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胆红素对红细胞毒性的评估。对新生儿黄疸管理的意义。

Assessment of bilirubin toxicity to erythrocytes. Implication in neonatal jaundice management.

作者信息

Brito M A, Silva R, Tiribelli C, Brites D

机构信息

University of Lisbon, Lisbon, Portugal, and; University of Trieste, Trieste, Italy.

出版信息

Eur J Clin Invest. 2000 Mar;30(3):239-47. doi: 10.1046/j.1365-2362.2000.00612.x.

Abstract

BACKGROUND

Neonatal hyperbilirubinaemia remains one of the most common clinical conditions requiring therapeutic intervention. Nevertheless, reliable indicators of bilirubin toxicity are still missing. This prompted us to investigate (a) the progression of cytotoxic events produced by increasing concentrations of bilirubin; (b) the relevance of the membrane lipid package on bilirubin binding to erythrocytes; and (c) the reliability of chloroform extraction compared with albumin extraction to evaluate erythrocyte-bound bilirubin and cytotoxicity.

MATERIALS AND METHODS

Morphological alterations, free bilirubin, erythrocyte-bound bilirubin (albumin- and chloroform-extractable), haemolysis and membrane-released lipids, were determined in human erythrocytes at 4 degrees C or 37 degrees C, after 4 h incubation at pH 7.4, with increasing molar ratios of bilirubin to albumin (0.5-5). The reversibility of cytotoxicity by albumin washing was assessed by morphological analysis.

RESULTS

Decreased free bilirubin, lower erythrocyte-bound bilirubin concentration by albumin extraction (superficial/non-aggregated bilirubin) and higher values by chloroform extraction (deep/aggregated bilirubin) were observed for 37 degrees C vs. 4 degrees C, at molar ratios > 1. Echinocytosis increased with bilirubin concentration and temperature and was not fully reversed by albumin washing. Haemolysis was already significant at a molar ratio of 1, and was enhanced by temperature at molar ratios 3 and 5 (P < 0.01). The loss of membrane lipids was remarkable at molar ratios > or = 0.5, both at 4 degrees C and 37 degrees C (P < 0.01), although correlation with bilirubin concentration was only significant at 37 degrees C (r = 0.971; P < 0.01).

CONCLUSIONS

These results suggest that increased lipid fluidity and high bilirubin concentrations promote membrane bilirubin translocation and toxicity. They also show that albumin is not able to displace the bilirubin located deeply or aggregated within the membrane, which in turn is removed by chloroform. Accordingly, chloroform-extractable rather than albumin-extractable bilirubin is a more accurate parameter to assess erythrocyte-bound bilirubin during severe hyperbilirubinaemia.

摘要

背景

新生儿高胆红素血症仍然是最常见的需要进行治疗干预的临床病症之一。然而,胆红素毒性的可靠指标仍然缺失。这促使我们研究:(a)胆红素浓度增加所产生的细胞毒性事件的进展;(b)膜脂质包裹对胆红素与红细胞结合的相关性;以及(c)与白蛋白提取相比,氯仿提取用于评估红细胞结合胆红素和细胞毒性的可靠性。

材料与方法

在pH 7.4条件下,于4℃或37℃对人红细胞进行4小时孵育,随着胆红素与白蛋白摩尔比(0.5 - 5)的增加,测定形态学改变、游离胆红素、红细胞结合胆红素(可被白蛋白和氯仿提取)、溶血和膜释放脂质。通过形态学分析评估白蛋白洗涤对细胞毒性的可逆性。

结果

在摩尔比>1时,与4℃相比,37℃时观察到游离胆红素降低,白蛋白提取的红细胞结合胆红素浓度较低(表面/非聚集胆红素),氯仿提取的浓度较高(深层/聚集胆红素)。棘红细胞增多症随胆红素浓度和温度升高而增加,且白蛋白洗涤不能使其完全逆转。在摩尔比为1时溶血就已显著,在摩尔比为3和5时温度会增强溶血作用(P < 0.01)。在4℃和37℃时,摩尔比>或 = 0.5时膜脂质损失显著(P < 0.01),尽管与胆红素浓度的相关性仅在37℃时显著(r = 0.971;P < 0.01)。

结论

这些结果表明,脂质流动性增加和高胆红素浓度会促进膜胆红素转运和毒性。它们还表明,白蛋白无法取代膜内深层或聚集的胆红素,而氯仿可将其去除。因此,在严重高胆红素血症期间,氯仿可提取的而非白蛋白可提取的胆红素是评估红细胞结合胆红素的更准确参数。

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