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Increased apoptosis and myocyte enlargement with decreased cardiac mass; distinctive features of the aging male, but not female, monkey heart.

Authors
  • Zhang, Xiao-Ping1
  • Vatner, Stephen F
  • Shen, You-Tang
  • Rossi, Franco
  • Tian, Yimin
  • Peppas, Athanasios
  • Resuello, Ranillo R G
  • Natividad, Filipinas F
  • Vatner, Dorothy E
  • 1 Cardiovascular Research Institute, Department of Cell Biology and Molecular Medicine, UMDNJ-New Jersey Medical School, 185 S. Orange Avenue, MSB G-609, Newark, NJ 07103, USA. , (Jersey)
Type
Published Article
Journal
Journal of molecular and cellular cardiology
Publication Date
Oct 01, 2007
Volume
43
Issue
4
Pages
487–491
Identifiers
PMID: 17720187
Source
Medline
License
Unknown

Abstract

We studied gender-specific changes in aging cardiomyopathy in a primate model, Macaca fascicularis, free of the major human diseases, complicating the interpretation of data specific to aging in humans. Left ventricular (LV) weight/body weight decreased, p<0.05, in old males but did not change in old females. However, despite the decrease in LV weight, mean myocyte cross-sectional area in the old males increased by 51%. This increase in myocyte size was not uniform in old males, i.e., it was manifest in only 20-30% of all the myocytes from old males. In old males there was a 4-fold increase in frequency of myocyte apoptosis without any increase in proliferation-capable myocytes assessed by Ki-67 expression. Apoptosis was unchanged in old female monkey hearts, whereas the frequency of myocytes expressing Ki-67 declined 90%. These results, opposite to findings from rodent studies, indicate distinct differences in which male and female monkeys maintain functional heart mass during aging. The old male hearts demonstrated increased apoptosis, which more than offset the myocyte hypertrophy. Interestingly, the hypertrophy was not uniform and there was no significant increase in myocyte proliferation.

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