Ahlfors C E, Bennett S H, Shoemaker C T, Ellis W G, Davis S L, Wennberg R P, Goetzman B W
Pediatr Res. 1986 Jun;20(6):511-5. doi: 10.1203/00006450-198606000-00005.
The auditory brainstem response (ABR) was monitored in nine infant rhesus monkeys during the intravenous infusion of 50-168 mg/kg of unconjugated bilirubin. Sulfisoxazole (200 mg/kg) was sometimes given near the end of or just before the bilirubin infusion if no obvious ABR change had yet occurred. Five of the animals were term gestation, four were preterm, and they ranged from 1 to 40 days of age at the time of study. The three oldest term animals, studied at 20, 35 and 40 days of age, respectively, showed variable changes in the ABR waves during bilirubin infusion and these changes were not altered further by sulfisoxazole administration. The other two term infants, studied at 1 and 6 days of age, respectively, showed sulfisoxazole enhanced ABR wave latency increase and amplitude reduction followed by loss of the ABR. Both of these animals became apneic following ABR loss and eventually died. The ABR reappeared in one animal prior to death. Minimal gross and microscopic changes were present in the brain of the 6-day-old animal at autopsy. The four preterm animals all had a progressive wave amplitude decrease followed by loss of the ABR with bilirubin alone. These preterm animals were sacrificed shortly after the ABR loss with only one showing yellow staining of the basal ganglia at autopsy. The infant rhesus monkey may be a useful paradigm for bilirubin-induced ototoxicity as manifested by potentially reversible ABR changes. The changes are dependent on gestational and chronological age of the animal and appear to occur in the peripheral eighth nerve or cochlea as well as in brainstem pathways.
在向9只恒河猴幼猴静脉输注50 - 168mg/kg未结合胆红素的过程中,对其听觉脑干反应(ABR)进行了监测。如果尚未出现明显的ABR变化,有时会在胆红素输注接近尾声或即将开始前给予磺胺异恶唑(200mg/kg)。其中5只动物为足月产,4只为早产,研究时它们的年龄在1至40天之间。3只年龄最大的足月动物,分别在20、35和40日龄时进行研究,在胆红素输注期间ABR波出现了不同变化,而给予磺胺异恶唑后这些变化并未进一步改变。另外2只足月婴儿,分别在1日龄和6日龄时进行研究,显示磺胺异恶唑使ABR波潜伏期延长、波幅降低,随后ABR消失。这两只动物在ABR消失后均出现呼吸暂停,最终死亡。其中一只动物在死亡前ABR再次出现。尸检时,6日龄动物的大脑仅有轻微的大体和微观变化。4只早产动物仅在输注胆红素后均出现ABR波幅逐渐降低,随后ABR消失。这些早产动物在ABR消失后不久被处死,尸检时只有一只显示基底神经节有黄色染色。恒河猴幼猴可能是胆红素诱导耳毒性的一个有用模型,表现为潜在可逆的ABR变化。这些变化取决于动物的胎龄和实际年龄,似乎发生在外周第八神经或耳蜗以及脑干通路中。