Cardiovascular Pharmacology Concepts

Richard E. Klabunde, Ph.D.


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Clinical Disorders:

Angina

Arrhythmias

Edema

Heart Failure

Systemic Hypertension

Pulmonary Hypertension

Hypotension

Myocardial Infarction


Therapeutic Classes:

Antianginal

Antiarrhythmic

Antihypertensive

Cardioinhibitory

Cardiostimulatory

Diuretic
Pressor

Thrombolytic

Vasoconstrictor

Vasodilator


Mechanism Classes:

Click here to see list

 


Click here for information on Cardiovascular Physiology Concepts, a textbook published by Lippincott Williams & Wilkins (2005)



 


Sympathomimetics

 

General Pharmacology

Sympathomimetic drugs mimic the effects of sympathetic activation on the heart and circulation. Like the sympathetic nerves innervating the heart, sympathomimetics stimulate the heart through activation of beta-adrenoceptors, and sympathomimetics cause vascular smooth muscle contraction and vasoconstriction through activation of alpha-adrenoceptors. Included in the list of sympathomimetic drugs are beta-adrenoceptor agonists and alpha-adrenoceptor agonists. Some sympathomimetics stimulate the release of norepinephrine from sympathetic nerves in addition to their receptor agonist activities.

Therapeutic Use and Rationale

Sympathomimetics are used in conditions where it is appropriate to raise blood pressure by stimulating the heart and inducing vasoconstriction. Because long-term use of sympathomimetics is deleterious (see Side Effects and Contraindications), they are used for short-term treatment of refractory heart failure, cardiogenic shock, and hypotension caused by hemorrhage or sepsis.

Drug Classes and General Mechanisms of Action

Many sympathomimetics are catecholamines or analogs of catecholamines that can be divided into two mechanistic classes: 1) alpha-adrenoceptor agonists (a-agonists), and 2) beta-adrenoceptor agonists (b-agonists). It is not uncommon because of their catecholamine structure for there to be mixed a-agonist and b-agonist properties. A third class of sympathomimetics that affects norepinephrine storage, release and uptake by sympathetic nerves are not used in cardiovascular drug therapy; however, they are used as research tools (e.g., tyramine, guanethidine) and are also used illicitly (e.g., amphetamine, methamphetamine, cocaine).

Click on the mechanistic class below for more details:

Side Effects and Contraindications

Because these drugs mimic sympathetic adrenergic stimulation, they can produce hypertension, excessive cardiac stimulation and cardiac arrhythmias. For these reasons, most of these drugs are only used for short-term cardiovascular therapy with clinical supervision and monitoring. Long-term use increases mortality in heart failure patients. These drugs are contraindicated in patients with coronary artery disease because of the risk of precipitating myocardial ischemia and angina due to decreased myocardial oxygen supply/demand ratio. These drugs can also precipitate myocardial infarction and cerebrovascular stroke.

 

 

Revised 03/15/07


DISCLAIMER: These materials are for educational purposes only, and are not a source of medical decision-making advice.

© 2005-2007  Richard E. Klabunde, all rights reserved.