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. 2010 Jul 26;588(Pt 18):3425–3443. doi: 10.1113/jphysiol.2010.195396

Table 2.

Effects of viral gene manipulation on the coupling between Inline graphic and discharge properties of inspiratory HMNs

Experimental conditions n SmFR (sp s−1%−1) SSB (sp burst−1%−1) SBR (bursts min−1%−1)
Intact (control) 44 9.2 ± 0.9 4.6 ± 0.4 5.6 ± 0.8
7 days post-crushing 44 3.5 ± 0.4* 1.5 ± 0.2* 4.1 ± 0.6
AVV-eGFP 25 10.1 ± 0.8 6.2 ± 0.6 4.1 ± 1.2
AVV-eGFP/AVV-nNOS 16 3.5 ± 0.5*# 1.7 ± 0.4*# 4.2 ± 2.3
AVV-eGFP/AVV-nNOS+L-NAME 16 8.2 ± 2.0§ 5.0 ± 1.1§ 3.1 ± 1.1
AVV-eGFP/AVV-nNOS+7-NI 10 10.7 ± 1.1§ 6.4 ± 1.3§ 4.1 ± 0.4
AVV-eGFP/AVV-nNOS+ODQ 12 13.4 ± 2.5§ 6.4 ± 1.1§ 6.2 ± 1.5
LVV-miR-shRNA/nNOS/AVV-nNOS 16 10.7 ± 1.0§ 6.3 ± 0.5§ 3.5 ± 1.6
LVV-miR-shRNA/nNOS/Crush 11 7.3 ± 0.9 3.7 ± 0.4 5.7 ± 0.9
LVV-miR-shRNA/nNOS/Crush +Dox 9 4.2 ± 1.2* 1.8 ± 0.5* 6.3 ± 3.2

Sensitivity (S) or gain parameters characterizing motoneuron activity were measured in response to Inline graphic changes from 3–3.5% to 5.5–6.0%. n represents the number of motoneurons included in the study. Data values are expressed as means ±s.e.m. At least 3 animals were used per experimental condition. Significant differences relative to intact/control

*

AVV-eGFP-

#

or AVV-eGFP/AVV-nNOS-injected

§

groups (P < 0.05; one-way ANOVA; post hoc Tukey's test).