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Digestion. Types of digestion systems. 2 /23. in unicellular and primitive multicellular organisms intracellular digestion in more developed multicellular organisms – extracellular digestion - PowerPoint PPT Presentation
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Digestion
Types of digestion systems
• in unicellular and primitive multicellular organisms intracellular digestion
• in more developed multicellular organisms – extracellular digestion
• diverse extracellular digestion systems exist in animals – there are three basic types based on the functioning of the „reactor”– intermittent, stirred – saclike; one portion in,
digestion, undigested remnants out (e.g. hydra)
– continuous flow, stirred – continuous intake, content mixed, continuous output (e.g. ruminant forestomach)
– plug-flow, unstirred – continuous input, continuous output, tubelike reactor, composition depends on place, but not on time (e.g. small intestine in vertebrates)
2/23
Alimentary canal in vertebrates
• topologically external to the body
• entrance and exit are protected by sphincters and other devices
• ingested material is subjected to various mechanical, chemical and bacterial effects
• digestive juices break down the ingested material chemically, nutrients are absorbed, undigested, unabsorbed material is expelled with the feces
• tubular organization allows for functional specialization (i.e. acidic and alkaline environment)
• parts of the alimentary canal: headgut,
foregut, midgut, hindgut
3/23
Headgut• food enters here – structures related to
feeding and swallowing: mouth-parts, buccal (oral) cavity, pharynx, bills, teeth, tongue, salivary glands, additional structures to direct the flow of ingested materials and inspired water or air
• most multicellular organisms have salivary glands to help swallowing (mucin - mucopolysaccharide)
• saliva may contain: enzymes, toxins, anticoagulants (vampires, leeches, etc.)
• tongue from chordates on – mechanical digestion, swallowing, grasping food (chameleon, anther), chemoreception (taste buds)
• snakes take olfactory samples from the air and wipe the samples in the Jacobson’s organ (vomeronasal organ)
4/23
Foregut• in most species it consists of the esophagus
and the stomach• esophagus carries food from headgut to
stomach• in infrequently feeding animals it can contain
a saclike expanded section – crop (leeches) to store food, birds might use it to feed nestlings
• digestion starts in the stomach• in most vertebrates: pepsinogen and HCl• monogastric stomach in omnivorous and
carnivorous vertebrates• invaginations with gastric pits with gland cells
• digastric stomach in ruminants: fermentative
(rumen + reticulum - cellulose) and digestive (omasum + abomasum [enzymes only here]) parts
• camel, llama, alpaca, vicuñas: similar stomach• fermentation occurs before the stomach also
in other species: kangaroo, chickenlike birds• birds might have a muscular gizzard following
the stomach – chyme moves back and forth
5/23
Midgut I.• in vertebrates it consists of the small
intestine (duodenum, jejunum, ileum), it is separated from the stomach by the pylorus
• shorter in carnivores, longer in herbivores – dynamic changes
• in tadpoles longer than in frogs relative to body size
• duodenum: production of mucus and fluids + receives secretions from liver and pancreas – neutralization of stomach acid and digestion
• jejunum: secretion of fluids, digestion, absorption
• ileum: mainly absorption, some secretion• small intestine is characterized by a large
surface epithelium: gross cylindrical surface would be 0.4 m2, but circular folds, intestinal villi, brush border - 200-300 m2
6/23
Midgut II.• circular folds also slow down the progress
of food – more time for digestion• each villus (approx. 1 mm long) sits in a
circular depression (crypt of Lieberkühn) – inside: network of arterioles, capillaries and venules, in the middle: central lacteal (lymph vessel)
• longitudinal smooth muscle fibers – their contraction empties the lymph vessels
• epithelium is made up of enterocytes (lifespan 3-6 days) proliferating at the bottom of the crypts (chemotherapy!) and bearing brush border (~1 long, 0.1 wide, 200,000/mm2); tight junctions, desmosome
• on the microvilli (brush border) glycocalyx: hydrolases (glycoproteins) and luminal transporters, inside actin filaments – in the basolateral membrane Na-K-pumps and different transporters
• among the enterocytes sporadic goblet cells (mucus)
7/23
Hindgut• stores remnants of digested food –
absorption of inorganic ions and water• in vertebrates it consists of the final
portion of small intestine and of the large intestine (colon)
• the hindgut is the major site of fermentation in many herbivores– colon fermentation (plug-flow reactor) – large
animals, like horses, zebras, elephants, rhinos, sirenians (sea cows), etc.
– cecal fermentation (continuous-flow, stirred reactor) - smaller animals, like rabbits, many rodents, koalas, opossums, etc.
