carbohydrates
monosaccharides - glucose, fructose, galactose
disaccharides - two monomers linked through glycosidic linkage
maltose (2 glucose)
alpha 1,4 glycosidic linkage
malted grain
partial digestion
sucrose (glucose,fructose)(table sugar)
alpha 1-beta-2 glycosidic linkage (unique among carbs)
non-reducing
consume roughly 100 lbs per year
sources - sugarcane, sugar beets, honey, maple syrup
processing of corn starch with enzymes produces high fructose corn syrup
lactose (galactose, glucose)
beta - 1,4 glycosidic bond
milk and milk products
lactose digestion
digestion challenges (lactose intolerance)
generally lack the ability to hydrolyze beta glycosidic linkages
amylose vs cellulose
start life with ability to digest lactose (enzyme lactase) but many people lose this ability
lactose broken down by gut bacteria, producing CO2 gas
dairy products
less present in hard aged cheese
lactose free milk already has lactase added
sweetness rank: fructose > sucrose > glucose > galactose > lactose
reducing and non reducing ends
sugar molecule with the free anomeric C is the reducing end and the other is the non reducing end
glycosidic bonds
linkage between sugar molecules
naming - configuration of anomeric C (alpha/beta) and number (C involved in linkage)
formation
condensation (water released)
breaking
hydrolysis (digestion - water is a reactant)
polysaccharides - amylose, amylopectin, glycogen
structural forms
open (fischer projection) - long chains
closed (haworth projection) - rings
SUMMARY/KEY TAKEAWAYS: small changes in structure between sugars make a lot of difference in their sweetness, their ability to be digested and how they are metabolized
CARBOHYDRATES 2
monosaccharides
glucose (dextrose), fructose (levulose)
double bonded O (aldose vs ketose)
disaccharides
bond orientation (alpha vs beta)
reducing and non-reducing ends
polysaccharides
starches - from plants
bead structure
amylose - linear chain of alpha 1,4 glucose molecules
1 reducing end and 1 non-reducing end
amylopectin - branching chain of alpha-1,4 glucose, with alpha-1,6 branches
1 reducing end and many non-reducing ends
absorb water - modified starches used for thickening agents
made of glucose
1 reducing end but branches provide many non reducing ends (glycogen as well)
important for digestion of starches and how quickly they lead to changes in blood sugar (glycemic index) and for maintenance of blood glucose by the liver
amylose vs amylopectin (quinoa vs short grain white rice)
glycogen - storage form of glucose in the body, found in muscle and liver
branching chain of alpha-1,4 glucose with alpha-1,6 branches (but generally more branches than amylopectin)
1 reducing end and many non-reducing ends
liver
helps maintain blood glucose (glycogen in liver can be mobilized and pushed out into circulation)
muscle
used for energy
DOES NOT contribute to maintenance of blood glucose
oligosaccharides
3-10 monosaccharides
raffinose
galactose-glucose-fructose
essentially sucrose plus galactose
starchyose
galactose-galactose-glucose-fructose
from legumes and role of microbiome
dietary fiber
cellulose - comes from minimally processed plant material
purest form: cotton
indigestible for humans, but ruminants (cows) can digest
insoluble fiber
hemicellulose
complex structures
soluble or insoluble, depending on type/structure
adds bulk to fecal material
lignins - polycyclic alcohol
insoluble fiber and mostly non-digestible
comes from woody parts of plants
provide bulk to fecal material
do not need to know structure
soluble fiber
pectins, gums, and mucilages
absorbs water (gel-like consistency)
softer, spongier parts of plants
mucilages, seaweeds
used as food additives, thickeners, etc
grains
wheat kernel comprised of
endosperm (83%)
starch, protein, and few fibres
bran (14%)
germ (3%)
lipids, plant sterols, antioxidants, vitamin E, B, minerals, enzymes
aleurone layer (6-9%)
insoluble dietary fibres and few soluble fibres
proteins, enzymes, phenolic compounds, lignans, vitamin E and B, minerals, phytic acid, lipids, plant sterols
testa (1%)
alkylresorcinols, sterols, steryl ferulates
outer pericarp
insoluble dietary fibres (xylans, cellulose, lignin)
antioxidants bound to cell walls (phenolic acids)
CARBOHYDRATES 3
~50% of that 100lb annual intake comes from processed foods
carbs that have been refined, concentrated and/or added to foods
potential link between high intake of sugar and fat storage
