Thiamin, Pantothenic Acid, Biotin

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35 Terms

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Thiamin

Vitamin B1 essential for energy metabolism, part of Kreb's Cycle, contains pyrimidine ring and thiazole moiety.

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Niacin

Vitamin B3, works alongside thiamin and riboflavin in the Kreb's Cycle.

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Riboflavin

Vitamin B2, works alongside thiamin and niacin in the Kreb's Cycle.

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Kreb's Cycle

Metabolic pathway for ATP production, involving thiamin, niacin, and riboflavin.

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Pyrimidine ring

Part of thiamin's structure, involved in energy metabolism.

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Thiazole moiety

Part of thiamin's structure, involved in energy metabolism.

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Methyl group

Found in the thiazole ring of thiamin, serves as the active site during enzyme interaction.

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Enzymes

Biological catalysts, often requiring thiamin for activation.

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Thiamin sources

Found in meat, whole grains, legumes, and yeast

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frequently enriched in grain products.

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Thiamin sensitivity

Sensitive to high temperatures and alkaline pH, protected by reducing reagents like vitamin C and citric acid.

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Thiamin absorption

Only free form can be absorbed, phosphorylated forms must be dephosphorylated by intestinal phosphatases.

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Thiamin storage

Absorbed into blood, taken up by the liver, phosphorylated to coenzyme form TDP/TPP.

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TDP/TPP

Most metabolically active form of thiamin, involved in energy metabolism and coenzyme function.

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Thiamin functions

Energy metabolism, pentose and NADPH synthesis, membrane and nerve conduction.

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Decarboxylase reactions

Essential for energy transformation, involve TDP/TPP and specific enzymes like pyruvate dehydrogenase.

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Pyruvate dehydrogenase

Enzyme complex involving TDP/TPP, responsible for converting pyruvate to acetyl CoA.

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Transketolase

Enzyme involved in pentose phosphate pathway, loosely binds to TDP/TPP.

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Thiamin in nerve conduction

TTP plays a role in nerve conduction, activates chloride transport and stimulates nerve impulses.

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Thiamin deficiency

Uncommon in developed world, can occur in alcoholism, liver damage, and diseases impairing absorption.

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Maple syrup urine disease

Genetic disease related to thiamin status, results in accumulation of branched-chain amino acids and keto acids in the blood.

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Thiamin toxicity

Parenteral exposure can cause headaches, cardiac arrhythmia, and convulsions.

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Thiamin assessment

Measured by urinary thiamin concentrations and red blood cell transketolase activity.

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Pantothenic acid

Vitamin B5, metabolically active form of coenzyme A, comprised of beta-alanine and D-pantoic acid.

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Pantothenic acid sources

Found in various foods, including brewer's yeast, corn, cauliflower, kale, egg yolk, organ meats, milk, and whole-grain breads.

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Pantothenic acid digestion

Hydrolyzed to free form before absorption through the enterocytes.

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Pantothenic acid absorption

Absorbed via sodium-dependent active multivitamin carrier in the jejunum.

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Pantothenic acid functions

Carries out acetyl and acyl transfer reactions, important for macronutrient and lipid metabolism.

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Biotin

Vitamin B7, composed of ureido and tetrahydrothiophene rings with a valeric acid side chain.

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Biotin sources

Found in meat products, soybeans, cereal products, and synthesized by intestinal bacteria.

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Biotin digestion and absorption

Requires digestion prior to absorption, absorbed in the small intestine via passive diffusion or carrier-mediated transport.

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Biotin functions

Covalently attaches to carboxylases, regulates gene expression, and plays a role in cellular division.

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Biotin deficiency

Can occur due to impaired absorption, inflammatory bowel diseases, alcoholism, or genetic mutations in biotin-dependent enzymes.

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Biotin toxicity

No reported toxic side effects, used in large amounts in skin and hair products.

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Biotin assessment

Blood and urine analysis, decreased urinary biotin excretion and greater excretion of 3-hydroxy isovaleric acid are markers of deficiency.