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Effects of S 38093, an antagonist/inverse agonist of histamine H3 receptors, in models of neuropathic pain in rats

机译：组胺H3受体拮抗剂/反向激动剂S 38093在大鼠神经性疼痛模型中的作用

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机译：国际观众

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Chaumette T.; Chapuy E.; Berrocoso E.; Llorca-Torralba M.; Bravo L.; Mico A.; Chalus M.; Eschalier A.; Ardid D.; Marchand F.; Sors A.;
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年度 2017
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1. Effects of S 38093, an antagonist/inverse agonist of histamine H3 receptors, in models of neuropathic pain in rats [J] . Chaumette T., Chapuy E., Berrocoso E., European journal of pain : . 2018,第1期

机译：S 38093，组胺H3受体的拮抗剂/逆激动剂，大鼠神经性疼痛模型的影响
2. S 38093, a histamine H3 antagonist/inverse agonist, promotes hippocampal neurogenesis and improves context discrimination task in aged mice [J] . Jean-Philippe Guilloux, Benjamin A. Samuels, Indira Mendez-David, Scientific reports. . 2017,第1期

机译：S 38093，组胺H3拮抗剂/反向激动剂，促进海马神经发生，并改善老年小鼠中的上下文鉴别任务
3. Mechanistic characterization of S 38093, a novel inverse agonist at histamine H3 receptors [J] . Sors Aurore, Panayi Fany, Bert Lionel, European Journal of Pharmacology: An International Journal . 2017,第期

机译：S 38093的机械表征，是组胺H3受体的新型逆激动剂
4. Design and Synthesis of Novel Blfunctional Ligands (Opioid Agonist and Bradykinin Antagonist) for Treatment of Chronic and Neuropathic Pain [C] . Srinivas Deekonda, David Rankin, Peg Davis American Peptide Symposium . 2011

机译：设计与合成新型血官能配体（阿片类激动剂和Bradykinin拮抗剂）治疗慢性和神经性疼痛
5. Cannabinoid 2 receptor (CB2R) agonists modulate neuropathic pain and cytokine expression. [D] . Wilkerson, Jenny L. 2012

机译：大麻素2受体（CB2R）激动剂可调节神经性疼痛和细胞因子的表达。
6. S 38093 a histamine H3 antagonist/inverse agonist promotes hippocampal neurogenesis and improves context discrimination task in aged mice [O] . Jean-Philippe Guilloux, Benjamin A. Samuels, Indira Mendez-David, -1

机译：S 38093一种组胺H3拮抗剂/反向激动剂可促进衰老小鼠的海马神经发生并改善背景识别任务
7. Effects of S 38093, an antagonist/inverse agonist of histamine H3 receptors, in models of neuropathic pain in rats [O] . Chaumette T., Chapuy E., Berrocoso E., 2017

机译：组胺H3受体拮抗剂/反向激动剂S 38093在大鼠神经性疼痛模型中的作用

Effects of S 38093, an antagonist/inverse agonist of histamine H3 receptors, in models of neuropathic pain in rats

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