• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Altered tryptophan hydroxylase 2 expression in enteric serotonergic nerves in Hirschsprung's-associated enterocolitis.先天性巨结肠相关小肠结肠炎中肠嗜铬细胞中色氨酸羟化酶2表达的改变
World J Gastroenterol. 2016 May 21;22(19):4662-72. doi: 10.3748/wjg.v22.i19.4662.
2
Expression of connexin 26 and connexin 43 is reduced in Hirschsprung's disease.在先天性巨结肠症中,连接蛋白26和连接蛋白43的表达降低。
J Surg Res. 2016 Nov;206(1):242-251. doi: 10.1016/j.jss.2016.08.010. Epub 2016 Aug 9.
3
Altered neurotransmitter expression profile in the ganglionic bowel in Hirschsprung's disease.先天性巨结肠症中神经节肠段神经递质表达谱的改变
J Pediatr Surg. 2016 May;51(5):762-9. doi: 10.1016/j.jpedsurg.2016.02.018. Epub 2016 Feb 12.
4
Reduction of hydrogen sulfide synthesis enzymes cystathionine-β-synthase and cystathionine-γ-lyase in the colon of patients with Hirschsprungs disease.先天性巨结肠症患者结肠中硫化氢合成酶胱硫醚-β-合酶和胱硫醚-γ-裂合酶的减少。
J Pediatr Surg. 2018 Mar;53(3):525-530. doi: 10.1016/j.jpedsurg.2017.06.011. Epub 2017 Jun 23.
5
Altered goblet cell function in Hirschsprung's disease.先天性巨结肠症中杯状细胞功能的改变。
Pediatr Surg Int. 2018 Feb;34(2):121-128. doi: 10.1007/s00383-017-4178-0. Epub 2018 Jan 30.
6
Use of anoctamin 1 (ANO1) to evaluate interstitial cells of Cajal in Hirschsprung's disease.使用八聚体通道蛋白1(ANO1)评估先天性巨结肠病中的 Cajal 间质细胞。
Pediatr Surg Int. 2016 Feb;32(2):125-33. doi: 10.1007/s00383-015-3822-9. Epub 2015 Oct 28.
7
Altered expression of IL36γ and IL36 receptor (IL1RL2) in the colon of patients with Hirschsprung's disease.先天性巨结肠症患者结肠中IL36γ和IL36受体(IL1RL2)的表达改变。
Pediatr Surg Int. 2017 Feb;33(2):181-186. doi: 10.1007/s00383-016-4011-1. Epub 2016 Nov 16.
8
Deficiency of platelet-derived growth factor receptor-α-positive cells in Hirschsprung's disease colon.先天性巨结肠症结肠中血小板衍生生长因子受体-α阳性细胞的缺乏。
World J Gastroenterol. 2016 Mar 28;22(12):3335-40. doi: 10.3748/wjg.v22.i12.3335.
9
Altered distribution of small-conductance calcium-activated potassium channel SK3 in Hirschsprung's disease.小电导钙激活钾通道SK3在先天性巨结肠病中的分布改变。
J Pediatr Surg. 2015 Oct;50(10):1659-64. doi: 10.1016/j.jpedsurg.2015.01.013. Epub 2015 Jan 29.
10
Reduced expression of the NLRP6 inflammasome in the colon of patients with Hirschsprung's disease.先天性巨结肠病患者结肠中 NLRP6 炎性小体表达减少。
J Pediatr Surg. 2019 Aug;54(8):1573-1577. doi: 10.1016/j.jpedsurg.2018.08.059. Epub 2018 Sep 7.

