Lecture 30 - Monogastric Secretions (Oral, Gastric) Flashcards

1
Q

what are the 4 functions of saliva

A

-moisten and lubricate bolus
-dilutes osmolarity of the ingested material
-digestion of carbs and fat
-anti-bacterial

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2
Q

what kind of cells are contained in salivary glands

A

acinar cells

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3
Q

what do acinar cells produce

A

proteins and antibacterial peptides

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4
Q

parasympathetic fibers have what effect on acinar cells and myoepithelial cells

A
  • increase production of acinar cells
  • contraction of myoepithelial cells
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5
Q

what do salivary ducts add

A

add an alkaline secretion

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6
Q

what is the effect of secretin on salivary duct cell secretion

A

increases

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7
Q

(lower/higher) pH in the duodenum increases secretin production

A

lower pH in the duodenum

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8
Q

what kind of drugs dry up secretions from the mouth

A

anticholinergic drugs

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9
Q

what toxin can make horses drool alot? by what mechanism?

A

toxin in mouldy red clover activates salivary muscarinic receptors

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10
Q

esophageal stomach is lined by what kind of epithelium

A

stratified squamous epithelium

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11
Q

is the esophageal stomach glandular or nonglandular

A

non glandular

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12
Q

does the esophageal stomach produce mucus, acid or enzymes?

A

no

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13
Q

is the cardiac stomach glandular

A

yes

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14
Q

what does the cardiac stomach produce and its function

A

mucus and buffer –> adheres to cells to protect epithelium from proteolytic enzymes and acid

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15
Q

is the fundic region of the stomach glandular or non glandular

A

glandular

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16
Q

what does the fundic region of the stomach produce

A

produces acid, proteolytic enzymes, hormones, mucus

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17
Q

which compartment of the stomach is generally the largest

A

fundic region of the stomach

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18
Q

is the pyloric region of the stomach glandular or non glandular

A

glandular

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19
Q

what does the pyloric stomach produce

A

produces mucus and buffer but not acid or proteolytic enzymes

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20
Q

what cells live in the pyloric region of the stomach

A

enteroendocrine cells and G cells that produce gastrin

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21
Q

what increases gastrin secretion from G cells in the pyloric stomach

A

high stomach distention and high stomach pH

22
Q

what are gastric pits lined with

A

lined with mucus secreting cells at the luminal surface

23
Q

what is the function of the mucus on the surface of gastric pits

A

forms a thick gel to protect stomach from acid and proteolytic enzymes

24
Q

where does each gastric pit lead into

A

leads into a gastric gland: very deep invagination in the submucosa

25
Q

function of chief cells

A

secrete proteolytic enzyme precursor pepsinogen into the stomach

26
Q

describe the activation of pepsinogen

A

pepsinogen is cleaved into pepsin by HCl

27
Q

what do chief cells also produce in neonates? what does it do>

A

also produces rennin in neonates, helps digest milk `

28
Q

effect of rennin on milk

A

converts liquid milk to semisolid for longer residence in the GI and better absorption

29
Q

what do parietal cells secrete? function?

A

acid to help hydrolytic breakdown of diet components and kills bacteria in ingesta

30
Q

how are parietal cell proton secretions increased

A

Hormonal and parasympathetic efferent innervation

31
Q

3 factors that activate mechanisms to increase proton secretions by parietal cells** (tAkE a DeEp BrEaTh:)

A
  • histamine produced by ECL cells when gastric gland fluid pH is too high, histamine then diffuses to reach nearby parietal cells and binds to receptors on parietal cell (on basolateral side)
  • hormone gastrin secreted into blood and reaches parietal cell on basolateral side
  • increases in stomach distention and osmolarity which then increases vagal afferent to medulla and then vagal efferent stimulation of parietal cells increases (Ach working on muscarinic receptors)
32
Q

describe the anticipation of food on vagal efferents to parietal cells

A

sight/smell/chewing/ swallowing of food increases parasympathetic activity which directly increases parietal and chief cell acivity
- increase in parasympathetic activity also increases gastrin secretion by G cells which then increases parietal and pepsinogen secretions

33
Q

why are there multiple mechanisms in the control of acid secretion

A

ensure acid production by parietal cell can be increased on demand

34
Q

mucous cells secrete…

A

mucus!!!! (shocker i know)

35
Q

parietal cells secrete…

A

HCl

36
Q

chief cells secrete…

A

pepsinogen

37
Q

G cells secrete

A

gastrin

38
Q

ECL cells secrete

A

histamine

39
Q

how can epithelial cells lining the stomach get damaged

A

excessively low pH or other trauma

40
Q

how do epithelial cells lining the stomach respond to damage

A

produce prostaglandin (requires function of cyclooxygenase (COX)-1

41
Q

actions of prostaglandin

A
  • reduce histamine and gastrin secretion by enteroendocrine cells (reduce acid secretion)
  • increases mucus secretion by nearby epithelial cells
  • increases blood flow to area: provides nutrients needed for rapid repair or replacement of damaged cells
42
Q

what are ulcers

A

erosions of the mucosal lining of the GI system

43
Q

clinical signs of GI ulceration

A

vomiting, anorexia, abdominal pain, weight loss

44
Q

what enzyme is expressed in arthritic joints

A

COX-2

45
Q

action of COX-2

A

catalyzes production of prostaglandins which are proinflammatory and activate nociceptors (pain) in affected region

46
Q

COX 2 inhibitors are…

A

NSAIDs: ex. aspirin, Ibuprofen

47
Q

COX 1 inhibitors

A

also NSAIDs :(

48
Q

function of NSAIDs on COX-1

A

prevents prostaglandin production by cells that are damaged within the digestive tract (decreases tissue homeostasis and increases risk of ulcer development)

49
Q

how can ulcers be treated

A

administer synthetic analogs of prostaglandins

50
Q

carprofen

A

major COX 2 inhibitor (good for arthritic ouchies) with minor effects on COX1 activity (allows digestive tract to keep producing prostaglandins

51
Q

what are other ways that ulcers can be treated

A

histamine receptor antagonists, muscarinic antagonists, proton pump inhibitors