Comprehensive Profiling of Dopamine Regulation in Substantia Nigra and Ventral Tegmental Area

Summary

Dopamine is distinctly regulated in the midbrain nuclei, which contain the cell bodies and dendrites of the dopamine neurons. Here we describe a dissection and sample-handling approach to maximize results, and thus conclusions and insights, on dopamine regulation in the midbrain nuclei of the substantia nigra (SN) and ventral tegmental area (VTA) in rodents.

Abstract

Dopamine is a vigorously studied neurotransmitter in the CNS. Indeed, its involvement in locomotor activity and reward-related behaviour has fostered five decades of inquiry into the molecular deficiencies associated with dopamine regulation. The majority of these inquiries of dopamine regulation in the brain focus upon the molecular basis for its regulation in the terminal field regions of the nigrostriatal and mesoaccumbens pathways; striatum and nucleus accumbens. Furthermore, such studies have concentrated on analysis of dopamine tissue content with normalization to only wet tissue weight. Investigation of the proteins that regulate dopamine, such as tyrosine hydroxylase (TH) protein, TH phosphorylation, dopamine transporter (DAT), and vesicular monoamine transporter 2 (VMAT2) protein often do not include analysis of dopamine tissue content in the same sample. The ability to analyze both dopamine tissue content and its regulating proteins (including post-translational modifications) not only gives inherent power to interpreting the relationship of dopamine with the protein level and function of TH, DAT, or VMAT2, but also extends sample economy. This translates into less cost, and yet produces insights into the molecular regulation of dopamine in virtually any paradigm of the investigators' choice.

We focus the analyses in the midbrain. Although the SN and VTA are typically neglected in most studies of dopamine regulation, these nuclei are easily dissected with practice. A comprehensive readout of dopamine tissue content and TH, DAT, or VMAT2 can be conducted. There is burgeoning literature on the impact of dopamine function in the SN and VTA on behavior, and the impingements of exogenous substances or disease processes therein ^1-5. Furthermore, compounds such as growth factors have a profound effect on dopamine and dopamine-regulating proteins, to a comparatively greater extent in the SN or VTA ^6-8. Therefore, this methodology is presented for reference to laboratories that want to extend their inquiries on how specific treatments modulate behaviour and dopamine regulation. Here, a multi-step method is presented for the analyses of dopamine tissue content, the protein levels of TH, DAT, or VMAT2, and TH phosphorylation from the substantia nigra and VTA from rodent midbrain. The analysis of TH phosphorylation can yield significant insights into not only how TH activity is regulated, but also the signaling cascades affected in the somatodendritic nuclei in a given paradigm.

We will illustrate the dissection technique to segregate these two nuclei and the sample processing of dissected tissue that produces a profile revealing molecular mechanisms of dopamine regulation in vivo, specific for each nuclei (Figure 1).

Protocol

1. Dissection

1. On a bed of wet-ice, chill a rodent brain matrix (coronal sections segregated 1 mm apart), a Petri dish containing 5 razors, and a #11 scalpel. In a separate container, place labeled 2 ml size microfuge tubes into dry ice.
2. The investigator will choose the method of euthanasia. We have reproducible results conducting a very brief anesthesia with isoflurane, Ideally, a vaporizer should be used. However, if not available, we use a large battery jar containing a platform. With the battery jar located in an approved ventilating hood, place an isoflurane-saturated gauze pad below the platform and wait 3-5 minutes to allow the isoflurane to saturate the battery jar. Place the rat inside and remove for decapitation as soon as the rat has lost consciousness. Rapidly remove the brain (ideally in under two minutes), rinse under cold water, and place immediately in the chilled rodent brain matrix.
3. One minute after positioning the brain into the matrix, insert cold razor blades into the cooled brain, beginning around 2 mm rostral to the optic chiasm if the striatum and nucleus accumbens are desired for analysis in addition to the midbrain nuclei. Continue inserting cold razor blades with each 1 mm section until arriving midway through the pons, staggering the placement of each subsequent razor blade so as to facilitate easier removal of each individual blade.
4. When pulling out the razors, look for the start of the hippocampus. When it has completely wrapped around the midbrain, begin to take sections using the #11 scalpel blade, as illustrated in Figure 2.
5. Immediately place the dissected tissue into the pre-cooled microfuge tube on the dry ice. In the rat, expect to be able to dissect SN and VTA from a minimum of two coronal slices and a maximum of three. Store tissues at -80 °C until ready for processing.

