1 sugar molecule and can be directly absorbed into bloodstream to be brought to liver for energy (ATP) or storage:
Glucose
Fructose
Galactose
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Disaccharides
2 sugar molecules:
Sucrose
Maltose
Lactose
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Complex Carbohydrates
Larger, several sugar molecules (vegetables), less sweet.
Starches
Fiber
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Glycogen
Not dietary, built in the body from carbs we eat, & is how carbs are stored. Process of production known as glycogenesis where glucose molecules are combined.
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Glucose
Basic unit of many sugars & primary energy source for all cells. Necessary for blood contents (blood sugar).
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Fructose
Naturally found in fruits, honey & some vegetables. Tastes sweeter than glucose, converted to glucose in the body.
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Galactose
Not commonly found in foods, except milk (component of lactose).
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Refined Sugars
Must be limited, less nutritional value, mostly added just for taste.
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Polysaccharides
10+ monosaccharides bound together (starches & fiber), nutritive.
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Nutritive
Contributes energy to our foods (4kcal for carbs).
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Carbohydrate Storage
Animals: glycogen, can only produce so much and will begin to store as fat when in excess.
Plants: starch/fiber
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Fiber
Supportive structures in plants, most are not digestible by the human body (cellulose, pectin, & lignins). Better to increase slowly.
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Functions of Fiber
Feeds gut bacteria
Reduces blood cholesterol
Slows glucose absorption
Reduces constipation
Prevents diverticulitis
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Soluble Fiber
Dissolves, forms a gel during digestion
Slows absorption of sugar
Delays stomach emptying so you feel fuller
Can lower blood cholesterol
(oatmeal, fruits, seeds)
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Insoluble Fiber
Does not dissolve well in water
Adds bulk to digestive tract
Helps movement through GI tract
Prevents or alleviates constipation
(rice, wheat, vegetables)
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Fermentability
Ability to be fermented/eaten by gut bacteria in order to provide energy for gut bacteria (not us), leading to a healthy gut microbiome. Byproducts may provide us with health benefits.
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Lactose
Disaccharide that is broken down by lactase in the small intestine to form glucose and galactose.
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Maltose
Disaccharide that is broken down by maltase in the small intestine to form glucose.
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Sucrose
Disaccharide that is broken down by sucrase in the small intestine to form glucose and fructose.
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Adipose Tissue
Carbohydrates are stored in this way when all glycogen has been made.
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Insulin
Hormone produced by the beta cells in the pancreas, travels through the bloodstream, and acts as a key to allow certain cells to absorb and store glucose. When in lack, glucose cannot enter certain cells, and as a result, collects in the blood.
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Glycogenesis
Production of glycogen to store extra glucose energy.
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Lipogenesis
Production of fat to store extra glucose.
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Blood Glucose
70/110 mg/dl, regulated by insulin. Cells need energy from glucose in the blood stream in order to function.
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Symptoms of High Blood Sugar
Thirst
Headaches
Trouble Concentrating
Blurred Vision
Frequent Urination
Fatigue
Can lead to diabetes, heart disease, or damage to blood vessels
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Symptoms of Low Blood Sugar
Shaking
Sweating
Headaches
Hunger
Fatigue
Fainting
Can lead to death in severe cases because cells need energy to function
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When Blood Glucose is Low
1) The pancreas is alerted of low glucose levels
2) Alpha cells in the pancreas release glucagon
3) Glucagon stimulates cells to release glucose (from glycogen) into the blood
4) Blood glucose is regulated
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When Blood Glucose is High
1) The pancreas is alerted of high glucose levels
2) Beta cells in the pancreas release insulin
3) Insulin stimulates cells to absorb glucose
4) Blood glucose is regulated
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Glucagon
Secreted by the alpha cells in the pancreas when glucose levels are low. Activates glycogen to be broken down and used to energize cells.
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Glycogenolysis
Breakdown of glycogen to form glucose.
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Lipolysis
Breakdown of fat molecules.
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AMDR for Carbohydrates
45-65% of total calories should come from carbohydrates (roughly half, or slightly more).
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Type I Diabetes
Autoimmune disease that damages beta cells of the pancreas, therefore, little to no insulin can be produced. Can continue to have a normal diet but must be conscious and use insulin.
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Hypoglycemia
Low blood glucose (< 70 mg/dl), can result from taking too much insulin.
