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Temporal Factors Alter Effects of Social Housing Conditions on Responses to Chemotherapy and Hormone Levels in a Shionogi Mammary Tumor Model

Leslie R. Kerr, PhD, Heather N. Andrews, PhD, Karen S. Strange, PhD, Joanne T. Emerman, PhD and Joanne Weinberg, PhD

From the Departments of Psychology and Biology, Trent University, Peterborough, Ontario, Canada (L.R.K.); the Department of Kinesiology, University College of the Fraser Valley (H.N.A., K.S.S.), Abbotsford, British Columbia, Canada; and the Department of Cellular & Physiological Sciences, Faculty of Medicine, University of British Columbia (J.T.E., J.W.), Vancouver, British Columbia, Canada.


Figure 121
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Figure 1. Experimental designs.

 

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Figure 2. Tumor growth in mice in the drug vehicle treatment condition. Tumor weights (mean ± standard error) from 11 to 18 days after tumor cell injection and formation of social housing conditions (n = 5, II; n = 10, IG; n = 6, GG; n = 5, GI). Tumor growth rates at 16 to 18 days after tumor cell injection and formation of social housing conditions: GI > II = GG > IG (p values <.05).

 

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Figure 3. Plasma hormone levels (mean ± standard error) in drug vehicle- (V) or chemotherapy- (C) treated mice at 0, 1, and 5 days after drug vehicle or chemotherapy injection. Significance symbols: treatment (•), group (*), and day ({diamondsuit}). (A) Corticosterone (CORT): CORT levels were significantly higher at 1 day for C-II than for V-II mice (p < .05; •). (B) Growth hormone (GH): before vehicle/chemotherapy injection (0 days), GH levels did not differ significantly among mice in the housing conditions. At 1 day after drug vehicle injection, GH levels were higher in GI mice compared with all other housing conditions (p values <.05; *). Also, GH levels in GI mice were significantly higher at 1 and 5 days than at 0 days (p values <.05; {diamondsuit}). Overall, GH levels were significantly higher in V-GI mice than in C-GI mice (p < .01; •). (C) Testosterone (T): for V mice, significant increases in T levels were seen at 5 days in GG mice compared with IG and GI mice (p values <.05; *). Also for GG mice, T levels were significantly higher at 5 days than those at 1 day (p < .01; {diamondsuit}). No significant differences in T levels were seen in C mice or between V and C mice.

 

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Figure 4. Tumor growth in mice in the drug vehicle treatment condition. Arrow represents formation of experimental housing conditions. Tumor weights (means ± standard error) from 11 to 18 days after tumor cell injection for drug vehicle-treated mice in the experimental housing conditions (n = 5, II; n = 9, IG; n = 6, GG; n = 6, GI). Tumor growth rates by 18 days after tumor cell injection (4 days after formation of experimental housing conditions): GI = GG > II = IG (p values <.05).

 

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Figure 5. Plasma hormone levels (mean ± standard error) in drug vehicle- (V) and chemotherapy- (C) treated mice at 0, 1, and 5 days after drug vehicle or chemotherapy administration. Significance symbols: treatment (•), group (*), and day ({diamondsuit}). (A) Corticosterone (CORT): at day 0 (1 day after experimental housing condition formation), CORT levels were significantly higher for IG mice than in mice in all other housing conditions (p values <.05; *). Also, CORT levels at day 0 were significantly higher than those at 1 and 5 days in V-IG mice and higher than those at 5 days in C-IG mice (p values <.05; {diamondsuit}). Accordingly, CORT levels at 1 day were significantly higher for C-IG than for V-IG mice (p < .01; •). (B) Growth hormone (GH): at day 0, GH levels were significantly higher for GI mice than in mice in all other housing conditions (p values <.01;*) as well as for II than for IG mice (p < .05; *). Also at day 0, GH levels in GI mice were significantly higher than those at 1 or 5 days (p values <.05; {diamondsuit}). GH levels at 5 days were significantly higher in C-GI mice than in C-IG mice (p < .05; *). Also, GH levels at 5 days were significantly higher for C-GI than for V-GI mice (p < .05; •). (C) Testosterone (T): for V mice, T levels, overall, were significantly higher in GI than in II mice (p = .01; *) and marginally higher in GI than in IG and GG mice (p = .060 and p = .086, respectively). T levels did not differ significantly for C mice or between the C and V conditions.

 





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