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. 2005 Jan 27;564(Pt 1):233–243. doi: 10.1113/jphysiol.2004.080051

Figure 7. Stimulation of nCRF increases orientation–time inseparability of cortical neurones.

Figure 7

A, TOM, its first singular vector reconstructed matrix, and the difference between these two matrixes for an example neurone at 1 × CRF (in unit of the percentage of the mean spike rate). Inseparability index was 1.71. B, same as A, but at 4 × CRF. The relatively high inseparability index (7.83) is largely caused by the tilt (upper-left to lower-right) of the TOM profile, which indicates a downward shift in the preferred orientation over time. C, inseparability index (see eqn (7) in Methods) as a function of stimulus size for 126 neurones. Error bar, ±s.e.m. The indices obtained with nCRF were significantly larger than those with CRF only, in all cortical layers; layer 2/3: 2.8 ± 0.5 for 1 × CRF versus 4.1 ± 0.7 (P < 0.001, paired t test) and 4.8 ± 0.7 (P < 10−4) for 2× and 4 × CRF, respectively, n = 44; layer 4: 5.1 ± 1.2 versus 6.2 ± 1.5 (P < 0.05) and 6.3 ± 1.5 (P < 0.05), n = 14; layer 5/6: 3.6 ± 0.5 versus 5.3 ± 0.7 (P < 0.001) and 5.3 ± 0.7 (P < 0.001), n = 33. This effect was also found for both simple and complex cells; simple cells: 4.7 ± 0.6 for 1 × CRF versus 6.5 ± 0.9 (P < 0.01, paired t test) and 6.2 ± 0.8 (P < 0.01) for 2× and 4 × CRF, respectively, n = 30; complex cells: 2.4 ± 0.3 versus 3.8 ± 0.4 (P < 10−8) and 4.3 ± 0.4 (P < 10−10) n = 96. Cells with or without inhibitory nCRF also had a similar effect. Inhibitory: 2.7 ± 0.3 for 1 × CRF versus 4.1 ± 0.4% (P < 10−5 paired t test) and 4.3 ± 0.4 (P < 10−6) for 2× and 4 × CRF, respectively, n = 68; facilitatory: 3.2 ± 0.6 for 1 × CRF versus 4.2 ± 0.7 (P < 0.001) and 4.9 ± 0.7 (P < 10−5) for 2× and 4 × CRF, n = 42; neither facilitatory nor inhibitory: 3.5 ± 1.0 for 1 × CRF versus 6.4 ± 1.6 (P < 0.001) and 6.5 ± 1.6 (P < 0.001) for 2× and 4 × CRF, n = 16.