Target intelligence / Profile preview

Fatty acid-binding protein, liver (FABP1)

Target
FABP1
Molecular classification
Lipid-binding protein, Cytoplasmic transport protein, Member of the intracellular lipid-binding protein (iLBP) family, Carrier/chaperone protein
01

Overview

Fatty acid-binding protein, liver (FABP1), or liver-type fatty acid-binding protein, is a 14-kDa cytosolic protein highly expressed in hepatocytes and also found in the intestine, kidney, and other tissues at lower levels[1][4][5]. FABP1 binds long-chain fatty acids, fatty acyl-CoAs, bilirubin, heme, and other hydrophobic ligands, playing a pivotal role in cellular uptake, intracellular transport, and metabolic compartmentalization of lipids and related molecules[1][2][4][5]. Unlike other family members, FABP1 can bind two fatty acid molecules simultaneously, which relates to its distinctive structural features[4]. It modulates lipid metabolism, supports antioxidant defense by binding potentially toxic hydrophobic molecules, regulates nuclear receptor activity (notably PPARs), and contributes to hepatic regeneration and inflammation modulation[1][5]. Deficiency or dysregulation of FABP1 is associated with metabolic diseases, inflammation, and liver dysfunction, and its expression is influenced by drugs targeting lipid metabolism such as PPAR agonists and statins[1][5]. FABP1 is considered both a cytoprotective chaperone and a potential therapeutic target in metabolic and hepatic disease contexts[1].

Other names
L-FABPLiver-type fatty acid-binding proteinFABPLFatty acid-binding protein 1LFABP
02

Mechanism of action

Modulation of lipid metabolism and transport in response to drug-induced gene expression changes (e.g., PPARα agonists upregulate FABP1, increasing lipid uptake/oxidation) Enhancement of statin hypolipidemic effects through increased intracellular fatty acid trafficking and PPAR cross-talk

03

Biological functions

Fatty acid uptake and intracellular transportRegulation of lipid metabolismRegulation of cellular signaling pathways (including via nuclear receptors such as PPARα and PPARγ)Cytoprotection against oxidative damageRegulation of heme and bilirubin metabolismModulation of enzyme activities and membrane structureCell proliferation and hepatic regeneration supportIntracellular trafficking/delivery of hydrophobic moleculesEnhancing fatty acid solubility and transportRegulation of cholesterol uptake in hepatocytes
04

Disease associations

Nonalcoholic fatty liver disease (NAFLD)Oxidative stressIschemia/reperfusion injuryInflammationLiver regeneration (biomarker/prognostic role)Metabolic disorders (e.g., dyslipidemia, hepatic steatosis)Potential role in infection (via inflammation modulation)Other hepatic and systemic metabolic diseases
05

Safety considerations

Potential for altered lipid handling/metabolism with modulation of FABP1 functionRisk of increased oxidative damage and impaired hepatic regeneration if FABP1 is deficient or inhibitedImpact on heme and bilirubin disposition with possible drug-drug or drug-disease interactions
06

Interacting drugs

Statins (indirectly, via impact on FABP1 expression and lipid metabolism)

2 more in the full profile.

07

Biomarkers

Elevated FABP1 levels as a marker of liver injury/regenerationPotential prognostic marker for hepatic surgery and liver regenerationInvestigated as a biomarker for nonalcoholic fatty liver disease and metabolic syndromes

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