引用本文的文献

1
The A328 V/E (rs2887147) polymorphisms in human tryptophan hydroxylase 2 compromise enzyme activity.人类色氨酸羟化酶2中的A328 V/E(rs2887147)多态性会损害酶活性。
Biochem Biophys Rep. 2023 Aug 15;35:101527. doi: 10.1016/j.bbrep.2023.101527. eCollection 2023 Sep.
2
Neuroimmune regulation in Hirschsprung's disease associated enterocolitis.先天性巨结肠相关性肠炎的神经免疫调控。
Front Immunol. 2023 Apr 17;14:1127375. doi: 10.3389/fimmu.2023.1127375. eCollection 2023.
3
Selective serotonin reuptake inhibitors and inflammatory bowel disease; Beneficial or malpractice.选择性 5-羟色胺再摄取抑制剂与炎症性肠病;是有益还是弊端?
Front Immunol. 2022 Oct 6;13:980189. doi: 10.3389/fimmu.2022.980189. eCollection 2022.
4
A Novel Method for Identifying the Transition Zone in Long-Segment Hirschsprung Disease: Investigating the Muscle Unit to Ganglion Ratio.一种识别长段先天性巨结肠症移行区的新方法:研究肌间神经节单位比率。
Biomolecules. 2022 Aug 10;12(8):1101. doi: 10.3390/biom12081101.
5
Exploring the role of survivin in neuroendocrine neoplasms.探讨生存素在神经内分泌肿瘤中的作用。
Oncotarget. 2020 Jun 9;11(23):2246-2258. doi: 10.18632/oncotarget.27631.
6
Altered expression of inflammasomes in Hirschsprung's disease.先天性巨结肠症中炎性小体的表达改变。
Pediatr Surg Int. 2019 Jan;35(1):15-20. doi: 10.1007/s00383-018-4371-9. Epub 2018 Nov 1.
7
Altered goblet cell function in Hirschsprung's disease.先天性巨结肠症中杯状细胞功能的改变。
Pediatr Surg Int. 2018 Feb;34(2):121-128. doi: 10.1007/s00383-017-4178-0. Epub 2018 Jan 30.

本文引用的文献

1
Trisomy 21--incidence and outcomes in the first year, in Ireland today.21三体综合征——当今爱尔兰第一年的发病率及预后情况。
Ir Med J. 2014 Sep;107(8):248-9.
2
Colonic migrating motor complexes, high amplitude propagating contractions, neural reflexes and the importance of neuronal and mucosal serotonin.结肠移行性运动复合波、高振幅传播收缩、神经反射以及神经元和黏膜 5-羟色胺的重要性。
J Neurogastroenterol Motil. 2014 Oct 30;20(4):423-46. doi: 10.5056/jnm14092.
3
Extensive projections of myenteric serotonergic neurons suggest they comprise the central processing unit in the colon.肌间神经丛5-羟色胺能神经元的广泛投射表明,它们构成了结肠的中央处理单元。
Neurogastroenterol Motil. 2014 Apr;26(4):556-70. doi: 10.1111/nmo.12302. Epub 2014 Jan 26.
4
Enteric nervous system abnormalities are present in human necrotizing enterocolitis: potential neurotransplantation therapy.肠神经系统异常存在于人类坏死性小肠结肠炎中:潜在的神经移植治疗。
Stem Cell Res Ther. 2013;4(6):157. doi: 10.1186/scrt387.
5
Serotonin signalling in the gut--functions, dysfunctions and therapeutic targets.肠道中的血清素信号传递——功能、功能障碍和治疗靶点。
Nat Rev Gastroenterol Hepatol. 2013 Aug;10(8):473-86. doi: 10.1038/nrgastro.2013.105. Epub 2013 Jun 25.
6
Serotonin is a sword and a shield of the bowel: serotonin plays offense and defense.血清素是肠道的一把剑和一面盾:血清素兼具攻击和防御作用。
Trans Am Clin Climatol Assoc. 2012;123:268-80; discussion 280.
7
5-Hydroxytryptamine (serotonin) in the gastrointestinal tract.胃肠道中的 5-羟色胺(血清素)。
Curr Opin Endocrinol Diabetes Obes. 2013 Feb;20(1):14-21. doi: 10.1097/MED.0b013e32835bc703.
8
Hirschsprung-associated enterocolitis: prevention and therapy.先天性巨结肠相关小肠结肠炎:预防与治疗
Semin Pediatr Surg. 2012 Nov;21(4):328-35. doi: 10.1053/j.sempedsurg.2012.07.007.
9
The pathogenesis of Hirschsprung's disease-associated enterocolitis.先天性巨结肠相关小肠结肠炎的发病机制。
Semin Pediatr Surg. 2012 Nov;21(4):319-27. doi: 10.1053/j.sempedsurg.2012.07.006.
10
Platelet-derived growth factor receptor α-positive cells in the tunica muscularis of human colon.人结肠固有肌层中血小板衍生生长因子受体α阳性细胞。
J Cell Mol Med. 2012 Jul;16(7):1397-404. doi: 10.1111/j.1582-4934.2011.01510.x.

