The acute effect of trimetazidine on the high frequency fatigue in the isolated Rat diaphragm muscle

被引:0
作者
Mustafa Emre
Ibrahim Karayaylali
Mustafa San
Ayşe Demirkazik
Servet Kavak
机构
[1] Medical School,Departments of Biophysics
[2] Medical School,Department of Nephrology
[3] Cukurova University,Department of Cardiology
[4] Medical School,Department of Biophysics
[5] Cukurova University,undefined
[6] Medical School,undefined
来源
Archives of Pharmacal Research | 2004年 / 27卷
关键词
Trimetazidine (TMZ); Isolated rat diaphragm muscle; Isometric contraction; Fatigue;
D O I
暂无
中图分类号
学科分类号
摘要
The objective of this study was to determine the acute effect of trimetazidine (TMZ) on the pre-fatigue, fatigue and post-fatigue contractile characteristics and tension-frequency relationships of isolated rat diaphragm muscle. Muscle strips were taken from the ventral-costal aspects of the diaphragm muscle of rats killed by decapitation. The muscle strips were suspended in organ baths containing Krebs solution, with a gas mixture of 95% O2 and 5% CO2 at 37°C and pH 7.35-7.45. After determining the thermoregulation and optimum muscle length the muscles were subjected to direct supramaximal stimulation with 0.05 Hz frequency square pulses for periods of 0.5 msec to obtain control values. After adding 5x10p-6 and 5x10p-5 M trimetazidine solution to the respective bath media, the contractile parameters of the muscles were recorded. The contractile parameters were also recorded for both the trimetazidine and tri-metazidine-free media after application of the high frequency fatigue protocols. Later, the tension-frequency relationship was determined by applying stimulating pulses of 10, 20, 50 and 100 Hz to the muscle strips. Whilst the twitch tension obtained from the 5x10p-6 and 5x10p-5 M trimetazidine media showed numerical increases compared to that of the controls, these were not statistically significant (p>0.05). The contraction time exhibited a dose dependent increase (p<0.001), whilst the contraction and relaxation rates did not differ significantly. The isometric contraction forces obtained with the different stimulating frequencies showed a significant increase in the tetanic contraction only at 100 Hz (p<0.05). A comparison of the pre-and post-fatigue twitch tensions in the trimetazidine media showed the postfatigue twitch tensions to be significantly higher than those of the pre-fatigue contraction forces (p<0.05). In the 5x10p-6 and 5x10p5 M trimetazidine media the increases in the post-fatigue contraction force were 22 and 30%, respectively. These results demonstrated that in isolated rat diaphragm muscle, TMZ significantly limited the mechanical performance decrease during fatigue. It is our opinion that trimetazidine contributed to the observed fatigue tolerance by eliminating the factors of fatigue, due to preservation of intracellular calcium homeostasis, provision of the ATP energy levels needed by ATPase dependent pumps and especially by keeping the intracellular pH within certain limits.
引用
收藏
页码:646 / 652
页数:6
相关论文
共 96 条
[1]  
Albengres E.(1998)Trimetazidine: Experimental and clinical update review Cardiovascular Drug Reviews 16 359-390
[2]  
Tillement J. P.(1989)Intracellular calcium and tension during fatigue in isolated single muscle fibers from Xenopus Laevis J. Physiol (Lond) 1415 433-458
[3]  
Louet H. L.(1992)Role of excitation-construction coupling in muscle fatigue Sports Med. 13 116-126
[4]  
Morin D.(1974)Nerve and muscle stimulation of the rat isolated phrenic nerve-diaphragm preparation Anesth. Analg. 53 594-596
[5]  
Allen D. G.(1984)Effects of hyperoxia and hypoxia on dynamic and sustained static performance of the human quadriceps muscle Acta Physiol. Scand. 122 629-633
[6]  
Lee J. A.(2003)Effects of trimetazidine and selenium on high-frequency fatigue in isolated rat diaphragm muscle Adv. Ther. 20 261-269
[7]  
Westerbland H.(1994)Role of adenosine in the depolarization of hypoxic hamster diaphragm membrane A J. Respir. Crit. Care Med. 149 910-914
[8]  
Allen D. G.(1994)Cellular mechanisms of muscle fatigue Physiol. Rev. 74 49-94
[9]  
Westerblad H.(1995)Effects of creatine phosphate and P J. Physiol., (Lond) 482 123-140
[10]  
Lee J. A.(1985) on Ca Br. J. Pharmacol. 84 517-524