2. Tissue Analysis: HPLC for Dopamine and Metabolites

For complete information on the HPLC equipment and maintenance, refer to HPLC analysis at the end of the manuscript.

1. Gently homogenize tissue immediately after removal from dry-ice using ice-cold 0.1 M HClO₄-EDTA solution (0.1 M HClO₄ & 0.1 mM EDTA) ⁹, which contains N-methyl dopamine at a concentration of 20 ng/mL that serves as an internal standard for recovery of sample during the HPLC analysis. The homogenizer we use is a Branson Sonifier 150, with the setting at 10% of full power (1 of 10). The following sonication volumes are recommended:
   In rat, SN = 250 μl (unilateral dissection), 400 μl (bilateral dissection), VTA = 200 μl (unilateral dissection), 400 μl (bilateral dissection).
   In mouse, (bilateral dissections only), SN = 200 μl, VTA = 200 μl.
2. After homogenization, hold samples on dry ice. Samples are then centrifuged (DuPont Sorvall Microspin 24S) at 12,000 RPM to sediment the protein pellet to be used for western blot determinations. The supernatants are injected directly into the HPLC. The following injection volumes are recommended for precise analysis in rat or mouse: SN = 150 (from either prep.), VTA = 160 μl (from either prep.)
3. The stock standard is prepared at 1 mg/ml by adding the appropriate amount of monoamines and metabolites* of dopamine component to 0.1 M perchloric acid 0.1 mM EDTA. The concentration of each compound is 1 mg/ml except tryptophan which is 5 mg/ml. The stock standard is divided into 10 μl aliquots and stored in the ultralow until needed.
   *All weights are corrected for the salt form of the compound if applicable.
   Prepare the working standard by diluting a 10 μl aliquot of stock standard to 100 ml of the perchloric acid solution. Concentration of the working standard is 0.1 μg/ml except tryptophan which is 0.5 μg/ml. 50 μl of this working standard is injected into the HPLC for an on-column amount of 5 ng of each component except tryptophan which is 25 ng.
4. Determination of dopamine recovery within sample aliquot:
   There are several steps involved to determine the dopamine recovery from a sample aliquot.
5. First, divide the dopamine peak height of the sample by the dopamine peak height of the standard and multiply this ratio by the total amount (ng) of dopamine in the standard. Our standard dopamine concentration is 0.1 ng/μL and 50 μL of standard is assayed. Thus, the quantity of dopamine in the standard is 5 ng. Thus, the equation below can be used to determined dopamine recovery in a given sample:
   (Dopamine peak height in sample/dopamine peak height in standard)*5 ng
6. Correcting for loss of sample using the internal standard N-methyl dopamine:
   The actual recovery of N-methyl dopamine is calculated in the same way as dopamine by dividing the N-methyl dopamine peak height in the sample by the N-methyl dopamine peak height of the standard and multiplying this ratio by the total amount (ng) of N-methyl dopamine in the standard. Like dopamine, our standard N-methyl dopamine concentration is 0.1 ng/μL. 50 μL of the standard is assayed. Thus, the amount of N-methyl dopamine in the standard is 5 ng. Thus, the equation below can be used to determine N-methyl dopamine recovery in a given sample:
   (N-methyl dopamine peak height in sample/N-methyl dopamine peak height in standard)*5ng
   However, because the N-methyl dopamine in each sample comes not from the sample itself but from the HPLC buffer, the amount of N-methyl dopamine expected in each sample is calculated. The N-methyl dopamine concentration in HPLC buffer is 20 ng/mL or 0.02 ng/μL, so the expected amount of N-methyl dopamine in each sample is found by multiplying the N-methyl dopamine concentration of the HPLC buffer by the aliquot volume of each sample used for HPLC analysis. This is demonstrated in the equation below:
   (0.02 ng/μL)*(aliquot volume of sample used for HPLC analysis)
7. The difference between the expected and recovered N-methyl dopamine can then be used to correct the for the amount of dopamine recovered by adjusting for any sample loss. Simply take the ratio of expected N-methyl dopamine/recovered N-methyl dopamine and multiply this by the amount of dopamine recovered. Thus, the overall equation for the amount of dopamine in a sample aliquot is given below:
   (Dopamine peak height in sample/dopamine peak height in standard)*(N-methyl dopamine peak height in standard/N-methyl dopamine peak height in sample)* (0.02 ng/μL)*(aliquot volume of sample used for HPLC analysis)
8. Total dopamine recovered from a sample:
   The value of dopamine recovered from a sample aliquot is then used to extrapolate the total amount of dopamine in a given sample. This is done by dividing the recovered amount (ng) of DA by the aliquot volume and multiplying this value by the total volume of HPLC buffer that the sample was sonicated in. This is given by the equation below:
   (amount (ng) of dopamine in sample aliquot/volume of sample aliquot)*(Total volume of HPLC buffer into which sample was sonicated).
   The reader is referred to the following studies ^2,4,10 for a comprehensive presentation of the assessment of dopamine and metabolites in conjunction with readouts from dopamine-regulating proteins in not only SN and VTA, but striatum and nucleus accumbens as well.

