Quantifying Acute Changes in Renal Sympathetic Nerve Activity in Response to Central Nervous System Manipulations in Anesthetized Rats

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Summary

Methods for measuring sympathetic and cardiovascular responses to central nervous system (CNS) manipulations are important for advancing neuroscience. This protocol was developed to assist scientists with measuring and quantifying acute changes in renal sympathetic nerve activity (RSNA) in anesthetized rats (non-survival).

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Fink, A. M., Dean, C. Quantifying Acute Changes in Renal Sympathetic Nerve Activity in Response to Central Nervous System Manipulations in Anesthetized Rats. J. Vis. Exp. (139), e58205, doi:10.3791/58205 (2018).

Abstract

Renal sympathetic nerve activity (RSNA) and mean arterial pressure are important parameters in cardiovascular and autonomic research; however, there are limited resources directing scientists in the techniques for measuring and analyzing these variables. This protocol describes the methods for measuring RSNA and mean arterial pressure in anesthetized rats. The protocol also includes the approaches for accessing the brain during RSNA recordings for central nervous system (CNS) manipulations. The RSNA recording technique is compatible with pharmacologic, optogenetic, or electrical stimulation of the CNS. The approach is useful when an investigator will measure short-term (min to h) autonomic responses in non-survival experiments to correlate anatomically with CNS nuclei. The approach is not intended to be used to obtain chronic (survival) recordings of RSNA in rats. Discharges in RSNA, averaged rectified RSNA, and mean arterial pressure can be quantified and analyzed further using parametric statistical tests. Methods for obtaining venous access, recording mean arterial pressure telemetrically, and brain fixation for future histological analysis are also described in the article.

Introduction

Pre-clinical discoveries about autonomic control of the cardiovascular system inform strategies for managing disorders such as hypertension, heart failure, and chronic kidney disease. Over-activity of the sympathetic nervous system and reduced vagal cardiac tone contribute to elevated blood pressure (BP)1. Chronically elevated renal sympathetic outflow enhances catecholamine secretion and decreases renal blood flow, with deleterious consequences to the cardiovascular/renal systems2,3. To define the neurobiological pathways leading to autonomic dysfunction, studies in rodents are important for determining how central nervous system (CNS) neurons regulate sympathetic parameters. The purpose of this protocol is to provide technical information about measuring renal sympathetic nerve activity (RSNA) and BP and to outline the techniques for quantifying acute sympathetic changes in response to CNS manipulations in anesthetized rats.

Acute (non-survival) RSNA measurements (lasting min to h) are useful when scientists will probe the CNS pharmacologically, electrically, or optogenetically in anesthetized rats to determine the functions of specific nuclei. Using these methods, structures such as the solitary nucleus, periaqueductal gray, pedunculopontine tegmentum, and rostral ventrolateral medulla have been investigated to define neurobiological pathways regulating sympathetic parameters4,5,6,7. This approach is important for identifying CNS targets to be investigated further in chronic models of autonomic dysfunction8,9. To complete these experiments, the laboratory requires a soldering iron, surgical microscope, stereotaxic frame, microelectrode amplifier, and audio monitor. Depending on the factors present in the laboratory that contribute to electrical noise, the surgical/recording area may require a Faraday cage/grounding strap to reduce electrical noise in the RSNA recording. If brain analyses will require tissue fixation, a perfusion pump and fume hood are required. Data can be digitized and recorded using multiple physiologic software/data acquisition (analogue-digital converter) units4,5, with different analysis options and compatibilities for incorporating telemetric signals.

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Protocol

All methods described were approved by the Institutional Animal Care Committee at the University of Illinois at Chicago.

