ANS Pharmacology: Intro to Atonomic Nervous System

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ANS Physiology and Pharmacology Overview | Review of Autonomic Nervous System

Widmaier, EP. Vander’s human physiology 14th Ed. New York: McGraw-Hill, 2016.

Marc Imhotep Cray, M.D.


Overall Goal

“ Deconstruction, Reconstruction, Integration and Relationships” The nineteenth-century physiologist Claude Bernard put it this way:

“After carrying out an analysis of phenomena, we must . . . always reconstruct our physiological synthesis, so as to see the joint action of all the parts we have isolated. . .” http://en.wikipedia.org/wiki/Claude_Bernard

Marc Imhotep Cray, M.D.

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Topics Outline  Homeostasis  Basic Neuroanatomy and Neurophysiology of ANS  Neurotransmitters  Receptors  Receptor-Ligand Interactions & Signal Transduction  Autonomic and Somatic Pharmacology Terminology Marc Imhotep Cray, M.D.

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Learning Objectives After this presentation the learner should be able: To describe the two divisions of the ANS and the main functions and effects of each division. To explain how sympathetic and parasympathetic nerves interact with each other to regulate organ function (maintain homeostasis) To describe the fight or flight reaction and explain how sympathetic activation affects the activities of the different organs To list the main organ effects caused by parasympathetic stimulation To describe the different autonomic receptors that are stimulated by acetylcholine, norepinephrine, and epinephrine To describe signaling mechanisms and pharmacology of ANS receptor subtypes Marc Imhotep Cray, M.D.

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Autonomic Nervous System (ANS)

 Autonomic nervous system (ANS) is part of

nervous system responsible for homeostasis

 Except for skeletal muscle, which gets its

innervation from somatomotor nervous system, innervation to all other organs is supplied by ANS

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ANS vs. Endocrine System in Homeostasis Autonomic nervous system (ANS) is moment-to-moment regulator of internal environment regulating specific functions that occur without conscious control:  respiration  circulation  digestion  body temperature  metabolism  sweating, secretions of certain endocrine glands Endocrine system, in contrast, provides slower, more generalized regulation by secreting hormones into the systemic circulation to act at distant, widespread sites over periods of minutes to hours to days Marc Imhotep Cray, M.D.

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ANS and Endocrine System [common properties]  high-level integration in the brain

 ability to influence processes in distant regions of body  extensive use of negative feedback 

maintaining homeostasis

 both systems use chemicals for transmission of information Marc Imhotep Cray, M.D.

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Walter Cannon coined word homeostasis  Referring to animal systems, 20th century physiologist Walter Cannon coined the word homeostasis in 1926  “Coordinated physiological reactions which maintain most of the steady states in the body are so complex, and are so peculiar to the living organism, that it was suggested (Cannon, 1929) that a specific designation for these states be employed – homeostasis”

Courtesy National Library of Medicine

Cannon, WB, Organization for Physiological Homeostasis.pdf Physiological Rev July 1, 1929 9:399-431 Also see: Cray MI. Walter Cannon, Homeostasis and the Physiological Response to Stress, A Web Interactive PowerPoint Presentation Marc Imhotep Cray, M.D.

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Homeostasis (1) ď Ž

ď Ž

The physiologic process of maintaining an internal environment (ECF environment) compatible w normal health Autonomic reflexes maintain set points and modulate organ system functions via negative feedback in pursuit of homeostasis

Marc Imhotep Cray, M.D.

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Homeostasis (2) A dynamic steady state of constituents in internal environment (ECF) that surrounds and exchanges materials with cells Factors homeostaticly maintained include: (Controlled Variables)  Concentration of nutrient molecules  Concentration of O2 and CO2  Concentration of waste products  pH  Concentration of water, salts, and other electrolytes  Temperature  Volume and pressure  GFR  …and others Marc Imhotep Cray, M.D.

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Homeostasis (3) Nervous

versus

Endocrine

Wired

Wireless

Neurotransmitters

Hormones Hormones

Short Distance Distance Short

Long Distance Distance Long

Closeness

Receptor Specificity

Rapid Onset

Delayed Onset

Short Duration

Prolonged Duration

Rapid Response

Regulation

Marc Imhotep Cray, M.D.

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Components of a negative feedback control system Recognizes deviation of normal set point value

Attempt to restore set point value

Measures control variable

COMPARATOR SENSOR stretch receptors, chemo-, baro-, osmo-, and thermoreceptors etc.

SET POINT

ERROR SIGNAL

EFFECTOR

CONTROLLED VARIABLE (SEE NEXT SLIDE)

Important variable maintained within a normal range Marc Imhotep Cray, M.D.

