Dissecting the Non-human Primate Brain in Stereotaxic Space

Summary

The non-human primate is an important translational species for our understanding of the normal processing of the brain. The anatomical organization of the primate brain can provide important insights into normal and pathological conditions in humans.

Abstract

The use of non-human primates provides an excellent translational model for our understanding of developmental and aging processes in humans^1-6. In addition, the use of non-human primates has recently afforded the opportunity to naturally model complex psychiatric disorders such as alcohol abuse⁷. Here we describe a technique for blocking the brain in the coronal plane of the vervet monkey (Chlorocebus aethiops sabeus) in the intact skull in stereotaxic space. The method described here provides a standard plane of section between blocks and subjects and minimizes partial sections between blocks. Sectioning a block of tissue in the coronal plane also facilitates the delineation of an area of interest. This method provides manageable sized blocks since a single hemisphere of the vervet monkey yields more than 1200 sections when slicing at 50μm. Furthermore by blocking the brain into 1cm blocks, it facilitates penetration of sucrose for cyroprotection and allows the block to be sliced on a standard cryostat.

Protocol

Part 1: Pre-processing of tissue

1. Tissue should be well perfused with paraformaldehyde, glutaraldehyde, or formalin. This can be achieved through standard transcardial perfusion typically used to harvest other organs. In the present study the subject was deeply sedated with ketamine hydrochloride (10 mg/kg, i.m.), euthanized with an overdose of sodium pentobarbital (25 mg/kg, i.v.) and perfused transcardially with 0.1 M PBS until completely exsanguinated.This is followed by a 4% paraformaldehyde solution in PBS for 5 min (~1 liter).

Part 2: Stereotaxic blocking

1. Prior to placing the head into the stereotaxic frame the coordinates of the Horsley-Clarke/interaural plane zero needs to be taken. This is the theoretical midpoint between the ears. To measure this plane, the ear bars need to be equally fitted in the apparatus, then place a scalpel blade in the stereotaxic manipulator arm and measure the midpoint between the ear bars. This is important for determining where to block the tissue based on research needs. Once this is completed the skull needs to be prepared for fixation into the stereotaxic apparatus.
2. In order to place the head into the stereotaxic frame the lower jaw will have to be removed with bone rongeurs and a scalpel. Additionally the skin, muscle, and connective tissue should be removed in order to expose the skull. Once the connective tissue is removed from the skull, expose the brain by chipping away the calvaria (the tabular portion of the occipital bone as well as the parietal, ad frontal bones). In the present experiment part of the calvaria has all ready been removed. Be careful not to completely remove the temporal bones because the ear canals will need to be intact to place the head into the stereotaxic frame. The remaining dura matter should be removed from the exposed brain. The skull is now ready to be placed into the stereotaxic frame.
3. In the same manner in which one would perform a stereotaxic surgery, adjust the eye, palate, and ear bars such that the head is securely fixed in the stereotaxic apparatus. Place the stereotaxic manipulator in the predetermined anterior/posterior (A/P) coordinates and move the manipulator to the lateral aspect of the brain. Slowly lower the blade into the brain, completely raise the blade from the brain, then move medially and lower the blade again. Repeat these two steps until the blade has reached the lateral aspect of the opposite hemisphere. This completes the first coronal block. For subsequent coronal blocks move the manipulator 1cm in the A/P axis and repeat until the entire brain has been blocked.

Part 3: Removing the brain from the skull

1. Remove the head from the stereotaxic frame and hold the exposed brain in the palm of your hand. Try to secure the brain by lightly placing coddling the brain in the palm of your hand and place your pinky finger across the frontal lobes, this minimizes movement of the brain in the skull. In order to prevent the drying of the pial surface of the brain, place a piece of PBS dampened gauze across the brain. Hold the head firmly by the skull and chip away the remaining occipital and temporal bones along with the spinal column. This exposes the base and lateral aspects of the brain. Lastly remove any remaining frontal bone and the nasal bone, which will allow access to the olfactory bulbs. It is important to remove the frontal bone last because as you remove the base of the skull the brain moves slightly and the frontal lobes can become damaged on the jagged edges of the fontal bone. Cut away and remove remaining dura matter. Carefully lift the front of the brain, slide the scalpel under the brain and free the brain from the skull.

Part 4: Measurements

1. There are a number of useful measurements that can be made prior to freezing. For example, the A/P axis of the brain with a caliper. Furthermore the specific density can be measured by weighing the brain, measuring volume by the displacement of water in a graduated cylinder then dividing weight by volume displacement (Table 1).

Part 5: Finish blocking the brain.

1. Typically when the scalpel blade is inserted into the brain it is not long enough to completely penetrate the full dorsal-ventral extent of the brain. Once the brain is removed and gross measurements are obtained, take a tissue-slicing blade and finish blocking the brain through to the ventral side of the brain (Figure 2).
2. Prior to freezing the blocks, it is necessary to cryoprotect the tissue in graded PBS-buffered sucrose solutions (10, 20, and 30%) maintained at 4˚C until the brain sinks. It typically takes an overnight incubation in 10%, 2-3 days in 20% and additional 3-5 days in 30% for the blocks to sink to the bottom of the container. A daily change of the 30% sucrose solution is recommended.

Part 6: Representative Results

There are a number of gross morphological measurements that can be made once the brain has been removed from the skull. These include A/P length, weight, and specific density (Table 1). We generally block the brain into 6-7 blocks measuring 1cm (Figure 1). Each piece is then photographed (Figure 2) and can be further dissected depending on research needs or prepared for freezing in graded sucrose solutions.

Subject	A/P  Length (mm)	Weight (grams)	Water Displacement (ml)	Specific Density (g/ml)
O2303-2-1-1	64.3	28.1	24	1.171
O5180-1	71.3	38.7	34	1.138
O2708-3-1	62.8	28.7	26	1.104
O9184-4-2	65.3	29.5	24	1.229
N459-1-14-2	68.2	31.6	26	1.215
AVERAGE	66.38	31.32	26.8	1.171
STD DEV	3.38	4.33	4.17	0.052

Table 1. Gross Morphological Measurements of the Right Hemisphere of 5 Month Old Vervets

Figure 1. Schematics for the coronal planes used for blocking the brain. This is an example of an externalized adult vervet brain. Example of the blocking procedure. The vertical lines here are spaced at 1cm, typically producing 7 coronal blocks from each hemisphere.

Figure 2. Blocks of brain tissue in stereotaxic space.Each block will yield approximately 200 sections taken at 50µm. With this sampling scheme over 1200 sections through the cortex will be taken and an additional 400-500 from the cerebellum when sliced in the coronal plane.

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Discussion

The St. Kitts vervet (Chlorocebus aethiops sabeus) is an Old World primate with similar patterns and rates of cortical and subcortical brain development to that of humans. This species has been used to model complex human behavioral disorders like anxious behavior, hypertension⁸, hemispherectomy⁹, Parkinson’s disease¹⁰, Alzhemier’s disease¹¹, and alcohol abuse¹². More recently, this species has been used to study the neuroanatomical effects of na...

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Materials

Name	Company	Catalog Number	Comments
Scalpel	Fine Science Tools	10003-12
Scalpel blades	Fine Science Tools	10011-00
Scissors	Fine Science Tools	14090-11	Any surgical scissors are sufficient
Rongeurs	Fine Science Tools	16121-14
Forceps	Fine Science Tools	11027-12
Filter paper	Fisher Scientific	09-924-150
Stereotaxic Frame	Kopf Instruments
Tissue slicing blade	Thomas Scientific