Autonomic Pharmacology Quiz
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Questions and Answers

What is the primary neurotransmitter used by sympathetic postganglionic neurons?

  • Noradrenaline (correct)
  • Dopamine
  • Acetylcholine
  • Serotonin

Which category do drugs that enhance the effect of noradrenaline fall into?

  • NAT inhibitors
  • Adrenergic antagonists
  • Muscarinic agonists
  • Adrenergic agonists (correct)

Which of the following is an example of a β-adrenoceptor antagonist?

  • Dopamine
  • Isoprenaline
  • Metoprolol (correct)
  • Phenylephrine

How are adrenoceptors primarily categorized?

<p>By the type of adrenoreceptor they act on (A)</p> Signup and view all the answers

Which type of drug acts on the sympathetic nervous system via catecholamine regulation?

<p>NAT inhibitors (B), MAO inhibitors (D)</p> Signup and view all the answers

What is the mechanism of action for α-adrenoceptor agonists?

<p>Stimulate α-adrenoceptors (A)</p> Signup and view all the answers

What distinguishes β-adrenoceptor antagonists from α-adrenoceptor antagonists?

<p>They bind to different types of receptors (B)</p> Signup and view all the answers

Which of the following is a primary use for muscarinic antagonists?

<p>Counteract cholinergic toxicity (A)</p> Signup and view all the answers

Which class of drugs primarily contains NAT inhibitors?

<p>Drugs that regulate catecholamines (A)</p> Signup and view all the answers

What is the primary role of MAO inhibitors in relation to noradrenaline?

<p>Prevent its breakdown (A)</p> Signup and view all the answers

What is the primary structural difference between nicotinic ACh receptors in skeletal muscle and those in the autonomic nervous system?

<p>Skeletal muscle receptors use α<del>1</del> subunits. (B)</p> Signup and view all the answers

Which drug is recognized as a non-competitive antagonist of autonomic nicotinic ACh receptors?

<p>Hexamethonium (B)</p> Signup and view all the answers

What type of receptors do postganglionic neurones of the parasympathetic nervous system predominantly act upon?

<p>Muscarinic receptors (A)</p> Signup and view all the answers

What is a prominent effect of muscarine poisoning?

<p>Bradycardia (B)</p> Signup and view all the answers

How does atropine counteract muscarine poisoning?

<p>By inhibiting muscarinic receptors competitively (C)</p> Signup and view all the answers

What is the therapeutic use of pilocarpine?

<p>To treat glaucoma (A)</p> Signup and view all the answers

Which aspect of hexamethonium limits its clinical use?

<p>It causes severe side effects due to broad receptor blocking. (B)</p> Signup and view all the answers

What type of receptor is primarily targeted by muscarinic agonists?

<p>G-protein coupled receptors (D)</p> Signup and view all the answers

Which of the following is NOT an effect associated with muscarinic stimulation?

<p>Mydriasis (dilated pupils) (B)</p> Signup and view all the answers

Which statement about muscarinic ACh receptors is incorrect?

<p>There are only two types of muscarinic receptors. (A)</p> Signup and view all the answers

Flashcards

Nicotinic ACh Receptor (nAChR)

A type of acetylcholine receptor found at the junction between preganglionic and postganglionic neurons in both the sympathetic and parasympathetic nervous systems.

Hexamethonium

A non-competitive antagonist of nicotinic ACh receptors in the autonomic nervous system. It blocks all the effects of autonomic stimulation, both sympathetic and parasympathetic.

Muscarinic ACh Receptor (mAChR)

A type of acetylcholine receptor found on postganglionic neurons in the parasympathetic nervous system. These receptors are responsible for mediating the effects of the parasympathetic nervous system.

Muscarinic Agonists

Drugs that activate muscarinic ACh receptors, mimicking the effects of parasympathetic stimulation.

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Muscarine poisoning

A condition caused by an over-consumption of muscarine-containing mushrooms. It leads to extreme parasympathetic effects, such as bradycardia, hypotension, increased gut motility, bronchoconstriction, and miosis of the pupils.

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Atropine

A competitive antagonist of muscarinic ACh receptors. Used to reverse the effects of muscarine poisoning and other muscarinic agonist overdoses.

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Pilocarpine

A muscarinic agonist used to treat glaucoma by targeting M3 receptors in the ciliary muscles of the eye, reducing intraocular pressure.

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Autonomic pharmacology

The use of drugs to influence the autonomic nervous system.

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Autonomic drugs

Drugs that specifically target the autonomic nervous system.

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Sympathetic Nervous System

The division of the autonomic nervous system responsible for 'fight or flight' responses.

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Muscarinic Antagonists

Muscarinic antagonists block the action of acetylcholine (ACh) at muscarinic receptors, which are found in the parasympathetic nervous system (PNS).

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Muscarinic Agonists and ACh Esterase Inhibitors

Muscarinic agonists can be used to counter the effects of ACh esterase inhibitors, which increase ACh levels in the synapse by preventing its breakdown.

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Adrenoceptors

Adrenoceptors are G-protein coupled receptors that bind to catecholamines, like norepinephrine (NE) and epinephrine. They are found in the sympathetic nervous system.