+

-

Negative feedback: Initiation of responses that counter deviations of controlled variables from their normal range

NEGATIVE FEEDBACK Effector opposes stimulus

Redrawn after: Kibble JD, Halsey CR, Homeostasis. In: Medical Physiology -The Big Picture; McGraw-Hill , 2009; 2.

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Examples of Physiologic Controlled Variables & Set Points Controlled Variable (Arterial Blood Sample)

Arterial O2 partial pressure Arterial CO2 partial pressure Arterial blood pH Glucose Core body temperature Serum Na+ Serum K+ Serum Ca2+ Mean arterial blood pressure Glomerular filtration rate

Typical Set Point Value 100 mm Hg 40 mm Hg pH 7.4 90 mg/dL (5 mM) 98.4°F (37°C) 140 mEq/L 4.0 mEq/L 4.5 mEq/L 90 mm Hg 120 mL /min

Adopted from: Kibble JD, Halsey CR, Homeostasis: In Medical Physiology :The Big Picture. New York, NY: McGraw-Hill , 2009; 3. Marc Imhotep Cray, M.D.

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Important Negative Feedback Control Systems

Modified from Carroll RG. Elsevier’s Integrated Physiology. Mosby, Inc. 2007; Table 1-3, Pg. 5.

Marc Imhotep Cray, M.D.

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Example: Baroreceptor Reflex control of blood pressure COMPARATOR SENSOR stretch receptors in Aortic arch and Carotid sinus

SET POINT

N 95 mm Hg

+

EFFECTOR

ERROR SIGNAL

cardiac contractility, vascular tone, urinary fluid excretion

CNS|

Medulla Oblongata

Mean Arterial Blood Pressure (MAP)

-

NEGATIVE FEEDBACK

Receptors: • Aortic arch transmits via vagus nerve to solitary nucleus of medulla (responds only to BP) • Carotid sinus transmits via glossopharyngeal nerve to solitary nucleus of medulla (responds to and in BP) Marc Imhotep Cray, M.D.

See Baroreflex pdf

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Baroreceptors & Chemoreceptors Baroreceptors: • Hypotension-

arterial pressure stretch afferent baroreceptor firing efferent sympathetic firing and efferent parasympathetic stimulation vasoconstriction, HR, contractility BP important in response to severe hemorrhage • Carotid massage - pressure on carotid artery stretch afferent baroreceptor firing HR Can by tried for Tachycardia (SVT) • Contributes to Cushing reaction (triad of hypertension, bradycardia, and respiratory depression) intracranial pressure constricts arterioles cerebral ischemia and reflex sympathetic increase in perfusion pressure ( hypertension) stretch reflex baroreceptor induced-bradycardia

Chemoreceptors:

• Peripheral—carotid and aortic bodies are stimulated by PO2 (< 60 mm Hg), PCO2, and pH of blood • Central—are stimulated by changes in pH and PCO2 of brain interstitial fluid, which in turn are influenced by arterial CO2 Do not directly respond to PO2 Marc Imhotep Cray, M.D.

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Baroreceptors & Chemoreceptors Mechanism Illustrated

Marc Imhotep Cray, M.D.

Le T., Bhushan V. First Aid for the USMLE Step 1 2017. New York, NY: M-H. 2017.

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Mean Arterial Pressure Control and Autonomic & Hormonal Feedback Loops

Katzung & Trevor. Pharmacology Examination & Board Review 10th Ed. New York: ; McGraw-Hill , 2014.

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Organization of Nervous System CENTRAL NERVOUS SYSTEM (CNS)

BRAIN & SPINAL CORD

AFFERENT

EFFERENT

(Sensory)

(Motor)

NERVES

NERVES

EXTEROCEPTORS

INTEROCEPTORS

EFFECTOR ORGANS

SKELETAL MUSCLES

VOLUNTARY Monosynaptic Marc Imhotep Cray, M.D.

PERIPHERAL NERVOUS SYSTEM (PNS)

SOMATIC

AUTONOMIC

SMOOTH MUSCLE, CARDIAC MUSCLES AND GLANDS INVOLUNTARY Pre & Post Ganglionic Fiber


Peripheral Nervous System (PNS) Peripheral nerves contain both motor and sensory neurons Motor neurons: somatic innervate skeletal muscles autonomic innervate smooth muscle, cardiac muscle, and glands (autonomic motor neurons) Sensory neurons are not subdivided into somatic and autonomic b/c there is overlap in function (input can be from either somatic or ANS) e.g., pain receptors can stimulate both somatic (withdrawal reflex) and autonomic reflexes (increased heart rate)

Marc Imhotep Cray, M.D.