dental problems
added and natural sugars can contribute to tooth decay
oral bacteria ferment the sugars and produce acid that erodes tooth enamel
recommended dietary intake
simple sugars
limit to 10% of total energy
low nutrient density, high caloric density
provides sweetness, texture, and color
fermentation
carbs overall
130 g/day for adults
starch not simple carbs
45-60% of total energy
300g in a 2000 kcal dietary intake
healthy effects of dietary fiber
insoluble fiber
contributes to regularity by increasing fecal bulk and decreasing intestinal transit time
too much fiber can BE BAD
proper hydration important for moving fiber through the body
over-intake can lead to intestinal blockages
soluble fiber
slows gastric emptying
increases viscosity of stomach contents
possibly helps prevent obesity
feel full for longer
diabetes
absorption of sugar is slowed, thus sharp spikes in blood glucose following a meal are minimized
may lower blood cholesterol through 2 mechanisms
soluble fiber blocks enterohepatic circulation of bile acids
soluble fiber is metabolized into short-chain fatty acids that travel to the liver and reduce cholesterol synthesis
digestive tract path
food moves stomach -> small intestine -> large intestine at the cecum and moves up the right side of the body, across the abdomen near the stomach, and down the left side of the body
diverticulosis
lining of the intestines
epithelial lining with finger like projections known as mucosa
underneath is muscle tissue
diverticula are little pouches of epithelial lining that pushes out in between the layers of muscle
asymptomatic until revealed by a colonoscopy
more common in elderly
diverticulitis
rare complication of diverticulosis
material (bacteria) from small intestine becomes trapped in the diverticula
can trigger inflammation and lead to internal bleeding because of the arrangement of small blood vessels in and around the smooth muscle tissue around the intestine
treatment
rest the colon with soft diet (broth) or surgery may be needed
cancer
polyps and diverticula are not the same thing, structures are opposite
polyps are outgrowths of the cells
often harmless but can develop into cancer
dietary fiber
some evidence that fiber protects against colorectal cancers
through the efficient dilution/binding/removal of any potential cancer-causing agent
can promote healthy microbiome
largely from observational studies
enterohepatic circulation - portal vein
absorbed nutrients pass through the liver first
carbs and proteins
fats are more complicated but still pass
LIPIDS 1
fatty acids
4-24 C long
16 and 18 most common in food
processed in 2-C units
methyl group (omega) at one end other end carboxylic acid (alpha)
saturation - refers to presence or absence of C=C
saturated fatty acids have no C=C
animal fats
Monounsaturated have a single C=C
olive oil
polyunsaturated have multiple C=C
seeds
most polyunsaturated fats liquid at room temp
saturated fats solid at room temp because they stack on top of each other
saturated and unsaturated fats don’t stack the same since there is a bend at the C=C
essential fatty acids
we lack the enzymatic machinery to place C=C
omega-6 and omega-3 must be from diet
deficiency
flaky skin, diarrhea, reduced healing, anemia, organ pace of cell turnover
Eicosanoids - 20-C polyunsaturated
act as hormones, regulate blood pressure/clotting, immune/inflammatory response, GI secretions
generally act locally
many classes
linoleic acid (omega-6) - group 1 and 2
1T per day plant oil
alpha linoleic acid (omega-3) - group 3
abuse may lead to hemorrhagic stroke
rich in fatty fish (salmon, tuna, sardines), canola or soybean oil
LIPIDS 2
Rancidity - process of autoxidation/hydrolysis of fats/oils (air, light, moisture, bacteria)
produces short chain aldehydes, ketones, and fatty acids
oxidation in lipids occurs at the unsaturations, more double bonds means more likely for this to occur
prevention
add antioxidants like Vitamin E, BHA, and BHT
hydrogenation or partial hydrogenation
adding back H to unsaturated fatty acids
altered structure can be useful
spreadable fats like imparting softer texture to butter (margarine) and shortening, used in baking
trans fat
most fatty acids with unsaturations are cis - the H are on the same side, and the chain is therefore kinked
a small percentage are trans, H atoms on opposite sides
chain is more linear and can behave more like a saturated fat
