🧈 Lecture 3: Part 1 - Fat-Soluble Vitamins

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Last updated 10:07 PM on 9/18/26
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14 Terms

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Vitamins

Definition
  • Organic compounds with a carbon skeleton

Solubility
  • Can be lipid-soluble or water-soluble
  • Solubility is important

Functions
  • Perform a variety of functions
  • Metabolic regulation
  • Coenzymes
  • Antioxidants

Essential Vitamins
  • May or may not be considered essential
  • Depends on the species

<p class="PDq2pG_selectionAnchorContainer"><strong>Definition</strong><br>  • <strong>Organic compounds</strong> with a <strong>carbon skeleton</strong></p><p><strong>Solubility</strong><br>  • Can be <strong>lipid-soluble</strong> or <strong>water-soluble</strong><br>  • <strong>Solubility is important</strong></p><p><strong>Functions</strong><br>  • Perform a variety of functions<br>  • <strong>Metabolic regulation</strong><br>  • <strong>Coenzymes</strong><br>  • <strong>Antioxidants</strong></p><p><strong>Essential Vitamins</strong><br>  • May or may not be considered <strong>essential</strong><br>  • Depends on the <strong>species</strong></p>
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Fat-Soluble Vitamins

Vitamin A
  • Retinol
  • Retinal (retinaldehyde)
  • Retinoic acid (retinol metabolite)
  • Retinyl esters (esterified retinol)
  • Beta-carotene (provitamin A carotenoid)

Vitamin E
  • Tocopherols: alpha, beta, gamma, delta
  • Tocotrienols: alpha, beta, gamma, delta

Vitamin K
  • K₁ (phylloquinone)
  • K₂ (menaquinone)
  • K₃ (menadione)

Vitamin D
  • D₂ (ergocalciferol)
  • D₃ (cholecalciferol)

Why is it important to know which vitamins are fat-soluble?
  • They can be stored in body fat, so they can accumulate to toxic levels

<p><strong>Vitamin A</strong><br>  • <strong>Retinol</strong><br>  • <strong>Retinal</strong> (retinaldehyde)<br>  • <strong>Retinoic acid</strong> (retinol metabolite)<br>  • <strong>Retinyl esters</strong> (esterified retinol)<br>  • <strong>Beta-carotene</strong> (provitamin A carotenoid)</p><p><strong>Vitamin E</strong><br>  • <strong>Tocopherols</strong>: alpha, beta, gamma, delta<br>  • <strong>Tocotrienols</strong>: alpha, beta, gamma, delta</p><p><strong>Vitamin K</strong><br>  • <strong>K₁</strong> (phylloquinone)<br>  • <strong>K₂</strong> (menaquinone)<br>  • <strong>K₃</strong> (menadione)</p><p><strong>Vitamin D</strong><br>  • <strong>D₂</strong> (ergocalciferol)<br>  • <strong>D₃</strong> (cholecalciferol)</p><p><strong>Why is it important to know which vitamins are fat-soluble?</strong><br>  • They can be <strong>stored in body fat</strong>, so they can <strong>accumulate to toxic levels</strong></p>
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Vitamin A

Functions
  • Vision
  • Growth
  • Tissue maintenance
  • Immune function
  • Embryonic development

Biologically Active Forms
  • Retinol
  • Retinal (retinaldehyde)
  • Retinoic acid

Storage Forms — Inactive
  • Retinyl ester
    • From animal products
    • Stored in the liver
  • Beta-carotene (mostly)
    • From plant products
    • Associated with red/orange pigmentation

Vitamin A Forms
  • Retinyl esters → Retinol → Retinaldehyde → Retinoic acid

<p><strong>Functions</strong><br>  • <strong>Vision</strong><br>  • <strong>Growth</strong><br>  • <strong>Tissue maintenance</strong><br>  • <strong>Immune function</strong><br>  • <strong>Embryonic development</strong></p><p><strong>Biologically Active Forms</strong><br>  • <strong>Retinol</strong><br>  • <strong>Retinal</strong> (retinaldehyde)<br>  • <strong>Retinoic acid</strong></p><p><strong>Storage Forms — Inactive</strong><br>  • <strong>Retinyl ester</strong><br>    • From <strong>animal products</strong><br>    • Stored in the <strong>liver</strong><br>  • <strong>Beta-carotene</strong> (mostly)<br>    • From <strong>plant products</strong><br>    • Associated with <strong>red/orange pigmentation</strong></p><p><strong>Vitamin A Forms</strong><br>  • <strong>Retinyl esters → Retinol → Retinaldehyde → Retinoic acid</strong></p>
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Vitamin A – Vision

