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Relaxin-3-Deficient Mice Showed Slight Alteration in Anxiety-Related Behavior

Relaxin-3 is a neuropeptide belonging to the relaxin/insulin superfamily. Studies using rodents have revealed that relaxin-3 is predominantly expressed in neurons in the nucleus incertus (NI) of the pons, the axons of which project to forebrain regions including the hypothalamus. There is evidence t...

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Autores principales: Watanabe, Yoshihisa, Tsujimura, Atsushi, Takao, Keizo, Nishi, Kazunori, Ito, Yasuaki, Yasuhara, Yoshitaka, Nakatomi, Yasuhito, Yokoyama, Chihiro, Fukui, Kenji, Miyakawa, Tsuyoshi, Tanaka, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156976/
https://www.ncbi.nlm.nih.gov/pubmed/21887138
http://dx.doi.org/10.3389/fnbeh.2011.00050
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author Watanabe, Yoshihisa
Tsujimura, Atsushi
Takao, Keizo
Nishi, Kazunori
Ito, Yasuaki
Yasuhara, Yoshitaka
Nakatomi, Yasuhito
Yokoyama, Chihiro
Fukui, Kenji
Miyakawa, Tsuyoshi
Tanaka, Masaki
author_facet Watanabe, Yoshihisa
Tsujimura, Atsushi
Takao, Keizo
Nishi, Kazunori
Ito, Yasuaki
Yasuhara, Yoshitaka
Nakatomi, Yasuhito
Yokoyama, Chihiro
Fukui, Kenji
Miyakawa, Tsuyoshi
Tanaka, Masaki
author_sort Watanabe, Yoshihisa
collection PubMed
description Relaxin-3 is a neuropeptide belonging to the relaxin/insulin superfamily. Studies using rodents have revealed that relaxin-3 is predominantly expressed in neurons in the nucleus incertus (NI) of the pons, the axons of which project to forebrain regions including the hypothalamus. There is evidence that relaxin-3 is involved in several functions, including food intake and stress responses. In the present study, we generated relaxin-3 gene knockout (KO) mice and examined them using a range of behavioral tests of sensory/motor functions and emotion-related behaviors. The results revealed that relaxin-3 KO mice exhibited normal growth and appearance, and were generally indistinguishable from wild genotype littermates. There was no difference in bodyweight among genotypes until at least 28 weeks after birth. In addition, there were no significant differences between wild-type and KO mice in locomotor activity, social interaction, hot plate test performance, fear conditioning, depression-like behavior, and Y-maze test performance. However, in the elevated plus maze test, KO mice exhibited a robust increase in the tendency to enter open arms, although they exhibited normal performance in a light/dark transition test and showed no difference from wild-type mice in the time spent in central area in the open field test. On the other hand, a significant increase in the acoustic startle response was observed in KO mice. These results indicate that relaxin-3 is slightly involved in the anxiety-related behavior.
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spelling pubmed-31569762011-09-01 Relaxin-3-Deficient Mice Showed Slight Alteration in Anxiety-Related Behavior Watanabe, Yoshihisa Tsujimura, Atsushi Takao, Keizo Nishi, Kazunori Ito, Yasuaki Yasuhara, Yoshitaka Nakatomi, Yasuhito Yokoyama, Chihiro Fukui, Kenji Miyakawa, Tsuyoshi Tanaka, Masaki Front Behav Neurosci Neuroscience Relaxin-3 is a neuropeptide belonging to the relaxin/insulin superfamily. Studies using rodents have revealed that relaxin-3 is predominantly expressed in neurons in the nucleus incertus (NI) of the pons, the axons of which project to forebrain regions including the hypothalamus. There is evidence that relaxin-3 is involved in several functions, including food intake and stress responses. In the present study, we generated relaxin-3 gene knockout (KO) mice and examined them using a range of behavioral tests of sensory/motor functions and emotion-related behaviors. The results revealed that relaxin-3 KO mice exhibited normal growth and appearance, and were generally indistinguishable from wild genotype littermates. There was no difference in bodyweight among genotypes until at least 28 weeks after birth. In addition, there were no significant differences between wild-type and KO mice in locomotor activity, social interaction, hot plate test performance, fear conditioning, depression-like behavior, and Y-maze test performance. However, in the elevated plus maze test, KO mice exhibited a robust increase in the tendency to enter open arms, although they exhibited normal performance in a light/dark transition test and showed no difference from wild-type mice in the time spent in central area in the open field test. On the other hand, a significant increase in the acoustic startle response was observed in KO mice. These results indicate that relaxin-3 is slightly involved in the anxiety-related behavior. Frontiers Research Foundation 2011-08-17 /pmc/articles/PMC3156976/ /pubmed/21887138 http://dx.doi.org/10.3389/fnbeh.2011.00050 Text en Copyright © 2011 Watanabe, Tsujimura, Takao, Nishi, Ito, Yasuhara, Nakatomi, Yokoyama, Fukui, Miyakawa and Tanaka. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Neuroscience
Watanabe, Yoshihisa
Tsujimura, Atsushi
Takao, Keizo
Nishi, Kazunori
Ito, Yasuaki
Yasuhara, Yoshitaka
Nakatomi, Yasuhito
Yokoyama, Chihiro
Fukui, Kenji
Miyakawa, Tsuyoshi
Tanaka, Masaki
Relaxin-3-Deficient Mice Showed Slight Alteration in Anxiety-Related Behavior
title Relaxin-3-Deficient Mice Showed Slight Alteration in Anxiety-Related Behavior
title_full Relaxin-3-Deficient Mice Showed Slight Alteration in Anxiety-Related Behavior
title_fullStr Relaxin-3-Deficient Mice Showed Slight Alteration in Anxiety-Related Behavior
title_full_unstemmed Relaxin-3-Deficient Mice Showed Slight Alteration in Anxiety-Related Behavior
title_short Relaxin-3-Deficient Mice Showed Slight Alteration in Anxiety-Related Behavior
title_sort relaxin-3-deficient mice showed slight alteration in anxiety-related behavior
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156976/
https://www.ncbi.nlm.nih.gov/pubmed/21887138
http://dx.doi.org/10.3389/fnbeh.2011.00050
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