Sphincter contractility after muscle-derived stem cells autograft into the cryoinjured anal sphincters of rats

Dis Colon Rectum. 2008 Sep;51(9):1367-73. doi: 10.1007/s10350-008-9360-y. Epub 2008 Jun 7.

Abstract

Purpose: This study was designed to determine whether the injection of muscle-derived stem cells into the anal sphincter can improve functional properties in a fecal incontinence rat model.

Methods: Cryoinjured rats were utilized as a fecal incontinence model. The gastrocnemius muscles of normal three-week-old female Sprague-Dawley rats were used for the purification of the muscle-derived stem cells. The experimental group was divided into three subgroups: normal control; cryoinjured; and muscle-derived stem cells (3 x 10(6) cells) injection group of cryoinjured rats. All groups were subsequently employed in contractility experiments using muscle strips from the anal sphincter, one week after preparation.

Results: Contractility in the cryoinjured group was significantly lower than in the control after treatment with acetylcholine and KCl. In the muscle-derived stem cells injection group, contraction amplitude was higher than in the cryoinjured group but not significantly (20.5 +/- 21.3 vs. 17.3 +/- 3.4 g per gram tissue, with acetylcholine (10(-4) mol/l); 31 +/- 14.2 vs. 18.4 +/- 7.9 g per gram tissue, with KCl (10(-4) mol/l)). PKH-26-labeled transplanted cells were detected in all of the grafted sphincters. Differentiated muscle masses stained positively for alpha smooth muscle actin and myosin heavy chain at the muscle-derived stem cells injection sites.

Conclusions: This is the first study reporting that autologous muscle-derived stem cell grafts may be a tool for improving anal sphincter function.

MeSH terms

  • Acetylcholine / pharmacology
  • Anal Canal / injuries*
  • Anal Canal / pathology
  • Anal Canal / physiopathology*
  • Animals
  • Cells, Cultured
  • Cholinergic Agents / pharmacology
  • Cold Temperature / adverse effects
  • Fecal Incontinence / etiology
  • Fecal Incontinence / therapy*
  • Female
  • Models, Animal
  • Muscle Contraction / physiology*
  • Muscle, Skeletal / cytology*
  • Rats
  • Rats, Sprague-Dawley
  • Stem Cell Transplantation*
  • Transplantation, Autologous

Substances

  • Cholinergic Agents
  • Acetylcholine