naltrexone and quinine

naltrexone has been researched along with quinine in 19 studies

Research

Studies (19)

TimeframeStudies, this research(%)All Research%
pre-19904 (21.05)18.7374
1990's3 (15.79)18.2507
2000's6 (31.58)29.6817
2010's6 (31.58)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Topliss, JG; Yoshida, F1
Lombardo, F; Obach, RS; Waters, NJ1
Ahlin, G; Artursson, P; Bergström, CA; Gustavsson, L; Karlsson, J; Larsson, R; Matsson, P; Norinder, U; Pedersen, JM1
Fisk, L; Greene, N; Naven, RT; Note, RR; Patel, ML; Pelletier, DJ1
Ekins, S; Williams, AJ; Xu, JJ1
Cantin, LD; Chen, H; Kenna, JG; Noeske, T; Stahl, S; Walker, CL; Warner, DJ1
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K1
Chipkin, RE; Rosecrans, JA1
Frenk, H; Rosen, JB1
Crebolder, J; Maier, S; Parker, LA; Rennie, M1
Cammera, P; Griffiths, W; Swift, RM1
Lynch, MR; Porter, JH; Rosecrans, JA1
Froehlich, JC; Krishnan-Sarin, S; Li, TK; Portoghese, PS1
Leeb, K; Parker, L1
Amit, Z; Babinska, I; Campisi, M; Goodwin, FL1
Coonfield, DL; Ferraro, FM; Hill, KG; Kaczmarek, HJ; Kiefer, SW1
Berridge, KC; Cooper, SJ; Reynolds, SM; Richardson, DK1
Badalia, A; Bodnar, RJ; Duenas, SM; Hossain, M; Rotella, FM; Saeed, S; Sclafani, A; Touzani, K1
Henderson-Redmond, AN; Lowe, TE; Morgan, DJ; Tian, XB1

Reviews

1 review(s) available for naltrexone and quinine

ArticleYear
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
    Drug discovery today, 2016, Volume: 21, Issue:4

    Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Drug Labeling; Humans; Pharmaceutical Preparations; Risk

2016

Other Studies

18 other study(ies) available for naltrexone and quinine

ArticleYear
QSAR model for drug human oral bioavailability.
    Journal of medicinal chemistry, 2000, Jun-29, Volume: 43, Issue:13

    Topics: Administration, Oral; Biological Availability; Humans; Models, Biological; Models, Molecular; Pharmaceutical Preparations; Pharmacokinetics; Structure-Activity Relationship

2000
Trend analysis of a database of intravenous pharmacokinetic parameters in humans for 670 drug compounds.
    Drug metabolism and disposition: the biological fate of chemicals, 2008, Volume: 36, Issue:7

    Topics: Blood Proteins; Half-Life; Humans; Hydrogen Bonding; Infusions, Intravenous; Pharmacokinetics; Protein Binding

2008
Structural requirements for drug inhibition of the liver specific human organic cation transport protein 1.
    Journal of medicinal chemistry, 2008, Oct-09, Volume: 51, Issue:19

    Topics: Cell Line; Computer Simulation; Drug Design; Gene Expression Profiling; Humans; Hydrogen Bonding; Liver; Molecular Weight; Organic Cation Transporter 1; Pharmaceutical Preparations; Predictive Value of Tests; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Structure-Activity Relationship

2008
Developing structure-activity relationships for the prediction of hepatotoxicity.
    Chemical research in toxicology, 2010, Jul-19, Volume: 23, Issue:7

    Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Humans; Structure-Activity Relationship; Tetracyclines; Thiophenes

2010
A predictive ligand-based Bayesian model for human drug-induced liver injury.
    Drug metabolism and disposition: the biological fate of chemicals, 2010, Volume: 38, Issue:12

    Topics: Bayes Theorem; Chemical and Drug Induced Liver Injury; Humans; Ligands

2010
Mitigating the inhibition of human bile salt export pump by drugs: opportunities provided by physicochemical property modulation, in silico modeling, and structural modification.
    Drug metabolism and disposition: the biological fate of chemicals, 2012, Volume: 40, Issue:12

    Topics: Animals; ATP Binding Cassette Transporter, Subfamily B, Member 11; ATP-Binding Cassette Transporters; Bile Acids and Salts; Cell Line; Chemical and Drug Induced Liver Injury; Humans; Quantitative Structure-Activity Relationship

2012
Aversiveness of oral methadone in rats.
    Psychopharmacology, 1978, May-31, Volume: 57, Issue:3

    Topics: Animals; Choice Behavior; Decision Making; Heroin Dependence; Humans; Male; Methadone; Models, Psychological; Naltrexone; Quinine; Rats; Self Administration; Taste; Time Factors

1978
Suppressant effects of naltrexone on water intake in rats.
    Pharmacology, biochemistry, and behavior, 1979, Volume: 11, Issue:4

