Seoul virus infection increases aggressive behaviour in male Norway rats

2004 ◽  
Vol 67 (3) ◽  
pp. 421-429 ◽  
Author(s):  
Sabra L. Klein ◽  
M.Christine Zink ◽  
Gregory E. Glass
2006 ◽  
Vol 20 (2) ◽  
pp. 182-190 ◽  
Author(s):  
Ella R. Hinson ◽  
Michele F. Hannah ◽  
Douglas E. Norris ◽  
Gregory E. Glass ◽  
Sabra L. Klein

2002 ◽  
Vol 16 (6) ◽  
pp. 736-746 ◽  
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Sabra L. Klein ◽  
Aimee L. Marson ◽  
Alan L. Scott ◽  
Gary Ketner ◽  
Gregory E. Glass

2017 ◽  
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Mary-Margaret A. Fill ◽  
Heather Mullins ◽  
Andrew Stephen May ◽  
Heather Henderson ◽  
Shelley M. Brown ◽  
...  
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2018 ◽  
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pp. 1099-1102 ◽  
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Jörg Hofmann ◽  
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Martin Kuhns ◽  
Annekathrin Zinke ◽  
Heike Heinsberger ◽  
...  
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2017 ◽  
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Yuan-Yuan Liu ◽  
Hai-Rong Xiong ◽  
...  

2008 ◽  
Vol 80 (7) ◽  
pp. 1308-1318 ◽  
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Judith D. Easterbrook ◽  
Sabra L. Klein

1979 ◽  
Vol 83 (1) ◽  
pp. 17-26 ◽  
Author(s):  
MARJORIE H. CHRISTIE ◽  
R. J. BARFIELD

SUMMARY Three experiments were used to test the applicability of the aromatization hypothesis of androgen action to aggressive behaviour among Norway rats. In Expt 1, administration of testosterone propionate was highly effective in restoring aggressive behaviour to castrated rats while 17β-hydroxy-5α-androstan-3-one was of intermediate effectiveness. Of the steroids tested in Expt 2, androstenedione and testosterone were highly effective, 17β, 19-dihydroxyandrost-4-en-3-one was of intermediate effectiveness and cholesterol was ineffective. The results of Expt 3 indicated that treatment with testosterone or oestradiol both resulted in increased aggression while treatment with (5α, 17β)-17, 19-bis(acetyloxy)-andostan-3-one diacetate (5α-19-hydroxytestosterone) was without effect. Androgens which were aromatizable and could be 5α reduced, i.e. testosterone, testosterone propionate and androstenedione, were highly effective in restoring aggressive behaviour; however, two other steroids, 5α, 19-hydroxytestosterone which is 5α reduced, and 19-hydroxytestosterone, which can be aromatized, were respectively of low or medium effectiveness on behaviour. However, oestradiol, which did not maintain sexual development of accessory glands, was highly effective in the restoration of aggressive behaviour. Since the behaviourally active steroids in the present experiments were not only those predicted by the aromatization hypothesis, it is proposed that several steroids are capable of activating aggressive behaviour and that the aromatization hypothesis does not adequately explain the hormonal basis of aggressive behaviour among Norway rats.


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