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57 Cards in this Set

  • Front
  • Back
Digestive tract
1. mouth
2. esophagus
3. stomach
4. small intestines (duodenum, ileum, jejunum)
5. large intestines (ascending colon, transverse colon, descending colon, sigmoid colon)
6. rectum
7. anus
Mouth
Digestion begins in the mouth with alpha-amylase contained in saliva

breakdown of starch

chewed food forms clump called bolus
alpha-amylase
contained in saliva

begins breakdown of starch (carbohydrates) into polysaccharides
esophagus
bolus is pushed into esophagus from mouth by swallowing

bolus is moved down esophagus by peristaltic action

saliva acts to lubricate esophagus to help food move down

no digestion occurs
peristaltic action
wave motion, similar to squeezing a tube of toothpaste at bottom and sliding fingers toward top to expel toothpaste

movement is performed by smooth muscles
stomach
bolus moves into stomach through lower esophageal sphincter (cardiac sphincter)

very flexible pouch that mixes and stores food

reduces bolus to semifluid mass called chyme

contains exocrine glands

begins protein digestion with enzyme pepsin

low pH assists by denaturing proteins (pH 2) and kills bacteria

no absorption occurs
chyme
semifluid mass of food in stomach
4 major cell types of stomach
1. mucous cell
2. chief (peptic) cell
3. parietal (oxyntic cells)
4. G cell
G cell
secrets gastrin into interstitium, which stimulates parietal cells to secrete HCl
Mucous cell
contains rough ER and golgi to make mucus, composed of glycoprotein and electrolytes

secretes mucus to lubricate stomach and protect epithelial lining

different types

line stomach wall and necks of exocrine glands

some secrete small amounts of pepsinogen
parietal (oxyntic) cell
many mitochondria to produce sufficient energy to establish proton gradient

found in exocrine glands of stomach

secrete HCl, which diffuses to lumen

used to lower pH of stomach and raise pH of blood

also secrete intrinsic factor, helps ileum absorb B12
Chief (peptic) cell
synthesizes pepsinogen on rough ER, which is later cleaved to active pepsin

deep in exocrine glands

secret pepsinogen, zymogen precursor of pepsin
epithelial lining
protected by mucus from acidic environment of stomach
pepsinogen
zymogen precursor to pepsin

activated to pepsin by low pH in stomach

once activated, pepsin beings protein digestion
gastrin
secreted by G cells into interstitium

large peptide hormone

absorbed into blood

stimulates parietal cells to secrete HCl
Major hormones affects secretion of stomach juices
1. acetylcholine: increases secretion of all cell types

2. gastrin: increase secretion of HCl

3. histamine: increase secretion of HCl
Small intestines
90% of digestion and absorption occurs in small intestines

3m in length

divided into 3 parts (smallest to largest):
1. duodenum (digestion)
2. jejunum (absorption)
3. ileum (absorption)
villi
finger-like projections that covers outermost layer of small intestines

increases surface area, allowing for greater digestion and absorption

each contain capillary network and lymph vessel (lacteal) through which absorbed nutrients pass
microvilli
on apical (lumen side) surface of cells of each villus (enterocytes)

smaller finger-like projections

increase surface area

appear as fuzzy covering
brush border
fuzzy covering of microvilli on villus

contains membrane bound digestive enzymes for carbohydrates, proteins, nucleotides
goblet cells
small intestine lining

epithelial cells

secrete mucus to lubricate intestines and help protect brush border from mechanical and chemical damage
Pancreas
secretes bicarbonate ion into duodenum to make pH 6

exocrine glands

also secretes enzymes:
trypsin, chymotrypsin, pancreatic amylase, lipase, ribonuclease and deoxyribonuclease

all enzymes are released as zymogens

activated trypsin, activates other enzymes
trypsin and chymotrypsin
degrade proteins into small polypeptides
pancreatic amylase
like salivary alpha-amylase, but more powerful

digests starch, carbohydrates

hydrolyzes polysaccharides to disaccharides and trisaccharides

degrades carbohydrates of chyme to small glucose polymers
lipase
degrades fats, specifically triglycerides

since intestinal fluid is aqueous solution, fat clumps together, reducing surface area, which makes degradation difficult, problem fixed by addition of bile
bile
produced by liver and stored in gall bladder

gall bladder releases bile into small intestines

needed to increase surface area of fat

physically separates fat molecules, but does not chemically break down fat

emulsifies fat, doesn't digest fat

reabsorbed by small intestine and transported back to liver
emulsification
what bile does to fat

breaking up of fat into small particles without changing it chemically

increases surface area of fat, allowing lipase to degrade it into fatty acids and monoglycerides
peristalsis
moves chyme through intestines

wave-motion
large intestines
site of water and electrolyte reabsorption

profuse water loss, diarrhea, results when there is a problem with large intestines

mutualistic symbiosis between humans and bacteria (E. coli) in large intestines, bacteria get our leftovers and we get vitamins (K, B12, thiamin and riboflavin)

made up of:
1. ascending colon
2. transverse colon
3. descending colon
4. sigmoid colon
glycogenesis
formation of glycogen from glucose

glycogen is stored

occurs when blood glucose levels increase

occurs in liver and muscle cells

all cells are capable of storing glycogen, liver and muscle cells store most glycogen
glycogenolysis
occurs when blood glucose levels decrease

glycogen in converted to glucose

takes place in the liver and glucose is returned to blood
urea
ammonia is converted to urea by liver and then excreted in urine by kidney
albumin
fatty acids combine with albumin in the blood

single molecule of albumin carried 3 fatty acid molecules, but is capable of carrying up to 30
vena cava
location where all blood that has passed through liver is deposited
functions of liver
1. blood storage
2. blood filtration
3. carbohydrate metabolism (gluconeogenesis, glycogenesis, storage of glycogen)
4. fat metabolism
5. protein metabolism (urea)
6. detoxification
7. erythrocyte destruction
8. vitamin storage

when liver mobilizes fat or protein for energy, blood acidity increases (acidosis)
Kidney function
1. excrete waste products (urea, uric acid, ammonia and phosphate)
2. maintain homeostasis of body fluid volume and solute composition
3. help control plasma pH
Kidney
2 fist-size organs

made up of:
1. outer cortex
2. inner medulla

creates urine, which empties into renal pelvis
cortex
outer part of kidney
medulla
inner part of kidney
renal pelvis
where urine is emptied to

emptied by ureter
ureter
carries urine to bladder
bladder
drained by urethra
nephron
functional unit of kidney

Made up of:
1. glomerulus
2. bowman's capsule
3. renal corpuscle
4. proximal tubule
5. loop of henle
6. distal tubule
7. collecting duct
8. juxtaglomerular apparatus
glomerulus
blood flows into the 1st capillary bed of nephron

contains fenestrations

hydrostatic pressure of glomerulus controls amount of filtrate
renal corpuscle
made up by bowman's capsule and glomerulus

where filtration occurs
hydrostatic pressure
forces plasma through fenestrations of glumerular endothelium and into bowman's capsule
fenestration
like a sieve

screens out blood cells and large proteins from entering bowman's capsule
bowman's capsule
fluid is called filtrate or primary urine

fluid from bowman's capsule to proximal tubule
proximal tubule
most reabsorption and secretion takes place

secondary active transport proteins in apical membranes of proximal tubule cells are responsible for reabsorption of:
glucose, proteins and other solutes

water is reabsorbed across relatively permeable tight junctions due to favorable osmotic gradient

net result:
reduce amount of filtrate in nephron, while changing solute composition without changing osmolarity
secreted
drugs, toxins and other solutes are secreted into filtrate by cells of proximal tubule

also secreted into proximal tubule:
uric acid, bile pigments, antibiotics and other drugs
antiport system
secretes H ions with Na+

driven by Na+ concentration gradient

similar to transport system of glucose with Na+, except H+ crosses membrane in opposite direction to Na+
loop of henle
filtrate flows to here from proximal tubule

dips into medulla

functions to increase solute concentration, thus osmotic pressure, of medulla

concentrates solute in medulla

water passively diffuses out and into medulla

2 parts:
1. descending loop of henle
2. ascending loop of henle
descending loop of henle
low permeability to salt

filtrate osmolarity goes up

permeable to water
ascending loop of henle
filtrate rises out of medulla into cortex

salt diffuses out, passively at first and then actively

impermeable to water

actively transports Na+ into kidney
distal tubule
reabsorbs Na+ and Ca +2

secretes K+, H+ and HCO3-

ADH acts on distal tubule cells to increase Na+ & K+ membrane transport proteins

net effect:
lower filtrate osmolarity

ADH acts to increase permeability of cells to water

presence of ADH, water flow from tubule, concentrating filtrate
collecting duct
where distal tubules empties

carries filtrate into highly osmotic medulla

impermeable to water and sensitive to ADH

presence of ADH, collecting duct becomes permeable to water allowing it to passively diffuse in medulla, concentrating urine

lead to renal pelvis
juxtaglomerular apparatus
monitors filtrate pressure in distal tubule

cells secrete renin enzyme, to initiate regulatory cascade which ultimately stimulates adrenal cortex to secrete aldosterone

aldosterone acts on distal tubule, stimulating formation of membrane proteins that absorb Na+ and secrete K+