3. Tissue Analysis: Total Protein and Final Normalization of TH and DAT Results

1. Place the precipitated protein pellets (derived from the HPLC buffer treatment) into wet ice to maintain 4 °C. Ensure that all buffer has been removed and archived (if confirmatory analysis is required). If the SN or VTA is to be processed bilaterally (rat only), add 300 μL (SN) or 200 μL (VTA) of 1% SDS containing 5 mM Tris (pH 8.3) and 1 mM EDTA to the pellet and sonicate. Add 150 μL of the SDS solution to SN pellets or 100 μl to VTA pellets if processing tissue from unilateral dissections.
2. Place the samples in near boiling water for ~5 minutes to complete protein denaturation and allow to cool to room temperature. Ensure caps are securely held at this step.
3. Determine protein concentration in the samples using the BCA assay, including a protein standard curve (albumin standard) range of 2 - 40 μg protein. Assay 5 μl volume of the sample in triplicate and use the median value to determine protein quantity against the standard curve. Divide by the assay volume for protein concentration. Note this is the first of two steps taken for normalizing total TH, DAT, and VMAT2 results to total protein recovery.
4. Prepare the samples with sample buffer (containing dithiothreitol) for reducing SDS-electrophoresis on 10% acrylamide gels. Ideally, the final total protein concentration should be ~2 μg/μl. The reason for this concentration selection is to reduce the sample volume necessary for the ultimate determination of TH phosphorylation, as ~100 μg of total protein will be necessary for loading to precisely quantify ser31 and ser40 TH phosphorylation. If yellow color is seen in sample after adding sample buffer, the sample is too acidic. Add 1 M Tris (pH 8.2) in 10 μl increments until blue color is restored.
5. Prepare the samples as follows for the following determinations of dopamine-regulating proteins:
6. TH: Against a calibrated standard for TH protein (as ng), the concentration of TH (as per ng TH per total μg protein) in the SN is expected to range from ~0.05-0.27 ng TH per μg total protein ^2,4,7,10,11. Against a linear TH standard curve, ranging from 0.5 - 5.0 ng TH and using primary antibody to TH (Millipore cat# AB152, 1:1000 dilution in PVP T-20 blocking solution) which produces a linear standard curve, the optimal load of total protein from the SN should be ~10 μg. The concentration of TH in the VTA ranges from ~0.4 to 1.0 ng TH per μg protein ^4,11. Thus, total protein load for VTA should be ~5 μg.
7. DAT: The relative quantities of DAT in SN or VTA are significantly less than that in the cognate terminal field regions of striatum and nucleus accumbens ⁴. The relative expression of DAT as normalized to recovered TH protein is also significantly lower in SN and VTA. Accordingly, protein loads for quantifying DAT protein in SN or VTA need to be much greater compared to sample loads of the terminal field regions. A minimum of 30 μg of total protein is needed for precision in DAT assessment in VTA and a nominal load of 50 μg total protein is need for assessment in the SN. The primary antibody used is Santa Cruz, cat# sc-1433.
8. VMAT2: The expression of VMAT2, as normalized to total protein, is greater in the mesoaccumbens than nigrostriatal regions. However, relative to TH expression, VMAT2 expression is greatest in SN and least in striatum ⁴. Using Santa Cruz cat# sc-15314, a nominal total protein load of ~40 μg to be best for quantification of VMAT2.
9. Run the appropriate quantity of total protein using SDS-PAGE on 10% acrylamide gels. The Bio-Rad Protean II electrophoresis unit is used for the determinations, which is a large gel format. Transfer the proteins onto 0.45 μm pore size nitrocellulose. For the transfer, a Hoeffer tank set to at least 27 Volts allows the transfer to take place over night.
10. Allow the blots to dry for at least 30 minutes and then stain with Ponceau S solution (1% Ponceau S in 5% glacial acetic acid) for ~5 minutes. De-stain vigorously with 0.2% HCl solution until individual protein bands clearly resolve and background staining is removed. Obtain an image of the Ponceau S staining using Image J to further quantify relative protein loads in each lane and normalize TH, DAT, or VMAT2 results (Figure 3).

