Andurkar, Shridhar V <br/><br/>
Tramadol antinociception is potentiated by clonidine through α₂-adrenergic and I₂-imidazoline but not by endothelin ET(A) receptors in mice.  [electronic resource] 

 -  European journal of pharmacology  May 2012 
 - 109-15 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1879-0712 
<br/><br/><label>Standard No.: </label>10.1016/j.ejphar.2012.03.016  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenergic alpha-2 Receptor Agonists--administration & dosage<br/>Adrenergic alpha-2 Receptor Antagonists--administration & dosage<br/>Analgesics--administration & dosage<br/>Analgesics, Opioid--administration & dosage<br/>Animals<br/>Clonidine--administration & dosage<br/>Dose-Response Relationship, Drug<br/>Drug Synergism<br/>Endothelin A Receptor Antagonists<br/>Imidazoline Receptors--antagonists & inhibitors<br/>Male<br/>Mice<br/>Mice, Inbred Strains<br/>Narcotic Antagonists--pharmacology<br/>Pain Measurement<br/>Random Allocation<br/>Receptor, Endothelin A--metabolism<br/>Receptors, Adrenergic, alpha-2--chemistry<br/>Receptors, Opioid, mu--agonists<br/>Tramadol--administration & dosage