Emmanuel Darcq
Biographic Data
| ID | 7387288 |
|---|---|
| NAME | Emmanuel Darcq |
| GIVEN NAMES | Emmanuel |
| FAMILY NAME | Darcq |
| SIGNATURE | DARCQ E |
| AFFILIATIONS | Douglas Mental Health University Institute |
| ORCID | 0000-0002-8377-8015 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2018 |
| LATEST PUBLICATION YEAR | 2023 |
| H-INDEX | 0 |
Chronic tianeptine induces tolerance in analgesia and hyperlocomotion via mu-opioid receptor activation in mice
These findings suggest that tianeptine's opioid-like effects require MOR and that chronic use could lead to tolerance
Deformation-based Morphometry MRI Reveals Brain Structural Modifications in Living Mu Opioid Receptor Knockout Mice
Mu opioid receptor (MOR) activation facilitates reward processing and reduces pain, and brain networks underlying these effects are under intense investigation. Mice lacking the MOR gene (MOR KO mice) show lower drug and social reward, enhanced pain sensitivity and altered emotional responses. Our previous neuroimaging analysis using Resting-state (Rs) functional Magnetic Resonance Imaging (fMRI) showed significant alterations of functional conne…
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Deformation-based Morphometry MRI Reveals Brain Structural Modifications in Living Mu Opioid Receptor Knockout Mice
Mu opioid receptor (MOR) activation facilitates reward processing and reduces pain, and brain networks underlying these effects are under intense investigation. Mice lacking the MOR gene (MOR KO mice) show lower drug and social reward, enhanced pain sensitivity and altered emotional responses. Our previous neuroimaging analysis using Resting-state (Rs) functional Magnetic Resonance Imaging (fMRI) showed significant alterations of functional conne…
Chronic tianeptine induces tolerance in analgesia and hyperlocomotion via mu-opioid receptor activation in mice
These findings suggest that tianeptine's opioid-like effects require MOR and that chronic use could lead to tolerance
Neuroscience (2 works) · Psychology (2 works) · Agonist (1 work) · Amygdala (1 work) · Analgesic (1 work) · Antidepressant (1 work) · Basal ganglia (1 work) · Central nervous system (1 work) · Chemistry (1 work) · Dopamine (1 work)