Olpin S E, Manning N J, Carpenter K, Middleton B, Pollitt R J
Neonatal Screening Laboratory, Children's Hospital, Sheffield, UK.
J Inherit Metab Dis. 1992;15(6):883-90. doi: 10.1007/BF01800227.
Intact cultured fibroblasts from patients with deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase release 3H2O from [9,10-3H]myristic acid and [9,10-3H]palmitic acid more slowly than normal. The ratio of activity (palmitate/myristate) is also low and the expression (rate with palmitate2/(rate with myristate) gives good differentiation between affected and unaffected cells. In some patients who have shown hydroxydicarboxylic aciduria when unwell there is reduced 3H2O production from [9,10-3H]myristic and [9,10-3H]palmitic acids by intact cultured fibroblasts but normal 3-hydroxyacyl-CoA dehydrogenase activities in disrupted cells. The palmitate/myristate ratio is higher than in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. The basic defect in these patients is still unknown but it is suggested that caution be used over the administration of medium-chain triglyceride.
长链3-羟基酰基辅酶A脱氢酶缺乏症患者的完整培养成纤维细胞从[9,10-³H]肉豆蔻酸和[9,10-³H]棕榈酸释放³H₂O的速度比正常情况慢。活性比(棕榈酸/肉豆蔻酸)也较低,并且表达(棕榈酸²的速率/肉豆蔻酸的速率)能很好地区分受影响和未受影响的细胞。在一些不适时出现羟基二羧酸尿症的患者中,完整培养的成纤维细胞从[9,10-³H]肉豆蔻酸和[9,10-³H]棕榈酸产生的³H₂O减少,但破碎细胞中的3-羟基酰基辅酶A脱氢酶活性正常。棕榈酸/肉豆蔻酸的比率高于长链3-羟基酰基辅酶A脱氢酶缺乏症患者。这些患者的基本缺陷仍然未知,但建议在给予中链甘油三酯时要谨慎。