naltrexone and n(6)-cyclopentyladenosine

naltrexone has been researched along with n(6)-cyclopentyladenosine in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Borghi, V; Ilona, O; Labuz, D; Maj, M; Pavone, F; Przewlocka, B	1
Dickenson, JM; Fretwell, L	1

Other Studies

2 other study(ies) available for naltrexone and n(6)-cyclopentyladenosine

Article	Year
Formalin-induced pain and mu-opioid receptor density in brain and spinal cord are modulated by A1 and A2a adenosine agonists in mice. Brain research, 2002, Nov-29, Volume: 956, Issue:2 Topics: Adenosine; Animals; Autoradiography; Central Nervous System; Fixatives; Formaldehyde; Male; Mice; Motor Activity; Naltrexone; Narcotic Antagonists; Pain; Periaqueductal Gray; Phenethylamines; Purinergic P1 Receptor Agonists; Receptor, Adenosine A2A; Receptors, Opioid, mu; Receptors, Purinergic P1; Spinal Cord; Thalamus	2002
Role of large-conductance Ca(2+) -activated potassium channels in adenosine A(1) receptor-mediated pharmacological preconditioning in H9c2 cells. European journal of pharmacology, 2009, Sep-15, Volume: 618, Issue:1-3 Topics: Adenosine; Adenosine A1 Receptor Agonists; Animals; Caspase 3; Cell Death; Cell Hypoxia; Cell Line; Enzyme Activation; Extracellular Signal-Regulated MAP Kinases; Gene Expression Regulation; Ion Channel Gating; Ischemic Preconditioning, Myocardial; L-Lactate Dehydrogenase; Large-Conductance Calcium-Activated Potassium Channels; Myoblasts, Cardiac; Naltrexone; Phosphorylation; Protein Subunits; Proto-Oncogene Proteins c-akt; Rats; Receptor, Adenosine A1; Time Factors	2009

Article

Year

Formalin-induced pain and mu-opioid receptor density in brain and spinal cord are modulated by A1 and A2a adenosine agonists in mice.

Brain research, 2002, Nov-29, Volume: 956, Issue:2

Topics: Adenosine; Animals; Autoradiography; Central Nervous System; Fixatives; Formaldehyde; Male; Mice; Motor Activity; Naltrexone; Narcotic Antagonists; Pain; Periaqueductal Gray; Phenethylamines; Purinergic P1 Receptor Agonists; Receptor, Adenosine A2A; Receptors, Opioid, mu; Receptors, Purinergic P1; Spinal Cord; Thalamus

2002

Role of large-conductance Ca(2+) -activated potassium channels in adenosine A(1) receptor-mediated pharmacological preconditioning in H9c2 cells.

European journal of pharmacology, 2009, Sep-15, Volume: 618, Issue:1-3

Topics: Adenosine; Adenosine A1 Receptor Agonists; Animals; Caspase 3; Cell Death; Cell Hypoxia; Cell Line; Enzyme Activation; Extracellular Signal-Regulated MAP Kinases; Gene Expression Regulation; Ion Channel Gating; Ischemic Preconditioning, Myocardial; L-Lactate Dehydrogenase; Large-Conductance Calcium-Activated Potassium Channels; Myoblasts, Cardiac; Naltrexone; Phosphorylation; Protein Subunits; Proto-Oncogene Proteins c-akt; Rats; Receptor, Adenosine A1; Time Factors

2009