4. Tissue Analysis: Site-specific TH Phosphorylation

The phosphorylation of TH at ser31 or ser40 can increase L-DOPA biosynthesis in catecholaminergic cells ¹². Although the amount of phosphorylation at each site necessary to increase L-DOPA biosynthesis in dopaminergic brain regions like SN and VTA is not established, there is evidence that ser31 phosphorylation plays a significant role in regulating L-DOPA biosynthesis ¹⁰ and co-varies with DA tissue content among the striatum, nucleus accumbens, SN, and VTA ^{2, 10}. Nonetheless, inclusion of ser40 determinations are necessary, as numerous studies show it can affect TH activity, particularly if a threshold of phosphorylation is reached ¹².

While ser19 phosphorylation does not affect TH activity alone ^13,14, it can be considered a sentinel for Ca²⁺-dependent signaling in the DA neuron, given that extracellular Ca²⁺ is necessary to increase ser19 phosphorylation under depolarizing conditions ¹². Furthermore, there is a significant positive correlation of ser19 phosphorylation with ser31 phosphorylation only in the SN and VTA ¹⁰, signifying that ser19 phosphorylation status could affect ser31 phosphorylation, and thus indirectly L-DOPA biosynthesis.

Sample load considerations for optimal quantification of site-specific TH phosphorylation stoichiometry: Below, the considerations required for accurate and precise determinations of site-specific TH phosphorylation in dissected tissues is presented. When possible, a calibrated TH phosphorylation standard should be included in the assessment of sample TH phosphorylation. The sample load must take into account inherent stoichiometry at each phosphorylation site so that the assay quantifies phosphorylation within the dynamic working range of the antibody being used. As a final note, the inherent total protein coming into the assay for each sample should be also loaded in the standard curve lanes. This is easily achieved with a carrier protein (such as rat liver) which does not express TH.

1. ser19. Of the three phosphorylation sites, ser19 phosphorylation stoichiometry levels are greatest in SN and VTA, ranging from 0.15 - 0.25 ^2,10,11. The other consideration is that by our detection method, ser19 ps is quantified in linear range between 0.5 and 5.0 ng phospho-ser19 ¹⁰. Given these considerations, a total TH protein load between 5 and 10 ng (thus giving an estimated 0.75 - 2.5 ng phospho-ser19 from the sample) would provide a reliable measure of ser19 TH phosphorylation. We use Phosphosolutions primary (Cat. #p1580-19) at 1:1000 dilution.
2. ser31. ser31 phosphorylation stoichiometry levels are comparatively less in SN and VTA compared to their cognate terminal field regions, ranging from ~0.04 - 0.10 ^2,4,10,11. By our detection method, ser31 ps is detected in linear range between 0.5 and 7.0 ng phospho-ser31 ¹⁰. Given these considerations, a total TH protein load between 10 and 30 ng (thus giving an estimated 0.50 - 3.0 ng phospho-ser31 from the sample) would provide a reliable measure of ser31TH phosphorylation. See Figure 4A for an example of ser31 quantification. Our primary antibody is an in-house affinity-purified antibody that was manufactured by 21^st Century Biochemicals, (Boston, MA), and validated for specificity the phospho-epitope using our in-house standards ².
3. ser40. ser40 phosphorylation stoichiometry levels in SN and VTA range from ~0.02 - 0.06 ^2,4,10,11. By our detection method, ser40 ps is detected in linear range between 0.2 and 2.0 ng phospho-ser40 ¹⁰. Given these considerations, a total TH protein load between 10 and 30 ng (thus giving an estimated 0.20 - 1.8 ng phospho-ser40 from the sample) would provide a reliable measure of ser40TH phosphorylation. See figure 4B for an example of ser40 quantification. We use Phosphosolutions primary (Cat. #p1580-40) at 1:1000 dilution.

