Literature DB >> 32248747

Characterisation of the pharmacodynamic effects of the P2X7 receptor antagonist JNJ-54175446 using an oral dexamphetamine challenge model in healthy males in a randomised, double-blind, placebo-controlled, multiple ascending dose trial.

Kasper Recourt1,2, Jasper van der Aart1, Gabriel Jacobs1,2, Marieke de Kam1, Wayne Drevets3, Luc van Nueten4, Kawita Kanhai1, Pieter Siebenga1, Rob Zuiker1, Paulien Ravenstijn4, Maarten Timmers4, Joop van Gerven1,2, Peter de Boer4.   

Abstract

BACKGROUND: This is the first report of the pharmacodynamic (PD) effects of the selective, potent and brain-penetrant P2X7 receptor (P2X7R) antagonist JNJ-54175446. Activation of the P2X7R, an adenosine triphosphate-gated ion channel, leads to the production of pro-inflammatory cytokines, which have been linked to neuroinflammation and play a role in the pathogenesis of mood disorders. Previous clinical studies with JNJ-54175446 demonstrated peripheral target engagement of JNJ-54175446 by assessing ex vivo lipopolysaccharide (LPS)-stimulated cytokine production. Blood-brain barrier penetration and a clear dose-receptor occupancy relationship was demonstrated using positron emission tomography. AIMS: The objectives of this double-blind, placebo-controlled, translational study were to assess the safety and tolerability of administering multiple doses of JNJ-54175446 and to explore its PD effects using a dexamphetamine challenge.
METHODS: Subjects (N = 64) were randomised to either JNJ-54175446 (50-450 mg; n = 48) or placebo (n = 16) and underwent a baseline oral 20 mg dexamphetamine challenge followed by 11 consecutive days q.d. dosing with JNJ-54175446/placebo and a randomised crossover dexamphetamine/placebo challenge.
RESULTS: At all doses tested, JNJ-54175446 was well tolerated and suppressed the ex vivo LPS-induced release of cytokines. At doses ⩾100 mg, JNJ-54175446 attenuated dexamphetamine-induced increases in locomotion and enhanced the mood-elevating effects of dexamphetamine, suggesting that a dose that is approximately twice as high is needed to obtain a central PD response compared to the dose needed for maximum peripheral occupancy.
CONCLUSION: Overall, the observed pharmacological profile of JNJ-54175446 in the dexamphetamine challenge paradigm is compatible with a potential mood-modulating effect.

Entities:  

Keywords:  P2X7; inflammation; major depressive disorder

Year:  2020        PMID: 32248747     DOI: 10.1177/0269881120914206

Source DB:  PubMed          Journal:  J Psychopharmacol        ISSN: 0269-8811            Impact factor:   4.153


  9 in total

1.  Agonists, Antagonists, and Modulators of P2X7 Receptors.

Authors:  Christa E Müller; Vigneshwaran Namasivayam
Journal:  Methods Mol Biol       Date:  2022

2.  Inhibition of P2X7 receptors by Lu AF27139 diminishes colonic hypersensitivity and CNS prostanoid levels in a rat model of visceral pain.

Authors:  Roland G W Staal; Adarsh Gandhi; Hua Zhou; Manuel Cajina; Anne-Marie Jacobsen; Sara Hestehave; Allen Hopper; Suresh Poda; Gamini Chandresana; Stevin H Zorn; Brian Campbell; Marta Segerdahl; Thomas Mӧller; Gordon Munro
Journal:  Purinergic Signal       Date:  2022-08-24       Impact factor: 3.950

Review 3.  P2X7 Receptor Antagonism as a Potential Therapy in Amyotrophic Lateral Sclerosis.

Authors:  Cristina Ruiz-Ruiz; Francesco Calzaferri; Antonio G García
Journal:  Front Mol Neurosci       Date:  2020-06-12       Impact factor: 5.639

4.  P2X3-selective mechanism of Gefapixant, a drug candidate for the treatment of refractory chronic cough.

Authors:  Wen-Wen Cui; Si-Yu Wang; Yu-Qing Zhang; Yao Wang; Ying-Zhe Fan; Chang-Run Guo; Xing-Hua Li; Yun-Tao Lei; Wen-Hui Wang; Xiao-Na Yang; Motoyuki Hattori; Chang-Zhu Li; Jin Wang; Ye Yu
Journal:  Comput Struct Biotechnol J       Date:  2022-03-31       Impact factor: 6.155

5.  Pharmacological profile of ALKS 7119, an investigational compound evaluated for the treatment of neuropsychiatric disorders, in healthy volunteers.

Authors:  Francis M Dijkstra; Rob G J A Zuiker; Pieter S Siebenga; Richard A Leigh-Pemberton; Lei Sun; Joan D Manthis; Marieke L de Kam; Richard Lin; Lisa L von Moltke; David Rezendes; Joop M A van Gerven
Journal:  Br J Clin Pharmacol       Date:  2022-01-31       Impact factor: 3.716

6.  Integration of healthy volunteers in early phase clinical trials with immuno-oncological compounds.

Authors:  Igor Radanovic; Naomi Klarenbeek; Robert Rissmann; Geert Jan Groeneveld; Emilie M J van Brummelen; Matthijs Moerland; Jacobus J Bosch
Journal:  Front Oncol       Date:  2022-08-29       Impact factor: 5.738

7.  Central nervous system effects of TAK-653, an investigational alpha-amino-3-hydroxy-5-methyl-4-isoxazole receptor (AMPAR) positive allosteric modulator in healthy volunteers.

Authors:  Francis Dijkstra; Patricio O'Donnell; Erica Klaassen; Derek Buhl; Mahnaz Asgharnejad; Laura Rosen; Rob Zuiker; Joop van Gerven; Gabriël Jacobs
Journal:  Transl Psychiatry       Date:  2022-09-24       Impact factor: 7.989

8.  P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular Dystrophy.

Authors:  Lizzia Raffaghello; Elisa Principi; Serena Baratto; Chiara Panicucci; Sara Pintus; Francesca Antonini; Genny Del Zotto; Andrea Benzi; Santina Bruzzone; Paolo Scudieri; Carlo Minetti; Elisabetta Gazzerro; Claudio Bruno
Journal:  Pharmaceuticals (Basel)       Date:  2022-01-13

Review 9.  The Role of Microglial Purinergic Receptors in Pain Signaling.

Authors:  Hidetoshi Tozaki-Saitoh; Hiroshi Takeda; Kazuhide Inoue
Journal:  Molecules       Date:  2022-03-16       Impact factor: 4.411

  9 in total

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