DiMauro S, Stern L Z, Mehler M, Nagle R B, Payne C
Muscle Nerve. 1978 Jan-Feb;1(1):27-36. doi: 10.1002/mus.880010105.
In a postmortem study of a patient with adult-onset acid maltase deficiency (AMD), morphological abnormalities were confined to skeletal muscle and consisted of a vacuolar myopathy. Acid maltase activity, however, was approximately 6% of normal in muscle, liver, and brain, and 3% of normal in heart. Kinetic characteristics, and inhibition by antibodies and Zn++, showed that the residual activity was "authentic" acid maltase. Neutral maltase activity was normal in muscle and liver, but decreased in brain (55% of normal) and heart (19% of normal). Although the relative decrease of acid maltase was similar in different tissues, absolute residual activity was lowest in skeletal muscle: this may explain the selective involvement of this tissue in late-onset AMD.
在一项对成年发病型酸性麦芽糖酶缺乏症(AMD)患者的尸检研究中,形态学异常仅限于骨骼肌,表现为空泡性肌病。然而,酸性麦芽糖酶活性在肌肉、肝脏和大脑中约为正常水平的6%,在心脏中为正常水平的3%。动力学特征以及抗体和锌离子的抑制作用表明,残余活性是“真正的”酸性麦芽糖酶。中性麦芽糖酶活性在肌肉和肝脏中正常,但在大脑中降低(为正常水平的55%),在心脏中降低(为正常水平的19%)。尽管不同组织中酸性麦芽糖酶的相对降低相似,但骨骼肌中的绝对残余活性最低:这可能解释了该组织在迟发性AMD中的选择性受累情况。