5. Representative Results

1. Dopamine in SN vs. VTA. There are three readouts of dopamine (or metabolites) that may be taken in quantitative analysis; as per total recovered from dissection, per protein, and per TH protein (demonstrated for striatum, SN, nucleus accumbens, and VTA in Table 1 below). Total dopamine recovery between SN and VTA is fairly comparable, ranging between 6-9 ng for two to three coronal slice dissections ². Normalizing dopamine recovery to total protein will show that, based upon the dissection method employed, that the VTA will have greater dopamine per total protein, averaging 6-8 ng / mg protein in SN and 9-10 ng / mg protein in VTA ^{2, 4}. Finally, normalization of dopamine to total TH recovered should also reveal a difference between SN and VTA, being greater in the VTA ¹⁰, and ranging between 0.2 and 0.8 ng dopamine per ng TH protein between the two regions ^2,10.

   DA region	Total DA recovered	DA per mg protein	DA per ng TH
   striatum	214 ± 16	165 ± 13	0.56 ± 0.11
   SN	8.4 ± 0.8	6.1 ± 0.5	0.18 ± 0.03
   Nucleus accumbens	60 ± 6	75 ± 4	0.77 ± 0.03
   VTA	6.0 ± 1.0	9.2 ± 1.4	0.22 ± 0.03

2. Total proteins: TH, DAT, VMAT2 Using the calibrated TH protein standard for quantification, more TH is recovered in SN than the VTA from the dissection (60 ng in SN and 26 ng in VTA ²). However, when normalized to protein, this relationship reverses, with TH per total protein in the VTA being ~3- to 5-fold greater than in the SN, (~0.32 ng / μg protein in VTA and ~0.09 in SN) ^4,10.
   The expected recovery of DAT in SN and VTA is similar, with slightly more recovery in the VTA as per total protein or as per total TH recovered ⁴. Notably, DAT protein is much less abundant in these regions compared to the cognate terminal field regions ⁴.
   VMAT2 recovery as per total protein is greater in the VTA versus SN ⁴. However, when normalized to TH protein, there is slightly greater recovery in the SN ⁴.
3. Site-specific TH phosphorylation From a number of studies, there have been consistent results in ser19, ser31, and ser40 phosphorylation quantity in the SN and VTA, and also in relation to the cognate terminal field regions. Ser19 phosphorylation is notably greater in the SN and VTA (~0.2-0.3) compared to striatum and nucleus accumbens (~0.05-0.15) ^2,4,7,10,11. Ser31 phosphorylation is significantly less in the SN and VTA compared to their cognate terminal field regions, being ~0.06 - 0.10 between these somatodendritic regions ^2,4,7,10,11. During inhibition of aromatic acid decarboxylase with NSD-1015, there is a 2-fold increase in ser31 phosphorylation in the VTA only ¹⁰. Ser40 phosphorylation ranges between 0.02 and 0.05 in the SN and VTA and generally this stoichiometry does not significantly differ from the cognate terminal field regions ^2,4,7,10,11.

Figure 1. Dopaminergic readouts from one tissue dissection.

Figure 2. Dissection Technique for isolating the midbrain dopaminergic neuropil. Technique for dissecting substantia nigra (SN) from ventral tegmental area (VTA). 1. Remove overlying cortex and hippocampus (these structures have already been removed in the above image). 2. Make a vertical cut separating the pigmented area of the SN from the VTA. 3. Make a horizontal cut at or near the midline just above the dorsal and lateral most part of the SN. 4. Tease the SN away from the rest of the brainstem. Once SN has been removed, similarly tease the VTA away from the rest of the midbrain. Note: this section is typically observed at coordinates, relative to Bregma, at AP 5.7.