1. Create Bipolar RSNA Electrodes

  1. To create the electrode, cut two pieces of stainless steel wire each approximately 18 mm long. Cut one piece of polyethylene (PE-50) tubing approximately 15 mm long. Feed both pieces of wire into the tubing, leaving the wire protruding from both ends.
  2. Remove the insulation from the ends of the wires; trim the wires leaving 2-3 mm of exposed wire. On one end, crimp male pins over the exposed wire. Solder the pins securely to the wire, secure the pins inside a connector strip, and cover the connection with epoxy.
    NOTE: An alternative approach that avoids soldering is to use quick connect/release alligator clips.
  3. On the opposite end of the electrode, remove the insulation from the ends of the wires, leaving 2-3 mm of exposed wire. Bend this portion of the wires to create small "V" shaped hooks in the uninsulated wire.
    NOTE: This is the portion of the electrode that will be in contact with the renal sympathetic nerve. It is important to seal this end to prevent fluids from entering the tubing. Silicone or epoxy effectively can be used.

2. Administer Anesthesia and Prepare Surgical Sites

  1. Administer anesthesia to a male Sprague Dawley rat (age 9-11 weeks, weighing 150-400 g). Administer pentobarbital sodium 50 mg/kg via an intraperitoneal (IP) injection. To assess a stable plane of anesthesia during surgery, check toe-pinch reflex every 15 min and re-dose anesthesia as needed.
    NOTE: Pentobarbital sodium (Nembutal) was used in previous studies to achieve a sustained plane of anesthesia without interfering with the modulation of RSNA4,5,6. This protocol is for non-survival surgery, so there is no recovery/post-operative monitoring period.
  2. Prepare the surgical site according to institutional animal care guidelines (i.e., shave the rat's abdomen, back, and head; cleanse the skin with 10% povidone-iodine solution; apply eye lubricant; and place the rat on a heating pad). Maintain the body temperature at 37 °C during the experiments.

3. Cannulate the Femoral Vein (for Intravenous Access)

  1. Add heparin to 0.9% sterile saline (to achieve 20 units/mL). Fill a 1 mL syringe with the heparinized saline through a 22G needle. Connect 15 cm of PE-50 tubing to the needle and fill tubing with the solution.
  2. With the rat lying supine, create a 2 cm horizontal incision through the inguinal area. Using cotton-tipped applicators, dissect the connective tissue to expose the femoral vein and artery. To hold the incision open, either apply single-hook elastic surgical stays secured to the surgical field with silk tape or use small hemostats.
  3. Use hemostats to bend the tip of a 22G needle at a 90° angle to serve as a catheter introducer10.
  4. Visualize the vessels under the microscope. Gently separate the vein and artery using curved forceps. Place two 12 cm long 5-0 silk suture beneath the vein (one distal and one proximal); place the suture in the same manner beneath the artery.
    1. Tie the distal (bottom) suture to occlude the vein; secure the edges of this suture to the surgical field using either silk tape or small hemostats. Gently pull the vein taut but not with so much force that the vessel will tear. Position the vein perpendicular to the surgeon's dominant hand.
  5. Use a loose overhand half knot in the proximal suture to briefly occlude the vein. With delicate hemostatic forceps, gently clamp this suture to occlude blood flow. Hold the 22G needle with the bent tip in the non-dominant hand; clasp the tubing with forceps using the dominant hand.
  6. Puncture a small hole in the vein with the catheter introducer (Step 3.3) and insert the PE-50 tubing (pre-filled with heparinized saline) into the vessel; use the bent needle to keep the opening in the vessel open and to assist in positioning the tip of the catheter into the vessel10.
    1. Release the proximal suture and gently flush 0.2 mL of heparinized saline into the vein; advance the catheter. Check the blood return from the vein to ensure proper placement. Complete the proximal knot and, with distal suture tie, secure the tubing inside the vein.
  7. Use venous access during the experiments for administering supplemental anesthesia or medications and for blood collection. Incorporate a 3-way connector if regular intravenous infusions and blood sampling will be necessary. Check noxious toe-pinch reflex every 15 min to titrate anesthesia.

