Ocular Kinematics Measured by In Vitro Stimulation of the Cranial Nerves in the Turtle

Podsumowanie

This protocol describes how to use an in vitro isolated turtle head preparation to measure the kinematics of their eye movements. After removal of the brain from the cranium, cranial nerves can be stimulated with currents to quantify rotations of the eye and changes in pupil sizes.

Streszczenie

After animals are euthanized, their tissues begin to die. Turtles offer an advantage because of a longer survival time of their tissues, especially when compared to warm-blooded vertebrates. Because of this, in vitro experiments in turtles can be performed for extended periods of time to investigate the neural signals and control of their target actions. Using an isolated head preparation, we measured the kinematics of eye movements in turtles, and their modulation by electrical signals carried by cranial nerves. After the brain was removed from the skull, leaving the cranial nerves intact, the dissected head was placed in a gimbal to calibrate eye movements. Glass electrodes were attached to cranial nerves (oculomotor, trochlear, and abducens) and stimulated with currents to evoke eye movements. We monitored eye movements with an infrared video tracking system and quantified rotations of the eyes. Current pulses with a range of amplitudes, frequencies, and train durations were used to observe effects on responses. Because the preparation is separated from the brain, the efferent pathway going to muscle targets can be examined in isolation to investigate neural signaling in the absence of centrally processed sensory information.

Wprowadzenie

Rationale for Using Red-eared Slider Turtles in Electrophysiological Experiments:

Red-eared slider turtles (Trachemys scripta elegans), are considered one of world's worst invasive species¹ and can indicate that an ecosystem is in trouble. The reason why red-eared slider turtles are so successful is poorly understood but it may in part be due to their tolerant physiology and possession of nervous tissues that can survive under hypoxic conditions^2,3,4. Using them for experimentation does not threaten their numbers and with minimal efforts, electrophysiological preparations can remain viable over extended durations, as long as 18 hours^5,6. The benefit is similar to the advantage of using invertebrate animals such as crayfish⁷, which also have the ability to withstand low levels of oxygen⁸.

Techniques for Measuring Eye Movements:

Approaches to measure eye movements in frontal-eyed animals using non-human primates have been well developed⁹. The eye rotates in the orbit around three axes: horizontal, vertical, and torsional. The magnetic search coil method is generally considered the most reliable for measuring rotations, but is invasive, requiring small coils to be inserted into the scleras of animals^10,11. Video-based systems also can measure rotations and have the advantage of being non-invasive. The development of better cameras along with innovative image processing have enhanced their functionality making video-based systems an attractive alternative to consider^12,13,14.

The techniques developed for measuring eye movements in nonmammals have been much less significant. Measures are either low resolution or describe only some of the rotations^15,16,17,18. The lack of development can be partially blamed on the difficulty in training nonmammals to follow visual targets. Although eye movements have been well studied in red-eared slider turtles^{19,20,21,22,23,24,25,26,27,28,29,30}, because of the challenge in training animals to track targets, the precise kinematics of their eye movements is poorly understood.

Red-eared slider turtles are generally considered lateral-eyed vertebrates, but because they can fully retract their heads into their shell³¹, significant occlusion of the lateral visual fields by the carapace occurs³². The result is that their visual line of sight is forced toward the front, making them behave more like frontal-eyed mammals. Therefore, their use as a model for developing approaches for measuring eye movements also offers a unique evolutionary perspective.

The protocol described in this work uses an in vitro isolated head preparation to identify the kinematics of the eye movements in red-eared slider turtles. Brains are dissected from the skulls leaving the cranial nerves intact. Heads are placed into a gimbal to calibrate eye movements and evoke responses by electrical stimulation of the cranial nerves innervating the eye muscles. Measures of rotations by the eyes are done by a video-based system, using software algorithms, which track the dark pupil and the markings of the iris. The preparation provides the opportunity to measure kinematics of both extraocular (i.e., horizontal, vertical, and torsional rotations)³² and intraocular (i.e., pupil changes)³³ movements.

