histamine and enkephalin, ala(2)-mephe(4)-gly(5)-

histamine has been researched along with enkephalin, ala(2)-mephe(4)-gly(5)- in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's1 (20.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Itoh, Y; Nishibori, M; Oishi, R; Saeki, K1
Chikai, T; Oishi, R; Saeki, K1
Edwards, T; Ko, MC; Lee, H; Naughton, NN; Song, MS1
Barr, T; de Esch, IJ; Hough, LB; Janssen, E; Kern, B; Nalwalk, JW; Phillips, JG; Shan, Z; Stadel, R; Wentland, MP1
Del Vecchio, G; Massaly, N; Meyer, J; Seitz, V; Stein, C1

Other Studies

5 other study(ies) available for histamine and enkephalin, ala(2)-mephe(4)-gly(5)-

ArticleYear
Involvement of Mu receptors in the opioid-induced increase in the turnover of mouse brain histamine.
    The Journal of pharmacology and experimental therapeutics, 1988, Volume: 244, Issue:3

    Topics: Animals; Brain; Enkephalin, Ala(2)-MePhe(4)-Gly(5)-; Enkephalin, Leucine; Enkephalin, Leucine-2-Alanine; Enkephalins; Histamine; Male; Methylhistamines; Methylhistidines; Mice; Naloxone; Oligopeptides; Receptors, Opioid; Receptors, Opioid, mu; Tetrodotoxin

1988
Increase in the extracellular histamine concentration in the rat striatum by mu-opioid receptor activation.
    Journal of neurochemistry, 1994, Volume: 62, Issue:2

    Topics: Animals; Corpus Striatum; Enkephalin, Ala(2)-MePhe(4)-Gly(5)-; Enkephalins; Extracellular Space; Histamine; Male; Methylhistidines; Morphine; Osmolar Concentration; Rats; Rats, Wistar; Receptors, Opioid, mu

1994
The role of central mu opioid receptors in opioid-induced itch in primates.
    The Journal of pharmacology and experimental therapeutics, 2004, Volume: 310, Issue:1

    Topics: Analgesics, Opioid; Animals; Disease Models, Animal; Enkephalin, Ala(2)-MePhe(4)-Gly(5)-; Histamine; Macaca mulatta; Morphine; Narcotic Antagonists; Narcotics; Pruritus; Receptors, Opioid, mu

2004
CC12, a high-affinity ligand for [3H]cimetidine binding, is an improgan antagonist.
    Neuropharmacology, 2007, Volume: 52, Issue:5

    Topics: Analgesics, Opioid; Animals; Autoradiography; Benzoxazines; Binding Sites; Cimetidine; Dose-Response Relationship, Drug; Enkephalin, Ala(2)-MePhe(4)-Gly(5)-; Guanosine 5'-O-(3-Thiotriphosphate); Histamine; Histamine H2 Antagonists; Imidazoles; Indicators and Reagents; Injections, Intraventricular; Ligands; Male; Membranes; Mice; Morpholines; Naloxone; Naphthalenes; Narcotic Antagonists; Pain Measurement; Rats; Rats, Sprague-Dawley; Receptors, Histamine H2; Sulfides

2007
Modulation of μ-opioid receptor activation by acidic pH is dependent on ligand structure and an ionizable amino acid residue.
    British journal of pharmacology, 2019, Volume: 176, Issue:23

    Topics: Cells, Cultured; Dose-Response Relationship, Drug; Enkephalin, Ala(2)-MePhe(4)-Gly(5)-; Fentanyl; HEK293 Cells; Histamine; Humans; Hydrogen-Ion Concentration; Ligands; Molecular Structure; Mutation; Naloxone; Receptors, Opioid, mu; Signal Transduction; Structure-Activity Relationship

2019