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Fully automated head-twitch detection system for the study of 5-HT2A receptor pharmacology in vivo

Mario de la Fuente Revenga, Jong M. Shin, Hiba Z. Vohra, Kelsey S. Hideshima, Matthew Schneck, Justin L. Poklis, Javier González-Maeso

Scientific Reports October 3, 2019 DOI: 10.1038/s41598-019-49913-4 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Mice
Interventions DOI LY341495 LY404039
Topics Serotonin
Keywords Agonist Metabotropic glutamate receptor Metabotropic receptor Pharmacology
Citations 57
Key findings The mGluR2/3 antagonist LY341495 potentiates DOI-induced head-twitch behavior, while the mGluR2/3 agonist LY404039 blocks it.

Abstract

Abstract Head-twitch behavior (HTR) is the behavioral signature of psychedelic drugs upon stimulation of the serotonin 5-HT 2A receptor (5-HT 2A R) in rodents. Following the previous report of a semi-automated detection of HTR based on the dynamics of mouse’s head movement, here we present a system for the identification of individual HTR events in a fully automated fashion. The validity of this fully automated HTR detection system was tested with the psychedelic drug DOI in 5-HT 2A R-KO mice, and via evaluation of potential sources of false-positive and false-negative HTR events. The increased throughput in data processing achieved via automation afforded the possibility of conducting otherwise time consuming HTR time-course studies. To further assess the versatility of our system, we also explored the pharmacological interactions between 5-HT 2A R and the metabotropic glutamate receptor 2 (mGluR2). Our data demonstrate the potentiation effect of the mGluR2/3 antagonist LY341495 on DOI-induced HTR, as well as the HTR-blocking effect of the mGluR2/3 agonist and antipsychotic drug in development LY404039. This fully automated system can contribute to speed up our understanding of 5-HT 2A R’s pharmacology and its characteristic behavioral outputs in rodents.

Comparable studies

Other preclinical and animal studies on serotonin, most cited first.

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