Title: Digestive System and Derivatives
1Digestive System and Derivatives
- Derivatives include respiratory system, liver,
pancreas, gall bladder and endocrine structures - All are endodermal in origin
- Digestive System includes digestive tract
- Mouth Pharynx Small Intestine
- Esophagus Large Intestine
- Stomach Cloaca (or derivative)
- Also includes associated digestive glands liver,
pancreas and gall bladder
2Figure 13.1
Fig 13.1 Digestive tract components
3Embryonic Origin of Digestive Tube
- Embryonic Origin of Digestive Tube by 2 Basic
Methods - Cyclostomes, Actinopterygians, and Amphibians
gastrulation provides a tube-within-a-tube
arrangement. Inner tube is endodermally derived
and becomes gut. - All other vertebrates have
- The epiblast oriented on top of the hypoblast in
flat sheets. The hypoblast is continuous
peripherally with the endoderm of the prospective
yolk sac. - Development of head, lateral body, and tail folds
separate the embryo from extraembryonic
membranes. - The endoderm folds upon itself to form a tube
continuous ventrally with the yolk sac ? forms
the gut.
4Development of Openings to Gut Tube
- Protostomes blastopore forms the mouth the
anus is derived secondarily - Includes Annelids, Molluscs, and Arthropods
- Deuterostomes blastopore becomes the anus the
mouth forms later as an independent perforation
of the body wall - Includes Echinoderms and Chordates
- In vertebrate development the head turns downward
over the surface of the yolk, forming an
ectodermal pocket (stomodeum) which represents
the primitive mouth cavity
5Development of Openings to Gut Tube
- Stomodeum is separated from the pharyngeal
region of the gut by a membrane (pharyngeal
membrane) that eventually breaks down so that the
oral cavity and pharynx become continuous. - Proctodeum is similar invagination at the
posterior end of the gut, separated from the gut
by the cloacal membrane that eventually
disappears, leaving a tube open at both ends. - The mouth and teeth are derived from ectoderm.
6Figure 13.2
Fig 13.2 Embryonic formation of the digestive
system
Early amniote embryo
Generalized amniote embryo
Ventral view of isolated gut
Lateral view of differentiating gut
7Development of Openings to Gut Tube
- The boundary of the mouth ideally is the junction
of the stomodeum (ectodermal) with the pharynx
(endodermal). - In practice, definite anterior and posterior
limits to the mouth are difficult to establish,
and differ among vertebrate groups. - Landmarks used in distinction as markers of the
mouth (ectodermally derived) include - Nasal Pits ( nasal placodes)
- Rathkes Pouch ( hypophyseal pouch)
- Evolutionary trend toward inclusion of more
ectoderm inside the mouth in advanced forms - Primitively, stomodeal structures are forced
outside the mouth through differential growth
8Figure 13.4
Fig 13.4 boundaries of the mouth cavity
9Mouth Cavity
- Lined by skin, includes teeth and salivary glands
as components - Teeth are homologous with the integument of some
fishes and placoid scales (denticles) of shark
skin - Location of teeth
- Fish found on palate (roof of mouth), margins
of jaw, gill arches - Amphibians/Reptiles found on some bones of the
palate and margins of maxillary, premaxillary and
dentary bones - Mammals found only on margins of maxillary,
premaxillary and dentary bones
10Mouth Cavity
- Evolutionary trend in mammals reduction in
numbers of teeth from primitive to advanced
mammals - Primitive mammal number is 44 (humans with 32)
- Whales have an increased number as a
specialization to their very large mouth - Birds have no teeth, except for primitive
Mesozoic forms (associated with reduced weight
for flight) - Turtles also lack teeth instead have a hard,
keratinized beak - Number of generations of teeth is reduced from
primitive (continuous replacement) to advanced (1
or 2 sets) vertebrates
11Degree of Tooth Differentiation
- Homodontous Condition all teeth are similar,
generally conical in shape - Most vertebrates
- Heterodontous Condition specialization of
teeth - Typical state for a few reptiles, Therapsids, and
Mammals - Teeth include
- Incisors (front) - used for cropping
- Canines - behind the incisors, used for tearing
- Molars (cheek teeth) - furthest back in mouth,
used for chewing - Teeth in heterodontous vertebrates are used for
capture or cropping of food and chewing - Chewing aids in digestion by increasing surface
area of food available for digestion - This increases digestive efficiency and provides
energy necessary to support high rates of
metabolism of mammals
12Homodontous Teeth from salamander
Heterodontous Teeth from fox
13Salivary Glands
- Formed from invaginations of the mouth lining
- Mucous Glands produce mucous lubrication of
food - Serous Glands watery secretion containing
enzymes initiates digestion of carbohydrates
(salivary amylase) - Mixed Glands mucous and serous secretions
- Snake venom glands are modified serous salivary
glands
14Fig 13.37 Salivary glands in a dog
15Fig 13.35 Oral glands of reptiles. Venom glands
derived from Duvernoys gland.
