Cocaine self-administration in mice with forebrain knock-down of trpc5 ion channels

Canonical transient receptor potential (TRPC) channels are a family of non-selective cation channels that play a crucial role in modulating neuronal excitability due to their involvement in intracellular Ca2+ regulation and dendritic growth. TRPC5 channels a) are one of the two most prevalent TRPC channels in the adult rodent brain; b) are densely expressed in deep layer pyramidal neurons of the prefrontal cortex (PFC); and c) modulate neuronal persistent activity necessary for working memory and attention. In order to evaluate the causal role of TRPC5 in motivation/reward-related behaviors, conditional forebrain TRPC5 knock-down (trpc5-KD) mice were generated and trained to nose-poke for intravenous cocaine. Here we present a data set containing the first 6 days of saline or cocaine self-administration in wild type (WT) and trpc5-KD mice. In addition, we also present a data set showing the dose-response to cocaine after both groups had achieved similar levels of cocaine self-administration. Compared to WT mice, trpc5-KD mice exhibited an apparent increase in self-administration on the first day of cocaine testing without prior operant training. There were no apparent differences between WT and trpc5-KD mice for saline responding on the first day of training. Both groups showed similar dose-response sensitivity to cocaine after several days of achieving similar levels of cocaine intake.


lters the exc
tability of the PFC by biasing neurons towards strong inputs, such as those associated with drug cues, which may diminish cognitive function 7 .Understanding the mechanism underlying how PFC excitability influences the behavioral responses to psychostimulants is fundamental to learning how to reverse these maladaptive alterations in order to treat addiction.

Canonical transient receptor potential (TRPC) channels are a family of non-selective cation channels that play a crucial role in modulating neuronal excitability due to their involvement in intracellular Ca 2+ regulation 8 .The TRPC5 isoform has been shown to play a role in dendritic growth and arborization through CaMKII-mediated mechanisms throughout the brain 9,10 , as well as the expression of fear conditioning in the amygdala 11 .TRPC5 channels a) are one of the two most prevalent TRPC channels in the adult rodent brain 12 ; b) are densely expressed in deep layer pyramidal neurons of the PFC 12 ; and c) modulate neuronal persistent activity necessary for working memory and attention 13 .

Since deep-layer pyramidal neurons of the PFC are known to project to limbic structures that subserve reward, such as the ventral tegmental area, nucleus accumbens, amygdala, laterodorsal tegmentum 14 , and the rostromedial tegmental nucleus 15 , TRPC5 channels may influence the ability of cortical networks to exert inhibitory control over these structures.Consequently, motivational and drug rewardseekin behaviors may be affected.In the present data sets, we gathered data from mice that lack functional TRPC5 channels in their forebrain CaMKII-expressing pyramidal neurons to measure their cocaine self-administration behavior as an index of cocaine reward.


Materials and methods

Subjects 19 adult (25-30 g) male C3H mice were group-housed until surgery.Mice were maintained in a reverse 12 hr light:dark cycle (lights off at 7:00 am) with access to food and water ad libitum.Using the cre-lox system, forebrain specific knock-down of trpc5 was achieved by crossing floxed trpc5 mice with mice that express Cre recombinase under the control of the aCaMKII promoter,

here Cre transgene exp
ession was restricted to excitatory neurons in the forebrain.Breeding pairs of the floxed trpc5 mice were initially obtained from Dr. Lutz Birnbaumer at the NIEHS and bred at the Institute for Behavioral Genetics.CaMKII-Cre mice were obtained from UTSW Medical Center, Dallas.All procedures were approved by the Institute for Animal Care and Use Committee of the University of Colorado Boulder.


Surgery

Prior to behavioral experimentation, mice were anaesthetized with a cocktail of 80 mg/mL ketamine and 6 mg/mL xylazine (Sigma Aldrich) and implanted with intravenous catheters as previously described 16 .Chronically implanted custom catheters consist of Silastic tubing that is affixed to 23-gauge steel tubing bent at a right angle and inserted into a plastic hypodermic needle hub bound to a circular p

yurethan
backmount and surgical mesh.Catheters were steam autoclaved and rinsed with 70% ethanol prior to surgery.The skin area on the back and above the jugular vein were shaved and prepared with Betadine scrub, 70% ethanol, and 1% Zephiran to prevent infection.Following incisions and exposure of the right external jugular vein, catheter tubing was channeled subcutaneously from the back out the chest above the exposed vein.Catheter tubing was inserted approximately 7 mm into the vein and secured to the vein and surrounding tissue with sterile suture.Following successful insertion and jugular attachment, the incisions were sutured, stapled, and fixed with Vetbond (3M).The neck of the needle hub contains the 23-gauge tubing that remains capped when animals are not connected to the intravenous self-administration apparatus.Catheters were flushed with heparinized pyrogen-free sterile physiological saline daily to detect resistance to flow and patency.If animals' nose-poking behavior deviated by >20% of mean responding, catheter integrity and access to the jugular vein was examined using 10 mg/kg Sodium Brevital.If animals did not exhibit sedation within 3 seconds they were omitted from the study.Requests for the customized mouse catheter system used in this study should be directed to http://neuro-cloud.net/nature-precedings/pomrenze 16.


