14 Regulation of Gut Function Flashcards

1
Q

Q: What are the 3 regulatory systems? 2 subs of 1.

A

A: Nervous stimulation: neurotransmitters released from neurones innervate target cells. -> intrinsic (enteric) and extrinsic (autonomic)

Paracrine : hormones released by cells in the vicinity of the target cell and reach target cell by diffusion.

Endocrine : hormones produced by endocrine cells, released into the blood where they reach their targets via the circulation.

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2
Q

Q: How many neurons do we have in the GIT wall? What do they communicate with? What system do they make and why is it referred to as the second brain? Independence?

A

A: totalling somewhere between 10 and 100 million nerve cells (compared with 300 billion in the brain)

cells in the autonomic nervous system (combined function)

enteric nervous system = integrating centre for coordinating function = similar to how the brain receives signals from different parts of the body (afferent signals), integrates them, and produces a response (efferent signals)

ENT can do so independent of the central nervous system

In experimental animal models, the independence of the enteric nervous system can be demonstrated by severing the sympathetic and parasympathetic nerves innervation to the gut. Afterwards, many motor and secretory activities continue unaffected.

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3
Q

Q: How are nerves in the GIT arranged? (3)

A

A: in rich plexuses (a dense local network of nerves and supporting cells)

of ganglia (nerve cells which carry signals, and glial cells which provide ((insulate, protective, nutritional and structural)) support)

These ganglia are interconnected by tracts of fine, unmyelinated nerve fibres

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4
Q

Q: What can cause dysfunction of the ENS? (4)

A

A: Inflammation (ulcerative colitis; Crohn’s disease)
Following invasive abdominal surgery
Irritable bowel syndrome
Ageing (constipation)

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5
Q

Q: What are the 2 main structures of the ENS? Where are they? Afferent/efferent functions? What does it allow/function?

A

A: gut wall has two main plexuses (plexi) - the myenteric plexus and the submucosal plexus -> both communicate

Myenteric plexus (also known as Auerbach’s plexus)
= located between the circular and longitudinal smooth muscle layers
=has efferent innervation of both
=careful control of the entire activity of muscularis externa 
=allows for coordinated control of motor function, and hence, motility
Submucosal plexus (also known as Meissner’s plexus)
=in submucosa
=has both afferent and efferent functions.
=Afferent: Senses the environment within lumen using mechanoreceptors, chemoreceptors and osmoreceptors.
=Efferent: Can fine tune local blood flow, epithelial transport and secretory/paracrine/endocrine cell function.
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6
Q

Q: What are the 5 key efferent functions of the ENS?

A

A: SPAMW

Secretion - 
Perfusion - blood flow 
Absorption - 
Motility - 
Water and electrolyte transport
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7
Q

Q: Describe secretion as a role of the ENS.

A

A: controlling the secretion of enzymes, paracrine signals and endocrine hormones to regulate local and non-local gut functions.

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8
Q

Q: Describe perfusion as a role of the ENS.

A

A: blood flow needs to be carefully controlled to ensure high perfusion in regions of the gut that are working (vascular smooth muscle cells [VSMC], submucosal glands) and/or absorbing (enterocytes)

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9
Q

Q: Describe absorption as a role of the ENS.

A

A: carefully controlling the absorption of nutrients, vitamins, minerals and ions by adjusting expression of luminal transport proteins

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10
Q

Q: Describe motility as a role of the ENS.

A

A: smooth muscle cells [SMCs] in the circular and longitudinal muscle layers can contract and relax to cause effective gut transit. It may be desirable to accelerate this (e.g. following a large meal) or stop it completely (e.g. during exercise)

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11
Q

Q: What are the 3 neuronal populations of the ENS? (describe) Most neurons are?

A

A: Most are neurons are multipolar (one axon, one cell body, multiple dendrites)

Sensory: respond to mechanical, thermal, osmotic and chemical stimuli.

Motor: axons terminate on smooth muscle cells of the circular or longitudinal layers, secretory cells of the gastrointestinal tract, or gastrointestinal blood vessels.

Interneurons: neurons between neurons integrate the sensory input and effector output

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12
Q

Q: What is the third plexus of the GIT? Where? (2)

A

A: Minor plexuses

including deep muscular plexus (inside circular muscle), and the ganglia supplying biliary system and pancreas

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13
Q

Q: What does the ANS regulate? (3) Control? (2) 2 branches? (what are they associated with) How do they differ?

What does central control interact with? why?

A

A: smooth muscle, cardiac muscle and glands

not under conscious control and cannot be activated voluntarily

  1. Sympathetic – associated with stress and the fight or flight response
  2. Parasympathetic – associated with sedate activities, including rest, repair and recuperation

structure and function of these braches is very different, as are the neurotransmitters they release.

enteric nervous system to control gut function.

