佳
Lung epithelial fucosylation promotes the development of house dust mite (HDM)-induced allergic airway inflammation
肺上皮岩藻糖基化促进屋尘螨(HDM)诱导的过敏性气道炎症的发展
  • DOI:
  • 发表时间:
    2017
  • 期刊:
  • 影响因子:
    0
  • 作者:
    SAKU Aiko;HIROSE Koichi;ITO Takashi;SATO Takashi;GOTO Yoshiyuki;KIYONO Hiroshi;NAKAJIMA Hiroshi
  • 通讯作者:
    NAKAJIMA Hiroshi

SATO Takashi的其他文献

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{{ truncateString('SATO Takashi', 18)}}的其他基金

Peptide ligand screening of transthyretin protein-protein interaction inhibitor using phage display system
利用噬菌体展示系统筛选转甲状腺素蛋白-蛋白质相互作用抑制剂的肽配体
  • 批准号:
    16K18875
  • 财政年份:
    2016
  • 资助金额:
    $ 0.13万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Study of nanoparticles-incorporating immune modulating oligodeoxynucleotide for the treatment of lung diseases
纳米颗粒掺入免疫调节寡脱氧核苷酸治疗肺部疾病的研究
  • 批准号:
    15K09224
  • 财政年份:
    2015
  • 资助金额:
    $ 0.13万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Evolution of the new competition policy by the open source strategy
开源战略演变新竞争政策
  • 批准号:
    25380313
  • 财政年份:
    2013
  • 资助金额:
    $ 0.13万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Development of drugs targeting secretory inhibition of transthyretin for familial amyloidotic polyneuropathy
开发针对家族性淀粉样变性多发性神经病的运甲状腺素蛋白分泌抑制药物
  • 批准号:
    24790079
  • 财政年份:
    2012
  • 资助金额:
    $ 0.13万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Study of inhaled nanoparticles incorporating synthetic oligodeoxynucleotides to treat lung diseases
掺入合成寡脱氧核苷酸的吸入纳米颗粒治疗肺部疾病的研究
  • 批准号:
    23790917
  • 财政年份:
    2011
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    $ 0.13万
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    Grant-in-Aid for Young Scientists (B)
A Study in Dynamics of BEI Expression in 3 Prefectures in Northern Kanto Region
北关东地区3县BEI表达动态研究
  • 批准号:
    23520564
  • 财政年份:
    2011
  • 资助金额:
    $ 0.13万
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    Grant-in-Aid for Scientific Research (C)
Investigation for the nuculear receptor functions to cure clonic inflammatory syndrome
核受体治疗阵挛炎症综合征功能的研究
  • 批准号:
    23591347
  • 财政年份:
    2011
  • 资助金额:
    $ 0.13万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Stabilization and Emergence of Rule Dynamics in Dynamic Cognitive Agents with Internal Dynamics
具有内部动力学的动态认知主体中规则动力学的稳定和出现
  • 批准号:
    22700242
  • 财政年份:
    2010
  • 资助金额:
    $ 0.13万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Oscillation characteristics improvement of a Vertical Cavity Surface Emitting Laser and consideration to its application
垂直腔面发射激光器振荡特性的改进及其应用思考
  • 批准号:
    22560035
  • 财政年份:
    2010
  • 资助金额:
    $ 0.13万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Molecular mechanisms of gefitinib-induced rash formation: Gefitinib augments lipogenesis and steroidgenesis in sebaceous glands
吉非替尼诱导皮疹形成的分子机制:吉非替尼增强皮脂腺的脂肪生成和类固醇生成
  • 批准号:
    22590506
  • 财政年份:
    2010
  • 资助金额:
    $ 0.13万
  • 项目类别:
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