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Generic Neuron Anatomy Basic structural unit of nervous system >>> neuron

http://en.wikipedia.org/wiki/Neuron

Marc Imhotep Cray, M.D.

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Autonomic (Visceral) Reflex

“Functional unit of the ANS”  Afferent fibers from periphery to CNS  CNS integration     

Cortex Thalamus Hypothalamus Medulla Spinal cord

Efferent fibers from CNS to periphery

Marc Imhotep Cray, M.D.

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Sympathetic Nervous System Wiring Dorsal root ganglion

Intermediolateral cell column (IML)

Sympathetic trunk Gray ramus White ramus

See: ANS Summary Notes Marc Imhotep Cray, M.D.

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Functional Unit of ANS >> Visceral Reflex Arc Afferent fibers from periphery to CNS CNS integration Spinal cord Medulla Hypothalamus Thalamus Cortex Efferent fibers from CNS to periphery Effector response

Organ receptors ( in viscus ) >>>> sensory (afferent ) neuron >>>>CNS lateral horn cell of spinal cord >>>> motor (efferent) neuron ( two neurons: pre & post ganglionic ) >>>> effector organ (smooth, cardiac muscle or gland)

Marc Imhotep Cray, M.D.

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Neurotransmitters  

Chemicals synthesized and stored in neurons Liberated from axon terminus in response to action potentials Interact with specialized receptors Evoke responses in innervated tissues

See: IVMS Neurotransmitters Notes

Marc Imhotep Cray, M.D.

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ANS Neurotransmitters Class

Chemical

Synthesis

Small molecule Transmitters Acetylcholine

Catecholamines

Dopamine

Norepinephrine

Choline + acetyl CoA, via enzyme Choline Acetyltransferase From the amino acid tyrosine via the enzyme Tyrosine hydroxylase in the catecholamine pathway From dopamine in the catecholamine pathway

Postsynaptic Receptors

Signal Termination

Functions ANS

Nicotinic (cation channel) Muscarinic (G-protein– coupled) D1 (stimulatory G- protein– coupled) D2 (inhibitory G-protein– coupled)

Extracellular hydrolysis by Acetylcholinestrase

Movement control Cognition

Reuptake

ANS Movement control General affect

α & β Adrenergic receptors

Reuptake or breakdown via the enzymes monoamine oxidase and catechol–Omethyltransferase

ANS Alertness General affect

NB: Epinephrine is a catecholamine released upon stimulation of SANS, produced in adrenal medulla. It is a neurohormone, not an ANS neurotransmitter Marc Imhotep Cray, M.D.

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Efferent autonomic nerves general arrangement 

Innervation of smooth muscle, cardiac muscle, and glands    

Preganglionic neuron Peripheral ganglion - axodendritic synapse Postganglionic neuron(s) Effector organ(s)

Post

Pre

Effector organ

Ganglion Marc Imhotep Cray, M.D.

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Anatomic Divisions of ANS 

Parasympathetic (PANS) (CN3,7,9,10) & (S2-S4)   

Sympathetic (SANS) T1-L2/L3   

Preganglionic axons originate in brain, and sacral spinal cord Peripheral ganglia are near, often within* the effector organs Ratio of postganglionic-to-preganglionic axons is small, resulting in discrete responses Preganglionic axons originate in the thoracic and lumbar cord Peripheral ganglia are distant from the effector organs Ratio of post-to-preganglionic axons is large, resulting in widely distributed responses

Enteric Nervous System (ENS) (Discussed in GI) Has been described as a "second brain" for several reasons:

 operate autonomous of SANS & PANS

 Vertebrate studies show when the vagus nerve is severed, ENS continues to function

* Exceptions are the four paired parasympathetic ganglia of head and neck Marc Imhotep Cray, M.D.

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Schematized Anatomic Comparison of PANS & SANS (1) (click to expand)

Marc Imhotep Cray, M.D.

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Schematized Anatomic Comparison of PANS & SANS (2) Effectors: cardiac muscle, smooth mm, vascular endothelium, exocrine glands, and presynaptic nerve terminals Cranial or sacral cord ANS functions:  circulation  digestion  respiration  temperature  sweating  metabolism  some endocrine gland secretions

Thoracic or lumbar cord Marc Imhotep Cray, M.D.

Parasympathetic Post

Pre Ganglion

Effector organ

Sympathetic Pre Ganglion

Post

Effector organ

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Cranial Nerve Parasympathetic Innervations

Marc Imhotep Cray, M.D.