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14
Q

Q: How do the PNS and SNS of the ANS differ in terms of neuronal cell bodies? (2,2)

A

A: SNS

  • Preganglionic cell bodies are located in the spinal cord in the lower thoracic and upper lumbar spinal cord
  • Postganglionic cell bodies are in the pre- and paravertebral ganglia

PNS

  • Preganglionic cell bodies are located in the brainstem and sacral spinal cord
  • Postganglionic cell bodies are located very close to the target organs.
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15
Q

Q: How do the PNS and SNS of the ANS differ in terms of neuron length? (2,2) Relate one to the neurons of the ENS.

A

A: SNS - Preganglionic nerves synapse with the postganglionic nerves close to the spine, which makes the preganglionic neurons relatively SHORT compared to the postganglionic neurons which extend from the sympathetic chain to the target organ and are relatively LONG.

PNS - Preganglionic nerves synapse with the postganglionic nerves close to the target organs, which could be as far from the brain as the rectal muscle wall. This makes the preganglionic neurons relatively LONG compared to the postganglionic neurons which are relatively SHORT, extending from ganglia outside of, or inside, the directly with gut plexus of the ENS.

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16
Q

Q: How do the PNS and SNS of the ANS differ in terms of innervation? (3,2) What does this reflect?

A

Q: SNS - Pre-ganglionic neurons are in the splanchnic nerves arising from the thoracic and lumbar regions. Thoracic branches innervate the foregut and associated organs, and the lumbar branches innervate the hindgut.
-> some post ganglionic N from sympathetic ganglia can directly act of blood vessels (while the rest go through ENS)

PNS - Most GI tract innervation in the branch of the ANS arises from the vagus nerve (CNX). Structures from the descending colon onwards receive innervation from the pelvic splanchnic nerves.

embryological origins of the gut

17
Q

Q: How do the PNS and SNS of the ANS differ in terms of neurotransmitter? Between pre and post?

A

A: SNS - The major neurotransmitter of the SNS is NOREPINEPHRINE/noradrenaline (NE). Although synapses in the sympathetic chain use acetylcholine (ACh) to communicate, most synapses between the SNS and the enteric nervous system use NE.

PNS - The major neurotransmitter of this branch of the ANS is acetylcholine.

always ACh

18
Q

Q: How do the PNS and SNS of the ANS differ in terms of gut function?

A

A: SNS - The general impact of the SNS on the gut function is to REDUCE ACTIVITY.

PNS - The general impact of the PNS on the gut function is to INCREASE ACTIVITY.

19
Q

Q: Majority sympathetic fibres… but… 3 examples.

A

A: do not directly innervate structures in the GI tract- terminate on neurons in the intramural plexuses.
BUT: Vasoconstrictor sympathetic fibers do directly innervate the blood vessels of the GI tract- coeliac, superior and inferior mesenteric.

20
Q

Q: Afferent signals? (2) Directly to ENS? To CNS (->PNS and ANS -> ENS)?

A

A: Chemo and mechanoreceptors in wall of GI tract

local afferents

Splanchnic and vagal afferents

21
Q

Q: What are the 2 types of innervation of the GIT? (2-1,2 examples) What does this allow?

A

A: Intrinsic innervation:
- Neurons of the enteric nervous system.

Extrinsic innervation:

  • Afferents (pain, nausea, fullness)
  • Efferents (coordination - sympathetic and parasympathetic nervous systems).

Complexity allows fine control of the GI tract.

22
Q

Q: What produces the gastrointestinal endocrine system? Can act as?

A

A: by (entero)endocrine cells in the mucosa or submucosa of the stomach, intestine and pancreas

paracrine or neurocrine factors

23
Q

Q: Name 3 hormones released by the duodenum.

A

A: Secretin
CCK
Somatostatin

24
Q

Q: Name 3 hormones released by the stomach. Effect of 2?

A

A: Gastrin*
Ghrelin
Somatostatin
*
Histamine***

paracrine signalling:

  • D-cells secrete somatostatin -> inhibits secretion of acid from parietal cells in the gastric pits.
  • enterochromaffin-like (ECL) cells secrete histamine -> binds to H2 receptors on the parietal cells, stimulating acid secretion.
25
Q

Q: Name a hormone released by the pancreas.

A

A: Insulin
Glucagon
Somatostatin** need
Pancreatic Polypeptide

26
Q

Q: Name a hormone released by the large intestine and small. Only small?

A
A: Somatostatin***
PYY
GLP1
Oxyntomodulin
Neurotensin

PYY
GIP (gastric inhibitory peptide)***

27
Q

Q: What are enteroendocrine cells? Structure (4).