consequences
raises LDL, promotes inflammation, promotes fat storage, stimulate cholesterol synthesis
triglycerides
storage form of lipids in our bodies
most abundant form of lipids in our bodies
glycerol head + 3 fatty acid chains
three fatty acids attached to a glycerol form triglyceride and each one yields a water molecule
do not cross cell membranes
free FAs, monoglycerides, and glycerol can
TGs must first be hydrolyzed (de-esterified) by a class of enzymes called lipases
function
provide energy, energy storage, insulation/protection, transport of fat-soluble vitamins
phospholipids
contain 2 fatty acid chains with the third position linked to a phosphate group
primary component of cellular membranes
useful as emulsifiers due to amphiphilic nature
emusifiers
phospholipids can organize in aq solution so that the hydrophilic head is oriented out towards water, with the interior becoming a hydrophobic core
organization important for digestion of TGs
emulsified by bile acids during digestion
following TG hydrolysis, micelles are formed which are essential in lipid digestion
sterols
from cholesterol
entirely from animal sources (don’t need to consume them)
important for cell membranes
precursor to steroid hormones and fat-soluble vitamins
corticosteroids, mineralocorticoids, estrogen, testosterone, Vitamin D, bile acids
dietary cholesterol
liver makes it
800-1500 mg per day
intake ~300mg per day
cholesterol can accumulate in the arterial walls and develop into atherosclerosis plaques
LIPIDS 3
lipoproteins - how lipids are moved throughout the body
phospholipid outer shells and TG interior that includes cholesterol
carries hydrophobic substance through aqueous system (blood)
chlyomicrons
transports diet derived lipids from small intestine to lymphatics then blood
least dense
VLDL
created in liver from dietary and newly synthesized lipids
carries lipids and cholesterol to tissues
LDL
bad cholesterol
derived from VLDL as cells remove TGs
mostly cholesterol
internalized by receptor pathway in liver and tissue
supplies cholesterol for growth and development of tissues
scavenged by white blood cells
attach to blood vessels and oxidize lipids (atherosclerosis)
HDL
“good” cholesterol
synthesized in liver and intestine
picks up cholesterol from dying cells and transfers to other lipoproteins and transport to liver for excretion
lipoprotein lipase
enzyme attached to blood vessels that hydrolyze TGs, yielding glycerol and FFAs => delivers lipids to surround tissue
adipose tissue
stores lipids and stored as TGs
blood lipids profiles
measurements conducted after fasting
fed state
clearance of blood lipids
lipoprotein lipase is insulin sensitive and acts on chylomicrons and VLDL
lipids delivered to adipose and muscle
fasting state
hormone sensitive lipase activated in adipose tissue
TG breakdown and mobilization of glycerol and FFAs
FFA from adipose delivered to liver and muscle via albumin
foam cells - when white blood cell tries to internalize a lot of cholesterol
stick to arterial walls can contribute to CVD
PROTEINS 1
functions - enzymes, structural scaffolds, signaling (hormones), immune system (antibodies), transport, buffering (fluids/electrolytes and pH)
source of Nitrogen
Amino acids are amphoteric meaning they can carry a positive and negative charge
L-isomers
R-groups
basic - lysine, arginine, histidine
acidic - aspartate, glutamate
sulfur containing - cysteine, methionine
aliphatic - glycine, alanine, valine, leucine, isoleucine
hydroxyl - serine, therine, tyrosine
aromatic - phenylalanine, tyrosine, tryptophan
nitrogen containing - asparagine, glutamine
unique - proline
essential aminos - Histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, valine
non-essential aminos - Alanine, arginine, asparagine, aspartate, glutamate, glutamine, glycine, proline, serine
Conditionally dispensable - Cysteine, tyrosine, Phenylketonuria
transamination
how we handle amino acids is strongly linked to the metabolism of Nitrogen
used to transfer nitrogen between amino acid backbones
used in synthesis of non-essential amino acids
deamination
removal of amino group
ammonia is a problem
toxic and must be eliminated
converted to urea in liver => to kidney => excreted in urine
keto acid
becomes fuel as glucose or fat
polypeptides are ordered from the amino-terminal residue on the left to the carboxyl terminal residue on the right
