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73 Cards in this Set

  • Front
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Proteins
large complex molecules composed of amino acids.
-Contain carbon, hydrogen, oxygen, nitrogen
-Primary source of nitrogen in our diets
-20 different amino acids are used to make proteins
Essential amino acids
-Cannot be produced by our bodies
-Must be obtained from food
Nonessential amino acids
Can be made by our bodies
How are Proteins Made?
Proteins are long chains of amino acids.

Amino acids are joined to each other by peptide bonds.

The structure of each protein is dictated by the DNA of a gene.
Protein Synthesis
Protein synthesis can be limited by missing amino acids
-if we do not consume adequate amounts of the essential amino acids, or do not consume adequate energy overall
Limiting amino acid
the amino acid that is missing or in the smallest supply
Incomplete protein:
does not contain all essential amino acids.
-Not sufficient for growth and health
-Considered a “low quality” protein
Complete protein
contains sufficient amounts of all 9 essential amino acids
-Considered a “high quality” protein
Mutual supplementation:
using two incomplete proteins together to make a complete protein.
Complementary proteins
two protein sources that together supply all 9 essential amino acids.
ex. beans and rice
Digestion of Proteins
Digestion of proteins begins in the stomach.
-Hydrochloric acid breaks down protein structure
-Hydrochloric acid activates pepsin
Digestion of proteins continues in the small intestines.
-Pancreatic enzymes called proteases complete the digestion of proteins into single amino acids
Pepsin
: an enzyme that breaks down proteins into short polypeptides and amino acids.
process of digestion of protetins
Absorption of Proteins
In the LIVER:
Absorbed amino acids are transported by blood to liver and taken up for conversion into whichever amino acids are needed for body

Excess amino acids can also be converted to fat or glucose and stored in the body, or broken down for energy
Absorption of Proteins
In the LARGE INTESTINE:
proteins from food are not present in large intestine

proteins present in feces come from bacterial cells and from sloughed intestine cells
Storage of Proteins
No storage, unlike that for carbohydrates and lipids

Used to build muscle and organ tissue

Contributes to amino acid pool
Functions of Proteins
Cell growth, repair, and maintenance:
Proteins in our bodies are constantly being broken down, repaired and replaced

Structures:
Important in cell membranes (as lipoproteins); bone and tooth matrix; collagen (skin, bone, muscle filaments, nails, hair)

Hormones :
act as messengers and regulators in the body

Enzymes:
a protein which serves to speed up a biochemical reaction
Most enzyme names end in –ase, such as lactase
Fluid Balance
(func. of pro)
-Protein works to keep a balance of fluid in the cells, the space surrounding the cells and in the blood.
-If the concentration of protein is too low to draw fluid from the tissues and across the blood vessel walls; it causes fluid to collect in the tissues, causing edema.
Electrolyte Balance
(func. of pro)
-Transport proteins maintain the proper balance of sodium and potassium throughout the body and across cell membranes
-If protein intake is insufficient, this balance may be lost, resulting in changes in the rhythm of the heart
Immune function
(func. of Pro)
Antibodies
-chemicals that attack invading cells or molecules)
made up of proteins
-If we do not consume enough protein, our resistance to certain diseases is weakened.
pH Balance
(func. of pro)
-Proteins act as buffers by helping to maintain proper acid-base balance
-Proteins attach or release hydrogen ions as the blood acidity changes
How Much Protein Should We Eat?
Recommended Dietary Allowance (RDA)
0.8 grams protein per kg body weight
12-20% of total energy intake should be from protein
Can You Eat Too Much Protein?
High cholesterol and heart disease
Diets high in protein from animal sources are associated with high cholesterol
Possible bone loss
High protein diets MAY cause excess calcium excretion leading to bone loss
-Kidney disease
Vegetarianism
restricting the diet to foods of plant origin.
Protein-energy malnutrition
: a disorder caused by inadequate intake of protein and energy.'
two forms:
Marasmus
Kwashiorkor
Marasmus
disease resulting from severely inadequate intakes of protein, energy, and other nutrients
symptoms:
Severe wasting of muscle tissue
Stunted physical growth
Stunted brain development
Anemia
Kwashiorkor
disease resulting from extremely low protein intake.
Genetic Disorders
Phenylketonuria (PKU)
Phenylketonuria:
Inherited disease
Individual cannot break down amino acid phenylalanine
Phenylalanine builds up in the body and can result in brain damage if untreated
Must follow diet that is very low in phenylalanine
Genetic Disorders
Sickle Cell Anemia
Inherited disorder
Causes red blood cells to be sickle- or crescent-shaped
Due to a change in an amino acid in hemoglobin
Cells rupture easily and become clogged in blood vessels
Genetic Disorders
Cystic Fibrosis
Inherited disease
Affects respiratory system and digestive tract
Caused by abnormal protein that prevents the normal passage of chloride into and out of cells
Lipids
diverse class of molecules that are insoluble in water.