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Somatic Nervous System (included for comparison) 

 

Efferent innervation of skeletal muscle No peripheral ganglia Rapid transmission, discrete control of motor units Striated muscle Voluntary Any spinal segment

Motor neuron

Myelinated with a high conduction velocity

In contrast

Postganglionic neurons of ANS are unmyelinated w a low conduction velocity

Marc Imhotep Cray, M.D.

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Neurochemical Transmission in Peripheral Nervous System (PNS) 

Cholinergic nerves  

Acetylcholine is neurotransmitter Locations of Ach 

Preganglionic neurons to all ganglia

Postganglionic, parasympathetic neurons

“Preganglionic” fibers to adrenal medulla

Postganglionic, sympathetic neurons to sweat glands in most species Somatic motor neurons

Marc Imhotep Cray, M.D.

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Cholinergic Neurotransmission Denotes ACh

Parasympathetic Cranial or sacral cord

Post

Pre Ganglion

Sympathetic Thoracic or lumbar cord Marc Imhotep Cray, M.D.

Pre Ganglion

Effector organ

Denotes ACh

Post

Effector organs

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Adrenergic Neurotransmission 

Adrenergic nerves  

Norepinephrine is the neurotransmitter Locations 

Postganglionic, sympathetic axons

Sympathetic Thoracic or lumbar cord

Pre Ganglion Denotes ACh

Marc Imhotep Cray, M.D.

Denotes Norepinephrine

Post

Effector organs 35


Adrenal Medulla  

Presynaptic nerves are cholinergic Medullary cells (*Chromaffin cells) synthesize and release two, related catecholamines into systemic circulation  

Epinephrine (adrenaline) Norepinephrine

Epi and NE stimulate adrenergic sites

*They release catecholamines: ~80% Epinephrine and ~20% Norepinephrine into systemic circulation for systemic effects on multiple organs (similarly to secretory neurons of the hypothalamus), can also send paracrine signals, hence they are called neuroendocrine cells Marc Imhotep Cray, M.D.

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Adrenal Medulla (2) Adrenal medulla Cholinergic neuron

Epi and NE released into systemic circulation

Denotes ACh

 Chromaffin cells are neuroendocrine cells found in the medulla of the adrenal glands  They are in close proximity to pre-synaptic sympathetic ganglia of sympathetic nervous system, with which they communicate  structurally similar to post-synaptic sympathetic neurons Marc Imhotep Cray, M.D.

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Summary of Actions of SANS & PANS (1) SYMATHETIC

PARASYMPATHETIC

widely distributed responses

discrete responses

Fright-Fight-or-Flight

Rest-Relax-Restoration

 increase in heart rate

 decrease in heart rate

 decrease in gastric motility

 increase in gastric motility

 decrease secretion of salivary and digestive glands

 increase in secretion of salivary and digestive glands

 dilation of pupils

 constriction of pupils

 ejaculation

 penile erection

 vasoconstriction

 contraction of smooth muscle in walls of bladder

 dilation of bronchioles  increased secretion of sweat glands Marc Imhotep Cray, M.D.

Of note: Cannon’s emergency reaction: An immediate sympathetic response to lifethreatening situations with both SANS and PANS overactivity. The PANS phenomenon includes vagal cardiac arrest with involuntary defecation and urination

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Summary of Actions of SANS and PANS (2) (click to expand)

Sympathetic Responses

Parasympathetic Responses

"fight, fright, flight" or fight or flight" system

 heart rate increases  blood pressure increases  blood is shunted from skin & viscera to skeletal muscles  blood glucose increase  bronchioles dilate  pupils dilate

"rest and digest" or "feed and breed" system

 slows heart rate  protects retina from excessive light (near  lowers blood pressure  empties the bowel and bladder  increases gastrointestinal motility  promotes absorption of nutrients

Toy E, Rosenfeld G, Loose D, Briscoe D. CASE 1, Autonomic Sympathetic Nervous System, In Case Files: Pharmacology 2 ed. McGraw-Hill 2008; 16.

Marc Imhotep Cray, M.D.

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ACh Synthesis, Release, and Fate (1)  

Synthesized from choline and acetyl-CoA Released in response to neuronal depolarization (action potential)  Calcium enters the nerve cell  Transmitter vesicles fuse with cell membrane  ACh released by exocytosis Inactivated by acetylcholinesterase (AChE)

Marc Imhotep Cray, M.D.

