Action potential and calcium dependence of tonic somatodendritic dopamine release in the Substantia Nigra pars compacta

Despite the importance of somatodendritic dopamine (DA) release in the Substantia Nigra pars compacta (SNc), its mechanism remains poorly understood. Using a novel approach combining fast‐scan controlled‐adsorption voltammetry (FSCAV) and single‐unit electrophysiology, we have investigated the mecha...

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Veröffentlicht in:Journal of neurochemistry 2019-02, Vol.148 (4), p.462-479
Hauptverfasser: Yee, Andrew G., Forbes, Blaze, Cheung, Pang‐Ying, Martini, Alessandro, Burrell, Mark H., Freestone, Peter S., Lipski, Janusz
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container_issue 4
container_start_page 462
container_title Journal of neurochemistry
container_volume 148
creator Yee, Andrew G.
Forbes, Blaze
Cheung, Pang‐Ying
Martini, Alessandro
Burrell, Mark H.
Freestone, Peter S.
Lipski, Janusz
description Despite the importance of somatodendritic dopamine (DA) release in the Substantia Nigra pars compacta (SNc), its mechanism remains poorly understood. Using a novel approach combining fast‐scan controlled‐adsorption voltammetry (FSCAV) and single‐unit electrophysiology, we have investigated the mechanism of somatodendritic release by directly correlating basal (non‐stimulated) extracellular DA concentration ([DA]out), with pharmacologically‐induced changes of firing of nigral dopaminergic neurons in rat brain slices. FSCAV measurements indicated that basal [DA]out in the SNc was 40.7 ± 2.0 nM (at 34 ± 0.5°C), which was enhanced by amphetamine, cocaine, and L‐DOPA, and reduced by VMAT2 inhibitor, Ro4‐1284. Complete inhibition of firing by TTX decreased basal [DA]out, but this reduction was smaller than the effect of D2 receptor agonist, quinpirole. Despite similar effects on neuronal firing, the larger decrease in [DA]out evoked by quinpirole was attributed to cell membrane hyperpolarization and greater reduction in cytosolic free Ca2+ ([Ca2+]in). Decreasing extracellular Ca2+ also reduced basal [DA]out, despite increasing firing frequency. Furthermore, inhibiting L‐type Ca2+ channels decreased basal [DA]out, although specific Cav1.3 channel inhibition did not affect firing rate. Inhibition of sarcoplasmic/endoplasmic reticulum Ca2+‐ATPase (SERCA) also decreased [DA]out, demonstrating the importance of intracellular Ca2+ stores for somatodendritic release. Finally, in vivo FSCAV measurements showed that basal [DA]out in the SNc was 79.8 ± 10.9 nM in urethane‐anesthetized rats, which was enhanced by amphetamine. Overall, our findings indicate that although tonic somatodendritic DA release is largely independent of action potentials, basal [DA]out is strongly regulated by voltage‐dependent Ca2+ influx and release of intracellular Ca2+. Open science badges This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/. The mechanism underlying tonic dopamine (DA) release from somata and dendrites of Substantia Nigra pars compacta (SNc) neurons remains poorly understood. We have directly correlated absolute extracellular DA concentration ([DA]out) with electrophysiological ac
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Using a novel approach combining fast‐scan controlled‐adsorption voltammetry (FSCAV) and single‐unit electrophysiology, we have investigated the mechanism of somatodendritic release by directly correlating basal (non‐stimulated) extracellular DA concentration ([DA]out), with pharmacologically‐induced changes of firing of nigral dopaminergic neurons in rat brain slices. FSCAV measurements indicated that basal [DA]out in the SNc was 40.7 ± 2.0 nM (at 34 ± 0.5°C), which was enhanced by amphetamine, cocaine, and L‐DOPA, and reduced by VMAT2 inhibitor, Ro4‐1284. Complete inhibition of firing by TTX decreased basal [DA]out, but this reduction was smaller than the effect of D2 receptor agonist, quinpirole. Despite similar effects on neuronal firing, the larger decrease in [DA]out evoked by quinpirole was attributed to cell membrane hyperpolarization and greater reduction in cytosolic free Ca2+ ([Ca2+]in). Decreasing extracellular Ca2+ also reduced basal [DA]out, despite increasing firing frequency. Furthermore, inhibiting L‐type Ca2+ channels decreased basal [DA]out, although specific Cav1.3 channel inhibition did not affect firing rate. Inhibition of sarcoplasmic/endoplasmic reticulum Ca2+‐ATPase (SERCA) also decreased [DA]out, demonstrating the importance of intracellular Ca2+ stores for somatodendritic release. Finally, in vivo FSCAV measurements showed that basal [DA]out in the SNc was 79.8 ± 10.9 nM in urethane‐anesthetized rats, which was enhanced by amphetamine. Overall, our findings indicate that although tonic somatodendritic DA release is largely independent of action potentials, basal [DA]out is strongly regulated by voltage‐dependent Ca2+ influx and release of intracellular Ca2+. Open science badges This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/. The mechanism underlying tonic dopamine (DA) release from somata and dendrites of Substantia Nigra pars compacta (SNc) neurons remains poorly understood. We have directly correlated absolute extracellular DA concentration ([DA]out) with electrophysiological activity of SNc neurons. We show that basal [DA]out is largely independent of action potentials, but is strongly regulated by intracellular Ca2+. These data shed new light on differences between somatodendritic DA release and axon terminal release, indicating that release from these sites can be controlled independently. Open Science: This manuscript was awarded with the Open Materials Badge. 