Daood Monica J, Watchko Jon F
Department of Pediatrics, Division of Newborn Medicine, University of Pittsburgh School of Medicine, Magee-Womens Research Institute, Pittsburgh, Pennsylvania 15213, USA.
Pediatr Res. 2006 Jul;60(1):44-9. doi: 10.1203/01.pdr.0000219561.07550.04. Epub 2006 May 11.
In vitro studies suggest a free bilirubin (B(F)) concentration in the range of 71-770 nmol/L can induce neurotoxicity. In vivo data regarding central nervous system (CNS) B(F) levels have not been determined. We calculated in vivo CNS B(F) levels in Gunn rat pups (15-19 d old; heterozygous nonjaundiced Gunn rats (J/j) and homozygous jaundiced Gunn rats (j/j); saline or sulfadimethoxine treated) based on 1) total brain bilirubin (TBB) content, 2) brain albumin level, 3) CNS bilirubin binding capacity attributable to brain albumin determined using an ultrafiltration technique, and 4) published Gunn rat albumin-bilirubin binding constants (k). Gunn rat brain bilirubin binding capacity was approximately 22 x 10(-3) micromol/g, of which two thirds was accounted for by brain albumin. Using a Gunn rat pup in vivo, k of 9.2 L/micromol, calculated CNS B(F) levels ranged from 72 to 112 nmol/L [95% confidence interval (CI)] in saline and from 59 to 156 nmol/L (95% CI) in sulfadimethoxine-treated J/j pups. These animals demonstrated no neurobehavioral abnormalities and normal cerebellar weight. Calculated CNS B(F) levels were severalfold higher (p < 0.001) in saline (95% CI: 556-1110 nmol/L) and sulfadimethoxine-treated (95% CI: 3461-8985 nmol/L) j/j pups; the former evidenced reduced cerebellar weight; the latter both reduced cerebellar weight and acute neurobehavioral abnormalities. We conclude that calculated CNS B(F) values in j/j pups are substantially higher than those in J/j animals. Given the absence of CNS abnormalities in J/j pups, the presence of such in j/j animals, and the CNS B(F) levels in these groups, we speculate that the CNS B(F) neurotoxicity threshold in vivo is subsumed within the range (71-770 nmol/L) reported in vitro.
体外研究表明,游离胆红素(B(F))浓度在71 - 770 nmol/L范围内可诱发神经毒性。关于中枢神经系统(CNS)B(F)水平的体内数据尚未确定。我们根据以下因素计算了冈恩大鼠幼崽(15 - 19日龄;杂合非黄疸冈恩大鼠(J/j)和纯合黄疸冈恩大鼠(j/j);生理盐水或磺胺二甲氧嘧啶处理)体内的CNS B(F)水平:1)全脑胆红素(TBB)含量,2)脑白蛋白水平,3)使用超滤技术测定的归因于脑白蛋白的CNS胆红素结合能力,以及4)已发表的冈恩大鼠白蛋白 - 胆红素结合常数(k)。冈恩大鼠脑胆红素结合能力约为22×10⁻³ μmol/g,其中三分之二由脑白蛋白构成。在冈恩大鼠幼崽体内,k为9.2 L/μmol,计算得出生理盐水处理组的CNS B(F)水平范围为72至112 nmol/L [95%置信区间(CI)],磺胺二甲氧嘧啶处理的J/j幼崽为59至156 nmol/L(95% CI)。这些动物未表现出神经行为异常且小脑重量正常。计算得出生理盐水处理组(95% CI:556 - 1110 nmol/L)和磺胺二甲氧嘧啶处理组(95% CI:3461 - 8985 nmol/L)的j/j幼崽体内CNS B(F)水平高出数倍(p < 0.001);前者小脑重量减轻;后者小脑重量减轻且出现急性神经行为异常。我们得出结论,j/j幼崽体内计算得出的CNS B(F)值显著高于J/j动物。鉴于J/j幼崽无CNS异常,j/j动物存在此类异常,以及这些组中的CNS B(F)水平,我们推测体内CNS B(F)神经毒性阈值包含在体外报告的范围(71 - 770 nmol/L)内。