The Digestive System Part I Flashcards

Refer to Course Notes

1
Q

Functions of Digestive System:

A

Absorb molecules into bloodstream

Produce hormones, neurotransmitters, hormone-like compounds, nutrient synthesis,

Remove toxins

Take in food

Digest

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2
Q

What major processes occur
during digestive system activity?

A

Ingestion: eating

propulsion: food through the alimentary canal, includes swallowing - oropharynx (voluntary),
- Peristalsis: contraction & relaxation of muscles (squeeze food along the tract, some mixing. It’s powerful even standing on your head, won’t stop it. Swallowing (oropharynx)
* Peristalsis (esophagus, stomach, small intestine, large intestine)

Mechanical breakdown/digestion:
increase surface area of food increase before digestion by enzymes.
Chewing (mouth)
* Churning (stomach) * Segmentation
(small intestine) - Segmentation, a type of mixing wave, mixes food with digestive juices against the intestinal wall.

Digestion: series of steps in which enzymes secreted into the lumen (cavity) of the alimentary canal, break down complex food molecules to their chemical building blocks.

  • How does a cell synthesize and store these enzymes without digesting itself? The answer is that the cell makes proenzymes, or zymogens. These are inactive forms of the enzymes that are only activated once they are released.

Absorption:
Defecation

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3
Q

Components of alimentary canal (gastrointestinal tract) vs. accessory digestive organ:

A

Major Organs of Digestive Tract:

Oral Cavity (Mouth)

Pharynx

Esophagus

Stomach

Small Intestine

Large intestine (dehydration & indigestible materials accumulate)

Accessory Organs of Digestive System:

Teeth

Tongue

Salivary Glands

Liver (secrete bile for lipid digestion)

Gallbladder

Pancreas (exocrine cells - buffers & digestive enzymes) (endocrine cells - secrete hormones)
Pancreas - also secret pancreatic juice.

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4
Q

Peristalsis vs. Segmentation

A

P.: adjacent segments of Alimentary canals contract and relax. Distally, primarily propulsion

S.: non-adjacent. Moves fwd. then bkw. some propulsion, mainly mixing.

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5
Q

Most digestive system organs reside in the abdominopelvic cavity.

A

ventral body cavities contain slippery serous membranes or peritoneum:

Two types of p. membranes:
- Visceral p.: covers external surface of digestive organs
- Parietal p.: lines the body wall

Btw. them is the parietal cavity - contains slippery fluid (serous) secreted by both membranes
- allows mobile digestive organs to glide easily.

Mesentery: double layer of
peritoneum. Both dorsal and ventral.
Function:
- routes for blood vessels, lymphatic, & nerves to reach digestive viscera.
- Hold organs in place
- Store fat

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6
Q

Peritoneum: Serous membranes (double membrane lines visceral and abdominal wall)

Types:

A

Visceral p. external surface of digestive organs

Parietal p.: lines body wall

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7
Q

q
Most digestive organs are intraperitoneal and are suspended from the body wall by a dorsal mesentery.
a
Some digestive organ mesenteries have specific names (such as the omenta)

Not all alimentary canal organs are suspended by a mesen- tery.
9
q
during development, some regions of the small intestine, pancreas, large intestine, duodenum, adhere to the dorsal abdominal wall, so they lose their mesentery and lie posterior to peritoneum
a
Retroperitoneal organs
10
q
Digestive organs (like the stomach) that keep their mesentery and are completely surrounded by the peritoneum are called intraperitoneal or peritoneal organs.
a
Peritonitis is inflammation of the peritoneum. From leaking juice, burst appendix (sprays bacteria-contained feces). often lethal.
11
q
Some intraperitoneal digestive organs are also suspended from the body wall by ventral mesenteries.
a
Some digestive organs are retroperitoneal because they have lost their mesentery during development
12
q
The walls of the alimen-tary canal have the same four basic layers, or tunics—mucosa, submucosa, muscularis externa, and serosa
a
The mucosa: Innermost layer, moist epithelial membrane mouth to anus.
Functions:
- secret mucus, digestive enzymes, hormones (lining epithelium)
- absorb end products of digestion into blood
- Protection from infection

Sublayers:
1) a lining epithelium,
(2) a lamina propria (areolar connective tissue) - underlies the epith. nourish epith. and absorb nutrients, part of MALT (protection)
(3) a muscularis mucosae (smooth muscle cells): external to LP, local movements of mucosa (absorption & secretion)

Not sure this is right - probably taken from online: The epithelium is usually a single layer of tall, column-shaped cells (simple columnar) in most places, but in areas with more mechanical stress (like the mouth and esophagus), the epithelium is tougher and stratified squamous (multiple flat cell layers, secretes mucus, protect digestive organs from being digested by organs.

