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Adrenergic receptor and mechanism of action
AUTONOMIC
NERVOUS SYSTEM
• Central Nervous System (CNS) - Brain and

spinal cord
• Peripheral Nervous System (PNS) - Located
outside the brain & spinal cord
* Autonomic Nervous System (ANS) &
the somatic
• The PNS receives stimuli from the CNS &
initiates responses to the stimuli after it’s
interpreted by the brain
AUTONOMIC NERVOUS SYSTEM
• ANS acts on smooth muscles & glands

•

- Controls & regulation of the heart, respiratory.
system, GI tract, bladder, eyes & glands
- Involuntary - person has little or no control
Somatic - voluntary - person has control (skeletal
muscle)
ANS
• ANS has 2 sets of neurons:
1. Afferent (sensory) - sends impulses to the CNS for
interpretation
2. Efferent - receives impulses (info.) from the brain &
transmits from the spinal cord to the effector organ
cells
- 2 branches - sympathetic &
parasympathetic nervous system
FIGURE 20-2.

SYMPATHETIC AND PARASYMPATHETIC EFFECTS ON BODY
TISSUES
ANS - SYMPATHETIC NERVOUS
SYSTEM
(ADRENERGIC)
• Sympathetic Nervous System (adrenergic)

Norepinephrine = neurotransmitter
- Drugs that mimic = adrenergic drugs,
sympathomimetics, or adrenomemetics
* Adrenergic agonists - Drugs initiate a
response
- Drugs that block = adrenergic blockers,
sympatholytics or adrenolytics
* Adrenergic antagonists - prevent a response
ANS
• 4 types of adrenergic receptor organ cells:

1. Alpha-1 = vasoconstriction of blood vessels
inc. blood return to heart, inc. circulation, inc. BP
2. Alpha-2 = inhibits release of norepinephrine
dec. in vasoconstriction, dec. BP
3. Beta-1 = inc. in heart rate & force on contraction
4. Beta-2 = relaxation of smooth muscle in bronchi, uterus,
peripheral blood vessels
Dopaminergic = dilate vessels, inc. in blood flow - only
dopamine activates this receptor
ANS - PARASYMPATHETIC
NERVOUS
SYSTEM
(CHOLINERGIC)
• Parasympathetic or Cholinergic Nervous

System
Acetylcholine = neurotransmitter
- Drugs that mimic = cholinergic drugs,
parasympathomimetics
Cholinergic agonists - initiates a response
- Drugs that block = anticholinergic,
parasympatholytics
Cholinergic antagonists - prevents a response
ANS
•

Sympathomimetic
pathway
Norepinephrine
From adrenergic fiber
Inc. heart rate
Pupil dilation
Adrenergic (sympathomimetic)
agents
Fight or Flight

•

Parasymathomimetic
pathway

Acetylcholine
From cholinergic fibers
Dec. heart rate
pupil constriction
Cholinergic
(parasympathomimetic
agents)
ADRENERGICS AND
ADRENERGIC BLOCKERS
• Drugs that Stimulate the sympathetic Nervous

System (adrenergics, adrenergic agonists,
sypathomimetics, or adrenomimetics)
• Mimic the sympathetic neruotransmitters
norepinephrine and epinephrine
• Act on one or more adrenergic receptor sites
located on the cells of smooth muscles - heart,
bronchioles, GI tract, bladder, eye
• 4 main receptors (alpha-1, alpha-2, beta-1,
beta-2)
SYMPATHETIC RESPONSES
MECHANISM OF ADRENERGIC
RECEPTORS
There are two main groups of adrenergic receptors, α and β, with
several subtypes.
•α receptors have the subtypes α1 (a Gq coupled receptor) and α2 (a
Gi coupled receptor). Phenylephrine is a selective agonist of the α
receptor.
•β receptors have the subtypes β1, β2 and β3. All three are linked to
Gs proteins (although β2 also couples to Gi),[2] which in turn are
linked to adenylate cyclase. Agonist binding thus causes a rise in
the intracellular concentration of the second messenger cAMP.
Downstream effectors of cAMP include
cAMP-dependent protein kinase (PKA), which mediates some of the
intracellular events following hormone binding. Isoprenaline is a
non-selective agonist.
Adrenaline or noradrenaline are
receptor ligands to either α 1, α 2 or β adrenergic receptors.
α 1 couples to Gq, which results in
increased intracellular Ca2+ and
subsequent smooth muscle
contraction. α 2, on the other hand,
couples to Gi, which causes a
decrease of cAMP activity and a
resulting smooth muscle relaxation.
β receptors couple to Gs, and
increases intracellular cAMP
activity, resulting in e.g.
heart muscle contraction, smooth
muscle relaxation and glycogenolysis
.
MOLECULAR MECHANICS OF ADRENRGIC
RECPTOR
Beta adrenergic receptor kinase (βARK) is a serine/threonine
intracellular kinase. It is activated by PKA and its target is the beta
adrenergic receptor.
βARK Activation :
1.Upon stimulation of the Beta adrenergic receptor by epinephrine, Gs will be activated.
2.Gs alpha will then stimulate adenyl cyclase to make cAMP.
3.cAMP will then activate cAMP-dependent kinase (PKA), which, among other proteins that
it acts on, will phosphorylate serine and threonine residues on β AR
K.