denaturation - unfolding of a protein due to exposure to heat, alkali, acid, or salts
disrupts the secondary, tertiary, and quaternary structure
makes proteins inactive and dysfunctional
PROTEINS 2
all or nothing rule - if an essential amino acid is deficient, you cannot make proteins that have that amino acid
RDA for protein
0.8 g/kg healthy weight in adults
eq: intake = output
positive balance - intake > output (children, pregnancy)
negative balance - intake < output (fasting, disease states)
Nitrogen Balance -
70 kg man needs ~56 g protein per day
55 kg women needs ~44 g/day
Nitrogen represents 16% of the weight of a protein
equation: N balance = (protein intake (g) / 6.25g) - urinary urea N - (0.2 X urinary urea N) - 2g
protein quality
limiting amino acid: an essential amino acid found in the shortest supply in a given protein source relative to the amounts needed for protein synthesis
if any one essential amino acid is limiting, existing proteins must be dismantled to obtain it
complete protein: contains all amino acids in sufficient quantities to support protein synthesis
animal proteins (meat, fish, eggs, and cheese) are complete
plant proteins likely incomplete
soy protein is complete
complementary proteins: proteins obtained from two sources of food that make up for each other’s inadequate supply of essential amino acids
equations and values for protein
protein digestibility - a measure of the amount of amino acids absorbed from a given protein source
reference protein - a standard used to measure the quality of other proteins (egg protein)
biological value (BV) - amount of protein nitrogen retained for growth and maintenance expressed as a % of protein nitrogen digested and absorbed
protein efficiency ratio is a determination of how well a given protein supports weight gain in growing rats over given period of time
PER = weight gain (g) of rats on standard diet/amount of protein consumed
chemical score - lowest ratio for any essential amino acid in a given protein source
protein digestibility corrected amino acid score (PDCAAS) - replaces PER evaluation for children over 1 year of age and non-pregnant adults
used to correct for protein quality on food labels when expressed as % DV
PDCAAS - chemical score * digestibility of a protein
chemical score [0 - 1]
digestibility [0.8 - 1]
protein lacking any essential amino = 0
absorption
specific transporters in the small intestine help move individual amino acids into the intestinal cells
amino acids that are not used by the intestinal cells are passed on to the liver
DIGESTION 1
digestive system
mouth
mucus, amylase, mastication
swallowing
voluntary movement of food from the mouth to the pharynx
reflex closes the epiglottis over the larynx
closes the trachea and allows food to move into the esophagus
esophagus
upper esophageal sphincter
peristalsis
lower esophageal sphincter => closes the distal end of the esophagus and blocks the reflux of stomach contents back into the esophagus
gastroesophageal reflux disease
lower esophageal sphincter is loose
stomach contents reflux back into esophagus
not heartburn
treatment
neutralize acid, block acid secretion, proton pump inhibitor
stomach
extremely muscular organ
gastric secretions (HCl) cause acidification of the meal
denatures proteins and proteases enzymes
pepsin secretion
unique protease that functions at low pH
begins to break up peptide bonds
gastric lipase
can start hydrolyzing fatty acids
intrinsic factor
vitamin B-12 absorption
muscle contractions grind and mix food to produce chyme
liver
produces bile acids that are stored in the gallbladder
central hub
pancreas
produces digestive enzymes
gastric emptying into small intestine
primary site of digestion and absorption
lumen
collectively called the mucosa
villi - small folds
rich blood supply
lined with a single layer of epithelial cells
highly pleated
increased surface area
increased interaction with food
compare with a smooth interior pipe
crypt cells
complex organization of cells as a result of the villi structure
don’t project out in lumen
epithelial cell turnover every 3-5 days
stem cells that replenish these epithelial cells are down at bottom of the crypt
cells migrate from crypt up to the lumen
cell types
enterocytes - majority; digestion/absorption
goblet cells - secrete mucin
enteroendocrine cells - hormone secretion
paneth cells - immune monitoring
receives digestive enzymes and bicarbonate from the exocrine pancreas