Lipids (fats) do not dissolve in water.
Three types of lipids
Triglycerides
Phospholipids
Sterols
Triglycerides composed of:
-Three fatty acid molecules
Fatty acids are long chains of carbon atoms surrounded by hydrogen atoms
*One glycerol molecule
Glycerol is a 3-carbon alcohol that is the backbone of a triglyceride
Saturated fatty acids
have hydrogen atoms surrounding every carbon in the chain.
Monounsaturated fatty acids
lack hydrogen atoms in only one region
Polyunsaturated fatty acids
lack hydrogen atoms in multiple locations.
Hydrogenation
The addition of hydrogen atoms to unsaturated fatty acids.
Coverts liquid fats (oils) into a more solid form
Used to create margarine from plant oil
Often creates trans fatty acids
Phospholipids
re composed of
Glycerol backbone
2 fatty acids
Phosphate
Are soluble in water
Are manufactured in our bodies so they are not required in our diet
Sterols
Lipids containing multiple rings of carbon atoms.

-Are essential components of cell membranes and many hormones
-Are manufactured in our bodies and therefore are not essential components of our diet
Digestion of Fats
Fats are not digested and absorbed easily because they are insoluble in water.

Very little digestion of fats occurs in the watery environments of the mouth or stomach.

Digestion of fats primarily begins in the small intestine.
Digestion of Fat diagram
Digestion of Fat in:
Small intestine
As fat enters the small intestine
Bile is secreted from the gall bladder into the small intestine
Bile is produced by the liver and stored in the gall bladder
Bile disperses fat into smaller fat droplets
Pancreatic enzymes break fat into 2 separate fatty acids and a monoglyceride
Single fatty acids and monoglycerides are packaged into micelles, along with bile, and taken to cell walls of small intestine.
Chylomicron:
A lipoprotein produced by cells lining the small intestine.
Essential fatty acids
Alpha-linolenic acid (omega-3 fatty acid)
Found in vegetables, fish and fish oils
Linoleic acid (omega-6 fatty acid)
Found in vegetable and nut oils
Fat-soluble vitamins
Vitamins A, D, E, and K are soluble in fat; fat is required for their transport
How Much Fat?
The Acceptable Macronutrient Distribution Range (AMDR) for fat:
20-35% of calories should be from fat
The type of fat consumed
-Saturated fat should be no more than 7% of total calories.
-Trans fatty acids should be reduced to the absolute minimum.
-Most fat in our diets should be from monounsaturated fats (eg., olive oil).
Health Problems from Fat
Cardiovascular disease
Dysfunction of the heart or blood vessels
Can result in heart attack or stroke
Blood lipids include
Chylomicrons
VLDLs – very low-density lipoproteins
LDLs – low-density lipoproteins
“bad cholesterol”
HDLs – high-density
EFFECTS of SATURATION on LIPOPROTEIN LEVELS
Saturated and trans fatty acids
- Increase LDL and decrease HDL cholesterol output
Polyunsaturated fatty acids
- Decrease LDL and HDL cholesterol levels
Monounsaturated fatty acids
-Decrease LDL without lowering HDL cholesterol
Vitamins
13 known vitamins.
Vitamins – Major Functions
Anitoxidation: the prevention of unwanted oxidation of compounds in body

production and release of energy

regulation of growth and development

Hematopoiesis: the production of red blood cells and the hemoglobin contained in them
Vitamin K
Phylloquinone – plant form of vitamin K
Menaquinone – form of vitamin K produced by bacteria in the large intestine
Functions of vitamin K
Blood coagulation
Bone metabolism


Recommended intake
There is no RDA for vitamin K.
AI values are 120 mg/day for men and 90 mg/day for women.

Sources of vitamin K
Green leafy vegetables, vegetable oils
Cancer
a group of related diseases characterized by cells growing out of control.