Figure 3. second (and final) normalization of total protein load-Ponceau S staining for Image J analysis. Ponceau S protein staining of a total TH determination in rat substantia nigra samples. The first five lanes form the left are the standard total TH curve, to which 28 μg protein from rat liver homogenate was added to mirror the protein load from the substantia nigra samples. The next lane contains molecular weight (MW) markers. The remaining lanes contain ~28μg protein from rat substantia nigra samples. The protein loads are based on the protein concentration of each sample as determined by the BCA method. However, despite what should be equal loads, there are variations in the darkness of Ponceau S staining between the samples indicating a slight variability in protein concentrations, which is corrected for by normalization using ImageJ analysis to analyze the amount of Ponceau S staining for each sample.

Figure 4. Representative TH phosphorylation results from controls and treatments. Representative ser31 phosphorylated tyrosine hydroxylase (pTH) and ser40 pTH Western blots from saline and methamphetamine treated Wistar rats from a previous study⁴. A. ser 31 pTH in rat substantia nigra samples. The calibrated ser 31 pTH standard curve ranges from 0.3 ng to 2.0 ng and is within the linear range of detection. Based on previous Western blot analysis of total TH levels, 6 ng of total TH were loaded for each sample. B. ser40 pTH in rat ventral tegmental samples. The calibrated ser40 pTH standard curve ranges from 0.2 ng to 1.5 ng and is within the linear range of detection. Based on previous Western blot analysis of total TH levels, 9 ng of total TH were loaded for each sample.

Discussion

As outlined in Figure 1, the methods detailed above should yield multiple readouts of dopamine and its regulating proteins TH, DAT, and VMAT2 from one sample of SN or VTA obtained from either the rat or mouse. Again, the benefits of carrying out this protocol are that the investigator can obtain operationally-matched readouts of how dopamine is regulated in vivo under virtually any experimental paradigm and, in doing so, save significant experimental resources by reducing the number of animals required in any experiment.

It is absolutely imperative that the investigator observe temperature requirements imposed during the dissection (4° C), storage of tissue (at least -70° C), tissue sonication (immediate sonication after removal from storage temperature) in ice-cold HPLC buffer and subsequent pellet formation and processing. Once the pellet is sonicated and boiled in SDS solution, the samples may continue to be further processed at room temperature. Storage of archived HPLC analyzed sample and the sample buffer prepared samples for protein analysis should be at -80° C.

Again, the major advantage of the protocol is the innate approach to operationally-match results pertaining to dopamine regulation in vivo. Furthermore, normalizing dopamine tissue readouts to markers of dopaminergic neuropil (TH, DAT) provide a large measure of assurance that the investigator is dissecting SN or VTA with consistency and accuracy. Given the involvement of dopamine in the addiction, psychiatric disorder, and locomotor arenas, this protocol could be employed in many experiments. One notable limitation is that the interpretation of TH phosphorylation results should be conservative, as it is not known at this time the extent to which an increase in phosphorylation at ser31 or ser40 is required in vivo to increase L-DOPA biosynthesis. However, as mentioned, there is evidence that ser31 phosphorylation appears to regulate L-DOPA biosynthesis and has a role in regulating total dopamine tissue content in the CNS ^2,10. At this time, standards for TH protein and TH phosphorylation are not commercially available. However, this laboratory has maintained and expanded such standards based upon those used when the first paper on TH phosphorylation regulation in vivo was published ¹¹. Still, it is possible to normalize dopamine tissue content to recovered TH protein in these discrete regions using this protocol.

