Back to Search
Start Over
N-acylhydrazone improves exercise intolerance in rats submitted to myocardial infarction by the recovery of calcium homeostasis in skeletal muscle.
- Source :
-
Life sciences [Life Sci] 2014 Jan 14; Vol. 94 (1), pp. 30-6. Date of Electronic Publication: 2013 Nov 21. - Publication Year :
- 2014
-
Abstract
- Aims: This work investigated the effects of 3,4-methylenedioxybenzoyl-2-thienylhydrazone (LASSBio-294) treatment on the contractile response of soleus (SOL) muscle from rats submitted to myocardial infarction (MI).<br />Main Methods: Following coronary artery ligation, LASSBio-294 (2mg/kg, i.p.) or vehicle was administrated once daily for 4 weeks.<br />Key Findings: The run time to fatigue for sham rats was 17.9 ±2.6 min, and it was reduced to 3.3 ± 0.8 min (P<0.05) in MI rats. In MI rats treated with LASSBio-294, the time to fatigue was 15.1 ± 3.6 min. During the contractile test, SOL muscles from sham rats showed a response of 7.12 ± 0.54N/cm(2) at 60 Hz, which was decreased to 5.45 ± 0.49 N/cm(2) (P<0.05) in MI rats. The contractility of SOL muscles from the MI-LASSBio-294 group was increased to 9.01 ± 0.65N/cm(2). At 16 mM caffeine, the contractility was reduced from 2.31 ± 0.33 to 1.60 ± 0.21 N/cm(2) (P<0.05) in the MI group. In SOL muscles from MI-LASSBio-294 rats, the caffeine response was increased to 2.62 ± 0.33 N/cm(2). Moreover, SERCA2a expression in SOL muscles was decreased by 0.31-fold (31%) in the MI group compared to the Sham group (P<0.05). In the MI-LASSBio-294 group, it was increased by 1.53-fold (153%) compared to the MI group (P<0.05). Meanwhile, the nuclear density in SOL muscles was increased in the MI group compared to the Sham group. Treatment with LASSBio-294 prevented this enhancement of cellular infiltrate.<br />Significance: LASSBio-294 treatment prevented the development of muscular fatigue and improved exercise intolerance in rats submitted to MI.<br /> (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Caffeine pharmacology
Disease Models, Animal
Exercise Tolerance physiology
Homeostasis
Male
Muscle Contraction drug effects
Muscle Contraction physiology
Muscle Fatigue physiology
Muscle, Skeletal metabolism
Muscle, Skeletal physiology
Physical Conditioning, Animal physiology
Rats
Rats, Wistar
Sarcoplasmic Reticulum Calcium-Transporting ATPases metabolism
Time Factors
Calcium metabolism
Exercise Tolerance drug effects
Hydrazones pharmacology
Muscle Fatigue drug effects
Myocardial Infarction physiopathology
Thiophenes pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0631
- Volume :
- 94
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Life sciences
- Publication Type :
- Academic Journal
- Accession number :
- 24269214
- Full Text :
- https://doi.org/10.1016/j.lfs.2013.11.012