Related Experiment Video
Updated: Jun 2, 2026

Assessment of Vascular Tone Responsiveness using Isolated Mesenteric Arteries with a Focus on Modulation by Perivascular Adipose Tissues
Published on: June 3, 2019
The physiologic implications of isolated alpha(1) adrenergic stimulation
Robert H Thiele1, Edward C Nemergut, Carl Lynch
1Department of Anesthesiology, University of Virginia Health System, P.O. Box 800710, Charlottesville, VA 22908, USA. rht7w@virginia.edu
Phenylephrine and methoxamine, alpha-1 adrenergic receptor agonists, increase cardiac afterload and decrease cardiac output. These drugs do not improve myocardial energetics despite raising blood pressure.
Area of Science:
- Pharmacology
- Cardiovascular Physiology
Background:
- Phenylephrine and methoxamine are direct-acting alpha-1 adrenergic receptor (AR) agonists.
- Understanding their physiological effects is crucial for clinical applications.
Purpose of the Study:
- To review the physiological effects of phenylephrine and methoxamine, focusing on alpha-1 AR agonism.
- To evaluate their impact on cardiac afterload, cardiac output, and myocardial energetics.
Main Methods:
- Systematic review of 463 articles from PubMed searches and citation tracking.
- Inclusion criteria: human, randomized studies published in English.
- Incorporation of relevant articles from the peer-review process.
Main Results:
- Both agents increase cardiac afterload through increased vascular resistance and decreased compliance.
- Pure alpha-1 agonism increases arterial blood pressure but does not improve myocardial energetics.
- Cardiac output is decreased, likely due to increased venous resistance, despite potential transient increases in venous return.
Conclusions:
- Alpha-1 AR agonists like phenylephrine and methoxamine increase cardiac workload and decrease cardiac output.
- Their net effect on cardiovascular hemodynamics is complex, with potential negative impacts on organ perfusion.
Related Concept Videos
Adrenergic Receptors: ɑ Subtype
Adrenaline ≥ Noradrenaline >> Isoprenaline
α-adrenoceptors are further divided into α1 and α2-adrenoceptors.
α1-Adrenoceptors: These receptors are located postsynaptically on the effector organs and cause constriction of smooth muscle mediated by activation of phospholipase C—inositol-1,4,5-trisphosphate...
Adrenergic Receptors: β Subtype
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors have equal affinities for...
Adrenergic Receptors (Adrenoceptors): Classification
α-Adrenoceptors
α-Adrenoceptors are classified into two main subtypes: α1 and α2. The α1 adrenoceptors, which are found on postsynaptic...
Sympathetic Signaling
Sympathetic preganglionic fibers release the neurotransmitter acetylcholine (ACh) onto the ganglionic neurons in the...
Adrenergic Antagonists: Pharmacological Actions of ɑ-Receptor Blockers
α1-blockers: These drugs inhibit α1-adrenoceptors on smooth muscle cells, resulting in vasodilation. This vasodilation lowers blood pressure, making α1-blockers valuable in treating hypertension. Additionally, α1-blockers effectively address urinary obstruction...
Sympathetic Activation

