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Presented here is a novel method for assessing metacognitive responding in rats using an odor-based DMTS task. Due to olfaction as rodents' primary sense, the use of odor is preferable to visual cues in rats and mice 20,21. The use of digging in the sand is a natural foraging behavior of rats, making the task ecologically-relevant for rodent species.
A crucial step in the protocol is ensuring that there is a hierarchy of food rewards, one of which is clearly preferred over the other. During early phases of the study, rats were required to choose between the presumed to be preferred reward, a piece of sweetened cereal, and small standard food pellet. However, preference testing yielded indiscriminate choice behavior, causing the use of quantity as the source of reward variation. Rats chose between a whole piece of cereal and a ¼ piece of cereal, and reliably favored the larger quantity. Without a preference, whether food quality or quantity, there is no incentive to take the test over declining it, so this step is crucial.
Another important aspect of the protocol is establishing proper RIs and ITIs so that MTS accuracy remains within the range of 40 to 70% correct. If delays are too short, and interference is minimal- due to long ITIs, rats never experience "forgetting" the sample. Conversely, if RIs are too long and the ITIs are too short, the test becomes too difficult and rats never remember the sample. Such responses can be detected not only by accuracy on forced trials but by decline rates that are either too high or too low. Subjects should decline about 10-50% of choice trials: if a subject declines every trial or never declines, data cannot be interpreted as positive or negative for the presence of metamemory and the relative value of the decline-test response needs to be re-evaluated. Throughout the experiment, average performance on forced trials is consistently calculated at the end of two days of testing. As rats' progress through more trials of DMTS, their performance may improve, which would initiate a return delay titration (see Figure 1B) such that delays can be appropriately increased such that accuracy remains below 70% correct. If memory for the sample is consistently above 70% consider decreasing the ITI. If memory for the sample is consistently below 40% consider increasing the ITI and/or increasing the odor sample size from four to 10-20 odors to decrease memory interference.
Depending on the strain of rats used, housing environment, and light-dark cycle animals are housed in, memory may be weaker or stronger. Compared to other laboratory rat strains, such as Wistar or Sprague Dawleys, Long Evans are known to acquire cognitive tasks with relatively fewer trials22,23. It may, therefore, take more stages of habituation, and more training for other rodents to learn the task. Rats in the present study were housed in highly enriched environments with access to exercise so it is possible their memories were relatively strong24,25,26. Rats used here were also housed on a reversed light-dark cycle which may increase cognitive performance since they were tested during their dark cycle.
Adaptive use of the decline-test response, indicated by significantly higher performance on choice as compared to forced tests suggests metacognitive responding. However, metacognitive responding could result from reliance on internal memory cues or external cues8. To determine if in fact adaptive use of the decline-test response is the result of internal memory cues, experimenters should aim to eliminate as many external cues as possible8,14. External cues are considered any publicly available test-specific stimuli or cues that subjects could use to guide decline-test use8. Potential external cues in this task include relative salience of individual odors, sample duration, response latency, and duration of RIs. Generalization tests as described here and in more detail the results paper19 are useful in ruling out behavioral responding based on external cues like environmental cue associations due to cue inconsistency in task parameters across experiments.
In this paradigm, the rat is required to make the decision to take or decline the test before the memory test is presented (see 8.2), largely eliminating the potential for response competition to control use of the decline-test response. Response competition is the propensity to take the test based on the sight or smell of the correct test option when the metacognitive choice is presented concurrently with the primary memory test8. Requiring rats to choose to take or decline the test before encountering the memory test itself significantly reduces the possibility that response competition controls use of the decline-test response. However, one improvement to this design would be to have rats choose to take or decline the test by making a particular response in a room separate from the memory test itself. This would further increase the prospective nature of this paradigm, which may allow for the more successful elimination of external cues8,19. An additional improvement for future studies is to, if possible, record response latency at the point when the rat enters the testing room to the time it takes for the subject to turn left or turn right (decline or take the test, respectively). This would allow the researchers to determine if response latency served as an external cue subjects learned to associate with particular responses overtime (see8). It would also be enlightening to record if and when subjects change their response (see 8.2; e.g. travel from the MTS choice side of the room to the decline test area or vice versa). As discussed in the results paper, we observed this behavior only once, which adds to the conclusion that rats made a decision to take or decline the test as soon as they entered the testing room and before they encountered the memory test itself, which they did by systematically sampling each choice odor.
Because rats tested in this paradigm transferred metacognitive responding across multiple generalization tests, it was concluded that rats were capable of metamemory- they could monitor their memories for the sample19. It will be important for other research groups to test this paradigm or similar adaptations of it as corroborating evidence from different laboratories is needed before it can be concluded with certainty that rats are capable of metacognitive responding and that behavior is controlled by an internal rather than external cue. Testing for the presence of this important mnemonic ability, which degrades with age, may prove useful in translational approaches to studying memory dysfunction, such as with transgenic mice and models of Alzheimer's disease. It would be especially fruitful for researchers to employ this behavioral paradigm in conjunction with brain lesions, temporary brain inactivation's or activations (e.g. optogenetics, chemogenetics), and with electrophysiological recordings, as these investigations may elucidate the neural mechanisms underlying metacognitive processes.