Adaptation capacity of small intestine in short bowel syndrome and criteria for small intestinal transplantation

短肠综合征小肠适应能力及小肠移植标准

基本信息

  • 批准号:
    12470373
  • 负责人:
  • 金额:
    $ 9.41万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    2000
  • 资助国家:
    日本
  • 起止时间:
    2000 至 2003
  • 项目状态:
    已结题

项目摘要

Background : Regarding complications associated with short bowel syndrome(SBS), progressive liver failure is one of most severe complications known to occur. Although several studies have suggested that many factors interactively influence on this clinical condition, we investigated the relationship between hepatic circulation and hepatic fibrosis, using a neonatal piglet SBS model.Materials & Methods : This study used the following four groups of neonatal piglets : a group with an 80% resection of the small bowel(SBS group), a group with a by-pass operation of the small bowel(functional SBS group), a group with only a laparotomy as a Sham operation(Sham group), and a no operative treatment group(Control group). We measured the hepatic circulation just before and after the reconstruction of the intestine, as well as on 7th and 14th postoperative day. In addition, both blood and hepatic tissue samples were collected to investigate them both biochemically and morphologicallyResults : In the biochemical liver function and the tissue blood flow of liver, there were no significant differences among all groups on any investigated days. However, on both the 7th and 14th postoperative day, the portal venous flow in the SBS group was significantly lower than that in other groups. According to a histological analysis, only hepatic samples on the 14th postoperative day showed mild hepatic fibrosis in the SBS group. In □-smooth muscle actin staining, which expresses active stellate cells, numerous positive cells were distributed in the perisinusoidal space on the 14th postoperative day in the SBS group.Conclusion : Based on our data, a decrease in the hepatic circulation, especially in the portal venous flow, after a massive resection of the intestine, may cause progressive liver dysfunction due to the activation of hepatic stellate cells.
背景:关于与短肠综合征(SBS)相关的并发症,进行性肝衰竭是已知发生的最严重并发症之一。 Although several studies have suggested that many factors interactively influence on this clinical condition, we investigated the relationship between hepatitic circulation and hepatitic fibrosis, using a neonatal piglet SBS model.Materials & Methods: This study used the following four groups of neonatal piglets: a group with an 80% resection of the small bowel(SBS group), a group with a by-pass operation of the small bowel(functional SBS group), a group with仅作为假手术(假手术组)和无手术治疗组(对照组)。我们在肠重建之前和之后测量了肝循环,以及术后第7和14日。此外,收集了血液和肝组织样品,以在生化和形态学上研究它们:在生化肝功能和肝脏的组织血流中,在任何研究的日子中,所有组之间均无显着差异。但是,在术后第7和14日,SBS组的门静脉流量明显低于其他组的静脉流量。根据组织学分析,仅在术后第14天,只有肝样品显示SBS组的轻度肝纤维化。在□ - 表达活跃的星状细胞的光滑肌肉肌动蛋白染色中,在SBS组的第14天,在术后第14天分布了许多阳性细胞。结论:基于我们的数据,肝循环的减少,尤其是在门静脉流动,导致渐进式渐进性,可能会导致渐进性,可能会导致渐进式渐进性,可能会导致渐进式渐进性。星状细胞。

项目成果

期刊论文数量(78)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
水田祥代: "標準小児外科第4版 3.出生前診断 pp35-42"監修:鈴木宏志,横山穣太郎、発行所:株式会社 医学書院. 300 (2000)
水田芳世:《标准小儿外科第4版3.产前诊断》第35-42页监督:铃木宏、横山光太郎、出版社:医学书院株式会社300(2000)
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Taguchi T, Suita S, Ohkubo K, Ono J: "Mutations in the sulfonylurea receptor gene in relation to the long-term outcome of persistent hyperinsulinemic hypoglycemia of infancy"J Pediatr Surg. 37. 593-598 (2002)
Taguchi T、Suita S、Ohkubo K、Ono J:“磺酰脲类受体基因突变与婴儿持续性高胰岛素性低血糖的长期结果相关”J Pediatr Surg。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Nishimoto Y, Suita S, Taguchi T, et al.: "Hepatic foreign body- a sewing needle- in a child"Asian J Surg. 26. 231-233 (2003)
Nishimoto Y、Suita S、Taguchi T 等人:“儿童的肝脏异物 - 缝衣针”《亚洲外科杂志》。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Suita S, Taguchi T: "Organ development of fetus in gastrointestinal tract and genitourinary tract"Shin-Joseiigaku-taikei 29. 345-371
Suita S、Taguchi T:“胎儿胃肠道和泌尿生殖道的器官发育”Shin-Joseiigaku-taikei 29. 345-371
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Taguchi T, Suita S: "Segmental small-intestinal transplantation : A comparison of jejunal And ileal grafts"Surgery. 131. S294-S300 (2002)
Taguchi T、Suita S:“节段性小肠移植:空肠和回肠移植物的比较”手术。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