Model System for Analysis of Efferent Neural Pathways:

More generally, the approach provides investigators the chance to study how efferent neural signals generate eye movements when muscles start from their relaxed states and in the absence of integrated sensory information processed by the brain^32,33. Therefore, the eye kinematics can be examined in a model system in which they are solely processed by the efferent neural pathway leaving the brain and synapsing onto the muscles.

Protokół

NOTE: Red-eared slider turtles, both male and female, were purchased from a vendor. Turtles were housed in a warm animal suite containing two 60-gallon tubs equipped with brick islands for sunning under 250-W infrared lights. The environment was maintained on a 14/10-h light/dark cycle with the water temperature at 22 °C. Lights were turned on at 6:00 am and turned off at 8:00 pm. The tanks equipped with filtering systems were cleaned weekly, and turtles were fed ad libitum every other day. The care of red-eared slider turtles and all of the following experimental procedures described here^32,33 were approved by the Institutional Animal Care and Use Committee (IACUC) at Lafayette College.

1. Equipment Setup

1. Prepare turtle Ringer's solution. Add the following to distilled water in this order: sodium chloride 96.5 mM (58.44 g/mol), potassium chloride 2.6 mM (74.56 g/mol), magnesium chloride 2.0 mM (203.31 g/mol), sodium bicarbonate 31.5 mM (84.01 g/mol), dextrose 20.0 mM (180.16 g/mol), concentrated hydrochloric acid to adjust the pH to 7.51, and calcium chloride 4.0 mM (110.98 g/mol) (see Table of Materials). Mix the solution while adding each salt.
   CAUTION: Concentrated HCl is hazardous (skin, eyes, inhalation, and ingestion hazards).
2. Make tips for the suction electrodes from 5-cm-long capillary glass (see Table of Materials), by fire-polishing to different sizes of inner diameters in order to accommodate cranial nerves of varying thickness.
   1. Use a small file to etch a line across a piece of capillary glass. Place in tissue paper and break in half.
   2. Slowly roll one of the ends of the capillary glass into the flame of a Bunsen burner. Periodically examine the tip for size, smoothness, and symmetry using a dissection scope and a fiber optic light source (see Table of Materials).
      NOTE: For turtles with head widths between 20 and 30 mm, optimal fitting inner diameter sizes typically range from 0.4 to 0.8 mm for the oculomotor nerve (nIII), 0.3 to 0.6 mm for the trochlear nerve (nIV), and 0.2 to 0.4 mm for the abducens nerve (nVI).
3. Clean and organize Rongeurs, a blunt dissection probe, microscissors, fine forceps, curved forceps, and a scalpel handle with blades (see Table of Materials) for the dissection.
   NOTE: Sterilization of instruments is optional.

2. Anesthesia and Euthanasia

1. Place the turtle in an ice bucket for 60 min to cryoanesthetize it.
2. Euthanize the turtle by decapitation using a small animal guillotine (see Table of Materials).
   1. Gently pry the jaws of the animal open with a small weighing spatula so that a hook can be inserted and turned to fit under the tip of the upper jaw.
   2. Pull with steady pressure to extend the animal's head through the guillotine. Swiftly decapitate the animal.
3. Place turtle head in a dissection dish. Have enough turtle Ringer’s solution on hand to irrigate the tissue. Oxygenize the solution with 95/5% O₂/CO₂ (see Table of Materials).
4. Maintain the tissue at 4 °C by placing ice around the outside of the dish.

