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. Author manuscript; available in PMC: 2009 Jul 7.
Published in final edited form as: Respir Physiol Neurobiol. 2008 Oct 11;165(1):40–48. doi: 10.1016/j.resp.2008.10.003

Table 1.

Ventilation at rest in adult wild-type (+/+) and homozygous (−/−) mice for deletions of intron 1 (i1RR knockout), of exons 5 and 6 (del E5+6 knockout) of the AChE gene, or of the anchor molecule PRiMA.

i1RR +/+ (n = 6) i1RR −/− (n=6) P % difference
E (mL/(g min−1)) 2.01 ± 0.1 2.65 ± 0.14 <0.01 +32.5
VT (µL/g) 10.9 ± 0.3 13.3 ± 0.7 <0.02 +22
fR (breaths/min) 185 ± 11 204 ± 19 NS +10
Ti (ms) 105 ±7 89 ±5 NS −15
TE (ms) 232 ± 18 222 ± 30 NS −4
TI/TTOT (%) 31.5 ± 1.10 30.0 ± 2.68 NS −5
VT/TI (µL/(g s−1)) 106 ± 5.9 153 ± 13.2 <0.01 +44
Weight (g) 19.4 ± 0.67 14.5 ± 1.07 <0.01 −25
Temperature (°C) 37.4 ± 0.21 38.1 ± 0.26 NS +2
Del E5+6 +/+ (n = 7) Del E5+6 −/− (n=7)

E (mL/(g min−1)) 1.81 ± 0.11 2.57 ± 0.12 <0.001 +42
VT (µL/g) 10.9 ± 0.42 13.8 ± 0.60 <0.01 +27
fR (breaths/min) 167 ± 11 188 ±9 NS +12
Ti (ms) 109 ±8 80 ± 1 <0.01 −27
TE (ms) 266 ± 21 244 ± 15 NS −8
TI/TTOT (%) 29.7 ± 1.6 26.8 ±2 NS −10
VT/TI (µL/(g s−1)) 104 ± 9.5 166 ± 13 <0.01 +59
Weight (g) 23.9 ± 1.0 17.6 ± 1.7 <0.01 −26.5
Temperature (°C) 37.8 ± 0.2 37.8 ± 0.1 NS 0
PRiMA +/+ (n = 6) PRiMA −/− (n=8)

E (mL/(g min−1)) 1.62 ± 0.16 1.48 ± 0.10 NS −9
VT (µL/g) 10.4 ± 0.58 10.4 ± 1.02 NS 0
fR (breaths/min) 154 ±8 148 ±8 NS −4
Ti (ms) 113 ±4 118 ± 9.0 NS +4.5
TE (ms) 293 ± 20 307 ± 23.0 NS +5
TI/TTOT (%) 28.8 ± 1.5 28.2 ± 1.6 NS −2
VT/TI (µL/(g s−1)) 94 ± 7.4 93 ± 13.2 NS −1
Weight (g) 28.5 ± 2.3 30.1 ± 3.5 NS +5.5
Temperature (°C) 37.2 ± 0.2 37.1 ± 0.2 NS 0
AChE +/+ (n = 9) AChE −/− (n=9)

E (mL/(g min−1)) 1.34 ± 0.12 2.28 ± 0.19 <0.001 +70
VT (µL/g) 9.6 ± 1.1 18.8 ± 1.60 <0.001 +96
fR (breaths/min) 144 ±7 130 ± 12 NS −10
Ti (ms) 130 ±5 74 ± 4 <0.001 −43
TE (ms) 301 ± 20 448 ± 47 <0.02 +49
TI/TTOT (%) 30.9 ± 1.4 15.5 ± 1.6 <0.001 −50
VT/TI (µL/(g s−1)) 76 ± 10 264 ± 31 <0.001 +247
Weight (g) 24.9 ± 0.83 16.3 ± 1.10 <0.001 −34.5
Temperature (°C) 36.7 ± 0.4 36.6 ± 0.27 NS 0

Values for mice with deletion of the AChE gene (Boudinot et al., 2004) are presented for reference.