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ACh Synthesis, Release, and Fate (2)  CHT - Choline transporter  ChAT - Choline acetyl transferase  VAT - Vesicle-associated transporter  VAMPs - Vesicle-associated membrance proteins  SNAP’s - Synaptosomeassociated proteins

Marc Imhotep Cray, M.D.

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Cholinergic Neuron Pharmacology

Marc Imhotep Cray, M.D.

From Le T., Bhushan V. First Aid 2017. New York, NY: M-H. 2017.

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NE Synthesis, Release, and Fate (1) 

Catecholamine - synthesized in a multistep pathway starting with tyrosine as the rate limiting step Released by exocytosis in response to axonal depolarization Duration of activity primarily limited by neuronal reuptake Minor metabolism by synaptic monoamine oxidase (MAO) and catechol-O-methyl transferase (COMT)

Marc Imhotep Cray, M.D.

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NE Synthesis, Release, and Fate (2) VMAT-Vesicular Monoamine transporter

Marc Imhotep Cray, M.D.

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Adrenergic Neuron Pharmacology

Marc Imhotep Cray, M.D.

From Le T., Bhushan V. First Aid 2017. New York, NY: M-H. 2017.

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Receptors* 

Specialized proteins that are binding sites for neurotransmitters and hormones  Postsynaptic cell membranes (neurotransmitters)  Cell nucleus (steroid hormones) Linked to one of many signal transduction mechanisms

“Receptor” (According to Rang & Dale Pharmacology): A target or binding protein for a small molecule (ligand), which acts as an agonist or antagonist. Rang HP, Maureen M. Dale MM, Ritter JM , Flower J Henderson G . Rang & Dale's Pharmacology, 7th ed. Churchill Livingstone; 2011.

*“not to be confuse with other drug targets such as enzymes etc.” Marc Imhotep Cray, M.D.

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Ligand-Receptor Interactions 

Complementary conformations in 3 dimensions 

Physiologic interactions are weak attractions 

Similar to enzyme-substrate interactions H-bonding, van der Waal’s forces

Drug mechanisms  

Agonists - bind and activate receptors Antagonists - bind but DO NOT activate receptors

"Receptor" according to IUPHAR: (International Union of Basic and Clinical Pharmacology)

“A cellular macromolecule, or an assembly of macromolecules, that is concerned directly and specifically in chemical signaling between and within cells. Combination of a hormone, neurotransmitter, drug, or intracellular messenger with its receptor(s) initiates a change in cell function.” See: Basic Receptor Pharmacology/ PDF Marc Imhotep Cray, M.D.

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Steps in Signal Transduction Process See: G-protein Signal Transduction (video animations)

 There are four general classes of signal transducing receptors:  G-proteins are one and are referred to as serpentine receptors

Binding of neurotransmitter, hormone or drug to receptor> signaling of Gprotein> enzyme activation> production of a second-messenger> protein kinase activation > phosphorylation of specific proteins (effect)>termination

See: Raffa RB. Netter's Illustrated Pharmacology,Updated Ed. Philadelphia, PA: Elsevier, 2014; Pgs. 15-17. (offline) Marc Imhotep Cray, M.D.

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GPCR structure & function (simplified) G-Protein Coupled Receptor Binding of NT, hormone or drug to receptor> signaling of Gprotein> enzyme activation> production of a secondmessenger> protein kinase activation >phosphorylation of specific proteins (effect) >termination

Mechanism of cAMP dependent signaling (offline video)

Neurohormone epinephrine and its receptor (pink) is used in tis example: Activated receptor releases the Gs alpha protein (tan) from the beta and gamma subunits (blue and green) in the heterotrimeric G-protein complex. The activated Gs alpha protein in turn activates adenylyl cyclase (purple) that converts ATP into the second messenger cAMP Marc Imhotep Cray, M.D.

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G Protein Messenger Pathways 3 major G-Protein class subtypes: Compose the largest class of *receptors: 1) Gq Messenger Pathway: (used by H1, Alpha 1, V1, M1, M3 Receptors) (HAVM1&3)

Receptor → Gq → Phospholipase C that turns Lipid into PIP2 that is split into IP3 (Increases IC Calcium) and DAG (Activates Protein Kinase C - PKC) 2) Gαs Messenger Pathway: (used by Beta 1, Beta 2, D1, H2, V2 Receptors) (1D2BHV)

Receptor → Gαs → Adenylyl Cyclase (AC) that turns ATP into cAMP that activates Protein Kinase A - PKA 3) Gαi Messenger Pathway: (used by M2, Alpha 2, and D2 Receptors) (2MAD)

Receptor → Gαi that inhibits Adenylyl Cyclase that in turn decreases cAMP , thus making less active Protein Kinase A * Remember there are four major classes of ligand–receptor interactions (more in Pharm.)

