Page last updated: 2024-10-24

vitamin A metabolic process

Definition

Target type: biologicalprocess

The chemical reactions and pathways involving any of the vitamin A compounds, retinol, retinal (retinaldehyde) and retinoic acid, all of which are derivatives of beta-carotene. [GOC:jl, http://www.dentistry.leeds.ac.uk/biochem/thcme/vitamins.html#k]

Vitamin A, also known as retinol, is a fat-soluble vitamin that plays a critical role in various physiological processes, including vision, cell growth and differentiation, immune function, and reproduction. The metabolic process of vitamin A involves a series of interconnected reactions that convert dietary precursors into active forms and regulate their availability in the body.

**Dietary Intake and Conversion:**
- Vitamin A is obtained from the diet in two forms: preformed vitamin A (retinol) found in animal products like liver, eggs, and dairy, and provitamin A carotenoids (beta-carotene, alpha-carotene, and beta-cryptoxanthin) found in plants like carrots, sweet potatoes, and spinach.
- Carotenoids are converted to retinol in the intestinal mucosa through a series of enzymatic reactions.

**Absorption and Transport:**
- Retinol and carotenoids are absorbed in the small intestine with the help of bile salts and dietary fat.
- Once absorbed, retinol is incorporated into chylomicrons, lipoproteins that transport lipids from the gut to the liver.
- In the liver, retinol is esterified to retinyl esters, the storage form of vitamin A, and stored in hepatic stellate cells.

**Retinol Metabolism:**
- Retinol is released from the liver as needed and transported bound to retinol-binding protein (RBP) in the bloodstream.
- RBP delivers retinol to target tissues, including the retina, skin, and reproductive organs.

**Retinol to Retinoid Conversion:**
- Retinol can be converted to retinaldehyde, an aldehyde form of vitamin A, by retinal dehydrogenase enzymes.
- Retinaldehyde is crucial for vision as it is the precursor to rhodopsin, the light-sensitive pigment in the retina.
- Retinaldehyde can also be converted to retinoic acid, the active form of vitamin A involved in cell growth and differentiation.

**Retinoic Acid Signaling:**
- Retinoic acid binds to nuclear receptors, retinoic acid receptors (RARs) and retinoid X receptors (RXRs), which regulate gene expression.
- Retinoic acid signaling plays a vital role in embryonic development, cell proliferation, and differentiation, immune function, and epithelial cell maintenance.

**Regulation of Vitamin A Metabolism:**
- Vitamin A metabolism is tightly regulated to maintain adequate levels in the body while preventing toxicity.
- Retinol storage and release are controlled by liver-specific mechanisms.
- Retinoid synthesis and degradation are regulated by feedback mechanisms involving retinoic acid receptors and other signaling pathways.

**Vitamin A Deficiency and Toxicity:**
- Deficiency in vitamin A can lead to various health problems, including night blindness, impaired immune function, skin disorders, and growth retardation.
- Excess vitamin A intake can cause toxicity, characterized by liver damage, bone pain, and birth defects.

The metabolic process of vitamin A is essential for maintaining overall health and well-being. It involves a complex series of reactions that ensure the availability of active forms of vitamin A to meet the diverse physiological needs of the body.'
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Proteins (3)

ProteinDefinitionTaxonomy
Lysosomal acid lipase/cholesteryl ester hydrolaseA lysosomal acid lipase/cholesteryl ester hydrolase that is encoded in the genome of human. [PRO:DNx, UniProtKB:P38571]Homo sapiens (human)
Lecithin retinol acyltransferaseA lecithin retinol acyltransferase that is encoded in the genome of human. [PRO:DNx, UniProtKB:O95237]Homo sapiens (human)
Retinal dehydrogenase 2A retinal dehydrogenase 2 that is encoded in the genome of human. [PRO:DNx, UniProtKB:O94788]Homo sapiens (human)

Compounds (7)

CompoundDefinitionClassesRoles
uvitex swnUvitex SWN: optical brightner from Ciba; structure7-aminocoumarinsfluorochrome
framycetinframycetin : A tetracyclic antibacterial agent derived from neomycin, being a glycoside ester of neamine and neobiosamine B.

Framycetin: A component of NEOMYCIN that is produced by Streptomyces fradiae. On hydrolysis it yields neamine and neobiosamine B. (From Merck Index, 11th ed)
aminoglycosideallergen;
antibacterial drug;
Escherichia coli metabolite
win 18446WIN 18446 : A carboxamide that is 1,8-diaminooctane in which a hydrogen attached to each of the amino groups has been replaced by a dichloroacetyl group. Inhibitor of aldehyde dehydrogenase 1a2 (ALDH1a2). Inhibits the biosynthesis of retinoic acid from retinol in neonatal and adult murine testis. It down-regulates sex related genes in zebrafish.organochlorine compound;
secondary carboxamide
EC 1.2.1.3 [aldehyde dehydrogenase (NAD(+))] inhibitor
neamineneamine : 2-Deoxy-D-streptamine glycosylated at the 4-oxygen with a 6-amino-alpha-D-glucosaminyl group.

neamine: fragment of NEOMYCIN B; structure in first source
2,6-dideoxy-alpha-D-glucoside;
aminoglycoside
antibacterial agent
daidzindaidzein 7-O-beta-D-glucoside : A glycosyloxyisoflavone that is daidzein attached to a beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage. It is used in the treatment of alcohol dependency (antidipsotropic).

daidzin: a potent, selective, and reversible inhibitor of human mitochondrial aldehyde dehydrogenase
7-hydroxyisoflavones 7-O-beta-D-glucoside;
hydroxyisoflavone;
monosaccharide derivative
plant metabolite
7-butyl-8-[[4-(3-chlorophenyl)-1-piperazinyl]methyl]-1,3-dimethylpurine-2,6-dionepiperazines
lalistat 2