16Palate
- Forms roof of mouth
- Composed of bone, lined by epithelium and
connective tissue - Fish, Amphibians and Birds have only a primary
palate present - Crocodilians and mammals also have a secondary
palate, which allows simultaneous chewing and
breathing in mammals, and breathing while mouth
is submerged in crocodiles - Secondary palate separates nasal passages from
mouth
17Fig 7.57 Primary and Secondary palates in
vertebrates
18Pharynx
- Shared region between digestive and respiratory
systems Respiratory system represents a
derivative of the digestive tract. - Other pharyngeal derivatives
- Thyroid - present in all vertebrates, always
derived as outpocketing from floor of 1st
pharyngeal pouch - Fish thyroid tissue becomes dispersed along
the ventral aorta in adults - Tetrapods remains as a single or bilobed gland
- Function produces Thyroid Hormones that
increase metabolic rate and regulate early
development and growth - C-cells are also present (only in mammals)
produce Calcitonin which decreases blood calcium
levels by reducing bone resorption
19Other Pharyngeal Derivatives
- Parathyroids - not present in fishes present in
all tetrapods - Amphibians and Reptiles derived from ventral
regions of pouches 2-4 - Birds from ventral regions of pouches 3-4
- Mammals from dorsal regions of pouches 3-.
- Secrete parathyroid hormone which increases blood
calcium levels by promoting bone resorption
20Other Pharyngeal Derivatives
- Thymus - found in all vertebrates except
Cyclostomes - Derived from various pouches in the different
vertebrate groups - Function immunological role, production of
T-lymphocytes ? cell-mediated immunity - Ultimobranchial Bodies derivatives of ventral
part of 5th pharyngeal pouch in all vertebrates
except mammals - Secrete Calcitonin, so they are presumably
homologous with C-cells of mammalian thyroid
gland - 1st Pharyngeal Pouch forms spiracle in
Elasmobranchs - Forms the tympanic cavity and Eustachian tubes in
Tetrapods
21Comparative Pharyngeal Pouch Derivatives in
Vertebrates
22Digestive Tube Proper
- General Sequence anterior to posterior is
Esophagus ? Stomach ? Intestine ? Cloaca (or
anus) - Esophagus
- Function food transport secretes mucus to aid
passage - Birds show specialized Crop sac-like structure
adapted for food storage
23Stomach
- None present in Cyclostomes, chimeras, lungfish,
and some teleosts (primitive condition) - When present, functions in food storage, physical
treatment of food, initiates digestion - Food storage is the primary function (and
probably the original evolutionary function) - Physical treatment evolved somewhat later as food
is taken in large chunks - Digestion probably is latest function to evolve
24Stomach
- Birds and Crocodiles
- Muscular tissue of stomach is concentrated
posteriorly as a gizzard - Anterior stomach is glandular (Proventriculus)
- Because birds lack teeth, many will swallow small
pebbles (grit) that lodge in the gizzard and aid
in grinding food - Functional analog to teeth in mammals
25Stomach
- Ruminant Mammals (Cud-chewing Ungulates)
- Possess ruminant stomach with 4 chambers
- When food is eaten it enters rumen and reticulum
which reduce the food to pulp - Microorganisms are present that aid in the
breakdown of complex carbohydrates in plant
material - The cud is then regurgitated for more chewing
- After chewing the cud, the remasticated material
passes to omasum and abomasum where physical and
chemical processing similar to normal mammalian
stomach occurs - The rumen, reticulum, and omasum are derived as
modifications of esophagus abomasum is the true
stomach - Ruminant-like digestion occurs in one bird, the
Hoatzin - Folivorous (eats leaves) bird with foregut
fermentation similar to ruminant digestion - Enlarged crop lower esophagus house symbiotic
bacteria
26Fig 13.42 Ruminant digestion in the bovine
stomach
27Foregut fermentation in Hoatzin digestive system
28Intestine
- Majority of digestion and absorption occurs here
- Sharks and some other fishes have a spiral
intestine cigar-shaped body with spiral valve
internally - Greatly increases surface area for absorption
- Increased surface area in Tetrapods is by
elongation and coiling of intestines along with
folding of internal surfaces - Intestine is longer in herbivores than in
carnivores because plant matter is more difficult
to digest
29Intestine
- Evolutionary Trend in intestine structure
increased intestinal surface area (primitive ?
advanced) associated with higher metabolic rates
in advanced vertebrates - Hagfish lack spiral valve poorly developed in
lampreys - Spiral valve is present in sharks and some other
fishes - Elongation and coiling with internal folding in
Tetrapods
30Fig 13.27 Stomach and Intestines in
non-mammalian vertebrates
31Figure 13.28
Fig 13.28 Stomach and Intestines in various
mammals
32Fig 13.29 Digestive tracts of various fishes.
Note spiral valves in several species and
elongation of intestine in perch