4. Cannulate the Femoral Artery for Mean Arterial Pressure Monitoring

  1. Visualize the artery under the microscope. Similar to the method used for venous cannulation, tie the distal suture (Step 3.4) to occlude the artery; secure the edges of this suture to the surgical field with silk tape and position the artery perpendicular to the surgeon's dominant hand.
  2. Arterial access if using a pressure transducer/infusion system
    1. Connect the pressure transducer/tubing to a 500 mL 0.9% saline bag. Flush the tubing with saline, removing all bubbles, and place the bag inside a pressure inducer bag to pressurize the system.
    2. As described in Step 3.1, fill a 1 mL syringe with the heparinized saline through a 22G needle and connect 15 cm of PE-50 to the needle (flush tubing with heparinized saline).
    3. Use a loose half knot in the proximal suture to briefly occlude the artery. Hold the catheter introducer (Step 3.3) in the non-dominant hand; hold the distal tip of the PE-50 with vessel cannulation forceps in the dominant hand. Puncture a hole in the artery with the bent 22G needle and insert the cannula into the vessel.
    4. Release the proximal suture, gently flush 0.2 mL of heparinized saline into the artery and advance the catheter as far as possible. Check for arterial blood return to ensure proper placement. Complete the proximal knot and, with distal suture tie, secure the tubing inside the artery. Connect the arterial line to the pressure transducer/tubing.
      NOTE: The distal portion of tubing can be taped to the rat's hindlimb to secure the arterial line. An alternative approach to vessel cannulation is described by Jespersen et al.;11 their protocol differs by using retractors to spread the incision, glue-rather than suture-to secure the tubing, and the approach does not include the bent needle introducer.
  3. Arterial access if using telemetry
    1. Inspect the pressure-sensing catheter under high magnification before arterial cannulation. Ensure that the catheter is free of bubbles/debris and has an intact meniscus between the fluid-filled (proximal) and gel-filled (distal) components. Prior to each implantation, refill the gel at the distal tip of the catheter. Turn on the transmitter using a magnet; monitor BP during the surgery to endure perfect placement.
    2. Use a loose overhand half knot in the proximal suture to briefly occlude the femoral artery. Hold the catheter introducer (Step 3.3) in the non-dominant hand. Hold the tip of the cannula of the telemetry unit with vessel cannulation forceps to avoid displacing gel from the tip.
    3. Puncture a hole in the artery with the bent 22G needle and insert the cannula into the artery using vessel cannulation forceps to avoid displacing gel from the tip. Advance the cannula as far as possible. Using the proximal and distal suture ties, secure the pressure catheter.
    4. Tuck the body of the telemetry implant inside the flank adjacent to the incision, and close this incision using 4-0 nylon suture on a cutting needle. Turn the telemetry devices off by magnet at the conclusion of the recording period to conserve battery life.

5. Position the Rat in the Stereotaxic Surgery Frame to Access the Brain

  1. Gently move the rat into the prone position in the stereotaxic surgery frame.
  2. Position the rat between the ear bars, and adjust the incisor bar to equalize the height of lambda and bregma. Positioning may depend on the rat strain, weight, and locations of CNS targets.
  3. Make a 2 cm rostrocaudal scalpel incision through the midline of the scalp. Using cotton-tipped applicators, firmly remove connective tissue from the skull surface. Apply hydrogen peroxide to the skull to assist in visualizing the bregma, lambda, and midline sutures.
  4. Using an atlas of the rat brain to guide targeting12, drill a burr hole osteotomy, sized for electrode access, through the skull.

