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. 2017 Mar 1;117(6):2179–2187. doi: 10.1152/jn.00935.2016

Table 1.

Cough parameters after kynurenic acid microinjections in rostral NTS

Control 5–15 min 15–25 min Recovery P Value
Cough number, motor drive, and mechanics
CN (per 20 s) 10.0 ± 1.2 4.1 ± 1.2***+++ 4.5 ± 0.7***+++ 9.8 ± 1.1 <0.001
ABD, % 100 40 ± 9***+++ 50 ± 7***+++ 87 ± 8 <0.001
PS, % 100 89 ± 11 90 ± 9 110 ± 11 >0.05
EP E, kPa 24.1 ± 5.2 5.8 ± 1.7***++ 8.1 ± 1.8***++ 20.0 ± 4.3 <0.001
EP I, kPa −5.6 ± 1.0 −5.4 ± 0.8 −5.5 ± 0.9 −6.5 ± 0.9 >0.05
Cough phase durations
CTI, s 1.08 ± 0.11 3.31 ± 0.68***++ 3.39 ± 0.52***++ 1.21 ± 0.10 <0.001
CTE, s 1.40 ± 0.14 2.76 ± 0.83 2.28 ± 0.43 1.32 ± 0.19 >0.05
CTE1, s 0.63 ± 0.07 2.24 ± 0.87 1.77 ± 0.42 0.75 ± 0.06 <0.05
CTE2, s 0.76 ± 0.12 0.52 ± 0.21 0.52 ± 0.26 0.57 ± 0.17 >0.05
Ttot, s 2.47 ± 0.24 6.07 ± 1.36**++ 5.47 ± 0.84*++ 2.53 ± 0.26 0.001
Tactive, s 1.71 ± 0.15 5.55 ± 1.43**++ 4.96 ± 0.88*+ 1.96 ± 0.13 <0.01
Other temporal metrics of cough
desI, s 0.14 ± 0.01 1.64 ± 0.73*+ 1.30 ± 0.40 0.21 ± 0.02 <0.05
dif, s 0.18 ± 0.01 1.65 ± 0.70*+ 1.19 ± 0.41 0.25 ± 0.02 <0.05
over, s 0.55 ± 0.08 3.14 ± 1.16*+ 2.96 ± 0.88*+ 0.66 ± 0.12 <0.01
TPS, s 1.21 ± 0.12 4.95 ± 1.31**++ 4.44 ± 0.86*++ 1.42 ± 0.11 <0.001
TABD, s 1.04 ± 0.12 3.73 ± 1.31*+ 3.48 ± 0.91*+ 1.21 ± 0.15 <0.05
Cardiorespiratory data
TI, s 0.77 ± 0.07 2.57 ± 0.57***++ 2.15 ± 0.32**++ 0.88 ± 0.11 <0.001
TE1, s 0.63 ± 0.09 2.64 ± 0.84*+ 2.30 ± 0.86 0.77 ± 0.19 <0.01
TE2, s 1.40 ± 0.18 0.96 ± 0.14* 1.13 ± 0.19 0.92 ± 0.11* <0.05
RR, min−1 22.6 ± 1.5 13.3 ± 2.3***+++ 14.0 ± 1.8***+++ 26.6 ± 3.0 <0.001
PS ampl, % 13.1 ± 2.2 24.3 ± 7.5 11.9 ± 2.4 18.4 ± 8.3 >0.05
EP ampl, kPa 0.33 ± 0.08 0.44 ± 0.17 0.43 ± 0.16 0.26 ± 0.06 >0.05
ETCO2, mmHg 31.7 ± 1.8 33.4 ± 2.4 35.0 ± 2.0 32.2 ± 2.1 >0.05
BP, mmHg 130 ± 5 175 ± 9***+++ 165 ± 7***+++ 126 ± 5 <0.001
HR, min−1 188 ± 10 213 ± 11*** 203 ± 11* 203 ± 11* <0.01

Values are means ± SE (n = 11). Data were pooled for both rNTS microinjection groups. Control, preinjection control; 5–15 min, 15–25 min, data within the time intervals after completion of microinjections; Recovery, data >90 min after microinjections; CN, number of coughs per 20-s stimulus duration (per 1 trial); ABD, amplitudes of abdominal muscle EMG; PS, amplitudes of parasternal muscle EMG; EP E, EP I, expiratory and inspiratory esophageal pressure amplitudes, respectively; CTI, duration of cough inspiratory phase; CTE, duration of cough expiratory phase; CTE1, duration of active cough expiratory phase; CTE2, duration of quiescent period of cough expiration; Ttot, total cough cycle duration; Tactive, duration of cough-related EMG activity; desI, descendent portion of cough parasternal bursting; dif, time interval between the peaks of parasternal and abdominal EMG activity; over, duration of parasternal and abdominal activity overlap; TPS, TABD, durations of cough-related parasternal and abdominal discharge, respectively; TI, inspiratory phase duration; TE1, postinspiratory phase duration; TE2, expiratory phase 2 duration; RR, respiratory rate; PS ampl, amplitudes of parasternal muscle EMG; EP ampl, amplitudes of esophageal pressure; ETCO2, end-tidal CO2 content; BP, mean arterial blood pressure; HR, heart rate. P value is for ANOVA.

*

P < 0.05,

**

P < 0.01,

***

P < 0.001 compared with preinjection control;

+

P < 0.05,

++

P < 0.01,

+++

P < 0.001 compared with recovery >90 min after injection.