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[31] Antioxidant activities of bile pigments: Biliverdin and bilirubin

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The results show that both biliverdin and conjugated bilirubin efficiently scavenge hypochlorous acid and act synergistically with vitamin E in protecting lipid membranes from peroxidation initiated within the lipid phase, adding further credit to the notion that the two bile pigments function as important physiological antioxidants.
Abstract
Publisher Summary This chapter discusses the antioxidant activities of bile pigments—biliverdin and bilirubin. Biliverdin and bilirubin are potent scavengers of singlet oxygen. The methods described in the chapter apply to the measurement of the peroxyl radical scavenging activity of biliverdin and the various biological forms of bilirubin. Most of the methods are applicable to testing the antioxidant activity of other compounds. The method is based on the thermal decomposition of an azo compound under aerobic conditions whereby peroxyl radicals are produced at a known and constant rate. In the presence of phospholipids containing polyunsaturated fatty acids (LH), the peroxyl radical will abstract a hydrogen atom to give rise to a lipid radical, thus initiating the chain reaction of lipid peroxidation. Because the peroxyl radical-mediated oxidation of polyunsaturated fatty acids initially results in quantitative formation of the corresponding lipid hydroperoxides, the extent of oxidation can be followed simply by measuring the accumulation of hydroperoxides. Any compound possessing peroxyl radical scavenging activity will compete with LH for the lipid peroxyl radical, resulting in inhibition of the chain reaction and hence inhibition of formation of lipid hydroperoxides. The results show that both biliverdin and conjugated bilirubin efficiently scavenge hypochlorous acid and act synergistically with vitamin E in protecting lipid membranes from peroxidation initiated within the lipid phase, this add further credit to the notion that the two bile pigments function as important physiological antioxidants.

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γ-Tocopherol traps mutagenic electrophiles such as NOx and complements α-tocopherol: Physiological implications

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Free and albumin-bound bilirubin are efficient co-antioxidants for alpha-tocopherol, inhibiting plasma and low density lipoprotein lipid peroxidation.

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TL;DR: Ascorbic acid is discussed in detail, and an analysis is made of whether it has the properties mentioned, and several water‐soluble candidates are mentioned, with most having no more than one or two of the attributes listed.
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Vitamin C: update on physiology and pharmacology

TL;DR: The increasing knowledge of the functions of ascorbate and of its molecular sites of action can mechanistically substantiate a place for asCorbate in the treatment of various diseases.
References
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Journal ArticleDOI

Bilirubin is an antioxidant of possible physiological importance

TL;DR: The data support the idea of a "beneficial" role for bilirubin as a physiological, chain-breaking antioxidant.
Journal ArticleDOI

Oxidative damage, lipid peroxidation and antioxidant protection in chloroplasts

TL;DR: The current controversy as to whether lipid peroxidation is a cause of cellular damage or merely a consequence of it is addressed by reference to several “oxidative stress” situations in plant tissues.
Journal ArticleDOI

Detection and characterization of lipid hydroperoxides at picomole levels by high-performance liquid chromatography.

TL;DR: A new method by combining an HPLC system with an ultrasensitive analytical system based on the detection of chemiluminescence emitted by isoluminol in the presence of hydroperoxide and microperoxidase to detect lipid hydroperoxides at the picomole level is developed.
Journal ArticleDOI

Oxidation of lipids. 7. Oxidation of phosphatidylcholines in homogeneous solution and in water dispersion.

TL;DR: In this paper, the rates and products of the oxidations of phosphatidylcholines (PCs) in organic homogeneous solutions and as multilamellar liposomes in an aqueous dispersion were studied at 50 degrees C initiated by oil-soluble and water soluble azo compounds and with the aim primarily of elucidating the effect of substrate and reaction medium.
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