Any of a group of predominantly unsaturated solid alcohols of the steroid group, such as cholesterol and ergosterol, present in the fatty tissues of plants and animals.
[Short for CHOLESTEROL.]
Dictionary:
ster·ol (stîr'ôl', -ōl', stĕr'-) ![]() |
[Short for CHOLESTEROL.]
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| Sci-Tech Encyclopedia: Sterol |
Any of a group of naturally occurring or synthetic organic compounds with a steroid ring structure, having a hydroxyl (OH) group, usually attached to carbon-3. This hydroxyl group is often esterified with a fatty acid (for example, cholesterol ester). The hydrocarbon chain of the fatty-acid substituent varies in length, usually from 16 to 20 carbon atoms, and can be saturated or unsaturated. Sterols commonly contain one or more double bonds in the ring structure and also a variety of substituents attached to the rings. Sterols and their fatty-acid esters are essentially water insoluble. For transport in an aqueous milieu (for example, the bloodstream of mammals), sterols and other lipids are bound to specific proteins, forming lipoprotein particles. These particles are classified based on their composition and density. One lipoprotein class is abnormally high in the blood of humans prone to heart attacks.
Sterols are widely distributed in nature. Modifications of the steroid ring structure are made by specific enzyme systems, producing the sterol characteristic for each species, such as ergosterol in yeast. The major regulatory step in the sterol biosynthetic pathway occurs early in the process. Drugs that lower blood cholesterol levels in humans are designed to inhibit this regulatory enzyme. In addition to their conversion to sterols, several intermediates in the pathway are precursors of other important biological compounds, including chlorophyll in plants, vitamins A, D, E, and K, and regulators of membrane functions and metabolic pathways.
A universal role of sterols is to function as part of membrane structures. In addition, some insects require sterols in their diets. Cholesterol also serves as a precursor of steroid hormones (estrogens, androgens, glucocorticoids, and mineralocorticoids) and bile acids. See also Cholesterol; Steroid.
| Food and Nutrition: sterols |
Alcohols derived from the steroids; including cholesterol, ergosterol in yeast (the precursor for synthetic vitamin D2), sitosterol and stigmasterol in plants, and coprosterol in faeces.
| Dental Dictionary: sterols |
Steroids having one or more hydroxyl groups and no carbonyl or carboxyl groups (for example, cholesterol).
| Sports Science and Medicine: sterol |
A group of chemicals derived from steroids. They include cholesterol and the several compounds which make up vitamin D.
| Veterinary Dictionary: sterol |
Any steroid, e.g. cholesterol and ergosterol, having long (8–10 carbons) aliphatic side-chains at position 17 and at least one alcoholic hydroxyl group; the sterols have lipid-like solubility.
| Wikipedia: Sterol |
Sterols are an important class of organic molecules. They occur naturally in plants, animals and fungi, with the most familiar type of animal sterol being cholesterol. Cholesterol is vital to cellular function, and a precursor to fat-soluable vitamins and steroid hormones.
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Sterols of plants are called phytosterols and sterols of animals are called zoosterols. Important zoosterols are cholesterol and some steroid hormones; notable phytosterols include campesterol, sitosterol, and stigmasterol. Ergosterol is a sterol present in the cell membrane of fungi, where it serves a role similar to cholesterol in animal cells.
Sterols and related compounds play essential roles in the physiology of eukaryotic organisms. For example, cholesterol forms part of the cellular membrane in animals, where it affects the cell membrane's fluidity and serves as secondary messenger in developmental signaling. In humans and other animals, corticosteroids, such as cortisol act as signaling compounds in cellular communication and general metabolism.
Phytosterols, more commonly known as plant sterols, have been shown in clinical trials to block cholesterol absorption sites in the human intestine, thus helping to reduce cholesterol in humans. [1] They are currently approved by the U.S. Food and Drug Administration for use as a food additive, however, there is some concern that they may block absorption, not only of cholesterol, but of other important nutrients as well. At present the American Heart Association has recommended that supplemental plant sterols be taken only by those diagnosed with elevated cholesterol, and has particularly recommended that they not be taken by pregnant women or nursing mothers. [2]
Sterols are also known as steroid alcohols. They are a subgroup of steroids with a hydroxyl group at the 3-position of the A-ring.[3] They are amphipathic lipids synthesized from acetyl-coenzyme A via the HMG-CoA reductase pathway. The overall molecule is quite flat. The hydroxyl group on the A ring is polar. The rest of the aliphatic chain is non-polar.
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