4.β ARK, itself a serine/
threonine kinase, will then phosphorylate serine and threonine
resides on the β -adrenergic receptor itself.

5.This will facilitate Beta-arrestin's binding to the receptor. Additional stimulation by
epinephrine will now be unable to activate Gs due to arrestin.
Therefore, β AR is a negative feedback enzyme that will prevent overstimulation of the β K
adrenergic receptor.
SYMPATHOMIMETICS/
ADRENOMIMETICS
• Stimulate adrenergic receptors: 3 categories
1. Direct-acting = directly stimulates receptors
(epinephrine or norepinephrine)
2. Indirect-acting = stimulates release of norep. from
terminal nerve endings (amphetamine)
3. Mixed-acting (indirect & direct) = stimulates
receptor sites & release of norep. from nerve
endings (Ephedrine)
SYMPATHOMIMETIC AGENTS/
ADRENERGICS
• Action - Many of the adrenergic drugs stimulate
more than one of the adrenergic receptor sites
(alpha & Beta)

• Response = Inc. BP, pupil dilation, inc. HR, &
bronchodilation

• Use = Cardiac stimulation, bronchodilator,
decongestant

• Side effects = Hyperness in body
SYMPATHOMIMETICS/ADRENER
GICS
•

Albuterol - Beta-2 agonist (bronchodilation)
Use - bronchospasm, asthma, bronchitis
SE - nervousness, restlessness
CI - severe cardiac disease, HTN

•

Epinephrine - stimulates alpha & beta
Use - allergic reaction, cardiac arrest
SE - nervousness, agitation
CI - cardiac dysrhythmias
ADRENERGIC AGENTS
• Dopamine - alpha-1 & beta-1 stimulation
Use - Hypotension, shock, inc. cardiac output,
improve perfusion to vital organs
SE - N & V, headache
CI - V. Tach
ADRENERGIC BLOCKERS
(ANTAGONISTS/SYMPATHOLYTI
CS)
• Block alpha & beta receptor sites
(nonselective)

• direct or indirect acting on the release of
norepinephrine and epinephrine

• Use - Cardiac arrthymias (HR), HTN

( cardiac output), angina (O2 demand)

• SE - CHF, bronchospasm, bradycardia,
wheezing
NONSELECTIVE VS SELECTIVE
BETA BLOCKERS
• Nonselective have an equal inhibitory effect on B1
& B2 receptors -

- Drugs have lots of interactions due to lots of
alpha/beta receptor sites throughout body
- use with caution on clients with cardiac
failure or asthma

• Selective B1 helpful in asthma clients
ADRENERGIC BLOCKING AGENTS
•

•
•

Inderal (Propranolol) - Nonselective
Use - angina, dysrhythmias, HTN, migraines
SE - Many d/t nonselective
CI - asthma, heart block > 1st degree

Minipress (Prazosin) - A blocker

Use - mild to mod. HTN
SE - orthostatic hypotension

Tenormin (Atenolol), Lopressor (Metoprolol)

B1 (cardio) selective
Use - mild to mod HTN, angina
CHOLINERGICS AND
ANTICHOLINERGICS parasympathetic
• Cholinergics stimulate the
nervous system

• Mimic the neurotransmitter acetylcholine
• 2 types of cholinergic receptors
1. muscarinic - stimulates smooth muscle &
slows HR
2. nicotinic - affect skeletal muscle

• Many = nonselective & affect both receptors
• Some affect only the muscarinic receptors and
not the nicotinic receptors
PARASYMPATHETIC RESPONSES
CHOLINERGIC AGENTS
• Direct acting - act on the receptors to activate a tissue
response