receives bile acids from the liver via the gallbladder
large intestine
large population of bacteria
they digest dietary fiber and can produce short chain fatty acids that can be absorbed into the bloodstream
water and some minerals are absorbed
rectum - stores and expels feces
transit of large intestine may take up to 3 days
regularity
does not mean a particular time period
everyone is different
frequency of bowel movements depends on microbiome, food, intake, genetics, etc
control of GI function
autonomic nervous system
branch of nervous system that regulates function of visceral organs
GI hormones
small polypeptides released from GI tract into blood
released in response to meals
travel to different regions of the digestive system to regulate GI function
secretion of various chemicals
digestive enzymes, mucus, water, bicarbonate, HCl, bile acids
regulation of GI motility
epithelial cell growth
regulated to maintain homeostasis
secretin and gastrin
GI motility
peristalsis
sweeping motion that propels food forward
swallowing, stomach, and some sections of small intestine
segmentation
closely spaced contractions in discrete areas of the intestine that act to mix the chyme with the digestive secretions and increase contact with the mucosal surface
mass movement
contractions that occur over a large area of intestine that act to move the waste towards the rectum
DIGESTION 2
carb digestion
salivary amylase - begins to break down alpha-1,4 glycosidic bonds from amylose and amylopectin
does not break alpha-1,6 bonds
most carb digestion occurs in the small intestine
also uses amylase from the pancreas
amylase converts amylose and amylopectin into dextrins
dextrins further broken down by the brush border enzymes
brush border
organization of microvilli on enterocytes looks like a fuzzy layer on a light microscope
microvilli membrane is studded with glycosidases that break down the dextrin
carb absorption
lactose intolerance
do not produce lactase
more frequent in asian, african, or mediterranean origin
only monosaccharides absorbed in the intestine
glucose and galactose are actively transported by the Na+ dependent transport protein
goes uphill against concentration gradients
fructose transported by a separate GLUT5 transporter
facilitated transport - moves with concentration gradient
GLUT2
basal transporter that moves glucose, galactose, and fructose out of the cell and into the blood
moves with the concentration gradient
protein digestion
stomach is where this largely starts
HCl denatures proteins
pepsin released
unique protease that is active at low pH
breaks apart proteins into pieces
pancreas secretes digestive enzymes and bicarbonate into small intestine
proteolytic enzymes are released from the pancreas as inactive proenzymes and are later activated in small intestine
majority done in small intestine
enzymes hydrolyze peptide bonds producing oligopeptides
amino acid absorption
brush border peptidases hydrolyze oligopeptides into di and tripeptides and individual amino acids
these are transported across the intestinal cell membrane by brush border transporters
active and facilitated transport
further breakdown can occur inside cells
transporters move amino acids and small peptides out of basal region of cell and into the blood
lipid digestion
largely starts in stomach
production of gastric lipase
hydrolyzes TG to FFA and monoglycerides
small intestine is major site of fat digestion and absorption
gallbladder stores and releases bile acids and lecithins
bile acids and lecithins emulsify lipids, facilitate breakdown and transport
lipid absorption
Pancreatic lipase acts together with the protein co-lipase to hydrolyze TGs
Emulsification of fat droplets by lecithins and bile acids gives the co-lipase and lipase enzymes access to the TGs. End products are FFA, monoglycerides, and glycerol
Micelles form from monoglycerides and FFA surrounded by bile acids
Gives the lipids access to the epithelial cells (and is needed for lipid soluble vitamin absorption)
Absorption of FFA, monoglycerides, and glycerol is by diffusion and
protein mediated transport
Bile acids: produced in liver, released from the gallbladder, and most are
reabsorbed (~98%) in the terminal ileum and travel in the blood back to
the liver (enterohepatic circulation – via the hepatic portal vein)
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