Department of Neurology, Medstar Georgetown University Hospital, 3800 Reservoir Rd NW, Washington, DC, 20007, USA.
Clinical Neurocardiology Section, CNP/DIR/NINDS/NIH, Bethesda, MD, 20892, USA.
Clin Auton Res. 2019 Feb;29(1):113-117. doi: 10.1007/s10286-018-0564-5. Epub 2018 Sep 18.
The pressor effect of L-threo-3,4-dihydroxyphenylserine (L-DOPS, droxidopa, Northera™) results from conversion of L-DOPS to norepinephrine (NE) in cells expressing L-aromatic-amino-acid decarboxylase (LAAAD). After L-DOPS administration the increase in systemic plasma NE is too small to explain the increase in blood pressure. Renal proximal tubular cells abundantly express LAAAD. Since NE generated locally in the kidneys could contribute to the pressor effect of L-DOPS, in this study we assessed renal conversion of L-DOPS to NE.
Ten patients who were taking L-DOPS for symptomatic orthostatic hypotension had blood and urine sampled about 2 h after the last L-DOPS dose. L-DOPS and NE were assayed by alumina extraction followed by liquid chromatography with electrochemical detection. Data were compared in patients off vs. on levodopa/carbidopa.
In patients off levodopa/carbidopa the ratio of NE/L-DOPS in urine averaged 63 times that in plasma (p = 0.0009 by t test applied to log-transformed data). In marked contrast, in the three patients on levodopa/carbidopa the ratio of NE/L-DOPS in urine did not differ from that in plasma.
There is extensive renal production of NE from L-DOPS. Carbidopa seems to attenuate the conversion of L-DOPS to NE in the kidneys. Further research is needed to assess whether the proposed paracrine effect of L-DOPS in the kidneys contributes to the systemic pressor response.
L-苏-3,4-二羟基苯丙氨酸(L-DOPS,droxidopa,Northera™)的升压作用源于在表达 L-芳香族氨基酸脱羧酶(LAAAD)的细胞中,L-DOPS 转化为去甲肾上腺素(NE)。在给予 L-DOPS 后,全身血浆 NE 的增加太小,无法解释血压的升高。肾近端小管细胞大量表达 LAAAD。由于肾脏中局部产生的 NE 可能有助于 L-DOPS 的升压作用,因此在这项研究中,我们评估了 L-DOPS 在肾脏中向 NE 的转化。
10 名因直立性低血压症状而服用 L-DOPS 的患者在最后一次 L-DOPS 剂量后约 2 小时采集血液和尿液样本。通过氧化铝提取后,用带有电化学检测的液相色谱法测定 L-DOPS 和 NE。将患者停药与用药时的数据进行比较。
在停药的患者中,尿液中 NE/L-DOPS 的比值平均为血浆中的 63 倍(通过对数转换数据的 t 检验,p=0.0009)。相比之下,在 3 名服用左旋多巴/卡比多巴的患者中,尿液中 NE/L-DOPS 的比值与血浆中无差异。
肾脏中大量产生 NE 来自 L-DOPS。卡比多巴似乎可减轻 L-DOPS 在肾脏中向 NE 的转化。需要进一步研究来评估 L-DOPS 在肾脏中的这种拟分泌作用是否有助于全身升压反应。