JOURNAL ARTICLE
RESEARCH SUPPORT, NON-U.S. GOV'T
Add like
Add dislike
Add to saved papers

Histological evidence for reversible cardiomyocyte changes and serum cardiac troponin T elevation after exercise in rats.

Physiological Reports 2016 December
This study characterized cardiac troponin T (cTnT) appearance and associated histological evidence of reversible or irreversible changes in myocardial ultrastructure, determined via electron microscopy, in rats undertaking isoproterenol (ISO) infusion or an endurance exercise challenge. Male rats were randomized into ISO and exercise groups. In ISO trials rats were killed 5 h (ISO-5H) and 24 h (ISO-REC19H) after a single ISO or saline injection (SAL-5H; SAL-REC19H). In the exercise trials rats were killed before, as a control (EXE-CON), immediately after (EXE-END5H) and 19 h after (EXE-REC19H) a 5-h bout of swimming with 5% body weight attached to their tail. Serum cTnT was quantified by electrochemiluminescence, and myocardial samples in ISO-REC19H, EXE-REC19H and SAL-REC19H were harvested for assessment of specific mitochondrial injury scores using electron-microscopy. cTnT was undetectable in all control animals (SAL-5H/SAL-REC19H and EXE-CON). cTnT increased in all animals after ISO and exercise but the response was significantly higher (P < 0.05) at ISO-5H (median [range]: 2.60 [1.76-6.18] μg · L-1 ) than at EXE-END5H (median [range]: 0.05 [0.02-0.14] μg · L-1 ). cTnT returned to baseline at EXE-REC19H, but had not completely recovered at ISO-REC19H (median [range]: 0.17 [0.09-1.22] μg · L-1 ). Mitochondrial "injury scores" were significantly higher (P < 0.05) in ISO-REC19H compared to EXE-REC19H and SAL-REC19H, with no difference between EXE-REC19H and SAL-REC19H. Mitochondria from EXE-REC19H appeared aggregated in nonlinear clusters in a small number of scans. These findings suggest that acute exercise-induced appearance of cTnT in this animal model is only associated with reversible changes in cardiomyocyte structure.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app