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"Ketosis-Lipolysis is not Ketoacidosis"

Maria C. Linder is on the faculty at California State University
Fullerton, California in the Department of Chemistry and Biochemistry.
All quotes are from her textbook; "Nutritional Biochemistry and
Metabolism: with clinical applications", Maria C. Linder. pages
87-109. Chapter Eight: Nutrition and Metabolism of Protein.

There is a difference between starvation, prolonged fasting and
controlled carbohydrate eating. There are similar metabolic mechanisms
at work, but the differences are key to understanding the safety
and efficacy of controlled carbohydrate diets.

"The whole process of muscle protein catabolism and liver
gluconeogenesis is regulated principally by glucocorticosteroids and
glucagon and a relative lack of insulin. Early in fasting glycogen
reserves are depleted, and protein (mainly from muscle) becomes the major
source of carbon for glucose production. Glucose is required in
substantial amounts by blood cells and the central nervous system on a
daily basis. There is also an initiation of ketone body production by
the liver to provide a more water soluble form of fat-derived fuel."

THIS IS WHERE THE CONFUSION BEGINS

"A very similar adaption of protein and energy metabolism
occurs in persons consuming diets very low in carbohydrates, where there
is little or no glycogen reserve. However, in this instance, DIETARY
PROTEIN largely or fully SUBSTITUTES for muscle protein in gluconeogenesis.

NOTE: "DIETARY PROTEIN LARGELY OR FULLY SUBSTITUTES FOR MUSCLE PROTEIN IN GLUCONEOGENESIS."

Even when discussing starvation many critics of lowcarb eating miss the proverbial
boat. "The body adapts to starvation and reduces the need for
protein-dependent gluconeogenesis by boosting its production of ketones,
a fuel ALTERNATIVE to glucose for MOST CELLS. Circulating ketones reach
maximum levels after about ten days and now substitute for
much of the glucose requirement of the central nervous system.
This drastically reduces the need for catabolism of muscle protein."

"With reduced protein catabolism, urinary nitrogen excretion also
declines. And there is a shift from the excretion of urea to a
predominance of ammonia loss. This shift toward ammonia versus urea
parallels the increased production and excretion of keto acids, and
serves to MAINTAIN ACID/BASE BALANCE."

"The overall point is that muscle is a valuable reserve of carbons
that can be used for glucose production when needed. However the body
prevents excessive losses of muscle protein over long periods of fasting
by adapting the central nervous system to utilization of ketone bodies
for fuel."

Adaptation avoids keto-acidosis in lowcarb dieters

"A parallel adaptation in the production and excretion of
ammonium ions by the kidney neutralizes the increased ketone bodies
(principally beta-hydroxybutyric and acetoacetic acids). Without the
latter adaptation, such large productions of keto acids would cause a
severe ketoacidosis, as well as a loss of large quantities of sodium and
potassium ions (accompanying ketones spilled into the urine)."

Therefore, unless one is an insulin dependent diabetic or literally starving
due to a lack of food, there is little or no danger from ketosis when it
is not characterized by a simultaneous RISE IN BLOOD GLUCOSE and BLOOD ACIDITY.

Miller-Keane Encyclopedia & Dictionary of Medicine, Nursing, & Allied Health
Miller-Keane Medical Dictionary, 2000

(ke-to´sis) accumulation in the blood and tissues of large quantities of the "ketone bodies"
KETONE BODIES: beta-hydroxybutyric acid, acetoacetic acid, and acetone. Because the first
two are acids, this results in metabolic "acidosis" ACIDOSIS. Thus, the condition is often referred to
as ketoacidosis. adj., ketot´ic.

When fatty acids are metabolized in the liver, an intermediate, acetylcoenzyme A (acetyl CoA), is
produced. Normally, acetyl CoA is condensed with oxaloacetic acid, a product of carbohydrate metabolism,
to form citric acid. This then enters the tricarboxylic acid cycle, the final common pathway of cellular energy
metabolism.

When oxaloacetate is not present, acetyl CoA is converted by another pathway to ketone bodies. These
compounds cannot be metabolized by the liver and are released into the blood stream. Other tissues, including
muscle, brain, heart, and kidneys, can convert ketone bodies back to acetyl CoA and metabolize them as an
energy source.

In acute starvation or in uncontrolled "diabetes mellitus" DIABETES MELLITUS, there is a great increase
in fatty acid metabolism and impaired or absent carbohydrate metabolism, which results in a greatly increased
production of ketone bodies. This can also occur when the diet is composed almost entirely of fat. The production
of ketone bodies is reduced to the normal low level and the ketoacidosis is reversed when adequate carbohydrate
metabolism is restored.

The patient with ketosis often has a sweet or "fruity" odor to his breath. This is produced by acetone, a ketone
body that is highly volatile and is blown off in small amounts with air expired from the lungs.


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