Physiology Flashcards
Functions of the stomach?
- Temporary storage: 1-2 liters
Receptive relaxation: regulation is thru NANC vago-vagal reflex and possibly VIP and NO, enteric innervation to proximal stomach is largely inhibitory
- Mixing of contents: semi liquid called CHYME mixed by the distal stomach
- Propulsion into duodenum: regulated by pyloric sphincter
- Gastric emptying
What happens in the proximal part of the stomach?
- Low stable RMP (~50mV)
- Partially contracted at RMP
- Length-tension relationship
- Primary enteric innervation is INHIBITORY (NANC)
- Predominant type of activity: variations in tone
What happens in the distal part of the stomach?
- Propagated contraction resulting from a series of enteric reflexes in response to local distension
- The MAGNITUDE of the stimulus (along with interaction of neural and hormonal factors) determines the AMPLITUDE of the peristaltic wave
- The ELECTRICAL CHARACTERISTICS OF THE SMOOTH MUSCLE determines the FREQUENCY, DIRECTION and VELOCITY of the wave
- Slow waves = ECA (electric control activity) or BER (basic electric rhythm)
- Spikes at the peak of BER = electrical response activity (ERA)
- This is coordinated by the interstitial cells of Cajal (stomach pacemaker)
What happens at the pyloric sphincter?
At the end of a peristalsis, the pyloric sphincter actually contracts and allows only small molecules of enter the duodenum. The liquids pass way faster.
Regulation:
- Vagus nerve (proximal innvervates proximal stomach and distal innervates the distal)
- Distension, pH < 3.5, osmolarity (fat >> proteins > carbs) will regulate antral peristalsis
By what is composed the mixed gastric juice?
- Volume: 1.5-2 L/d
- Ions: Isotonic fluids with Na+, K+, Cl- and H+ (precipitates soluble proteins, denatures proteins, activates pepsin and provides optimal pH for its activity)
- pH = 1-2
- Pepsinogen (converter to pepsin by HCL, autocatalysis and breaks protein to polypeptides)
- Intrinsic factor: glycoprotein and absorption of B12
- Gelatinase and lipase
- Mucin: mucin-bicarb layer, gastric mucosal barrier, effective blood glow, rapid cell turnover
- Prostaglandins (cyto-protection) increase mucin and bicarb secretion, increases blood flow and decreases acid production
Cardiac and pyloric tubular glands secrete what?
alkaline mucin-rich fluid
Parietal (oxyntic) cells secrete what?
- secretes acids after a meal (changes phase)
- glycoprotein (B12 absorption)
Chief cells secrete what?
pepsinogen converter to pepsin by HCL
Surface epithelial cells secrete what?
bicarb and mucus
What are the 3 regulatory postprandial state?
- Cephalic (psychic and gustatory) – 30%
Parietal, peptic and mucoses secretions + vasodilation
Mediated by vagus, vagotomy abolishes cephalic phase s
- Gastric 60%
Due to food in the stomach
Local enteric, neuro (vagal) and hormonal (gastrin +, histamine - and somatostatin -) regulation
- Intestinal 10%
Secretagogues in duodenum Inhibit acid secretion via neuro and hormonal pathways
Major regulatory factors of the stomach pH?
- gastrin (+)
- somatostatin (-)
- histamine (potentialize +)
- vagus (+/-)
Digestive enzymes secreted by the pancreas?
- Amylase: polysaccharides ®disaccharides
- Protease: proteins and activation of proenzymes into enzymes such as trypsinogen ® trypsin (which will also activate other proenzymes into enzymes)
- Lipase: fats
What are the 2 structures that contribute to the exocrine function of the pancreas?
- Acinar cell: ENZYMES
Has zymogens (inactive pancreatic enzymes); when enzymes are produced, they are formed as zymogens (cannot be active in pancreas because they will digest the pancreas), and they become active enzymes in the duodenum
- Centroacinar duct cells: ALKALINE FLUID
Are filled with mitochondria for energy
Regulation of the pancreas?
- Neuronal mechanism (vagal nerve)
- Hormonal mechanism:
- Secretin: will increase pH (decrease acidity)
- CCK: triggered by fat and protein to release pancreatic enzymes via vagal nerve
Pancreatic exocrine insufficiency causes?
- Chronic Pancreatitis: slow chronic fibrosis due to ductal obstruction, ATROPHY
- Cystic Fibrosis: CFTR gene mutation (Na+/ CL-+ HCO3- transport problem)
- Bowel or pancreatic resection: affects CCK and secretin synthesis
- Pancreatic duct obstruction: cancer
- Shwachman-Diamon Syndrome: autosomal recessive, bone problems, short stature, can be secondary to CF