This research was supported by the Israel Science Foundation (grant No. 592/12) to DJ

NOTE: All experimental protocols conformed to the guidelines of the Institutional Animal Care and Use Committee of Tel Aviv University, Israel, and to the guidelines of the NIH. All efforts were made to minimize the number of animals used and their suffering.
1. Animal Preparation
<ol>
	<li>House rats in a room with a 12 hr light/dark cycle.</li>
	<li>During the experimental procedures maintain rats on a 22 hr food restriction schedule with freely available water.</li>
	<li>Weigh the rats twice a week to ensure that their body weight is not reduced below 90% of the weight of free-feeding rats, based on growth curves (e.g., Harlan, <a href="http://www.harlan.com/models/spraguedawley.asp" target="_blank">http://www.harlan.com/models/spraguedawley.asp</a>). Exclude rats whose body weight is reduced.</li>
</ol>
2. Set-up
<ol>
	<li>Use two adjacent rooms. One to be used as a &#8220;waiting room&#8221; for holding rats prior to behavioral testing, and the other for carrying out the procedure. This room will house the operant chambers. 
	NOTE: Make sure that rats in the waiting room are not exposed to the tones generated by the operant chambers.</li>
	<li>Use operant chambers with grid floor and a food magazine, which delivers one 45 mg food pellet accessible through a hinged Perspex panel. 
	NOTE: Opening of the hinge activates a micro-switch; a 3 W light to illuminate the food magazine; two retractable levers (4 cm wide, positioned 2.8 cm from the side walls, 7.5 cm on each side of the food magazine and 5 cm from the floor); a house light located on the ceiling to illuminate the chambers; an audio signal device to produce a 80 dB, 2.8 kHz tone.</li>
	<li>Seat the operant chambers in sound-attenuated boxes with ventilating fans mounted on the side of each box.</li>
	<li>Prior to the beginning of the experiment, pre-program all training stages with the exact session parameters relevant for each stage using a designated software, which computer-controls and activates the operant chambers as well as automatically records all the relevant data accumulated during the running of the experiment. 
	NOTE: The parameters for each training stage (magazine training, lever-press training, signal attenuation, test) are fully detailed below. The exact fashion in which these parameters are pre-programmed is dependent upon the software and hardware in use.</li>
</ol>
3. Handling and Food Restriction
<ol>
	<li>Handle rats for about 2 min daily, 5 days prior to the beginning of the experimental procedure.</li>
	<li>Launch a 22 hr food restriction schedule beginning on the first day of handling. Allow rats access to food for 2 hr in their home cages no sooner than half an hour after the end of handling/behavioral training. 
	NOTE: Ensure that rats have water ad libitum when in their home cages, and especially during the 2 hr feeding period, as they will not eat properly without water.</li>
	<li>On the last 3 days of handling, place 20 - 30 food pellets on a small tray and place the tray in the rats home cage. Remove the tray from the cage only after each rat has been observed to consume at least two pellets. 
	NOTE: Later, use the pellets as reinforcement for operant training.</li>
</ol>
4. Training Procedure
<ol>
	<li>In order for the rats to get acclimated to the testing environment, transport the rats in their home cages at least 15 min prior to behavioral testing in the waiting room.</li>
	<li>Magazine training (days 1 - 3).
	<ol>
		<li>On the 1st day of magazine training, put a sufficient amount of food pellets in the food magazine so that they are visible to the rat. 
		NOTE: One way to do so is to place the pellets so that they cause the hinged Perspex panel to remain slightly open.</li>
		<li>Compute the magazine training program so that the house light is turned on automatically at the start of each trial and a single food pellet is dropped into the food magazine following a 5 sec variable delay, simultaneously with the onset of a compound stimulus consisting of the magazine light and a tone.</li>
		<li>Compute the compound stimulus and house light to turn off after the rat&#39;s head enters the food magazine (collected trial) or after 15 sec (uncollected trial), whichever comes first. Define each trial to be followed by a 30 sec inter-trial interval.</li>
		<li>Place the rats into the operant chambers and 5 min later verify manually that all of the rats have collected the pellets. If so, activate the training program. If not, allow an extra 5 min.</li>
		<li>Program the magazine training session to stop running either after the rat has completed 30 collected trials or after a total of 40 trials has been attained.</li>
		<li>On the 3rd day of magazine training ensure that the rats perform 30 collected trials out of a total of 32 trials at the most. Return rats that fail to attain this criterion to the operant chambers for another full training session at the end of the training day. 
		NOTE: Run rats that fail to reach this criterion following an extra session on the last day of magazine training on the morning of the first day of lever-press training. Exclude rats that fail to reach criterion.</li>
	</ol>
	</li>
	<li>Lever-press training - Pre-training stage (day 4): Lever-pressing on a free-operant schedule.
	<ol>
		<li>Activate the training program before placing the rats in the operant chambers. Compute the program so that the reinforced lever is present in the chamber and the house light is on during the whole training session and that the non-reinforced lever is always retracted. 
		NOTE: Counterbalance the side of the lever (left/right) across rats and keep constant for each rat throughout the experimental procedure.</li>
		<li>Put some pellets on the lever and place a rat into the chamber.</li>
		<li>Allow the rat to explore the lever area until it incidentally presses the lever while collecting the pellets, triggering the delivery of a single food pellet and the onset of the compound stimulus.</li>
		<li>Compute the program so that the compound stimulus is turned off after the rat&#39;s head enters the food magazine (completed trial) or after 15 sec (uncompleted trial), whichever comes first.</li>
		<li>Program the session to stop running after the rat has reached 30 completed trials.</li>
		<li>If a rat does not reach this criterion within 30 min, put 3 - 4 pellets on the lever and wait for another 20 min. If a rat fails to complete 30 trials, return it to the operant chamber for additional training at the end of the training day. 
		NOTE: Run rats that fail to reach this criterion following the extra pre-training session again on the morning of the first day of lever-press training. Exclude rats that fail to reach criterion. Generally, almost all rats acquire lever-pressing after 3 sessions of pre-training (most do within the first session). However, if the animals have more difficulties in acquiring lever-pressing, use shaping.</li>
