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BIO202 Anatomy & Physiology
Lecture Outline 7: Digestive System
B. Accessory Structures
1. assist in digestion
2. includes teeth, salivary glands, liver, gall bladder, pancreas
C. Four Major Layers of GI Tract
1. mucosa - innermost lining of GI organs
a. epithelium
b. lamina propria – areolar CT,
MALT, blood vessels, lymph vessels
c. thin muscularis layer
2. submucosa
a. areolar CT
b. blood vessels
c. autonomic nerves
3. muscularis
a. smooth & skeletal muscles
4 serosa - outermost lining of GI organs
a. CT + simple squamous epithelium
(mesothelium)
b. peritoneum
i. visceral
– mesothelium on organ surface
ii. parietal
– mesothelium on abdominal wall
iii. major periotoneal
folds – extensions of peritoneum layers
aa. mesentary – attaches SI to posterior wall
bb. mesocolon – attaches LI to posterior wall
cc. falciform ligament – attaches liver to anterior wall
dd. lesser omentum – attaches stomach & duodenum to liver
ee. greater omentum – attaches transv. colon & SI to stomach
& duodenum
D. Oral Cavity Structures
1. deciduous teeth (20)
2. permanent teeth (32)
3. tongue
a. skeletal muscles
b. moves food mass “bolus”
c. appropriate use of “lingual”
terminology
4. salivary glands (3 pair)
a. parotid
b. submandibular
c. sublingual
d. parasympathetic innervation
(activation)
5. saliva
a. amylase - begins starch
digestion (not very significant amount)
b. lysozyme - protective,
digests bacterial cell walls
c. lingual lipase - begins
lipid digestion (not very significant amount)
6. appropriate use of “buccal” terminology
E. Pharynx
1. oropharynx
2. esophagus - connects pharynx to stomach
3. peristalsis - rhythmic smooth muscle contractions
propel material inside
II. Major Organs of Digestion and Absorption
A. Stomach
1. general anatomic regions
a. cardia
b. fundus
c. body
d. pyloric region
2. stomach is important in the process of physical
digestion
3. rugae are undulations in stomach wall
to help grind
4. gastric pits contain four major secretory
cells:
a. chief cells
i. pepsinogen
aa. activation of pepsinogen by low pH to form pepsin
bb. pepsin is a protease for protein digestion
b. parietal cells
i. HCl
aa. secretion enhanced by histamine via H2 receptors
bb. Tagamet blocks H2 histamine receptors to inhibit HCl secretion
ii. intrinsic
factor
aa. binds to and allows B12 absorption in intestines
c. G-cell
i. secretes gastrin hormone
aa. gastrin activates gastric juice secretion & gastric smooth muscle
“churning”
bb. gastrin activates gastroileal reflex which moves chyme from
ileum to colon
d. mucus cell
i. protective role of mucus against acids and digestive enzymes
5. pyloric sphincter regulates entry
into the duodenum
6. chyme is liquified digested material
B. Gastric Activity
1. major action in the stomace are secretion of
gastric juice & contraction of smooth muscle
2. three major mechanisms of gastric regulation
a. cephalic phase
i. initiated
by parasympathetic activation (vagal innervation)
ii. cortical
(smell, thoughts, etc.) activation of medulla
iii. medulla
activates gastric juice secretion
iv. medulla
activates gastrin secretion
v. medulla activates
smooth muscle “churning”
b. gastric phase
i. food mass
and chemicals trigger parasympathetic reflex
ii. enhance
parasympathetic activation of stomach
iii. activate
& enhance emptying of chyme into duodenum
c. intestinal phase – will
cover later in outline
C. Small Intestine
1. major site of chemical digestion & absorption
2. approx. 21 ft long/ 1inch diameter
3. three major segments
a. duodenum ~10 inches
b. jejunum ~8 ft
c. ileum ~ 12 ft
4. histology
a. mucosa has intestinal glands
(cavities) for secretion of intestinal juice
b. mucosa also has circular
folds, villi & microvilli for increased surface area
c. “brush border” has many
enzymes embedded in plasma membranes
i. several carbohydrate-digesting
enzymes
ii. peptidases
iii. nucleosidases
iv. enterokinase
is released by epithelial cell “shedding”
aa. important enzyme activator – see later
D. Intestinal Phase of Regulating Digestion
1. chyme enters duodenum
2. three hormones secreted from SI mucosa
a. gastric inhibitory peptide
