Gallant E M, Donaldson S K
Department of Veterinary Biology, College of Veterinary Medicine, Minneapolis, MN 55455.
Pflugers Arch. 1989 May;414(1):24-30. doi: 10.1007/BF00585622.
Bundles of cells, intact from tendon to tendon, were dissected from muscles of normal and malignant hyperthermia susceptible (MHS) pigs. Intact bundles were stimulated either (1) electrically, to elicit twitches and tetani, or (2) ionically with elevated extracellular K+ (K+0), to elicit K-contractures. Maximal tetanic force was the same for MHS and normal intact bundles. In MHS muscles, when responses were elicited from control resting plasmalemma polarization (4 mM K+0), twitches and K-contractures were significantly larger and the K-contracture activation curve was shifted towards lower [K+]0 with respect to normal bundles. Resting hyperpolarization (2 mM K+0) selectively reduced MHS twitch force to normal and K-contracture force toward normal. For K-contracture and twitches, there was a range of K+0 concentrations (7-10 mM), representing resting depolarization, which enhanced subsequent twitch and K-contracture magnitude in both MHS and normal intact bundles as compared to responses elicited from control (4 mM K+0). These results are consistent with the hypothesis that resting plasmalemma voltage sets the gain of sarcoplasmic reticulum calcium release in MHS and normal intact bundles independent of type of stimulation and suggest that a defect in this mechanism may be responsible for the enhanced twitches and K-contractures of MHS muscles.
从正常猪和恶性高热易感(MHS)猪的肌肉中解剖出从肌腱到肌腱完整的细胞束。完整的细胞束通过以下两种方式之一进行刺激:(1)电刺激,引发抽搐和强直收缩;(2)用细胞外钾离子浓度升高(K+0)进行离子刺激,引发钾离子收缩。MHS和正常完整细胞束的最大强直收缩力相同。在MHS肌肉中,当从对照静息质膜极化(4 mM K+0)引发反应时,抽搐和钾离子收缩明显更大,并且相对于正常细胞束,钾离子收缩激活曲线向较低的[K+]0偏移。静息超极化(2 mM K+0)选择性地将MHS抽搐力降低至正常水平,并将钾离子收缩力降低至接近正常水平。对于钾离子收缩和抽搐,存在一系列K+0浓度(7 - 10 mM),代表静息去极化,与从对照(4 mM K+0)引发的反应相比,这增强了MHS和正常完整细胞束中随后的抽搐和钾离子收缩幅度。这些结果与以下假设一致,即静息质膜电压设定了MHS和正常完整细胞束中肌浆网钙释放的增益,与刺激类型无关,并表明该机制的缺陷可能是MHS肌肉抽搐和钾离子收缩增强的原因。