		<li>During shaping, keep the door of the sound-attenuated box open and observe the rat in the operant chamber. When the rat approaches the lever use the software to activate the delivery of a food pellet and the onset of the compound stimulus. Do so repeatedly.</li>
		<li>In the beginning, reinforce the rat when it is in the vicinity of the lever, but gradually start reinforcing it only when it makes actual physical contact with the lever, and finally reinforce only attempts to press it. 
		NOTE: Shaping may take a while. Be as quiet as possible.</li>
	</ol>
	</li>
	<li>Lever press training (days 5 - 7): Lever-pressing on a discrete trial schedule.
	<ol>
		<li>Compute the program so that the start of each trial is signaled by the onset of the house light and 5 sec later, both levers are introduced into the chamber.</li>
		<li>Ensure that responses on the non-reinforced lever (NRL) have no programmed consequences and presses on the reinforced lever trigger the delivery of a single food pellet into the magazine, together with the presentation of the compound stimulus.</li>
		<li>After the rat&#8217;s head enters the food magazine or after 15 sec have elapsed the levers are retracted and the compound stimulus and house light are turned off.</li>
		<li>Define each trial so that it is followed by a 30 sec inter-trial interval. On the first day of lever-press training (day 5) define the compound stimulus to be turned off after 15 sec in order to facilitate acquisition of the lever-press response. On the following two days (days 6 - 7) define the compound stimulus to last only 10 sec in order to ensure that magazine entry closely follows the lever-press responses.</li>
		<li>Place the rats in the operant chambers, and then activate the training program.</li>
		<li>Program the lever-press training session to stop running either after a rat has pressed the reinforced lever (RL) and collected the food pellet (completed trial) 40 times or after a total of 60 trials has been attained.</li>
		<li>On the last day of lever-press training make sure rats complete 40 trials out of a total of 42 total trials at the most. If a rat fails to reach this criterion, return it to the operant chamber for an additional training session at the end of the day. 
		NOTE: Exclude rats that fail to reach this criterion following an extra session on the last day of lever-press training.</li>
		<li>On the last day of lever-press training record the number of unrewarded lever presses on each trial, i.e., the number of presses following the first response on the RL (extra lever-presses).</li>
		<li>Randomly allocate rats to the experimental groups.</li>
		<li>When conducting the experimental manipulation at the time of the Test stage (e.g., in studies testing the acute effect of a drug), use analysis of variance (ANOVA) with main factors of manipulation (with manipulation/without manipulation) and Procedure (post-training signal attenuation, PTSA/regular extinction, RE, see section 4.5) to analyze the number of excessive lever presses followed by pellet collection (named excessive lever-presses-completed, ELP-C) and unpressed trials on the last day of lever-press training before the beginning of the signal attenuation stage.</li>
		<li>Ensure that there are no statistically significant differences between the groups in this measure. 
		NOTE: Typically, there are only a few rats with a high number of extra lever-presses, so compare the groups without these rats. In addition, make sure that rats that underwent extra-training are distributed between the groups as evenly as possible.</li>
	</ol>
	</li>
	<li>Signal attenuation/Regular extinction (days 8 - 10).
	<ol>
		<li>Run the procedure in an identical manner to magazine training on days 1 - 3 with two exceptions:
		<ol>
			<li>Empty the pellet dispenser so that no food pellet is delivered to the food magazine following the onset of the compound stimulus.</li>
			<li>Program the relevant stage so that the compound stimulus is turned off after 10 sec and not after 15 sec.</li>
		</ol>
		</li>
		<li>Make sure both the RL and NRL remain retracted during the training session.</li>
		<li>Ensure each signal attenuation training session to consist of 30 trials. On the last day of training make sure rats attempt to collect a food pellet (i.e., insert their head into the food magazine following the onset of the compound stimulus) no more than 14 times.</li>
		<li>Return rats that failed to attain this criterion to the operant chambers for an additional training session at the end of the day. 
		NOTE: Do not exclude rats that fail to reach criterion at this stage.</li>
		<li>Bring the rats undergoing regular extinction to the &#8220;waiting room&#8221; and leave them in their home cages for a period equivalent to the average duration of the signal attenuation stage.</li>
		<li>Use a mixed ANOVA with main factors of manipulation (with manipulation/without manipulation) and Procedure (PTSA/RE) and a repeated measures factor of Session (sessions 1 - 3) to analyze the number of completed trials on the three sessions of the signal attenuation stage.</li>
		<li>Ensure that differences in performance at the test stage are not a result of an earlier difference.</li>
	</ol>
	</li>
	<li>Test (day 11): Run the procedure in an identical manner to lever-press training, but under extinction conditions, i.e., pressing the RL results in the presentation of the compound stimulus, but no food is delivered to the food magazine because the pellet dispenser is empty.
	<ol>
		<li>Compute the test session to consist of 50 trials for males and 60 trials for females, because usually females still respond after 50 trials. However, if both sexes are used in the same study (recommended), then give 60 trials to all subjects.</li>
		<li>Collect the the number of excessive lever-presses that were not followed by magazine entry (named excessive lever-presses-uncompleted, ELP-U); the number of excessive lever-presses that were followed by magazine entry (i.e., ELP-C); the number of lever presses on the NRL; and the number of nose-pokes (i.e., the number of times the rat inserted its head into the food magazine.</li>
		<li>Analyze rats&#8217; performance on the Test stage using analysis of variance (ANOVA) with main factors of manipulation (with manipulation/without manipulation) and Procedure (PTSA/RE) performed on the number of ELP-C, ELP-U, the number of completed, uncompleted and unpressed trials, and the number of nose-pokes and presses on the non-reinforced lever.</li>
		<li>Follow significant interactions with post hoc analysis comparing the treated group with the non-treated/control group, within each procedure. 
		NOTE: When the exact parameters of the manipulation are not known (e.g., the relevant drug dose, the parameters of electrical stimulation) and in order to reduce the number of animals, test the effects of the manipulation in the PTSA procedure only, using different parameters (e.g., using several drug doses).</li>
		<li>Find the optimal parameters, that is, the parameters that exert the greatest effect on the number of ELP-U, without abolishing behavioral responding, and then run a full experimental design (PTSA and RE).</li>
	</ol>
	</li>
</ol>

