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Vitamin B5

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Vitamin B5
(Pantothenic Acid)
HISTORY AND DEVELOPMENT
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Pantothenic Acid was isolated in 1938 by Dr. R. J. Williams
and synthesized by other investigators in 1940. Although its
vitamin nature was demonstrated by its ability to prevent
certain deficiencies in animals, little interest was shown in
this vitamin until about a decade later.
In 1946, Lipmann and his associates showed that coenzyme
A was essential for acetylation reactions in the body, and in
1950 reports from this same laboratory showed pantothenic
acid to be a constituent of coenzyme A.
HISTORY AND DEVELOPMENT
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The name for this vitamin is derived from the
Greek word panthos, meaning “everywhere”.
The universal distribution of this vitamin in
biologic materials suggests the key role that it
plays in metabolism.
CHEMISTRY AND CHARACTERISTICS
• PANTOTHENIC
Acid, as the free acid, is an unstable, viscous yellow
oil, soluble in water.
• Commercially it is available as the sodium or calcium salt, which is
slightly sweet, water soluble and quite soluble.
• There is little loss of the vitamin with ordinary cooking procedures,
except in acid and alkaline solutions.
• The pantothenic acid content of tissues and foods is determined by
microbiologic, chemical or radioimmunoassay methods; values are
expressed in milligrams or micrograms.
Body Distribution
• Pantothenic acid along with 4’-phosphopantothenate and
pantothenic may be found in the body’s cells.
• Free Pantothenic acid is found in plasma, however, higher
concentrations are found intracellularly:
•
Mainly in RBC’s
• Most ingested pantothenic acid is used to synthesize or resynthesize
CoA
• Found in fairly high concentrations in the:
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Liver
Adrenal gland
Kidney
Brain
Heart
DIGESTION, ABSORPTION AND TRANSPORT
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85% of the pantothenic acid found in foods is bound to CoA.
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During digestion, CoA is hydrolyzed in the lumen to pantothenic acid
Via phosphatases and pyrophosphatases.
Free pantothenic acid can then be absorbed (mainly in the jejunum)
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High concentrations by passive diffusion
Low concentrations via a Na+ dependent transport system
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40 to 61% of pantothenic acid is absorbed.
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From the intestinal cell, it will enter the portal blood for transport
to body cells.
•
Pantothenic acid is found free in blood plasma/serum; however,
higher concentrations are found intracellularly (specifically within
red blood cells) than extracellularly (in plasma/serum).
EXCRETION
• Pantothenic acid does not appear to undergo metabolism
prior to excretion.
• Pantothenic acid is excreted intact primarily in the urine, with
only small amounts excreted in the feces.
• No metabolites of the vitamin have been identified in the
urine or feces.
• Urinary excretion of the vitamin usually ranges from about 2
to 7 mg/day.
FUNCTIONS OF PANTOTHENIC ACID
• Pantothenic acid functions in the body as a component of
COENZYME A (CoA) and as a prosthetic group on the acyl carrier
protein.
• CoA is a complex molecule consisting of a sulfur containing
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compound, adenine, ribose, phosphoric acid and pantothenic acid.
The sulfur linkage is highly reactive.
• The part of the acyl carrier protein containing pantothenic acid has
a structure similar to part of CoA.
• CoA functions in reactions that accept or remove the acetyl group
(-CH3CO). One of these reactions is the formation of acetyl choline,
a substance of importance in the transmission of the nerve
impulse.
FUNCTIONS OF PANTOTHENIC ACID
• CoA participates in the oxidation of pyruvate, α-keto-glutarate and
fatty acids.
• CoA reacts with pyruvic acid to form acetyl CoA, which, in turn,
combines with oxaloacetate to form citrate thus initiating the TCA
cycle for the release of energy.
• CoA is also involved in the synthesis of cholesterol and other
sterols, and porphyrin in the hemoglobin molecule. The acyl carrier
protein has an essential role in fatty acid synthesis.
• CoA is synthesized in all cells and apparently does not cross cell
membranes. Liver, kidney, brain, adrenal and heart tissues, being
metabolically active, contain high concentrations.
PANTOTHENIC ACID RECOMMENDATIONS
• An Adequate Intake (AI) for pantothenic acid has been set. It
reflects the amount needed to replace daily losses.
RECOMMENDED DIETARY ALLOWANCES
(ADEQUATE INTAKE (MG/DAY)
• Infants (Birth -1 year)
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• Infants (0-0.5 yr): 1.7 mg/day
• Infants (0.5-1 yr): 1.8 mg/day
Children (1-8 year)
• Children (1-3 yr): 2 mg/day
• Children (4-8 yr): 3 mg/day
Males
• 9-13 years: 4 mg/day
• 14-70 years: 5mg/day
• >70 years: 5 mg/day
Females
• 14-18 years: 4 mg/day
• 19-70 years: 5 mg/day
• >70 years: 5 mg/day
• Pregnancy: 6 mg/day
• Lactation: 7 mg/day
FOOD SOURCES
• Pantothenic acid is widespread in
foods, and typical diets seem to provide
adequate intakes.
• Beef, poultry, liver, egg yolk, whole
grains, potatoes, tomatoes, and broccoli
are particularly good sources.
• Losses of pantothenic acid during food
production can be substantial because it
is readily destroyed by the freezing,
canning, and refining processes.
PANTOTHENIC ACID DEFICIENCY
• Pantothenic acid deficiency is rare.
• Its symptoms involve a general failure of all the body’s systems and
include fatigue, GI distress, and neurological disturbances.
• The “burning feet” syndrome that affected prisoners of war in Asia
during World War II is thought to have been caused by pantothenic acid
deficiency.
• “Burning feet syndrome” is characterized by numbness of the toes and a
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sensation of burning in the feet.
The condition is exacerbated by warmth and diminished with cold and is
thought to result from pantothenic acid deficiency.
The syndrome can be corrected with calcium pantothenate
administration.
PANTOTHENIC ACID DEFICIENCY
• Other symptoms of deficiency
include vomiting, fatigue, weakness,
restlessness, and irritability.
• A metabolic inhibitor of
pantothenate, omega
methylpantothenate, has been used
in studies to induce low
pantothenate status in humans.
• Deficiency of pantothenic acid is
thought to occur more often in
conjunction with multiple nutrient
deficiencies, as for example in
malnutrition.
PANTOTHENIC ACID DEFICIENCY
• Some conditions that may increase the need for the vitamin
include alcoholism, diabetes mellitus, and inflammatory
bowel diseases.
• Increased excretion of the vitamin has been shown in people
with diabetes mellitus. Absorption is likely to be impaired
with inflammatory bowel diseases.
• Intake of the vitamin typically is low in people with excessive
alcohol intake.
PANTOTHENIC ACID TOXICITY
• No toxic effects have been reported, and no UL
has been established.
INTERACTION WITH OTHER NUTRIENTS
• In animal studies, vitamin B12, folate and biotin
are required for proper use of vitamin B5 in the
body’s biochemical pathways.
• In addition, vitamin C appears to help prevent
B5 deficiency.
DIAGNOSIS OF PANTOTHENIC ACID
• Blood pantothenic acid concentrations <100 mg/dL are
thought to reflect low dietary pantothenate intakes; however,
blood concentrations do not correlate well with changes in
dietary pantothenate intake and status.
• Urinary pantothenate excretion is considered to be a better
indicator of status, with excretion of <1 mg/day considered
indicative of poor status.
REFERENCES
• Gropper, S., Smith, J., & Groff, J. (2009). Advanced Nutrition
and Human Metabolism. Belmont, CA: Wadsworth, Cengage
Learning.
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