Donaldson S K, Gallant E M, Huetteman D A
Department of Physiology, School of Medicine, Minneapolis, MN 55455.
Pflugers Arch. 1989 May;414(1):15-23. doi: 10.1007/BF00585621.
Porcine skeletal muscle fibers were studied to determine if the defect in malignant hyperthermia involves transverse tubule (TT) to sarcoplasmic reticulum (SR) communication. Peeled (mechanically skinned) skeletal muscle fibers from normal and malignant hyperthermia susceptible (MHS) pigs were stimulated with Cl- to ionically depolarize transverse tubules and thereby trigger Ca2+ release from SR. Caffeine was used to directly stimulate the Ca2+-induced Ca2+ release mechanism (CaIR) of the sarcoplasmic reticulum. Calcium released from internal fiber stores was monitored as Ca2+-activated isomeric force generation in the form of tension transients. Cl- -induced tension transients result from a primary component of Ca2+ release which triggers a secondary CaIR component; CaIR and caffeine contractures were eliminated by procaine. The primary component of Cl- -induced SR Ca2+ release was indistinguishable for MHS and normal skeletal peeled fibers at all TT resting and Cl- stimulation conditions. Only the magnitude of the secondary CaIR component was significantly larger in MHS fibers. The [Ca2+] threshold for secondary CaIR was lowered by resting TT depolarization in both normal and MHS fibers. Conditions for resting TT hyperpolarization selectively reduced the magnitude of the secondary CaIR component of MHS fibers, making them indistinguishable from normal.
对猪骨骼肌纤维进行了研究,以确定恶性高热的缺陷是否涉及横管(TT)与肌浆网(SR)之间的通讯。用氯离子刺激来自正常猪和恶性高热易感(MHS)猪的去皮(机械去表皮)骨骼肌纤维,使横管发生离子去极化,从而触发肌浆网释放钙离子。使用咖啡因直接刺激肌浆网的钙诱导钙释放机制(CaIR)。从纤维内部储存释放的钙以张力瞬变的形式作为钙激活的异构力产生进行监测。氯离子诱导的张力瞬变源于钙离子释放的主要成分,该成分触发了次要的CaIR成分;普鲁卡因消除了CaIR和咖啡因挛缩。在所有横管静息和氯离子刺激条件下,MHS和正常去皮骨骼肌纤维中氯离子诱导的肌浆网钙离子释放的主要成分没有区别。只有次要CaIR成分的幅度在MHS纤维中显著更大。在正常和MHS纤维中,静息横管去极化都会降低次要CaIR的钙离子阈值。静息横管超极化的条件选择性地降低了MHS纤维次要CaIR成分的幅度,使其与正常纤维无法区分。