Cholinergic System: Acetylcholine – Neurotransmitter for ganglionic synapse between preganglionic and postganglionic fibers of both the sympathetic and parasympathetic NS’s. Neurotransmitter at the junction between the parasympathetic postganglionic fiber and the effecter cells Adrenergic system: Norepinephrine – Neurotransmitter between the sympathetic postganglionic fiber and the effector cell. Fibers that release norepinephrine and called adrenergic fibers. Stimulation of sympathetic and parasympathetic fibers stimulate certain organs and inhibit others. Divisions of ANS A. Parasympathetic a. Concerned with vegetative functions i. Less kinetic ii. Concerned with conservation and restoration of function b. Cholinergic nervous systems i. Acetylcholine is chemical mediator ii. Cholinergic nerves 1. Nerves releasing acetylcholine at their receptor terminal c. Acetylcholinesterase i. After chemical mediator transmits stimulus to receptor it is then broken down (metabolized) by enzyme ii. Acetylcholine – acetylcholinesterase d. Epinephrine and norepinephrine (sympathetic NS) i. Metabolized in liver or bowel ii. Amine oxidase e. Vagus nerve is primary mode of parasympathetic transmission i. 80% f. stimulation i. Slower cardiac rate ii. Decrease stroke volume iii. Decrease cardiac output (HR X SV = CO) iv. Decrease blood pressure v. Increase peristalsis and digestion KEYPOINT: adverse effects of vagus nerve is decreased HR, SV, and CO. g. Dominant nervous system of cardiac muscle h. Two portions or receptors i. Muscarinic – involved with organs innervated by 10th cranial nerve 1. Stimulation lower HR and BP ii. Nicotinic 1. Motor nerves to skeletal muscles 2. Muscle relaxants act on these receptors B. Sympathetic a. Fight or flight syndrome i. Protect integrity ii. Maintains safety of organism b. Prepares body to respond to stress c. Adrenergic nervous system i. Nerves whose impulses act through release of catecholamine ii. Chemical mediators 1. Epinephrine 2. Norepinephrine 3. Produced by medulla of adrenal glands iii. Stimulation 1. Increase cardiac rate 2. Increase stroke volume 3. Increase cardiac output 4. Aids O2 demands of tissues C. Response a. Sympathetic and parasympathetic are antagonist to each other b. Action maintains a constant tone D. Medications can act in four ways upon ANS a. Stimulate sympathetic nervous system i. Sympathomimetic b. Inhibit sympathetic nervous system i. Sympatholytic c. Stimulate parasympathetic i. Parasympathomimetic d. Inhibit parasympathetic i. Parasympatholytic E. Receptors sites of sympathetic nervous system a. Alpha adrenergic receptors i. Alpha 1 and 2 receptors ii. Located in vascular smooth muscle and skeletal muscle iii. Stimulation 1. Contraction of vascular smooth muscle 2. Vasoconstriction 3. Increase SVR 4. Increase BP 5. Little or no bronchoconstriction Alpha 1 primary neurotransmitter is norepinephrine (Levifed) 6. Alpha 2 inhibits the release of norepinephrine from adrenal gland b. Beta adrenergic receptors i. Beta 1 1. Located in myocardial muscle and electrical cells 2. Increase cardiac rate; increase stroke volume or contraction 3. Increase automaticity 4. Increase conductivity 5. Increase cardiac output 6. Increase myocardial O2 requirements 7. Main drug = Epinephrine ii. Beta 2 1. Located bronchial smooth muscle 2. Located skeletal vascular muscle 3. Relaxes bronchial smooth muscle resulting in bronchodilation 4. Relaxes vascular smooth muscle; decreases PVR 5. Mechanism of bronchodilation a. Smooth muscle cells of tracheobronchial tree contain intracellular enzyme C-AMP b. Increase levels of C-AMP cause chemical reaction relaxing bronchial musculative c. Bronchodilation results d. Decrease levels of C-AMP result bronchoconstriction e. Bronchodilators cause increase in C-AMP i. Increased production – catecholamines – bronchodilation ii. Decreased breakdown – methylronthines – bronchodilation iii. Cyclic 3,5 AMP bronchodilation mecanism 1. Cathecholimines (sympathminetrics) stimulate Beta 2 receptors 2. Beta 2 receptors releases adenylcyclase 3. ATP to C3,5 AMP = bronchodilation 4. Phosphodiesterase breaks down C3,5 AMP c. Dopaminergic i. Located coronary blood vessels ii. Located in renal and mesenteric blood vessels iii. Stimulation causes dilation iv. Dopamine F. Alpha and beta drug agents a. Knowledge of whether a sympathetic drug is an alpha or beta agent one can predict its physiological affects i. Cardiac effects ii. Arterial effects iii. Lung effects b. Medication examples i. Isoproterenol 1. Pure beta agent 2. Stimulates hearts 3. Dilates bronchi 4. Dilates arteries ii. Phenylephrine (Neo-Synephrine) 1. Pure alpha 2. No cardiac stimulation 3. Little or no bronchoconstriction 4. Vasoconstriction iii. Epinephrine 1. Combination alpha and beta 2. Predominately beta 3. High dose alpha effects iv. Norepinephrine 1. Predominantly alpha v. Dopamine (Intropin) 1. Low dose dopaminergic 2. Middle beta 3. High alpha vi. Metaraminol (anamine) 1. Pedominately alpha vii. Metaprotarenol (alupent) 1. Beta c. Sympathetic blockers i. Block sympathetic agents by beating them and occupying receptor sites 1. Inderal a. Sympathetic beta blocker (sympatholytic) b. Opposes beta effects c. Slow heartrate d. Prevents vasodilation and bronchodilation 2. Atropine a. Parasympathetic blocker (parasympatholytic) b. Accelerates heart rate ii. Indication of stimulating or blocking agents 1. Epinephrine 2. Norepinephrine 3. Isuprel 4. Dopamine Thanks to Michael Vance for this document!