• Indirect acting - inhibit the action of the enzyme
cholinesterase (acetylcholinesterase - ACH)

• Major uses = Stimulate bladder & GI tone, constrict
pupils (miosis),

neuro-

muscular transmission
DIRECT-ACTING
PARASYMPATHOMIMETIC
(CHOLINERGIC DRUGS)
CHOLINERGIC AGENT
(PARASYMPATHOMIMETICS)
• Bethanechol (Urecholine) selective to

muscarinic receptors, mimic action of
acetylcholine
Use - For urinary retention
* Take on an empty stomach d/t inc. peristalsis
* Alert- Never give IM or IV – circulatory
collapse, hypotension, shock & cardiac arrest
poss.
• Pilocarpine (Pilocar) - Ophthalmic - direct acting
CHOLINERGIC BLOCKING AGENTS

ANTICHOLINERGICS/PARASYMP
ATHOLYTICS
• Drugs that inhibit action of acetylcholine

(ACH) receptors
• Affects the heart, resp. tract, GI tract, bladder,
eye, & exocrine glands.
• Allows the sympathetic nervous system to
dominate
• Anticholinergic & cholinergic drugs have
opposite effects
• Major responses = dec. in GI motility, dec. in
salivation, dilation of pupil (mydriasis), inc.
pulse rate
ANTICHOLINERGICS
• Uses: Pre-op meds,bradycardia, GI/urinary
antispasmodic

• SE: Dry mouth/mucus membranes
blocks vagal
• Atropine Sulfate - Inhibits ACH
effects on SA & AV nodes
inc. HR

inc. conduction &

Use = Bradycardia, pre-up to dec. secretions,
peptic ulcer disease
SE = Many. Most frequent = dry mouth,
ANTICHOLINERGICS
• Bentyl (Dicyclomine) - Inhibits ACH on muscarinic
receptors & dec. GI motility

Use - Irritable bowel syndrome
SE - constipation, urinary retention, dry mouth

• Robinul (Glycopyrrolate) - Similar to above
Use - pre-op to dec. secretions, GI disorders
SE - Similar to above
ANTICHOLINERGICS
• Anticholinergics effect the CNS & benefit
people prone to motion sickness

• Scopolamine Patch - Classified as an
antihistamine for motion sickness

- Topical skin patch behind the ear x3 days
Use = cruising on water, flying, car sickness
Other drugs = Dramamine, Bonine
SE = Dry mouth, visual disturbances d/t pupil
dilation

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Adrenergic receptor and mechanism of action by yehia matter

