muscle enzyme activities
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2014 ◽  
Vol 174 (6) ◽  
pp. 145-145 ◽  
Author(s):  
S. J. Mack ◽  
K. Kirkby ◽  
F. Malalana ◽  
C. M. McGowan

2009 ◽  
Vol 181 (2) ◽  
pp. 227-232 ◽  
Author(s):  
R. DIMBERG ◽  
R. HED ◽  
G. KALLNER ◽  
A. NYGREN

2008 ◽  
Vol 105 (6) ◽  
pp. 1746-1753 ◽  
Author(s):  
Inge D. Wijnberg ◽  
Klien G. van Dam ◽  
Ellen de Graaf-Roelfsema ◽  
Hans A. Keizer ◽  
Mireille M. E. van Ginneken ◽  
...  

Too intensive training may lead to overreaching or overtraining. To study whether quantitative needle electromyography (QEMG) is more sensitive to detect training (mal)adaptation than muscle enzyme activities, 12 standardbred geldings trained for 32 wk in age-, breed-, and sex-matched fixed pairs. After a habituation and normal training (NT) phase ( phases 1 and 2, 4 and 18 wk, respectively), with increasing intensity and duration and frequency of training sessions, an intensified training (IT) group ( phase 3, 6 wk) and a control group (which continued training as in the last week of phase 2) were formed. Thereafter, all horses entered a reduced training phase ( phase 4, 4 wk). One hour before a standardized exercise test (SET; treadmill), QEMG analysis and biochemical enzyme activity were performed in muscle or in biopsies from vastus lateralis and pectoralis descendens muscle in order to identify causes of changes in exercise performance and eventual (mal)adaptation in skeletal muscle. NT resulted in a significant adaptation of QEMG parameters, whereas in muscle biopsies hexokinase activity was significantly decreased. Compared with NT controls, IT induced a stronger adaptation (e.g., higher amplitude, shorter duration, and fewer turns) in QEMG variables resembling potentially synchronization of individual motor unit fiber action potentials. Despite a 19% decrease in performance of the SET after IT, enzyme activities of 3-hydroxyacyl dehydrogenase and citrate synthase displayed similar increases in control and IT animals. We conclude that 1) QEMG analysis is a more sensitive tool to monitor training adaptation than muscle enzyme activities but does not discriminate between overreaching and normal training adaptations at this training level and 2) the decreased performance as noted in this study after IT originates most likely from a central (brain) rather than peripheral level.


2005 ◽  
Vol 2 (3) ◽  
pp. 153-157 ◽  
Author(s):  
CA Williams ◽  
DS Kronfeld ◽  
TM Hess ◽  
KE Saker ◽  
JE Waldron ◽  
...  

AbstractThis study tested our hypothesis that during an 80-km Research Ride in 2002 (R2) horses that did not finish (NF) the ride would have elevated muscle enzyme activities in the blood and changes in biomarkers of oxidative stress as compared to horses that finished (F) the ride. These results were then compared to previous rides – Old Dominion (OD) and the Research Ride 2001 (R1). For R2, 40 mostly Arabian horses competed and had blood samples collected before, at 27, 48 and 80 km, and 170 to 190 min after the 80-km race. Blood was collected similarly in R1 and OD. Blood was analysed for plasma lipid hydroperoxides (LPO), α-tocopherol (TOC), creatine kinase (CK), aspartate aminotransferase (AST), red and white blood cell total glutathione (GSH-T) and glutathione peroxidase (GPx). Data were analysed using a repeated measure ANOVA in SAS. Associations between muscle enzymes and antioxidant status were determined using Pearson's or Spearman's correlations. Activities of CK and AST were higher (P<0.05) before, during and after the ride in NF than in F; however, TOC, LPO, GSH-T and GPx were not different. In R2, negative correlations were found with GPx and CK (r = −0.21; P = 0.005), GPx and AST (r = −0.15; P = 0.05), and a positive correlation was found with GSH-T and CK (r = 0.18; P = 0.02). Values of CK, LPO, GPx and GSH-T were higher (P<0.05) in R2 than in R1 or OD. The overall comparison of 80-km endurance races suggests the importance of considering the horse's fitness, terrain, ambient conditions and calibre of race when interpreting results from markers of oxidative stress and muscle enzyme leakage.


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