6. Isolating the Renal Sympathetic Nerves

  1. Connect the wire RSNA electrode (Steps 1.1-1.3) to a 10X pre-amplifier and microelectrode amplifier.
  2. Isolate the renal nerves through a retroperitoneal incision prior to, or after, the rat is secured in the stereotaxic frame. Position the RSNA electrodes once the rat is in the stereotaxic frame. Make a scalpel incision extending from 4-5 cm below the ribs in the caudal direction, slightly lateral to the spine. Blunt dissect the incision to visualize the paraspinal muscles.
  3. Use scissors to make a very superficial 1-2 cm rostrocaudal incision where the fat meets the muscle. Using cotton-tipped applicators, spread the fat away from the muscle to visualize the kidney. It is important not to enter the peritoneal space.
  4. Use retractors to gently separate the kidney from the paraspinal muscles to visualize the renal artery and abdominal aorta. Do not stretch the vessels excessively to avoid damaging the renal nerves. Use a 2" x 2" cotton gauze pad soaked in saline to protect the kidney from injury.
  5. Under high magnification, identify the renal nerves in the incision pocket. The nerve bundles are most easily visible in the right angle formed by the aorta and the renal artery. The renal nerves closely follow the renal artery from the aorta to the kidneys.
  6. Select a segment of the nerve bundle that will be placed on the recording electrode. Gently dissect the nerve fibers from the surrounding tissue/vessel using micro-dissecting tweezers.
  7. Secure the wire RSNA electrode in a holder (e.g., an alligator clip attached to a support stand). Lower the electrode to the level of the nerve segment. Use a nerve hook to gently lift the segment of the renal nerve onto the electrode without stretching the nerve.
    NOTE: The nerve should rest inside both "V" shaped hooks in the uninsulated wire, parallel to the nerve. The electrode wires must not touch any other tissue, blood, or lymph fluid.
  8. Fill the incision with mineral oil to prevent the exposed renal sympathetic nerve from becoming dry. Use a grounding clip with one end on the skin of the incision and the other attached to the Faraday cage.
  9. Direct the signal to the amplifiers using high- and low-pass filtering (10 Hz and 3 kHz). Adjust the gain up to 10 K. Include an audio monitor to assess the bursting pattern of the RSNA. Use sampling rates ranging between 2,000-10,000 Hz4,5,6,7,8. Use an increased sampling rate when a CNS manipulation is hypothesized to cause rapid/brief sympathetic responses.

7. Record Data

  1. Assess the quality of the RSNA recording by evoking the baroreflex with a bolus injection of 1 mL of saline or 10 µg/mL phenylephrine (in 0.1 mL) intravenously. As illustrated in Figure 1, the infusion should increase BP and inhibit RSNA. An increase in mean arterial pressure of 60-80 mmHg is sufficient for renal sympathoinhibition4,13,14.
  2. Adjust the position of the electrodes to improve the signal if necessary. Repositioning is required if the nerve is not in contact with both hooks on the electrode or if any tissue, blood, or lymph fluid is in contact with the wires.
    NOTE: The need for repositioning is based on the auditory characteristics of the nerve discharges.
    1. If the bursts of RSNA are not occurring cyclically with the cardiac cycle, and if there is any interference in the recording, then carefully reposition the electrode.
    2. As respiratory movements can also affect the quality of the RSNA recording, improve the signal by gently moving the electrode into a position where the muscle movements do not disrupt the electrode during breathing.
  3. Once a clear signal is obtained, secure the RSNA electrode in place by withdrawing mineral oil and applying a silica gel to cover the nerve/electrode connection in the incision pocket. Do not move the rat before the gel has set completely.
  4. Perform CNS manipulation protocols while continuously recording RSNA and mean arterial pressure. If a microinjector/pulser is used for brainstem manipulations, a logic signal from this device can be introduced into the RSNA/BP recordings to document the timing of CNS manipulations.
  5. When the experiment is complete, determine the noise level by crushing the nerve proximal to the recording electrodes between the silica gel and the spinal muscle. Record at least 30 s of this "zero" value for RSNA4,5,6. As an alternative approach for quantifying noise, administer a short-acting ganglionic blocker such as atropine, hexamethonium, chlorisondamine, or pentolinium tartrate8,15,16,17.
  6. Carefully remove the RSNA electrode and remove any traces of silica gel from the wire electrodes. Save the electrode for re-use. Turn off the telemetry transmitter and remove it, taking care not to damage the tip of the catheter.

