Literature DB >> 23481590

Testosterone modulates spatial recognition memory in male rats.

Wayne R Hawley1, Elin M Grissom, Ryan C Martin, Miklos B Halmos, Corrine L S Bart, Gary P Dohanich.   

Abstract

A growing body of research indicates that testosterone influences spatial cognition in male rats; however, the overwhelming majority of studies have been conducted on tasks motivated by either food deprivation or water escape. The hippocampus-dependent version of the Y-maze task, which characterizes spatial recognition memory, capitalizes on the propensity of rats to gravitate toward novel spatial environments and is not contingent upon either appetite or the stress associated with water escape, two factors also affected by testosterone. Accordingly, the aim of the current study was to examine the effects of orchidectomy and subsequent testosterone treatment on spatial recognition memory. Orchidectomy did not impact spatial recognition memory when the delay between the information and retention trials of the Y-maze task was 24h. Alternatively, on the second Y-maze task, which featured a 48-h delay between trials, orchidectomy reduced, and treatments that produced higher levels of testosterone restored, preference for the arm associated with the novel spatial environment. Importantly, there were no differences in activity levels as a function of orchidectomy or testosterone treatment on either of the two tasks. Consistent with previous findings, orchidectomy attenuated, and testosterone treatment restored, both body weight gain and the relative weight of the androgen-sensitive ischiocavernosus muscle, which confirmed the efficacy of orchidectomy and testosterone treatments on physiological outcomes. Therefore, testosterone influenced spatial cognition on a task that minimized the influence of non-mnemonic factors and took advantage of the innate preference of rodents to seek out novel spatial environments.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23481590     DOI: 10.1016/j.yhbeh.2013.02.007

Source DB:  PubMed          Journal:  Horm Behav        ISSN: 0018-506X            Impact factor:   3.587


  22 in total

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2.  Sex differences in the neural substrates of spatial working memory during adolescence are not mediated by endogenous testosterone.

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Journal:  Brain Res       Date:  2014-10-12       Impact factor: 3.252

3.  Local N-methyl-d-aspartate receptor antagonism in the prefrontal cortex attenuates spatial cognitive deficits induced by gonadectomy in adult male rats.

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Review 4.  Androgen Modulation of Hippocampal Structure and Function.

Authors:  Sarah Atwi; Dallan McMahon; Helen Scharfman; Neil J MacLusky
Journal:  Neuroscientist       Date:  2014-11-21       Impact factor: 7.519

5.  Assessment of the effects of sex and sex hormones on spatial cognition in adult rats using the Barnes maze.

Authors:  M N Locklear; M F Kritzer
Journal:  Horm Behav       Date:  2014-06-14       Impact factor: 3.587

6.  Pair bonding prevents reinforcing effects of testosterone in male California mice in an unfamiliar environment.

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Journal:  Proc Biol Sci       Date:  2014-08-07       Impact factor: 5.349

7.  Effects of testosterone dose on spatial memory among castrated adult male rats.

Authors:  Benjamin A Wagner; Valerie C Braddick; Christopher G Batson; Brendan H Cullen; L Erin Miller; Mark D Spritzer
Journal:  Psychoneuroendocrinology       Date:  2017-12-29       Impact factor: 4.905

8.  Short-term testosterone manipulations do not affect cognition or motor function but differentially modulate emotions in young and older male rhesus monkeys.

Authors:  Brian Kelly; Vanessa Maguire-Herring; Christian M Rose; Heather E Gore; Stephen Ferrigno; Melinda A Novak; Agnès Lacreuse
Journal:  Horm Behav       Date:  2014-10-13       Impact factor: 3.587

9.  Gonadal Hormones Rapidly Enhance Spatial Memory and Increase Hippocampal Spine Density in Male Rats.

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Review 10.  Recognition memory tasks in neuroendocrine research.

Authors:  Victoria Luine
Journal:  Behav Brain Res       Date:  2014-05-13       Impact factor: 3.332

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