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Neuwirth-Brown™ Attention Set-shift Test (ASST)

An advanced adaptation of the Attention Set-shift Test, designed to study rodent cognition, attentional flexibility, and fronto-executive function.

Overview

The Neuwirth-Brown™ Attention Set-shift Test (ASST) is an adaptation of the traditional Attentional Set-shifting (ID/ED) Chamber and Digging Task, developed to better assess attentional flexibility and executive functions in rodents.

Originally adapted from Birrell and Brown’s (2000) paradigm, this apparatus integrates scent and texture discrimination while expanding behavioral measures to include latency to retrieve and consume food rewards. By addressing limitations of the original ASST, the Neuwirth-Brown™ ASST captures nuanced relationships between prefrontal attentional mechanisms, frontal executive behavior, and neurochemical processes, providing a more complete model of goal-directed cognition.

Market Opportunity

Cognitive flexibility and executive dysfunction are central to many conditions, including ADHD, schizophrenia, dementia, and toxicological exposures (e.g., lead). The Neuwirth-Brown™ ASST:

  • Expands on the classic ASST by measuring additional behavioral parameters.

  • Provides a validated translational model cited in over 135 publications.

  • Enables sensitive detection of neurotoxic, pharmacological, and developmental effects on attentional function.

  • Supports preclinical studies for treatments targeting executive dysfunction.

Invention & Advantages

Expanded paradigm

4-day testing protocol instead of a single 10-hour session.

Reduced stress:

Increases motivation, minimizes exhaustion.

New parameters

Includes latency to eat, time holding food, and reward consumption metrics.

Versatile discrimination tasks

Uses odor cues, tactile media, and reversal learning.

Species adaptable

Configurable for both mice and rats.

Well-cited tool:

Over 135 publications validate its research utility.

Applications

  • Study of attentional flexibility and executive function.

  • Evaluation of fronto-executive dysfunctions from neurodevelopmental lead exposure.

  • Pharmacological studies of drugs targeting cognition.

  • Modeling of psychiatric and neurodevelopmental disorders.

  • Research into sex, age, and strain-specific behavioral differences.

Apparatus & Equipment

Mouse ASST – $2,990
Rat ASST – $3,290

Training Protocol

  • Food restriction for 2 weeks under NIH guidelines to ensure steady metabolic state and motivation.

  • Dig training with incremental shredded paper depths (25% → 100%) until rodents complete 10 successful retrievals.

Four-day testing protocol:

  • Day 1: Two-choice stimuli (odor or texture) paired with food reward.

  • Day 2: New stimuli sets, discrimination reversals.

  • Day 3: Interdimensional shifts and reversals.

  • Day 4: Extradimensional shifts and reversals.

  • Time to reach food bowl.

  • Latency to approach/eat.

  • Correct vs incorrect discriminations.

  • Time holding and consuming reward.

Strengths & Limitations

Strengths
Limitations

Principal Investigator

Contact

Neil Veloso

Executive Director, Brown Technology Innovations ✉ [email protected]

References
  • Birrell JM, & Brown VJ. Medial frontal cortex mediates perceptual attentional set-shifting in the rat. J Neurosci. 2000.

  • Tait, D. S., Bowman, E. M., Neuwirth, L. S., & Brown, V. J. (2018). Assessment of intradimensional/extradimensional attentional set-shifting in rats. Neurosci Biobehav Rev, 89, 72-84.

  • Neuwirth, L.S. et al. (2019a). Sex-based impairments in executive functions after developmental lead exposure in rats. Behav Brain Res, 366, 126-134.

  • Neuwirth, L.S. et al. (2019b). Taurine rescues fronto-executive dysfunctions from low-level lead exposure in rats. Adv Exp Med Biol, 1155: 821-846.

  • Neuwirth, L.S. et al. (2020). Low-level lead exposure impairs fronto-executive functions: A call to update DSM-5. Psychol Neurosci, 13(3), 299–325.

  • Neuwirth, L.S. et al. (2022). Need for standardization of light stimuli in rodent anxiety tests. Front Mol Neurosci, 15.

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