In vitro Brainstem-spinal Cord Preparation from Newborn Rat

Materials and Reagents

1. Needles (25 G) (Henke-Sass Wolf, catalog number: 4710005016 )
   
2. Neonatal rat (0-2 days old)
   
3. Sodium chloride (NaCl) (Sigma-Aldrich, catalog number: S3014 )
   
4. Potassium chloride (KCl) (Sigma-Aldrich, catalog number: P3911 )
   
5. Sodium phosphate monobasic (NaH₂PO₄) (Sigma-Aldrich, catalog number: S0751 )
   
6. Calcium chloride dihydrate (CaCl₂·2H₂O) (Sigma-Aldrich, catalog number: C5080 )
   
7. Magnesium chloride hexahydrate (MgCl₂·6H₂O) (Sigma-Aldrich, catalog number: M2670 )
   
8. Sodium bicarbonate (NaHCO₃) (Sigma-Aldrich, catalog number: S8875 )
   
9. D-glucose (Thermo Fisher Scientific, Fisher Scientific, catalog number: AC410950010 )
   
10. Sodium hydroxide (NaOH) (1 N) (Sigma-Aldrich, catalog number: 795429 )
    
11. Hydrochloric acid (HCl) (37%) (Sigma-Aldrich, catalog number: 258148 )
    
12. Isoflurane (Piramal Enterprises, Piramal HealthCare, catalog number: Isoflurane )
    
13. Vaseline (Sigma-Aldrich, catalog number: 16415 )
    
14. Artificial cerebro-spinal fluid (aCSF) solution (see Recipes)

Equipment

1. Fisherbrand^TM beaker (1 L) (Thermo Fisher Scientific, Fisher Scientific, catalog number: 15449083 )
   
2. Ice bucket (SP Scienceware - Bel-Art Products - H-B Instrument, catalog number: M18848-2001 )
   
3. Induction chamber for inhalational anesthesia (TemSega, catalog number: chamber )
   
4. Isoflurane vaporizer (TemSega, model: Isoflurane vaporizer )
   
5. Carbogen, 95% O₂, 5% CO₂ (The Linde Group, Linde Gaz, model: Carbogen B50 )
   
6. Scalpel blade (LCH MEDICAL PRODUCTS, catalog number: SCX23 ) (Figure 1a)
   
7. Small scissors (Moria, model: MC26B ) (Figure 1a)
   
8. Fine forceps (Fine Science Tools, Dumont, model: 55 ) (Figure 1a)
   
9. Dissection chamber (plastic box, 100 ml) with 2 mm layer of silicone elastomer
   
10. Binocular microscope (Olympus, model: SZX7 )
    
11. Recording chamber (10 ml) composed by a standard petri dish (60 mm) with 2 mm layer of silicone elastomer
    
12. Peristaltic pump (Gilson, model: Minipuls^® 3 )
    

Procedure

1. Artificial cerebro-spinal fluid (aCSF)
   For the preparation, see explanation in the Recipes section below. Once prepared, place a beaker containing aCSF in an ice bucket throughout experience.
   
   
2. Dissection and isolation of the brainstem-spinal cord
   
   1. Place a neonatal rat (0-2 days old) in an induction chamber for inhalational anesthesia. Animal is anesthetized with 4% isoflurane until the loss of reflex responsiveness to tail pinching (during 7 to 10 min).
      
   2. Using a scalpel, swiftly euthanize the animal by decapitation (incision must be performed in front of the ears) (Figure 1b). This allows decerebration just rostrally to the fifth cranial nerves.
      
   3. Remove the skin and muscles covering the back with forceps and scissors (Figure 1c).
      
   4. Transfer the preparation into a dissection chamber filled with aCSF at 4 °C and insert needle in each fore- and hind-limb to hold the preparation (slightly stretched) with the dorsal surface upwards (Figure 1d).
      
   5. Under binocular microscope, hold and lift up the skull bones with fine forceps. Using small scissors, cut the skull bones on both sides in order to expose the brainstem (Figure 1e).
      
   6. Using the same procedure along vertebral column, cut each vertebra on both sides to expose the spinal cord (dorsal laminectomy) (Figure 1f).
      
   7. Turn the preparation over in order to maintain its ventral surface upwards (Figure 1g).
      
   8. Hold and lift up the skull bones with fine forceps (Figure 1h) and cut all ventral and dorsal spinal roots leaving as much length as possible. The inset in Figure 1h shows how the skin, muscles and bones are removed to allow laminectomy to be performed. To avoid damage of brainstem and/or spinal cord, it is crucial to never hold nervous tissue with forceps.
      
