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. Author manuscript; available in PMC: 2007 Jul 2.
Published in final edited form as: Pharmacol Biochem Behav. 2006 Dec 28;85(4):769–779. doi: 10.1016/j.pbb.2006.11.012

TABLE 1. Changes in baseline latencies following chronic morphine administration.

Baseline latencies (± S.E.M.) are listed for each strain, treatment condition, and nociceptive assay following one of two published morphine regimens (Bryant et al. 2006; Kest et al. 2002). "B6" = C57BL/6J.

Strain Regimen Treatment Assay Latency
129S6 Bryant saline
morphine
HP 16.7±1.6
22.0±1.7*
129S6 Bryant saline
morphine
TW 3.3±0.4
3.9±0.2
129P3 Bryant saline
morphine
HP 17.6±1.1
16.7±1.3
129P3 Bryant saline
morphine
TW 3.5±0.2
3.1±0.5
129P3 Kest day 1
day 4
TW 2.9±0.2
2.7±0.3
129P3 Kest saline
morphine
TW 2.9±0.2
2.5±0.2
B6 Kest day 1
day4
TW 2.1±0.2
1.7±0.2*
B6 Kest saline
morphine
TW 2.3±0.2
1.5±0.08*
129S6 Bryant saline
morphine
MK+mor
MK-801
HP 14.9±1.6
16.1±1.1
20±1.2*
17.7±1.3
CD-1 Bryant saline
morphine
MK+mor
MK-801
HP 16.3±1.7
16.0±1.1
23.4±2.7*
25.7±1.9*
*

significantly different from control mice receiving chronic saline or from day 1. A p-value of 0.05 was considered significant.