Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Protocol
  • Published:

Assessing spatial pattern separation in rodents using the object pattern separation task

A Publisher Correction to this article was published on 10 October 2018

Abstract

Pattern separation is the process of transforming highly similar sensory inputs into distinct, dissimilar representations. It takes place in the hippocampus and is thought to be used in episodic memory. Impaired pattern separation performance has been recognized as a predictor for the development of cognitive impairments such as dementia in humans and as being present in patients with schizophrenia and post-traumatic stress disorder (PTSD). In this protocol, we describe how to implement a simple and robust object pattern separation (OPS) task in mice and rats that we have previously established and validated. This two-trial memory task uses specific object locations so differences in performance can be calibrated with the extent of object movement. Changes in performance are indicative of spatial pattern separation. In contrast to other pattern separation tasks, the OPS task allows detection of spatial pattern separation performance bidirectionally. Furthermore, the OPS task is cheaper and easier to use and interpret than other tasks that use more than two objects or that are touch-screen based. The entire protocol, from vivarium acclimatization to training of the animals, takes ~35–41 d. After successful training, the animals can be tested repeatedly, and three OPS experiments (n = 20–24 per experimental day) can be performed per week. A standard level of expertise in behavioral studies in rodents is sufficient to successfully integrate this paradigm into an existing rodent test battery.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Objects, base plate and testing arena used for rats in the OPS paradigm.
Fig. 2: An example of object placement in both the learning trial (T1) and the test trial (T2).
Fig. 3: Flowchart of the OPS task procedure.
Fig. 4: Characteristic OPS task results, showing the d2 indices (mean + s.e.m.) for all five positions of untreated 4-month-old male Wistar rats (average weight = 393 g).

Similar content being viewed by others

References

  1. Clelland, C. et al. A functional role for adult hippocampal neurogenesis in spatial pattern separation. Science 325, 210–213 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Kheirbek, M. A., Klemenhagen, K. C., Sahay, A. & Hen, R. Neurogenesis and generalization: a new approach to stratify and treat anxiety disorders. Nat. Neurosci. 15, 1613–1620 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Reagh, Z. M. et al. Spatial discrimination deficits as a function of mnemonic interference in aged adults with and without memory impairment. Hippocampus 24, 303–314 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  4. Schreiber, R. & Newman-Tancredi, A. Improving cognition in schizophrenia with antipsychotics that elicit neurogenesis through 5-HT1A receptor activation. Neurobiol. Learn. Mem. 110, 72–80 (2014).

    Article  CAS  PubMed  Google Scholar 

  5. Das, T., Ivleva, E. L., Wagner, A. D., Stark, C. E. L. & Tamminga, C. A. Loss of pattern separation performance in schizophrenia suggests dentate gyrus dysfunction. Schizophr. Res. 159, 193–197 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  6. Tamminga, C. A., Stan, A. D. & Wagner, A. D. The hippocampal formation in schizophrenia. Am. J. Psychiatry 167, 1178–1193 (2010).

    Article  PubMed  Google Scholar 

  7. Bekinschtein, P. et al. BDNF in the dentate gyrus is required for consolidation of ‘pattern-separated’ memories. Cell Rep. 5, 759–768 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Oomen, C. A. et al. The touchscreen operant platform for testing working memory and pattern separation in rats and mice. Nat. Protoc. 8, 2006–2021 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Sahay, A., Wilson, D. A. & Hen, R. Pattern separation: a common function for new neurons in hippocampus and olfactory bulb. Neuron 70, 582–588 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Lacy, J. W., Yassa, M. A., Stark, S. M., Muftuler, L. T. & Stark, C. E. L. Distinct pattern separation related transfer functions in human CA3/dentate and CA1 revealed using high-resolution fMRI and variable mnemonic similarity. Learn. Mem. 18, 15–18 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  11. van Goethem, N. P., Schreiber, R., Newman-Tancredi, A., Varney, M. & Prickaerts, J. Divergent effects of the “biased”, 5-HT1A receptor agonists F15599 and F13714 in a novel object pattern separation task. Br. J. Pharmacol. 172, 2532–2543 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Ennaceur, A. & Delacour, J. A new one-trial test for neurobiological studies of memory in rats. 1: behavioral data. Behav. Brain Res. 31, 47–59 (1988).

    Article  CAS  PubMed  Google Scholar 

  13. Leger, M. et al. Object recognition test in mice. Nat. Protoc. 8, 2531–2537 (2013).

    Article  CAS  PubMed  Google Scholar 

  14. Antunes, M. & Biala, G. The novel object recognition memory: neurobiology, test procedure, and its modifications. Cogn. Process 13, 93–110 (2012).

    Article  CAS  PubMed  Google Scholar 

  15. van Hagen, B. T. J., van Goethem, N. P., Lagatta, D. C. & Prickaerts, J. The object pattern separation (OPS) task; a behavioral paradigm derived from the object recognition task. Behav. Brain Res. 285, 44–52 (2015).

    Article  PubMed  Google Scholar 

  16. van Goethem, N. P. et al. Object recognition testing: rodent species, strains, housing conditions, and estrous cycle. Behav. Brain Res. 232, 323–334 (2012).

    Article  PubMed  Google Scholar 

  17. Heyser, J. & Chemero, A. Novel object exploration in mice: not all objects are created equal. Behav. Process. 89, 232–238 (2012).

    Article  Google Scholar 

  18. Prusky, G. T., Harker, K. T., Douglas, R. M. & Whishaw, I. Q. Variation in visual acuity within pigmented, and between pigmented and albino rat strains. Behav. Brain Res. 136, 339–348 (2002).

    Article  PubMed  Google Scholar 

  19. Roedel, A., Storch, C., Holsboer, F. & Ohl, F. Effects of light or dark phase testing on behavioural and cognitive performance in DBA mice. Lab. Anim. 40, 371–381 (2006).

    Article  CAS  PubMed  Google Scholar 

  20. Akkerman, S. et al. PDE5 inhibition improves object memory in standard housed rats but not in rats housed in an enriched environment: implications for memory models? PLoS ONE 9, e111692 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Bartolomucci, A. et al. Individual housing induces altered immuno-endocrine responses to psychological stress in male mice. Pyschoneuroendocrinology 28, 540–558 (2003).

    Article  CAS  Google Scholar 

  22. Arndt, S. S. et al. Individual housing of mice – impact on behaviour and stress responses. Physiol. Behav. 97, 385–393 (2009).

    Article  CAS  PubMed  Google Scholar 

  23. Castelhano-Carlos, M. J. & Baumans, V. The impact of light, noise, cage cleaning and in-house transport on welfare and stress of laboratory rats. Lab. Anim. 43, 311–327 (2009).

    Article  CAS  PubMed  Google Scholar 

  24. Ameen-Ali, K. E., Eacott, M. J. & Easton, A. A new behavioural apparatus to reduce animal numbers in multiple types of spontaneous object recognition paradigms in rats. J. Neurosci. Methods 211, 66–76 (2012).

    Article  CAS  PubMed  Google Scholar 

  25. Ameen-Ali, K. E., Easton, A. & Eacott, M. J. Moving beyond standard procedures to assess spontaneous recognition memory. Neurosci. Biobehav. Rev. 53, 37–51 (2015).

    Article  CAS  PubMed  Google Scholar 

  26. Albasser, M. M. et al. New behavioral protocols to extend our knowledge of rodent object recognition memory. Learn. Mem. 17, 407–419 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  27. Kinnavane, L., Albasser, M. M. & Aggleton, J. P. Advances in the behavioural testing and network imaging of rodent recognition memory. Behav. Brain Res. 285, 67–78 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  28. Sorge, R. E. et al. Olfactory exposure to males, including men, causes stress and related analgesia in rodents. Nat. Methods 11, 629–632 (2014).

    Article  CAS  PubMed  Google Scholar 

  29. Ennaceur, A. One-trial object recognition in rats and mice: methodological and theoretical issues. Behav. Brain Res. 215, 244–254 (2010).

    Article  CAS  PubMed  Google Scholar 

  30. Akkerman, S. et al. Methodological considerations on discrimination and exploration measures in object recognition. Behav. Brain Res. 232, 335–347 (2012).

    Article  PubMed  Google Scholar 

  31. Bruno, O. et al. GEBR-7b, a novel PDE4D selective inhibitor that improves memory in rodents at non-emetic doses. Br. J. Pharmacol. 164, 2054–2063 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Vanmierlo, T. et al. Liver X receptor activation restores memory in aged AD mice without reducing amyloid. Neurobiol. Aging 32, 1262–1272 (2009).

    Article  CAS  PubMed  Google Scholar 

  33. Zeef, D. H. et al. Memory deficits in the transgenic rat model of Huntington’s disease. Behav. Brain Res. 227, 194–198 (2012).

    Article  CAS  PubMed  Google Scholar 

  34. Rutten, K. et al. Automated scoring of novel object recognition in rats. J. Neurosci. Methods 171, 72–77 (2008).

    Article  CAS  PubMed  Google Scholar 

  35. Akkerman, S., Prickaerts, J., Steinbusch, H. W. M. & Blokland, A. Object recognition testing: statistical considerations. Behav. Brain Res. 232, 317–322 (2012).

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

N.P.v.G. is financially supported by Alzheimer Nederland (grant no. WE.03-2017-11).

Author information

Authors and Affiliations

Authors

Contributions

N.P.v.G. and J.P. designed the general OPS procedure for measuring pattern separation performance in rodents. B.T.J.v.H. and N.P.v.G. performed the experiments and analyzed the data. N.P.v.G. and B.T.J.v.H wrote the manuscript with input from J. P.

Corresponding author

Correspondence to Jos Prickaerts.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Related links

Key references using this protocol

1. van Hagen, B. T. J. et al. Behav. Brain Res. 285, 44–52 (2015): https://doi.org/10.1016/j.bbr.2014.10.041

2. van Goethem, N. P. et al. Br. J. Pharmacol. 172, 2532–2543 (2015): https://doi.org/10.1111/bph.13071.

Electronic supplementary material

Supplementary Data

This Excel file shows scoring of the supplementary video files; output and calculations of the parameters are outlined in the troubleshooting table

Supplementary Video 1

An example of a T1 OPS trial of a mouse. Trial duration is 4 min starting immediately upon placement of the mouse in the testing arena. Position 1 is utilized. The same mouse undertaking the T2 trial is shown in Supplementary Video 2 and the scoring and analysis of this trial is shown in the Supplementary Data

Supplementary Video 2

An example of a T2 OPS trial of a mouse. Trial duration is 4 min starting immediately upon placement of the mouse in the testing arena. Position 4 is utilized as a novel object location (right object moved backward to position 4). The same mouse undertaking the T1 trial is shown in Supplementary Video 1 and the scoring and analysis of this trial is shown in Supplementary the Data

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

van Goethem, N.P., van Hagen, B.T.J. & Prickaerts, J. Assessing spatial pattern separation in rodents using the object pattern separation task. Nat Protoc 13, 1763–1792 (2018). https://doi.org/10.1038/s41596-018-0013-x

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41596-018-0013-x

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing