Chapter 51
fueling the body: digestion and
nutrition
I.
Types
of Digestion
A.
single
cell organisms digest intracellularly
B.
multicellular
organisms digest extracellularly
1.
two
way digestive tract: (flatworm)one
opening, no specialization due to exposure to particles at all levels of
digestion. (gastrovascular cavity)
2.
One
way digestion: specialized regions for
specialized breakdown.
Nematode(roundworm)èannelida(earthworm)èèhigher vertebrates
3.
ingestion,
storage, fragmentation, digestion, absorption.
II.
ingestion:
A.
teeth: tear or grind
carnivors:
specialized ripping/tearing
omnivores:
tearing and grinding
herbivores:
specialized grinding
B.
gizzard
of birds grind
C.
structures
of mouth
1. tongue
D. enzymes
of mouth:
1. salivary glands
III.
Transport
to stomach
A. Esophagus
1. Peristalsis: rythmic contractions initiated by swallowing
B. Cardiac
sphincter: to the stomach
C. Stomach
Gastric
juice
Protease (pepsin) è pepsinogen
HCL (activates pepsin, denatures
proteins, kills bacteria
D. Pyloric sphincter: to the SI
IV.
Small
vs. large intestine
A.
divided
into duodenum, jejunum, ileum
B.
enzymes
of the small intestine: brush
border
1.
peptidaseè short polypeptides into amino acids
2. nucleases è nucleotides into sugars and nucleic acid bases
3. lactase, maltase, sucraseè disaccharides into monosaccharides
4. lipase è triglycerides into fatty acid and glycerol
C.
absorption
by small intestine
1.
into
blood: amino acids and monosaccharides.
2.
Into lymphatic: fatty acids and
monoglycerides
A.
absorption
of water, sodium and potassium.
B.
Vestigeal
structure: appendix serves a function
in some mammals, but none in humans
C.
Bacterial
flora present in LI aids digestion in some mammals through fermentation, but
due to lack of absorption in humans only produces gas.
V.
Accessory
organs
A.
pancrease: secrete enzymes into and activated by brush
border of SI
1.
pancreatic
fluid secreted through pancreatic duct:
from
pancreatic cells
a.
trypsin
& chymostrypsin è protein breakdown
b.
pancreatic
amylase è
starch breakdown
c.
lipase
è fat
breakdown
from acini
d.
bicarbonate
è
neutralize HCl from stomach
from islets
of langerhans (not a digestive function)
e.
glucagon
from alpha cells (increase sugar in blood)
f.
insulin
from beta cells (decrease sugar in blood)
B.
liver: produces bile
1. bile
pigments: come from breakdown of RBC;s è waste only
2.
bile
salts: emulsifies fats in small
intestine
C.
gall
bladder: stores bile
1.
delivers
through common bile duct into SI
D. Regulation for homeostasis:
1.
hepatic
portal vein takes blood from stomach/intestine directly to liverè takes out alcohol, drugs, steroid hormones, poisons and converts to
less toxic forms. Converts ammonia
(from intestinal bacteria) è urea for kidney removal.
2.
Insulin
and glucagon regulate blood sugar levels by Ièstoring sugar in liver as
glycogen, Gè releasing sugar from liver stores. (fasting can cause gluconeogenesis from
amino acids/lactic acid from muscle cells =
burning muscle.) (insulin ineffectivenessè diabetes mellitus)
VI.
digestive
systems variation:
A.
ruminants: stomach divisions (cow/deer)
1.
1st
chamber partially digests
2.
regurgitated
for more chewing
3.
2nd
, 3rd chambers further digest
4.
4th
chamber has gastric juices like stomach.
B.
other
herbivores (horses, rodents, rabbits)
1.
enlarged
cecum that has bacteria that ferment to breakdown cellulose
2.
eating
of feces to pass nutrients though a second time
C.
wax
eaters(birds/some fish/crustaceans)
1.
rely
on bacteria to breakdown wax
D. most
animals rely on microorganisms to make vitamin K (for blood clotting)
VII.
nutrition
1. satiety
factor: ob/ob gene translates into a mutated form of leptin released by
adipocytes which do not cause satietation as does the normal form of leptin.
2. essential nutrients: must be obtain through dietè vitamins, minerals, amino acids, some cant produce fatty acids.