  • 1. Adrenergic receptor and mechanism of action
  • 2. AUTONOMIC NERVOUS SYSTEM • Central Nervous System (CNS) - Brain and spinal cord • Peripheral Nervous System (PNS) - Located outside the brain & spinal cord * Autonomic Nervous System (ANS) & the somatic • The PNS receives stimuli from the CNS & initiates responses to the stimuli after it’s interpreted by the brain
  • 3. AUTONOMIC NERVOUS SYSTEM • ANS acts on smooth muscles & glands • - Controls & regulation of the heart, respiratory. system, GI tract, bladder, eyes & glands - Involuntary - person has little or no control Somatic - voluntary - person has control (skeletal muscle)
  • 4. ANS • ANS has 2 sets of neurons: 1. Afferent (sensory) - sends impulses to the CNS for interpretation 2. Efferent - receives impulses (info.) from the brain & transmits from the spinal cord to the effector organ cells - 2 branches - sympathetic & parasympathetic nervous system
  • 5. FIGURE 20-2. SYMPATHETIC AND PARASYMPATHETIC EFFECTS ON BODY TISSUES
  • 6. ANS - SYMPATHETIC NERVOUS SYSTEM (ADRENERGIC) • Sympathetic Nervous System (adrenergic) Norepinephrine = neurotransmitter - Drugs that mimic = adrenergic drugs, sympathomimetics, or adrenomemetics * Adrenergic agonists - Drugs initiate a response - Drugs that block = adrenergic blockers, sympatholytics or adrenolytics * Adrenergic antagonists - prevent a response
  • 7. ANS • 4 types of adrenergic receptor organ cells: 1. Alpha-1 = vasoconstriction of blood vessels inc. blood return to heart, inc. circulation, inc. BP 2. Alpha-2 = inhibits release of norepinephrine dec. in vasoconstriction, dec. BP 3. Beta-1 = inc. in heart rate & force on contraction 4. Beta-2 = relaxation of smooth muscle in bronchi, uterus, peripheral blood vessels Dopaminergic = dilate vessels, inc. in blood flow - only dopamine activates this receptor
  • 8. ANS - PARASYMPATHETIC NERVOUS SYSTEM (CHOLINERGIC) • Parasympathetic or Cholinergic Nervous System Acetylcholine = neurotransmitter - Drugs that mimic = cholinergic drugs, parasympathomimetics Cholinergic agonists - initiates a response - Drugs that block = anticholinergic, parasympatholytics Cholinergic antagonists - prevents a response
  • 9. ANS • Sympathomimetic pathway Norepinephrine From adrenergic fiber Inc. heart rate Pupil dilation Adrenergic (sympathomimetic) agents Fight or Flight • Parasymathomimetic pathway Acetylcholine From cholinergic fibers Dec. heart rate pupil constriction Cholinergic (parasympathomimetic agents)
  • 10. ADRENERGICS AND ADRENERGIC BLOCKERS • Drugs that Stimulate the sympathetic Nervous System (adrenergics, adrenergic agonists, sypathomimetics, or adrenomimetics) • Mimic the sympathetic neruotransmitters norepinephrine and epinephrine • Act on one or more adrenergic receptor sites located on the cells of smooth muscles - heart, bronchioles, GI tract, bladder, eye • 4 main receptors (alpha-1, alpha-2, beta-1, beta-2)
  • 12. MECHANISM OF ADRENERGIC RECEPTORS There are two main groups of adrenergic receptors, α and β, with several subtypes. •α receptors have the subtypes α1 (a Gq coupled receptor) and α2 (a Gi coupled receptor). Phenylephrine is a selective agonist of the α receptor. •β receptors have the subtypes β1, β2 and β3. All three are linked to Gs proteins (although β2 also couples to Gi),[2] which in turn are linked to adenylate cyclase. Agonist binding thus causes a rise in the intracellular concentration of the second messenger cAMP. Downstream effectors of cAMP include cAMP-dependent protein kinase (PKA), which mediates some of the intracellular events following hormone binding. Isoprenaline is a non-selective agonist.
  • 13. Adrenaline or noradrenaline are receptor ligands to either α 1, α 2 or β adrenergic receptors. α 1 couples to Gq, which results in increased intracellular Ca2+ and subsequent smooth muscle contraction. α 2, on the other hand, couples to Gi, which causes a decrease of cAMP activity and a resulting smooth muscle relaxation. β receptors couple to Gs, and increases intracellular cAMP activity, resulting in e.g. heart muscle contraction, smooth muscle relaxation and glycogenolysis .
  • 14. MOLECULAR MECHANICS OF ADRENRGIC RECPTOR Beta adrenergic receptor kinase (βARK) is a serine/threonine intracellular kinase. It is activated by PKA and its target is the beta adrenergic receptor. βARK Activation : 1.Upon stimulation of the Beta adrenergic receptor by epinephrine, Gs will be activated. 2.Gs alpha will then stimulate adenyl cyclase to make cAMP. 3.cAMP will then activate cAMP-dependent kinase (PKA), which, among other proteins that it acts on, will phosphorylate serine and threonine residues on β AR K. 4.β ARK, itself a serine/ threonine kinase, will then phosphorylate serine and threonine resides on the β -adrenergic receptor itself. 5.This will facilitate Beta-arrestin's binding to the receptor. Additional stimulation by epinephrine will now be unable to activate Gs due to arrestin. Therefore, β AR is a negative feedback enzyme that will prevent overstimulation of the β K adrenergic receptor.
