Yannick Goumon

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France

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Modernisation du plateau technique mutualisé participatif de spectrométrie de masse de l’UPR3212 pour la détection et la quantification des hormones et des neuromédiateurs en conditions physiologiques et pathologiques

Open Date: 2023-01-01

Close Date: 2023-01-01

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Cofinancement pour l'achat d'un robot d'aide au pipetage

Open Date: 2022-08-01

Close Date: 2022-08-01

Grant: Close

Cofinancement pour l'achat d'un robot d'aide au pipetage

Open Date: 2022-08-01

Close Date: 2022-08-01

Grant: Close

Identification and validation of the crealgin receptor for therapeutic purposes: anti-pain and anti-inflammation

Open Date: 2021-04-01

Close Date: 2022-04-01

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STUDY OF THE IMPACT OF PARACETAMOL AND CODEINE ON THE METABOLIC TRACKS OF TAMOXIFENE AND ANASTROZOLE

Open Date: 2021-03-01

Close Date: 2022-12-01

Articles (10)

Central metabolism as a potential origin of sex differences in morphine antinociception but not induction of antinociceptive tolerance in mice

Background and Purpose In rodents, morphine antinociception is influenced by sex. However, conflicting results have been reported regarding the interaction between sex and morphine antinociceptive tolerance. Morphine is metabolised in the liver and brain into morphine‐3‐glucuronide (M3G). Sex differences in morphine metabolism and differential metabolic adaptations during tolerance development might contribute to behavioural discrepancies. This article investigates the differences in peripheral and central morphine metabolism after acute and chronic morphine treatment in male and female mice. Experimental Approach Sex differences in morphine antinociception and tolerance were assessed using the tail‐immersion test. After acute and chronic morphine treatment, morphine and M3G metabolic kinetics in the blood were evaluated using LC‐MS/MS. They were also quantified in several CNS regions. Finally, the blood–brain barrier (BBB) permeability of M3G was assessed in male and female mice. Key Results This study demonstrated that female mice showed weaker morphine antinociception and faster induction of tolerance than males. Additionally, female mice showed higher levels of M3G in the blood and in several pain‐related CNS regions than male mice, whereas lower levels of morphine were observed in these regions. M3G brain/blood ratios after injection of M3G indicated no sex differences in M3G BBB permeability, and these ratios were lower than those obtained after injection of morphine. Conclusion These differences are attributable mainly to morphine central metabolism, which differed between males and females in pain‐related CNS regions, consistent with weaker morphine antinociceptive effects in females. However, the role of morphine metabolism in antinociceptive tolerance seemed limited. LINKED ARTICLES This article is part of a themed issue on Advances in Opioid Pharmacology at the Time of the Opioid Epidemic. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v180.7/issuetoc

Year:

2022

Collaborators (10)

Katia Befort

University of Strasbourg

FRANCE

Sylvain Hugel

CNRS Délégation Alsace

FRANCE

Perrine Inquimbert

Assistant professor

-

FRANCE

Benjamin Boutrel

Senior Lecturer

Lausanne University Hospital

SWITZERLAND

Ron Stoop

University of Lausanne

SWITZERLAND

Jan Siemens

Professor

Ruprecht-Karls-Universität Heidelberg Medizinische Fakultät Mannheim

GERMANY

Emeline TANGUY

Maitre de Conférences (lecturer)

University of Strasbourg

FRANCE

Pascal Darbon

Associate professor

University of Strasbourg

FRANCE

Albano C. Meli

-

FRANCE

Pierrick Poisbeau

Full Professor (PU)

University of Strasbourg

FRANCE
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