Linear Stimulus Isolator

$1,581.00
Order code
VAR-2275

Replicates a programmed waveform of any shape or polarity

  • Creates a constant current replica of analog waveforms
  • Amplitude of the output current is voltage controlled
  • Input voltage from –10V to +10V
  • 3 current ranges from 100 μA to 10 mA
  • Built-in test resistors
  • Digital display shows current being delivered for non-varying currents of adequate duration
  • Output offset adjustment ±70 V compliance range
  • Choose batteries: NiMH with Charger (A395RC), Alkaline (SYS-A395D), NiMH (SYS-A395R)

Options

Part # Description Battery Type Includes Charger
A395RC A395R with an A362 Battery Charger 17 NiMH 9V Rechargeable Batteries Yes
SYS-A395R Linear Stimulus Isolator 17 NiMH 9V Rechargeable Batteries No
SYS-A395D Linear Stimulus Isolator 17 Alkaline 9V Batteries _

Benefits

  • Amplitude of current is voltage controlled
  • Built-in test resistances
  • Error LEDs illuminate when current is less than commanded by control voltage

Applications

  • Neuroscience

All WPI stimulus isolators are designed to supply constant current, because current threshold (not voltage) is the most quantitatively reproducible parameter for stimulation of nerve and muscle. Model A395 dispenses current reproducibly from its Output terminals; the amplitude being determined by the selected current RANGE and the input voltage. Current amplitude is “constant”, that is, load resistance independent, provided that the I x R (load) product does not exceed the available battery supply voltage. A visual indicator (the compliance LEDs) displays if I x R reaches this limit. When the unit is out of compliance, one of the two LEDs (labeled - and +) illuminate, depending in which direction the current is flowing. Model A395D can generate a voltage of 70Vor more across its OUTPUT terminals. You can be sure that the amplitude of the current is as dialed as long as the voltage drop across the load (stimulus electrode path) does not reach the magnitude of the supply voltage. The compliance LEDs will then be visible. Then, you would know that:

• Too much current was dialed for a given load or

• Inter-electrode resistance was too high or the electrode circuit path was open.

User defined output current of various forms

Model A395 generates a user-defined output current of wave shape; DC, AC, pulse and combinations. Battery operated, pho­to­elec­tri­cal­ly-isolated from the input voltage drive, the instrument regen­er­ates out­put currents which are linearly proportional to the analog voltage wave­forms pro­vid­ed by your D/A con­vert­er or sig­nal generator (see diagram below).

The A395 is ideally suited for data acquisition and stimulator generators.

Current delivery for selected ranges

A 10 V input produces the maximum output current for the current range selected. (For example, 100 µA, 1 mA, or 10 mA) Front panel controls allow DC current to be generated. Externally applied signals can be superimposed si­mul­ta­neous­ly (DC offset). Warning lamps indicate open circuit or ex­ces­sive current conditions.

Digital meter shows DC or average output

The digital display meter shows the measures DC current or the average output current. Overload lamps indicate when output voltage has reached positive or negative compliance voltage limit.
a395io.jpg

NOTE: Not intended for human use.

OUTPUT CURRENT, Imax 3 ranges: 100 μA, 1 mA, and 10 mA
OUTPUT VOLTAGE RANGE ±70 V
OUTPUT BANDWIDTH 10 kHz (measured across 1 KΩ load R)
INPUT RESISTANCE >20 MΩ
INPUT VOLTAGE @ Imax ±10 V
INPUT/OUTPUT LINEARITY ERROR <0.5%
RISE, FALL TIME 26 μs @ 10 KΩ
POWER: Model A395D 17 alkaline 9 V batteries
POWER: Model A395R 17 rechargeable NiMH 9 V batteries
DIMENSIONS 6.5 x 4 x 3.5 in. (16 x 10 x 9 cm)
SHIPPING WEIGHT 4 lb. (1.8 kg)

Chemla, S., Witharana, W. K. L., & McNaughton, B. L. (2016). Spatiotemporal after-effects of transcranial direct current stimulation on sensory-evoked activity in rat S 1 : A pilot VSDI study. Retrieved from https://www.semanticscholar.org/paper/Spatiotemporal-after-effects-of-transcranial-direct-Chemla-Witharana/ebfca5444c8b7c0133217e62756e75f4c0c727d5

