Potential role of conjugated bilirubin and copper in the metabolism of lipid peroxides in bile.

Потенциальная роль конъюгированного билирубина и меди в метаболизме липидных пероксидов в желчи
Roland Stocker, B N Ames
1987-11-01

conjugated bilirubincopper ionslinoleic acid hydroperoxidelipid peroxidationperoxyl radical scavenging
Conjugated bilirubin and copper ions at their physiological concentrations in bile may play an important role in hydroperoxide and other detoxification. Conjugated bilirubin may also be an important chain-breaking antioxidant preventing lipid peroxidation. Bilirubin ditaurine (BR-DT), a water-soluble model compound of conjugated bilirubin, completely prevents the peroxyl radical-induced oxidation of phosphatidylcholine in either multilamellar liposomes or micelles. This antioxidant activity is associated with the bilirubin moiety of BR-DT, since taurine alone is inefficient in scavenging peroxyl radicals. The number of peroxyl radicals trapped per molecule of BR-DT is 1.9, compared to 4.7 trapped per molecule of biliverdin, the water-soluble physiological precursor of bilirubin. Peroxyl radical-induced oxidation of BR-DT results in a spectral shift in maximal absorbance toward shorter wavelengths; biliverdin is not formed as a major oxidation product. BR-DT, but neither taurine nor biliverdin, greatly accelerates the cupric ion-catalyzed decomposition of linoleic acid hydroperoxide. In the presence of ferric ion, BR-DT shows no lipid hydroperoxide-degrading activity. Addition of cupric ion to BR-DT results in formation of a complex with spectral features similar to that of a biliverdin-cupric ion complex, indicating that BR-DT and cupric ion undergo redox reactions.
1
Bilirubin ditaurine completely prevents peroxyl radical-induced phosphatidylcholine oxidation in multilamellar liposomes and micelles, whereas taurine alone is ineffective.
2
Bilirubin ditaurine strongly accelerates cupric-ion-catalyzed linoleic acid hydroperoxide decomposition, but shows no hydroperoxide-degrading activity with ferric ions, consistent with redox complex formation with copper.
3
Bilirubin ditaurine traps 1.9 peroxyl radicals per molecule, compared with 4.7 for biliverdin, indicating weaker radical-scavenging capacity than its precursor.
4
Conjugated bilirubin may contribute to bile lipid-peroxide detoxification through both chain-breaking antioxidant activity and copper-dependent hydroperoxide decomposition.
5
Peroxyl-radical oxidation of bilirubin ditaurine shifts its absorbance maximum toward shorter wavelengths without producing biliverdin as a major product.

Conjugated bilirubin, represented by bilirubin ditaurine (BR-DT), and copper ions in bile, including their interactions with lipid hydroperoxides and phosphatidylcholine lipid systems

The antioxidant, lipid-peroxide-degrading, radical-scavenging, and redox properties of conjugated bilirubin and its interactions with cupric ions

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1987-11-01
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Roland Stocker
B N Ames
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