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. 2014 Jan 10;306(5):H690–H698. doi: 10.1152/ajpheart.00901.2013

Table 3.

Spinotrapezius muscle PO2mv kinetics following the onset of contractions under control, SNP, and l-NAME conditions in CHF and CHF + EXT rats

Control
SNP
l-NAME
CHF CHF + EXT CHF CHF + EXT CHF CHF + EXT
PO2mv(BL), mmHg 24.3 ± 2.3 22.6 ± 1.9 33.7 ± 2.3* 35.3 ± 2.9* 23.5 ± 2.4 21.3 ± 1.0
Δ1PO2mv, mmHg 10.3 ± 1.0 9.5 ± 1.1 8.8 ± 0.8 10.4 ± 2.1 11.9 ± 1.6 11.6 ± 1.0
Δ2PO2mv, mmHg 1.9 ± 0.3 2.2 ± 0.4 2.4 ± 0.4 2.3 ± 0.4
ΔTotalPO2mv, mmHg 8.8 ± 1.0 8.7 ± 1.0 8.8 ± 0.8 10.4 ± 2.1 9.7 ± 1.3 10.6 ± 0.8
PO2mv(SS), mmHg 15.5 ± 1.8 13.9 ± 1.2 24.9 ± 2.2* 24.9 ± 2.2* 13.7 ± 1.2 10.7 ± 0.6*
TD1, s 8.9 ± 1.5 12.6 ± 1.3# 4.0 ± 1.7* 5.7 ± 2.1*# 6.7 ± 0.7 11.9 ± 2.1
TD2, s 45.7 ± 5.7 83.3 ± 10.5 35.4 ± 4.7 60.5 ± 15.5
τ1, s 11.9 ± 1.3 19.7 ± 3.0# 39.0 ± 6.5* 49.8 ± 8.3* 10.1 ± 1.4 19.1 ± 2.9#
τ2, s 41.2 ± 12.6 57.0 ± 9.9 59.3 ± 9.1 38.0 ± 13.5
T63, s 20.4 ± 1.2 31.2 ± 2.3 42.2 ± 7.7* 55.0 ± 7.1* 17.4 ± 1.6 31.3 ± 3.4

Values are means ± SE. PO2mv(BL), resting PO2mv; Δ1PO2mv, amplitude of the first component; Δ2PO2mv, amplitude of the second component; ΔTotalPO2mv, overall amplitude regardless of one- or two-component model fit; PO2mv(SS), contracting steady-state PO2mv; TD1, time delay for the first component; TD2, time delay for the second component; τ1, time constant for the first component; τ2, time constant for the second component; T63, time to reach 63% of the primary amplitude as determined independent of modeling procedures. The one-component exponential model was used to analyze the PO2mv kinetics in the following conditions: CHF control (2/10), CHF SNP (10/10), CHF l-NAME (1/10), CHF + EXT control (7/10), CHF + EXT SNP (7/7), CHF + EXT l-NAME (5/11). Significantly different from:

*

control within group;

SNP within group;

CHF within superfusion condition;

#

P = 0.05–0.1 vs. CHF within condition.