BackChapter 14: The Autonomic Nervous System – Structure, Function, and Regulation
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Autonomic Nervous System (ANS)
Overview of the ANS
The Autonomic Nervous System (ANS) is a division of the peripheral nervous system responsible for regulating involuntary physiological functions. It primarily controls smooth muscle, cardiac muscle, and glands, ensuring optimal support for body activities through subconscious control.
Effectors: Smooth muscle, cardiac muscle, glands
Control: Operates via subconscious mechanisms
Effectors Location: Most effectors are viscera (internal organs)
Organization of the Nervous System
ANS in the Nervous System
The nervous system is divided into the central nervous system (CNS) and peripheral nervous system (PNS). The PNS is further divided into sensory and motor divisions. The motor division includes the somatic nervous system (SNS) and the autonomic nervous system (ANS), which is subdivided into sympathetic and parasympathetic divisions.
Somatic Nervous System (SNS): Controls voluntary movements (skeletal muscle)
Autonomic Nervous System (ANS): Controls involuntary functions (smooth/cardiac muscle, glands)
Sympathetic vs Parasympathetic Divisions
Functional Differences
Sympathetic Division: "Fight or flight" – prepares the body for emergency situations
Parasympathetic Division: "Rest and digest" – conserves energy and maintains routine functions
ANS Versus Somatic Nervous System (SNS)
Key Differences
Effectors: SNS targets skeletal muscle; ANS targets smooth muscle, cardiac muscle, and glands
Efferent Pathways: SNS uses a single, heavily myelinated neuron; ANS uses a two-neuron chain (preganglionic and ganglionic neurons)
Target Organ Responses: SNS always excitatory; ANS can be excitatory or inhibitory depending on neurotransmitter and receptor
Effectors
SNS Effectors: Skeletal muscles
ANS Effectors: Cardiac muscle, smooth muscle, glands
Functional Role: Sympathetic division activates the organism; parasympathetic division restores normalcy
Efferent Pathways
SNS: Single, heavily myelinated axon from CNS to effector
ANS: Two-neuron chain:
Preganglionic neuron: Lightly myelinated
Ganglionic neuron: Unmyelinated, extends to effector organ
Comparison of Somatic and Autonomic Systems
System | Neurotransmitter | Effector Organs | Pathway |
|---|---|---|---|
Somatic | Acetylcholine (ACh) | Skeletal muscle | Single neuron, heavily myelinated |
Autonomic – Sympathetic | ACh (preganglionic), NE/EPI (postganglionic) | Smooth muscle, glands, cardiac muscle | Two-neuron chain |
Autonomic – Parasympathetic | ACh (both pre- and postganglionic) | Smooth muscle, glands, cardiac muscle | Two-neuron chain |
Neurotransmitter Effects
SNS: All motor neurons release ACh (always excitatory)
ANS:
Preganglionic fibers: Release ACh
Postganglionic fibers: Release NE or ACh (effect can be stimulatory or inhibitory)
Effect depends on neurotransmitter and receptor type
Divisions of the ANS: Functions
Sympathetic: Mobilizes body during extreme situations (fight, flight, fright, sex)
Parasympathetic: Maintains body functions and conserves energy (rest and digest)
The two divisions counterbalance each other
Role of the Parasympathetic Division
Maintains low energy use
Involves "D" activities: digestion, defecation, diuresis
Illustrated by relaxation after a meal: low blood pressure, heart rate, and respiratory rate; high GI activity; warm skin; constricted pupils
Role of the Sympathetic Division
"Fight-or-flight" system
Involves "E" activities: exercise, excitement, emergency, embarrassment
Promotes increased blood flow to muscles, increased heart rate, rapid breathing, cold/sweaty skin, dilated pupils
Anatomy of the ANS
Division | Origin of Fibers | Length of Fibers | Location of Ganglia |
|---|---|---|---|
Sympathetic | Thoracolumbar region of spinal cord | Short preganglionic, long postganglionic | Close to spinal cord |
Parasympathetic | Brain and sacral spinal cord (craniosacral) | Long preganglionic, short postganglionic | In visceral effector organs |
Parasympathetic Division Outflow
Cranial Nerve | Ganglion | Effector Organ(s) |
|---|---|---|
Oculomotor (III) | Ciliary | Eye |
Facial (VII) | Pterygopalatine, Submandibular | Salivary, nasal, lacrimal glands |
Glossopharyngeal (IX) | Otic | Parotid salivary glands |