The authors have nothing to disclose.

The signal attenuation rat model of OCD is a powerful behavioral model for the study of compulsive-like behavior. The model displays high face, predictive and construct validity20,21, and has been extensively used to study the neural substrates of this behavior39,43-45,48, its response to pharmacological manipulations38,39,43,47,53,54 and to deep brain stimulation40,46,50 and its modulation by ovarian hormones51. Thus, this model is a useful animal model for the study of OCD.
Compulsive lever-pressing in the signal attenuation model has several advantages over other experimentally induced repetitive behaviors (such as extinction burst and perseverative behaviors). First, the relevance of compulsive lever-pressing to compulsive behaviors in humans has been well established whereas the validity of other repetitive behaviors, which are often referred to as compulsive-like, is low or has never been tested20-22. Notably, behavioral repetition/perseveration is a phenomenon shared by various psychiatric disorders55-62 and therefore, proper validation of the target behavior as compulsive-like is crucial. In addition, the various behavioral measures collected during the PTSA procedure (i.e., the number of presses on the non-reinforced lever or the general number of nose-pokes the rats perform during the Test stage) help in eliminating alternative explanations for differences in compulsive lever-pressing between the groups being tested. For example, excessive lever-pressing can reflect a general increase in motor activity, in which case it will most likely be accompanied by an increase in the number of presses on the non-reinforced lever (thus, this measure also eliminates the need to test the rats in additional procedures such as the open-field test). On the other hand, manipulations which lead to a general increase in the number of nose-pokes the rats perform are likely to lead to a reduction in compulsive lever-pressing, even if they do not possess a genuine anti-compulsive effect. Additional measures collected even before the Test (excessive lever-presses during the lever-press training stage, completed trials during the signal attenuation stage) allows the experimenter to eliminate the possibility that any differences between the groups on the Test stage stem from prior differences in learning. Notably, all measures collected during the various stages of the procedure are quantitative, and therefore unbiased, not given to subjective interpretation and unaffected by inter-experimenter variability.
A disadvantage of the signal attenuation model is the fact that it requires special equipment (computer-operated operant boxes, appropriate software for the operation of these boxes, etc.). This makes it both costly and somewhat complex to perform, requiring skilled personnel, proficient both in ad-hock troubleshooting and in the day-to-day maintenance of the equipment. In addition, because the model is based on learned rather than spontaneous behavior, and because it consists of multiple stages, it is relatively time-consuming (11 days) when compared to some of the other animal models of OCD. However, in our experience, with the proper training the expertise required for performing the procedure are quite easily acquired. Also, because all equipment is computer-controlled and almost fully automatic, large groups of rats can be run efficiently and simultaneously, reducing its time-cost. In addition, results are easily calculated and do not require manual coding or any special processing. Finally, operant boxes are highly versatile, and once acquired, they can be used for various behavioral procedures in addition to signal attenuation, making them extremely cost-effective.
Another consideration, which should be taken into account when using the model, is that due to its lengthy and multi-staged nature, it may not be well suited for chronic treatments or developmental studies. In order not to affect rats&#8217; learning in the initial stages of the behavioral procedure, administration of a chronic treatment requires a break in the procedure, which makes the procedure even more time-costly. Moreover this break cannot take place immediately before the test stage, and thus, rats administered the chronic treatment will undergo the signal attenuation stage while under the influence of the treatment, which may alter their behavior even before the test stage and make any interpretation of the results problematic. Regarding developmental studies, again, because of the model&#8217;s lengthy nature, it is impossible to use it for extremely young rats (e.g., younger than 46-day old rats on test day). In addition, rats cannot be re-tested, making in necessary to train new rats at each age studied, and excluding the possibility of using longitudinal designs.
An important aspect of the signal attenuation model which has been mentioned above is the fact that compulsive lever-pressing is modulated by fluctuations in ovarian hormone levels along the rat estrous cycle51. This aspect is important for researchers interested in studying the mechanisms by which female gonadal hormones affect compulsive behaviors. Although the effects of male gonadal hormones on compulsive lever-pressing have not been tested, these or other factors are affecting male performance in the model, as the variability of the different response measures in the model is similar in male and female rats51. Therefore, researchers, who do not aim to study the role of gonadal hormones, may use both male and female rats without measuring the level of these hormones.
In summary, despite some shortcomings of the signal attenuation rat model of OCD such as its length and the fact that it requires special equipment and some technical knowledge, it provides a sensitive and reliable way of assessing compulsive behaviors in rats. Moreover, it can differentiate between these behaviors and other repetitive/perseverative behaviors, which are not truly compulsive in nature. As such, it is an excellent model for the assessment of putative anti-compulsive therapies, and studies employing it can be used to expand our knowledge of the neural substrates of OCD, which are still not well understood.