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Type II Diabetes
Beta cells can successfully produce insulin, but cells do not respond and are unable to absorb glucose (insulin resistance). No certain cause, but it’s necessary to be conscious that carb intake is spread throughout the day. Diet and exercise is also beneficial.
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Hyperglycemia
High blood glucose; can cause complications and lead to blood vessel damage in untreated cases.
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Gestational Diabetes
Diabetes formed during pregnancy. Often resolves post-partum, but increases the risk of developing type II diabetes.
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Lipids
Not soluble in water and associates with self (in droplets). Oils, spreads, dairy, fatty fish, avocados, and nuts.
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Functions of Lipids
Reserves energy \n Cushions organs \n Insulation \n Signal transduction \n Cell membrane structure & function \n Component of other compounds (e.g., bile, \n vitamin D) \n Absorption & transport of fat-soluble vitamins
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Fatty Acids
Chains of carbon, hydrogen & oxygen that can be saturated of unsaturated.
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Short-Chain Fatty Acids
SCFA, 2-4 carbons.
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Medium-Chain Fatty Acids
MCFA, 6-10 carbons.
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Long-Chain Fatty Acids
LCFA, 12-24 carbons. Most naturally-occurring fatty acids in food are long-chain with an even number of carbons.
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Saturated Fat
Full, no room for more hydrogens. There are no double bonds in the fat molecule, meaning molecules can lay flat against one another and form a solid substance.
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Unsaturated Fat
The fat molecule has one or more double bonds, creating a bend in the molecule’s shape and a more liquified substance.
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Monounsaturated Fat
MUFA, there is one double bond and is liquid at room temperature, but will become solid if refrigerated (olive oil, canola oil, peanut oil, sesame oil).
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Polyunsaturated Fatty Acids
PUFA, two or more double bonds resulting in a liquid substance at room temperature or when refrigerated. Usually of plant origin (corn oil, safflower oil).
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Essential Fatty Acids
Long-Chain, PUFA fatty acids that must be obtained from the diet. Omega-3 and Omega-6 help with cell communication, inflammation, and blood clotting.
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Omega-3
Linolenic acid; mostly anti-inflammatory and prevents blood clotting (poultry, eggs, avocado, nuts, cereals, whole-grain breads, and vegetable oils). 0.6-1.2% of daily kcals.
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Omega-6
Linoleic acid; pro-inflammatory, anti-inflammatory, and promotes blood clotting (fatty fish, human milk, fortified eggs, flaxseed, walnut, canola, and soybean). 5-10% of daily kcals.
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Trans Fatty Acids
Unsaturated; do not serve a useful purpose in the body but used for rancidity resistance, spreadability, and higher smoking point in food production.
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Partial Hydrogenation
Process of forming trans fats, adding hydrogen to the molecule to flip the double bond and make the shape more straight.
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Total Fat
AMDR is 20-35% of daily calories.
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Triglycerides
TG; major form of fat in foods and storage of lipids. Contains 3 fatty acids and can be broken down to form ATP.
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Glycerol
3 carbon molecule that binds tryglycerides.
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Functions of Tryglycerides
Provides energy (9 kcal/gram)
Allows body to store energy
Pads organs
Insulates the body
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Visceral Fat
Fat surrounding the organs.
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Phospholipids
Forms structure of cell membrane (lipid bilayer). Facilitates nerve function, transportation of fat-soluble nutrients, and emulsification. Head is hydrophilic (interacts with water), and tails are hydrophobic (repels water).
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Sterol
Large, lipid molecules. Gives cell membranes flexibility and makes bile, vitamin D, and hormones.
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Cholesterol
No specific recommendation, but minimize intake within context of a healthy diet. Body can make its own cholesterol (made by liver).
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Stomach
Begins lipid digestion by clumping contents together through mechanical digestion.
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Lingual Lipase
Enzyme that leads to minor lipid digestion in the mouth (mostly in infants).
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Small Intestine
Where most lipid digestion occurs. Lipids are emulsified by bile and digested by lipase into absorbable fatty acids.
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Emulsification
Breaking lipids down into smaller droplets.
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Micelles
Emulsified lipid droplets surrounded by water in the small intestine.
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Bile
Made up of cholesterol and phospholipids to emulsify lipids.
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Pancreatic Lipase
Made in the pancreas and active in the small intestine to break triglycerides into fatty acids and then glycerol.
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Chylomicron
Lipoprotein package of reassembled lipids made up of cholesterol, proteins, and phospholipids to transport lipids to lymphatic system and ultimately the blood stream.
