FUNCTION
Organization and Integration
The sympathetic system, in response to internal or external challenges,
acts to increase heart rate, blood pressure, and cardiac output; to dilate the bronchial
tree; and to shunt blood away from the intestines and other viscera to voluntary
muscles. Teleologically, the body is then better prepared to deal with the challenge.
Parasympathetic nervous input acts primarily to conserve energy and
TABLE 16-1 -- Responses elicited in effector organs by stimulation of sympathetic and parasympathetic
nerves
Effector Organ |
Adrenergic Response |
Receptor Involved |
Cholinergic Response |
Dominant Response (A or C) |
Heart |
|
|
|
|
Rate of contraction |
Increase |
β1
|
Decrease |
C |
Force of contraction |
Increase |
β1
|
Decrease |
C |
Blood vessels |
|
|
|
|
Arteries (most) |
Vasoconstriction |
α1
|
|
A |
Skeletal muscle |
Vasodilation |
β2
|
|
A |
Veins |
Vasoconstriction |
α2
|
|
A |
Bronchial tree |
Bronchodilation |
β2
|
Bronchoconstriction |
C |
Splenic capsule |
Contraction |
α1
|
|
A |
Uterus |
Contraction |
α1
|
Variable |
A |
Vas deferens |
Contraction |
α1
|
|
A |
Prostatic capsule |
Contraction |
α1
|
|
A |
Gastrointestinal tract |
Relaxation |
α2
|
Contraction |
C |
Eye |
|
|
|
|
Radial muscle, iris |
Contraction (mydriasis) |
α1
|
|
A |
Circular muscle, iris |
|
|
Contraction (miosis) |
C |
Ciliary muscle |
Relaxation |
β |
Contraction (accommodation) |
C |
Kidney |
Renin secretion |
β1
|
|
A |
Urinary bladder |
|
|
|
|
Detrusor |
Relaxation |
β |
Contraction |
C |
Trigone and sphincter |
Contraction |
α1
|
Relaxation |
A, C |
Ureter |
Contraction |
α1
|
Relaxation |
A |
Insulin release from pancreas |
Decrease |
α2
|
|
A |
Fat cells |
Lipolysis |
β1
|
|
A |
Liver glycogenolysis |
Increase |
α1
|
|
A |
Hair follicles, smooth muscle |
Contraction (piloerection) |
α1
|
|
A |
Nasal secretion |
|
|
Increase |
C |
Salivary glands |
Increase secretion |
α1
|
Increase secretion |
C |
Sweat glands |
Increase secretion |
α1
|
Increase secretion |
C |
A, adrenergic; C, cholinergic. |
From Ruffolo R: Physiology and biochemistry of the
peripheral autonomic nervous system. In Wingard
L, Brody T, Larner J, et al (eds): Human Pharmacology: Molecular to Clinical.
St. Louis, Mosby-Year Book, 1991, p. 77. |
maintain organ function and to support the vegetative processes.
Most organs of the body exhibit dual innervation, with input from
the sympathetic and parasympathetic systems frequently mediating opposing effects
[22]
( Table
16-1
). Stimulation of one system may have an excitatory effect on the
end organ, whereas stimulation of the other system may have an inhibitory effect.
The eye, heart, bronchial tree, and gastrointestinal and genitourinary systems are
innervated. For example, sympathetic stimulation acts on the heart to increase rate
and vigor of contraction and to enhance conduction through the atrioventricular node,
whereas parasympathetic stimulation acts to decrease rate and contractility and to
slow conduction through the atrioventricular node. One of the two systems normally
dominates the organ's function, providing its "resting tone" ( Table
16-2
). In a few organs, the sympathetic system alone provides innervation;
certain blood vessels, the spleen, and piloerector muscles are examples.
To predict the effects of drugs, the interaction of the sympathetic
and parasympathetic system in different organs must be understood. Blockade of sympathetic
function unmasks preexisting parasympathetic activity, and the converse relation
also is true. For example, administration of atropine blocks the resting muscarinic
tone of the parasympathetically dominated heart, and unopposed sympathetic tone then
causes tachycardia. Autonomic denervation, which may occur with neuraxial anesthesia,
diabetes, and myocardial infarction (MI), can be assessed by traditional methods,
such as orthostatic hypotension, or by changes in the time interval between successive
heart beats (i.e., beat-to-beat or heart rate variability) as a measure of sympathovagal
balance.[23]