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Classification and Structure of Lipids

For medical students2 min readUpdated 2026-10-10

Lipids are a diverse group of organic compounds united by a common physicochemical property: they are hydrophobic or amphiphilic. Due to their tendency to avoid contact with water, they form the essential non-aqueous structures of our body—from cell membranes to energy-storing adipose depots.

Carbon ParityHuman fatty acids always contain an even number of carbon atoms due to the specifics of their synthesis.
Energy ReserveTriacylglycerol (TAG) stores in adipocytes (6–10 kg) can sustain an adult for 40–50 days of total starvation.
Alveolar SurfactantPhosphatidylcholine containing palmitic acid prevents pulmonary alveoli from collapsing.
Vitamin EA powerful antioxidant that inhibits dangerous lipid peroxidation (LPO).

Fatty Acids as Structural Building Blocks

Most lipids contain fatty acids (FAs), which share a general structural scheme: a hydrocarbon chain and a carboxyl group (R-COOH). In cells, they rarely exist in a free state, more often acting as components of more complex molecules or as vital 'fuel molecules' competing with glucose.

Based on the degree of carbon chain saturation with hydrogen, they are divided into three groups:

Special nomenclatures are used to precisely record the structure of FAs:

  1. $\Delta$-nomenclature (delta): the position of double bonds is counted starting from the carboxyl carbon atom. For example, $18:2 \Delta 9, 12$ means the chain has 18 carbons and 2 double bonds at positions 9 and 12.
  2. $\omega$-nomenclature (omega): indicates the position of only the first double bond, but counting starts from the opposite end—the methyl group ($CH_3$). This is the origin of the well-known $\omega-3$ and $\omega-6$ families.

Major Classes of Complex Lipids

Fatty acids can bind to various alcohols to form functionally distinct classes of substances.

Triacylglycerols (TAGs) Consist of a glycerol molecule esterified with three fatty acid residues. This is the most compact and energy-dense form of calorie storage. TAGs are located primarily in adipose tissue (adipocytes). In addition to their energy function, they provide thermal insulation and mechanical protection for internal organs.

Glycerophospholipids Have an amphiphilic structure: two fatty acids are attached to glycerol, and the third position is occupied by a phosphate group linked to an alcohol (choline, ethanolamine, serine, or inositol bisphosphate). They form the lipid bilayers of cell membranes and the monolayer on the surface of lipoproteins.

Sphingolipids Their core is not glycerol, but the amino alcohol sphingosine. Sphingolipids are abundant in nervous tissue, forming the myelin sheaths of neurons, and are also components of cell receptors.

Steroids and Essential Nutritional Factors

Cholesterol is the body's primary steroid. It is an essential component of cell membranes, regulating the rigidity of their hydrophobic core, and serves as the basic substrate for the synthesis of bile acids and all steroid hormones.

Certain lipids cannot be synthesized by the human body and are therefore recognized as essential dietary factors:

Mnemonic

How to remember essential acids: The word 'Linoleic' is shorter and has 2 double bonds ($C_{18:2}$). The word 'Linolenic' is longer and has 3 double bonds ($C_{18:3}$).

Frequently asked questions

What is the chemical structure of sphingolipids?

Sphingolipids are structurally based on the amino alcohol sphingosine. A fatty acid radical attaches to the amino group of sphingosine, forming ceramide (acylated sphingosine), which is the precursor for more complex sphingolipids. Various groups attach to the hydroxyl group of ceramide (the polar 'head'):

  • Sphingomyelins (sphingophospholipids) — contain a phosphoric acid residue and choline (or ethanolamine or serine).
  • Glycolipids (cerebrosides and gangliosides) — contain a carbohydrate residue (mono- or oligosaccharide in cerebrosides, branched oligosaccharide with N-acetylneuraminic acid in gangliosides).
Which classes of substances are synthesized from essential fatty acids?

Other polyunsaturated acids are synthesized from essential fatty acids (linoleic and linolenic); for example, arachidonic acid is synthesized from linoleic acid. Essential fatty acids (polyunsaturated acids with two or more double bonds) are also substrates for the synthesis of local-acting hormones—eicosanoids. Eicosanoids include prostaglandins, leukotrienes, and thromboxanes.

Specifically, which lipids form the myelin sheaths of neurons?

The myelin sheaths of neurons are formed by sphingolipids, primarily sphingophospholipids (sphingomyelins).

What is the difference between omega- and delta-nomenclature of fatty acids?

In delta-nomenclature ($\Delta$), double bonds are counted from the carboxyl carbon, and all positions are listed. In omega-nomenclature ($\omega$), the position of only the first double bond is indicated, and counting starts from the opposite (methyl) end.

Why is arachidonic acid not always considered truly essential?

Although it is vital, the body can synthesize arachidonic acid on its own if an adequate amount of its precursor—essential linoleic acid—is supplied in the diet.

What are the functions of glycerophospholipids?

They are the main structural components of cell membranes. Additionally, phosphatidylcholine is the basis of pulmonary surfactant, which prevents alveoli from sticking together during expiration.

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