Marc Imhotep Cray, M.D.

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G-protein-linked 2nd messenger mechanisms (1) Sympathetic (Adrenergic-Noradrenergic-R) Receptor

G-Protein Class

Major Function

Alpha 1 Receptor - q - Vasoconstriction and Pupillary Dilator Muscle contraction (Mydriasis), and increased Intestinal Sphincters and Bladder Sphincter contraction  Via PLC-IP3-DAG

Alpha 2 Receptor - i - Decreased Sympathetic Outflow, and decreased Insulin release  Via Inhib. AC-cAMP

Beta 1 Receptor - s - Increase Heart Rate, Increase Contractility, Increase Renin release, and increase Lipolysis  Via Stim. AC-cAMP

Beta 2 Receptor - s - Vasodilation, Bronchodilation, Increase Heart Rate, Increase Contractility, Increase Lipolysis, Increase Insulin release, Decrease Uterine Muscle tone  Via Stim. AC-cAMP

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G-protein-linked 2nd messenger mechanisms (2) Parasympathetic (Ach-Cholinergic-R) Receptor

G-Protein Class

Major Function

M1 Receptor - q - found in CNS and Enteric Nervous System M2 Receptor - i - Decrease Heart Rate and Contractility of Atria

M3 Receptor - q - Increase Exocrine Gland secretions (Sweat Gland, Parietal Cells), Increase Gut Peristalsis, Increase Bladder Contraction, Bronchoconstriction, Increase Pupillary Sphincter Muscle Contraction (Miosis), Ciliary Muscle Contraction (Accommodation) N.B. Nicotinic ACh receptors are ligand-gated Na+/K+ channels Offline video

Marc Imhotep Cray, M.D.

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G-protein-linked 2nd messenger mechanisms (3) Receptor

G-Protein Class

Major Function

 Dopamine: D1 Receptor - s - Relax Renal Vascular Smooth Muscle D2 Receptor - i - Modulate Neurotransmitter release (espec. in Brain)

"For sake of completeness"

 Histamine: H1 Receptor - q - Increase Mucus production in Nose and Bronchi, Bronchiole Constriction, Pruritis, Pain H2 Receptor - s - Increase Gastric Acid secretion (Parietal Cells)  Vasopressin: V1 Receptor - q - Increase Vasoconstriction V2 Receptor - s - Increase Water Permeability and Water Reabsorption in Collecting Tubule (V2 in 2 Kidneys)

Marc Imhotep Cray, M.D.

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Cholinergic Receptors  

Activated by ACh and cholinergic drugs Anatomic distribution 

Postganglionic, parasympathetic neuroeffector junctions All autonomic ganglia, whether parasympathetic or sympathetic Somatic neuromuscular junctions

Marc Imhotep Cray, M.D.

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Schematic of Cholinergic Receptor Locations Denotes ACh receptors

Parasympathetic Cranial or sacral cord

Post

Pre Ganglion

Sympathetic

Thoracic or lumbar cord Marc Imhotep Cray, M.D.

Pre Ganglion

Effector organ

Denotes ACh receptors

Post

Effector organs

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Cholinergic Receptor Subtypes 

Muscarinic  Postganglionic, parasympathetic, neuroeffector junctions (M1-M5) Nicotinic  Distinction of two different subtypes  Ganglia - type II or type NG  Neuromuscular junctions - type I or type NM  N.B.-Nicotinic ACh receptors are ligand-gated Na+/K+ channels

Marc Imhotep Cray, M.D.

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Schematic representation of Cholinergic Receptor Subtype Locations Parasympathetic M

N1

Cranial or sacral cord

Post

Pre Ganglion

Effector organ

Sympathetic Thoracic or lumbar cord Marc Imhotep Cray, M.D.

Pre

N1

Ganglion

Post

Effector organ

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Adrenergic Receptors  

Activated by NE, Epi, and adrenergic drugs Anatomic distribution 

Postganglionic, sympathetic, neuroeffector junctions

Subtypes 

Alpha-1, 2; Beta-1, 2, 3

Marc Imhotep Cray, M.D.

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Schematic representation of Adrenergic Receptor Locations

Alpha or Beta adrenergic receptors

Sympathetic Thoracic or lumbar cord

Pre Ganglion paravertebral , prevertebral or lateral

Marc Imhotep Cray, M.D.

