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Monosaccharies
Glucose
Fructose
Galactose
Disaccharides
Maltose
Sucrose
Lactose
high fructose corn syrup
syrup obtained from the processing of corn
nutritive sweeteners
substances that sweeten and contribute energy to foods
Added sugars
sugars added to foods during processing or preparation
Alternative/Artificial sweeteners
substances that sweeten food and provide few to no calories
sugar alcohols
used to replace sucrose in some sugar-free foods
sorbitol, xylitol, mannitol
nonnutritive sweeteners (high-intensity)
group of compounds that are intensely sweet tasting compared to sugar
PKU
Improper phenylalanine metabolism
testing in all infants born in the US
Oligosaccharides
3-10 monosaccharides bonded together
Polysaccharides
10+ monosaccharides
starch
glycogen
dietary fiber
Fiber AI
38 g for men
25 g for women
typical americans 16 g
Whole grains vs refined grains
the FDA allows products made from ground cereal grains to be labeled as whole grains if they contain the same proportions as in the intact grain
tips to reduce sugar intake
replace sugar drinks with water
add fruit to drinks
read labels
replace drinks with naturally flavored water
salivary amylase
enters the stomach acidic environment to aid starch digestion
Pancreatic amylase
enzyme secreted by the pancreas that breaks down starch
maltose monosaccarides
Glucose and glucose
Sucrose monosaccharides
glucose and fructose
lactose monosaccharides
glucose and galactose
transport of monosaccharides to the liver
monosaccharides enter capillary network of villus
transported to the liver via hepatic portal vein
used by liver to make glycogen or fat
released into bloodstream
insulin
hormone secreted from the BETA cells of the pancreas that contributes to a decrease in blood glucose levels
Glucagon
hormone secreted from the ALPHA cells of the pancreas that contributes to an increase in blood glucose levels
Lipolysis
breaking down stored triglycerides in adipose tissue into free fatty acids and glycerol to provide energy, primarily during fasting or exercise
Ketogenic diet
high-fat, moderate-protein, and very low-carbohydrate eating plan designed to shift the body’s metabolism into a state of ketosis, where it burns fat for fuel instead of glucose.
ketosis
state where the body burns fat for fuel instead of carbohydrates (glucose), producing ketones in the liver
Ketone bodies
molecules formed from fat metabolism that can be used as an alternative fuel for certain cells in the body when glucose levels are low
ketogenesis
metabolic pathway in liver mitochondria that produces ketone bodies
ketoacidosis
condition in which ketone bodies accumulate in the blood
excessive ketone boides acidify the blood
symptoms
vomoting
exessive thirst
sudden weight loss
stomach pain
loss of consciousness
diabetes mellitus
group of chronic conditions characterized by abnormal glucose, fat and protein metabolism
hyperglycemia
typical symptoms of poorly controlled type 1 rather than type 2 diabetes
Normal levels of glucose
70-99
pre diabetes glucose levels
100-125
diabetes glucose levels
126
Type 1 diabetes
autoimmune disease that results in destruction of the beta cells of the pancreas
insulin must be supplied
Type 2 diabetes
treatment may involve diet, exercise, insulink injections, and oral medications
GLP 1s
stimulate insulin release and inhibit glucagon release
lowering of blood glucose
Carbohydrate counting
diabetes management tool in which an individual tracks his or her daily carb intake
meal should focus on
whole grains
veggies
fruit
poultry
fish
etc
Glycemic index
anks carbohydrate-containing foods from 0 to 100 based on how quickly they raise blood sugar levels
low <55
medium 56-69
high 70>
hypoglycemia
a condition that occurs when blood glucose level is too low
Epinephrine
hormone produced by the adrenal glands
secreted in response to decreasing blood glucose
metabolic syndrome
cluster of conditions that increases the risk of type 2 diabetes and CVD
large waist circumference
high fasting blood glucose
chronically elevated blood pressure
chronically elevated fasting blood fats