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Adrenergic Agonists

Drugs that bind to adrenoceptors and mimic the effects of norepinephrine (NE) or epinephrine. They activate the sympathetic nervous system.

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Adrenergic Antagonists

Drugs that bind to adrenoceptors and block the effects of norepinephrine (NE) or epinephrine. They inhibit the actions of the sympathetic nervous system.

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α-Adrenoceptor Agonists

α-adrenoceptor agonists activate α-adrenoceptors, which are involved in vasoconstriction, pupil dilation, and other sympathetic effects.

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α-Adrenoceptor Antagonists

α-adrenoceptor antagonists, also known as alpha-blockers, block the effects of NE and epinephrine at α-adrenoceptors. They are used to treat conditions like high blood pressure and benign prostatic hyperplasia (BPH).

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β-Adrenoceptor Agonists

β-adrenoceptor agonists activate β-adrenoceptors, which are involved in bronchodilation (opening airways), increasing heart rate, and other sympathetic effects.

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β-Adrenoceptor Antagonists

β-adrenoceptor antagonists, also known as beta-blockers, block the effects of NE and epinephrine at β-adrenoceptors. They are used to treat conditions like high blood pressure and angina (chest pain).

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NAT Inhibitors

NAT inhibitors, such as pargyline, inhibit the enzyme norepinephrine transporter (NAT), which is responsible for the reuptake of norepinephrine from the synapse. This leads to increased levels of norepinephrine in the synapse, enhancing sympathetic activity.

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Study Notes

Autonomic Pharmacology

  • Drugs targeting the entire autonomic nervous system affect both sympathetic and parasympathetic systems.
  • Nicotinic ACh receptors are present at synapses between pre- and post-ganglionic neurons in both systems.
  • Skeletal muscle AChRs are pentameric, while ANS AChRs have 2-7 subunits.
  • Hexamethonium is a non-competitive antagonist of nicotinic AChRs. It blocks all autonomic effects, but has many side effects.

Drugs Targeting Parasympathetic Nervous System

  • Postganglionic parasympathetic neurons use muscarinic ACh receptors to affect organs.
  • Muscarinic ACh receptors are G-protein coupled receptors (7 transmembrane domains).
  • Five types of muscarinic receptors exist (M1-M5).
  • M1 receptors are in the stomach and salivary glands (Gq).
  • M2 receptors are in cardiac muscle (Gi).
  • M3 receptors are in smooth muscles and glands (Gq).

Muscarinic Agonists/Parasympathomimetics

  • These drugs activate muscarinic receptors, mimicking parasympathetic stimulation.
  • Effects include decreased heart rate, vasodilation, smooth muscle contraction (gut/respiratory), salivation, and tearing.

Muscarinic Antagonists

  • These drugs block muscarinic receptors, opposing parasympathetic effects.
  • Uses include asthma treatment (ipratropium/tiotropium), increasing heart rate, widening pupils, treating bladder issues, and motion sickness.
  • Pilocarpine is an example and is used in glaucoma treatment.

Drugs Targeting Sympathetic Nervous System

  • Sympathetic postganglionic neurons use noradrenaline (NA).
  • Adrenoceptors are G-protein coupled receptors (5 types).
  • α1 receptors cause smooth muscle contraction (vasoconstriction, etc.).
  • α2 receptors also cause contraction and inhibit NA release.
  • β1 receptors increase heart rate and contractility.
  • β2 receptors relax smooth muscle (e.g., bronchi, blood vessels).
  • β3 receptors stimulate lipolysis and relax smooth muscle (e.g., bladder).

Adrenoceptor Agonists (Sympathomimetics)

  • Used in vasoconstriction, nasal decongestion, hypertension treatment, and facial erythema.

Adrenoceptor Antagonists (Alpha-blockers)

  • Used in hypertension and benign prostatic hyperplasia.

β-Adrenoceptor Antagonists (Beta-blockers)

  • Used in angina, cardiac arrhythmias, heart failure, hypertension, anxiety and glaucoma.

Drugs Affecting Catecholamine Regulation

  • Noradrenaline (NA) is synthesized from tyrosine.
  • NA is stored in vesicles and released in the synapse.
  • The action of NA is terminated by reuptake via the Noradrenaline transporter (NAT).
  • Some NA is broken down by monoamine oxidase (MAO).

NAT Inhibitors

  • Inhibit noradrenaline reuptake to increase its effect on the synapse.
  • Examples include desipramine and cocaine.

MAO Inhibitors

  • Inhibit the breakdown of noradrenaline, increasing its levels.
  • Side effects include hypotension, weight gain, restlessness, insomnia and 'cheese reaction' (hypertensive crisis with cheese).

Sympathetic Amines

  • Structurally similar to NA, they are transported into neurons, displacing NA and causing similar effects.
  • Examples include amphetamines, ephedrine, tyramine.

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Autonomic Pharmacology PDF

Description

Test your knowledge on autonomic pharmacology, focusing on drugs impacting the sympathetic and parasympathetic nervous systems. This quiz includes information about nicotinic and muscarinic receptors, their functions, and the drugs that affect them. Understand the mechanisms of action and clinical implications of various autonomic drugs.

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