Bibliographic Details
| Title: |
Inhibition of striatal dopamine release by the L‐type calcium channel inhibitor isradipine co‐varies with risk factors for Parkinson's. |
| Authors: |
Brimblecombe, Katherine R.1,2,3 (AUTHOR) katherine.brimblecombe@dpag.ox.ac.uk, Connor‐Robson, Natalie1,2 (AUTHOR), Bataille, Carole J. R.4,5 (AUTHOR), Roberts, Bradley M.1,2 (AUTHOR), Gracie, Caitlin1 (AUTHOR), O'Connor, Bethan1 (AUTHOR), te Water Naude, Rebecca1 (AUTHOR), Karthik, Gayathri1 (AUTHOR), Russell, Angela J.4,5 (AUTHOR), Wade‐Martins, Richard1,2,3 (AUTHOR), Cragg, Stephanie J.1,2,3 (AUTHOR) |
| Source: |
European Journal of Neuroscience. Mar2024, Vol. 59 Issue 6, p1242-1259. 18p. |
| Subject Terms: |
*DOPAMINERGIC neurons, *RYANODINE receptors, *PARKINSON'S disease, *CALCIUM channels, *DOPAMINE receptors, *DOPAMINE, *SEX (Biology), *SUBSTANTIA nigra |
| Abstract: |
Ca2+ entry into nigrostriatal dopamine (DA) neurons and axons via L‐type voltage‐gated Ca2+ channels (LTCCs) contributes, respectively, to pacemaker activity and DA release and has long been thought to contribute to vulnerability to degeneration in Parkinson's disease. LTCC function is greater in DA axons and neurons from substantia nigra pars compacta than from ventral tegmental area, but this is not explained by channel expression level. We tested the hypothesis that LTCC control of DA release is governed rather by local mechanisms, focussing on candidate biological factors known to operate differently between types of DA neurons and/or be associated with their differing vulnerability to parkinsonism, including biological sex, α‐synuclein, DA transporters (DATs) and calbindin‐D28k (Calb1). We detected evoked DA release ex vivo in mouse striatal slices using fast‐scan cyclic voltammetry and assessed LTCC support of DA release by detecting the inhibition of DA release by the LTCC inhibitors isradipine or CP8. Using genetic knockouts or pharmacological manipulations, we identified that striatal LTCC support of DA release depended on multiple intersecting factors, in a regionally and sexually divergent manner. LTCC function was promoted by factors associated with Parkinsonian risk, including male sex, α‐synuclein, DAT and a dorsolateral co‐ordinate, but limited by factors associated with protection, that is, female sex, glucocerebrosidase activity, Calb1 and ventromedial co‐ordinate. Together, these data show that LTCC function in DA axons and isradipine effect are locally governed and suggest they vary in a manner that in turn might impact on, or reflect, the cellular stress that leads to parkinsonian degeneration. [ABSTRACT FROM AUTHOR] |
|
Copyright of European Journal of Neuroscience is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
| Database: |
Academic Search Complete |
|
Full text is not displayed to guests. |
Login for full access.
|