3. Dissection

1. Use the dissection scope with a fiber optic light source to carry out the dissection.
2. Remove the lower jaw. Place a blunt dissection probe through the mouth to provide easier handling of the head. Cut the joint connecting the dentary bone to the cranium with a scalpel. Use rongeurs to pull the lower jaw away from the cranium. Use rongeurs to pull off the skin and muscles from their attachments at the dorsal and lateral regions of the cranium.
3. Remove the vertebral column.
   1. Identify the vertebral column at the caudal end of the cranium. Bend the vertebral column ventrally to expose the spinal cord. Use microscissors to snip the spinal cord. Use rongeurs to remove the vertebral column and other tissue from the cranium by pulling caudally.
4. Remove the brain from the cranium after cutting the cranial nerves.
   1. Starting at the foramen magnum, use rongeurs to cut two incisions on the dorsal cranium. Make cuts superficial to avoid damaging the brain beneath.
   2. Use rongeurs to carefully pull off the dorsal cranium. Use microscissors to remove the meninx to expose the rest of the brain. Remove enough meninx until the olfactory bulbs, in the anterior cranial cavity, can be identified (see Figure 1A). Continue to irrigate the brain with turtle Ringer's solution, as necessary.
   3. Use curved forceps to gently pull the cerebrum caudally and produce slight tension on the cranial nerves. Carefully cut away and remove the olfactory bulbs and cerebrum with curved forceps.
   4. Use microscissors to gently push the midbrain toward the midline to expose the cranial nerves; nIII, about 0.6 mm, can be seen in front of nIV, and the diameter of nIV will be slightly less than nIII. Cut nIII and nIV where they attach to the midbrain (see Figure 1B). Repeat this on the other side.
   5. Cut the left and right optic nerve (nII) with microscissors. Then tilt the brainstem to one side. Observe nVI emerging from the ventral surface near the junction of the pons and the medulla (see Figure 1C); the diameter of nVI is small and approximately 0.3 mm. Cut both the left and right nVI.
   6. Remove the remaining parts of the brainstem from the turtle with fine forceps and microscissors. Once the cranium is empty, examine the cranial cavity floor. Identify nIII, nIV, and nVI.
5. Remove the upper and lower eye-lids with fine forceps and microscissors.

