Literature DB >> 7147162

Histologic and embryologic studies on the innervation of the pelvic viscera in patients with Hirschsprung's disease.

E Okamoto, M Satani, K Kuwata.   

Abstract

On the specimens taken at autopsy from three newborns with Hirschsprung's disease and three newborns in the control group, the innervation of the pelvic organs was histologically studied. The authors found that all the pelvic organs, except for the rectum in patients with Hirschsprung's disease, preserved a completely normal innervation not only of pelvic autonomic nerve plexuses, but also of sensory nerves of spinal origin. Even in the wall of the aganglionic rectum, the extrinsic sympathetic as well as parasympathetic nerve fibers were preserved, which showed a marked proliferative change due to the absence of target nerve cells upon which they otherwise terminated. An additional embryologic study was performed upon 20 human embryos. The results revealed that the pelvic nerve plexuses were formed during the six to ten gestational week period by neural cells migrating along the pelvic visceral branches of sacral nerves, while none of these neural cells was found to enter the rectum. The enteric plexuses of the rectum were formed later by neural cells that migrated down along the alimentary tract in a craniocaudal manner. The two separate origins, the sacral for the pelvic nerve plexuses and the vagal for the enteric plexuses of the rectum, seem to be the reason why innervation of the genitourinary organs, which are located in front of the aganglionic rectum, is normal in those patients with Hirschsprung's disease.

Entities:  

Mesh:

Year:  1982        PMID: 7147162

Source DB:  PubMed          Journal:  Surg Gynecol Obstet        ISSN: 0039-6087


  8 in total

1.  Increased neuropeptide Y-immunoreactive innervation of aganglionic bowel in Hirschsprung's disease.

Authors:  Y Hamada; A E Bishop; G Federici; M Rivosecchi; I C Talbot; J M Polak
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1987

2.  Anorectal neural crest derived cell behavior after the migration of vagal neural crest derived cells is surgically disrupted: implications for the etiology of Hirschsprung's disease.

Authors:  Katsumi Miyahara; Yoshifumi Kato; Ryota Suzuki; Chihiro Akazawa; Nana Tanaka; Hiroyuki Koga; Takashi Doi; Geoffrey J Lane; Atsuyuki Yamataka
Journal:  Pediatr Surg Int       Date:  2013-01       Impact factor: 1.827

3.  Three serial neurones in the innervation of the colon by the sacral parasympathetic nerve of the dog.

Authors:  K Fukai; H Fukuda
Journal:  J Physiol       Date:  1985-05       Impact factor: 5.182

4.  Bioengineering of physiologically functional intrinsically innervated human internal anal sphincter constructs.

Authors:  Robert R Gilmont; Shreya Raghavan; Sita Somara; Khalil N Bitar
Journal:  Tissue Eng Part A       Date:  2014-02-03       Impact factor: 3.845

5.  Nerve growth factor receptor immunostaining suggests an extrinsic origin for hypertrophic nerves in Hirschsprung's disease.

Authors:  H Kobayashi; D S O'Briain; P Puri
Journal:  Gut       Date:  1994-11       Impact factor: 23.059

6.  An immunohistochemical study of glial fibrillary acidic (GFA) protein and S-100 protein in the colon affected by Hirschsprung's disease.

Authors:  T Kawana; O Nada; K Ikeda
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

7.  Three- and four-dimensional analysis of altered behavior of enteric neural crest derived cells in the Hirschsprung's disease mouse model.

Authors:  Nana Nakazawa-Tanaka; Katsumi Miyahara; Naho Fujiwara; Masahiko Urao; Chihiro Akazawa; Atsuyuki Yamataka
Journal:  Pediatr Surg Int       Date:  2015-11-06       Impact factor: 1.827

8.  Laminin-1 promotes enteric nervous system development in mouse embryo.

Authors:  Nana Nakazawa; Katsumi Miyahara; Manabu Okawada; Atsuyuki Yamataka; Ryota Suzuki; Chihiro Akazawa; Naoki Tomikawa-Ichikawa; Eri Arikawa-Hirasawa
Journal:  Pediatr Surg Int       Date:  2013-11       Impact factor: 1.827

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.