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大鼠中的吐根碱肌病

Emetine myopathy in the rat.

作者信息

Bradley W G, Fewings J D, Harris J B, Johnson M A

出版信息

Br J Pharmacol. 1976 May;57(1):29-41. doi: 10.1111/j.1476-5381.1976.tb07653.x.

Abstract

1 (-)Emetine (0.25-2.0 mg/kg i.p.) was administered to rats for up to 220 days. 2 At doses of 1.0 mg/kg or less, the animals continued to gain weight but more slowly than the untreated control animals. The physiological changes in the muscles from these animals were minimal; there was a small reduction in both the resting membrane potential and in the maximum rate of rise of the action potential. There was no atrophy or loss of muscle fibres although in the occasional muscle, hyaline fibres, necrotic fibres and split fibres were observed. There was a focal loss of myofibrillar adenosine triphosphatase (ATPase) and nicotinamide adenine dinucleotide tetrazolium reductase (NADH-TR) in Type II and Type III fibres, but no such loss in Type I fibres. 3 The animals receiving 2.0 mg/kg of (-)emetine gained weight slowly for up to 20 days but then rapidly lost weight and by 30 days they were weak and emaciated. The muscles from these animals were severly atrophied and the total muscle wet weight was reduced by almost 20%. 4 The strength of the muscles from these animals was measured in vitro using direct stimulation. They were weaker than normal both in absolute terms and when expressed in terms of tension developed/unit wet weight. 5 There was no evidence of either functional or structural denervation but surgically denervated muscles from animals in this group were indistinguishable from denervated muscles from normal rats. 6 Severe structural damage was obvious in the fibres of both extensor digitorum longus and soleus. Necrotic, hyaline and splitting fibres were common and the focal loss of myofibrillar ATPase and NADH-TR activity was extensive and occurred in Type I fibres as well as in Type II and Type II fibres. 7 It is concluded that the muscular weakness induced by (-)-emetine is due to a direct effect on the muscle fibres and that this occurs at a subcellular level. There is no evidence that functional or structural denervation plays any role in the aetiology of emetine myopathy in the rat.

摘要
  1. 给大鼠腹腔注射(-)吐根碱(0.25 - 2.0毫克/千克),持续220天。2. 剂量为1.0毫克/千克及以下时,动物继续增重,但比未处理的对照动物慢。这些动物肌肉的生理变化很小;静息膜电位和动作电位最大上升速率均有小幅降低。虽然偶尔在肌肉中观察到透明纤维、坏死纤维和分裂纤维,但没有肌肉纤维萎缩或丢失。II型和III型纤维中肌原纤维三磷酸腺苷酶(ATPase)和烟酰胺腺嘌呤二核苷酸四唑还原酶(NADH - TR)有局灶性丧失,但I型纤维中没有这种情况。3. 接受2.0毫克/千克(-)吐根碱的动物在长达20天的时间里体重缓慢增加,但随后迅速减重,到30天时变得虚弱消瘦。这些动物的肌肉严重萎缩,肌肉总湿重减少了近20%。4. 使用直接刺激在体外测量这些动物肌肉的力量。无论从绝对值还是以单位湿重产生的张力来表示,它们都比正常情况弱。5. 没有证据表明存在功能性或结构性去神经支配,但该组动物手术去神经支配的肌肉与正常大鼠去神经支配的肌肉没有区别。6. 趾长伸肌和比目鱼肌的纤维中明显存在严重的结构损伤。坏死、透明和分裂纤维很常见,肌原纤维ATPase和NADH - TR活性的局灶性丧失广泛存在,且发生在I型纤维以及II型和III型纤维中。7. 得出结论,(-)吐根碱诱导的肌肉无力是由于对肌肉纤维的直接作用,且这种作用发生在亚细胞水平。没有证据表明功能性或结构性去神经支配在大鼠吐根碱肌病的病因学中起任何作用。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e46/1667020/4fbbe743f014/brjpharm00505-0044-a.jpg

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