scholarly journals Presynaptic Dopamine Dynamics in Striatal Brain Slices with Fast-scan Cyclic Voltammetry

Author(s):  
Francis K. Maina ◽  
Madiha Khalid ◽  
Aaron K. Apawu ◽  
Tiffany A. Mathews
BIO-PROTOCOL ◽  
2018 ◽  
Vol 8 (19) ◽  
Author(s):  
Madelyn Mauterer ◽  
Paige Estave ◽  
Katherine Holleran ◽  
Sara Jones

The Analyst ◽  
2016 ◽  
Vol 141 (23) ◽  
pp. 6416-6421 ◽  
Author(s):  
R. Asri ◽  
B. O'Neill ◽  
J. C. Patel ◽  
K. A. Siletti ◽  
M. E. Rice

The study of transmitter interactions in the brain requires methodology to detect stimulus-driven neurotransmitter release. This report introduces an enzyme-coated 7 μm carbon-fiber microelectrode used with fast-scan cyclic voltammetry to detect evoked acetylcholine release in mouse brain slices.


Antioxidants ◽  
2020 ◽  
Vol 9 (12) ◽  
pp. 1285
Author(s):  
David M. Hedges ◽  
Jordan T. Yorgason ◽  
Andrew W. Perez ◽  
Nathan D. Schilaty ◽  
Benjamin M. Williams ◽  
...  

Parkinson’s disease is associated with degeneration of neuromelanin (NM)-containing substantia nigra dopamine (DA) neurons and subsequent decreases in striatal DA transmission. Dopamine spontaneously forms a melanin through a process called melanogenesis. The present study examines conditions that promote/prevent DA melanogenesis. The kinetics, intermediates, and products of DA conversion to melanin in vitro, and DA melanogenesis under varying levels of Fe3+, pro-oxidants, and antioxidants were examined. The rate of melanogenesis for DA was substantially greater than related catecholamines norepinephrine and epinephrine and their precursor amino acids tyrosine and l-Dopa as measured by UV-IR spectrophotometry. Dopamine melanogenesis was concentration dependent on the pro-oxidant species and Fe3+. Melanogenesis was enhanced by the pro-oxidant hydrogen peroxide (EC50 = 500 μM) and decreased by the antioxidants ascorbate (IC50 = 10 μM) and glutathione (GSH; IC50 = 5 μM). Spectrophotometric results were corroborated by tuning a fast-scan cyclic voltammetry system to monitor DA melanogenesis. Evoked DA release in striatal brain slices resulted in NM formation that was prevented by GSH. These findings suggest that DA melanogenesis occurs spontaneously under physiologically-relevant conditions of oxidative stress and that NM may act as a marker of past exposure to oxidative stress.


2010 ◽  
Vol 113 (3) ◽  
pp. 656-665 ◽  
Author(s):  
Christoph J. Griessenauer ◽  
Su-Youne Chang ◽  
Susannah J. Tye ◽  
Christopher J. Kimble ◽  
Kevin E. Bennet ◽  
...  

Object The authors previously reported the development of the Wireless Instantaneous Neurotransmitter Concentration System (WINCS) for measuring dopamine and suggested that this technology may be useful for evaluating deep brain stimulation–related neuromodulatory effects on neurotransmitter systems. The WINCS supports fast-scan cyclic voltammetry (FSCV) at a carbon-fiber microelectrode (CFM) for real-time, spatially resolved neurotransmitter measurements. The FSCV parameters used to establish WINCS dopamine measurements are not suitable for serotonin, a neurotransmitter implicated in depression, because they lead to CFM fouling and a loss of sensitivity. Here, the authors incorporate into WINCS a previously described N-shaped waveform applied at a high scan rate to establish wireless serotonin monitoring. Methods Optimized for the detection of serotonin, FSCV consisted of an N-shaped waveform scanned linearly from a resting potential of +0.2 to +1.0 V, then to −0.1 V and back to +0.2 V, at a rate of 1000 V/second. Proof-of-principle tests included flow injection analysis and electrically evoked serotonin release in the dorsal raphe nucleus of rat brain slices. Results Flow cell injection analysis demonstrated that the N waveform, applied at a scan rate of 1000 V/second, significantly reduced serotonin fouling of the CFM, relative to that observed with FSCV parameters for dopamine. In brain slices, WINCS reliably detected subsecond serotonin release in the dorsal raphe nucleus evoked by local high-frequency stimulation. Conclusions The authors found that WINCS supported high-fidelity wireless serotonin monitoring by FSCV at a CFM. In the future such measurements of serotonin in large animal models and in humans may help to establish the mechanism of deep brain stimulation for psychiatric disease.


2021 ◽  
Vol MA2021-02 (55) ◽  
pp. 1606-1606
Author(s):  
Alexander George Zestos ◽  
Favian Alberto Liu ◽  
Thomas Asrat ◽  
Harmain Rafi

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