Márquez-Ruiz, J., Ammann, C., Leal-Campanario, R., Ruffini, G., Gruart, A., & Delgado-García, J. M. (2016). Synthetic tactile perception induced by transcranial alternating-current stimulation can substitute for natural sensory stimulus in behaving rabbits. Scientific Reports, 6(1), 19753. https://doi.org/10.1038/srep19753

Kim, H. N., Jung, W. B., Kang, M. J., Im, G. H., Lee, J. H., & Choe, B.-Y. (2015). Cerebral glucose metabolism changes in rat brain upon forepaw electrical stimulation at different frequencies. NeuroReport, 26(4), 197–205. https://doi.org/10.1097/WNR.0000000000000327

Madison, R. D., Robinson, G. A., Krarup, C., Moldovan, M., Li, Q., & Wilson, W. A. (2014). In vitro electrophoresis and in vivo electrophysiology of peripheral nerve using DC field stimulation. Journal of Neuroscience Methods, 225, 90–96. https://doi.org/10.1016/j.jneumeth.2014.01.018

Ali, M. M., Sellers, K. K., & Fröhlich, F. (2013). Transcranial alternating current stimulation modulates large-scale cortical network activity by network resonance. The Journal of Neuroscience : The Official Journal of the Society for Neuroscience, 33(27), 11262–11275. https://doi.org/10.1523/JNEUROSCI.5867-12.2013

Ayata, C., Shin, H. K., Dileköz, E., Atochin, D. N., Kashiwagi, S., Eikermann-Haerter, K., & Huang, P. L. (2013). Hyperlipidemia Disrupts Cerebrovascular Reflexes and Worsens Ischemic Perfusion Defect. Journal of Cerebral Blood Flow & Metabolism, 33(6), 954–962. https://doi.org/10.1038/jcbfm.2013.38

Vastani, N., Seifert, B., Spahn, D. R., & Maurer, K. (2013). Sensitivities of rat primary sensory afferent nerves to magnesium. European Journal of Anaesthesiology, 30(1), 21–28. https://doi.org/10.1097/EJA.0b013e32835949ab

Jacob, S., Johansson, C., & Fridberger, A. (2013). Noise-induced alterations in cochlear mechanics, electromotility, and cochlear amplification. Pflügers Archiv - European Journal of Physiology, 465(6), 907–917. https://doi.org/10.1007/s00424-012-1198-4

Pothmann, L., Wilkens, L. A., & Hofmann, M. H. (2012). Two modes of information processing in the electrosensory system of the paddlefish (Polyodon spathula). Journal of Comparative Physiology A, 198(1), 1–10. https://doi.org/10.1007/s00359-011-0681-2

Couchman, K., Grothe, B., & Felmy, F. (2010). Medial Superior Olivary Neurons Receive Surprisingly Few Excitatory and Inhibitory Inputs with Balanced Strength and Short-Term Dynamics. Journal of Neuroscience, 30(50), 17111–17121. https://doi.org/10.1523/JNEUROSCI.1760-10.2010

Tai, C., Wang, J., Wang, X., Roppolo, J. R., & de Groat, W. C. (2007). Voiding reflex in chronic spinal cord injured cats induced by stimulating and blocking pudendal nerves. Neurourology and Urodynamics, 26(6), 879–886. https://doi.org/10.1002/nau.20430

Lang, P. M., Burgstahler, R., Haberberger, R. V, Sippel, W., & Grafe, P. (2005). A conus peptide blocks nicotinic receptors of unmyelinated axons in human nerves. Neuroreport, 16(5), 479–483. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/15770155

Irnich, D., Tracey, D. J., Polten, J., Burgstahler, R., & Grafe, P. (2002). ATP stimulates peripheral axons in human, rat and mouse--differential involvement of A(2B) adenosine and P2X purinergic receptors. Neuroscience, 110(1), 123–129. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/11882377

Irnich, D., Burgstahler, R., Bostock, H., & Grafe, P. (2001). ATP affects both axons and Schwann cells of unmyelinated C fibres. Pain, 92(3), 343–350. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/11376907

 

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