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Arginine Vasotocin, the Social Neuropeptide of Amphibians and Reptiles
Arginine vasotocin (AVT) is the non-mammalian homolog of arginine vasopressin (AVP) and, like vasopressin, serves as an important modulator of social behavior in addition to its peripheral functions related to osmoregulation, reproductive physiology, and stress hormone release. In amphibians and rep...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545607/ https://www.ncbi.nlm.nih.gov/pubmed/28824546 http://dx.doi.org/10.3389/fendo.2017.00186 |
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author | Wilczynski, Walter Quispe, Maricel Muñoz, Matías I. Penna, Mario |
author_facet | Wilczynski, Walter Quispe, Maricel Muñoz, Matías I. Penna, Mario |
author_sort | Wilczynski, Walter |
collection | PubMed |
description | Arginine vasotocin (AVT) is the non-mammalian homolog of arginine vasopressin (AVP) and, like vasopressin, serves as an important modulator of social behavior in addition to its peripheral functions related to osmoregulation, reproductive physiology, and stress hormone release. In amphibians and reptiles, the neuroanatomical organization of brain AVT cells and fibers broadly resembles that seen in mammals and other taxa. Both parvocellular and magnocellular AVT-containing neurons are present in multiple populations located mainly in the basal forebrain from the accumbens–amygdala area to the preoptic area and hypothalamus, from which originate widespread fiber connections spanning the brain with a particularly heavy innervation of areas associated with social behavior and decision-making. As for mammalian AVP, AVT is present in greater amounts in males in many brain areas, and its presence varies seasonally, with hormonal state, and in males with differing social status. AVT’s social influence is also conserved across herpetological taxa, with significant effects on social signaling and aggression, and, based on the very small number of studies investigating more complex social behaviors in amphibians and reptiles, AVT may also modulate parental care and social bonding when it is present in these vertebrates. Within this conserved pattern, however, both AVT anatomy and social behavior effects vary significantly across species. Accounting for this diversity represents a challenge to understanding the mechanisms by which AVT exerts its behavioral effects, as well are a potential tool for discerning the structure-function relationships underlying AVT’s many effects on behavior. |
format | Online Article Text |
id | pubmed-5545607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55456072017-08-18 Arginine Vasotocin, the Social Neuropeptide of Amphibians and Reptiles Wilczynski, Walter Quispe, Maricel Muñoz, Matías I. Penna, Mario Front Endocrinol (Lausanne) Endocrinology Arginine vasotocin (AVT) is the non-mammalian homolog of arginine vasopressin (AVP) and, like vasopressin, serves as an important modulator of social behavior in addition to its peripheral functions related to osmoregulation, reproductive physiology, and stress hormone release. In amphibians and reptiles, the neuroanatomical organization of brain AVT cells and fibers broadly resembles that seen in mammals and other taxa. Both parvocellular and magnocellular AVT-containing neurons are present in multiple populations located mainly in the basal forebrain from the accumbens–amygdala area to the preoptic area and hypothalamus, from which originate widespread fiber connections spanning the brain with a particularly heavy innervation of areas associated with social behavior and decision-making. As for mammalian AVP, AVT is present in greater amounts in males in many brain areas, and its presence varies seasonally, with hormonal state, and in males with differing social status. AVT’s social influence is also conserved across herpetological taxa, with significant effects on social signaling and aggression, and, based on the very small number of studies investigating more complex social behaviors in amphibians and reptiles, AVT may also modulate parental care and social bonding when it is present in these vertebrates. Within this conserved pattern, however, both AVT anatomy and social behavior effects vary significantly across species. Accounting for this diversity represents a challenge to understanding the mechanisms by which AVT exerts its behavioral effects, as well are a potential tool for discerning the structure-function relationships underlying AVT’s many effects on behavior. Frontiers Media S.A. 2017-08-07 /pmc/articles/PMC5545607/ /pubmed/28824546 http://dx.doi.org/10.3389/fendo.2017.00186 Text en Copyright © 2017 Wilczynski, Quispe, Muñoz and Penna. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Wilczynski, Walter Quispe, Maricel Muñoz, Matías I. Penna, Mario Arginine Vasotocin, the Social Neuropeptide of Amphibians and Reptiles |
title | Arginine Vasotocin, the Social Neuropeptide of Amphibians and Reptiles |
title_full | Arginine Vasotocin, the Social Neuropeptide of Amphibians and Reptiles |
title_fullStr | Arginine Vasotocin, the Social Neuropeptide of Amphibians and Reptiles |
title_full_unstemmed | Arginine Vasotocin, the Social Neuropeptide of Amphibians and Reptiles |
title_short | Arginine Vasotocin, the Social Neuropeptide of Amphibians and Reptiles |
title_sort | arginine vasotocin, the social neuropeptide of amphibians and reptiles |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545607/ https://www.ncbi.nlm.nih.gov/pubmed/28824546 http://dx.doi.org/10.3389/fendo.2017.00186 |
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