• hindgut terminates in the cloaca in many vertebrates (cyclostomes, sharks, amphibians, reptiles, birds and egg laying mammals), or in the rectum
• defecation and urination are under behavioral control
• the alimentary canal in invertebrates have many differences, but similarities as well
8/23
Motility of alimentary canal I.
• motility is the ability of the alimentary canal to contract
• its roles:– propulsion of food from intake to excretion– grinding and kneading the food to mix it with
digestive juices and to convert it to a soluble form– stirring the gut contents to ensure the continuous
renewal of material in contact with the epithelium
• in arthropods and chordates it is achieved exclusively by muscular motility, in other animal groups ciliary motility might play a supplemental or exclusively role
• in vertebrates at the entrance (buccal cavity, pharynx, first third of the esophagus) and exit (external anal sphincter) of the alimentary canal striated muscles – providing an at least partial voluntary control, in other places smooth muscles and the enteric nervous system dominates
9/23
Motility of alimentary canal II.• layers of the alimentary canal in vertebrates:
serosa, longitudinal and circular muscle, submucosa, muscularis mucosa, lamina propria, epithelium
• there are two basic forms of motility: peristalsis (longitudinal and circular muscles) and segmentation (circular muscles)
• sphincters: upper and lower esophageal, cardia (functional), pylorus, ileocecal valve (between the small and large intestine), internal and external anal
• swallowing is a complex reflex: tongue presses the food to the palate, soft palate closes the nasal cavity, food is propelled into the pharynx, mechanoreceptors induce the reflex, swallowing is unstoppable
• upper esophageal sphincter relaxes, peristalsis moves the food toward the stomach, lower esophageal sphincter relaxes, cardia opens, food enters the stomach
10/23
Motility of alimentary canal III.
• vomiting – complex reflex, helped by the respiratory muscles – reverse peristalsis in the small intestine, inspirational muscles contract – negative pressure in the chest, abdominal muscles contract – large pressure difference – lower esophageal sphincter relaxes, chyme enters the esophagus
• chyme returns to the stomach during retching
• during vomiting expiratory muscles contract, upper esophageal sphincter relaxes
• centers in the medulla: central vomiting (without retching), retching (without vomiting), chemoreceptive trigger zone
• stimuli: direct (meningitis, disgust), chemical (e.g. apomorphine), mechanical (back of the throat), visceral (peritoneum, uterus, renal pelvis, testis), organ of equilibrium
• reflux – cardia is leaking, acidic chyme reenters the esophagus – can lead to inflammation, cancer
• regurgitation: in ruminants – chyme reenters the buccal cavity without vomiting
11/23
Motility of alimentary canal IV.• peristalsis in the stomach by partially
closed contraction ring - mixing, but it is not complete – rat experiment with differently colored food
• small intestine – circumscribed expansion induces peristalsis
• obstruction of passage – very dangerous• causes: mechanical (e.g. tumor),
physiological (sympathetic hyperactivity – caused by peritoneal excitation) - mechanism not completely clear
• large intestine absorption of water and ions, excretion of feces
• following eating gastrocolic reflex distal movement of the chyme – might involve mass movement – frequently occurs in babies: eating leads to defecation
• defecation is a complex process: posture, contraction of abdominal wall, sphincters
• internal sphincter autonomic, external voluntary regulation
12/23
Regulation of the intestines I.
• intrinsic control: contraction is myogenic in the alimentary canal – smooth muscle is capable of inducing electrical activity (rhythmic hypo-, and repolarization – might lead to Ca-spike and contraction; influenced by stretching and chemical stimuli from the chyme
• extrinsic control: enteric nervous system, central nervous system, peptide hormones
• enteric nervous system– myenteric (Auerbach's) and submucosal
(Meissner’s) neuronal networks– local reflexes– sensory neurons: transmit information of
mechano-, chemo-, and osmoreceptors - substance-P
– interneurons: n-Ach (excitatory), enkephalinergic, somatostatin releasing (inhibitory)
– effector neurons: excitatory: colocalized ACh and tachykinin (e.g. substance-P); inhibitory: VIP, NO, ATP - morphine excites the latter neurons, long-lasting contraction, constipation; on glands VIP can also be excitatory
13/23
Regulation of the intestines II.
