Pharmacokinetics and effect of cocaine on cerebral blood flow in the newborn.

E K Anday, R Lien, J M Goplerud, C D Kurth, L M Shaw
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引用次数: 13

Abstract

The present study investigated the effect of cocaine (COC) on cerebral circulation (CBF) and oxidative metabolism (CMRO2) in the newborn piglet and aimed to relate pharmacokinetics of cocaine to cerebrovascular effects. COC decreased CBF and CMRO2 from 75 to 64 and 4.27 to 3.91 ml/min/100 g, respectively, at 4 min with reduced flow to all brain regions (p < 0.05) which returned to baseline by 10 min. COC was rapidly metabolized with a t1/2 of 43 min and peak plasma concentration of 1,172 ng/ml. Norcocaine (NOR) appeared in plasma and CSF within 3 min of cocaine administration and remained elevated for the duration of the study along with COC in the CSF. These data show that the timing of the peak plasma COC level is associated with maximal decreased CBF. Further, the stable elevated level of COC and NOR in the CSF suggests that biotransformation does not occur in the brain. As a result, accumulation of these drugs may occur in the brain with successive COC use and affect the developing CNS in a deleterious manner.

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可卡因对新生儿脑血流的药代动力学及影响。
本研究研究了可卡因(COC)对新生仔猪脑循环(CBF)和氧化代谢(cmo2)的影响,旨在探讨可卡因的药代动力学与脑血管效应的关系。COC使CBF和cmor2在4分钟内分别从75降至64和4.27降至3.91 ml/min/100 g,所有脑区流量减少(p < 0.05), 10分钟后恢复到基线水平。COC在43分钟的1/2内迅速代谢,血药浓度峰值为1172 ng/ml。诺古柯碱(NOR)在给药后3分钟内出现在血浆和脑脊液中,并在研究期间与脑脊液中的COC一起保持升高。这些数据表明,峰值血浆COC水平的时间与最大CBF下降有关。此外,脑脊液中COC和NOR水平的稳定升高表明脑内没有发生生物转化。因此,随着COC的连续使用,这些药物可能在大脑中积累,并以有害的方式影响发育中的中枢神经系统。
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