8. Euthanasia (Transcardiac Perfusion)

  1. Identify the locations of CNS manipulations by injecting dyes or fluorochromes, creating electrolytic lesions, or by detecting of c-fos expression.
  2. If brain analyses will require fixation, prepare the rat for transcardiac perfusion. Assess the toe-pinch reflex to ensure that the rat remains deeply anesthetized. Provide supplemental anesthesia if needed. Perform transcardiac perfusion of paraformaldehyde fixative in a fume hood.
    CAUTION: Avid skin/eye irritant.
  3. Insert tubing into the perfusion pump and prime with 0.9% normal saline.
  4. Make a 5-6 cm lateral incision through the skin and abdominal wall immediately beneath the rib cage and open the chest cavity. Carefully separate the liver from the diaphragm. Make a small incision in the diaphragm using curved blunt scissors. Inject 0.1 mL of heparin directly into the left ventricle.
  5. Pass a perfusion needle into the left ventricle (a stainless steel gavage needle works well for this step) by either puncturing it into the heart or by cutting a small incision using sharp scissors and passing the gavage needle through so the tip is visible through the wall of the aorta (but does should not reach the aortic arch). Use a surgical or electrical clip to secure the needle in place.
  6. Using an infusion pump, administer 0.9% normal saline (room temperature). Immediately create a 2-3 mm incision in the right atrium to create an outlet for the saline rinse. Do not cut the descending aorta. Continue the saline rinse until the liver changes color from red/brown to pale yellow, an infusion of approximately 400 mL over 2-3 min.
  7. Stop the pump. Switch the perfusate to the fixative (e.g., 10% formalin or 4% paraformaldehyde); infuse 400 mL over 2-3 min. Remove the brain and store the specimen in fixative solution overnight at 4 °C before transferring the tissue to 30% sucrose (30 mL of sucrose dissolved in 100 mL of 0.1 M phosphate-buffered saline) for at least 3 days or until the brain sinks, for cryoprotection before cryogenetic sectioning18.

9. Analyze Data

  1. Full-wave rectify the raw RSNA to obtain absolute values. Full-wave rectify a 10 s segment of the raw noise signal. It is important to exclude any studies that were affected by a low signal-to-noise ratio. In studies quantifying RSNA, investigators applied a priori criteria such as requiring signal to noise ratios to exceed 2:1 to 6:117,19,20.
  2. Calculate the mean rectified RSNA for non-overlapping segments (µV) and subtract the noise estimate (µV). Depending on the aims of the experiment, investigators may select intervals such as 10 s (Figure 1) or 1 s. Calculate means by using waveform analysis options in the physiologic software or exporting the data into spreadsheets to calculate averages for selected time intervals.
  3. To normalize across different animals, express values for further analysis as the percent change from baseline. Use parametric statistics to conduct group comparisons.

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Representative Results

Figure 1 illustrates a sample RSNA and BP recording from a Nembutal-anesthetized rat. An intravenous injection of phenylephrine was used to induce an increase in mean arterial pressure and to evoke the baroreflex and transient sympathoinhibition4,6. To quantify RSNA, the raw RSNA was rectified and averaged for non-overlapping 10 s segments; the noise estimate was subtracted from each segment.

Figure 1
Figure 1: RSNA and BP in response to phenylephrine injection IV. The raw RSNA (A) was full-wave rectified (B); rectified crushed "zero" RSNA is shown in inset C. Non-overlapping 10 s averages (minus noise) were calculated (D). To evoke the baroreflex, 0.1 mL of phenylephrine (1 µg/mL) was injected intravenously (at arrow). The bolus infusion elicited an abrupt increase in BP and transient inhibition of RSNA. This figure was adapted from Fink AM, Dean C, Piano MR, Carley DW. The pedunculopontine tegmentum controls renal sympathetic nerve activity and cardiorespiratory activities in Nembutal-anesthetized rats. PLoS One. 2017;12(11):e01879564. Please click here to view a larger version of this figure.

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Discussion

Critical steps for measuring RSNA include: (1) avoiding stretching of the renal artery and nerves when separating the kidney from the paraspinal muscle and when placing the nerve segment on the recording electrodes, (2) carefully dissecting the renal nerve fibers from the surrounding tissue/vessel, (3) ensuring that the electrode wires are free of tissue, blood, or lymph fluid, and (4) preventing the nerve from drying out by applying mineral oil to the renal nerve and silica gel to the nerve-electrode unit. For troubleshooting, it is important to ensure that the recording system is adequately grounded. To obtain a clear RSNA signal, the position of the electrode can be carefully adjusted while visualizing and listening to the raw RSNA signal, prior to embedding in silica gel. Successful completion of the surgery results in a RSNA signal that can be modulated by CNS manipulations for the experiments lasting several hours.