• central nervous system– parasympathetic innervation (preganglionic):
• acting mostly on interneurons of the enteric nervous system – excitatory effect
• to a smaller extent on efferent neurons – stomach functions, sphincter relaxation (e.g. esophagus)
– sympathetic innervation (postganglionic): • vasoconstriction• pre-, and postsynaptic inhibition through 2-receptors• direct excitatory effect on sphincters through 1
receptors
• local peptide hormones– proved hormones: secretin, gastrin, CCK, GIP
(glucose-dependent insulinotropic peptide (formerly: gastric inhibitory peptide) – many more candidates
– hormonal role is difficult to prove: measurement of levels, administration (physiological vs. pharmacological dose), antagonists
– gastrin family - five C-terminal amino acids of gastrin and CCK are the same, both are active at different lengths
– secretin family – secretin, GIP, glucagon, VIP– produced by unicellular glands detecting the
composition and pH of the chyme directly – neuronal regulation in some of them 14/23
Gastrointestinal hormones
cell
hormone stimulus stomach bile pancreas
G gastrin
peptides,amino acids
in the stomach
HCl producti
on, motility
up
CCK
cholecystokinin
lipids, proteins in the small intestine
motility, emptyin
g inhibite
d
emptying the
gall bladder
increased enzyme
production
S secretinacid in the
small intestine
emptying
inhibited
increased HCO3
- secretion
GIP
glucose-dependent
insulinotropic peptide
carbohydrates in the
small intestine
HCl producti
on, emptyin
g inhibite
d
glucose dependent
insulin secretion
15/23
Gastrointestinal secretions• three types of secretion exist:
– secretion-reabsorption type – proteins, water, electrolytes secreted in the acinus, reabsorption in the secretory duct, e.g. salivary glands
– sequential secretion type – protein secretion in the acinus, water and electrolytes in the secretory duct, e.g. pancreas, liver
– parallel secretion type – e.g. stomach; chief cells: pepsinogen, parietal cells: HCl, intrinsic factor, goblet cells: mucin and HCO3
–
• in one day about 5-6 l digestive secretions • production of saliva
– three pairs of large salivary glands: parotid, submandibular, sublingual + many small ones in the buccal cavity
– function: lubrication (dry mouth - thirst), mucin, lysozyme, IgA, rinsing (dog-breath), amylase
– serous and mucous acinus cells– saliva is hyposmotic because of the reabsorption
of NaCl – mostly parasympathetic innervation,
sympathetic activation results in thick, viscous saliva
– unconditional and conditional reflexes – trumpet player and licking of lemon
16/23
Secretion in the stomach
• secretion is parallel in the stomach; in addition, G-cells produce gastrin
• fluid is acidic and isosmotic• functions of the low pH: optimal environment
for pepsin, chemical degradation of the food (denaturation), killing of bacteria
• large invaginations (canaliculi) in the membrane of the parietal cells with H-K-ATPase molecules - 106 concentration gradient – “world” record (exit of Cl– and K+ through channels)
• source of H+: CO2 and water (carbonic anhydrase, HCO3
–/Cl– exchange) • facilitation: vagus nerve (m-ACh), gastrin,
histamine• cephalic, gastric, intestinal phase• inhibition: HCl level, fatty acids longer than
10 C in the small intestine• secretion of chief cells increased by n-ACh,
HCl
17/23
Secretion of the pancreas• indispensable for digestion• sequential secretion
– acinus cells: • active enzymes (-amylase, lipase, DNAase, RNAase)• proenzymes (trypsinogen, chymotrypsinogen,
procarboxipeptidases, prophospholipases, etc.)
– secretory duct: • large amount of fluid with high HCO3
– content (alkaline)
• CO2 - HCO3– and H+ (carbonic anhydrase), Na+/H+
antiporter, Na+-pump, apical HCO3– exit
• secretory duct enters the duodenum along with the bile duct at the ampulla of Vater
• enteropeptidase (enterokinase) secreted by the duodenum activates trypsin, which in turn activates all the other (there is also a trypsin inhibitor in the pancreas) – during inflammation early activation, necrosis and death can occur
• activation of acinus cells: CCK, m-ACh, VIP• activation of HCO3
– secretion - secretin
18/23
Functions of the liver• secretion (bile acids) and excretion (bilirubin,
cholesterol, poisons, medicines, hormones, etc.)