Vagus (X) | Located within walls of target organs | Heart, lungs, most visceral organs |
S2–S4 (sacral) | Located within walls of target organs | Large intestine, urinary bladder, ureters, reproductive organs |
Sympathetic Trunks and Pathways
Preganglionic fibers may:
Synapse with ganglionic neuron in the same ganglion
Ascend/descend the sympathetic chain to another ganglion
Pass through the chain ganglion and emerge without synapsing
Adrenal Medulla Pathway
Thoracic splanchnic nerve fibers pass directly to the adrenal medulla
Stimulation causes secretion of norepinephrine (NE) and epinephrine (EPI) into the blood
Referred Pain
Pain from viscera perceived as somatic in origin
Occurs because visceral pain afferents travel along the same pathways as somatic pain fibers
Neurotransmitters and Receptors
Acetylcholine (ACh) and norepinephrine (NE) are the main ANS neurotransmitters
Cholinergic fibers: Release ACh
Adrenergic fibers: Sympathetic postganglionic axons that release NE
Effects depend on receptor type (can be excitatory or inhibitory)
Cholinergic Receptors
Two types: nicotinic and muscarinic
Named after drugs that mimic ACh (nicotine, muscarine)
Nicotinic Receptors
Found on motor end plates, all ganglionic neurons, adrenal medulla cells
ACh binding is always stimulatory
Muscarinic Receptors
Found on all effector cells stimulated by postganglionic cholinergic fibers
ACh binding can be inhibitory or excitatory, depending on target organ receptor type
Adrenergic Receptors
Two main types: alpha (α) and beta (β), each with subclasses (α1, α2, β1, β2, β3)
NE binding to α receptors is generally stimulatory; to β receptors is generally inhibitory (except β1 in the heart, which is stimulatory)
Effects of Drugs on the ANS
Atropine: Blocks parasympathetic effects (opposes ACh)
Neostigmine: Inhibits acetylcholinesterase, increasing ACh effects (used for myasthenia gravis)
Tricyclic antidepressants: Prolong NE activity
OTC cold/allergy drugs: Stimulate α-adrenergic receptors (vasoconstriction, less mucus)
Beta-blockers: Attach to β1 receptors, reduce heart rate, prevent arrhythmias
Interactions of the Autonomic Divisions
Most visceral organs receive dual innervation (sympathetic and parasympathetic)
Dynamic antagonism allows precise control of visceral activity
Sympathetic: Increases heart/respiratory rates, inhibits digestion/elimination
Parasympathetic: Decreases heart/respiratory rates, allows digestion/waste elimination
Sympathetic Tone
Maintains blood vessel constriction (vasomotor tone)
Increases blood pressure as needed; prompts dilation if pressure must decrease
Alpha-blockers treat hypertension by interfering with vasomotor fibers
Parasympathetic Tone
Slows the heart
Controls normal digestive and urinary system activity
Sympathetic division can override during stress
Drugs blocking parasympathetic responses increase heart rate, block fecal/urinary retention
Cooperative Effects
Seen in control of external genitalia
Parasympathetic: Vasodilation, erection of penis/clitoris
Sympathetic: Ejaculation in males, reflex peristalsis in females
Unique Roles of the Sympathetic Division
Regulates functions not influenced by parasympathetic division (adrenal medulla, sweat glands, arrector pili, kidneys, most blood vessels)
Controls thermoregulation, renin release, metabolic effects
Thermoregulatory Responses to Heat
Heat causes reflex dilation of blood vessels
Elevated body temperature leads to widespread vasodilation and sweating
Cold causes vasoconstriction, retaining blood in vital organs
Release of Renin from the Kidneys
Sympathetic impulses trigger renin release
Renin increases blood pressure
Metabolic Effects
Increases metabolic rate
Raises blood glucose
Mobilizes fat as energy
Stimulates reticular activating system (RAS) for alertness
Localized vs Diffuse Effects
Parasympathetic: Short-lived, localized control
Sympathetic: Long-lasting, diffuse effects (due to slower NE inactivation, second-messenger systems, and adrenal medulla hormone release)
Levels of ANS Control
Hypothalamus: Main integration center for ANS activity
Receives input from limbic system, cerebral cortex, reticular formation, and spinal cord
Controls heart activity, blood pressure, body temperature, water balance, endocrine activity, emotional states, biological drives, and fear responses