Skip to main content
Possible Molecular Mechanisms Underlying Age-Related Cardiomyocyte Apoptosis in the F344XBN Rat Heart
Biological Sciences Faculty Research
  • Sunil K. Kakarla, Marshall University
  • Kevin M. Rice, Marshall University
  • Anjaiah Katta, Marshall University
  • Satyanarayana Paturi, Marshall University
  • Miaozong Wu
  • Madhukar Kolli, Marshall University
  • Saba Keshavarzian, Marshall University
  • Kamran Manzoor
  • Paulette S. Wehner, Marshall University
  • Eric R. Blough, Marshall University
Document Type
Publication Date
Despite advances in treatment, age-related cardiac dysfunction still remains a leading cause of cardiovascular death. Recent data have suggested that increases in cardiomyocyte apoptosis may be involved in the pathological remodeling of heart. Here, we examine the effects of aging on cardiomyocyte apoptosis in 6-, 30-, and 36-month-old Fischer344xBrown Norway F1 hybrid rats (F344XBN). Compared with 6-month hearts, aged hearts exhibited increased TdT-mediated dUTP nick end labeling–positive nuclei, caspase-3 activation, caspase-dependent cleavage of α-fodrin and diminished phosphorylation of protein kinase B/Akt (Thr 308). These age-dependent increases in cardiomyocyte apoptosis were associated with alterations in the composition of the cardiac dystrophin glycoprotein complex and elevated cytoplasmic IgG and albumin immunoreactivity. Immunohistochemical analysis confirmed these data and demonstrated qualitative differences in localization of dystrophin–glycoprotein complex (DGC) molecules with aging. Taken together, these data suggest that aging-related increases in cardiac apoptotic activity model may be due, at least in part, to age-associated changes in DGC structure.

This article is freely available through PubMed Central at

Copyright © The Author 2010. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved.

Citation Information
Kakarla, S. K., Rice, K. M., Katta, A., Paturi, S., Wu, M., Kolli, M., ... & Blough, E. R. (2010). Possible molecular mechanisms underlying age-related cardiomyocyte apoptosis in the F344XBN rat heart. The Journals of Gerontology Series A: Biological Sciences and Medical Sciences, 65A(2), 147-155.