Florentin Allemand
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Florentin Allemand has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
- Alexandre Bonet
PEPITE EA4267, laboratoire de Toxicologie Cellulaire, Univ. Bourgogne Franche-Comté, F-25000 Besançon, France
1 shared publication - Barbara Dehecq
Université de Franche-Comté, UMR RIGHT, EFS, INSERM, F-25000 Besançon, France
1 shared publication - Bernard Refouvelet
INSERM UMR1322 LINC, Université Marie et Louis Pasteur, F-25000 Besançon, France
1 shared publication - Bruno Cardey
Université de Franche-Comté, CNRS, CHRONO-E (UMR 6249), F-25000, Besançon, France
1 shared publication - Chloé Richet
Department of Micro Nano Sciences and Systems (MN2S), Université Franche-Comté, UMR 6174 CNRS, FEMTO-ST Institute, F-25000 Besançon, France
1 shared publication Christophe Ramseyer
Université de Franche-Comté, CNRS, Chrono-environnement, F-25000 Besançon, France
1 shared publication
Latest Publications
- 16 November 2024
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Biomembranes
- Vol. 1867 (1) , 184402
Nanodomains enriched in arachidonic acid promote P2Y12 receptor oligomerization in the platelet plasma membrane
- 16 November 2024
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Biomembranes
- Vol. 1867 (1) , 184402
Nanodomains enriched in arachidonic acid promote P2Y12 receptor oligomerization in the platelet plasma membrane
- Open Access
- 31 August 2024
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 112, 129938
Synthesis and evaluation of lipoic acid – donepezil hybrids for Alzheimer’s disease using a straightforward strategy
- 31 August 2024
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 112, 129938
Open AccessSynthesis and evaluation of lipoic acid – donepezil hybrids for Alzheimer’s disease using a straightforward strategy
- Open Access
- 31 January 2021
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 22 (3) , 1432
Influence of Antiplatelet Agents on the Lipid Composition of Platelet Plasma Membrane: A Lipidomics Approach with Ticagrelor and Its Active Metabolite
Lipids contained in the plasma membrane of platelets play an important role in platelet function. Modifications in the lipid composition can fluidify or rigidify the environment around embedded receptors, in order to facilitate the access of the receptor by the drug. However, data concerning the lipid composition of platelet plasma membrane need to be updated. In addition, data on the impact of drugs on plasma membrane composition, in particular antiplatelet agents, remain sparse. After isolation of platelet plasma membrane, we assessed, using lipidomics, the effect of ticagrelor, a P2Y12 antagonist, and its active metabolite on the lipid composition of these plasma membranes. We describe the exact lipid composition of plasma membrane, including all sub-species. Ticagrelor and its active metabolite significantly increased cholesterol and phosphatidylcholine ether with short saturated acyl chains 16:0/16:0, and decreased phosphatidylcholine, suggesting overall rigidification of the membrane. Furthermore, ticagrelor and its active metabolite decreased some arachidonylated plasmalogens, suggesting a decrease in availability of arachidonic acid from the membrane phospholipids for synthesis of biologically active mediators. To conclude, ticagrelor and its active metabolite seem to influence the lipid environment of receptors embedded in the lipid bilayer and modify the behavior of the plasma membrane.
- 31 January 2021
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 22 (3) , 1432
Open AccessInfluence of Antiplatelet Agents on the Lipid Composition of Platelet Plasma Membrane: A Lipidomics Approach with Ticagrelor and Its Active Metabolite
Lipids contained in the plasma membrane of platelets play an important role in platelet function. Modifications in the lipid composition can fluidify or rigidify the environment around embedded receptors, in order to facilitate the access of the receptor by the drug. However, data concerning the lipid composition of platelet plasma membrane need to be updated. In addition, data on the impact of drugs on plasma membrane composition, in particular antiplatelet agents, remain sparse. After isolation of platelet plasma membrane, we assessed, using lipidomics, the effect of ticagrelor, a P2Y12 antagonist, and its active metabolite on the lipid composition of these plasma membranes. We describe the exact lipid composition of plasma membrane, including all sub-species. Ticagrelor and its active metabolite significantly increased cholesterol and phosphatidylcholine ether with short saturated acyl chains 16:0/16:0, and decreased phosphatidylcholine, suggesting overall rigidification of the membrane. Furthermore, ticagrelor and its active metabolite decreased some arachidonylated plasmalogens, suggesting a decrease in availability of arachidonic acid from the membrane phospholipids for synthesis of biologically active mediators. To conclude, ticagrelor and its active metabolite seem to influence the lipid environment of receptors embedded in the lipid bilayer and modify the behavior of the plasma membrane.