Materials

Name	Company	Catalog Number	Comments
HPLC system:
The basic system consists of a Shimadzu LC10-ADvp HPLC pump, a Waters WISP 717 automatic sample injector, a 250 X 4.4 mm 5 micron Spherosorb ODS-1 C18 reverse-phase column (Waters), a Bioanalytical Systems (BAS) TL12 dual glassy carbon electrode, two BAS LC4B electrochemical detectors, and a Waters Empower 2 data collection and integration system.
The column is maintained at 30-45 °C (BAS LC22A column heater). The mobile phase is 0.1 M sodium phosphate (pH 3.0), 0.1 mM EDTA, 0.2-0.4 mM 1-Octane Sulfonic Acid (Eastman-Kodak), and 0.35% acetonitrile (v/v), filtered through a 0.45 micron filter. Flow rate is of 1.2 ml/min. Four liter batches of mobile phase are optimized for separations by adjusting the pH, Octane Sulfonic Acid and column temperature. The mobile phase is recycled, and is continuously purged with helium gas to remove dissolved oxygen. Recycling of the mobile phase is almost essential to maintain good resolution for a reasonable period of time. The mobile phase shelf-life is maintained by using a flow switch (controlled by the integrator) to divert to waste the first 2-7 min of each run.
The electrodes are maintained at potentials of approximately 0.78 and 0.95V with respect to a Ag/AgC1 reference electrode. The electrode at the higher potential is used exclusively for the determination of tryptophan (and the NMDA internal standard). The 0.78 V potential provides a superior signal to noise ratio for detection of the monoamines and compounds, other than tryptophan. The chromatograms are stored on the hard drive of the Empower workstation, and subsequently processed and the data transferred directly into an Excel spreadsheet for computation of metabolite amounts and compilation of group data.
Pump: Shimadzu LC-10AD Cell: BAS Cross Flow. Glassy carbon working electrode at 0.780 and 0.950 V potential. Detector: BAS LC-4B operated in dual channel mode. Data Acq. System: Waters Empower Pro 2. Injector: Waters WISP 717 Column: Waters Spherosorb ODS-1, 5 μM particle, 4.4 mm X 250 mm.
Sodium Dodecyl Sulfate (SDS)	J.T. Baker	4095-02
Trizma Base	Sigma	T1503-1KG
Trizma HCl	Sigma	T3253-1KG
Glycerol	Sigma	G8773-500 mL
PVP-40	Sigma	PVP40-1KG
dPBS	Gibco	21600-069
Tween20	Sigma	P1379-500 mL
Glycine	Sigma	G8898-1KG
Ponceau S	Fluka	81460
Bromophenol Blue	Sigma	B8026-5G
Dithiothreitol	Sigma	D-9163
Protein Standard 2 mg BSA	Sigma	P5619-25VL
Pierce BCA Protein Assay Reagent A	Thermo-Fisher Scientific	23223
Precision Plus Protein Standard	Bio Rad	161-0373
[125I]-protein A, specific activity	Perkin-Elmer
Table 2. Specific reagents.
10% SDS			10 g SDS, 100 mL DI H20
1% SDS (pH to 8.2)			10 mL 10%SDS 60.5 mg Trizma Base 37.22 mg EDTA 90 mL DI H20
Copper II Sulfate Solution			1 g Copper II sulfate 25 mL DI H20
3X Sample Buffer			Trizma Base 2.27 g SDS 6 g Dithiothreitol 0.463 g Glycerol 30 g Bromophenol Blue 10 mg D I H20 (initially add above reagents to 40 mL of H20 in a graduated cylinder; then add H20 until volume reaches 100 mL) HCl (add as needed to reach pH of 6.85) Freeze solution in 50 2.0 mL tubes. (makes 100 mL): Volume of 3X Sample Buffer needed = ½ volume of SDS used in sample.
1X Sample Buffer			Dilute 3X Sample Buffer down to 1X sample buffer using DI H20
10X Running Buffer (Makes 4 L)			Trizma Base 121.1 g Glycine 577 g SDS 40 g
10X Transfer Buffer: (Makes 4 L)			Glycine 360 g Trizma Base 96 g
Ponceau			Ponceau S. 0.5 g Acetic Acid 5 mL DI H20 95 mL
.2% HCl Solution			5.2 mL HCl in 500mL of DI H20
PVP-T20 Blocking Soln. (Makes 4 L)			PVP-40 40 g dPBS 38.2 g Tween20 2 g Thimerisol 0.4 g 1M Tris pH 7.6 (60.6 g Tris HCl + 13.9 g Tris Base in 500 mL DI H20)- 50 mL
10X Blot Buffer (Makes 4 L)			Tween 20 20 g Tris Base 14 g Tris HCl 61 g
Table 3. Protein Assay and Western Blotting Formulas.
Tyrosine hydroxylase standards: The calibrated TH protein and phosphorylation standards used by this laboratory are derived from PC12 cell extracts, which were analyzed for TH protein content and phosphorylation stoichiometries against a previously calibrated TH standards that ultimately originated from the laboratory of Dr. John Haycock 11.