[Cellular mechanism of heart injury in the early stage of crush injury in rats]

Fa Yi Xue Za Zhi. 2006 Apr;22(2):90-2.
[Article in Chinese]

Abstract

Objective: To study cellular mechanism of cardiomyocytes injury in the early stage of crush injury by observing some effects of crush injury rat sera on cultured neonatal rat cardiomyocytes.

Methods: One to three days old neonatal rat cardiomyocytes were cultured in vitro and some effects of crush injury rat sera on beating rate, cell surface area, total protein content, 3H-Leu incorporation, intracellular calcium concentration ([Ca2+]i) and Fos protein expression were observed in cultured rat cardiomyocytes.

Results: Compared with normal rat serum group, crush injury rat sera decreased beating rate(beats/min) of cardiomyocytes from 88.3 to 26.4, cell surface area, total protein content, 3H-Leu incorporation, [Ca2+]i (nmol/L) and PI of Fos protein expression were increased.

Conclusion: Crush injury rat sera suppress cell beating, increase intracellular calcium, induce Fos protein synthesis and cause cell hypertrophy, which may cause cardiac injury in the early stage of rush injury.

Publication types

  • English Abstract

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Cell Size / drug effects
  • Cells, Cultured
  • Disease Models, Animal
  • Extremities / injuries
  • Heart Injuries / metabolism
  • Heart Injuries / pathology*
  • Heart Rate / drug effects
  • Immune Sera / pharmacology*
  • Myocytes, Cardiac / drug effects*
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / pathology
  • Proto-Oncogene Proteins c-fos / metabolism*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Immune Sera
  • Proto-Oncogene Proteins c-fos
  • Calcium