Submucosa:
13
q
Particularly large collections of lymphoid follicles occur within the pharynx (as the tonsils) and in the appendix.

A

Except for that of the mouth, parts of the pharynx, the esophagus, and the anus where it is stratified squamous, the epithelium of the mucosa is a simple columnar epithelium rich in mucus-secreting cells

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8
Q

Fluid-filled space btw. two peritoneum

Lubricates mobile organs

A

Peritoneal cavity

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9
Q

The digestive system’s organs are related to the peritoneum in the following ways:

A

Intraperitoneal organs: These are located within the peritoneum, suspended by the mesentery. Examples include the stomach, liver, and small intestine.

Retroperitoneal organs: These are located outside or behind the peritoneum. No mesentery. Examples include parts of the pancreas, duodenum, and large intestine.

Mesentery: A double layer of peritoneum that supports and anchors organs to the posterior body wall. It provides structural support, holds vessels and nerves, and stores fat.

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10
Q

Most digestive organs are intraperitoneal

A
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11
Q

The alimentary canal has four basic histological layers:

A

Mucosa: Lines the lumen; made of epithelium (secretes mucus, enzymes, hormones), lamina propria (supports absorption and immunity), and muscularis mucosae (local movements).

Submucosa: Areolar tissue with blood/lymph vessels, lymphoid follicles, and elastic fibers for shape recovery.

Muscularis Externa: Controls segmentation and peristalsis with circular/longitudinal muscle layers and sphincters. nerve plexus.

Serosa: Outermost layer of areolar tissue and mesothelium; replaced by fibrous adventitia in the esophagus.

Retroperitoneal Organs: Have both serosa (peritoneal side) and adventitia (dorsal side).

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12
Q

Blood Flow to Digestive Organs:
Oxygen-rich blood comes from the aorta.
It travels through specific arteries:
Hepatic artery: Supplies the liver.
Celiac artery: Branches into three main arteries:
Splenic artery: Supplies the spleen and pancreas.
Left gastric artery: Supplies the stomach.
Hepatic artery: same

Superior mesenteric artery: Supplies the pancreas, small intestines, and colon.
Inferior mesenteric artery: Also supplies the colon.
Blood Flow from Digestive Organs:
Blood from the digestive organs is drained via veins
.
The blood collects in the hepatic portal vein:
This carries nutrient-rich blood from the digestive organs (such as intestines) to the liver.
From the liver, blood is sent to the hepatic veins, then into the inferior vena cava, returning to the heart.
Why the Hepatic Portal Circulation?
The hepatic portal circulation allows the liver to process and filter nutrients, toxins, and other substances absorbed from the digestive system before they enter the general circulation. This ensures proper nutrient management and detoxification.

A
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13
Q

The digestive system receives 20-25% of cardiac output, which increases after a meal and decreases during exercise.

A
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14
Q

Peristalsis and segmentation both occur throughout the GI tract, with peristalsis primarily moving food forward in a wave-like motion, while segmentation mainly mixes food and digestive enzymes, especially in the small intestine.

A
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15
Q

In the GI tract, peristalsis propels food forward by contracting circular muscles behind the bolus and relaxing longitudinal muscles ahead, while segmentation mainly mixes food with digestive juices by contracting circular muscles at intervals. Peristalsis moves food along, while segmentation ensures thorough digestion through mixing.

A
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16
Q

3-5 pounds of food daily per each person but may differ from one person to another.

Bloodstream - major transportation system in the body. Need oxygen as well.

