Gender-typical olfactory regulation of sexual behavior in goldfish

It is known that olfaction is essential for the occurrence of sexual behavior in male goldfish. Sex pheromones from ovulatory females elicit male sexual behavior, chasing and sperm releasing act. In female goldfish, ovarian prostaglandin F2α (PGF) elicits female sexual behavior, egg releasing act. I...

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Main Author: Makito eKobayashi
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-04-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnins.2014.00091/full
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spelling doaj-6a3a084aebc541cc91321ca79be0a1eb2020-11-24T21:39:29ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2014-04-01810.3389/fnins.2014.0009182513Gender-typical olfactory regulation of sexual behavior in goldfishMakito eKobayashi0International Christian UniversityIt is known that olfaction is essential for the occurrence of sexual behavior in male goldfish. Sex pheromones from ovulatory females elicit male sexual behavior, chasing and sperm releasing act. In female goldfish, ovarian prostaglandin F2α (PGF) elicits female sexual behavior, egg releasing act. It has been considered that olfaction does not affect sexual behavior in female goldfish. In the present study, we reexamined the involvement of olfaction in sexual behavior of female goldfish. Olfaction was blocked in male and female goldfish by two methods: nasal occlusion (NO) which blocks the reception of olfactants, and olfactory tract section (OTX) which blocks transmission of olfactory information from the olfactory bulb to the telencephalon. Sexual behavior of goldfish was induced by administration of PGF to females, an established method for inducing goldfish sexual behavior in both sexes. Sexual behavior in males was suppressed by NO and OTX as previously reported because of lack of pheromone stimulation. In females, NO suppressed sexual behavior but OTX did not affect the occurrence of sexual behavior. Females treated with both NO and OTX performed sexual behavior normally. These results indicate that olfaction is essential in female goldfish to perform sexual behavior as in males but in a different manner. The lack of olfaction in males causes lack of pheromonal stimulation, resulting in no behavior elicited. Whereas the results of female experiments suggest that lack of olfaction in females causes strong inhibition of sexual behavior mediated by the olfactory pathway. Olfactory tract section is considered to block the pathway and remove this inhibition, resulting in the resumption of the behavior. By subtract sectioning of the olfactory tract, it was found that this inhibition was mediated by the medial olfactory tracts, not the lateral olfactory tracts. Thus, it is concluded that goldfish has gender-typical olfactory regulation for sexual behavior.http://journal.frontiersin.org/Journal/10.3389/fnins.2014.00091/fullGoldfishOlfactory BulbSexual BehaviorOlfactionprostaglandinsex pheromone
collection DOAJ
language English
format Article
sources DOAJ
author Makito eKobayashi
spellingShingle Makito eKobayashi
Gender-typical olfactory regulation of sexual behavior in goldfish
Frontiers in Neuroscience
Goldfish
Olfactory Bulb
Sexual Behavior
Olfaction
prostaglandin
sex pheromone
author_facet Makito eKobayashi
author_sort Makito eKobayashi
title Gender-typical olfactory regulation of sexual behavior in goldfish
title_short Gender-typical olfactory regulation of sexual behavior in goldfish
title_full Gender-typical olfactory regulation of sexual behavior in goldfish
title_fullStr Gender-typical olfactory regulation of sexual behavior in goldfish
title_full_unstemmed Gender-typical olfactory regulation of sexual behavior in goldfish
title_sort gender-typical olfactory regulation of sexual behavior in goldfish
publisher Frontiers Media S.A.
series Frontiers in Neuroscience
issn 1662-453X
publishDate 2014-04-01
description It is known that olfaction is essential for the occurrence of sexual behavior in male goldfish. Sex pheromones from ovulatory females elicit male sexual behavior, chasing and sperm releasing act. In female goldfish, ovarian prostaglandin F2α (PGF) elicits female sexual behavior, egg releasing act. It has been considered that olfaction does not affect sexual behavior in female goldfish. In the present study, we reexamined the involvement of olfaction in sexual behavior of female goldfish. Olfaction was blocked in male and female goldfish by two methods: nasal occlusion (NO) which blocks the reception of olfactants, and olfactory tract section (OTX) which blocks transmission of olfactory information from the olfactory bulb to the telencephalon. Sexual behavior of goldfish was induced by administration of PGF to females, an established method for inducing goldfish sexual behavior in both sexes. Sexual behavior in males was suppressed by NO and OTX as previously reported because of lack of pheromone stimulation. In females, NO suppressed sexual behavior but OTX did not affect the occurrence of sexual behavior. Females treated with both NO and OTX performed sexual behavior normally. These results indicate that olfaction is essential in female goldfish to perform sexual behavior as in males but in a different manner. The lack of olfaction in males causes lack of pheromonal stimulation, resulting in no behavior elicited. Whereas the results of female experiments suggest that lack of olfaction in females causes strong inhibition of sexual behavior mediated by the olfactory pathway. Olfactory tract section is considered to block the pathway and remove this inhibition, resulting in the resumption of the behavior. By subtract sectioning of the olfactory tract, it was found that this inhibition was mediated by the medial olfactory tracts, not the lateral olfactory tracts. Thus, it is concluded that goldfish has gender-typical olfactory regulation for sexual behavior.
topic Goldfish
Olfactory Bulb
Sexual Behavior
Olfaction
prostaglandin
sex pheromone
url http://journal.frontiersin.org/Journal/10.3389/fnins.2014.00091/full
work_keys_str_mv AT makitoekobayashi gendertypicalolfactoryregulationofsexualbehavioringoldfish
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