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Carnitine palmitoyl transferase deficiency in malignant hyperthermia

机译:恶性高热中的肉碱棕榈酰转移酶缺乏症

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AbstractThe activity of carnitine palmitoyl transferase, an enzyme that catalyzes the transport of long‐chain acylcarnitines into mitochondria, was quantitated in EB‐virus‐transformed lymphoblasts from 7 patients with susceptibility for malignant hyperthermia. Immunoreactive enzyme protein was also measured using an enzyme‐linked immunosorbent assay. Cell lines derived from patients with carnitine palmitoyl transferase deficiency of muscle and from normal individuals were used as positive and negative controls, respectively. One patient with malignant hyperthermia had a deficiency in the enzyme activity which was comparable with that of the known carnitine palmitoyl transferase deficient patients. This individuaľs lymphoblasts were also deficient in immunoreactive enzyme protein. All of the remaining patients with malignant hyperthermia were deficient only when the backward assay for carnitine palmitoyl transferase was used for quantitation. It is likely that a subset of individuals with a malignant hyperthermia phenotype have a primary deficiency of carnitine palmitoyl transferase and that others have a milder enzyme deficiency secondary to the primary defect in malignant hyperthermia. © 1993 John WileyS
机译:摘要对7例恶性高热易感患者的EB病毒转化淋巴母细胞中肉碱棕榈酰转移酶(一种催化长链酰基肉碱转运至线粒体的酶)的活性进行定量。还使用酶联免疫吸附测定法测量免疫反应性酶蛋白。分别使用来自肌肉肉碱棕榈酰转移酶缺乏症患者和正常个体的细胞系作为阳性和阴性对照。一名恶性高热患者存在酶活性缺陷,与已知肉碱棕榈酰转移酶缺乏症患者相当。这种个体淋巴母细胞也缺乏免疫反应性酶蛋白。其余的恶性高热患者仅在使用肉碱棕榈酰转移酶的反向测定进行定量时才出现缺陷。一部分恶性高热表型个体可能原发性肉碱棕榈酰转移酶缺乏,而其他人则有继发于恶性高热原发性缺陷的轻度酶缺乏。© 1993 约翰·威利

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