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Digestive System 1

The digestive system breaks down food into smaller molecules that can be absorbed and used by the body. The main organs involved include the mouth, esophagus, stomach, and small intestine. In the mouth, chewing and saliva begin breaking down food. Swallowing moves food to the stomach through the esophagus. The stomach stores and further breaks down food using gastric juices. Digestion is regulated by neural and hormonal signals to prepare the digestive organs and respond to food.

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dmutethia68
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0% found this document useful (0 votes)
21 views

Digestive System 1

The digestive system breaks down food into smaller molecules that can be absorbed and used by the body. The main organs involved include the mouth, esophagus, stomach, and small intestine. In the mouth, chewing and saliva begin breaking down food. Swallowing moves food to the stomach through the esophagus. The stomach stores and further breaks down food using gastric juices. Digestion is regulated by neural and hormonal signals to prepare the digestive organs and respond to food.

Uploaded by

dmutethia68
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd
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Digestive system

Objectives
1. Introduction
2. Define the digestive processes
3. Discuss functional anatomy of GIT
i. Mouth
ii. Pharynx
iii. Esophagus
iv. Stomach
Objectives: Introduction
• The alimentary canal, also called the
gastrointestinal (GI) tract
• It digests food
• Absorbs the digested fragments through its lin
ing into the blood.
• The accessory digestive glands produce a
variety of secretions that help break down
foodstuffs.
Objective 2: Digestive processes
• Ingestion: taking food into the digestive tract
(eating)
• Propulsion: moving food through the
alimentary canal (swallowing, peristalsis,
segmentation)
• Mechanical breakdown: Increase S/A for
digestion (chewing, mixing with saliva,
churning in the stomach and segmentation of
small intestines)
• Digestion: break down complex food
molecules to their chemical building blocks
(catabolism)
• Absorption: digested end products (plus
vitamins, minerals, and water) move from the
lumen of the GI cells by active or passive
transport into the blood or lymph.
• Defecation: eliminates indigestible substances
from the body
Stimuli and control of digestive activity
• All digestive tract regulatory mechanisms
control luminal conditions so that digestion
and absorption can occur there as effectively
as possible.
• This is accomplished through enteric nervous
system/gut brain
• Digestive activity is provoked by chemical and
mechanical stimuli
• Effectors of digestive activity are smooth
muscles and glands
• Neurons and hormones control the digestive
activity
Objective 3: Discuss Functional
anatomy of GIT
i. Mouth
• Ingests food
• Begins mechanical digestion by chewing
• Mixes food with saliva
• Saliva contains enzymes that begin the
process of digestion.
• The mouth also begins the propulsive process
of swallowing
• Absorption does not occur in the mouth
• except for a few drugs that are absorbed
through the oral mucosa
• (for example, nitroglycerine used to alleviate
the pain of angina)
Saliva
• Cleanses the mouth
• Dissolves food chemicals so they can be tasted
• Moistens food and helps compact it into a
bolus
• Contains the enzyme amylase that begins the
digestion of starchy foods
Composition
• 97 to 99% water and therefore is
hypoosmotic.
• Slightly acidic (pH 6.75 to 7.00)
• Electrolytes (Na+, K+, c1-, P0 43-, and HC03-)
• The digestive enzymes salivary amylase and
lingual lipase
• The proteins mucin, lysozyme, and lgA
• Metabolic wastes (urea and uric acid)
• Lysozyme-a bactericidal enzyme that inhibits
bacterial growth in the mouth and may help
prevent tooth decay.
• When dissolved in water, the glycoprotein
mucin forms thick mucus that lubricates the
oral cavity and hydrates foodstuffs
Control of salivation
• Minor salivary glands secrete saliva
continuously in amounts just sufficient to keep
the mouth moist.
• When food enters the mouth, the major
glands are activated and large amounts of
saliva pour out
• Average output of saliva is about 1500 ml per
day
• Salivation is controlled primarily by the