A

Nutrient molecules are small enough to be absorbed by the body, though fiber, which is not digestible, cannot be processed. The gut microbiome plays a significant role in health, influencing functions such as regulating blood sugar in diabetes, supporting the nervous system, and aiding in weight management, according to research. Additionally, gut bacteria produce certain vitamins, like Vitamin K, which is crucial for the formation of clotting factors. Nutrients are absorbed both from the food we eat and the byproducts produced by gut bacteria.

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17
Q

Peritonitis

A

Inflammation of peritoneum

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18
Q

Four types of tissues: epithelial, connective, nervous, and muscle tissues.

Mucosa (lines the lumen of the GI tract) has 3 layers:

Epithelial: Avascular (relies on underlying connective tissue for blood supply).

Lamina propria: Contains blood vessels, glands, and immune cells.
Muscularis mucosa: Responsible for local movements within the mucosa.

Muscularis externa: Controls global movements in the GI tract.

Villi and microvilli: Increase surface area for nutrient absorption.

Mucosa-associated lymphoid tissue (MALT): Traps harmful substances and provides immune defense.

A
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19
Q

The Enteric Nervous System (ENS), or “gut brain,” is a network of neurons that controls GI motility and is connected to the central nervous system via the autonomic nervous system.

A

Study diagram

20
Q

The Enteric Nervous System has two main plexuses (or intrinsic nerve plexuses):

Submucosal plexus: Regulates glands and smooth muscle in the mucosa.
Myenteric plexus: Controls GI motility through pacemaker cells and local reflex arcs.

A

Neurons (intrinsic and extrinsic) and hormones control digestive activity. The nervous system controls digestive activity via both intrinsic controls (involving short reflexes entirely within the enteric nervous system as described above) and extrinsic controls (involving long reflexes).

21
Q

External stimuli - CNS - local intrinsic plexus -effectors - response

Internal stimuli chemo, osmo, mechano receptors - CNS (short reflexes)

or instead of CNS - local intrinsic plexus - effectors - response

(long reflexes)

A

Digestive activity is regulated by both the nervous system and hormones.

Nervous system:
Intrinsic controls (short reflexes): Managed by the Enteric Nervous System (ENS) alone.

Extrinsic controls (long reflexes): Involve the central nervous system.

Hormonal controls: Hormones from the stomach and small intestine regulate muscles and glands to affect secretion and contraction.

Digestive activity is triggered by mechanical and chemical stimuli (e.g., stretch, pH, and substrate presence), which activate reflexes that stimulate smooth muscles (SM) and digestive glands to mix food, move contents, and secrete digestive juices or hormones.

22
Q

Oral Cavity: Bounded by lips, cheeks, palate, and tongue; lined with stratified squamous epithelium; where digestion begins with chewing and saliva.

Lips and Cheeks: Lips (orbicularis oris muscle); cheeks (buccinator muscles); oral vestibule (space inside lips and cheeks); oral cavity proper (between teeth and gums).

Tongue: Repositions and mixes food; aids in swallowing, speech, and taste; divided into anterior 2/3 (oral cavity) and posterior 1/3 (oropharynx); has papillae with taste buds (filiform (this), fungiform (this), circumvallate, foliate (this)). The tongue has intrinsic and intrinsic muscles (change shape of tongue), extrinsic m. (alter tongue’s position.

Palate: Hard palate (palatine bones) for friction; soft palate (skeletal muscle) with uvula to close nasopharynx during swallowing.

Ankyloglossia: Condition where the lingual frenulum is short, causing “tongue-tied.”

A

See diagrams

The uvula extends out from and past the soft palate area of the palatopharyngeal arch.

23
Q

Salivary Glands:
Function: Secrete saliva for mouth cleaning, taste, food moistening, and starch breakdown.

Types:
Serous cells (submandibular, parotid): Produce watery secretion with enzymes.

Mucous cells (in sublingual): Produce mucus.

Major Glands: Sublingual, submandibular, parotid (main saliva producers).

Saliva: Contains water, electrolytes, enzymes (amylase, lipase), proteins (IgA, lysozyme, mucin), and wastes (urea).

Protection: Defends against microbes with IgA, lysozyme, defensins.

Xerostomia: Dry mouth due to low saliva production.

Teeth:
Location: In sockets of the mandible and maxilla.
Types:
Deciduous: 20 baby teeth, lost by age 12.
Permanent: 32 adult teeth.
Structure: Crown (above gum) and root (in jawbone).
Classification:
Incisors: Cutting.
Canines: Tearing.
Premolars: Grinding.
Molars: Best for grinding.

A

Mumps - viral infection affects salivary glands

Salivation Control:
1500 ml/day of saliva produced.
Minor glands/intrinsic: Continuously moistens mouth.
Major glands/extrinsic: Activated by PNS.
Chemo- & mechanoreceptors: In mouth detect food.
Signals sent to salivatory nuclei in brainstem.
Cranial nerves VII (facial) & IX (glossopharyngeal): Stimulate salivary glands.

Salivation is controlled primarily by the parasympathetic division of the autonomic nervous system.

Crown: Enamel-covered, exposed part.
Root: Embedded in jawbone, with cement and periodontal ligament.
Dentin: Shock-absorbing material beneath enamel.
Pulp: Contains nerves, blood vessels.
Enamel: Hardest body substance, cannot regenerate.

24
Q

Digestive Processes of the Mouth:
Ingestion: Food enters the mouth.
Mechanical Breakdown: Teeth and tongue grind food into a bolus.
Propulsion: Swallowing moves food down.
Chemical Breakdown: Salivary amylase starts starch digestion (polysaccharides), and lingual lipase starts fat digestion.
Mastication:
Mechanical: Teeth grind, tongue mixes food with saliva.
Chemical: Enzymes begin breaking down starches and fats.

A

Only polysaccharides are digested in the mouth, the rest in the stomach.

25
Q

Function: Allows passage of food, fluids, and air.

Pathway: Food passes from the mouth → oropharynx → laryngopharynx.

Lining: Stratified squamous epithelium with mucus-producing glands.

Muscle layers:
Inner layer: Longitudinal skeletal muscles.
Outer layer: Pharyngeal constrictors that encircle the pharynx.

A

The Pharynx

26
Q

Esophagus: 25 cm muscular tube from laryngopharynx to stomach.

Collapsed when not involved in food movement.
Passes through diaphragm at esophageal hiatus (opening in the diaphragm).

Joins stomach at cardial orifice.

Surrounded by lower esophageal sphincter (gastroesophageal or cardiac sphincter).
Keeps orifice closed when not swallowing, thus prevent reflux.

Mucus cells protect against acid reflux.

A

Heartburn is a burning sensation in the chest caused by stomach acid refluxing into the esophagus.

27
Q

Esophagus Structure:

Contains all four alimentary canal layers:

Mucosa: Stratified squamous epithelium transitioning to columnar at the stomach.

Glands in submucosa secrete mucus for bolus movement.

Muscularis: Skeletal (superior), mixed (middle), smooth (inferior).

Adventitia instead of serosa.

Swallowing (Deglutition):
Phases: Buccal (voluntary) and pharyngeal-esophageal (involuntary) - see slide for steps.

Controlled by the tongue, pharynx, esophagus, and muscle groups.
Food Passage Regulation:
Sphincters: Upper and lower esophageal sphincters.
Peristalsis: Involuntary muscle contractions, aided by mucus.

A

See diagrams

28
Q

Gross Anatomy of the Stomach:

Function: Storage and breakdown of food into chyme.

Capacity: Expands from 50 mL to 4L.

Structure: Rugae, regions: cardia, fundus, body, pylorus, greater/lesser curvatures.

Omenta: Lesser (liver to stomach), Greater (covers intestines).
Nerve & Blood Supply: Sympathetic (splanchnic),
Parasympathetic (vagus), Celiac trunk arteries, hepatic portal veins.

Mesenteries: Lesser omentum (to liver), Greater omentum (over intestines, spleen). Contain fat deposits & lymph nodes.

Innervation & Blood Supply: Sympathetic (celiac plexus), Parasympathetic (vagus nerve), Blood from celiac trunk.

A

Microscopic Anatomy of the stomach:

Muscularis Externa: Three smooth muscle layers (circular, longitudinal, oblique).

