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*Whole (unrefined), enriched or fortified grains
*Yeast
*Wheat germ
*Meat (Pork)
*Legumes
*Nuts
*Green vegetables (peas, asparagus, okra)
*Supplements: thiamin HCL, thiamin nitrate
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*In our body, thiamin exists as free thiamin and various phosphorylated forms:
*Thiamin monophosphate (TMP)
*Thiamin pyrophosphate (TPP) or thiamin diphosphate (TDP)
*Thiamin triphosphate (TTP)
*Free form in plants
*~95% of thiamin occurs in phosphorylated form with 80-85% as TPP in animal products |
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*TPP is hydrolyzed by intestinal phosphatases to free thiamin b4 absorption
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*Absorption rate from foods is high
*Anti-thiamin factors:
*Thiaminases- cleave thiamin, make it inactive (raw fish, shellfish) (thermolabile- cooking inactivates it so thiamin can be absorbed)
*Thiamin antagonists- inactivate thiamin by oxyreductive process (caffeine and tannic acid) (thermostable) |
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*Free thiamin absorbed in small intestine
*Low concentrations: active transport (ThTr1 and ThTr2 found in variety of tissues: thiamin/H+ antiport carrier system)
*At high concentrations: passive diffusion |
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*Transport across basolateral membrane: thiamin/H+ antiport system
*In the blood, 90% of thiamin is transported by RBCs
*Once in RBC, thiamin is phosphorylated to TPP
*Remaining 10% is found as free thiamin bound to albumin or as TMP |
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*Little storage, most is functional
*Half is in skeletal muscle |
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*Excess thiamin, TPP, TMP are excreted either intact or catabolized for urinary excretion
*Methylene bridge btwn pyrimidine and thiazole is catabolized generating metabolites |
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*Coenzyme function
-Energy transformation
-Synthesis of pentoses and NADPH
*Noncoenzyme function
-TPP is important in membrane and nerve conduction: important in transmission of Na+/K+ channels and aCH receptors
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Thiamin – coenzyme function |
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*TPP functions in energy transformation as a coenzyme with:
-Pyruvate DH
-Alpha-KG DH
-BC alpha-KA DH
-Transketolases (for NADPH and pentose synthesis) |
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TPP coenzyme in Energy Transformation |
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*Thiamin catalyzes the oxidative decarboxylation rxns for:
Pyruvate DH, alpha-KG DH, BC alpha-KAD |
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TPP oxidative phosphorylation |
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Oxidative decarboxylation of pyruvate by PDH |
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Decarboxylation of BCAA in skeletal muscle requires TPP |
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What happens if TPP-required rxns are inhibited? |
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*ATP synthesis and Acetyl CoA needed for FA and cholesterol synthesis is decreased
*Accumulation of pyruvate, alpha-KG, and BCAAs in blood
*This accumulation can lead to ketoacidosis |
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About 50% of Body Thiamin is in Skeletal Muscle—Why? |
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*Because that's where BCAA are metabolized
*Skeletal Muscle is very metabolically active (PDH, TCA need Thiamin) |
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Synthesis of Pentoses and NADPH
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*TPP is a coenzyme for transketolase
*A key enzyme in PPP- necessary for making ribose and regenerating NADPH
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Pentose Phosphate Pathway |
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TPP Involvement in Pathways |
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*RDA Men: 1.2mg/d
*RDA Women: 1.1mg/d
*Determined:
-RDA= EAR + 20%
*Men have more muscle, are more metabolically active
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*Erythrocyte transketolase activity:
-Stimulate activity by adding the substrate ribose-5-p or xyulose-5-p w/ or w/o thiamin
-If an increase in enzymatic activity by >25% with thiamin supplementation = deficiency
*Blood pyruvate, alpha-KG, or thiamin
*Thiamin in urine |
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*Early symptoms= vague
-Fatigue, irritability, poor memory, loss of appetite, sleep disturbances, abdominal discomfort, weight loss
*As deficiency worsens
-Cardiovas sys and neurological symptoms
*Dry, Wet, Acute
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*Found mostly in older adults bc of chronic low thiamin intakes
*Nerve and muscle abnormalities
-Prickling sensation in toes
-Burning sensation in feet, leg cramps, pain
-Muscles my become weak and atrophy |
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*Heart abnormalities
*Heart pumps more blood and beats faster
-Blood vessels widen= edema in legs/lungs = decrease in blood pressure = shock and death |
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Acute (aka infantile) BeriBeri |
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*In infants who are breastfed by a mom who has a thiamin def
*Symptoms in baby:
-Anorexia, vomiting, lactic acidosis, altered heart rate, lack of reflexes |
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Wernicke – Korsakoff syndrome |
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*Thiamin def is often associated with alcoholism in western countries:
-Due to decrease in food intake, liver damage and a decrease in thiamin absorption
*Causes brain abnormalities:
-Wernickes: ophthalmoplegia, nystagmus, ataxia
-Korsakoff: loss of short-term memory, confusion
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*Ophthalmoplegia: paralysis of ocular muscles
*Nystagmus: constant involuntary eye movement
*Ataxia: impaired muscle coordination |
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*Low risk of toxicity- due to limit on absorption by brush border
*UL: not established |
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