Obsessive-compulsive disorder (OCD) is a major psychiatric disorder that manifests in 1 - 3% of the general population1,2. People suffering from OCD have recurrent, intrusive and unwanted thoughts (obsessions) and/or repetitive ritualistic behaviors (compulsions)3. The specific neuropathological mechanisms underlying OCD are still not fully understood. However, the involvement of the serotonergic4-7, dopaminergic8,9 and glutamatergic10 systems has been demonstrated in this disorder. In addition, the orbitofrontal cortex, the cingulate cortex, the basal ganglia and regions within the parietal lobe have been implicated in its pathophysiology7,11-13. Finally, life events related to fluctuations in the level of ovarian hormones (e.g., child birth, ovulation) have been reported to trigger or exacerbate OCD in women patients14-16, suggesting that ovarian hormones play a modulatory role in OCD17.
Because the mechanisms underlying OCD are poorly understood, the use of appropriate animal models that closely mimic its behavioral and neural manifestations is essential for advancing our knowledge of its biological basis. In addition, such models contribute to the development of new lines of treatment. This is especially relevant in the case of OCD, because many patients are either treatment-resistant or experience only a partial alleviation of symptoms18,19. Indeed, in recent years, genetic, pharmacological and behavioral animal models of OCD (reviewed in 20-28) have expanded and advanced our knowledge of this disorder.
One of the most extensively used behavioral animal models of OCD is the signal attenuation rat model (for review, see 29). The theoretical assumption behind the model is that a deficit in the feedback associated with a successful performance of goal-directed behaviors leads to compulsive responses30-37. The model, developed by Joel and colleagues28, is based on operant behavior in rats. During initial training, rats are rewarded with a food pellet after pressing a lever. A successful lever-press triggers in addition the onset of a magazine light and a tone. This provides the rat with feedback that the lever-press response has led to the delivery of food. Next, the ability of the stimulus to signal the delivery of the reward is intentionally decreased by repeatedly presenting it without reward (importantly, there are no levers in the box at this stage). Compulsive-like behavior emerges on the last stage of training. During this test stage, which is carried out under extinction conditions, a lever press is followed by the presentation of the stimulus but not of the food reward. &#8220;Compulsive&#8221; behavior is expressed as multiple lever-presses after which the rat does not try to collect the reward. An anti/pro-compulsive effect is expressed as a decrease/increase in the number of &#8220;compulsive&#8221; lever-presses. Since signal attenuation involves extinction, it is important to distinguish between the effects of signal attenuation and of extinction per se. Therefore in a control group (the Regular extinction group) the compound stimulus is not attenuated prior to the test stage. Treatment that has an anti/pro compulsive effect should not alter the number of &#8220;compulsive&#8221; lever-presses in this group. (for additional details, see 29).
&#8220;Compulsive&#8221; lever-presses mimic the exaggerated and unnecessary nature of compulsive behaviors displayed by OCD patients. Therefore, the signal attenuation model displays good face validity. In addition, studies conducted with this model show that it has good predictive and construct validity (reviewed in 20,21). The model&#8217;s predictive validity derives from studies showing that the compulsive lever-pressing is attenuated by drugs known to ameliorate obsessive-compulsive symptoms38,39, as well as by high frequency stimulation of the subthalamic nucleus40, which has been found to have an anti-compulsive effect in human OCD patients41,42. Moreover, several drugs that are inefficient in the treatment of OCD have been found not to exert an anti-compulsive effect in the model38,39. The model also displays good construct validity, because studies indicate that similar neural mechanisms are involved both in OCD symptomatology and in the compulsive-like behavior induced by signal attenuation in rats. Thus, the involvement of the serotonergic43-46, dopaminergic39,46 and glutamatergic47 systems, as well as the involvement of OCD-related brain areas40,44,48-50 has been demonstrated in compulsive lever-pressing. In addition, ovarian hormones have been found to modulate compulsive lever-pressing in females51. Therefore, the signal attenuation model is a powerful tool for exploring the neural substrates of OCD and for screening novel anti-compulsive therapies. For a thorough discussion of the signal attenuation model&#8217;s clinical correlates and its usefulness and application in OCD research, see 20-22,29.

<table border="0" cellpadding="0" cellspacing="0" width="625">
	<tbody>
		<tr height="42">
			<td height="42" style="height:42px;width:204px;">Name of the Material/Equipment</td>
			<td style="width:173px;">Company</td>
			<td style="width:131px;">Catalog Number</td>
			<td style="width:119px;">Comments/ Description&#160;</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:204px;">Modular Test Chamber for Rats</td>
			<td style="width:173px;">Campden Instruments Ltd.</td>
			<td style="width:131px;">Model 80003M</td>
			<td></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:204px;">Pellet Trough for Modular Chamber with Head Entry and Door</td>
			<td style="width:173px;">Campden Instruments Ltd.</td>
			<td style="width:131px;">Model 80210M-R</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:204px;">Low Profile Retractable Response Lever&#160;</td>
			<td style="width:173px;">Campden Instruments Ltd.</td>
			<td style="width:131px;">Model CI4460-M</td>
			<td style="width:119px;">2 levers per chamber</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:204px;">Stimulus Lights</td>
			<td style="width:173px;">Campden Instruments Ltd.</td>
			<td style="width:131px;">Model 80221</td>
			<td></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:204px;">Pellet Dispenser with 45mg Interchangeable Pellet Size Wheel</td>
			<td style="width:173px;">Campden Instruments Ltd.</td>
			<td style="width:131px;">Model 80209-45</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:204px;">Mouse Nosepoke with Stimulus Light</td>
			<td style="width:173px;">Campden Instruments Ltd.</td>
			<td style="width:131px;">Model 80116S</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:204px;">Sonalert Audible Stimulus System</td>
			<td style="width:173px;">Campden Instruments Ltd.</td>
			<td style="width:131px;">Model SC628</td>
			<td></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:204px;">ABET II Complete Starter Package with 220VAC/50Hz Power Supply</td>
			<td style="width:173px;">Campden Instruments Ltd.</td>
			<td>Model 88501*C</td>
			<td></td>
		</tr>
		<tr height="105">
			<td height="105" style="height:105px;width:204px;">Sound Attenuating Chamber</td>
			<td style="width:173px;">Campden Instruments Ltd.</td>
			<td style="width:131px;">Model&#160;80600A-SAC</td>
			<td style="width:119px;">Equipped with a peephole and a 28 volt DC ventilation fan pannel</td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:204px;">Animal Behavior Environment Test system (ABET) II</td>
			<td style="width:173px;">Lafayette Instrument Neuroscience, Indiana, USA</td>
			<td>Model 89501</td>
			<td></td>
		</tr>
		<tr height="92">
			<td height="92" style="height:92px;width:204px;">Personal computer with a minimum 1.8 GHz Processor</td>
			<td style="width:173px;"></td>
			<td></td>
			<td style="width:119px;">Running Microsoft Windows XP (SP3), or Win7</td>
		</tr>
		<tr height="105">
			<td height="105" style="height:105px;width:204px;">45-mg dust-free precision pellets</td>
			<td style="width:173px;">PMI Nutrition International, Indiana, USA</td>
			<td style="width:131px;">Formula. P/AlN-76A</td>
			<td style="width:119px;">Keep the containers tightly closed to protect from moisture.</td>
		</tr>
	</tbody>
</table>