parasympathetic division
• When we ingest food, chemoreceptors and
mechanoreceptors in the mouth send signals
to the salivatory nuclei in the brain stem (Pons
and medulla)
• Parasympathetic nervous system activity
increases.
• Impulses sent via motor fibers in the facial
(VII) and glossopharyngeaL (IX) nerves
dramatically increase the output of watery
(serous), enzyme-rich saliva.
• The chemoreceptors are activated most
strongly by acidic substances
• The mechanoreceptors are activated by
virtually any mechanical stimulus in the mouth
• The thought, sight or smell of food is enough
to stimulate salivation
• Irritation of the lower GI tract by bacterial
toxins, spicy foods, or hyperacidity also
increases salivation.
• This response may help wash away or
neutralize the irritants.
• The sympathetic division (specifically fibers in
T1-T3) causes release of a thick, mucin-rich saliva
• Strong activation of the sympathetic division
constricts blood vessels serving the salivary
glands and almost completely inhibits saliva
release, causing a dry mouth
• Dehydration also inhibits salivation because low
blood volume reduces filtration pressure at
capillary beds.
ii.Pharynx
• the pharyngeal constrictor muscles Contract
and propel food into the esophagus below.
iii. Esophagus
• As food moves through the laryngopharynx,
the epiglottis closes off the larynx and
incoming food is routed posteriorly into the
esophagus.
• Gastroesophageal or cardiac sphincter is
closed when food is not being swallowed
• Mucous cells on both sides of the sphincter
help protect the esophagus from reflux of
stomach acid.
Swallowing
• Mouth and esophagus help in food propulsion
• This is accomplished through
deglutition/swallowing
• Food is first compacted by the tongue into a
bolus and is then swallowed.
• Deglutition phases include: Buccal phase &
pharyngeal-esophageal phase
Buccal phase
• Occurs in the mouth and is voluntary.
• The upper esophageal sphincter is contracted
(closed)
• The tongue presses against the hard palate
forcing the food bolus into the oropharynx
• Ends when a food bolus or a "bit of saliva"
leaves the mouth and stimulates tactile
receptors in the posterior pharynx, initiating
the next phase.
Pharyngeal-esophageal phase
• Is involuntary
• Controlled by the swallowing center in the brain
stem (medulla and lower pons).
• Vagus nerves, transmit motor impulses from
the swallowing center to the muscles of the
pharynx and esophagus
• The tongue blocks the mouth
• The soft palate and its uvula rise, closing off the
nasopharynx.
• The larynx rises so that the epiglottis blocks the
trachea.
• The upper esophageal sphincter relaxes; food
enters the esophagus.
• The constrictor muscles of the pharynx
contract, forcing food into the esophagus
inferiorly.
• The upper esophageal sphincter contracts after
food enters.
• Peristalsis moves food through the esophagus
to the stomach.
• The gastroesophageal sphincter surrounding
the cardial orifice opens.
• After food enters the stomach, the sphincter
closes, preventing regurgitation.
• Solid foods pass from the oropharynx to the
stomach in about 8 seconds, and fluids, aided
by gravity, pass in I to 2 seconds.
iv. Stomach
• A holding area for ingested food
• Degrades food both physically and chemically
• Food is converted into a slurry called chyme
• Gastric glands produce the stomach secretion
called gastric juice
• Secretory cells of gastric glands include
mucous neck cells, parietal, chief and
enteroendocrine cells
• Mucus neck cells-produce thin soluble mucus
• Parietal cells-produce HCL and intrinsic
factor(HCL enhances the activity of pepsin,
denatures proteins and kills bacteria while
intrinsic factor is a glycoprotein required for
vitamin B 12 absorption in the small intestine)
• Chief cells produce pepsinogen and lipases
that account for 15% of lipolysis
• Pepsinogen is converted to pepsin by HCL
• The produced pepsin also converts
pepsinogen to pepsin through a positive
feedback mechanism
• Enteroendocrine cells: they produce
serotonin, histamine, somatostatin and gastrin
• Stomach is protected from autodigestion by
the mucosal barrier
• Barrier is created through:
– A thick coating of bicarbonate-rich mucus
– Tight junctions on epithelial mucosa
– High rate of replacement of damaged mucosal
cells (every 3-6days)
Digestive processes in the stomach
• Propulsion
• Mechanical breakdown
