DIMINISHED HEAT-SHOCK PROTEIN-70 MESSENGER-RNA INDUCTION IN AGED RAT HEARTS AFTER ISCHEMIA

被引:68
作者
NITTA, Y
ABE, K
AOKI, M
OHNO, I
ISOYAMA, S
机构
[1] TOHOKU UNIV, SCH MED, DEPT INTERNAL MED 1, AOBA KU, SENDAI, MIYAGI 980, JAPAN
[2] TOHOKU UNIV, SCH MED, INST BRAIN DIS, DEPT NEUROL, SENDAI, MIYAGI 980, JAPAN
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1994年 / 267卷 / 05期
关键词
AGING; HEAT SHOCK PROTEIN 72; HEAT SHOCK PROTEIN 73;
D O I
10.1152/ajpheart.1994.267.5.H1795
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vulnerability of aged hearts to ischemia may be due to defects in protective mechanisms provided by heat shock proteins (HSPs). To determine whether there is a defect in the induction of HSPs by ischemia in old hearts, HSP72 and HSP73 (inducible and constitutive HSP70, respectively) mRNA induction was examined in young (2-mo-old; n = 36) and old (18-mo-old; n = 32) rat hearts. Transient (10- or 20-min) ischemia was applied by tightening a snare placed around left coronary arterial branches 3 days before examination to avoid the effect of operation on induction. HSP72 mRNA was induced markedly in young hearts after 10-min ischemia, peaked at 2 h, but was induced only slightly in old hearts. HSP73 mRNA was also induced in young hearts, peaked at 4 h, but was not induced in old hearts. The mRNAs were markedly induced in old hearts as well after 20-min ischemia, which was accompanied by the induction of HSP72 protein. Thus the age-related modulation of HSP72 and HSP73 mRNAs suggests a defective sensing mechanism for ischemia in old hearts.
引用
收藏
页码:H1795 / H1803
页数:9
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