signal attenuation as a rat model of obsessive compulsive disorder

In the signal attenuation rat model of obsessive-compulsive disorder (OCD), lever-pressing for food is followed by the presentation of a compound stimulus which serves as a feedback cue. This feedback is later attenuated by repeated presentations of the stimulus without food (without the rat emitting the lever-press response). In the next stage, lever-pressing is assessed under extinction conditions (i.e., no food is delivered). At this stage rats display two types of lever-presses, those that are followed by an attempt to collect a reward, and those that are not. The latter are the measure of compulsive-like behavior in the model. A control procedure in which rats do not experience the attenuation of the feedback cue serves to distinguish between the effects of signal attenuation and of extinction. The signal attenuation model is a highly validated model of OCD and differentiates between compulsive-like behaviors and behaviors that are repetitive but not compulsive. In addition the measures collected during the procedure eliminate alternative explanations for differences between the groups being tested, and are quantitative, unbiased and unaffected by inter-experimenter variability. The major disadvantages of this model are the costly equipment, the fact that it requires some technical know-how and the fact that it is time-consuming compared to other models of OCD (11 days). The model may be used for detecting the anti- or pro-compulsive effects of pharmacological and non-pharmacological manipulations and for studying the neural substrate of compulsive behavior.

The following results are based on Brimberg et al., 200752. All figures are re-printed with permission from Elsevier.
In this study we tested the behavior of Sprague Dawley (SD) male rats in the signal attenuation model. First, in experiment 1, we tested the effects of 3 doses of the selective serotonin reuptake inhibitor (SSRI) paroxetine in the PTSA procedure (n per group = 10). In the Test, paroxetine dose-dependently decreased the number of ELP-C (Figure 1A; ANOVA yielded a signi&#64257;cant main effect of Dose, F(3,22) = 5.15, p &#60; 0.01) and ELP-U (Figure 1B; ANOVA yielded a signi&#64257;cant main effect of Dose, F(3,22) = 7.99, p &#60; 0.001).
<img alt="Figure 1" src="/files/ftp_upload/52287/52287fig1highres.jpg" /> 
Figure 1. This figure shows a representative dose response experiment comparing the effects of various doses of the SSRI Paroxetine on ELP-C and ELP-U of male rats following signal attenuation. Mean and standard error of the number of extra lever presses that (A) were followed by magazine entry (extra lever presses in completed trials; ELP-C) and (B) were not followed by magazine entry (extra lever presses in uncompleted trials; ELP-U) of rats treated with vehicle or 1, 5 or 10 mg/kg of paroxetine on the test day of the PTSA procedure. Re-printed with permission from 52.
In experiment 2 we tested the drug dose that was the most effective in experiment 1 (5 mg/kg), in both the PTSA and RE procedures (n per group = 10). In the Test, paroxetine decreased the number of ELP-C in both the PTSA and RE procedures (Figure 2A; two-way ANOVA, main effect of Procedure, F(1,32) = 6.50, p &#60; 0.05; main effect of Drug, F(1,32) = 8.69, p &#60; 0.01; Procedure X Drug interaction, F(1,32) = 0.43, p = 0.52) and in addition exerted an anti-compulsive effect, i.e., decreased the number of ELP-U in the PTSA but not in the RE procedure (Figure 2B; main effect of Procedure, F(1,32) = 9.60, p &#60; 0.005; main effect of Drug, F(1,32) = 5.75, p &#60; 0.05; Procedure X Drug interaction, F(1,32) = 4.83, p &#60; 0.05).
<img alt="Figure 2" src="/files/ftp_upload/52287/52287fig2highres.jpg" /> 
Figure 2. This figure shows a representative experiment comparing the effects of signal attenuation and regular extinction on ELP-C and ELP-U of saline- and paroxetine-exposed male rats. Mean and standard error of the number of (A) ELP-C and (B) ELP-U of rats treated with vehicle or 5 mg/kg of paroxetine on the test day of the PTSA and RE procedures. Re-printed with permission from 52.

Watch this Scientific Journal Video about Signal Attenuation as a Rat Model of Obsessive Compulsive Disorder at JoVE.com

Signal Attenuation as a Rat Model of Obsessive Compulsive Disorder

The goal of the protocol described in this paper is to induce compulsive-like behavior in rats for the study of obsessive-compulsive disorder (OCD). This behavior is precipitated by attenuating a signal indicating that a lever-press response was effective in producing food.