to be diagnosed you need 3 signs
Lactose intolerance
the inability to digest lactose (milk sugar) due to insufficient lactase enzymes in the small intestine
functions of lipids
cushion the body
insulation
produce steroid hormones
provide and store energy
fatty acid
hydrocarbon chain found in lipids
short chain fatty acid
2-4 carbons
medium chain
6-12 carbons
long chain
14-24 carbons
fatty acids are identified by
number of double bonds and type of bond
saturated fatty acid
hydrocarbon chain is filled with hydrogen
solid at room temo
unsaturated fatty acid
monounsaturated: 1 double bond
polyunsaturated: 2+ double bond
Omega 6 (linoleic)
18 carbon polyunsaturated with 2 double bonds
omega 3
18 carbon polyunsaturated with 3 double bonds
essential fatty acids
omega 3s and 6s
deficiency signs
scaly skin, hair loss, poor wound healing
cis fatty acids
most naturally occuring unsaturated fatty acid
trans fatty acid
have hydrogen atoms of the double bonded carbons on opposite sides of hydrocarbon chain
partial hydrogenation
manufacturing process that adds hydrogen atoms to liquid veg oil forming trans fats
triglycerides
3 fatty acids + glycerol
glycerol
a three carbon alcohol that forms the backbone of fatty acids
emulsifier
substance that keeps water soluble and water insoluble components mixed
cholesterol
lipid found in animal foods
needed to produce steroid homorones, bile and vitamin D
sterols
lipids with a more complex structure than triglycerides and phospholipids
plant sterols
chemical found in plants that are structurally similar to cholestorol
lipases
inguinal lipase
acidity of the stomach activates the lipase which begins fat digestion
small intestine
primary site of lipid digestion
secretin
stimulates the liver to produce bile and the pancrease to screte bicarbonate pancreatic juice
cholecystokinin (CCK)
stimulates bile release
bile salts
a component of bile, aids in lipid digestion by emulsifying
pancreatic lipase
absorbed as fatty acids, monoglycerides, cholesterol, and phospholipid fragments
end procdues of lipid digestion
free fatty acids, monoglycerides, glycerol, cholesterol, and phospholipid fragement
after absorption the contents are reassembled into tri and phospholipids
lipoproteins
water soluble molecules that transport lipids through the blood
chylomicron
type of lipoprptein formed in enterocytes, but are too large for blood stream
lacteal
to the thoracic duct, entering the blood stream through the left subclavian vein
Very low density lipoprotein
made in the liver
carries much of the triglycerides in the bloodstream
low density lipoprotein
carries cholesterol into tissues
high density lipoprotein
transports cholesterol away from tissues and to the liver for elimination, ,and contains the most protein
total fat percent
20-35 % of calories
saturated fat percent
less than 10%
polypeptides
50+ amino acids
functions of protein
enzymes
clotting compounds
movement
energy source
builds new cells
amino acid structure
amino or nitrogen containing group
carbon skeleton
legumes
plants that produce pods with a ingle row of seeds
complete protein
adequate proportion of the 9 essential amino acids
high quality protein
complete proteins that have high bioavailiability
protein digestions begins where
in the stomach
trypsin and chymotrypsin
break down polypeptides into shorter peptides and amino acids
gluconeogeneisis
if not enough carbs are ingested, the body will turn to this process.
creating new glucose from non carb sources
fate of extra amino acids
unnecessary amino acids are borken down forming waste products
ammonia
urea
Blood urea nitrogen
assess kidney function
urine urea nitrogen
a marker of protein intake
complementary protein combinations
combining certain plant foods to provide all essential amino acids
maramus
results from starvation
diet lacks energy and nutrients
Kwashiokor
results from consuming adequate energy but low protein
maramic kwashiorkor
child with kwash who then starts to under consume energy
PKU
genetic metabolic disorder characterized by the inability to convert the amino acid phenylalanine resulting in accumulation of protein the the brain