(GIP)
i. fatty acids
in chyme induce GIP secretion
ii. GIP inhibits
gastric secretion
iii. GIP inhibits
gastric “churning”
iv. GIP activates
insulin secretion
b. secretin
i. secretin
inhibits gastric secretion
c. cholecystokinin (CCK)
i. CCK fatty
acids in chyme induce CCK secretion
ii. CCK slows
gastric emptying
3. receptors in SI mucosa sense food/chemical presence
in duodenum
4. neuronal activation of sympathetic NS/ inhibiton
of parasympathetic NS
E. Role Of The Pancreas In Digestion
1. approx 1.5L/day pancreatic secretions produced
2. secretions enter duodenum via two pancreatic
ducts
3. many different components in these secretions
a. NaHCO3 – buffers pH of chyme
b. pancreatic amylase
c. trypsinogen, chymotrypsinogen,
carboxypeptidase
i. trypsinogen
activated by enterokinase to become trypsin
ii. trypsin
acts on other proteases to activate them
d. lipases
e. ribonucleases
G. Regulation Of Pancreatic Secretions
1. neuronal regulation
a. initiated by parasympathetic
activation (vagal innervation)
b. same stimuli as with cephalic
and gastric phases
2. hormonal regulation
a. CCK stimulates pancreatic enzyme
secretions
b. secretin stimulates bicarbonate
secretions
H. Role Of The Liver
1. liver is largest gland in body
2. overall function to “filter” and process nutrient-rich
blood delivered to it
3. receives nutrient-rich blood from SI via the
hepatic portal vein
4. many functions to liver besides aiding in digestion
5. regulates carbohydrate metabolism
a. glucose secretion into blood/absorption
from blood into glycogen storage
b. regulated by insulin &
glucagon (endocrine review)
6. regulates many aspects of lipid metabolism
a. chemical digestion of fatty
acids (B-oxidation) for entry into Krebs cycle
i. release of
ketones as metabolic waste product of fatty acid metabolism
b. cholesterol synthesis
7. detoxifies blood
a. ETOH detoxification
b. other dietary toxins neutralized
by liver
8. bile synthesis (approx 1L/day)
a. bile salts (cholesterol
derivatives) function to emulsify fats to aid enzymatic digestion
i. bile salts
are recycled (are not excreted) from colon back into liver for reuse
b. main bile pigment is bilirubin
– derived from RBC heme
i. bilirubin
and other neutral fats in bile do not aid in digestion; they are excreted
e. bile is synthesized in liver,
stored in gall bladder
f. release of bile from gall bladder
stimulated by CCK and vagus nerve
i. CCK also
causes hepatopancreatic sphincter to relax – allows bile to enter
duodenum
ii. secretin
also stimulates bile synthesis
iii. bile salts
also act as positive feedback activator to enhance more bile synthesis
g. “gallstones” are concentrated
precipitates of cholesterol
i. gallstones
form when bile is too rich in cholesterol or lacking bile salts
I. Large Intestine
1. major function to absorb water and eliminate
indigestable matter
2. major structures
a. cecum with vermiform appendix
b. ascending, transverse, descending
colon
c. sigmoid colon, rectum
d. haustra are pouches in wall
of large intestine
i. haustral
churning is sequential movement of contents from one haustra to the
next
ii. gastrocolic
reflex is rapid peristalsis in LI triggered by food in stomach
3. normal bacterial flora colonize colon
a. vitamin K synthesis by E.
coli bacterium
4. vermiform appendix
a. lymphatic structure attached
to cecum
J. Nutrient Absorption
1. carbohydrates
a. enzymatically digested to form
monosaccharides (glucose, fructose, galactose)
b. absorbed in SI by active transport
or facilitated diffusion
c. enter blood capillary in villi,
then directed to hepatic portal vein
2. proteins
a. enzymatically digested to amino
acids or di- and tri-peptides
b. absorbed in SI by active transport
or facilitated diffusion
c. enter blood capillary in villi,
then directed to hepatic portal vein
3. lipids
a. enzymatically digested to short
or long chain fatty acids
b. suspended in SI in form of
micelles with bile salts
c. micelle formation aids lipid
diffusion into SI epithelial lining
d. inside epithelial cells, lipids
bound into chylomicrons for transport
e. chylomicrons transported to
lacteal villi; then into lymphatics and then to venous
blood