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无肛畸形胎鼠盆底横纹肌复合体m-ATPase组织化学研究 被引量:3

The m-ATPase Histochemical Study of Striomuscular Complex in Murine Fetus with Anorectal Malformation
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摘要 目的:为了解无肛畸形胎鼠盆底横纹肌复合体的组织化学特征。方法:对39只无肛畸形胎鼠(高位8只、中位10只、低位21只)盆底横纹肌复合体进行 ATP 酶染色,光镜下观察单位面积内肌纤维数及Ⅰ、Ⅱ型肌纤维所占比例。结果:中、高位无肛畸形单位面积肌纤维数和Ⅰ型肌纤维所占比例较正常鼠明显减少(P<0.001),而低位无肛则与正常鼠近似。结论:横纹肌复合体肌纤维组化类型异常也是无肛畸形的一种病理改变。 Objective:To study the histochemical characteristics of striomuscular complex in murine fetus with anorectal malformation.Methods:The striomuscular complex of pelvic floor of 39 murine fetus(high 8,intermediate 10,low 21)were stained with ATPase and observed under microscope.The total of muscular fiber per unit area and the percentage of type Ⅰ and Ⅱ fibers were calculated.Results:The total of muscular fibers and percentage of type Ⅰ fibers in the high and intermediate type was lower than that in the normal mice group,while in the low type the to- tal was almost equal to that of the normal.Conclusions:The histochemical abnormality of stri- omuscular complex of the pelvic floor is one of the pathologic changes in anorectal malformations.
出处 《中华小儿外科杂志》 CSCD 1997年第6期354-356,共3页 Chinese Journal of Pediatric Surgery
基金 国家自然科学基金(NO39370696)
关键词 无肛畸形 横纹肌复合体 ATP 组织化学 Anorectal malformation Striomuscular complex ATPase Histochemistry
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参考文献1

  • 1凌启波,实用病理特殊染色和组化技术,1989年,262页

同被引文献19

  • 1于明,李正.肛门直肠畸形儿肛门外括约肌肌电图的应用[J].中华小儿外科杂志,1989,10(3):129-131. 被引量:3
  • 2刘颖,王练英,李正,王伟.先天性肛门直肠崎形鼠仔的病理特点[J].中华小儿外科杂志,1996,17(1):37-39. 被引量:21
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  • 4王燕霞.一穴肛畸形[J].中华小儿外科杂志,1988,9:48-50.
  • 5张志波,中华小儿外科杂志,1997年,18卷,354页
  • 6刘颖,中华小儿外科杂志,1996年,17卷,37页
  • 7凌启波,实用病理特殊染色和组化技术,1989年,262页
  • 8王燕霞,中华小儿外科杂志,1988年,9卷,48页
  • 9Iwai N, Iwata G, Kimura O, et al. Is a new biofeedback therapy effective for fecal incontinence in patients who have anorectal malformations? J Pediatr Surg, 1997, 32: 1626- 1629.
  • 10Glia A, Gylin M, Akerlund JE, et al. Biofeedback training in patients with fecal incontinence. Dis Colon Rectum, 1998, 41:359 - 362.

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