Please use this identifier to cite or link to this item:
Title: Role of oxytocin in mate-choice copying of female rats
Authors: Chua, Chelsea
Keywords: Science::Biological sciences::Zoology::Animal behavior
Issue Date: 2019
Publisher: Nanyang Technological University
Source: Chua, C. (2019). Role of oxytocin in mate-choice copying of female rats. Master's thesis, Nanyang Technological University, Singapore.
Abstract: Mate-choice copying occurs when animals made decisions based on the mate choice of the conspecifics. Mate copying in rats is currently understudied. Past studies in oxytocin-knockout mice suggested the involvement of oxytocin, but the neurobiological mechanisms underlying mate choice have not been fully elucidated. Building on this, we investigated if female rats in oestrous exhibit mate-choice copying and whether oxytocin plays a role. The rats were injected with oxytocin (1 mg/kg), a cocktail of oxytocin (1 mg/kg) and its antagonist L-368,899 hydrochloride (5 mg/kg), or saline as control. We observed that both oxytocin and its antagonist reduced mate-choice copying instead of enhancing it. Furthermore, these treatments resulted in sedated behaviour up to 1h after injection. Locomotor activity recovered 24h post-injection. On the other hand, control rats showed mate-choice copying and no loss of locomotor activity. However, any learned mate choices did not seem to be strong enough to induce short- (30 min) and long-term (24h) memory. This might be due to a lack of information provided to the observer rat. To fill the gap in the proximate mechanisms behind Toxoplasma infections in female rats, the behaviours of oxytocin-treated and Toxoplasma-infected rats were compared. Toxoplasma infection leaves mate-choice copying behaviours intact and unchanged in female rats. Strangely, cat odour aversion was not observed in all tested rats (oxytocin-treated, Toxoplasma-infected, and their controls). The current findings suggest a possible role for oxytocin in mate-choice copying, but further investigation is required.
DOI: 10.32657/10356/136851
Rights: This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SBS Theses

Files in This Item:
File Description SizeFormat 
MSc thesis_final submission.pdf1.19 MBAdobe PDFView/Open

Page view(s)

Updated on Feb 7, 2023

Download(s) 50

Updated on Feb 7, 2023

Google ScholarTM




Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.