• Protein digestion through pepsin and rennin in
children acts on milk protein casein
• Fat digestion through lingual and gastric lipase
• Absorption of alcohol and aspirin
• NB: The only gastric fx essential to life is intrinsic
factor production(production of mature
erythrocytes-pernicious anemia)
Regulation of gastric secretion
• Gastric mucosa pours out as much as 3 L of
gastric juice
• Both neural and hormonal mechanisms
control gastric secretion.
• Neural controls consist of both long (vagus
nerve-mediated) and short (local enteric)
nerve reflexes
• In each case, acetylcholine (ACh) is released,
stimulating the output of gastric juice
• When the stomach is stimulated by the vagus
nerves (which are parasympathetic) secretory
activity of virtually all of its glands increases
• Activation of sympathetic nerves depresses
secretory activity
• Hormonal control of gastric secretion is largely
through gastrin
• It stimulates secretion of HCl by the stomach
• Control of HCL-secreting parietal cells is
stimulated by Ach, gastrin and histamine
• Gastric secretion phases include: cephalic,
gastric and intestinal phases
Cephalic phase
• Occurs before food enters the stomach
• Triggered by the aroma, taste, sight, or
thought of food
• These triggers act via the vagus nerve to
stimulate gastric glands, getting the stomach
ready for its digestive chore.
Gastric phase
• Local neural and hormonal mechanisms
initiate the gastric phase once food reaches
the stomach
• This phase lasts three to four hours and
provides about two-thirds of the gastric juice
released.
• Secretory stimuli are distension, peptides, and
low acidity
Stimulation of gastric phase
• Stomach distension activates stretch receptors
and initiates both short and long reflexes.
• In the long reflexes, impulses travel to the
medulla and then back to the stomach via
vagal fibers.
• Chemical stimuli provided by partially digested
proteins, caffeine, and rising pH directly
activate gastrin-secreting enteroendocrine
cells called G cells in the stomach antrum
• Gastrin plays a major role in stimulating
parietal cells to secrete HCL
• When protein foods are in the stomach, the
pH of the gastric contents generally rises
because proteins act as buffers to tie up H+
• The rise in pH stimulates gastrin secretion and
subsequently HCI release, which in turn
provides the acidic conditions needed to
digest proteins
• The more protein in the meal, the greater the
amount of gastrin and HCL released
• As proteins are digested, the gastric contents
gradually become more acidic, which again
inhibits the gastrin-secreting cells.
• This negative feedback mechanism helps
maintain optimal pH and working conditions
for gastric enzymes.
Inhibition of gastric phase
• Highly acidic (pH below 2) gastric contents
inhibit gastrin secretion
• Stress, fear, anxiety, or anything that triggers
the fight-or-flight response inhibits gastric
secretion because the sympathetic division
overrides parasympathetic (vagal) controls of
digestion
Intestinal phase
Stimulation:
• partially digested food fills the first part
(duodenum) of the small intestine
• This stimulates intestinal mucosa cells to
release intestinal (enteric) gastrin, a hormone
that encourages the gastric glands to continue
their secretory activity.
Inhibition
• Distension of the duodenum or the presence
of acidic, fatty, or hypertonic chyme inhibit
gastric secretion trigger neuronal and
hormonal controls
• Enterogastric reflex: The duodenun inhibits
acid secretion in the stomach by short reflexes
through the enteric nervous system and by
long reflexes involving sympathetic and vagus
nerves.
Enterogastrones:
• Hormones produced by duodenum.
• The two most important enterogastrones
• are secretin (se-kre'tin) and cholecystokinin
(CCK)
• The enterogastrones inhibit gastric secretion
Mechanism of HCL production :
STEPS
• Interstitial co2 diffuses into parietal cell, combines with
water to form carbonic acid
• Carbonic acid dissociates into bicarbonate and hydrogen
ions due to carbonic anhydrase
• H+-K+ atpase pumps potassium into the parietal cells and
H+ into the stomach lumen
• Bicarbonate leaves the cells and enters the blood stream
(alkaline tide)
• Cl- from interstitial fluid enters the parietal cell in return
• Cl- diffuses through the membrane channels into the
lumen

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