• bile is produced by the parenchyma cells (75%) and by the epithelium (25%) lining the bile ducts the latter secretes electrolytes
• sinusoids with large-pored endothelium, between them one-cell-thick parenchyma sheets – between neighboring hepatocytes bile canaliculi, surrounded by tight junctions – if damaged bile enters circulation
• bile is concentrated in the gallbladder, emptied three times a day (20-30 ml)
• 95% of bile acids are reabsorbed from the gut• bilirubin is transformed by bacteria to
stercobilin giving the brown color of the stool
19/23
Digestion and absorption I.• carbohydrates completely, while lipids and
proteins up to more than 90% are digested and absorbed from the gut
• digestion of carbohydrates and proteins is a two-step process: luminal digestion is completed by enzymes (oligosaccharidases, exopeptidases) on the surface (glycocalyx) of enterocytes
• absorption is mostly energized by the Na+ gradient that in turn is rebuild by the K+-Na+-pump in the basolateral membrane
• carbohydrates: -amylase can break the 1-4 bond, but not the 1-6– it is unable to break the -glycosidic bond in
lactose, this bond gets broken by the lactase (-galactosidase) – the lack of this enzyme leads to lactose intolerance
– uptake of glucose and galactose is accomplished by a Na+ cotransporter, fructose enters the cell using GLUT-5 – it is slower, as it is a passive process
– all sugars are transported through the basolateral membrane by GLUT-2
– part of the plant fibers (cellulose) are fermented by bacteria – not much usable energy is released, but huge amount of CH4, CO2 is produced
20/23
Digestion and absorption II.• proteins:
– luminal endopeptidases (pepsin, trypsin, chymotrypsin, elastase) and exopeptidases (carboxypeptidases) digest proteins to amino acids and smaller peptides
– enterocyte glycocalyx: different membrane peptidases
– membrane transport as amino acids (70-75%) or di-, and tripeptides (25-30%), mainly by group-specific Na+ cotransporters (active transport), partly through facilitated diffusion
– at the basolateral membrane: facilitated diffusion
• vitamin B12:– absorbed in protein-associated form– demand: 1-2 microgram/day – reserves in liver are
sufficient for several years– B12 binds to R-protein in the stomach, R is digested
in the duodenum, B12 binds to intrinsic factor– in the ileum, receptor induced endocytosis, in
blood transported by transcobalamin II– B12 is needed for erythropoiesis – anemia is most
frequently caused by the lack of the intrinsic factor
21/23
• lipids:– hydrophobic character, digestion is only
possible at the lipid-water border – micelles formed with the help of bile acids
– most important enzyme: pancreatic lipase; in general it cuts off 1,3 fatty acids
– fatty acids, 2-monoglycerids enter the enterocytes from the micelles
– micelles also contain lipid-soluble vitamins (DEKA) – lack of bile acids leads to low vitamin K levels and disturbances in hemostasis
– lipids are reformed in the endoplasmic reticulum of enterocytes and form lipoproteins containing triglycerides, phospholipids, cholesterol and its esters as well as apolipoproteins
– lipoproteins are classified according to their density: VLDL, LDL, HDL – the largest are the chylomicrons
– lipoproteins are transported from the Golgi to the lymphatic vessels through exocytosis
– lipoproteins are also produced in the liver
Digestion and absorption III.
22/23
• calcium:– reabsorbed partly by paracellular diffusion, but
mostly by active transport– regulation: parathormone and calcitriol (1,25-
dihidroxi-D3-vitamin)– entrance by unknown mechanism – calcium
binding protein – active transport through the basolateral membrane
• iron:– stored in the enterocytes in the form of ferritin,
transported in the blood bonded to transferrin – if the enterocyte is saturated absorption stops
– demand: in men 1 mg/day, in women (because of blood loss during menses) 2-3 mg/day – iron is needed mainly because of the renewal of enterocytes
• water and NaCl:– Na+ channels in the apical membrane (their
number is regulated by aldosterone) - Na+-pump in the basolateral membrane
– Cl– and water follows passively
Digestion and absorption IV.
23/23
End of text
Reactor types
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-13.
Parts of the digestive tract
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-15.
Monogastric stomach
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-18.
Anatomy of the small intestine
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-20.
Structure of a villus
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-21a,b.
Brush border
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-21c,d.
Colon and cecal fermenters
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-22.
Behavioral control
The Far Side Gallery 3, G.Larson, Andrews and McMeel, Kansas City. 1994, p..21.
Digestive systems in vertebrates
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-17.
Cross-section of the intestine
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-22.
Motility of the intestine
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-24.
Basic membrane potential rhythm
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-25.
Autonomic innervation
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-26.
Gastrointestinal hormones
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-34.
Digestive secretions
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-29.
Rinsing function of saliva
The Far Side Gallery 3, G.Larson, Andrews and McMeel, Kansas City. 1994, p..24.
Production of saliva
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-28.
HCl secretion in the stomach
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-32.
Pepsin secretion in the stomach
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-33.
Sugar transport in the intestine
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-35.
Lipid transport in the intestine
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-36.
Digestive fluid movements
Eckert: Animal Physiology, W.H.Freeman and Co., N.Y.,2000, Fig. 15-37.