Composed of three steps:
Initiation
Promotion
Progression
Antioxidants may work by
Antioxidants may contribute to reducing the risk of cancer.

Enhancing the immune system
Inhibiting growth of cancer cells
Preventing oxidation damage to cells
Cardiovascular disease (CVD)
The leading cause of death
Includes heart disease, hypertension, atherosclerosis
Can lead to heart attack or stroke
Risk factors include smoking, obesity, hypertension, high LDL levels, low HDL levels, inactivity, diabetes
4 major functions if Vitamins:
-Serving as antioxidants to prevent unwanted oxidation of other compounds
-Regulation of growth and development
-Hematopoiesis (production of red blood cells)
-Production or release of energy from other substances such as lipids, carbohydrates, and proteins (vitamins do NOT supply energy themselves)
Vitamins Fat soluable
A, D, E, K
regulate and promote growth and development; antioxidant
Water soluble vitamins
B, C
energy production, hematopoiesis, antioxidant, regulate metabolism
Provitamin
can be converted to active vitamin in the body
Where does most absorption of vitamins take place?
Small intestine – almost all absorption takes place here
Vitamin E
Primary role is as an antioxidant
Protects poly-unsaturated fatty acids (PUFAs)
Protects low-density lipoproteins (LDLs)

Recommended Intake
15mg alpha-tocopherol per day
Upper limit (UL) is 1,000 mg per day

Sources of Vitamin E
Vegetable oils, nuts, seeds, wheat germ, soybeans
Vitamin C
Vitamin C is a water-soluble vitamin that must be consumed in the human diet.

Functions of Vitamin C
Antioxidant
Synthesis of collagen
Prevents the disease scurvy
Enhances the immune system

Recommended intake
90 mg/day for men; 75 mg/day for women
Smokers need an extra 35 mg/day

Sources of vitamin C
Fresh fruits and vegetables
(Cooking destroys the vitamin C)
Beta-carotene
provitamin
Functions of beta-carotene
A weak antioxidant
Effective against oxidation in cell membranes and LDLs
Carotenoids in general are known to
Enhance the immune system
Protect skin from damage by UV light
Protect eyes from damage
Vitamin A
Excess vitamin A is stored in the liver, adipose tissue, kidneys, and lungs.
There are 3 active forms of Vitamin A:
Retinol
Retinal
Retinoic acid

Functions of vitamin A
Essential to proper vision
Antioxidant, protecting LDL cholesterol
Cell differentiation – the process by which cells mature and specialize
Sperm production and fertilization
Bone growth

Recommended intake
RDA is 900 mg/day for men; 700 mg/day for women

Sources of vitamin A
Obtained from animal sources (liver, eggs) and plant sources (dark green, orange, and deep yellow fruits and vegetables)

-highly toxic
Antioxidation
is the prevention of “unwanted” oxidation of compounds in the body
B-complex vitamins
are especially important for energy metabolism
Beriberi
deficiency of thiamin resulting
Riboflavin
Is part of coenzymes involved in oxidation-reduction reactions
Is part of the antioxidant enzyme glutathione peroxidase
Milk is a good source of riboflavin
Ariboflavinosis – riboflavin deficiency; sore throat, swollen mucous membranes
Niacin
Coenzyme assisting with metabolism of carbohydrates and fatty acids
Good sources: meat, fish, poultry, enriched bread products
Toxicity can result from supplements
Pellagra – severe niacin deficiency
Folate
Involved in DNA synthesis, amino acid metabolism
Critical for cell division of very early embryos
Good sources: ready-to-eat cereals, enriched bread products
Toxicity can mask vitamin B12 deficiency
Pantothenic acid
Component of coenzymes for fatty acid metabolism
Required for building new fatty acids
Good sources: chicken, beef, egg yolk, potatoes, oat cereals, tomato products
No toxicity from excess pantothenic acid
Deficiencies are very rare
Vitamin D
Excess is stored in liver and fat tissue
Can be synthesized by the body by exposure to UV light from the sun
Is a hormone since it is synthesized in one location and acts in another location

Functions of vitamin D
Required for calcium and phosphorus absorption
Regulates blood calcium levels
Stimulates osteoclasts
Necessary for bone calcification

The RDA for vitamin D ranges from 400 – 600 IU a day depending on age and gender.