TY - JOUR
T1 - Validation of a Portable Low-Power Deep Brain Stimulation Device Through Anxiolytic Effects in a Laboratory Rat Model
AU - Kouzani, Abbas Z.
AU - Kale, Rajas P.
AU - Zarate-Garza, Pablo Patricio
AU - Berk, Michael
AU - Walder, Ken
AU - Tye, Susannah J.
N1 - Funding Information:
Manuscript received December 23, 2015; revised October 5, 2016; accepted November 8, 2016. Date of publication November 15, 2016; date of current version September 2, 2017. The work of M. Berk was supported by a NHMRC Senior Principal Research Fellowship under Grant 1059660.
Publisher Copyright:
© 2001-2011 IEEE.
PY - 2017/9
Y1 - 2017/9
N2 - Deep brain stimulation (DBS) devices deliver electrical pulses to neural tissue through an electrode. To study the mechanisms and therapeutic benefits of deep brain stimulation, murine preclinical research is necessary. However, conducting naturalistic long-term, uninterrupted animal behavioral experiments can be difficult with bench-top systems. The reduction of size, weight, power consumption, and cost of DBS devices can assist the progress of this research in animal studies. A low power, low weight, miniature DBS device is presented in this paper. This device consists of electronic hardware and software components including a low-power microcontroller, an adjustable current source, an n-channel metal-oxide-semiconductor field-effect transistor, a coin-cell battery, electrode wires and a software program to operate the device. Evaluation of the performance of the device in terms of battery lifetime and device functionality through bench and in vivo tests was conducted. The bench test revealed that this device can deliver continuous stimulation current pulses of strength 200μA, width 90μs, and frequency 130 Hz for over 22 days. The in vivo tests demonstrated that chronic stimulation of the nucleus accumbens (NAc) with this device significantly increased psychomotor activity, together with a dramatic reduction in anxiety-like behavior in the elevated zero-maze test.
AB - Deep brain stimulation (DBS) devices deliver electrical pulses to neural tissue through an electrode. To study the mechanisms and therapeutic benefits of deep brain stimulation, murine preclinical research is necessary. However, conducting naturalistic long-term, uninterrupted animal behavioral experiments can be difficult with bench-top systems. The reduction of size, weight, power consumption, and cost of DBS devices can assist the progress of this research in animal studies. A low power, low weight, miniature DBS device is presented in this paper. This device consists of electronic hardware and software components including a low-power microcontroller, an adjustable current source, an n-channel metal-oxide-semiconductor field-effect transistor, a coin-cell battery, electrode wires and a software program to operate the device. Evaluation of the performance of the device in terms of battery lifetime and device functionality through bench and in vivo tests was conducted. The bench test revealed that this device can deliver continuous stimulation current pulses of strength 200μA, width 90μs, and frequency 130 Hz for over 22 days. The in vivo tests demonstrated that chronic stimulation of the nucleus accumbens (NAc) with this device significantly increased psychomotor activity, together with a dramatic reduction in anxiety-like behavior in the elevated zero-maze test.
KW - Brain
KW - deep brain stimulation (DBS)
KW - device
KW - low-power circuit
KW - miniature
KW - neurology
KW - preclinical
KW - psychiatry
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U2 - 10.1109/TNSRE.2016.2628760
DO - 10.1109/TNSRE.2016.2628760
M3 - Article
C2 - 28113945
AN - SCOPUS:85029572980
SN - 1534-4320
VL - 25
SP - 1365
EP - 1374
JO - IEEE Transactions on Neural Systems and Rehabilitation Engineering
JF - IEEE Transactions on Neural Systems and Rehabilitation Engineering
IS - 9
M1 - 7744659
ER -