Relevant bibliographies by topics / NLX-204

Contents

  1. Journal articles

Academic literature on the topic 'NLX-204'

Author: Grafiati
Published: 24 April 2022
Last updated: 30 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'NLX-204.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "NLX-204"

1

Gruca, P., E. Litwa, M. Lason, A. Newman-Tancredi, R. Depoortère, and M. Papp. "Ketamine and the 5-HT1A receptor biased agonists, NLX-204 and NLX-101, share common cortical efficacious rapid acting antidepressant mechanisms in rat cms depression model." Neuroscience Applied 2 (2023): 102777. http://dx.doi.org/10.1016/j.nsa.2023.102777.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Papp, Mariusz, Piotr Gruca, Magdalena Lason, Ewa Litwa, Adrian Newman-Tancredi, and Ronan Depoortère. "The 5-HT1A receptor biased agonists, NLX-204 and NLX-101, display ketamine-like RAAD and anti-TRD activities in rat CMS models." Psychopharmacology, June 13, 2023. http://dx.doi.org/10.1007/s00213-023-06389-5.

Full text
Abstract:
Abstract Objectives NLX-101 and NLX-204 are highly selective serotonin 5-HT1A ‘biased’ agonists, displaying potent and efficacious antidepressant-like activity upon acute administration in models such as the forced swim test. Methods we compared the effects of repeated administration of NLX-101, NLX-204 and ketamine in the chronic mild stress (CMS) model of depression, considered to have high translational potential, on sucrose consumption (anhedonia measure), novel object recognition (NOR; working memory measure) and elevated plus maze (EPM; anxiety measure) in male Wistar and Wistar-Kyoto ra
APA, Harvard, Vancouver, ISO, and other styles
3

Papp, Mariusz, Piotr Gruca, Ewa Litwa, Magdalena Lason, Adrian Newman-Tancredi, and Ronan Depoortère. "The 5-HT1A receptor biased agonists, NLX-204 and NLX-101, like ketamine, elicit rapid-acting antidepressant activity in the rat chronic mild stress model via cortical mechanisms." Journal of Psychopharmacology, June 2, 2024. http://dx.doi.org/10.1177/02698811241254832.

Full text
Abstract:
Background: The highly selective 5-HT1A serotonin receptor “biased” agonists NLX-101 and NLX-204 display, like ketamine, potent and efficacious rapid-acting antidepressant (RAAD) activity in the rat chronic mild stress (CMS) model with systemic (i.p.) administration. They rapidly (within 1 day) reverse anhedonia (i.e., CMS-induced sucrose consumption deficit), attenuate working memory deficit (novel object recognition: NOR), and decrease anxiety behavior in the elevated-plus maze (EPM). Aims: Here, we sought to explore the contribution of prefrontal cortex (PFC) 5-HT1A receptor activation in t
APA, Harvard, Vancouver, ISO, and other styles
4

Richin, Violette, Marco Valdebenito, Caroline Bouillot, et al. "Multimodal Neuroimaging for the PK/PD Profile of NLX-204: A Biased 5-HT1A Receptor Agonist." ACS Chemical Neuroscience, June 30, 2025. https://doi.org/10.1021/acschemneuro.5c00342.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Głuch-Lutwin, Monika, Kinga Sałaciak, Karolina Pytka, et al. "The 5-HT1A receptor biased agonist, NLX-204, shows rapid-acting antidepressant-like properties and neurochemical changes in two mouse models of depression." Behavioural Brain Research, November 2022, 114207. http://dx.doi.org/10.1016/j.bbr.2022.114207.

Full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography