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355 Cards in this Set

  • Front
  • Back
What do protiens contain
C H N O and maybe S
Briefly describe protiens
extremly complex molecules witha a wide variety of functions
What are all protiens composed of
amino acids
What links proteins and amino acids?
peptide bonds
What is used to classify protiens
structure or function
How many different protien structures are there? What are they?
four
primary
secondary
teritary
quatrinary
Describe a primary protein structure
a long one dimensional chain of amino acids joined by peptide bonds
Describe a secondary protein structure
when amino acid chain folds into a pleated sheet or coils into a helix
Describe a teritery protein structure
when the amino acid chain folds back on itself so that amino acids that were on opposite ends end up next to eachother
describe quatrinary protein structure
2 or more amino acid chains that twist together
What happens to a secondary, teritary or quatrinary protein when it encounters a hostile environment?
it unravels and loses its structure becoming a primary chain
what is a denatured protein?
when a protein enters a hostile environment and unravels into a primary structure. This renders the protein usless and it cannot function.
How many protein function classifications are there? Name them
5
catalytic proteins
transport proteins
immunilogical proteins
structural proteins
contractual proteins
Catalytic proteins
enzymes that speed up chemical reactions
transport proteins
carry substance in the body

ex: hemoglobin carries O2 into blood
Immunilogical proteins
enzymes that fight infection
structural proteins
build body structures

ex: collagen
contractual proteins
actin and myocin (located in the sarcomere)
What are enzymes
specialized proteins that speed up chemical reactions by lowering the activation energy needed for the reaction to occur. (lowers ATP)
What is a complete enzyme called/.
holoenzyme
What does a complete enzyme consist of?
a protein and non-protein part
What is the protein part of an enzyme called
apoenzyme
what is the non protein part of an enzyme called?
either a coenzyme in an organic enzyme or a cofactor in a metal ion enzyme
most enzymes end with the suffix
-ase
substrates
molecules in the body that enzymes are specialized to react to in the body. The enzyme will ignore everything else but the substrate.
Active site
located on the surface of the substrate (cell) where the substrate and an enzyme combine
induced fit
the process of the substrate and the enzyme combining together.

Like a lock and key
what happens when induced fit occurs
products are produced and reactions occur.
what happens after the induced fit reaction
the enzyme and substrate split and the enzyme is free to cause another reaction.
What is the biggest molecule in our body?
Nucleic Acids
What is the basic unit of structure for a Nucleic Acid
nucleotide
What makes up the nucleotide structure
pentosugar
phosphate group
nitrogen base
What is a pentosugar
Part of the nucleotide structure made up of either deoxyribose (DNA) or ribose (RNA)
what is a phosphate group?
part of the nucleotide structure. It forms the backbone of the nucleic acid
What is a nitrogen base
the third part of the nucleotide structure. Can be thyamine, uracil, adenine, guanine, cytosine.
Describe and compare the size and location of both DNA vs RNA
DNA: an extremly large molecule that is only found in the nucleus. It can never leave.

RNA: about 1/2 the size of DNA but is still big. Found in both nucleus and cytoplasm.
Compare the function of DNA vs RNA
DNA: controls our heredity or genetic makeup. It contains the instructions for making every protein in our body. Everyones is unique except identical twins.

RNA: Carries out DNA's instructions for making protein. Forms the small subunit of the ribosome. Brings amino acids into the ribosome so proteins can be made.
Compare the shape of DNA vs RNA
DNA: is a double stranded molecule twisted in to a helix.

RNA: always a single strand that can be long or folded.
Compare the sugars that make up DNA vs RNA
DNA: deoxyribose

RNA: ribose

Both are a pentose and a carbohydrate.
compare the nucleic bases used in DNA vs RNA
DNA: A,G,C,T

RNA: A, G, C, U

*T and U are the same thing.
Compare the nucleic base pairing in DNA vs RNA
DNA: A=T; G=C

RNA: A=U; G=C
What links bases in both DNA and RNA
Hydrogen bonds which are weak and easily break
What are the 3 types of RNA
mRNA
rRNA
tRNA
mRNA
messenger RNA the copy of DNA that carries the genetic code to the ribosome
rRNA
ribosomal RNA. small subunit of the ribosome
tRNA
transfer RNA. transfers amino acids from cytoplasm to ribosome so protein can be made.
What does C H N O P stand for
C= carbohydrate - the deoxyribose or ribose

H= Hydrogen

N= Nitrogen base

O= Oxygen

P= Phosphate group
What determines our genetic make-up
the proteins that make up DNA. conatins the blueprint for making every protien in our body.
How is it determined what protein will be made?
The number, kind and order of our amino acids.
How many amino acids are in our body.
20
How many amino acids are typically in a protein?
4 So they show up many times.
1 amino acids is coded by
3 bases
triplets
3 bases found on DNA
codons
3 bases on mRNA
anticodons
3 bases on tRNA
transcription
the 1st step in making a protein
Where does transcription occur?
always in the nucleus
how does DNA start copying
by forming a strand of mRNA
What is this a picture of
A single DNA strand
What do the letters stand for in 2?
Deoxyribose and Phosphate
RNAP does....
RNA polymerase: attaches to a receptor site on the end of DNA
What happens after rNAP attaches to DNA
causes the DNA molecule to uncoil from its helix, breaks the hydrogen bond between the nitrogen bonds resulting in 2 seperate strands.
How is mRNA constructed.
RNAP reads 1 of the strands and contructs a complimentary strand.
What is the complimentary mRNA strand called?
the sense strand
anti-sense
the DNA strand that is not read by RNAP
How does RNAP read the DNA strand?
It is non selective and intially copys everything from DNA
exons
info in DNA that codes for protein.
introns
Infor that odes not code for protein on DNA. It stays in the nucleus and disintigrates.
SNURPS and function
Subnuclear Ribonucleic Proteins.

cut introns out of the mRNA strand and splice the exons together.
What is contained on mRNA after it leaves the nucleus
exons aka only info containing proteins.
Biochemistry
the study of organic chmeicals
Every organic material contains
some carbon and hydrogen
What are the 5 types of organic molecules
carbons
lipids
proteins
nucleic acids
ATP
What are the 3 main stages of protein synthesis
transcription
translation
termination
How does transcription end?
the sense and antisense strand swing back together and the hydrogen bond reforms between the bases. DNA then twists back into a helix
what is the initiator codon?
AUG
What are the stop codons
UAA
UAG
UGA

When the ribosome reads any one of those it stops making protein.
Translation
when the genetic code that is now carried in mRNA is translated into a protein.
Where does translation occur
in the cytoplasm at the ribosome.
How does trnaslation start
mRNA comes out to the ribosome rRNA and attaches to a receptor stie on the end of mRNA
Initiation
when rRNA reads the codon "AUG" the large and the small subunits (protein and rRNA) lock together and start making protein.
What completes initiation?
the first tRNA and its amino acid enter the p-site of the ribosome and the codon and anti codon bind.
What is the first protein made in the body?
methionine
What is the 2nd stage of translation?
elongation
Elongation
the lengthening of the aa chain
How does elongation begin?
the 2nd codon is read and the 2nd tRNA and its amino acid enther the a-site. Codon and anticodon bind and
during elongation, what happens after the codon and anitcodon bind?
a peptide bond forms between aa1 and aa2 thus filing the ribosome
When the ribosome is filled what happens to the 1st tRNA and its aa?
the ribosome then jumps to the 3rd codon and the tRNA that was in the psite is now in the cytoplasm
what happens to the tRNA after it leaves the p-site
The hydrogen bond between the 1st aa and tRNA break and the tRNA is free to grab another methionine.
When the p-site "space" becomes available what happens to it?
the 2nd tRNA and its aa that were in the a site move to the p site, leaving the a site empty.
Termination
eventually the ribosome reads one of the stop codons
release factor
activated when a stop codon is read. Once activated the enzyme splits the ribosome back into 2 subunits and then cuts the protein away.
2 ribosome subunits
protein and rRNA
ATP
the prefered source of energy for our body.
How is ATP made?
its generated in the mitochondria from the oxidation of sugar, aa's fatty aids and glycerol.
Digestion
both the chemical and physical breakdown of complex food into its component parts.
What happens to the component parts in digestion
some of it is reabsorbed and some of it is removed.
2 groups of digestive organs
alimentary canal
accessory structures
alimentary canal
mouth
pharynx
esophagus
stomach
SI
LI
Accessory structures
teeth
toungue
salivary glands
liver
gall bladder
pancreas
histology of the Alimentary canal (4 parts
mucosa
submucosa
muscularis
serosa
mucosa
the inner lining. simple columnar with goblets and lymph nodes
submucosa
its a vascular CT membrane. Binds the mucosa to the muscularis
muscularis
skeletal muscle tissue. Mostly outermostly in the mouth throat and esophogus. produces the voluntary movement of swallowing.
serosa
the outer layer the visceral peritineum.
What are the 5 membranes of the digestive system
peritineum
mesentary
mesocolon
greater omentum
falciform ligament
mesentary
binds the SI's together in the DS.
mesocolon
binds the LI to the posterior body wall in the DS
greator omentum
a large apron of fat that hangs down from the stomach over the intestines. contains mostly adipose and lymph nodes
falciform ligament
attaches liver to the diaphram and to the anterior body wall.
Food intake is controlled by
the hypothalamus
2 regions of hypothalamus for food intake
feeding center
satiety center
feeding center
region of the hypothalamus that, when active, you cannot stop eating even if you are full.
satiety center
you wont eat even if you are starving.
What are the 2 types of digestion
physical and chemical
physical/mechanical digestion (5)
chewing
moving
swallowing
mixing
churning
chemical digestion
consists of all the reactions that that break food down into its component parts
the bucal cavity
the mouth
major tissue in the mouth
stratified squamous non keratinzed and completly covered with mucous membrane
vestibule
the space between the lips teeht and cheeks
mechanical digestion in the mouth
when you chew food and mix it with saliva to form a bolus
bolus
food chewed and mixed with saliva
chemical digestion in the mouth
initial digestion of starch with salivary amylase
lingual lipase
enzyme secreted by glands in the tongue that begin the digestion of fat. However, in most cases the food is swallowed too quickly and the enzymes are denatured before digestion is complete.
3 types of salivary glands
parotid
sublingual
submandibular and submaxillary
parotid
the largest salivary gland slightly in front of and below each ear. produces most of our saliva
sublingual
salivary glands underneath the tongue, toward the front. Produce thick mucus like saliva. Very active under stress
submandibular and submaxillary
salivary glands at the junction of the maxilla dn mandible. Produce a thin watery saliva
Saliva
99.5% water .5% solute
Solutes in saliva
Na, K, chloride, bicarbonate, phosphate ions. Lysozyme, salivary amylase, and ligual lipase.
lysozyme
an enzyme that kills bacteria
Tongue
located in the mouth. anchored by the hyoid bone.
tongue is made of
skeletal muscle tissue covered by mucous membrane
papillae on tongue.
bumps on the surface that make up the taste buds
5 taste senses
salt
sour
bitter
sweet
umami
lingual septum
divides the tongue in 1/2
lingual frenulum
a mucous membrane underneath the tongue
2 muscles associated with the tongue
extrinsic
intrinsic
extrinsic tongue muscles
in and out
up and down
intrinsic tongue muscles
alters size and shape of tongue during speech and swallowing.
what is this a picture of
an mRNA strand
What does the orange circle/curves represent
protein
What does the green circle/curve represent?
rRNA
What do both the orange circle and green circle make up together
a ribosome
Which codon is the stop codon?
UAG
What are the codons on top of the mRNA strand refered to?
anti codons
what do the purple circles represent
amino acids
What does the Orange line (connected to the purple circle down to the strand) represent?
tRNA
What does the blue line between the purple circles represent
the hydrogen bond.
What are the four types of teeth and how many do we have of each?
incissors 4
canine 2
premolars/bicuspids 4
molars 6
How do childrens teeth differ from an adult
children have no bicuspids and only 4 molars
crown
part of the tooth above the gum line covered with enamel
enamel
hardest substance in the body. Covers teeth
root
between 1 and 3 projections called root canals, covered by cementum
what are teeth made of
calcified connective tissue, called dentin
pulp cavity
deep in the crown of the tooth where blood vessels and nerves are located
apical foramen
a tiny hole in the base of each root canal where blood vessels and verves enter and exit the tooth.
alveolar process
the socket in which the tooth sits
peiodontal ligaments
line the alveolar process
gomphosis
the joint formed by a tooth in a socket
the neck
the junction point of the crown and the root, located at or slightly below gum line.
deglutition
swallowing
swallowing
the process that moves bolus from the mouth to the esophogus, requires both saliva and mucous
3 stages of swallowing
voluntary
pharyngeal
esophageal
voluntary swallowing
the movement of bolus from the mouth to the throat
pharyngeal swallowing
the involuntary movement of bolus through the throat and into the esophagus
What 2 things should occur during pharyngeal swallowing?
-soft palette should rise closing off the nasal region.