SUITA Sachiyo其他文献

SUITA Sachiyo的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('SUITA Sachiyo', 18)}}的其他基金

Effect of growth factor regarding lung development of congenital diaphragmatic hernia
生长因子对先天性膈疝肺发育的影响
  • 批准号:
    16390504
  • 财政年份:
    2004
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)

相似国自然基金

CLMP介导Connexin45-β-catenin复合体对先天性短肠综合征的致病机制研究
  • 批准号:
    82370525
  • 批准年份:
    2023
  • 资助金额:
    49 万元
  • 项目类别:
    面上项目
肠道菌群调控 FXR-FGF15 信号通路参与短肠综合征肠衰竭相关性肝损害发病的机制研究
  • 批准号:
    81900464
  • 批准年份:
    2019
  • 资助金额:
    21.0 万元
  • 项目类别:
    青年科学基金项目
痛泻要方靶向miR-144调控肠道黏膜通透性治疗肝郁脾虚型肠易激综合征分子机制研究
  • 批准号:
    81804047
  • 批准年份:
    2018
  • 资助金额:
    21.0 万元
  • 项目类别:
    青年科学基金项目
SCFA-GPR41/43-AMPAR/NMDAR免疫神经轴介导肠易激综合征内脏高敏感机制研究
  • 批准号:
    81800476
  • 批准年份:
    2018
  • 资助金额:
    22.0 万元
  • 项目类别:
    青年科学基金项目
短链脂肪酸参与肠道菌群与宿主互动致IBS-D内脏高敏感的外周机制及肠安I号方的作用研究
  • 批准号:
    81804089
  • 批准年份:
    2018
  • 资助金额:
    21.0 万元
  • 项目类别:
    青年科学基金项目

相似海外基金

The role of intestinal microbiota in intestinal adaptation in patients with pediatric short bowel syndrome.
肠道微生物群在小儿短肠综合征患者肠道适应中的作用。
  • 批准号:
    23K15426
  • 财政年份:
    2023
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Establishing the relationship between the intestinotrophic factor glucagon like peptide-2 and the microbiome in neonatal piglets with short bowel syndrome
建立短肠综合征新生仔猪肠营养因子胰高血糖素样肽-2 与微生物组之间的关系
  • 批准号:
    468344
  • 财政年份:
    2022
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Operating Grants
Role of intestinal microbiota in driving injury mechanisms in short bowel syndrome
肠道微生物群在驱动短肠综合征损伤机制中的作用
  • 批准号:
    10580044
  • 财政年份:
    2022
  • 资助金额:
    $ 9.41万
  • 项目类别:
Role of intestinal microbiota in driving injury mechanisms in short bowel syndrome
肠道微生物群在驱动短肠综合征损伤机制中的作用
  • 批准号:
    10433531
  • 财政年份:
    2022
  • 资助金额:
    $ 9.41万
  • 项目类别:
Study of Pathway-Dependent Effects of Luminal Microbial Metabolites Including Short Chain Fatty Acids and Bile Acids in Irritable Bowel Syndrome Through Meta-omics Analysis of Fecal Specimens
通过粪便样本的元组学分析研究肠道微生物代谢物(包括短链脂肪酸和胆汁酸)对肠易激综合征的途径依赖性影响
  • 批准号:
    10993051
  • 财政年份:
    2022
  • 资助金额:
    $ 9.41万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了