When interpreting the results, the investigators should consider the influence of anesthesia on mean arterial pressure and RSNA. This protocol uses barbiturate anesthesia (pentobarbital sodium), which can reduce mean arterial pressure and modify autonomic responses21. Depending on the experiment aims, other injectable formulations or inhalation anesthesia (via nose-cone or tracheostomy) can be used22. Researchers may consider the alternatives such as urethane23 and alpha-chloralose24. These agents have less impact on blunting cardiovascular reflexes but can pose potential health hazards to the investigator.

In addition to the methods described in this protocol, alternative approaches have been employed by other laboratories for recording and fabricating electrodes. RSNA can be recorded using stainless steel4,9, silver25, or platinum26 wire. In addition to lifting the exposed nerve segment onto the electrode wire, scientists have successfully recorded monophasic RSNA at the central ends of cut renal sympathetic nerves26. Flexibility differs based on the tensile strength of the wire (measured with kPSI units). Higher kPSI wire is more brittle but retains its shape; low kPSI wire is more flexible and less likely to break when bent, repetitively. For RSNA recordings, it is important to select a wire that can be easily bent and repositioned during recordings. The wire should not be too flexible, making it difficult to create hooks to position under the nerve, but not too stiff. The latter increases the risk of stretching and damaging the nerves. Our laboratory uses stainless steel wire with 155-185 kPSI.

Many approaches for RSNA analysis are available. Rather than quantifying the averages for 10 s recording segments and calculating the differences as the percent change, RSNA can be determined by quantifying burst frequency4,26,27. This approach may be preferred when the baseline levels and magnitudes of RSNA responses differ among rats in a study15,26. Another approach involves the rectification and integration of the RSNA signal; the RSNA amplitude (measured in mV) is summed over a selected interval of time (e.g., 20 ms)15,26. An integrator applies a low-phase filter and provides the average discharge amplitude during bursts of activity exceeding the time constant (e.g., > 20 s)15,27. Integrated signals are useful for examining the amplitude and phase of the RSNA, but this approach does not provide information about oscillatory changes. Frequency domain and time domain methods have been applied when researchers examine RSNA oscillations. The approach frequently used for RSNA is the fast Fourier transformation (FFT), which categorizes a signal into its sinusoidal oscillations, each with a distinct amplitude and phase20,26. FFT is a useful approach for examining the low- and high-frequency bursts in the RSNA and for studying respiratory and cardiac modulation of the RSNA signal.

The methods in this protocol are important for addressing hypotheses about the functional significance of CNS nuclei. Renal sympathetic nerves direct neural communication between the CNS and kidney, and therefore, acute changes in RSNA represent an important variable in cardiovascular research. Defining CNS mechanisms regulating sympathetic outflow is a priority research area, considering that renal sympathoexcitation contributes to the pathophysiology and clinical presentation of many diseases (e.g., chronic kidney disease, heart failure, arrhythmias, diabetes mellitus, and obstructive sleep apnea)28,29. Indirect measures of sympathetic nerve activity (e.g., BP, heart rate variability, catecholamine levels) are not always suitable for the studies on the functional significance of CNS nuclei. Therefore, the direct measurement of RSNA and mean arterial pressure in anesthetized rats represents a valuable method for functionally, anatomically defining the sources of aberrant renal sympathetic function.

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Disclosures

Anne M. Fink is a member of the Customer Advisory Board for Data Sciences International.

Acknowledgements

This study was supported by the National Institute for Nursing Research (K99/R00NR014369).