  • 15.
  • 16. SYMPATHOMIMETICS/ ADRENOMIMETICS • Stimulate adrenergic receptors: 3 categories 1. Direct-acting = directly stimulates receptors (epinephrine or norepinephrine) 2. Indirect-acting = stimulates release of norep. from terminal nerve endings (amphetamine) 3. Mixed-acting (indirect & direct) = stimulates receptor sites & release of norep. from nerve endings (Ephedrine)
  • 17. SYMPATHOMIMETIC AGENTS/ ADRENERGICS • Action - Many of the adrenergic drugs stimulate more than one of the adrenergic receptor sites (alpha & Beta) • Response = Inc. BP, pupil dilation, inc. HR, & bronchodilation • Use = Cardiac stimulation, bronchodilator, decongestant • Side effects = Hyperness in body
  • 18. SYMPATHOMIMETICS/ADRENER GICS • Albuterol - Beta-2 agonist (bronchodilation) Use - bronchospasm, asthma, bronchitis SE - nervousness, restlessness CI - severe cardiac disease, HTN • Epinephrine - stimulates alpha & beta Use - allergic reaction, cardiac arrest SE - nervousness, agitation CI - cardiac dysrhythmias
  • 19. ADRENERGIC AGENTS • Dopamine - alpha-1 & beta-1 stimulation Use - Hypotension, shock, inc. cardiac output, improve perfusion to vital organs SE - N & V, headache CI - V. Tach
  • 20. ADRENERGIC BLOCKERS (ANTAGONISTS/SYMPATHOLYTI CS) • Block alpha & beta receptor sites (nonselective) • direct or indirect acting on the release of norepinephrine and epinephrine • Use - Cardiac arrthymias (HR), HTN ( cardiac output), angina (O2 demand) • SE - CHF, bronchospasm, bradycardia, wheezing
  • 21. NONSELECTIVE VS SELECTIVE BETA BLOCKERS • Nonselective have an equal inhibitory effect on B1 & B2 receptors - - Drugs have lots of interactions due to lots of alpha/beta receptor sites throughout body - use with caution on clients with cardiac failure or asthma • Selective B1 helpful in asthma clients
  • 22. ADRENERGIC BLOCKING AGENTS • • • Inderal (Propranolol) - Nonselective Use - angina, dysrhythmias, HTN, migraines SE - Many d/t nonselective CI - asthma, heart block > 1st degree Minipress (Prazosin) - A blocker Use - mild to mod. HTN SE - orthostatic hypotension Tenormin (Atenolol), Lopressor (Metoprolol) B1 (cardio) selective Use - mild to mod HTN, angina
  • 23. CHOLINERGICS AND ANTICHOLINERGICS parasympathetic • Cholinergics stimulate the nervous system • Mimic the neurotransmitter acetylcholine • 2 types of cholinergic receptors 1. muscarinic - stimulates smooth muscle & slows HR 2. nicotinic - affect skeletal muscle • Many = nonselective & affect both receptors • Some affect only the muscarinic receptors and not the nicotinic receptors
  • 25. CHOLINERGIC AGENTS • Direct acting - act on the receptors to activate a tissue response • Indirect acting - inhibit the action of the enzyme cholinesterase (acetylcholinesterase - ACH) • Major uses = Stimulate bladder & GI tone, constrict pupils (miosis), neuro- muscular transmission
  • 27. CHOLINERGIC AGENT (PARASYMPATHOMIMETICS) • Bethanechol (Urecholine) selective to muscarinic receptors, mimic action of acetylcholine Use - For urinary retention * Take on an empty stomach d/t inc. peristalsis * Alert- Never give IM or IV – circulatory collapse, hypotension, shock & cardiac arrest poss. • Pilocarpine (Pilocar) - Ophthalmic - direct acting
  • 28. CHOLINERGIC BLOCKING AGENTS ANTICHOLINERGICS/PARASYMP ATHOLYTICS • Drugs that inhibit action of acetylcholine (ACH) receptors • Affects the heart, resp. tract, GI tract, bladder, eye, & exocrine glands. • Allows the sympathetic nervous system to dominate • Anticholinergic & cholinergic drugs have opposite effects • Major responses = dec. in GI motility, dec. in salivation, dilation of pupil (mydriasis), inc. pulse rate
  • 29. ANTICHOLINERGICS • Uses: Pre-op meds,bradycardia, GI/urinary antispasmodic • SE: Dry mouth/mucus membranes blocks vagal • Atropine Sulfate - Inhibits ACH effects on SA & AV nodes inc. HR inc. conduction & Use = Bradycardia, pre-up to dec. secretions, peptic ulcer disease SE = Many. Most frequent = dry mouth,
  • 30. ANTICHOLINERGICS • Bentyl (Dicyclomine) - Inhibits ACH on muscarinic receptors & dec. GI motility Use - Irritable bowel syndrome SE - constipation, urinary retention, dry mouth • Robinul (Glycopyrrolate) - Similar to above Use - pre-op to dec. secretions, GI disorders SE - Similar to above
  • 31. ANTICHOLINERGICS • Anticholinergics effect the CNS & benefit people prone to motion sickness • Scopolamine Patch - Classified as an antihistamine for motion sickness - Topical skin patch behind the ear x3 days Use = cruising on water, flying, car sickness Other drugs = Dramamine, Bonine SE = Dry mouth, visual disturbances d/t pupil dilation