the epiglottis should tip upward and close off the trachea
esophageal swallowing
the movement of bolus through the esophagus and into the stomach
the esophogus is coated with
mucous
peristalsis
movement through the esophogus. A contraction of the muscularis that moves contents through the GI tract. It is always strongest proximal and weakens as you move distal
3 subdivisions of the throat/pharynx
nasopharynx
oropharynx
laryngopharynx
nasopharynx
part of throat that is up behind the nose. A passageway for air only
oropharynx
the part behind the mouth. the passageway for food and air
laryngopharynx
between the mouth and the superior trachea
esophagus
a 10 inch collapsed tube posterior to the trachea. It connects the throat to the stomach
stomach
muscular J shaped organ. Mostly on the let side of the abdominal cavity.
Rugae
folds that allow for expansion and contraction of the stomach
Histology of the stomach
simple columnar epithelium, goblet cells secrete mucus onto surface of the tissue
gastric pits
open in to the gastric glands, contain cheif cells, mucous cells, parietal cells, G cells.
cheif cells
secrete pepsinogen and gastric lipase
parietal cells
secrete hydrochloric acid and intrinsic factor
mucous cells
secrete mucous
G cells
gastrin. only found in pyloric antrum.
mechanical digestion in stomach
major mechanical movement is mixing waves. Occurs every 15-20 secs.
Purpose of mixing waves
mix bolus with gastric juice forming a thinner solution called chyme.
When do mixing waves increase
as bolus moves from proximal to distal. Its the opposite of peristalsis.
chemical digestion in the stomach
bile stomach ph is 2.0 or less. The most acidic in the body.
acidic ph function
kills bacteria in food and other microbes that could reach the stomach.
Hcl:
kills bacteria, denatures ingested proteins, and stimulates the release of hormones that cause bile and pancreatic juice to be secreted.
pepsine
an enzyme that converts protein into peptides
pepsin is secreted as
pepsinogen which is inactive.
when does pepsinogen become active
when it mixes with Hcl
pepsin must be produced
in an inactive form or it would eat the cells that made it
Why is pepsin not denatured by Hcl
its in its primary structure
Gastric lypase
digests fat.
when does gastric lypase work best.
at a ph of 6. Therefore it does not work well in adult stomachs but an infants stomach is more alkaline so it digests milk fat in infants.
mucus
coaqts the entire lining of the stomach. About a 1 inch layer. It prevents digestion of the stomach by pepsin and destruction by Hcl
intrinsic factor
chemical that is required for the proper absorption of it. B12
gastrin
helps control stomach emptying. A hormone
3 stages of gastric juice production
reflex/cephalic
gastric phase
intestinal phase
reflex/cephalic phase occurs when
you see, smell think about, or taste food. But the stomach is still empty
What happens in the feeding center during the reflex phase
It send info to the MO which then send impulses to all the cells telling them to secrete
gastric phase occurs when
when food actually enters the stomach
gastric phase is controlled by
controlled by the autonomic nervous system and by hormones
process of gastric phase
when food enter the stomach it stretches the stomach wall, activating the stretch receptors. Also rasies stomach ph going from 2 to 4 or 5.
chemo receptors
monitors the ph level raise during the gastric phase. causeing the cells to make gastric juice and initiate peristalsis.
Process of gastrin
constricts the cardiac sphincter and relaxes the pylonic sphincter.
Intestinal phase
when chyme leaves the stomach and enters the SI. Causes the release of hormones
Hormones released during the intestinal phase
secretin
GIP
CCK
secretin
slow down production of gastrin juice
GIP
same as secretin
CCK
slows down emptying and cuases the release of bile and pancreatic juice.
vomiting
forcable expulsion of stomach contents through the mouth
vomit center is in the
MO
prolonged chronic vomting causes
acid base imbalance,
destrucion of esophagus, and breakdown of tooth enamel
type of gland of the pnacreas
endocrine and exocrine
appearance of pancreas
extremley large and flat.
has a head, body and tail.
Islets of langerhans
the endocrine part of the pancreas.