4. Calibration of Eye Movements

1. Use a rigid table (see Table of Materials) to support the placement of the gimbal and other instruments. Place the turtle head into the gimbal chuck so that the dorsal surface of the head is parallel to the horizon using a small bubble-level resting across the skull. Roughly position one of the eyes at the center of the gimbal's horizontal and vertical rotations.
2. Place the infrared camera, fitted with an infrared light emitting diode (LED), which is part of the video-based eye tracking system (see Table of Materials), at a viewing distance of approximately 12 cm from the turtle's eye.
   1. Angle the camera 45 degrees above the line of sight of the eye. The LED should be at the 11 o’clock position when looking at the camera lens. Center the LED along the optical axis of the eye. The camera will be slightly off axis (as viewed from above the eye).
   2. Adjust the distance of the camera from the eye so that the camera view is maximally filled by the eyeball. Ensure that the corners of the eyes (canthi) are at the edges of the horizontal view.
3. Connect the camera to the video-based eye tracking system to process the data. Split the signal to a DVD-recorder to capture the raw video. Focus the camera to obtain a clear image of the eye. Take care to fine-position the eye at the center of the camera view using the three degrees of linear adjustment (x, y, z) provided with the gimbal.
4. Detect the dark pupil by setting the threshold and contrast appropriately using the program provided with the video-based eye tracking system.
   1. Using the mouse, click on the "Video" menu and under "Mode" select "High Precision" to capture images at a sampling rate of 30 Hz (resolution of 640 pixels x 480 lines). Also under "Video", select "Dark Pupil" for "Pupil Type" and "Ellipse (rotated ellipse)" for "Pupil Segmentation Method".
   2. In the "EyeCamera" window, click on the "Pupil Search Area Adjustment" icon (small vertical rectangle with a dot in the center). Use the mouse to drag out a rectangle that limits an area around the pupil. Avoid dark areas that could be confused with the pupil.
   3. In the "Controls" window, confirm that boxes for "Auto Image" and "Positive-Lock Threshold-Tracking" are checked. Click on "Auto-Threshold" to optimize the density of scanning, which will show as green dots over the dark pupil.
5. Calibrate the video-display of the video-based eye tracking program to the rotations of the gimbal 12.5 ° (+/-) around its horizontal axis and 10 ° (+/-) around its vertical axis.
   1. In the "Controls" window, click on "Display". Check the boxes under both "Gaze" and "Stim" for "Gaze Point", "Calib Region", and "Geometry Grid". After checking the boxes under "Geometry Grid", a window will pop up and say, "The stimulus display geometry must be measured before the geometry grid can be displayed. Do you wish to do this now?" Select "Y" for yes.
   2. Using the mouse, click on the "Windows" menu and select "Stimulus". The "Stimulus" window will open showing a vertical and horizontal line crossing at the center of the display. Measure the lengths of the lines to the nearest mm. Press "Esc" on the keyboard to exit the "Stimulus" window.
   3. Using the mouse, click on the "Stimulus" menu and select "Geometry Setup". Input the lengths of the lines that were just measured. Adjust the viewing distance so that the degrees/line equal 25 ° for the horizontal line and 20 ° for the vertical line. Click on the "Store" button and close the window.
   4. In the "EyeSpace" window, select the number of calibration "Data Point" to be "9". With the turtle's eye positioned at the center, click on the center data point and click the "Re-present" button.
      NOTE: The "Stimulus" window will open, and "Get Ready" will appear at the center of the screen. A box will appear at the center location and then disappear. On its disappearance, the "Stimulus" window will close. The center position should now be calibrated.
   5. Repeat the procedure by rotating the gimbal right/left, +12.5 °/-12.5 °, and up/down +10 °/-10 ° to calibrate the remaining data points.
6. To calibrate torsional rotation, use the template fitting algorithm provided with the video-based eye tracking program. The algorithm sets a zero position based on markings of the iris and computes an angle of rotation when the markings become offset from the centroid of the pupil.
   1. Using the mouse pointer, click on the "Windows" menu and select "Torsion". Click the "START" button in the "Torsion" window. In the "EyeCamera" window, an arc will appear over the image of the eye.
   2. Adjust the radius, the angle, and the length of the arc using the sliders at a location where irregular markings are present in the iris. Check the boxes for "Real-time graphics" and "Auto-Set after adjust". If necessary, adjust the brightness and contrast in the Controls window and re-threshold the dark pupil (see step 4). Click the "Set Template" button.
7. Place a ruler in the same focal plane as the pupil and record the width of the full camera view. The value will be used later to determine the actual width of the pupil.

5. Positioning of Suction Electrode on Cranial Nerve to Evoke Eye Movements

1. Carefully place a pin reference electrode into the connective or muscle tissue remaining on the head.
2. Place the suction electrode (see Table of Materials) on the cranial nerve using a micromanipulator and dissection scope mounted on a boom. Use a fiber optic light source to view and guide the placement.
   1. Match the size of a nerve to a capillary glass tip. Trial and error is necessary to obtain a best fit around the diameter of a nerve (see step 1.2 for size recommendations). Place the glass tip onto the suction electrode. Fill the suction electrode with Ringer's solution and adjust the volume within the syringe to about half of its capacity.
   2. Carefully move the glass tip of the electrode using the micromanipulator to a position above the cut-end of the selected nerve. Ensure that Ringer's solution fills the cranium and the tip is below its surface. If necessary, use modeling clay to dam up locations where the Ringer's solution is leaking out of the cranium.
   3. Pull back on the plunger of the syringe.
      NOTE: The vacuum will draw the nerve into the end of the capillary tip. A good fit is indicated by the nerve remaining within the tip with little or no additional vacuum applied.

6. Stimulation of Cranial Nerve and Analysis of Eye Movements

1. Use a general purpose nerve/muscle stimulator with a current isolation device (see Table of Materials) to stimulate the cranial nerve via the suction electrode.
   1. Connect the suction electrode to the current isolation device using a cable. Connect the lead from the pin reference electrode to the ground connection of the isolation device.
   2. Select parameters of the currents using the dials and switches on the stimulator and isolation device. Use a range of currents from 1 to 100 µA, with frequency of 10 to 400 Hz. Use 1- or 2-ms pulses in trains lasting 100, 500, or 1,000 ms.
2. Record the timing of stimulations.
   NOTE: Transistor-transistor-logic (TTL) pulses are synchronized with the deliveries of the currents from the stimulator and communicate in real-time via a cable to input channels of the video-based eye tracking system. A software module provided with the video-based eye tracking program controls the communication.
   1. To visualize the timing of the current applications and their influence on eye movements, click on the "PenPlots" menu. Select "X Gaze Position", "Y Gaze Position", "Torsion", and "Pupil Width" to show real time raw data plots for X and Y eye positions, torsion, and pupil width. Also select the "Seconds & Markers" from the "PenPlots" menu to show a timing plot with tick marks, which appear at 1 s intervals.
      NOTE: A capital letter "T" will appear marking the onset of the TTL pulse, occurring simultaneously with the current application.
   2. To store the data of eye movements evoked by currents, click on the "File" menu and select "New Data File" under "Data". Input a file name and press "Enter". Saving data can be paused and then restarted using the combination of key commands, "Ctrl" + "p". When an experimental session is completed, select "Close Data File" off "File" menu under "Data".
   3. To help keep track of the type of currents applied, click on the "Windows" menu and select "Data Pad". The "KeyPad/DataMarker" window will appear. Click on a letter or a number to identify parameters of the current stimulations being delivered to the nerve.
      NOTE: For example, "X" could stand for 10 µA. Clicking on "X" stores its entry into the data file in real time for post hoc analysis. It also appears on the "PenPlot" for "Seconds & Markers" for ongoing observation.
3. Analyze data from the eye tracker system.
   1. Open the saved data file, which is in a text delimited format, into a spread sheet program of choice to organize the data and carry out statistical analysis.
      1. Convert the pupil width values stored in the file to real sizes in mm.
      2. Convert the values of X and Y eye positions and torsions to units of degree and use conventions for describing eye movements; therefore, positive directions of rotations: intorsion, elevation, and adduction; and negative directions of rotations: extorsion, depression, and abduction.
   2. Copy the header information onto a new worksheet. This will include values for the screen size (width and height) and the viewing distance. Eight columns of data collected at a rate of 30 Hz will follow below the header information.
   3. Go back to the worksheet containing the raw data. Do a "Find" for "X" in the last column titled "Marker" to locate where stimulation was applied with 10 µA. Find incidence of "T", marking the beginning of the current stimulation. Copy 15 rows (0.5 s) of data occurring before "T" and 90 frames after "T" (3.0 s); i.e., 3.5 s total. Paste the data in the new worksheet below the header information.
   4. Insert a blank column after "PupilWidth". In the blank column, convert to the calibrated dimension in mm:
      Horizontal pupil diameter = "PupilWidth" × the dimension of camera view width
   5. Insert 2 blank columns after both "X_Gaze" and "Y_Gaze". Normalize positions to the dimensions of the viewing screen: coordinates (0, 0) at the top left of the screen extending to (1, 1) at the bottom right. In the first blank column, translate positions to a coordinate system having (0, 0) at the center of the screen. Include the conversion to the dimensions of the screen in mm:
      X = (0.5 × width)  – ("X_Gaze" × width); Y = (0.5 × height) – ("Y_Gaze" × height)
      NOTE: The sequence of operation is for the left eye. The sequence will need to be reversed for the right eye in order to follow convention of negativity for abduction and positivity for adduction.
   6. In the second columns, use trigonometry functions to convert to angles (°) of rotation:
      horizontal rotation = arctan (X/viewing distance);vertical rotation = arctan (Y/viewing distance)
   7. Torsion is already shown in units of degrees, but to conform to convention of positivity for intorsion, if measuring is done on the left eye, multiply by -1. For the right eye, no multiplication is necessary. The program codes clockwise rotation as positive.
   8. Plot the pupil diameter and rotations as a function of time.