Self-administration

Seven days following catheter implantation mice (Saline -trpc5-KD (n = 8), trpc5-WT (n = 8); Cocaine -trpc5-KD (n = 9), trpc5-WT (n = 10)) were individually housed in self-administration operant chambers that contain two identical nose-poke portals (active and inactive).For acquisition and maintenance of cocaine (unit dose = 0.75 mg/kg/infusion; compounded in pyrogen-free sterile physiological saline;

IDA) self-administra
ion, mice received continuous reinforcement (fixed-ratio 1) of cocaine paired with a 10-second LED illumination and 10-second time-out following a nose-poke into the "active" portal.Inactive portals yielded no consequence.All studies were done without prior operant training.Infusions of 50 uL were delivered over a 4-second time period.For the data set presented mice were exposed to a 3-hr saline self-administration pretest on the first day.Subsequent cocaine daily 3-hr sessions continued until stable responding (> 20 infusions, < 20% variability in number of infusions across three daily sessions, > 70% discriminative responding in "active" portal vs "inactive" portal) was achieved in both groups.All genotypes were blind to the investigators.


Dose-response

After acquisition of cocaine self-administration and stable maintenance for ≥ 6 days, mice (trpc5-KD (n = 9), trpc5-WT (n = 10)) were challenged with a dose-response schedule of varying unit doses (0.05, 0.1, 0.75, and 2.0 mg/kg/infusion) of cocaine (one unit dose per session).The mean number of cocaine infusions at each unit dose was determined during two separate consecutive sessions.


Results

All mice were ex

sed to the sel
-administration chambers to nosepoke for light and saline on their first day of training to establish their baseline levels of exploratory behavior between treatment groups.Cocaine replaced saline thereafter and mice were trained to self-administer cocaine (0.75 mg/kg/infusion) without prior operant training for natural rewards (food pellets).Mice acquired cocaine  self-administration by

eting ou
stated criteria and subsequently exhibited stable self-administration maintenance for ≥ 6 days.WT and trpc5-KD mice demonstrated identical cocaine responding during the maintenance phase.The trpc5-KD mice reached the criteria by the first session and continued stable responding for the duration of the experiments, whereas WT took several days to catch up to KD responding.WT and trpc5-KD mice exhibited similar responding for saline, yet infusions earned by trpc5-KD surpassed WT for cocaine on the first session (Figure 1a).The mouse trpc5-KD nosepoking showed a similar pattern on the first session, surpassing WT nose-pokes (Figure 1b).

After the maintenance phase of self-administration training, separate groups of mice were taken through a dose-response.The sessions leading up to the dose response tests demonstrate similar responding between genotypes (Figure 2a).Dose-response functions demonstrated no difference between genotypes (Figure 2b).This is an interesting study, showing the role of TRPC5 channels in the forebrain, on cocaine self-administration.The experiments are described well.The dose-response curve is convincing, as it shows the characteristic inverted-U-shaped curve.In line with the journal's guidelines, no statistical results and/or interpretations are provided for any result.However, this makes it difficult to assess the reliability of data, so my comments address this concern.

An analysis of drug intake using repeated measures ANOVA with genotype as between-subject factor and days (cocaine 1-6) as the repeated measure does not yield any significant effects (effect of genotype, main effect of days, or interaction genotype x days).Only a t test on day 1 yields a significant genotype effect.I therefore understand that the authors refer to an "apparent" initial increase in drug intake (abstract).It would be important to replicate this finding in the future, to ascertain that it is a true result, rather than variability in initial intake across mice.

An analysis of active/inactive hole discrimination

inactive) as the repeated measure yields a trend for an interaction genotype x hole (p=0.068).It therefore appears that the -/-might have better
iscrimination.This could be reported.The authors could also consider if there is insufficient power for this difference to be significant.

The animals were trained first with saline.Could this have influenced their subsequent intake, and could the initial difference in intake (day 1 of cocaine) be the consequence of differences in the ability to switch across genotypes?

From the data, it appears that not all mice were tested for initial saline intake.Could this have influenced the results?

The authors should describe (methods) how they ran the dose-response curve (descending doses?Random doses?Etc…)


I hav read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

No competing interests were disclosed.Acquisition studies are notorious for variability, and differences between genotypes were observed only on Day 1 of acquisition and throughout the large majority of the study were identical for the two genotypes; A slight hyperactivity especially under reinforced conditions is a fairly common observation with a variety of manipulations, and nose pokes in Figure 1B are suggestive of such a phenomenon (i.e., higher nose pokes during timeouts as well as during reinforcer availability in the active nose poke hole for KD mice than for WT); There are no data addressing whether similar results would be obtained with other reinforcers, such as food.

I have read this submission.I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

No competi