Photoreceptors
  • Retinal + opsin (light-sensitive protein) = rhodopsin and iodopsin

Rhodopsin
  • Photoreceptor found in rod cells of the retina
  • Responsible for black and white vision
  • Works in dim light → “night vision”

Iodopsin
  • Photoreceptor found in cone cells of the retina
  • Responsible for colour vision
  • Works in bright light

<p><strong>Photoreceptors</strong><br>  • <strong>Retinal + opsin</strong> (light-sensitive protein) = <strong>rhodopsin</strong> and <strong>iodopsin</strong></p><p><strong>Rhodopsin</strong><br>  • <strong>Photoreceptor</strong> found in <strong>rod cells</strong> of the retina<br>  • Responsible for <strong>black and white vision</strong><br>  • Works in <strong>dim light</strong> → “night vision”</p><p><strong>Iodopsin</strong><br>  • <strong>Photoreceptor</strong> found in <strong>cone cells</strong> of the retina<br>  • Responsible for <strong>colour vision</strong><br>  • Works in <strong>bright light</strong></p>
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Vitamin A – Toxicity and Deficiency

Toxicity
  • Hypervitaminosis A → too much vitamin A in the body
  • Caused by excess preformed vitamin A, not beta-carotene

Deficiency
  • Fetal abnormalities
  • Impaired growth
  • Night blindness

<p><strong>Toxicity</strong><br>  • <strong>Hypervitaminosis A</strong> → too much vitamin A in the body<br>  • Caused by excess <strong>preformed vitamin A</strong>, not <strong>beta-carotene</strong></p><p><strong>Deficiency</strong><br>  • <strong>Fetal abnormalities</strong><br>  • <strong>Impaired growth</strong><br>  • <strong>Night blindness</strong></p>
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Vitamin A – Essentiality

Preformed Vitamin A is Essential For
  • Felids
  • Marine birds
  • Most carnivorous mammals
  • These animals lack sufficient amounts of 15,15′-dioxygenase, an enzyme needed to convert beta-carotene into vitamin A

Not Essential For
  • Canids → foxes, coyotes, wolves
  • Most herbivores
  • Most omnivores
  • These animals can readily convert beta-carotene into vitamin A

<p><strong>Preformed Vitamin A is Essential For</strong><br>  • <strong>Felids</strong><br>  • <strong>Marine birds</strong><br>  • <strong>Most carnivorous mammals</strong><br>  • These animals lack sufficient amounts of <strong>15,15′-dioxygenase</strong>, an enzyme needed to convert beta-carotene into vitamin A</p><p><strong>Not Essential For</strong><br>  • <strong>Canids</strong> → foxes, coyotes, wolves<br>  • <strong>Most herbivores</strong><br>  • <strong>Most omnivores</strong><br>  • These animals can readily convert <strong>beta-carotene</strong> into <strong>vitamin A</strong></p>
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Vitamin D

Functions
  • Homeostatic regulation of calcium and phosphorus → keeps calcium and phosphorus levels balanced
  • Growth
  • Bone remodeling → changes and maintains bone tissue
  • Eggshell formation

Sources

Vitamin D₂ – Ergocalciferol
  • Very few natural sources
  • Foods are often fortified with D₂

Vitamin D₃ – Cholecalciferol
  • Sunlight → UV-B exposure
  • Phytoplankton
  • Zooplankton
  • Marine fish

<p><strong>Functions</strong><br>  • <strong>Homeostatic regulation</strong> of calcium and phosphorus → keeps calcium and phosphorus levels balanced<br>  • <strong>Growth</strong><br>  • <strong>Bone remodeling</strong> → changes and maintains bone tissue<br>  • <strong>Eggshell formation</strong></p><p><strong>Sources</strong></p><p><strong>Vitamin D₂ – Ergocalciferol</strong><br>  • Very few <strong>natural sources</strong><br>  • Foods are often <strong>fortified with D₂</strong></p><p><strong>Vitamin D₃ – Cholecalciferol</strong><br>  • <strong>Sunlight</strong> → UV-B exposure<br>  • <strong>Phytoplankton</strong><br>  • <strong>Zooplankton</strong><br>  • <strong>Marine fish</strong></p>
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Vitamin D – Activation

Inactive Forms
  • D₂ → obtained from the diet
  • D₃ → obtained from sunlight and diet
  • D₂ and D₃ are biologically inactive

Active Form
  • Calcitriol → 1,25-dihydroxycholecalciferol
  • Also called 1,25-dihydroxyvitamin D₃ or 1,25(OH)₂D
  • Calcitriol is the biologically active form

Vitamin D Activation
  1. UV-B radiation reaches the skin
  2. UV-B initiates conversion of 7-dehydrocholesterol → vitamin D₃ (cholecalciferol)
  3. In the liver, vitamin D₃ → 25-hydroxyvitamin D₃ (calcidiol or 25(OH)D3)
  4. In the kidney, 25-hydroxyvitamin D₃ → 1,25-hydroxyvitamin D₃ (calcitriol or 1,25(OH)₂D3)

Main Function of Calcitriol
  • Calcitriol regulates calcium and phosphorus (Ca/P)

<p><strong>Inactive Forms</strong><br>  • <strong>D₂</strong> → obtained from the diet<br>  • <strong>D₃</strong> → obtained from <strong>sunlight</strong> and diet<br>  • D₂ and D₃ are <strong>biologically inactive</strong></p><p><strong>Active Form</strong><br>  • <strong>Calcitriol</strong> → <strong>1,25-dihydroxycholecalciferol</strong><br>  • Also called <strong>1,25-dihydroxyvitamin D₃</strong> or <strong>1,25(OH)₂D</strong><br>  • <strong>Calcitriol</strong> is the biologically active form</p><p><strong>Vitamin D Activation</strong><br>  1. <strong>UV-B</strong> radiation reaches the <strong>skin</strong><br>  2. UV-B initiates conversion of <strong>7-dehydrocholesterol → vitamin D₃</strong> (cholecalciferol)<br>  3. In the <strong>liver</strong>, vitamin D₃ → <strong>25-hydroxyvitamin D₃</strong> (calcidiol or <strong>25(OH)D<sub>3</sub></strong>)<br>  4. In the <strong>kidney</strong>, 25-hydroxyvitamin D₃ → <strong>1,25-hydroxyvitamin D₃</strong> (calcitriol or <strong>1,25(OH)₂D<sub>3</sub></strong>)</p><p><strong>Main Function of Calcitriol</strong><br>  • <strong>Calcitriol regulates calcium and phosphorus (Ca/P)</strong></p>
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Vitamin D – Dietary Requirement

Mammals
  • Vitamin D is only required in the diet for mammals with insufficient sun exposure
  • Polar regions
  • Fossorial/subterranean → live or spend most time underground
  • Nocturnal → active at night

Vitamin D₃
  • Essential for amphibians, birds, and reptiles
  • These animals cannot use vitamin D₂

Mammals
  • Can use vitamin D₂ or D₃

<p><strong>Mammals</strong><br>  • Vitamin D is only required in the <strong>diet</strong> for mammals with <strong>insufficient sun exposure</strong><br>  • <strong>Polar regions</strong><br>  • <strong>Fossorial/subterranean</strong> → live or spend most time underground<br>  • <strong>Nocturnal</strong> → active at night</p><p><strong>Vitamin D₃</strong><br>  • <strong>Essential</strong> for <strong>amphibians, birds, and reptiles</strong><br>  • These animals <strong>cannot use vitamin D₂</strong></p><p><strong>Mammals</strong><br>  • Can use <strong>vitamin D₂ or D₃</strong></p>
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Vitamin D – Toxicity and Deficiency

Toxicity
  • Hypervitaminosis D → too much vitamin D, causing hypercalcemia
  • Calcium builds up in soft tissues and organs

Deficiency
  • Rickets → soft bones in young animals
  • Osteomalacia → brittle bones in adults

