Anders A Jensen, Claudia R Cecchi, Meghan Hibicke, Astrid H Bach, Erik Kaadt, Emil Märcher-Rørsted, Charles D Nichols, Betina Elfving, Jesper L Kristensen
{"title":"选择性5-羟色胺5‑HT2A受体激动剂(S)‑3-(2,5-二甲氧基-4-(三氟甲基)苯基)哌啶(LPH-5)在啮齿动物中诱导持久和强大的抗抑郁样作用。","authors":"Anders A Jensen, Claudia R Cecchi, Meghan Hibicke, Astrid H Bach, Erik Kaadt, Emil Märcher-Rørsted, Charles D Nichols, Betina Elfving, Jesper L Kristensen","doi":"10.1021/acsptsci.5c00208","DOIUrl":null,"url":null,"abstract":"<p><p>Psychedelics have emerged as a promising treatment for mental health disease, and the therapeutic potential of psilocybin and lysergic acid diethylamide (LSD) is presently being pursued in numerous clinical trials. This has prompted a search for novel agents with more specific pharmacological activities than the rather promiscuous classical psychedelics. Here we present the detailed pharmacological characterization of one such compound, LPH-5 [(<i>S</i>)-3-(2,5-dimethoxy-4-(trifluoromethyl)-phenyl)-piperidine]. LPH-5 was found to be a potent partial agonist at the 5-HT<sub>2A</sub> receptor (5-HT<sub>2A</sub>R) with pronounced selectivity for 5-HT<sub>2A</sub>R over the related 5-HT<sub>2B</sub>R and 5-HT<sub>2C</sub>R in a range of functional assays. LPH-5 dose-dependently induced head-twitch responses (HTR) as well as robust acute and persistent antidepressant-like effects in rats. These results suggest that selective 5-HT<sub>2A</sub>R activation holds antidepressant potential and indicate that this activity component is key for the therapeutics effects of classical psychedelics.</p>","PeriodicalId":36426,"journal":{"name":"ACS Pharmacology and Translational Science","volume":"8 6","pages":"1791-1803"},"PeriodicalIF":4.9000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12171885/pdf/","citationCount":"0","resultStr":"{\"title\":\"The Selective Serotonin 5‑HT<sub>2A</sub> Receptor Agonist (<i>S</i>)‑3-(2,5-Dimethoxy-4-(trifluoromethyl)phenyl)piperidine (LPH-5) Induces Persistent and Robust Antidepressant-Like Effects in Rodents.\",\"authors\":\"Anders A Jensen, Claudia R Cecchi, Meghan Hibicke, Astrid H Bach, Erik Kaadt, Emil Märcher-Rørsted, Charles D Nichols, Betina Elfving, Jesper L Kristensen\",\"doi\":\"10.1021/acsptsci.5c00208\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Psychedelics have emerged as a promising treatment for mental health disease, and the therapeutic potential of psilocybin and lysergic acid diethylamide (LSD) is presently being pursued in numerous clinical trials. This has prompted a search for novel agents with more specific pharmacological activities than the rather promiscuous classical psychedelics. Here we present the detailed pharmacological characterization of one such compound, LPH-5 [(<i>S</i>)-3-(2,5-dimethoxy-4-(trifluoromethyl)-phenyl)-piperidine]. LPH-5 was found to be a potent partial agonist at the 5-HT<sub>2A</sub> receptor (5-HT<sub>2A</sub>R) with pronounced selectivity for 5-HT<sub>2A</sub>R over the related 5-HT<sub>2B</sub>R and 5-HT<sub>2C</sub>R in a range of functional assays. LPH-5 dose-dependently induced head-twitch responses (HTR) as well as robust acute and persistent antidepressant-like effects in rats. These results suggest that selective 5-HT<sub>2A</sub>R activation holds antidepressant potential and indicate that this activity component is key for the therapeutics effects of classical psychedelics.</p>\",\"PeriodicalId\":36426,\"journal\":{\"name\":\"ACS Pharmacology and Translational Science\",\"volume\":\"8 6\",\"pages\":\"1791-1803\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-05-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12171885/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Pharmacology and Translational Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1021/acsptsci.5c00208\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/13 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Pharmacology and Translational Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/acsptsci.5c00208","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/13 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
The Selective Serotonin 5‑HT2A Receptor Agonist (S)‑3-(2,5-Dimethoxy-4-(trifluoromethyl)phenyl)piperidine (LPH-5) Induces Persistent and Robust Antidepressant-Like Effects in Rodents.
Psychedelics have emerged as a promising treatment for mental health disease, and the therapeutic potential of psilocybin and lysergic acid diethylamide (LSD) is presently being pursued in numerous clinical trials. This has prompted a search for novel agents with more specific pharmacological activities than the rather promiscuous classical psychedelics. Here we present the detailed pharmacological characterization of one such compound, LPH-5 [(S)-3-(2,5-dimethoxy-4-(trifluoromethyl)-phenyl)-piperidine]. LPH-5 was found to be a potent partial agonist at the 5-HT2A receptor (5-HT2AR) with pronounced selectivity for 5-HT2AR over the related 5-HT2BR and 5-HT2CR in a range of functional assays. LPH-5 dose-dependently induced head-twitch responses (HTR) as well as robust acute and persistent antidepressant-like effects in rats. These results suggest that selective 5-HT2AR activation holds antidepressant potential and indicate that this activity component is key for the therapeutics effects of classical psychedelics.
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