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Phytosterol

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  • 6 chapters

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Phytosterol-enriched foods and dietary supplements have been marketed for decades. Despite well-documented LDL cholesterol-lowering effects from long-term consumption of phytosterols, there is insufficient evidence for an effect on cardiovascular diseases, fasting blood sugar, glycated hemoglobin, or overall mortality rate.

Structure

They have a fused polycyclic structure and vary in carbon side chains and / or presence or absence of a double bond (saturation). They are divided into 4,4-dimethyl phytosterols, 4-monomethyl phytosterols, and 4-desmethyl phytosterols based on the location of methyl groups at the carbon-4 position. Stanols are saturated sterols, having no double bonds in the sterol ring structure.

The molecule in the article lead is β-sitosterol. The nomenclature is shown on the right.

  • By removing carbon 242, campesterol is obtained.
  • By removing carbons 241 and 242, cholesterol is obtained.
  • Removing a hydrogen from carbons 22 and 23 yields stigmasterol (stigmasta-5,22-dien-3β-ol).
  • By hydrogenating the double bond between carbons 5 and 6, β-sitostanol (Stigmastanol) is obtained.
  • By hydrogenating the double bond between carbons 5 and 6 and removing carbon 242, campestanol is obtained.
  • Removing carbon 242 and hydrogens from carbons 22 and 23, and inverting the stereochemistry at C-24 yields brassicasterol (ergosta-5,22-dien-3β-ol).
  • Further removal of hydrogens from carbons 7 and 8 from brassicasterol yields ergosterol (ergosta-5,7,22-trien-3β-ol). Important: Ergosterol is not a plant sterol. Ergosterol is a component of fungal cell membranes, serving the same function in fungi that cholesterol serves in animal cells.

In addition:

  • Esterification of the hydroxyl group at carbon 3 with fatty/organic acids or carbohydrates results in plant sterol esters, i.e. oleates, ferulates and (acyl) glycosides.

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