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Using a novel approach combining fast‐scan controlled‐adsorption voltammetry (FSCAV) and single‐unit electrophysiology, we have investigated the mechanism of somatodendritic release by directly correlating basal (non‐stimulated) extracellular DA concentration ([DA]out), with pharmacologically‐induced changes of firing of nigral dopaminergic neurons in rat brain slices. FSCAV measurements indicated that basal [DA]out in the SNc was 40.7 ± 2.0 nM (at 34 ± 0.5°C), which was enhanced by amphetamine, cocaine, and L‐DOPA, and reduced by VMAT2 inhibitor, Ro4‐1284. Complete inhibition of firing by TTX decreased basal [DA]out, but this reduction was smaller than the effect of D2 receptor agonist, quinpirole. Despite similar effects on neuronal firing, the larger decrease in [DA]out evoked by quinpirole was attributed to cell membrane hyperpolarization and greater reduction in cytosolic free Ca2+ ([Ca2+]in). Decreasing extracellular Ca2+ also reduced basal [DA]out, despite increasing firing frequency. Furthermore, inhibiting L‐type Ca2+ channels decreased basal [DA]out, although specific Cav1.3 channel inhibition did not affect firing rate. Inhibition of sarcoplasmic/endoplasmic reticulum Ca2+‐ATPase (SERCA) also decreased [DA]out, demonstrating the importance of intracellular Ca2+ stores for somatodendritic release. Finally, in vivo FSCAV measurements showed that basal [DA]out in the SNc was 79.8 ± 10.9 nM in urethane‐anesthetized rats, which was enhanced by amphetamine. Overall, our findings indicate that although tonic somatodendritic DA release is largely independent of action potentials, basal [DA]out is strongly regulated by voltage‐dependent Ca2+ influx and release of intracellular Ca2+. Open science badges This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/. The mechanism underlying tonic dopamine (DA) release from somata and dendrites of Substantia Nigra pars compacta (SNc) neurons remains poorly understood. We have directly correlated absolute extracellular DA concentration ([DA]out) with electrophysiological activity of SNc neurons. We show that basal [DA]out is largely independent of action potentials, but is strongly regulated by intracellular Ca2+. These data shed new light on differences between somatodendritic DA release and axon terminal release, indicating that release from these sites can be controlled independently. Open Science: This manuscript was awarded with the Open Materials Badge. 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Using a novel approach combining fast‐scan controlled‐adsorption voltammetry (FSCAV) and single‐unit electrophysiology, we have investigated the mechanism of somatodendritic release by directly correlating basal (non‐stimulated) extracellular DA concentration ([DA]out), with pharmacologically‐induced changes of firing of nigral dopaminergic neurons in rat brain slices. FSCAV measurements indicated that basal [DA]out in the SNc was 40.7 ± 2.0 nM (at 34 ± 0.5°C), which was enhanced by amphetamine, cocaine, and L‐DOPA, and reduced by VMAT2 inhibitor, Ro4‐1284. Complete inhibition of firing by TTX decreased basal [DA]out, but this reduction was smaller than the effect of D2 receptor agonist, quinpirole. Despite similar effects on neuronal firing, the larger decrease in [DA]out evoked by quinpirole was attributed to cell membrane hyperpolarization and greater reduction in cytosolic free Ca2+ ([Ca2+]in). Decreasing extracellular Ca2+ also reduced basal [DA]out, despite increasing firing frequency. Furthermore, inhibiting L‐type Ca2+ channels decreased basal [DA]out, although specific Cav1.3 channel inhibition did not affect firing rate. Inhibition of sarcoplasmic/endoplasmic reticulum Ca2+‐ATPase (SERCA) also decreased [DA]out, demonstrating the importance of intracellular Ca2+ stores for somatodendritic release. Finally, in vivo FSCAV measurements showed that basal [DA]out in the SNc was 79.8 ± 10.9 nM in urethane‐anesthetized rats, which was enhanced by amphetamine. Overall, our findings indicate that although tonic somatodendritic DA release is largely independent of action potentials, basal [DA]out is strongly regulated by voltage‐dependent Ca2+ influx and release of intracellular Ca2+. Open science badges This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/. The mechanism underlying tonic dopamine (DA) release from somata and dendrites of Substantia Nigra pars compacta (SNc) neurons remains poorly understood. We have directly correlated absolute extracellular DA concentration ([DA]out) with electrophysiological activity of SNc neurons. We show that basal [DA]out is largely independent of action potentials, but is strongly regulated by intracellular Ca2+. These data shed new light on differences between somatodendritic DA release and axon terminal release, indicating that release from these sites can be controlled independently. Open Science: This manuscript was awarded with the Open Materials Badge. 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subjects Action potential
Adenosine triphosphatase
Amphetamines
Brain
Brain slice preparation
Ca2+ imaging
Ca2+-transporting ATPase
Calcium
Calcium (extracellular)
Calcium (intracellular)
Calcium (reticular)
Calcium channels
Calcium channels (voltage-gated)
Calcium influx
Calcium ions
Cell membranes
Cocaine
Dependence
Dihydroxyphenylalanine
Dopamine
Dopamine D2 receptors
electrochemistry
Electrophysiology
Endoplasmic reticulum
Ethyl carbamate
Firing rate
FSCAV
Hyperpolarization
Inhibition
Intracellular
Levodopa
Pharmacology
Quinpirole
rat brain
Reduction
Substantia nigra
Tetrodotoxin
title Action potential and calcium dependence of tonic somatodendritic dopamine release in the Substantia Nigra pars compacta
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