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Adipocytes
Adipose/fat cells; we can continue to store almost endless amounts of fat as energy. Fat cells continue to grow until they divide to form new ones.
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Fed State
Anabolic (building up) state after a meal. Excess energy, increased glucose levels, and insulin released. Insulin encourages adipocyte production/lipid storage.
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Fasting State
Catabolic (breaking down) state between meals or during exercise. Lack of energy and glucagon released. Glucagon encourages lipolysis and ATP production.
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Lipogenesis
The creation of fat storage (adipocytes).
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Lipolysis
The break down of fat storage.
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LDL Lipoproteins
Low-density lipoproteins; carry cholesterol and are harmful in excess. Releases cholesterol into the bloodstream for cells to absorb.
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HDL Lipoproteins
High-density lipoproteins; carry cholesterol and are less detrimental to health when in excess. Fill up with cholesterol to transport excess in the bloodstream.
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Consequences of Too Little Fat
Infertility
Amenorrhea
Decreased bone density
Poor cognitive development & concentration
Decreased immunity & growth
Poor vision
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Consequences of Too Much Fat
Cardiovascular Disease (leading cause of death in U.S.)
Diabetes
Cancer
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Cardiovascular Disease
Leading cause of U.S. adults (1/4). Characterized by blood vessels clogged with excess lipid, damaged vessels, or other heart issues.
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Atherosclerosis
First stage of CVD. Buildup of fats, cholesterol, and other \n substances in and on artery walls; forming “plaques” and restricting blood flow.
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Cardiovascular Disease Risk Factors
High blood pressure
High LDL cholesterol
Smoking
Diabetes (blood vessel damage)
Overweight and obesity
Poor diet (high trans/sat fat, high cholesterol, low omega 3)
Physical inactivity
Excessive alcohol use
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Protein
Made up of amino acids, about 50,000 kinds in our bodies. Is not stored beyond body’s usage, but made whenever necessary. 1+ polypeptides linked and folded into a 3D shape.
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Function of Proteins
Structure/movement
Molecule/nutrient transport
Facilitate chemical reactions
Support immune system
Allow body to adapt
Maintain fluid balance in bloodstream
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Protein Recommendations
Vary sources
5\.5oz daily
8oz seafood weekly
5oz nuts/seeds/soy products weekly
lbs / 2.2 = kg, kg x 0.8 = #g
Athletes, malnourished, energy restrictive diets, and older adults need more
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Sources of Protein
Meat
Fish
Dairy
Eggs
Soy
Quinoa
Amaranth
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Typical Protein Intake (for Americans)
Males: >100g/day
Females: >70g/day
Too much!!!
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Protein Deficiency Diseases
Occur when there is a lack of protein in the diet (Protein Malnutrition). Common in those with wasting diseases, with anorexia, in impoverished areas, U.S. homeless, children of the working class/poor.
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Kwashiorkor
Type of protein energy malnutrition where there is an inadequate protein intake or severe infection. It is acute and more common in young children. Caloric/other macronutrient intake may be adequate, but protein is not. Symptoms include:
Muscle wasting
Edema
Fatty liver
Inability to heal wounds
Loss of hair pigmentation
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Edema
Build up of fluid in the interstitial space (between blood and cells) that leads to swelling when there is a lack of protein. Protein creates pressure in the bloodstream and maintains the distribution of fluids.
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Marasmus
Chronic protein energy malnutrition characterized by a general lack of food/energy intake, not just protein. Symptoms include:
Impaired growth
Little subcutaneous fat\*
Slowed metabolism/lower body temp
Impaired brain development
Impaired immunity
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Amino Acids (AA)
Amino “nitrogen containing” acids are the basic unit of proteins. 20 are essential (from diet), 11 are made in the body. Every protein you eat is digested into amino acids. Each amino acid has a very specific structure and function.
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Amino Acid Structure
Contain an amino group, an acid, a carbon, and an “R Group” that determines the type of amino acid.
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Methionine
Usually first AA in a protein, donor of methyl groups.
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Phenylalanine/Tyrosine
AA that makes epinephrine, melanine, and thyroid hormone.
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Tryptophan
Synthesizes serotonin into melatonin.
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Peptide Bonds
Bind amino acids together to form a peptide; which is then folded into a protein.
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Transcription
Creating a copy of the DNA with mRNA and transporting it out of the nucleus so that the DNA does not have to leave the nucleus.
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Translation
A ribosome binds to the RNA at a specific codon to use tRNA to make amino acids.