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Assessment of bilirubin toxicity to erythrocytes. Implication in neonatal jaundice management
M A Brito1, R Silva, C Tiribelli
1University of Lisbon, Lisbon, Portugal, and; University of Trieste, Trieste, Italy.
Insights
Chloroform extraction accurately measures erythrocyte-bound bilirubin, indicating toxicity in neonatal hyperbilirubinaemia. This method is superior to albumin extraction for assessing deep or aggregated bilirubin within red blood cell membranes.
Area of Science:
- Biochemistry
- Cell Biology
- Neonatal Medicine
Background:
- Neonatal hyperbilirubinaemia is common, yet lacks reliable indicators of bilirubin toxicity.
- Understanding bilirubin's cytotoxic effects on erythrocytes is crucial for effective intervention.
Purpose of the Study:
- To investigate bilirubin-induced cytotoxic events at increasing concentrations.
- To determine the role of erythrocyte membrane lipids in bilirubin binding.
- To compare chloroform and albumin extraction methods for assessing erythrocyte-bound bilirubin and cytotoxicity.
Main Methods:
- Human erythrocytes were incubated with varying bilirubin-to-albumin ratios at 4°C and 37°C.
- Morphological changes, hemolysis, lipid loss, and bilirubin binding (albumin- and chloroform-extractable) were measured.
- Reversibility of cytotoxicity was assessed via albumin washing and morphological analysis.
Main Results:
- Higher temperatures and bilirubin concentrations increased echinocytosis and hemolysis.
- Significant membrane lipid loss occurred at low bilirubin concentrations.
- Chloroform extraction revealed higher 'deep/aggregated' bilirubin compared to albumin extraction's 'superficial' bilirubin.
Conclusions:
- Increased membrane lipid fluidity and high bilirubin concentrations drive bilirubin translocation and toxicity.
- Albumin cannot remove deeply bound or aggregated bilirubin from erythrocyte membranes.
- Chloroform-extractable bilirubin is a more accurate measure of erythrocyte-bound bilirubin in severe neonatal hyperbilirubinaemia.
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.