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. 2019 Dec 25;123(2):670–681. doi: 10.1152/jn.00500.2019

Table 1.

Properties of low- and high-amplitude IPSCs in control conditions in the presence of drugs as well as the difference between them

Amplitude, pA Rise Time, ms Decay Time, ms Half Width, ms
Control IPSCs
    High 167.2 ± 7.5* 1.91 ± 0.15 17.3 ± 1.5 14.3 ± 1.0
    Low 92.3 ± 3.8* 2.21 ± 0.13 20.6 ± 1.2 16.2 ± 0.9
Drug-resistant component
    High 120.0 ± 9.3* 1.76 ± 0.16 13.7 ± 1.5 12.5 ± 0.9
    Low 54.7 ± 4.4* 2.05 ± 0.18 15.5 ± 1.2 14.0 ± 0.8
Drug-sensitive component
    High 51.5 ± 5.2 2.64 ± 0.35 24.9 ± 3.7 19.7 ± 2.9
    Low 39.1 ± 3.6 2.32 ± 0.22 28.1 ± 1.9 20.1 ± 1.6

Values are means ± SE for control conditions in the presence of drugs (5-HT or CP93129; drug-resistant component) and the difference between them (drug-sensitive component); n = 14. In cells with low- and high-amplitude inhibitory postsynaptic currents (IPSCs), the 5-HT-sensitive component had a slower decay time than the 5-HT-resistant component (P < 0.001; see detailed statistics in main text). Whereas the amplitude of the 5-HT-sensitive current did not differ between the 2 subsets of cells, that of the 5-HT-resistant component was significantly higher in cells with high than low IPSC amplitudes (P < 0.001). CP93129 also shortened the decay time of GABAA IPSCs (P < 0.002).

*

P < 0.05, statistically significant differences between high vs. low.