secretes insulin
glucagon
somatostotin
acini cells
exocrine part of pancreas
pancreas produces
about 1 1/2 quarts of pancreatic juice daily.
ph of pancreatic juice
7.1-8.2
pnacreatic juice is made up of
water, salt, sodium bicarbonate, and a large group of enzymes
why is alkalinity critical in pancreatic juice
it buffers the acidic chyme that enters the SI. It stops the digestice actio of pepsin and creates the proper ph for digestio in the SI
Enzymes in pancreatic juice
p. amylase startch to sugar
p lypase- bile-lipids-fatty acid and glucerol
deoxribonuclease-dna-sugar,phosphate and bases
ribonuclease-rna and sameas dna
pancreatic secretions controlled by
the parasympathetic nervous system in response to the release of CCK
function of the liver
detoxes everyting
location of liver
right hypochondriac area, upper gastric just below the diaphram. Largest internal organ
histology of liver
completly covered by peritineum, followed by dense irregular connective tissue.
falciform ligament
seperates 2 lobes of the liver. Right and left.
right lobe of liver
divided in to the quadratic and caudate lobes
lobules
division of the the entire liver, tiny lobes containing hepatic cells
hepatic cells
produce blood proteins.
produce bile
heparin
stores glycogen, vitamins and minerals
sinusoids
spaces in the liver lined with kuppfer cells
kuppfer cells
in the liver:

destroy bacteria
neutralize toxins
breakdown and remove old red blood cells
bile
bwonish green liquid with slightly alkaline ph
make about a quart a day
bile is made of
bile salts
cholesteral
lipids
pigment
ions
biliruben
major pigment in bile.
produced when red blood cells break down
function of bile
emulsification of fat.
process of fat emulsification
a large globule of fat is acted on by bile which breaks it down into numerous small blobs of fat called micelles which gives a greator surface area for the digestive action of lypase
gall bladder
a sac under the right lobe of the liver
function of gall bladder
to store and concentrate bile
hystology of gall bladder
simple columnar with rugae that allow for expansion and contraction
What happens when chyme containing fat enters the SI
concentrated bile leaves the GB enters the systic duct, enters the common bile duct into the SI and the sphyncter of oddi is opened
when bile is not needed....
the sphyincter of oddi is closed bile leaves the liver and goes up the common bile duct up the cystic duct into the GB where its stored
SI appearance
a tube about 20 ft long and 1 inch in diameter
3 parts of SI
duodenum
jejenum
illium
Histology of SI
simple columnar. Has villi and micro villi that increase the surface area for reabsorption
Crypts of lieberkohn
throughout the entire intestine. Produce intestinal juice
Brunners glands
only in dudenum,
secrete an alkaline fluid that helps nutralize the aidic ph of chyme
panath cells
secrete lysozyme - kills bacteria
Mechanical digestion in the SI
parastalsis
segmentation
segmentation
locaized contraction in a region that conatins chyme.
segmentation works by
mixing chyme with gastric juice and brings it into contact with the mucosa to help with absorption
picae circulares
circular bands that help segmentation. Allow chyme to spiral through the intestine rather than move straight through.
segmentation occurrence
12-16 segmentations every minute.
picae allows for
greator absorption
chemical digestion in the SI
over 90% of all digestion
pancreatic enzymes break all carbs into
monosaccarides and are absorbed as such
pancreatic enzymes break all proteins
into peptides and then aa. absorbed as such
pancreatic enzymes
with the help of bile into fatty acids and glycerol and are absorbed as such
electrohepatic circulation
when the contents of the SI reach the Illium. 95% of bile salts that entered the duodenum will be reabsorbed by the blood and liver.
histology of the colon
simple columnar with goblets and haustra
Mechanical digestion in the LI (3)
parastalsis
haustra churning
mass parastalsis
haustrol churning
when haustra cells relax, fill and contract pushing contents through the intestine
mass parastalsis
strong contraction begining inthe transverse colon.
rapidly pusch contents to the rectum
when does mass parastalsis occur
after a meal or 3-4 times a day
What initiates mass parastalsis
gastrocolic reflex
chemical digestion in LI controlled by
the action of bacteria. very few enzymes.
Breaks down waste
helps in absorption of vitamins, minerals and water
where is absorption the greatest in the LI
in the cecum and the ascending colon
feces
anything not absorbed. composed of non digested food, bacteria, mucus, epithelium and water
diarrhea
liquid feces frequently expelled because contents move through the Gi tract too quickly and too little H2O is absorbed.
constipation
dry hard feces difficult to expell becuase too much H20 has been reabsorbed
defication
reflex that emptys the rectum
process of defication
must inhale
voluntarily contract your diaphram and abdominal muscles, anal sphincter relaxes and defication occurs
what happens if defication does not occur
feces stays in sigmoid colon till the next mass peristalsis
metabolism
all of the reactions in the body that generate energy in the form of ATP
chemical reactions in metabolism
energy transformations where stored enrgy is released and transfered to other substances
Re-Dox
the most common metabolic reaction. A combination of oxidation and reducion
when something is reduced it
is gaining energy in the form of electrons or H ions.
oxidation and reduction must occur. Which forms a...
together.

Red-ox reaction
Carbohydrate metabolism
during digestion poly and di's become mono's.
all monos become glucose
3 parts of the oxidation of glucose
glycolisis
Krebs
ETC
glycolisis
a series of 10 chemical reactions each catalyzed by enzymes
where do the chemical reactions for glycolisis occur
in the cytoplasm and can be aerobic or anerobic
What must happen for the glucose cycle to begin
the cell must invest 2 molecules of ATP.
glucose has a potential of releaseing
36-38 ATP's into the cell
1st step of glucose cycle
glucose enters the cell by facilitated diffusion and it becomes fructose and it phosphoratlates
phosphoralate
a phosphate group attaches to the glucose making it bigger so it does not lide out of the cell.
After phosphoralation
2 intermediate compounds form, DHP g-3p
once dhp and g-3p forms
the are oxidized and other compounds are reduced and eventually 2 molevules of pyruvic acid form.
How many carbons does each pyruvic acid have
3 and 4 ATP are released in the cell
phosphofructokinase
the most importan enzyme in glycolisis it catalyzes step 3 which controls the speed of the cycle
What happens if O2 is not present in pyruvic acid
it turns to lactic acid
location of lactic acid
it can stay till O2 is restored or can move to the liver, where its converted back to pyruvic acid
transitional step
step between glycolisis and krebs cycle.

