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BI4.1-8 | Chemistry and Metabolism of Lipids — Glossary
Lipid
A diverse group of biomolecules that are insoluble in water but soluble in organic solvents; includes fats, oils, phospholipids, steroids, and waxes
Triacylglycerol (triglyceride)
A simple lipid consisting of three fatty acids esterified to a glycerol backbone; the body's primary energy storage molecule providing ~9 kcal/g
Fatty acid
A long-chain carboxylic acid that can be saturated (no double bonds) or unsaturated (one or more double bonds); building block of most lipids
Essential fatty acid
A fatty acid that the human body cannot synthesise and must be obtained from diet; includes linoleic acid (omega-6) and alpha-linolenic acid (omega-3)
Beta-oxidation
The mitochondrial metabolic pathway that breaks down fatty acids by sequentially removing 2-carbon acetyl-CoA units, generating FADH2 and NADH for ATP production
Carnitine shuttle
The transport system (CPT-I, translocase, CPT-II) that transfers long-chain acyl-CoA across the inner mitochondrial membrane using carnitine as a carrier
CPT-I (Carnitine palmitoyltransferase I)
The enzyme on the outer mitochondrial membrane that transfers the acyl group from CoA to carnitine; inhibited by malonyl-CoA, the rate-limiting step of fatty acid entry
Acetyl-CoA
A 2-carbon unit linked to coenzyme A; the universal metabolic intermediate formed from fatty acid oxidation, glucose oxidation, and amino acid catabolism
Lipogenesis
The de novo synthesis of fatty acids from acetyl-CoA in the cytoplasm, catalysed by fatty acid synthase, producing palmitate (C16:0)
Acetyl-CoA carboxylase (ACC)
The biotin-dependent enzyme catalysing the rate-limiting step of lipogenesis: acetyl-CoA + CO2 → malonyl-CoA; activated by insulin and citrate, inhibited by glucagon and palmitoyl-CoA
Fatty acid synthase (FAS)
The large multi-enzyme complex in the cytoplasm that catalyses the synthesis of palmitate from acetyl-CoA and malonyl-CoA using NADPH
Cholesterol
A 27-carbon sterol essential for cell membrane fluidity, steroid hormone synthesis, bile acid formation, and vitamin D production; synthesised mainly in the liver
HMG-CoA reductase
The rate-limiting enzyme of cholesterol synthesis that converts HMG-CoA to mevalonate; the target of statin drugs
Statin
A class of lipid-lowering drugs that competitively inhibit HMG-CoA reductase, reducing hepatic cholesterol synthesis and upregulating LDL receptor expression
Phospholipid
An amphipathic lipid with a glycerol or sphingosine backbone, two fatty acid tails, and a phosphate-linked head group; major component of cell membrane bilayers
Sphingomyelin
A sphingophospholipid (ceramide + phosphocholine) abundant in the myelin sheath of nerve fibres; deficiency of sphingomyelinase causes Niemann-Pick disease
Lipoprotein
A spherical particle with a phospholipid/apolipoprotein shell and a hydrophobic core of triglycerides and cholesterol esters, enabling lipid transport in aqueous blood
LDL (Low-density lipoprotein)
The major cholesterol-carrying lipoprotein that delivers cholesterol to peripheral tissues; elevated LDL is a primary risk factor for atherosclerosis ('bad cholesterol')
HDL (High-density lipoprotein)
The lipoprotein responsible for reverse cholesterol transport — collecting excess cholesterol from tissues and returning it to the liver ('good cholesterol')
Apolipoprotein
A protein component of lipoproteins that provides structural stability and serves as enzyme cofactors or receptor ligands (e.g. ApoB-100 for LDL receptor, ApoCII for LPL activation)
Atherosclerosis
A chronic inflammatory disease of arterial walls characterised by the accumulation of oxidised LDL, foam cell formation, and fibrous plaque development, leading to luminal narrowing
Foam cell
A macrophage engorged with oxidised LDL cholesterol via scavenger receptors (SR-A, CD36); the hallmark cell of atherosclerotic fatty streaks
Dyslipidaemia
An abnormality in plasma lipoprotein levels — elevated LDL, elevated triglycerides, or decreased HDL — that increases cardiovascular disease risk
Familial hypercholesterolaemia
An autosomal dominant disorder caused by defective LDL receptors, resulting in markedly elevated LDL cholesterol, tendon xanthomas, and premature coronary artery disease
Ketone bodies
Water-soluble molecules (acetoacetate, beta-hydroxybutyrate, acetone) produced in the liver from acetyl-CoA during fasting or uncontrolled diabetes; serve as alternative fuel for the brain and heart