In the signal attenuation rat model of obsessive-compulsive disorder (OCD), lever-pressing for food is followed by the presentation of a compound stimulus ...

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15.3K Views.  Tel-Aviv University. The goal of the protocol described in this paper is to induce compulsive-like behavior in rats for the study of obsessive-compulsive disorder (OCD). This behavior is precipitated by attenuating a signal indicating that a lever-press response was effective in producing food.

Video: Signal Attenuation as a Rat Model of Obsessive Compulsive Disorder

Meal Duration as a Measure of Orofacial Nociceptive Responses in Rodents

A lengthening in meal duration can be used to measure an increase in orofacial mechanical hyperalgesia having similarities to the guarding behavior of humans with orofacial pain. To measure meal duration unrestrained rats are continuously kept in sound attenuated, computerized feeding modules for days to weeks to record feeding behavior. These sound-attenuated chambers are equipped with chow pellet dispensers. The dispenser has a pellet trough with a photobeam placed at the bottom of the trough and when a rodent removes a pellet from the feeder trough this beam is no longer blocked, signaling the computer to drop another pellet. The computer records the date and time when the pellets were taken from the trough and from this data the experimenter can calculate the meal parameters. When calculating meal parameters a meal was defined based on previous work and was set at 10 min (in other words when the animal does not eat for 10 min that would be the end of the animal&#39;s meal) also the minimum meal size was set at 3 pellets. The meal duration, meal number, food intake, meal size and inter-meal interval can then be calculated by the software for any time period that the operator desires. Of the feeding parameters that can be calculated meal duration has been shown to be a continuous noninvasive biological marker of orofacial nociception in male rats and mice and female rats. Meal duration measurements are quantitative, require no training or animal manipulation, require cortical participation, and do not compete with other experimentally induced behaviors. These factors distinguish this assay from other operant or reflex methods for recording orofacial nociception.

A lengthening in meal duration represents orofacial nociceptive behavior in rodents similar to the guarding behavior of humans with orofacial pain. Eating is a behavior that requires no training or animal manipulation, requires cortical participation, and is not competing with other experimentally induced behaviors, distinguishing this assay from alternative reflex or operant measurements.

A lengthening in meal duration can be used to measure an increase in orofacial mechanical hyperalgesia having similarities to the guarding behavior of ...

Marble Burying and Nestlet Shredding as Tests of Repetitive, Compulsive-like Behaviors in Mice

Obsessive-compulsive disorder (OCD) and autism spectrum disorders (ASD) are serious and debilitating psychiatric conditions and each constitutes a significant public health concern, particularly in children. Both of these conditions are highlighted by the repeated expression of meaningless behaviors. Individuals with OCD often show checking, frequent hand washing, and counting. Children with ASDs also engage in repetitive tapping, arm or hand flapping, and rocking. These behaviors can vary widely in intensity and frequency of expression. More intense forms of repetitive behaviors can even result in injury (e.g.&#160;excessive grooming, hand washing, and self-stimulation). These behaviors are therefore very disruptive and make normal social discourse difficult. Treatment options for repetitive behaviors in OCD and ASDs are somewhat limited and there is great interest in developing more effective therapies for each condition. Numerous animal models for evaluating compulsive-like behaviors have been developed over the past three decades. Perhaps the animal models with the greatest validity and ease of use are the marble burying test and the nestlet shredding test. Both tests take advantage of the fact that the target behaviors occur spontaneously in mice. In the marble burying test, 20 marbles are arrayed on the surface of clean bedding. The number of marbles buried in a 30 min session is scored by investigators blind to the treatment or status of the subjects. In the nestlet shredding test, a nestlet comprised of pulped cotton fiber is preweighed and placed on top of cage bedding and the amount of the nestlet remaining intact after a 30 min test session is determined. Presently, we describe protocols for and show movie documentation of marble burying and nestlet shredding. Both tests are easily and accurately scored and each is sensitive to small changes in the expression of compulsive-like behaviors that result from genetic manipulations, disease, or head injury.

Disease, head injury, genetic modifications, and treatment of mice with drugs can have profound effects on behavior. Utilizing well-characterized and validated approaches such as marble burying and nestlet shredding, compulsive-like behaviors can be documented accurately in mice as models of human obsessive-compulsive disorder and autism spectrum disorder.

Obsessive-compulsive disorder (OCD) and autism spectrum disorders (ASD) are serious and debilitating psychiatric conditions and each constitutes a ...

The Forced Swim Test as a Model of Depressive-like Behavior

The goal of the present protocol is to describe the forced swim test (FST), which is one of the most commonly used assays for the study of depressive-like behavior in rodents. The FST is based on the assumption that when placing an animal in a container filled with water, it will first make efforts to escape but eventually will exhibit immobility that may be considered to reflect a measure of behavioral despair. This test has been extensively used because it involves the exposure of the animals to stress, which was shown to have a role in the tendency for major depression. Additionally, the FST has been shown to share some of the factors that are influenced or altered by depression in humans, including changes in food consumption, sleep abnormalities and drug-withdrawal-induced anhedonia. The main advantages of this procedure are that it is relatively easy to perform and that its results are easily and quickly analyzed. Moreover, its sensitivity to a broad range of antidepressant drugs that makes it a suitable screening test is one of the most important features leading to its high predictive validity. Despite its appeal, this model has a number of disadvantages. First, the issue of chronic augmentation is problematic in this test because in real life patients need to be treated for at least several weeks before they experience any relief from their symptoms. Last, due to the aversiveness of the FST, it is important to take into account possible influences it might have on brain structure/function if brain analyses are to be carried out following this procedure.

This protocol describes the forced swim test, which is used for the study of depressive-like behavior in rodents. This procedure involves placing an animal in a container filled with water that eventually will lead to the exhibition of immobility behavior, which is considered to reflect behavioral despair.