Wyniki

Figure 1 shows stills of images taken from a video describing the dissection. Images provide typical locations of the nerves prior to cutting from the brain.

Figure 1: Stills of images captured from the video of the dissection to show locations of the optic nerve (nII), oculomotor nerve (nIII), trochlear...

Dyskusje

Critical Steps:

The critical steps within this protocol are the following: 1) the dissection and the care taken to maintain the viability of the transected nerves; 2) the matching of sizes by the suction electrodes to cranial nerves to provide consistent responses; and 3) the placement of the head in the gimbal to provide adequate calibration of the rotations of the eye.

Troubleshooting:

The dissection can be challenging, but after completing i...

Materiały

Name	Company	Catalog Number	Comments
Red-eared slider turtles	Kons Scientific	Trachemys scripta elegans	Large size (carapace length 15-20 cm)
Sodium chloride	Sigma-Aldrich Co. LLC.	S5886
Potassium chloride	Sigma-Aldrich Co. LLC.	P5405
Magnesium choride	Sigma-Aldrich Co. LLC.	M7304
Sodium bicarbonate	Sigma-Aldrich Co. LLC.	S5761
Dextrose	Sigma-Aldrich Co. LLC.	C5767
Concentrated hydrochloric acid	Sigma-Aldrich Co. LLC.	H7020
Calcium chloride	Sigma-Aldrich Co. LLC.	C7902
pH meter	Oakton	pH 6+
Suction stimulation electrode	A-M Systems	573000	Bipolar suction electrode. Note that 573000 has been replaced with 573050.
Capillary glass	A-M systems	626000	Single-barrel borosilicate capillary glass without microfilament, length 10 cm, outside diameter 1.0 mm, inner diameter 0.50 mm
Alternative suction stimulation electrode	A-M Systems	573050	Bipolar suction electrode. Requires larger diameter capillary glass: 627000, outside diameter 1.2 mm, inner diameter 0.68 mm
Stereoscope	Lieca	GZ7	Magnification range, 10x – 70x
Fiber optic light source	Amscope	HL250-A	150W Fiber optical microscope illuminator light box
Rongeurs	Carolina Biological Supply Company	625654	stainless steel, straight spring, 5.25"
Blunt dissection probe	Carolina Biological Supply Company	627405	Huber mall probe, double-ended probe and seeker, 6"
Microscissors	Carolina Biological Supply Company	623555	Iris microdissecting scissors, stainless steel, 0.5" blades, 4.75" long
Fine forceps	Sigma-Aldrich Co. LLC.	F6521	Jewelers forceps, dumont No. 5, inox alloy, 4.25"
Curved forceps	Sigma-Aldrich Co. LLC.	Z168696	Medium tip, curved forceps, stainless steel, 4"
Scalpel handle	Sigma-Aldrich Co. LLC.	S2896	Scalpel handles, No. 3, stainless steel
Scalpel blade	Sigma-Aldrich Co. LLC.	S2771	Scalpel blades, No. 11, steel
Guillotine	Harvard Apparatus	73-1918	Kleine guillotine type 7575
Spatula	Sigma	Z648299	Micro spoon and spatula weighing set. Use small spatula: 5.9” long x 0.07” diameter handle with square end: 0.17” x 1.3” long, other end round: 0.17” x 1.27” long
Hook	Autozone	98069	SureBilt hook and pick set. Use grinder to dull sharp points of hook to prevent injury to animals mouth.
95/5% O2/CO2	Airgas, Inc.	X02OX95C2003102	5% Carbon dioxide balance oxygen certified standard gas mixture, size 200 Cylinder, CGA-296
Regulator	Airgas, Inc.	Y11244D296-AG	Single stage brass 0-100 psi analytical cylinder regulator CGA-296 with needle outlet. Use brass adjustable airline pipe valve to go from 3/8", inner diameter, vinyl airline tubing connected to regulator to a 3/16", inner diameter, airline connection going to airstone or glass pasteur pipette.
Adjustable airline pipe valve	Doctors Foster and Smith	CD-12061	Brass valve
Rigid table	Unknown	Unknown	Auto-clave door laid on top of a sturdy table. Nine 5" diameter tennis balls isolate vibrations from the top surface of the table.
5" tennis ball	Petco Animal Supplies, Inc.	712868	Petco Jumbo Pet Tennis Ball: balls are unsliced and held within an integrated frame on the underside part of the autoclave door.
Alternative vibration isolation table	Newport Corporation	INT1-36-6-N	Rigid vibration control system, integrity 1: Surface dimensions, 3' x 6'
Gimbal	ISI, International Scientific Instruments, Inc.	Stage from SUPER III-A Scanning EM	5-axis eucentric stage: X, Y, and Z linear movements, ±20 mm, 0.1 mm precision; Rotations, vertical, ±10°, and horizontal, ±12.5°, with 1.25° precision. Note: from decommission instrument.
Chuck for gimbal	Unknown	Unknown	Chuck from an old microtome of unknown manufacture was machined to fit the shaft of the specimen holder of the Scanning EM stage
Alternative gimbal	ThorLabs, Inc.	GN2/M with MBT602/M	Dual-axis goniometer (GN2/M) mounted on 3-axis microblock stage with thumbscrew adjusters (MBT602/M): design a chuck to hold turtle head with eye at 12.7 mm above top surface of goniometer (distance to point of rotation)
Video-based eye tracking system	Arrington Research, Inc.	ViewPoint EyeTracker, PC-60	Tracking method: Infrared video by dark pupil; Black and white camera (Item BC02): 30 Hz, 640 x 480; System requirements: Windows 2000, XP, 7, 8, 8.1, 10; Visual range: Horizontal +/- 44°; vertical +/- 20°; Accuracy ~0.5°; Spatial resolution ~0.15°; Pupil size resolution ~0.03 mm; Eye data: X, Y position of gaze, pupil height and width, torsion, delta time, total time, and regions of interest (ROI); Real-time communication (Item 0022): 4-Channel AnalogOut with eight TTL input channels to mark codes into the data file
Multi-position magnetic base	Harbor Freight Tools	Pittsburg, item #5645	Magnetic holder reaches up to 12" and produces 45 lbs. of magnetic pull. Use to position camera. Machine thread holes onto the end of the rod to mount cameras.
Micromanipulator	Kopf	900	5 axis manipulation for mount of suction electrode: X, Y, Z linear travel, 2 axis of rotation
Dissection scope on boom	Lieca	GZ6	Magnification range, 6.7x – 40x
Nerve/muscle stimulator	Astro-Med Grass Telefactor	Grass S88	Dual pulse voltage stimulator: two output channels that can be operated independently or synchronized to generate non-isolated constant voltage pulses (10 mv to 150 V). Pulses can be single (10 μsec to 10 sec), repetitive (0.01 Hz to 1 KHz), and trains (1 ms to 10 s) and synchronized with TTL inputs and output. Send TTL outputs via the output channels of a DB25 connector to the TTL input channels of the ViewPoint EyeTracker. Note: Astro-Med Grass Telefactor is no longer in business.
Current isolation device	Astro-Med Grass Telefactor	PSIU6	Current stimulus isolation unit: enables safe delivery of constant currents by the S88 to the preparation. The PSIU6 connects by a BNC cable to one of the output channels of the S88. Multiplier switches on the PSIU6 allow the S88 to generate a wide array of current amplitudes ranging from 0.1 µA to 15 mA.
Alternative nerve/muscle stimulator with isolation	A-M Systems	2100	Isolated Pulse Stimulator: Unit has built-in isolator to produce constant currents.