[Myocardial expression of Spry1 and MAPK proteins of viral myocarditis]

Fa Yi Xue Za Zhi. 2013 Jun;29(3):164-7.
[Article in Chinese]

Abstract

Objective: To discuss the myocardial expression of Spry1 and MAPK proteins of viral myocarditis (VMC), to reveal its mechanism of sudden death, and to provide guides for forensic identification of sudden cardiac death.

Methods: Thirty Balb/c male mice were randomly divided into VMC group and control group, inoculated intraperitoneally with Coxsackievirus B3 and Eagel's solution, respectively. After the mice were sacrificed, the cardiac tissues of the mice were taken to proceed regular pathological examination. The changes of Spry1 protein, Spry1 mRNA and MAPK protein were detected by immunohistochemistry, Western blotting and real-time PCR.

Results: Under light microscope, the pathologic changes included myocardial interstitial edema, inflammatory cells infiltration, myocardial necrosis, and focal and patchy necrosis of myocardial fiber in VMC group. The expression of Spry1 protein in VMC group was lower than that in control group (P < 0.05). There was slightly decreased expression of Spry1 of the mRNA level in VMC group (P > 0.05). But the MAPK protein expression in VMC group was higher than that in control group (P < 0.05).

Conclusion: The pathway of MAPK/ERK involving Spry1 protein accelerates the expression of collagen, which may contribute to arrhythmia, heart failure and even sudden cardiac death.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Coxsackievirus Infections / metabolism
  • Coxsackievirus Infections / pathology
  • Death, Sudden, Cardiac / pathology
  • Disease Models, Animal
  • Immunohistochemistry
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Mitogen-Activated Protein Kinases / genetics
  • Mitogen-Activated Protein Kinases / metabolism*
  • Myocarditis / metabolism*
  • Myocarditis / pathology
  • Myocarditis / virology
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Random Allocation
  • Real-Time Polymerase Chain Reaction

Substances

  • Adaptor Proteins, Signal Transducing
  • Membrane Proteins
  • Phosphoproteins
  • RNA, Messenger
  • Spry1 protein, mouse
  • Mitogen-Activated Protein Kinases