King R G, Di Iulio J L, Gude N M, Brennecke S P
Department of Perinatal Medicine, Royal Women's Hospital, Carlton, Vic., Australia.
Reprod Fertil Dev. 1995;7(6):1581-4. doi: 10.1071/rd9951581.
An endogenous inhibitor of nitric oxide synthase (NOS), NG,NG dimethylarginine (asymmetric dimethylarginine, ADMA), which is present in human plasma and urine, has been reported to be elevated in the plasma of women with pre-eclampsia. As ADMA inhibition may contribute to reduced placental NOS activity observed in pre-eclampsia, the aim of this study was to compare the effects of ADMA on placental NOS activity from pre-eclamptic and normal pregnancies (gestational ages 38.4 +/- 0.9 and 38.3 +/- 0.3 weeks respectively). NOS activity was determined by measuring the conversion of [3H]L-arginine to [3H]L-citrulline in homogenates of normal and pre-eclamptic placentae in the absence and presence of increasing concentrations of ADMA (1-100 microM). The IC50 for ADMA for the pre-eclamptic placentae (22.1 +/- 2.1 microM, n = 6) was not significantly different from that for the normal placentae (18.8 +/- 1.4 microM, n = 6). When ADMA and L-arginine in homogenates was removed by ion exchange chromatography and exogenous L-arginine replaced (32 microM), the IC50 for the pre-eclamptic placentae (19.5 +/- 1.8 microM, n = 6) was not significantly different than that for the normal placentae (20.9 +/- 1.0 microM, n = 6), and NOS activity in the absence of endogenous and exogenous ADMA was still reduced in pre-eclamptic placentae. These results provide no evidence that the sensitivity of placental NOS to ADMA is affected by pre-eclampsia, or that placental ADMA contributes to the reduction of placental NOS in pre-eclampsia.
一氧化氮合酶(NOS)的内源性抑制剂,NG,NG - 二甲基精氨酸(不对称二甲基精氨酸,ADMA),存在于人体血浆和尿液中,据报道,子痫前期妇女血浆中该物质水平升高。由于ADMA抑制可能导致子痫前期胎盘NOS活性降低,本研究旨在比较ADMA对子痫前期妊娠和正常妊娠(分别为孕龄38.4±0.9周和38.3±0.3周)胎盘NOS活性的影响。通过测量在有无浓度递增的ADMA(1 - 100微摩尔)情况下,正常胎盘和子痫前期胎盘匀浆中[3H]L - 精氨酸向[3H]L - 瓜氨酸的转化来测定NOS活性。子痫前期胎盘匀浆中ADMA的半数抑制浓度(IC50)为(22.1±2.1微摩尔,n = 6),与正常胎盘的(18.8±1.4微摩尔,n = 6)无显著差异。当通过离子交换色谱法去除匀浆中的ADMA和L - 精氨酸并替换为外源性L - 精氨酸(32微摩尔)时,子痫前期胎盘匀浆的IC50为(19.5±1.8微摩尔,n = 6),与正常胎盘的(20.9±1.0微摩尔,n = 6)无显著差异,且在无内源性和外源性ADMA时,子痫前期胎盘的NOS活性仍然降低。这些结果表明,没有证据显示子痫前期会影响胎盘NOS对ADMA的敏感性,也没有证据表明胎盘ADMA会导致子痫前期胎盘NOS活性降低。