Post

Effector organs

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Functional Significance of ANS (1) “Organ system integration & Dual innervation”

Organ system integration  Parasympathetic  

Discrete innervation Energy conservation

Sympathetic   

Marc Imhotep Cray, M.D.

Highly distributed innervation, global responses Energy expenditure Fight or flight responses 60


Functional Significance of ANS (2) Dual innervation 

Organ responses moderated by both parasympathetic and sympathetic influences Parasympathetic dominant at rest 

Predominate tone

Balance of opposing neurologic influences determines physiologic responses

Marc Imhotep Cray, M.D.

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Alpha-1 Adrenergic Receptor 

 

Vascular smooth muscle contraction  Arterioles, veins  Increased arterial resistance  Decreased venous capacitance Agonists support systemic blood pressure  Increased resistance  Redistribution of blood toward heart, increased cardiac output Antagonists decrease blood pressure Iris  Pupillary dilation (mydriasis)

Marc Imhotep Cray, M.D.

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Alpha-2 Adrenergic Receptor 

postsynaptic α2-adrenoceptors (located in bld vessels) cause constriction Modulation of NE release  Presynaptic receptors on axon terminus Spinal alpha-2 receptors mediate analgesia  Agonists used clinically as epidural and spinal analgesics Sedation

Marc Imhotep Cray, M.D.

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Beta-1 Adrenergic Receptor  

To myocardium (renal-renin and fat cell also) Agonists  Increase HR, contractility, and impulse conduction speed  May be arrhythmogenic Antagonists  Decrease HR, contractility, and impulse conduction speed  Used clinically as antiarrhythmics

Marc Imhotep Cray, M.D.

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Beta-2 Adrenergic Receptor 

Vascular smooth muscle in skeletal muscle 

Agonists evoke active vasodilation, increased blood flow

Bronchial smooth muscle 

Agonists evoke bronchodilation, decreased airway resistance

Marc Imhotep Cray, M.D.

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Muscarinic Cholinergic Receptor (mAChR) 

Myocardium  Agonists decrease HR, contractility and AV conduction velocity  Antagonists used clinically to increase HR & facilitate AV conduction such as in heart block Iris sphincter muscle  Agonists evoke pupillary constriction (miosis)  Antagonists evoke mydriasis Gastrointestinal tract  Agonists increase peristalsis and relax sphincter Urinary bladder  Agonists evoke urination  Detrusor muscle (bladder) contraction  Trigone (sphincter) relaxation

Marc Imhotep Cray, M.D.

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Effect of ANS on Organ Systems (1) Sympathetic (NE) Receptor Îą1

Function Constriction of smooth muscles

Distribution Blood vessels and piloerectors in skin (vasoconstriction and goose bumps) Sphincters (bladder, gastrointestinal [GI])

Îą2

Inhibition of sympathetic autonomic ganglia (decreases SANS)

Marc Imhotep Cray, M.D.

Uterus and prostate (contraction) Eye (contraction of the radial muscle = pupillary dilation/mydriasis) Presynaptic ganglionic neurons GI tract (less important pharmacologically)

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Effect of ANS on Organ Systems (2) Sympathetic (NE) Receptor β1

Function

Distribution|Organ

Increase cardiac performance Heart-most important (increased and liberation of energy chronotropy, inotropy, dromotropy) Fat cells (release fat for energy via lipolysis) Kidney (release renin to conserve water)

β2

Relaxation of smooth muscles Lungs (bronchodilation) and liberation of energy Blood vessels in muscles (vasodilation) Uterus (uterine relaxation) GI (intestinal relaxation) Bladder (bladder relaxation) Liver (to liberate glucose via glycogenolysis)

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Effect of ANS on Organ Systems (3) Parasympathetic (Ach) Receptor

Function

N (Nicotinic)

"Nerve to nerve" & SANS & PANS ganglia "nerve to muscle" Neuromuscular junction (NMJ) communication To oppose most Lung (bronchoconstriction) sympathetic actions Heart (slower rate, decreased conduction, decreased at the level of the contractility) organs Sphincters of GI and bladder (relax)

M (Muscarinic)

Distribution|Organ

Bladder (constriction) GI (intestinal contraction) Eye (contraction of the circular muscle = pupillary constriction or miosis) Eye (contraction of the ciliary muscle = focus for near vision) Marc Imhotep Cray, M.D.


Acetylcholine receptors Nicotinic ACh receptors are ligand-gated Na+/K+ channels Two subtypes: NN (found in autonomic ganglia, adrenal medulla) and NM (found in NMJ of skeletal muscle) Muscarinic ACh receptors are G-protein–coupled receptors that usually act through 2nd messengers Five subtypes: M1–5 found in heart, smooth muscle, brain, exocrine glands, and on sweat glands (cholinergic sympathetic)

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Exception Sympathetic innervation of adrenal medulla is direct from spinal cord and uses ACh as neurotransmitter Adrenal gland functions as a special form of ganglion that secretes Epi & NE in a 4 to 1 ratio directly into the bloodstream Sympathetic postganglionic neurons that innervate renal vascular smooth muscle release dopamine rather than norepinephrine Important note: There is no parasympathetic fiber innervation of blood vessels, but bld vessels do have muscarinic receptors For example, in coronary arteries stimulation M3 receptors cause release of NO which result in vasodilation Sweat glands are innervated by sympathetic nerves, but paradoxically use mAChR Sexual arousal is parasympathetic, but orgasm is sympathetic Marc Imhotep Cray, M.D.

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Autonomic and Somatic NS Pharmacology Terminology 

Many drugs evoke effects by interacting with receptors  Affinity  Efficacy or (synonym) Intrinsic activity Agonists  Mimic physiologic activation  Have both high affinity and efficacy Antagonists  Block actions of neurotransmitters or agonists  Have high affinity, but no efficacy  Often used as pharmacologic reversal agents

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Signaling Mechanisms and Pharmacology of ANS Receptor Subtypes- SANS AdrenergicReceptor Type

Physiologic Agonist

Signaling Mechanism

Pharmacologic Agonist

Pharmacologic Antagonist

α1

Norepi ≥ Epi

IP3/DAG/Ca2+

Phenylephrine

Prazosin

α2

Norepi ≥ Epi

↓ [cAMP]

Clonidine, methyldopa

Yohimbine

β1

Epi > Norepi

↑ [cAMP]

Dobutamine (β1 > β2), isoproterenol (β1 = β2)

Metoprolol

β2

Epi > Norepi

↑ [cAMP]

Albuterol, isoproterenol (β1 = β2)

Propranolol (nonselective β1 and β2)

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Signaling Mechanisms and Pharmacology of ANS Receptor Subtypes- PANS CholinergicReceptor Type

Physiologic Agonist

Signaling Mechanism

Pharmacologic Agonist

Pharmacologic Antagonist

N1=NM

Acetylcholine

Ionotropic receptor

Nicotine

D-Tubocurarine

N2=NG

Acetylcholine

Ionotropic receptor

Nicotine

Hexamethonium, mecamylamine

M1–5

Acetylcholine

Various

Marc Imhotep Cray, M.D.

Bethanechol, methacholine, pilocarpine

Atropine, benztropine, ipratropium

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PNS summary schematic

Le T., Bhushan V. First Aid for the USMLE Step 1 2017. New York, NY: M-H. 2017.

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Summary: Take Home Points (1)  ANS functions involve a variety of effector tissues, including: cardiac muscle, smooth mm, vascular endothelium, exocrine glands, and presynaptic nerve terminals  To understand ANS function , and by extension how to pharmacologically manipulate ANS, you will need understand how two divisions of ANS coexist and function, how each subdivision exerts its effects, and finally what physiologic and pharmacologic mechanisms exist to increase or decrease each subdivision’s activity

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Summary: Take Home Points (2) ďƒ˜ By using drugs that mimic or block actions of chemical transmitters and / or their receptor mechanisms, we can selectively modify autonomic functions ďƒ˜ Autonomic drugs are useful in many clinical conditions, however a large number of drugs used for other clinical purposes have unwanted effects on autonomic function; and because of ubiquitous nature of ANS, autonomic drugs are frequently non-selective and thus can be assoc. w side effects

Bottom line| memorization of receptors, their distribution, signal transduction mechanisms and their effects is mandatory and will enable you to accurately predict effects, side effects, potential toxicities and interactions of ANS drugs

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THE END

See next slide for further study tools. Marc Imhotep Cray, M.D.

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Further study: Companion notes ANS Summary Notes Articles Laurie Kelly McCorry. Physiology of the Autonomic Nervous System Am J Pharm Educ. 2007 August 15; 71(4): 78. Goldstein DS, Robertson D, Straus SE, et al. Dysautonomias: clinical disorders of the autonomic nervous system. Ann Intern Med 2002;137(9):753–63.

Cannon, WB, Organization for Physiological Homeostasis. PDF Physiological Rev July 1, 1929 9:399-431 PowerPoint Presentation: Cray MI. Walter Cannon, Homeostasis and the Physiological Response to Stress. A Web Interactive PowerPoint Presentation , 2014

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