Mathews K P, Curd J G, Hugli T E
J Clin Immunol. 1986 Jan;6(1):87-91. doi: 10.1007/BF00915368.
Serum carboxypeptidase N (SCPN) is the primary inactivator of the C3a, C4a, and C5a anaphylatoxins as well as an inactivator of bradykinin. Thus SCPN deficiency potentially could result in significant pathophysiologic consequences. Previous studies identified a deficient subject afflicted with frequent episodes of angioedema, and other family members also had SCPN deficiency. To delineate this abnormality further, the fractional catabolic rate (FRC) and enzyme synthesis were determined in three members of the afflicted kindred as well as in five normal persons following the infusion of homogeneous 125I-SCPN. The mean FCR and synthesis rates for SCPN in the normal subjects were 1.3%/hr and 20,793 U/kg/hr, respectively. Reduced synthesis was concluded to be primarily responsible for the low SCPN levels in the afflicted kindred. The high FRC of SCPN discourages attempted maintenance therapy with infusions of enriched SCPN preparations.
血清羧肽酶N(SCPN)是C3a、C4a和C5a过敏毒素的主要灭活剂,也是缓激肽的灭活剂。因此,SCPN缺乏可能会导致严重的病理生理后果。先前的研究发现一名患有频繁血管性水肿发作的缺陷患者,其他家庭成员也存在SCPN缺乏。为了进一步阐明这种异常情况,在输注同源125I-SCPN后,测定了患病家族的三名成员以及五名正常人的分数分解代谢率(FRC)和酶合成。正常受试者中SCPN的平均FCR和合成率分别为1.3%/小时和20,793 U/kg/小时。得出结论,合成减少是患病家族中SCPN水平低的主要原因。SCPN的高FRC不鼓励尝试用富集的SCPN制剂进行维持治疗。