Mucosa: Simple columnar epithelium with mucus cells.

Gland Cells:

Mucous neck cells: Secrete acidic mucus.

Parietal cells: Secrete HCl and intrinsic factor.

Chief cells: Secrete pepsinogen and lipases.

Enteroendocrine cells: Secrete hormones like gastrin - (enteroendocrine G cells specifically) (for HCL secretion, pyloric spchinter, stomach’s motility) and ghrelin appetite, opening, gastric motility), somatostatin and paracrines: histamine & serotonin.

29
Q

Mechanism of HCl Formation:
Carbonic acid (H2CO3) dissociates into H+ and HCO3−.
H+ is pumped into the lumen via H+/K+ ATPase, while K+ moves into the parietal cells.
Cl− is exchanged for HCO3− and then diffuses into the lumen.
H+ and Cl− combine in the lumen to form HCl.
Alkaline Tide: As H+ is pumped into the lumen, HCO3− is released into the blood, raising blood pH.

A

Mucosal Barrier:
Protection: Bicarbonate mucus, tight junctions, rapid epithelial cell turnover (every 3-6 days)
Here’s a shorter version for studying:

Carbonic Acid Dissociation:
H₂CO₃ → HCO₃⁻ + H⁺ (Carbonic acid breaks into bicarbonate and hydrogen ions).
H⁺/K⁺ ATPase Pump:
H⁺ moves into the lumen.
K⁺ moves into the cell, then returns to lumen via channels.
Cl⁻/HCO₃⁻ Exchange:
Cl⁻ from interstitial fluid exchanges with HCO₃⁻ inside the cell.
Cl⁻ Diffusion:
Cl⁻ moves through membrane channels into the lumen.
This is the process related to acid secretion and ion exchange in cells like those in the stomach lining.

30
Q

Digestive Processes in the Stomach:
Storage: Holds food and begins digestion.
Mechanical breakdown: Churning action of peristalsis.
Protein digestion: HCl denatures proteins; pepsin digests them.
Milk digestion (in infants): Rennin breaks down casein.
Absorption: Lipid-soluble substances like alcohol and aspirin.
Essential function: Secretion of intrinsic factor for Vitamin B12 absorption (necessary for RBC maturation).

A

Online source:
Pepsinogen, the inactive precursor of pepsin (gastric enzyme), plays a crucial role in the stomach’s digestive process. When exposed to the acidic environment created by hydrochloric acid (HCl), pepsinogen is converted into its active form, pepsin. Pepsin then functions as a protease enzyme that breaks down proteins into smaller peptides, facilitating their further digestion and absorption in the small intestine. This enzymatic action is especially important for digesting protein-rich foods, contributing to the overall mechanical and chemical digestion of food in the stomach.

Mechanical digestion: Churns food into chyme via peristalsis.
Chemical digestion: HCl denatures proteins and activates pepsin.
Protein digestion: Pepsin breaks down proteins into smaller peptides.
Absorption: Absorbs alcohol and aspirin (not nutrients).
Intrinsic factor: Essential for Vitamin B12 absorption.
Chyme delivery: Transfers processed food to small intestine.

31
Q

Regulation of Gastric Secretion:
Neural Mechanisms:
Vagus nerve: Stimulates secretion.
Sympathetic nerve: Inhibits secretion.
Hormonal Mechanisms:
Gastrin: Stimulates enzyme and HCl secretion.
Histamine and acetylcholine (ACh) enhance gastric acid production.
Drugs blocking H2 histamine receptors reduce acid secretion.

32
Q

Phases of Gastric Secretion:
Cephalic Phase: Triggered by sensory input (sight, smell, taste, thought).

Gastric Phase:
Stimulated by stomach distention and partially digested proteins.
Buffering effect increases PH - then gastrin secretion -
Inhibition occurs with low pH (<2), sympathetic NS.

Intestinal Phase:
Partially digested food enters the small intestine, releasing intestinal gastrin (gastric secretion)
Inhibition as intestine fills, from duodenal stretch, acidity, and fatty chyme.
Enterogastric reflex: Reduces acid secretion via neural and hormonal signals (secretin, CCK).

