With test mice excluded from model fitting, reverse excitation gave no clear added strength prediction gain after same-PV calibration in 53 mouse V1 pairs
Can reverse excitation help predict a missing inhibitory response? We tested open mouse V1 PV–pyramidal recordings. We recalculated responses from source traces and reproduced the reported sample counts and strength relation. The main test used 53 reciprocal pairs from 23 PV cells in 16 mice. Each target inhibitory response was hidden. Other outputs of its PV cell supplied calibration. All fitted coefficients came from other mice. Adding reverse excitation decreased squared log prediction error by 14.8%. The 95% mouse resampling range was −61.6% to +52.3%, with all model fits repeated. Planned controls left this added gain uncertain. Removing the weakest inhibitory responses changed the point decrease to −10.7%. A planned second test used all 88 pairs from 29 mice, with soma distance and no peer calibration. Adding reverse excitation decreased error by 30.2%, with a range of +8.1% to +47.8%. An added check on the same 53 pairs gave lower errors with the global models than with the tested peer rules. Thus, reverse strength helped prediction across mice in this dataset. Its added value beyond the tested same-PV calibration rule remains uncertain. The test concerns detected slice responses, not conductance, complete anatomical wiring, or circuit stability. The package preserves code, compact derived data, source hashes, predictions, resampling draws, figures, checks, and repeat steps.
reciprocal connections · synaptic strength · PV interneurons · mouse visual cortex · prediction · multipatch recordings · excitatory inhibitory circuits · reproducible research
References
5- usesdoi:10.1016/j.neuron.2023.12.013
We use the source response method and test whether its reported reciprocal strength relation helps predict a missing response.
- usesdoi:10.25418/crick.23295188.v1
This fixed dataset version supplies the original connection traces and cell annotations.
- doi:10.1371/journal.pbio.0030068
This study reported correlated strengths in reciprocal excitatory cortical connections.
- Other outputs of the same neuron gave no clear strength prediction gain in shrinkage tests of 934 human layer 2–3 connections sci:sha256:748c9cedeba3841b13637e1d3ceeafee3278fdf1ccc5b88c28dfd48378e3eb8f
This prior SCI study tested missing strength prediction from shared cell identity in human cortical recordings. Our source data, code, and reverse-strength task are different.
- Recording and cell class controls left no clear added agreement in initial 50 Hz responses of 144 mouse reciprocal pairs sci:sha256:68f047b73392ee440a4b219b558a0865646d318aefb1f1a5714bfcad248cb881
This prior SCI study tested paired initial response changes in Allen reciprocal pairs. It did not test our missing inhibitory strength task.
Cited by
4 publicationsPublic catalog entries on Sciscape.
- Free factors for both cells left three strength contrasts in 88 reciprocal mouse V1 pairs
Prior same-PV calibration test. Our new test permits free factors for both endpoint cells and uses only nonbridge pairs.
- Reverse current gave no clear added strength prediction in 69 reciprocal mouse V1 pairs with test mice excluded
Its calibration control shows that the available reference information changes the reverse-strength question.
- usesWith matched windows, response timing cut error by 0.8 to 1.8% in fixed ridge tests of 52 mouse V1 inhibitory connections
We use the checked shared connectivity source-member cache documented by this record. Our visual-response window tests use the same source experiment, with new features and analysis code.
- usesWith each mouse excluded from ridge fitting, visual similarity reduced mean squared log voltage error by 3.64% in 92 mouse V1 connections
We reuse its checked cache of the unchanged raw patch source. Its prediction task uses reverse excitation; ours adds matched visual data and tests visual similarity. No prior analysis code or derived values are reused.