   9. Using a spoon, carefully transfer the brainstem-spinal cord with its ventral and dorsal spinal roots still attached in a 10 ml recording chamber containing circulating aCSF (flow rate, 3-5 ml/min adjusted with the peristaltic pump) (Figure 1i).
      
   10. In order to ensure mechanical stability, the preparation is pinned down with its ventral surface upward by several pins inserted through the meninges surrounding the brainstem and the spinal cord.
       
   11. To assess the quality of the procedure, motor output activity in spinal ventral roots is recorded with glass suction electrodes filled with aCSF solution (Figure 2a). Signals (burst of action potentials) are amplified (10,000 times) by differential AC amplifiers (low cutoff, 100 Hz; high cutoff, 1 kHz), digitized and acquired via an analogical/digital interface, and finally stored on a computer. The dissection is successful when motor activities are spontaneously generated by the isolated preparation (Figures 2b-2c).
       
       
       Figure 1. Illustrations of brainstem-spinal cord dissection. a. Tools used for dissection; b. Neonatal rat (2 days old) and level of incision for decerebration; c. After decerebration, skin and muscles covering the back are removed; d-f. The dorsal surface of the brainstem and the spinal cord is first exposed; g and h. The ventral surface; i. Image showing the isolated brainstem-spinal cord preparation with its spinal roots still attached.
       
       
       Figure 2. Motor output activity in spinal ventral roots from in vitro newborn rat preparation. a. Image of an isolated brainstem-spinal cord (from a P2 newborn animal) in a recording chamber. When required, the recording chamber is partitioned either 2 or 3 compartments with barriers of syringe-ejected Vaseline to permit differential exposure of selected spinal cord regions to pharmacological treatment. b. Simultaneous recordings are made from the 4th cervical (C4) and the 1st lumbar (L1) ventral roots. Respiratory-like rhythm is spontaneously generated, showing clear inspiratory (Insp) C4 and pre-inspiratory/expiratory (pre-I; Exp) L1 alternated phases. c. Blind techniques (with sharp or patch electrodes) were used to record rhythmic activity of brainstem and spinal respiratory neurons. Here, the firing of the impaled neuron is in synchrony with L1 ventral root discharge and therefore is identified as an expiratory motoneuron (MN).
       

Data analysis

1. Respiratory and locomotor-related activities in spinal ventral roots can be recorded using glass suction electrodes filled with aCSF solution. The motor outputs generated for these two functions consist in rhythmic bursting activities, allowing several types of analysis. Thus, by recording the respiratory motor outputs (see Giraudin et al., 2008), it is possible to determine the respiratory frequency before, during and after pharmacological or lesion experiments. In order to quantify the modulation of the respiratory rhythm between different conditions, statistical analyses are performed using dedicated software, such as SigmaPlot 11.0 (Systat). The results are expressed as mean ± SEM (or SD), and Student’s t-test is used to compare the means of two groups, whereas repeated measures ANOVA and subsequent Tukey’s post hoc tests are used to compare more than two groups. The differences are considered statistically significant when P ˂ 0.05.
   
2. It is also possible to establish the phase relationship between motor-related bursting activities, such as respiratory vs. locomotor, or locomotor vs. locomotor bursting activities. In order to calculate the phase relationship, several burst activities of a given ventral root are selected and taken as reference. The phase values of burst onsets in a second ventral root are calculated by dividing the duration between the onsets of two consecutive burst onsets of each motor output by the reference cycle period. The phase values are then plotted on a circular phase diagram with a scale ranging from 0 to 1. A phase value approaching 0 or 1 indicates synchrony, whereas values close to 0.5 reflects alternation.
   

Recipes

1. Artificial cerebro-spinal fluid (aCSF) solution
1. Add 7.305 g NaCl (final concentration 100 mM), 0.249 g KCl (4 mM), 0.069 g NaH₂PO₄ (1.2 mM), 0.185 g CaCl₂ (2 mM), 0.233 g MgCl₂ (1.3 mM), 1.764 g NaHCO₃ (25 mM), 5.406 g D-glucose (30 mM) in a beaker filled with 1 L of distilled water
   
2. Mix the solution with a magnetic stirrer
   
3. Place the beaker in an ice bucket and perfuse the aCSF with 95% O₂ and 5% CO₂ for at least 30 min before use
   
4. Adjust the pH to 7.4 (use NaOH or HCl)

Acknowledgments

This protocol was adapted from our published paper: Le Gal et al. (2016), J-P. Le Gal and A. Nicolosi were supported by a doctoral studentship from the French “Ministère de l’Enseignement Supérieur et de la Recherche”. Authors thank R. Anselm for his comments and for English revision.

References

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