A

Gastric phase: Gastrin directly (and indirectly via triggering histamine release)
stimulates parietal cells to secrete HCl

33
Q

Gastric Motility & Emptying:
Response to Filling:
Receptive relaxation: Reflex relaxation of smooth muscle.
Gastric accommodation: Muscle adjusts without increased tension.
Peristaltic Waves: 3/min, strongest near pylorus, pushing chyme into duodenum.
Gastric Emptying: Takes 4 hours; fatty chyme delays it, carbohydrate-rich chyme moves quickly.
Duodenal Feedback: Receptors inhibit gastric secretion and control chyme entry.

34
Q

Palatine and Lingual Tonsils are part of the immune system:

35
Q

Salivary Glands:
Major glands (parotid) external, produce watery saliva.
Minor glands: constant low-level saliva.
Contains amylase (digests carbs), mucin (mucus), urea & uric acid.
Dry mouth impedes digestion.
Cranial Nerve IX triggers saliva with smells.

A

Teeth:
Located in mandible and maxilla.
Deciduous teeth: temporary, for permanent ones.
Crown: Enamel, can’t regenerate.
Dentin: Protein-rich, holds nerves & blood vessels.
Root canal can get infected.

36
Q

Pharynx:
Oropharynx & laryngopharynx: for both breathing & digestion.
Orifice: Any opening.

A

Esophagus:
Lower esophageal sphincter: Controls food passage.
Muscles help push food down.

37
Q

Stomach:
pH ~2 for protein breakdown.
Rugae: Stomach folds for expansion.
Cardia: Near esophagus.
Pyloric sphincter: Controls chyme entry into small intestine.
Mesenteries: the greater omentum Attach stomach, more to intestine, spleen, colon and lesser to liver.
Celiac artery: Supplies blood.
Vagus nerve: Regulates digestion.
Oblique muscle: Aids food breakdown.
Stress (Sympathetic activation (T1−T3) releases thick, mucin-rich saliva or inhibits salivation (dry mouth) and dehydration - reduce saliva production due to low blood volume.

A

Gastric Secretions:
Intrinsic factor: Absorbs B12. Lack causes anemia.
Pepsinogen turns into pepsin to digest proteins.
GI Mucosa:
Esophagus: Stratified squamous.
Stomach: Simple columnar.
Colon: Stratified squamous at anus.

The vagus nerve (Cranial Nerve X) is one of the 12 cranial nerves. It is unique because, unlike most cranial nerves that primarily serve the head and neck, the vagus nerve extends far beyond the neck. It controls functions in the chest and abdomen, including heart rate, digestion, and respiratory rate.

38
Q

Swallowing irritating foods can upset GI and act as a stimulus.

39
Q

Gomphosis. It is a type of fibrous joint where the teeth fit into sockets in the gum-covered margins of the mandible and maxilla.

A

blood Supply:
Celiac trunk: Gastric & splenic branches.
Veins: Hepatic portal system.

40
Q

bloodstream: pH 7.4
Mucous cells: Secrete HCO₃⁻ (bicarbonate)
Mucus gel: pH 7.0 (near neutral)
Neutralization zone: H⁺ (acid) from gastric lumen reacts with HCO₃⁻ (bicarbonate) in mucus gel
Gastric lumen: pH 1.5 (highly acidic)
[HCO₃⁻] = 0, [H⁺] = 20mM in gastric lumen
H⁺ enters mucus gel: Reacts with HCO₃⁻ to form H₂CO₃ (carbonic acid)
H₂CO₃ breaks down into CO₂ and H₂O
Function: Protects stomach lining from acid damage through buffering system.

41
Q

Textbook - Summary Below

42
Q

Organs of digestive system fall into two main groups: alimentary canal and accessory digestive organs:

A

Alimentary canal (GI tract) or gut is continuous muscular tube (mouth to anus)

  • are the mouth, pharynx, esophagus, stomach, small intestine, and large intestine.

Accessory digestive organs: are the teeth, tongue, gall- bladder, and a number of large digestive glands—the salivary glands, liver, and pancreas.

