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. Author manuscript; available in PMC: 2007 Mar 7.
Published in final edited form as: Endocrinology. 2006 Jan 5;147(4):2008–2017. doi: 10.1210/en.2005-1041

TABLE 1.

Effect of CVS on physiological measures in experiment 1

BW change
(%)
Thymus weight
(mg)
Thymus weight
(mg/g BW) × 100
Adrenal weight
(mg)
Adrenal weight
(mg/g BW) × 100
16 h
 Control (n = 24) 14.3 ± 0.6 521 ± 20 184 ± 6 43.5 ± 1.0  15.5 ± 0.3
 CVS (n = 24)  4.8 ± 0.6a 460 ± 17 179 ± 7 44.8 ± 0.9  17.4 ± 0.3a
4d
 Control (n = 12) 18.5 ± 0.8 537 ± 34  189 ± 12 41.2 ± 0.9 14.1 ± 0.3
 CVS (n = 12)  11.4 ± 1.3a 493 ± 34  177 ± 10  46.6 ± 1.4a  16.8 ± 0.3a
7d
 Control (n = 12) 22.0 ± 1.0 498 ± 22 163 ± 5 42.6 ± 1.6 14.0 ± 0.4
 CVS (n = 24)  17.3 ± 0.8a 489 ± 17 167 ± 4  46.5 ± 0.6a  15.9 ± 0.2a
30 d
 Control (n = 12) 50.3 ± 3.7 430 ± 22 117 ± 5 46.8 ± 2.0 12.7 ± 0.4
 CVS (n = 12) 49.0 ± 1.7 444 ± 21 122 ± 5 47.9 ± 1.5 13.3 ± 0.5

Rats were exposed to CVS for 7 d or were unhandled controls. At each recovery time point, six rats per group received novel environment exposure (5 min), whereas a different set of six rats per group were exposed to hypoxia (20 min). The total number of rats in each group is listed. Unstressed rats from the 16 h control (n = 12), 16 h CVS (n = 12), and 7 d CVS (n = 12) groups are included in this table. Time points reflect length of time after cessation of stress, and values represent the mean ± SEM of each group.

a

CVS is significantly different from corresponding control group (P < 0.05).