Bilirubin chemistry and metabolism; harmful and protective aspects
Language English Country United Arab Emirates Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
- MeSH
- Bilirubin blood chemistry metabolism MeSH
- Biological Transport MeSH
- Heme metabolism MeSH
- Hyperbilirubinemia complications metabolism MeSH
- Liver metabolism MeSH
- Humans MeSH
- Molecular Structure MeSH
- Central Nervous System Diseases etiology metabolism MeSH
- Infant, Newborn MeSH
- Hyperbilirubinemia, Neonatal complications metabolism MeSH
- Oxidation-Reduction MeSH
- Oxidative Stress MeSH
- Structure-Activity Relationship MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Infant, Newborn MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Bilirubin MeSH
- Heme MeSH
Unconjugated bilirubin (UCB), the principal mammalian bile pigment, is the end product of heme catabolism. Both belong to the superfamily of tetrapyrrolic compounds that serve multiple biological functions in animals and plants. Its six internal hydrogen bonds give UCB a unique structure responsible for its physico-chemical properties and biological effects. Like many weakly-polar, poorly-soluble compounds, UCB is transported in blood tightly bound to albumin, with less than 0.01% of total bilirubin circulating in an unbound form (free bilirubin, Bf). This fraction governs the diffusion of UCB into tissues, and therefore Bf is responsible for both its beneficial and toxic effects on cells. Although, UCB was long thought to be a non-functional waste product, recent studies have shown that the antioxidant effects of mildly elevated serum bilirubin levels, as well as activation of heme oxygenase, may protect against diseases associated with oxidative stress, such as atherosclerosis. By contrast, markedly elevated serum UCB levels may cause severe neurological damage, especially in neonates. The regulation of cellular UCB content, by its conjugation, oxidation, and export, are, therefore of paramount importance to cellular health.
References provided by Crossref.org
The physiology of bilirubin: health and disease equilibrium
Serum Bilirubin Concentrations and the Prevalence of Gilbert Syndrome in Elite Athletes
The Role of Bilirubin and the Other "Yellow Players" in Neurodegenerative Diseases
Heme Oxygenase-1 May Affect Cell Signalling via Modulation of Ganglioside Composition
Hyperbilirubinemia Protects against Aging-Associated Inflammation and Metabolic Deterioration
The role of bilirubin in diabetes, metabolic syndrome, and cardiovascular diseases