<p><strong>Toxicity</strong><br>  • <strong>Hypervitaminosis D</strong> → too much vitamin D, causing <strong>hypercalcemia</strong><br>  • <strong>Calcium builds up</strong> in soft tissues and organs</p><p><strong>Deficiency</strong><br>  • <strong>Rickets</strong> → <strong>soft bones</strong> in young animals<br>  • <strong>Osteomalacia</strong> → <strong>brittle bones</strong> in adults</p>
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Vitamin E

Function
  • Antioxidant
  • Inhibits or prevents oxidative damage
  • Scavenges free radicals → unstable or reactive atoms

Forms

Tocopherols
  • Alpha, beta, gamma, delta
  • Organic compounds with various methylated phenols
  • Alpha-tocopherol = most active form of vitamin E

Tocotrienols
  • Alpha, beta, gamma, delta

<p><strong>Function</strong><br>  • <strong>Antioxidant</strong><br>  • Inhibits or prevents <strong>oxidative damage</strong><br>  • <strong>Scavenges free radicals</strong> → unstable or reactive atoms</p><p><strong>Forms</strong></p><p><strong>Tocopherols</strong><br>  • <strong>Alpha, beta, gamma, delta</strong><br>  • Organic compounds with various <strong>methylated phenols</strong><br>  • <strong>Alpha-tocopherol</strong> = most active form of vitamin E</p><p><strong>Tocotrienols</strong><br>  • <strong>Alpha, beta, gamma, delta</strong></p>
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Vitamin E – Toxicity and Deficiency

Toxicity
  • Hypervitaminosis E → too much vitamin E
  • Can counteract vitamin K actions → affects blood coagulation

Deficiency
  • Muscular dystrophy → muscle weakness and paralysis
  • Nerve damage
  • Infertility in rats and birds

<p><strong>Toxicity</strong><br>  • <strong>Hypervitaminosis E</strong> → too much vitamin E<br>  • Can <strong>counteract vitamin K</strong> actions → affects <strong>blood coagulation</strong></p><p><strong>Deficiency</strong><br>  • <strong>Muscular dystrophy</strong> → muscle weakness and paralysis<br>  • <strong>Nerve damage</strong><br>  • <strong>Infertility</strong> in rats and birds</p>
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Vitamin K

Function
  • Coagulation → blood clotting

Sources

Vitamin K₁ – Phylloquinone
  • Found in leaves of green plants

Vitamin K₂ – Menaquinone
  • Found in animal tissue and gut bacteria
  • Animal tissue and gut bacteria can convert K₁ → K₂

Vitamin K₃ – Menadione
  • Synthetic precursor
  • Inactive in its synthetic form
  • Plants and bacteria can activate it
  • Animals cannot activate it

<p><strong>Function</strong><br>  • <strong>Coagulation</strong> → blood clotting</p><p><strong>Sources</strong></p><p><strong>Vitamin K₁ – Phylloquinone</strong><br>  • Found in <strong>leaves of green plants</strong></p><p><strong>Vitamin K₂ – Menaquinone</strong><br>  • Found in <strong>animal tissue</strong> and <strong>gut bacteria</strong><br>  • Animal tissue and gut bacteria can convert <strong>K₁ → K₂</strong></p><p><strong>Vitamin K₃ – Menadione</strong><br>  • <strong>Synthetic precursor</strong><br>  • Inactive in its <strong>synthetic form</strong><br>  • <strong>Plants and bacteria</strong> can activate it<br>  • <strong>Animals cannot</strong> activate it</p>
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Vitamin K – Toxicity and Deficiency

Toxicity
  • K₁ and K₂ are innocuous → not harmful, even in very large amounts
  • K₃ can be toxic
  • K₃ is no longer used as a supplement

Deficiency
  • Increased risk of hemorrhage or excessive bleeding

<p><strong>Toxicity</strong><br>  • <strong>K₁ and K₂</strong> are <strong>innocuous</strong> → not harmful, even in very large amounts<br>  • <strong>K₃</strong> can be <strong>toxic</strong><br>  • K₃ is <strong>no longer used as a supplement</strong></p><p><strong>Deficiency</strong><br>  • Increased risk of <strong>hemorrhage</strong> or <strong>excessive bleeding</strong></p>