記事
Inhibitory Effects of a Novel μ-Opioid Receptor Nonpeptide Antagonist, UD-030, on Morphine-Induced Conditioned Place Preference
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CiNii Research
Inhibitory Effects of a Novel μ-Opioid Receptor Nonpeptide Antagonist, UD-030, on Morphine-Induced Conditioned Place Preference
- 資料種別
- 記事
- 著者
- Soichiro Ideほか
- 出版者
- MDPI AG
- 出版年
- 2023-02-08
- 資料形態
- デジタル
- 掲載誌名
- International Journal of Molecular Sciences 24 4
- 掲載ページ
- p.3351-
資料詳細
要約等:
- <jats:p>Although opioids are widely used to treat moderate to severe pain, opioid addiction and the opioid overdose epidemic are becoming more serious...
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デジタル
- 資料種別
- 記事
- 出版年月日等
- 2023-02-08
- 出版年(W3CDTF)
- 2023-02-08
- タイトル(掲載誌)
- International Journal of Molecular Sciences
- 巻号年月日等(掲載誌)
- 24 4
- 掲載巻
- 24
- 掲載号
- 4
- 掲載ページ
- 3351-
- 掲載年月日(W3CDTF)
- 2023-02-08
- 出版事項(掲載誌)
- MDPI AG
- 件名標目
- 対象利用者
- 一般
- 標準番号(その他)
- PMID : 36834763
- DOI
- 10.3390/ijms24043351
- 作成日(W3CDTF)
- 2023-02-08
- オンライン閲覧公開範囲
- インターネット公開
- 著作権情報
- https://creativecommons.org/licenses/by/4.0/
- 参照
- Inhibitory effects of the selective μ‐opioid receptor antagonist <scp>UD</scp>‐030 on methamphetamine‐induced conditioned place preferenceEffects of the novel selective κ-opioid receptor agonist NP-5497-KA on morphine-induced reward-related behaviors
- 参照
- (−)-Pentazocine Induces Visceral Chemical Antinociception, but not Thermal, Mechanical, or Somatic Chemical Antinociception, in μ-Opioid Receptor Knockout MiceOpiate receptor knockout mice define μ receptor roles in endogenous nociceptive responses and morphine-induced analgesiaMu-Opioid receptor biased ligands: A safer and painless discovery of analgesics?Effects of test conditions on the outcome of place conditioning with morphine and naltrexone in miceNaltrexone shortened opioid detoxification with buprenorphineDeveloping a novel treatment for patients with chronic pain and Opioid User DisorderPharmacological Properties of Bivalent Ligands Containing Butorphan Linked to Nalbuphine, Naltrexone, and Naloxone at μ, δ, and κ Opioid ReceptorsIncreased Attributable Risk Related to a Functional μ-Opioid Receptor Gene Polymorphism in Association with Alcohol Dependence in Central SwedenBuprenorphine initiation strategies for opioid use disorder and pain management: A systematic reviewNaltrexone for the Management of Alcohol DependenceNalmefene for the management of alcohol dependence: review on its pharmacology, mechanism of action and meta-analysis on its clinical efficacyAbolished thermal and mechanical antinociception but retained visceral chemical antinociception induced by butorphanol in μ-opioid receptor knockout miceOpiate Aromatic Pharmacophore Structure−Activity Relationships in CTAP Analogues Determined by Topographical Bias, Two-Dimensional NMR, and Biological Activity AssaysChemical Interventions for the Opioid Crisis: Key Advances and Remaining ChallengesDynorphin/Kappa Opioid Receptor Signaling in Preclinical Models of Alcohol, Drug, and Food AddictionSynthesis and opioid receptor binding properties of a highly potent 4-hydroxy analogue of naltrexoneConstitutively Active Mu Opioid Receptors Mediate the Enhanced Conditioned Aversive Effect of Naloxone in Morphine-Dependent MiceGenetic susceptibility of opioid receptor genes polymorphism to drug addiction: A candidate-gene association studyThe Effects of Naltrexone on Subjective Response to Methamphetamine in a Clinical Sample: a Double-Blind, Placebo-Controlled Laboratory StudyMethylnaltrexone for Opioid-Induced Constipation in Advanced IllnessDesign and synthesis of conformationally constrained somatostatin analogs with high potency and specificity for .mu. opioid receptorsExploring the opioid system by gene knockoutBuprenorphine: A Unique Drug with Complex PharmacologyOpioid receptor subtypes: fact or artifact?Attenuation of methamphetamine-induced behavioral sensitization in mice by systemic administration of naltrexoneThe irreversible narcotic antagonistic and reversible agonistic properties of the fumaramate methyl ester derivative of naltrexoneBuprenorphine Antinociception is Abolished, but Naloxone-Sensitive Reward is Retained, in μ-Opioid Receptor Knockout MiceMeasuring reward with the conditioned place preference paradigm: a comprehensive review of drug effects, recent progress and new issuesMethylnaltrexone in the treatment of opioid-induced constipationNovel peptidic mu opioid antagonists: Pharmacologic characterization in vitro and in vivoLinkage disequilibrium and association with methamphetamine dependence/psychosis of mu-opioid receptor gene polymorphisms
- 連携機関・データベース
- 国立情報学研究所 : CiNii Research
- 提供元機関・データベース
- Crossref科学研究費助成事業データベース科学研究費助成事業データベースCrossrefCrossref