Literature DB >> 10642450

Sexual dimorphism in numbers of vasotocin-immunoreactive neurons in brain areas associated with reproductive behaviors in the roughskin newt.

F L Moore1, C Richardson, C A Lowry.   

Abstract

Vasotocin (VT) and vasopressin control many endocrine and neuroendocrine functions, including the regulation of reproductive behaviors. In the roughskin newt (Taricha granulosa), VT administration can enhance courtship behaviors in males and egg-laying behaviors in females. This study used immunohistochemistry to investigate whether there are sex differences in VT in specific brain areas, and whether these differences persist in nonbreeding animals. Numbers of VT immunoreactive (ir) cell bodies were counted in males and females collected in February, April, June, and August. Radioimmunoassay of plasma samples confirmed that testosterone and 5alpha-dihydrotestosterone concentrations were higher in males than females, and that 17beta-estradiol concentrations were higher in females than males. In 11 brain areas, no sexual or seasonal differences in the number of VTir cells were found. But in 3 brain regions-the bed nucleus of the stria terminalis (BNST), the nucleus amygdalae dorsolateralis (AMYG), and the anterior preoptic area (aPOA)-there were significantly greater numbers of VTir cells in males than in females, and these differences did not change seasonally. In the aPOA, an area important to male sex behaviors, the sexual dimorphism in VTir was particularly pronounced. In four brain regions, there were significantly greater numbers of VTir cells in females than males, but only in specific seasons. In April-collected (breeding) animals, more VTir cells were found in females than in males in the populations of VT cells within the pars dorsalis hypothalami and ventromedial hypothalamus, brain regions frequently associated with stress responses and female mating behaviors. In August-collected (nonbreeding) animals, more VTir cells were found in females than in males, in the region of the bed nucleus of the decussation of the fasciculus lateralis telencephali and in the nucleus visceralis superior, nucleus isthmi region. Significantly greater numbers of VTir cells were observed in the magnocellular preoptic area of males and females collected in February. These results indicate that the functional interactions between gonadal steroid hormones and VT are complex and appear to involve site-, sex-, and season-specific regulatory mechanisms. Furthermore, it seems likely that populations of VT neurons in the BNST, AMYG, and aPOA are involved in regulating male-specific behaviors, and that the VT neurons in the pars dorsalis hypothalami/ventromedial hypothalamus may be involved in female-specific behaviors. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10642450     DOI: 10.1006/gcen.1999.7424

Source DB:  PubMed          Journal:  Gen Comp Endocrinol        ISSN: 0016-6480            Impact factor:   2.822


  9 in total

1.  Cryptic regulation of vasotocin neuronal activity but not anatomy by sex steroids and social stimuli in opportunistic desert finches.

Authors:  David Kabelik; Jenilee A Morrison; James L Goodson
Journal:  Brain Behav Evol       Date:  2010-03-19       Impact factor: 1.808

2.  Sexual differentiation of vasopressin innervation of the brain: cell death versus phenotypic differentiation.

Authors:  Geert J de Vries; Michelle Jardon; Mohammed Reza; Greta J Rosen; Eleanor Immerman; Nancy G Forger
Journal:  Endocrinology       Date:  2008-05-22       Impact factor: 4.736

3.  Pheromones enhance somatosensory processing in newt brains through a vasotocin-dependent mechanism.

Authors:  R R Thompson; P S Dickinson; J D Rose; K A Dakin; G M Civiello; A Segerdahl; R Bartlett
Journal:  Proc Biol Sci       Date:  2008-07-22       Impact factor: 5.349

4.  Unexpected effects of perinatal gonadal hormone manipulations on sexual differentiation of the extrahypothalamic arginine-vasopressin system in prairie voles.

Authors:  Joseph S Lonstein; Benjamin D Rood; Geert J De Vries
Journal:  Endocrinology       Date:  2004-12-09       Impact factor: 4.736

Review 5.  Species, sex and individual differences in the vasotocin/vasopressin system: relationship to neurochemical signaling in the social behavior neural network.

Authors:  H Elliott Albers
Journal:  Front Neuroendocrinol       Date:  2014-08-04       Impact factor: 8.606

6.  Neuroanatomical evidence for reciprocal regulation of the corticotrophin-releasing factor and oxytocin systems in the hypothalamus and the bed nucleus of the stria terminalis of the rat: Implications for balancing stress and affect.

Authors:  Joanna Dabrowska; Rimi Hazra; Todd H Ahern; Ji-Dong Guo; Alexander J McDonald; Franco Mascagni; Jay F Muller; Larry J Young; Donald G Rainnie
Journal:  Psychoneuroendocrinology       Date:  2011-04-09       Impact factor: 4.905

Review 7.  Sexual differentiation of central vasopressin and vasotocin systems in vertebrates: different mechanisms, similar endpoints.

Authors:  G J De Vries; G C Panzica
Journal:  Neuroscience       Date:  2005-11-28       Impact factor: 3.590

8.  Testosterone stimulates mounting behavior and arginine vasotocin expression in the brain of both sexual and unisexual whiptail lizards.

Authors:  K D Hillsman; N S Sanderson; D Crews
Journal:  Sex Dev       Date:  2007       Impact factor: 1.824

Review 9.  Arginine Vasotocin, the Social Neuropeptide of Amphibians and Reptiles.

Authors:  Walter Wilczynski; Maricel Quispe; Matías I Muñoz; Mario Penna
Journal:  Front Endocrinol (Lausanne)       Date:  2017-08-07       Impact factor: 5.555

  9 in total

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