先天性巨结肠相关小肠结肠炎中肠嗜铬细胞中色氨酸羟化酶2表达的改变

Altered tryptophan hydroxylase 2 expression in enteric serotonergic nerves in Hirschsprung's-associated enterocolitis.

作者信息

Coyle David, Murphy Justin M, Doyle Brian, O'Donnell Anne Marie, Gillick John, Puri Prem

机构信息

David Coyle, John Gillick, Temple Street Children's University Hospital, Dublin 1, Ireland.

出版信息

World J Gastroenterol. 2016 May 21;22(19):4662-72. doi: 10.3748/wjg.v22.i19.4662.

DOI:10.3748/wjg.v22.i19.4662
PMID:27217698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4870073/
Abstract

AIM

To determine if expression of colonic tryptophan hydroxylase-2 (TPH2), a surrogate marker of neuronal 5-hydroxytryptamine, is altered in Hirschsprung's-associated enterocolitis.

METHODS

Entire resected colonic specimens were collected at the time of pull-through operation in children with Hirschsprung's disease (HSCR, n = 12). Five of these patients had a history of pre-operative Hirschsprung's-associated enterocolitis (HAEC). Controls were collected at colostomy closure in children with anorectal malformation (n = 10). The distribution of expression of TPH2 was evaluated using immunofluorescence and confocal microscopy. Protein expression of TPH2 was quantified using western blot analysis in the deep smooth muscle layers.

RESULTS

TPH2 was co-expressed in nitrergic and cholinergic ganglia in the myenteric and submucosal plexuses in ganglionic colon in HSCR and healthy controls. Co-expression was also seen in submucosal interstitial cells of Cajal and PDGFRα(+) cells. The density of TPH2 immuno-positive fibers decreased incrementally from ganglionic bowel to transition zone bowel to aganglionic bowel in the myenteric plexus. Expression of TPH2 was reduced in ganglionic bowel in those affected by pre-operative HAEC compared to those without HAEC and healthy controls. However, expression of TPH2 was similar or high compared to controls in the colons of children who had undergone diverting colostomy for medically refractory HAEC.

CONCLUSION

Altered TPH2 expression in colonic serotonergic nerves of patients with HSCR complicated by HAEC may contribute to intestinal secretory and motor disturbances, including recurrent HAEC.

摘要

目的

确定作为神经元5-羟色胺替代标志物的结肠色氨酸羟化酶-2(TPH2)的表达在先天性巨结肠相关小肠结肠炎中是否发生改变。

方法

在先天性巨结肠(HSCR,n = 12)患儿行拖出式手术时收集完整切除的结肠标本。其中5例患者有术前先天性巨结肠相关小肠结肠炎(HAEC)病史。对照组取自肛门直肠畸形患儿结肠造口关闭时(n = 10)。使用免疫荧光和共聚焦显微镜评估TPH2的表达分布。在深层平滑肌层中通过蛋白质印迹分析对TPH2的蛋白表达进行定量。

结果

在HSCR和健康对照的神经节性结肠的肌间神经丛和黏膜下神经丛中的含氮能和胆碱能神经节中,TPH2共表达。在黏膜下Cajal间质细胞和PDGFRα(+)细胞中也可见共表达。在肌间神经丛中,TPH2免疫阳性纤维的密度从神经节段肠到过渡区肠再到无神经节段肠逐渐降低。与未患HAEC的患者和健康对照相比,术前患HAEC的患者神经节段肠中TPH2的表达降低。然而,对于因药物难治性HAEC而行转流性结肠造口术的患儿,其结肠中TPH2的表达与对照组相似或较高。

结论

HSCR合并HAEC患者结肠5-羟色胺能神经中TPH2表达的改变可能导致肠道分泌和运动紊乱,包括复发性HAEC。