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Updated: Sep 11, 2025

Transcranial Electrical Brain Stimulation in Alert Rodents
Published on: November 2, 2017
No observation of DIANA signals in rats at 7.0 and 17.2 Tesla
Martijn A Cloos1, Erwan Selingue2, Shota Hodono1
1Australian Institute for Bioengineering and Nanotechnology, University of Queensland, St. Lucia, Australia.
Abstract:
Recently, a new method was introduced to detect neuronal activity using Magnetic Resonance Imaging (MRI). The method, referred to as DIANA, showed MRI signals with millisecond temporal resolution that correlated with local field potentials measured invasively in mice. Troublingly, attempts by other groups to detect the DIANA signals in humans at 7 Tesla and mice at 15.2 Tesla have failed. So far, attempts to reproduce DIANA in small rodents have focused on paradigms using whisker pad stimulation, which were expected to produce a 0.1-0.15% signal change. However, the Supplementary Material accompanying the original DIANA paper showed that visual stimulation produced a three times larger signal, which should be much easier to detect. Therefore, we attempted to find the DIANA signal in rats using a visual stimulation paradigm. Experiments were performed at 17.2 Tesla but also at 7.0 Tesla to see if the DIANA signal appears at a lower field strength where T2 is longer and BOLD contributions are reduced. In addition, simulations were performed to investigate the theoretical detectability of synthetic DIANA signals in noisy data. Although our data indicated that a 0.1% signal change would have been detectable, we did not observe a DIANA signal. We did observe neuronally driven hemodynamic signal variations that were much larger than the anticipated DIANA signal. The amplitude of these signal changes was relatively similar at 7.0 and 17.2 Tesla (0.7% vs 1.1%). Numerical simulations indicated, however, that the measured hemodynamic signal changes would not interfere with the detection of DIANA signals. Therefore, it is reasonable to expect that measurements at higher field strength with improved SNR would have a better chance to detect the DIANA signal. Yet, we, among others, were unable to find it.
Insights
Researchers attempted to replicate the DIANA method for detecting neuronal activity using Magnetic Resonance Imaging (MRI). Despite using visual stimulation and high field strengths, the DIANA signal could not be detected, raising questions about its reproducibility.
Area of Science:
- Neuroimaging
- Magnetic Resonance Imaging (MRI)
- Neuronal Activity Detection
Background:
- A novel Magnetic Resonance Imaging (MRI) method, DIANA, was reported to detect neuronal activity with millisecond resolution.
- Previous attempts to reproduce DIANA signals in humans and rodents have been unsuccessful.
- The original DIANA study suggested visual stimulation yields larger signals than whisker stimulation.
Purpose of the Study:
- To investigate the detectability of the DIANA signal in rats using visual stimulation.
- To assess DIANA signal presence at different field strengths (7.0T and 17.2T).
- To evaluate the theoretical detectability of synthetic DIANA signals via simulations.
Main Methods:
- Experiments conducted on rats at 7.0T and 17.2T MRI scanners.
- Utilized a visual stimulation paradigm to elicit neuronal activity.
- Performed numerical simulations to assess signal detectability in noisy data.
Main Results:
- No DIANA signal was detected despite the study's sensitivity to a 0.1% signal change.
- Significant neuronally driven hemodynamic signals (0.7%-1.1%) were observed, larger than expected DIANA signals.
- Simulations confirmed that observed hemodynamic signals would not impede DIANA signal detection.
Conclusions:
- The DIANA signal, as reported, was not reproducible in this study using visual stimulation in rats.
- Larger hemodynamic signals were observed but did not preclude potential DIANA signal detection.
- Further investigation at higher field strengths with improved signal-to-noise ratio may be necessary, but reproducibility remains a concern.