Materials

Name Company Catalog Number Comments
Stainless steel wire A-M Systems; Sequim, WA 791000 RSNA electrode
Polyethylene (PE-50) tubing VWR; Radnor, PA 63019-048 RSNA electrode; vessel cannulation
Miniature pin connector A-M Systems; Sequim, WA 520200 RSNA electrode
Crimping tool Daniels Manufacturing Corp.; Orlando, FL M22520 RSNA electrode
Connector strip Amphenol; Clinton Township, MI 221-2653 RSNA electrode
J-B Kwik Epoxy J-B Weld, Sulphur Springs, TX 8270 RSNA electrode
Silicone Permatex; Hartford, CT 2222 RSNA electrode
Heparin sodium; Injectable (10 mL vial, 1000 U/mL) KV Veterinary Supply; David City, NE P03466 Venous line patency
Phenylephrine HCl; Injectable (1 mL vial; 10 mg/mL) ACE Surgical Supply; Brockton, MA 950-6312 Testing renal sympathoinhibition
Single-hook elastic surgical stays Harvard Apparatus; Holliston, MA 72-2595 Incision
Silk surgical tape 3M, Minneapolis, MN 1538-0 Secure surgical stays
Needles, 20 G Sigma-Aldrich; St. Louis, MO Z192554-100EA Vessel cannulation
Dumont #7 curved forceps Fine Science Tools; Foster City, CA 11274-20 Vessel cannulation
5-0 silk suture ties Braintree Scientific; Braintree, MA SUT-S 106 Vessel cannulation
Delicate hemostatic forceps Roboz Surgical Instrument Co.; Gaithersburg, MD RS-7117 Vessel cannulation and RSNA surgery
Crile Hemostatic forceps Fine Science Tools; Foster City, CA 13004-14 Needle bending
Telemetry transmitter Data Sciences International; Minneapolis, MN PA-10 Mean arterial pressure monitoring (telemetry)
Re-gel syringe Data Sciences International; Minneapolis, MN 276-0038-001 Transmitter reuse (telemetry)
Disposable pressure transducer Transpac; San Clemente, CA MI-1224 Mean arterial pressure monitoring
Clear-Cuff pressure infuser MILA International Inc.; Florence, KY 2281339 Mean arterial pressure monitoring
Vessel cannulation forceps Fine Science Tools; Foster City, CA 00574-11 Catheter insertion
Black monofilament nylon 4-0 suture on reverse cutting needle McKesson Medical-Surgical; San Francisco, CA S661GX Secure telemetry transmitter
Telemetry receiver Data Sciences International; Minneapolis, MN RPC-1 Mean arterial pressure monitoring (telemetry)
LabChart Pro (software), PowerLab (acquisition hardware) AD Instruments; Colorado Springs, CO ML846, MX2 matrix 2.0 (Compatible with Data Science International telemetry) 3 options for software/acquisition hardware
SciWorks (software), DataWave (acquisition hardware) DataWave Technologies, Loveland, CO N/A
Spike 2 (software), Micro1401-3 Cambridge Electronic Design Ltd., London UK 1401-3
Micro-drill Roboz Surgical Instrument Co.; Gaithersburg, MD RS-6300 CNS surgery
Stereotaxic surgery frame Stoelting; Wood Dale, IL 51600 CNS surgery
Microelectrode amplifier with 10X pre-amplifier A-M Systems; Sequim, WA 1800-2 RSNA recording
Retractors Fine Science Tools; Foster City, CA 17009-07 RSNA surgery
Micro-dissecting tweezers Fine Science Tools; Foster City, CA 11251-10 RSNA surgery
Micro-hook Fine Science Tools; Foster City, CA 10064-14 RSNA surgery
Mineral oil Fisher Scientific; Waltham, MA 8042-47-5 RSNA surgery
Audio monitor A-M Systems; Sequim, WA 3300 RSNA surgery
Silica gel Wacker, Munchen; Germany RT601A-B RSNA surgery
Electrical clips Tyco Electronics; Schaffhausen, Switzerland EB0283-000 Grounding or securing perfusion needle
Bonn scissors, straight/sharp points Roboz Surgical Instrument Co; Gaithersburg, MD RS-5840 Perfusion
Gavage needle Harvard Apparatus; Holliston, MA 75-0286 Perfusion
Masterflex perfusion pump Cole-Parmer; Vernon Hills, IL 7524-10 Perfusion
Masterflex platinum-cured silicone tubing Cole-Parmer; Vernon Hills, IL 96410-15 Perfusion
Formalin (10% buffered solution; 4 L) Sigma-Aldrich; St. Louis, MO HT501128 Perfusion
Sucrose Sigma-Aldrich; St. Louis, MO S0389 Cryoprotection

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