The goal of the present protocol is to describe the forced swim test (FST), which is one of the most commonly used assays for the study of depressive-like ...

Testing Sensory and Multisensory Function in Children with Autism Spectrum Disorder

In addition to impairments in social communication and the presence of restricted interests and repetitive behaviors, deficits in sensory processing are now recognized as a core symptom in autism spectrum disorder (ASD). Our ability to perceive and interact with the external world is rooted in sensory processing. For example, listening to a conversation entails processing the auditory cues coming from the speaker (speech content, prosody, syntax) as well as the associated visual information (facial expressions, gestures). Collectively, the &#8220;integration&#8221; of these multisensory (i.e., combined audiovisual) pieces of information results in better comprehension. Such multisensory integration has been shown to be strongly dependent upon the temporal relationship of the paired stimuli. Thus, stimuli that occur in close temporal proximity are highly likely to result in behavioral and perceptual benefits &#8211; gains believed to be reflective of the perceptual system&#39;s judgment of the likelihood that these two stimuli came from the same source. Changes in this temporal integration are expected to strongly alter perceptual processes, and are likely to diminish the ability to accurately perceive and interact with our world. Here, a battery of tasks designed to characterize various aspects of sensory and multisensory temporal processing in children with ASD is described. In addition to its utility in autism, this battery has great potential for characterizing changes in sensory function in other clinical populations, as well as being used to examine changes in these processes across the lifespan.

We describe how to implement a battery of behavioral tasks to examine the processing and integration of sensory stimuli in children with ASD. The goal is to characterize individual differences in temporal processing of simple auditory and visual stimuli and relate these to higher order perceptual skills like speech perception.

In addition to impairments in social communication and the presence of restricted interests and repetitive behaviors, deficits in sensory processing are ...

Errors as a Means of Reducing Impulsive Food Choice

Nowadays, the increasing incidence of eating disorders due to poor self-control has given rise to increased obesity and other chronic weight problems, and ultimately, to reduced life expectancy. The capacity to refrain from automatic responses is usually high in situations in which making errors is highly likely. The protocol described here aims at reducing imprudent preference in women during hypothetical intertemporal choices about appetitive food by associating it with errors. First, participants undergo an error task where two different edible stimuli are associated with two different error likelihoods (high and low). Second, they make intertemporal choices about the two edible stimuli, separately. As a result, this method decreases the discount rate for future amounts of the edible reward that cued higher error likelihood, selectively. This effect is under the influence of the self-reported hunger level. The present protocol demonstrates that errors, well known as motivationally salient events, can induce the recruitment of cognitive control, thus being ultimately useful in reducing impatient choices for edible commodities.

Giving in to temptation of tasty food may result in long-term overweight problems. This protocol describes how to reduce imprudent preference for edible commodities during hypothetical intertemporal choices in women by associating them with errors.

Nowadays, the increasing incidence of eating disorders due to poor self-control has given rise to increased obesity and other chronic weight problems, and ...

Wheel Running and Environmental Complexity as a Therapeutic Intervention in an Animal Model of FASD

Aerobic exercise (e.g., wheel running (WR) extensively used in animal research) positively impacts many measures of neuroplastic potential in the brain, such as rates of adult neurogenesis, angiogenesis, and expression of neurotrophic factors in rodents. This intervention has also been shown to mitigate behavioral and neuroanatomical aspects of the negative impacts of teratogens (i.e., developmental exposure to alcohol) and age-related neurodegeneration in rodents. Environmental complexity (EC) has been shown to produce numerous neuroplastic benefits in cortical and subcortical structures and can be coupled with wheel running to increase the proliferation and survival of new cells in the adult hippocampus. The combination of these two interventions provides a robust &#34;superintervention&#34; (WR-EC) that can be implemented in a range of rodent models of neurological disorders. We will discuss the implementation of WR/EC and its constituent interventions for use as a more powerful therapeutic intervention in rats using the animal model of prenatal exposure to alcohol in humans. We will also discuss which elements of the procedures are absolutely necessary for the interventions and which ones may be altered depending on the experimenter&#39;s question or facilities.

Cardiovascular exercise and stimulating experiences in a complex environment have positive benefits on multiple measures of neuroplasticity within the rodent brain. This article will discuss the implementation of these interventions as a &#34;superintervention&#34; which combines wheel running and environmental complexity and will address the limitations of these interventions.

Aerobic exercise (e.g., wheel running (WR) extensively used in animal research) positively impacts many measures of neuroplastic potential in the brain, ...

Neurodevelopmental Reflex Testing in Neonatal Rat Pups

Neurodevelopmental reflex testing is commonly used in clinical practice to assess the maturation of the nervous system. Neurodevelopmental reflexes are also referred to as primitive reflexes. They are sensitive and consistent with later outcomes. Abnormal reflexes are described as an absence, persistence, reappearance, or latency of reflexes, which are predictive indices of infants that are at high risk for neurodevelopmental disorders. Animal models of neurodevelopmental disabilities, such as cerebral palsy, often display aberrant developmental reflexes, as would be observed in human infants. The techniques described assess a variety of neurodevelopmental reflexes in neonatal rats. Neurodevelopmental reflex testing offers the investigator a testing method that is not otherwise available in such young animals. The methodology presented here aims to assist investigators in examining developmental milestones in neonatal rats as a method of detecting early-onset brain injury and/or determining the effectiveness of therapeutic interventions. The methodology presented here aims to provide a general guideline for investigators.

Behavioral testing is the gold standard for determining outcomes following brain injury, and can identify the presence of developmental disabilities in infants and children. Neurodevelopmental reflexes are an early indicator of these abnormalities. A host of easily accomplished developmental reflex tests in the neonatal rodent were developed and described here.

