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帕金森病的“开-关”现象:与血浆中多巴浓度的相关性

"On-off" phenomenon in Parkinson's disease: correlation to the concentration of dopa in plasma.

作者信息

Eriksson T, Magnusson T, Carlsson A, Linde A, Granérus A K

出版信息

J Neural Transm. 1984;59(3):229-40. doi: 10.1007/BF01250010.

Abstract

To investigate the relation between "on-off" fluctuations in symptomatology and bioavailability of dopa in patients with Parkinson's disease, five Parkinsonian patients with pronounced "on-off" symptoms were studied. Continuously during the study the degree of disability in the patients was registered. Every one hour, and in addition, whenever there was a change from "on" to "off" or vice versa, a blood sample was collected for dopa determination. Since dopa is transported from plasma into the brain by a saturable carrier for which it has to compete with endogenous large neutral amino acids (LNAA), the concentrations of these competitors were measured too. In four of the patients there were considerable oscillations in the plasma dopa concentration during the day; in one of these patients the highest value was as much as 12 times higher than the lowest value. These dramatic fluctuations in the absolute concentration of dopa in plasma had a major influence on the relative dopa concentrations (calculated as the ratio dopa/sum of LNAA) as the fluctuations in the concentrations of LNAA in plasma were much less pronounced. Consequently, the absolute and the relative concentrations of dopa in plasma were highly parallelled. In four of the five patients "on"-periods began within one hour after a peak in the concentration of dopa in plasma and in the fifth patient five out of seven "on"-periods were preceded by a rise in plasma dopa concentration within the same time interval. From the present data it could be concluded that the "on-off" phenomenon in Parkinson's disease, at least partly, is due to oscillations in the concentration of dopa in plasma. A reduction in the variations of the concentration of dopa in plasma seems to be necessary to overcome the "on-off" problem. The introduction of a slow release preparation of dopa is therefore urgently warranted. The concentration of LNAA in plasma must, however, also be considered in this context.

摘要

为研究帕金森病患者症状的“开-关”波动与多巴生物利用度之间的关系,对5例有明显“开-关”症状的帕金森病患者进行了研究。在研究过程中持续记录患者的残疾程度。每1小时,此外,每当出现从“开”到“关”或反之的变化时,采集血样测定多巴。由于多巴通过一种可饱和载体从血浆转运至脑内,且它必须与内源性大中性氨基酸(LNAA)竞争该载体,因此也测定了这些竞争物的浓度。4例患者血浆多巴浓度在白天有显著波动;其中1例患者的最高值比最低值高12倍。血浆中多巴绝对浓度的这些剧烈波动对相对多巴浓度(计算为多巴/LNAA总和的比值)有重大影响,因为血浆中LNAA浓度的波动不太明显。因此,血浆中多巴的绝对浓度和相对浓度高度平行。5例患者中有4例的“开”期在血浆多巴浓度达到峰值后1小时内开始,第5例患者7个“开”期中有5个在同一时间间隔内血浆多巴浓度升高之前出现。从目前的数据可以得出结论,帕金森病的“开-关”现象至少部分是由于血浆中多巴浓度的波动所致。减少血浆中多巴浓度的变化似乎是克服“开-关”问题所必需的。因此,迫切需要引入多巴缓释制剂。然而,在这种情况下也必须考虑血浆中LNAA的浓度。

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