Vockley J, Vockley C M, Lin S P, Tuchman M, Wu T C, Lin C Y, Seashore M R
Yale University School of Medicine, Department of Human Genetics, New Haven, Connecticut 06510.
Biochem Med Metab Biol. 1992 Feb;47(1):38-46. doi: 10.1016/0885-4505(92)90006-k.
N-Acetyl-L-glutamate synthetase (NAG synthetase) is a mitochondrial matrix enzyme which catalyzes the synthesis of N-acetyl-Lglutamate (NAG), a physiologic activator of the urea cycle enzyme carbamylphosphate synthetase I. Deficiency of NAG synthetase in humans has been reported only three times previously. Two cases presented with uncontrolable neonatal hyperammonemia leading to death, while a third child presented with hyperammonemia and a neurodegenerative picture at 15 months of age after previously being healthy. We report here a new case of NAG synthetase deficiency who presented at 4 years, 10 months of age with an episode of hyperammonemia. Diagnosis was made at age 5 years, 6 months when a liver biopsy showed 9.7% of normal activity. Urine orotic acid was low, and total NAG content in liver was normal. Liver pathology revealed micro- and macrovesicular fat and mitochondria of irregular size and shape with intracristae crystallizations. NAG content in liver in patients with NAG synthetase deficiency has not previously been reported. Its normal value in the face of NAG synthetase deficiency suggests an abnormal localization of NAG to the cytoplasm and the likelihood of aberrant cytoplasmic synthesis of this compound. Additional physiologic implications of this speculative abnormal compartmentalization are discussed.
N-乙酰-L-谷氨酸合成酶(NAG合成酶)是一种线粒体基质酶,它催化N-乙酰-L-谷氨酸(NAG)的合成,NAG是尿素循环酶氨甲酰磷酸合成酶I的生理激活剂。此前,人类NAG合成酶缺乏症仅被报道过三次。两例表现为无法控制的新生儿高氨血症并导致死亡,而第三例患儿在之前健康的情况下,15个月大时出现高氨血症和神经退行性病变。我们在此报告一例新的NAG合成酶缺乏症病例,该患儿4岁10个月时出现高氨血症发作。5岁6个月时通过肝活检显示活性为正常的9.7%而确诊。尿乳清酸水平较低,肝脏中总NAG含量正常。肝脏病理学显示有微泡和大泡脂肪,以及大小和形状不规则且有嵴内结晶的线粒体。此前尚未报道过NAG合成酶缺乏症患者肝脏中的NAG含量。在NAG合成酶缺乏的情况下其值正常,提示NAG在细胞质中的定位异常以及该化合物在细胞质中异常合成的可能性。本文讨论了这种推测性异常区室化的其他生理意义。