A

A: large family of cells that are each specialised for their own stimuli and secretions

  • typically has a small apical membrane
  • with a lot of sensory apparatus (receptors and intracellular signalling techniques) that can sense changes in the gut contents eg fats, proteins (or activation by neurotransmitters)
  • broad basolateral surface, close to blood vessels for rapid distribution
  • near the basolateral membrane they have vesicles with their secretory products ready for exocytosis.
28
Q

Q: What are the functions of the gastrointestinal endocrine system? (4) An example for each.

A

A: Regulation of the mechanical processes of digestion (e.g. smooth muscle of GI tract and sphincters, gall bladder).

Regulation of the chemical and enzymatic processes of digestion (e.g. secretory cells located in the wall of the GI tract, pancreas and liver).

Control of post absorptive processes involved in the assimilation of digested food and CNS feedback regulating intake (e.g. GIP stimulates insulin release from pancreatic beta cells, PYY3-36 acts on the CNS to suppress appetite).

Effects on the growth and development of the GI tract (e.g. GLP-2 promotes small intestinal growth).

29
Q

Q: Which cell secretes gastrin? Where? (2) What stimulates secretion? (3)

A

A: G-cells

  • distal end of the stomach (gastric antrum)
  • proximal duodenum
  • presence of single amino acids and small peptides in the stomach
  • mechanoreceptors in the stomach wall that detect the presence of a meal (inferred by gastric stretching)
  • parasympathetic nervous system can release gastrin-releasing peptide from vagal efferents
30
Q

Q: In what form is gastrin secreted in? Role? Feedback? why?

A

A: It is secreted in three lengths, mostly as a 34 amino-acid peptide, but also with shorter chains of 17 and 14 amino acids.

Gastrin causes an increase in gastric acid secretion from parietal cells in the stomach.

There is a negative feedback loop built into gastrin secretion; if the pH of chyme in the duodenum drops below 3 (pH<3), secretion will be reduced. This is to protect the duodenal mucosa.

31
Q

Q: Which cell secretes somatostatin? Where? (3) Secreted in response to? Role? Examples (4). How can their role be used in terms of treatment?

A

A: D (delta) cells

stomach, pancreas and small intestine

Somatostatin is secreted in response to a mixed meal.

enormous number of inhibitory functions, somatostatin is often described as the UNIVERSAL INHIBITOR.

  • decreases secretion of gastric acid via two mechanisms
    i) It inhibits G-cells form secreting gastrin (which promotes acid secretion)
    ii) inhibits ECL cells from secreting histamine
  • decreases motility of the gut and decreases gastric emptying.

Analogues used to treat neuroendocrine tumours

32
Q

Q: Which cell secretes secretin? Where? (2) What stimulates secretion? What does secretin do?

A

A: S-cells

proximal small intestine (duodenum and the jejunum).

drop in pH in the duodenal lumen (usually following acid chyme leaving the stomach through the pyloric sphincter)

stimulates the secretion of bicarbonate rich juice from the exocrine pancreas (to neutralise the acid)

33
Q

Q: What does excess secretin do? why?

A

A: -inhibit the secretion of acid by the stomach
-inhibit gastric emptying
(to prevent further exacerbation of the acidic environment in the small intestine, as this will be causing mucosal damage).

34
Q

Q: What is GIP? (2) Which cell secretes it? Where? (2) Involved in? Stimulus? Main physiological effect? In high concentrations?

A

A: Glucose-dependent insuliotropic peptide
Also called Gastric inhibitory peptide​

K cells
duodenum and jejunum

-peptide hormone is involved with glucose storage

high glucose concentration in the small intestine

upregulation of insulin secretion in response to

inhibitory effects on stomach function.

35
Q

Q: What is CCK? Which cell secretes it? Where? Stimulation? Effects? (4) What doesn’t it need?

A

A: Cholecystokinin

I-cells

small intestine

detection of small peptides and fats (i.e. a mixed meal) in the lumen

This triggers a number of effects, including:

  • stimulates pancreatic enzyme release
  • delays gastric emptying
  • stimulates gallbladder contraction.
  • decreases food intake and meal size (and appetite)

CCK is able to be secreted and triggers these effects without any input from the autonomic nervous system.

36
Q

Q: What is PYY? Which cells secrete it? Where? (3) When is it secreted? Role? (4) Subtype role.

A

A: peptide YY

L cells

Cells found throughout the mucosa of the terminal ileum, colon and rectum.

post prandially (particularly protein)

  • reduces intestinal motility
  • reduces gallbladder contraction
  • reduces pancreatic exocrine secretion
  • Inhibitor of intestinal fluid and electrolyte secretion.
  • PYY3-36 (truncated version) inhibits food intake.