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硝苯地平可减轻小鼠运动诱导的肌肉损伤。

Nifedipine diminishes exercise-induced muscle damage in mouse.

作者信息

Duarte J A, Soares J M, Appell H J

机构信息

Department of Sport Biology, Faculty of Sport Sciences, University of Porto.

出版信息

Int J Sports Med. 1992 Apr;13(3):274-7. doi: 10.1055/s-2007-1021266.

DOI:10.1055/s-2007-1021266
PMID:1601565
Abstract

The purpose of this study was to evaluate the effects of a calcium channel blocker (nifedipine) on the severity of muscle damage induced by intensive exercise. Male Charles River mice were assigned to four groups (8 mice/group): normal control (C), nifedipine (N), nifedipine and exercise (N + E) and exercise (E). The animals of the C group were not submitted to any exercise nor to drug administration. The animals of the N group received 1 mg.kg-1 per day of nifedipine (Adalat 10 mg, Bayer AG), per os, during 3 days. The mice of the N + E group were submitted to a treadmill run (0 degree slope) at 1000 m.h-1 (80% of their maximal speed) for 1 hour. In this group, the administration of the drug was under the same conditions as for the N group. The administration started 24 h before the run. The E group was submitted to the same exercise protocol as the animals of N + E group. The soleus muscle was excised for light and electron microscopic evaluation using routine histological techniques. In the C and N groups no morphological alterations were detected. In the E group the number of alterations of striated pattern was twice that in the N + E group. The number of fibres with central nuclei was 35% in the E group but only 8% in the N + E group. The total number of damaged fibres was significantly higher in the E group. The results suggest that nifedipine may give protection to exercise-induced skeletal muscle damage in mouse, probably because the blocking of channels impaired Ca2+ influx; and the results of this study therefore confirm earlier contentions about the possible role of calcium ions in producing muscle damage after work.

摘要

本研究的目的是评估钙通道阻滞剂(硝苯地平)对高强度运动所致肌肉损伤严重程度的影响。将雄性查尔斯河小鼠分为四组(每组8只):正常对照组(C)、硝苯地平组(N)、硝苯地平运动组(N + E)和运动组(E)。C组动物既不进行任何运动也不给予药物。N组动物在3天内每天经口给予1 mg·kg-1硝苯地平(拜耳公司的拜新同10 mg)。N + E组小鼠以1000 m·h-1(其最大速度的80%)在跑步机上(0度坡度)跑步1小时。该组药物给药条件与N组相同,在跑步前24小时开始给药。E组的运动方案与N + E组动物相同。切除比目鱼肌,采用常规组织学技术进行光镜和电镜评估。在C组和N组未检测到形态学改变。在E组,横纹模式改变的数量是N + E组的两倍。E组中央核纤维的数量为35%,而N + E组仅为8%。E组受损纤维的总数明显更高。结果表明,硝苯地平可能对小鼠运动诱导的骨骼肌损伤具有保护作用,这可能是因为通道阻断减少了Ca2+内流;因此,本研究结果证实了早期关于钙离子在运动后肌肉损伤中可能作用的观点。

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