Neurodevelopmental reflex testing is commonly used in clinical practice to assess the maturation of the nervous system. Neurodevelopmental reflexes are ...

Establishment of a Valuable Mimic of Alzheimer's Disease in Rat Animal Model by Intracerebroventricular Injection of Composited Amyloid Beta Protein

Alzheimer&#39;s disease (AD) is an irreversible, progressive brain disease that slowly destroys memory and is accompanied by neuron loss and structure change. With the increase of AD patients worldwide, the pathology and treatment of the disease has become a focus in the International Pharmaceutical Industry. Thus, the establishment of the animal model to mimic AD in the laboratory is of great importance.
Here, we describe a detailed protocol for establishing a mimic of AD in a rat animal model though intracerebroventricular injection of amyloid beta protein 25-35 (A&#946;25-35) combined with aluminum trichloride (AlCl3) and anterodorsal thalamic nucleus injection of recombinant human transforming growth factor-&#946;1 (RHTGF-&#946;1) to rats. The related markers of AD were measured, including: spatial memory, neuronal structure and substructure, neuronal A&#946;, and neurofibrillary tangles (NFT) production. This rat model demonstrates spatial memory impairment, neuronal structure and substructure pathological changes, neuron intracellular A&#946; burden, and NFT aggregation, and provides a close mimic of the neuronal structure and function disorder to that of clinical AD patients. Thus, the presented AD rat modelprovides a valuable in vivo tool for exploring neuronal function, neuronal pathology, and drug screening of AD.

Establishment of a Valuable Mimic of Alzheimer&#039;s Disease in Rat Animal Model by Intracerebroventricular Injection of Composited Amyloid Beta Protein

This is a protocol to mimic Alzheimer&#39;s Disease in rats by evaluation of spatial memory impairment, neuronal pathological changes, neuronal amyloid beta protein (A&#946;) burden, and neurofibrillary tangles aggregation, induced by the injection of A&#946;25-35 combined with aluminum trichloride and recombinant human transforming growth factor-&#946;1.

Alzheimer&#39;s disease (AD) is an irreversible, progressive brain disease that slowly destroys memory and is accompanied by neuron loss and structure ...

Clinical-oriented Three-dimensional Gait Analysis Method for Evaluating Gait Disorder

Three-dimensional gait analysis (3DGA) is shown to be a useful clinical tool for the evaluation of gait abnormality due to movement disorders. However, the use of 3DGA in actual clinics remains uncommon. Possible reasons could include the time-consuming measurement process and difficulties in understanding measurement results, which are often presented using a large number of graphs. Here we present a clinician-friendly 3DGA method developed to facilitate the clinical use of 3DGA. This method consists of simplified preparation and measurement processes that can be performed in a short time period in clinical settings and intuitive results presentation to facilitate clinicians&#39; understanding of results. The quick, simplified measurement procedure is achieved by the use of minimum markers and measurement of patients on a treadmill. To facilitate clinician understanding, results are presented in figures based on the clinicians&#39; perspective. A Lissajous overview picture (LOP), which shows the trajectories of all markers from a holistic viewpoint, is used to facilitate intuitive understanding of gait patterns. Abnormal gait pattern indices, which are based on clinicians&#39; perspectives in gait evaluation and standardized using the data of healthy subjects, are used to evaluate the extent of typical abnormal gait patterns in stroke patients. A graph depicting the analysis of the toe clearance strategy, which depicts how patients rely on normal and compensatory strategies to achieve toe clearance, is also presented. These methods could facilitate implementation of 3DGA in clinical settings and further encourage development of measurement strategies from the clinician&#39;s point of view.

In this study, a clinician-friendly three-dimensional gait analysis method, which was designed to be performed in the rehabilitation clinic, is presented. The method consists of a simplified measurement method and intuitive figures to facilitate clinicians&#39; understanding of the results.

Three-dimensional gait analysis (3DGA) is shown to be a useful clinical tool for the evaluation of gait abnormality due to movement disorders. However, ...

Stress-Enhanced Fear Learning, a Robust Rodent Model of Post-Traumatic Stress Disorder

Fear behaviors are important for survival, but disproportionately high levels of fear can increase the vulnerability for developing psychiatric disorders such as post-traumatic stress disorder (PTSD). To understand the biological mechanisms of fear dysregulation in PTSD, it is important to start with a valid animal model of the disorder. This protocol describes the methodology required to conduct stress-enhanced fear learning (SEFL) experiments, a preclinical model of PTSD, in both rats and mice. SEFL was developed to recapitulate critical aspects of PTSD, including long-term sensitization of fear learning caused by an acute stressor. SEFL uses aspects of Pavlovian fear conditioning but produces a distinct and robust sensitized fear response far greater than normal conditional fear responses. The trauma procedure involves placing a rodent in a conditioning chamber and administering 15 unsignaled shocks randomly distributed over 90 minutes (for rat experiments; for mouse experiments, 10 unsignaled shocks randomly distributed over 60 minutes are used). On day 2, rodents are placed in a novel conditioning context where they receive a single shock; then, on day 3 they are placed back in the same context as on day 2 and tested for changes in freezing levels. Rodents that previously received the trauma display enhanced levels of freezing on the test day compared to those that received no shocks on the first day. Thus, with this model, a single highly stressful experience (the trauma) produces extreme fear of the stimuli associated with the traumatic event.

Here we describe the detailed methodology required to conduct stress-enhanced fear learning (SEFL) experiments, a preclinical model of post-traumatic stress disorder, in both rats and mice. The model utilizes aspects of Pavlovian fear conditioning and freezing as an index of enhanced fear in rodents.

Fear behaviors are important for survival, but disproportionately high levels of fear can increase the vulnerability for developing psychiatric disorders ...