Saturday, August 29, 2009
Understanding acidifiers
Understanding acid-forming foods
Acid and human health
In contrast to strong acids, organic acids are classified as weak acids because they donate only a portion of their hydrogen ions, lower the pH to a lesser degree, and are less dangerous to tissues.
Many compounds in foods are weak acids, including CITRIC ACID, ACETIC ACID, and TARTARIC ACID. Several weak acids are used as FOOD ADDITIVES, including benzoic acid, CARBONIC ACID, and alginic acid. As food additives and recipe ingredients, weak acids add tartness to foods. Weak acids are common intermediates, products of cellular processes that sustain life, including LACTIC ACID, KETONE BODIES, PYRUVIC ACID, acetic acid, FATTY ACIDS, SUCCINIC ACID, citric acid, even the nucleic acids DNA and RNA. GLUTAMIC ACID and ASPARTIC ACID (two common AMINO ACIDS) are classified as acidic amino acids, and are more acid than most.
In the body, weak acids characteristically have lost all their hydrogen ions and exist as a family of anions (negatively charged ions) classified as “conjugate bases” because they have been completely neutralized by the buffer systems of blood. In the blood, lactic acid exists as its anion, lactate; acetoacetic acid (a ketone body) as acetoacetate; citric acid as citrate, and so on. Often the names of acids and their anions are interchanged in nutrition literature.
Tuesday, July 28, 2009
What is achlorhydria?
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What is acetoacetic acid (acetoacetate)
The most prevalent of the KETONE BODIES, which are acids produced by the liver. Acetoacetic acid is a useful fuel; it is readily oxidized by the heart and brain for the production of ATP, the energy currency of cells.
Though small amounts of ketone bodies are normally produced by liver metabolism, an excessive buildup of acetoacetic acid and its derivative, BETA HYDROXYBUTYRIC ACID, in the blood (ketonemia) can occur during excessive fat breakdown, when the liver cannot completely oxidize massive amounts of fatty acids released from fat (ADIPOSE TISSUE). Conditions conducive to excessive acetoacetic acid production include STARVATION (prolonged FASTING), crash DIETING, uncontrolled DIABETES MELLITUS, and chronic ALCOHOLISM.
Ketone body production serves an important role in the physiologic adaptation to starvation. With prolonged starvation, the blood levels of ketone bodies rise, and more of them cross the BLOOD-BRAIN BARRIER to be taken up by nerve tissue, where they are burned for energy. Consequently, the brain requires less blood glucose (blood sugar) for energy at a time when this fuel is at a premium. The sustained build-up of acetoacetic acid in the blood (KETOSIS) can acidify the blood, leading to metabolic ACIDOSIS, and alter the acid-base balance of the body, a potentially dangerous condition.
What is acetic acid?
During fermentation, certain bacteria produce acetic acid by oxidizing alcohol when exposed to air. VINEGAR contains 4 percent to 6 percent acetic acid, which gives vinegar its characteristic sour taste. As vinegar, acetic acid is a common ingredient in food preparation.
One of the simplest organic acids, acetic acid contains only two carbon atoms. It is classified as a weak acid because it is only partially ionized, unlike strong mineral acids, such as hydrochloric acid.
Acetic acid plays a pivotal role in metabolism. To be metabolized, acetic acid must be activated as acetyl CoA, in which acetic acid is bound to a carrier molecule, COENZYME A, which is in turn derived from the B vitamin PANTOTHENIC ACID. Metabolic pathways that oxidize fatty acids, carbohydrate, and amino acids for energy, all yield acetyl CoA, the common intermediate by which carbons from these fuels enter the KREB’S CYCLE to be oxidized to carbon dioxide. Alternatively, acetyl CoA can be used as a building block. It forms saturated fatty acids, cholesterol, and ketone bodies. Nerve cells can use it to form the NEUROTRANSMITTER, ACETYLCHOLINE. Tissues combine acetic acid with amino sugars to form a family of sugar derivatives like Nacetylglucosamine and N-acetylgalactosamine that help define recognition sites on the surface of cells and blood group specificities, such as the A, B, O, and Lewis blood groups used in blood typing.
Sunday, June 28, 2009
Acesulfame-K (acesulfame potassium; Sunett)
This non-caloric, ARTIFICIAL SWEETENER tastes approximately 200 times sweeter than table sugar (SUCROSE) and lacks the bitter aftertaste of SACCHARIN. The United Nations Food and Agriculture Organization endorsed acesulfame-K as a satisfactory artificial sweetener in 1983. Acesulfame-K was approved in 1988 by the U.S. FDA as a sugar substitute to be used in packets or as tablets and now is approved for use in chewing gum and in powdered drink mixes. Unlike ASPARTAME, acesulfame-K can be used in cooking because it does not break down at oven temperatures. Blending Sunett with other low-calorie sweeteners creates a beverage with a more sugarlike taste than one sweetened with any single low-calorie sweetener.
The Center for Science in the Public Interest has raised questions about Sunett’s safety, saying a few tests on rats indicated a possibility of cancer, although this was not proof that the sweetener could cause cancer. The Calorie Control Council counters that the safety of acesulfame potassium has been confirmed by more than 90 studies, and it is endorsed by a committee of the World Health Organization. Theoretically, it would not be expected to be absorbed by the body. Nonetheless, some studies suggest that large doses raise blood CHOLESTEROL levels in diabetic laboratory animals and increase the number of lung and mammary tumors in other animals.
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