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咖啡因和高钾对不同发育阶段正常和营养不良小鼠趾长伸肌的影响。

Effect of caffeine and high potassium on normal and dystrophic mouse EDL muscles at various developmental stages.

作者信息

Dangain J, Neering I R

机构信息

School of Physiology and Pharmacology, University of New South Wales, Kensington, Australia.

出版信息

Muscle Nerve. 1993 Jan;16(1):33-42. doi: 10.1002/mus.880160108.

Abstract

EDL muscles from normal and dystrophic (dy2j) mice of various ages were examined. Muscles were divided into three groups according to age: 7 to 14 days postnatal, 16 to 21 days postnatal, and 6 months old, to assess age and/or phenotype related differences in the muscle response to caffeine or high K+. The response of normal muscles to caffeine decreased with age and reached adult characteristics between the second and third week of postnatal life. Their response to high K+ also changed during postnatal development; specifically, the time taken to recover to 50% pretest twitch tension decreased with age, probably reflecting developmental changes in Cl- conductance. Up to 21 days of age, the sensitivity of dystrophic muscles to both caffeine and high K+ was essentially similar to normal, while marked differences were observed in the adult. Taken altogether, our results suggest that while the maturation of a number of systems might be delayed in dystrophic muscles at preclinical stages of the disease, their e-c coupling and SR function (Ca2+ release and reuptake) appear to be quite normal. Our results further suggest that the "abnormal" responses of dystrophic muscles at more advanced stages of the disease, when challenged by drugs acting on either of these systems, may be explained in terms of changes in muscle fiber type proportions.

摘要

对不同年龄的正常小鼠和营养不良(dy2j)小鼠的趾长伸肌(EDL)进行了检查。根据年龄将肌肉分为三组:出生后7至14天、出生后16至21天和6个月大,以评估肌肉对咖啡因或高钾离子反应中与年龄和/或表型相关的差异。正常肌肉对咖啡因的反应随年龄增长而降低,并在出生后第二周和第三周之间达到成年特征。它们对高钾离子的反应在出生后发育过程中也发生了变化;具体而言,恢复到测试前抽搐张力50%所需的时间随年龄增长而减少,这可能反映了氯离子电导的发育变化。在21日龄之前,营养不良肌肉对咖啡因和高钾离子的敏感性与正常肌肉基本相似,而在成年期观察到明显差异。综上所述,我们的结果表明,虽然在疾病临床前阶段营养不良肌肉中许多系统的成熟可能会延迟,但其电-机械偶联和肌浆网功能(钙释放和再摄取)似乎相当正常。我们的结果进一步表明,在疾病更晚期阶段,当受到作用于这些系统中任何一个的药物挑战时,营养不良肌肉的“异常”反应可能可以用肌纤维类型比例的变化来解释。

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