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小鼠肠神经丛的选择性化学消融

Selective chemical ablation of the enteric plexus in mice.

作者信息

Yoneda Akihiro, Shima Hideki, Nemeth Laszlo, Oue Takaharu, Puri Prem

机构信息

Children's Research Centre, Our Lady's Hospital for Sick Children, Crumlin, Dublin 12, Ireland.

出版信息

Pediatr Surg Int. 2002 May;18(4):234-7. doi: 10.1007/s003830100681.

Abstract

Although genetically aganglionic mice such as piebald lethal and lethal spotted mice exhibit striking similarities to the human condition of Hirschsprung's disease (HD), the aganglionic segment is very short and always located in the distal part of the rectum. Topical application of benzalkonium chloride (BAC) to the rectum of rats has been reported to result in segmental aganglionosis. To induce chemical ablation of the enteric plexus in mice to produce an aperistaltic narrow segment simulating HD, 32 mice were divided into three groups: (1) abdominal (n=12), for sigmoid colon treatment; (2) rectal (n=10), for rectum treatment; and (3) controls (n=10). For groups 1 and 2, 0.1% BAC was applied to a 1-cm serosal surface of the bowel for 15 min. In the controls, isotonic saline was applied in this fashion. A detailed histologic examination was performed using hematoxylin and eosin staining and acetylcholinesterase histochemistry. Ten animals (9 in group 1 and 1 in group 2) died 1 to 9 weeks after BAC treatment. Autopsy revealed a narrow segment of bowel at the site of BAC treatment and marked dilatation of the bowel proximal to the narrow segment. The remaining animals were killed 12 weeks after BAC treatment. Histologic examination demonstrated normal myenteric and submucous plexuses in the controls, whereas there was a total lack of innervation in the BAC-treated segments.Topical application of BAC thus successfully produced a narrow aganglionic segment of bowel in normal mice. This model provides the basis for future studies to investigate the pathophysiology of HD and megacolon and for comparison with genetically aganglionic mice.

摘要

尽管诸如花斑致死和致死斑点小鼠等基因无神经节小鼠与人类先天性巨结肠症(HD)表现出惊人的相似性,但无神经节段非常短,且总是位于直肠远端。据报道,将苯扎氯铵(BAC)局部应用于大鼠直肠可导致节段性无神经节症。为了诱导小鼠肠神经丛化学消融以产生模拟HD的无蠕动狭窄段,将32只小鼠分为三组:(1)腹部组(n = 12),用于乙状结肠治疗;(2)直肠组(n = 10),用于直肠治疗;(3)对照组(n = 10)。对于第1组和第2组,将0.1%的BAC应用于1 cm肠浆膜表面15分钟。在对照组中,以这种方式应用等渗盐水。使用苏木精和伊红染色以及乙酰胆碱酯酶组织化学进行详细的组织学检查。10只动物(第1组9只和第2组1只)在BAC治疗后1至9周死亡。尸检显示在BAC治疗部位有一段肠狭窄,且狭窄段近端肠管明显扩张。其余动物在BAC治疗后12周处死。组织学检查显示对照组的肌间神经丛和黏膜下神经丛正常,而BAC处理段完全缺乏神经支配。因此,局部应用BAC成功地在正常小鼠中产生了一段狭窄的无神经节肠段。该模型为未来研究HD和巨结肠的病理生理学以及与基因无神经节小鼠进行比较提供了基础。

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