No ATP is released in this step
where does transistional step occur
in the cytoplasm which occurs in the mitochondria.
process of transitional step
2 molecules of pyruvic acid is decaboxylized and converts to pyruvic acid into an acetyl group having 2 carbons
in the transitional step what happens to the acetyl group
it combines with coenzyme A forming acetylcoenzyme A which can enter the Krebs cycle
Krebs cyle
series of redox reactions plus many others
process of krebs cycle
acetylcoenzyme A combines ocaloacetic acid forming citric acid
what happens when citric acid is formed in the transitional step
it oxidizes and other molecules are reuced
What are the end products of Krebs
4 Co2
2 GTP (ATP)
6 NaDH
2 FaDa
the Krebs cycle occurs
on the outer membrane of the mitrochondria and O2 is required
Where does the Electron Transport Chain (ETC) take place
the inner membrane of the mitchondria

requires O2
During ETC when the coenzymes are reduced
they go through a series of electron moelcules.
What is the last substance to accept electrons or H ions
Oxugen. Therefore at the end of the ETC h2O is always produced
Lipids turn into
fatty acids and glycerol
what chemical reactions does glycerol undergo
becomes G-3P
When does glycerol enter the cycle
halfway through.
continues through the carb cycle
beta oxidations
a series of reactions that fatty acids undergo.
What do the reactions turn fatty acid into
acetyl coenzyme A and then enters Krebs
What happens when a fat breaks down too much acetyl coenzyme A
the extra acetyl coenzyme A i s converted into ketone bodies in the liver
ketogenesis
when acetyl coenzyme A is converted into ketone
When acetyl coenzyme A levels, after ketogenesis, returns to normal what happen
the ketones are changed back into acetyl coenzyme A and they reenter the system.
glycogenesis
conversion of glucose into glycogen.
when does glycogenesis occur
when one eats too many carbs
glycogenolysis
when stored glycogen is converted back into glucose.
when does glycogenolysis occur
when one ingests too few carbs
gluconeogenesis
when stored fat or protein is converted back into glucose
when does gluconeogenesis occur
when dieting or starving
lipogenesis
when extra glucose is converted to fat.
when does lipogenesis occur
when liver and skeletal muscle cells are full of glycogen
during digestion what do proteins become
peptides which are then converted to amino acids.
before an amino acid can be converted it must be
deaminated
deamination
an amino group is removed from the amino acid. It enters the liver where it is then conveted to amonia then amonium then urinated out
what is the fate of the remaining amino acids
it depends on which amino acid it is. So there are 20 possibilities.
an amino acid will always...
turn into something after deamniation, pre-Krebs, and then contiue through that cycle
there are ____ amino acids in the body
20
there are _______ essential amino acids
10
there are __ non-essential amino acids
10
transamnination
a process in the body where non-essential amino acids are produced.
proteins are easily produced when
both essential and non essential amino acids are present.
insulin (functions)
causes the movement of facilitated diffusion into cells and it converts extra glucose into glycogen and fat
glucagon
converts non carbohydrates back into glucose
HGH and Thyroxine
both hormones initiate protein synthesis and are needed to convert stored fat back into glucose
metabolic rate/metabolism
the production of enrgy in the form of ATP which comes from ingested food
BMR - Basil Metabolic Rate
a measurement of the rate at which the body uses energy to maintain itself. ie. the rate the body breaks down food and releases ATP
What does BMR depend on
the surface area, age and sex.
BMR is never influenced by
weight
BMR is higher in
Men, - more muscle mass
Tall people- more surface area
and very hugh in young children
how is BMR measured
have to be lying down at complet rest and no food for 24 hours.
Homeotherm
maintain a constant body temp with a slight range.

humans
when is body temp the lowest
the morning
heat produced must
equal heat lost
when you produce more heat than you lost
you have a fever
if you lose more heat than you produce then
you have hypothermia
4 major ways heat is generated
contraction of skeletal muscles
T4
SNS
vasconstriction
T4
thyroxine a hormone, increases metabolic rate which increases temp
SNS
sympathetic nervous system, in flight or fight response
vasoconstriction
goosebumps,
causes blood to flow to interior of the body
4 ways heat is lost
radiation
conduction
convection
evaporation
radiation
transfer of body heat ot a cooler substance that is not in direct contact with the body
conduction
transfer of body heat to a cooler substance that is in difrect contact witht the body
convection
transfer of body heat to a gas that is different tempurature than the body
ex a fan
evaporation
sweat liquid to vapor which cools the body