43
Q

See table 23.1

A

Gastric Pits & Glands: Pits lead to glands producing gastric juice, with different cell types in different regions.

44
Q

Gastritis/Ulcers: Inflammation and ulcers caused by H. pylori or NSAIDs. Symptoms: pain, risk of perforation.
Digestion: Protein and fat digestion, minimal absorption (only alcohol, aspirin).
Intrinsic Factor: Essential for B12 absorption, prevents pernicious anemia.
Secretion Control: Regulated by neural and hormonal mechanisms.

A

HCl Mechanism: Proton pumps release acid, creating an alkaline tide.
Motility: Stomach stretches to accommodate food, and peristalsis mixes and propels it.

45
Q

Teeth & Function:
Location: Teeth in gum-covered sockets of mandible and maxilla.
Function: Chewing breaks food down, aided by the tongue.
Dentition & Dental Formula:
Deciduous Teeth: 20 teeth by age 2, replaced by permanent teeth.
Formula: 2I, 1C, 2M (upper/lower jaw).
Permanent Teeth: 32 teeth, including wisdom teeth (17-25 years).
Formula: 2I, 1C, 2PM, 3M (upper/lower jaw).
Tooth Types:
Incisors: For cutting.
Canines: For tearing.
Premolars: For grinding.
Molars: For crushing.
Tooth Structure:
Crown: Enamel-covered, above gums.
Root: Embedded in bone, held by cement and ligament.
Dentin: Shock-absorbing, beneath enamel.
Pulp: Contains nerves and blood vessels.
Tooth Diseases:
Cavities: Caused by bacterial plaque; prevent with brushing.
Tartar: Hardened plaque, leads to gum disease (gingivitis, periodontitis).
Periodontal Disease: Leads to tooth loss, linked to heart disease and diabetes.
Mouth in Digestion:
Functions: Ingestion, chewing, swallowing, and digestion of starch.
Absorption: Only some drugs, like nitroglycerin.
Mastication (Chewing):
Process: Cheeks, lips, and tongue position food; teeth grind it.
Control: Both voluntary and reflexive movements.
This version captures the essentials of teeth, their function, and their role in digestion.

46
Q

Hormones & Functions
Cholecystokinin (CCK)
Site: Duodenum
Stimulus: Fatty chyme, proteins
Targets: Stomach, liver, pancreas, gallbladder
Action: Inhibits stomach, stimulates pancreatic enzymes, bile release.

GIP (Gastric Inhibitory Peptide)
Site: Duodenum
Stimulus: Glucose, fatty chyme
Targets: Stomach, pancreas
Action: Inhibits HCl, stimulates insulin.

GLP-1 (Glucagon-like Peptide-1)
Site: Intestines
Stimulus: Carbs, fats, proteins
Targets: Pancreas, stomach, brain
Action: Stimulates insulin, decreases gastric emptying and food intake.

Gastrin
Site: Stomach
Stimulus: Food, acetylcholine
Targets: Stomach, intestines
Action: Increases HCl, stimulates gastric motility and muscle contraction.

Histamine
Site: Stomach
Stimulus: Food
Target: Stomach
Action: Stimulates HCl release.

Intestinal Gastrin
Site: Duodenum
Stimulus: Acid/food in duodenum
Target: Stomach
Action: Stimulates gastric glands.

Motilin
Site: Duodenum
Stimulus: Fasting
Target: Duodenum
Action: Stimulates migrating motor complex.

Secretin
Site: Duodenum
Stimulus: Acidic chyme
Targets: Stomach, pancreas, liver
Action: Inhibits gastric secretion, increases bicarbonate and bile output.

Serotonin
Site: Stomach
Stimulus: Food
Target: Stomach
Action: Stimulates muscle contraction.

Somatostatin
Site: Stomach, duodenum
Stimulus: Food, nerves
Targets: Stomach, pancreas, intestines
Action: Inhibits secretion, absorption, blood flow, and bile release.

VIP (Vasoactive Intestinal Peptide)
Site: Enteric neurons
Stimulus: Chyme
Targets: Intestines, pancreas, stomach
Action: Increases blood flow, relaxes smooth muscle, inhibits acid secretion.