    Topics: Animals; Body Weight; Depression, Chemical; Drinking Behavior; Female; Naloxone; Naltrexone; Pain; Quinine; Rats; Self Administration; Sensory Thresholds; Time Factors; Water Deprivation

1979
Morphine- and naltrexone-induced modification of palatability: analysis by the taste reactivity test.
    Behavioral neuroscience, 1992, Volume: 106, Issue:6

    Topics: Animals; Arousal; Avoidance Learning; Brain; Dose-Response Relationship, Drug; Male; Morphine; Naltrexone; Quinine; Rats; Receptors, Opioid; Sucrose; Taste; Taste Threshold

1992
False positive urine drug screens from quinine in tonic water.
    Addictive behaviors, 1989, Volume: 14, Issue:2

    Topics: Adult; Alcoholism; Heroin; Heroin Dependence; Humans; Male; Middle Aged; Mineral Waters; Naltrexone; Patient Compliance; Quinine

1989
Latent inhibition in the aversion to oral methadone.
    Pharmacology, biochemistry, and behavior, 1984, Volume: 20, Issue:3

    Topics: Animals; Avoidance Learning; Extinction, Psychological; Female; Male; Methadone; Naltrexone; Quinine; Rats; Rats, Inbred Strains; Time Factors

1984
The delta 2-opioid receptor antagonist naltriben selectively attenuates alcohol intake in rats bred for alcohol preference.
    Pharmacology, biochemistry, and behavior, 1995, Volume: 52, Issue:1

    Topics: Alcohol Deterrents; Alcohol Drinking; Animals; Brain Chemistry; Male; Naltrexone; Quinine; Rats; Rats, Wistar; Receptors, Opioid, delta

1995
Amphetamine-induced modification of quinine palatability: analysis by the taste reactivity test.
    Pharmacology, biochemistry, and behavior, 1994, Volume: 47, Issue:3

    Topics: Animals; Dextroamphetamine; Drinking Behavior; Male; Morphine; Motor Activity; Naltrexone; Pimozide; Quinine; Rats; Rats, Sprague-Dawley; Sucrose; Taste

1994
Effects of naltrexone on the intake of ethanol and flavored solutions in rats.
    Alcohol (Fayetteville, N.Y.), 2001, Volume: 25, Issue:1

    Topics: Alcohol Drinking; Animals; Beverages; Drinking; Drug Combinations; Ethanol; Male; Naltrexone; Narcotic Antagonists; Quinine; Rats; Rats, Long-Evans; Rats, Wistar; Saccharin; Solutions

2001
Naltrexone modifies the palatability of basic tastes and alcohol in outbred male rats.
    Alcohol (Fayetteville, N.Y.), 2002, Volume: 27, Issue:2

    Topics: Alcohol Drinking; Animals; Dose-Response Relationship, Drug; Drinking; Male; Naltrexone; Quinine; Rats; Rats, Long-Evans; Sodium Chloride; Sucrose; Taste

2002
Endogenous opioids are necessary for benzodiazepine palatability enhancement: naltrexone blocks diazepam-induced increase of sucrose-'liking'.
    Pharmacology, biochemistry, and behavior, 2005, Volume: 81, Issue:3

    Topics: Analysis of Variance; Animals; Behavior, Animal; Benzodiazepines; Diazepam; Food Preferences; Male; Naltrexone; Narcotic Antagonists; Opioid Peptides; Quinine; Rats; Rats, Sprague-Dawley; Solutions; Sucrose; Taste; Taste Threshold; Time Factors

2005
Role of NMDA, opioid and dopamine D1 and D2 receptor signaling in the acquisition of a quinine-conditioned flavor avoidance in rats.
    Physiology & behavior, 2014, Apr-10, Volume: 128

    Topics: Animals; Avoidance Learning; Benzazepines; Conditioning, Psychological; Dizocilpine Maleate; Dopamine D2 Receptor Antagonists; Fructose; Male; Naltrexone; Narcotic Antagonists; Quinine; Raclopride; Rats; Rats, Sprague-Dawley; Receptors, Dopamine D1; Receptors, Dopamine D2; Receptors, N-Methyl-D-Aspartate; Saccharin; Signal Transduction; Taste

2014
Increased ethanol drinking in "humanized" mice expressing the mu opioid receptor A118G polymorphism are mediated through sex-specific mechanisms.
    Brain research bulletin, 2018, Volume: 138

    Topics: Alcohol Drinking; Alleles; Analgesics, Non-Narcotic; Analysis of Variance; Animals; Choice Behavior; Conditioning, Operant; Dose-Response Relationship, Drug; Ethanol; Female; Genotype; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mutagenesis, Site-Directed; Naltrexone; Narcotic Antagonists; Polymorphism, Single Nucleotide; Quinine; Receptors, Opioid, mu; Reflex; Reward; Self Administration; Self Stimulation; Sex Characteristics

2018