Mahone P R, Scott K, Sleggs G, D'Antoni T, Woods J R
Department of Obstetrics and Gynecology, University of Rochester School of Medicine and Dentistry, NY.
Am J Obstet Gynecol. 1994 Aug;171(2):465-9. doi: 10.1016/0002-9378(94)90284-4.
Cocaine and metabolites can be found in the amniotic fluid after maternal use, presumably as a result of fetal urination. The fetus may be repeatedly exposed to the effects of these drugs through contact with amniotic fluid that contains these substances. The purpose of this study was to determine whether the naive fetal lamb generates detectable fetal blood levels of cocaine and metabolites when cocaine is placed directly into the amniotic fluid and, if so, whether fetal swallowing accounts for these findings.
Six pregnant ewes with singleton fetuses of 120 to 125 days' gestation were chronically catheterized for daily sampling of cocaine and metabolite levels in maternal venous plasma, fetal venous plasma, and amniotic fluid over a 7-day period. Esophageal ligation was performed in three additional animals similarly instrumented to evaluate the role of fetal swallowing in the distribution of amniotic fluid cocaine and its metabolites. In each case, at the time of surgery, an Alzet osmotic pump delivering cocaine at 0.5 mg/kg estimated fetal weight per hour into the amniotic fluid was secured to the fetal back. Cocaine and metabolites (benzoylecgonine, ecgonine methyl ester, and norcocaine) were measured daily in material and fetal plasma, amniotic fluid, and meconium by solid-phase extraction and derivatization and quantified by high-performance gas chromatographic techniques.
The concentrations of ecgonine methyl ester were highest in the amniotic fluid followed by cocaine and benzoylecgonine. In the normal and esophagus-ligated groups, cocaine, benzoylecgonine, and norcocaine were found in fetal plasma in concentrations of approximately 3% that of amniotic fluid. Ecgonine methyl ester was not detected in fetal plasma from either group. Meconium samples from sheep with and without esophageal ligation demonstrated high levels of norcocaine.
We conclude that cocaine and metabolites in amniotic fluid enter the fetal circulation to produce detectable plasma levels through routes other than swallowing. Moreover, the results of meconium analyses in the two groups of fetuses suggest that fetal swallowing is not the primary mechanism by which cocaine and metabolites enter the intestine.
母体使用可卡因后,羊水内可发现可卡因及其代谢物,推测这是胎儿排尿的结果。胎儿可能会通过接触含有这些物质的羊水而反复受到这些药物的影响。本研究的目的是确定当将可卡因直接注入羊水时,未经接触过药物的胎羊是否会在胎儿血液中产生可检测到的可卡因及其代谢物水平,如果是,胎儿吞咽是否可以解释这些结果。
六只怀有单胎、妊娠120至125天的怀孕母羊被长期插管,以便在7天内每日采集母体静脉血浆、胎儿静脉血浆和羊水内的可卡因及其代谢物水平。另外三只同样插管的动物进行了食管结扎,以评估胎儿吞咽在羊水可卡因及其代谢物分布中的作用。在每种情况下,手术时将一个Alzet渗透泵固定在胎儿背部,该泵以每小时0.5毫克/千克估计胎儿体重的速度将可卡因注入羊水。通过固相萃取和衍生化,每日测量母体和胎儿血浆、羊水及胎粪中的可卡因及其代谢物(苯甲酰爱康宁、爱康宁甲酯和去甲可卡因),并通过高效气相色谱技术进行定量分析。
爱康宁甲酯在羊水中的浓度最高,其次是可卡因和苯甲酰爱康宁。在正常组和食管结扎组中,胎儿血浆中可卡因、苯甲酰爱康宁和去甲可卡因的浓度约为羊水浓度的3%。两组胎儿血浆中均未检测到爱康宁甲酯。食管结扎和未结扎的绵羊的胎粪样本中均显示出高水平的去甲可卡因。
我们得出结论,羊水中的可卡因及其代谢物通过吞咽以外的途径进入胎儿循环,从而产生可检测到的血浆水平。此外,两组胎儿胎粪分析的结果表明,胎儿吞咽不是可卡因及其代谢物进入肠道的主要机制。