Literature DB >> 3392529

Sex differences in the motor nucleus of cranial nerve IX-X in Xenopus laevis: a quantitative Golgi study.

D B Kelley1, S Fenstemaker, P Hannigan, S Shih.   

Abstract

In the clawed frog (Xenopus laevis), motor neurons in cranial nerve nucleus IX-X control contraction of laryngeal muscles responsible for sexually dimorphic vocal behaviors. We examined sex differences in dendritic arbors of n.IX-X cells using the Golgi-Cox method. Three morphological classes of somal types (ovoid, triangular, and elongate) are present in similar frequencies in n.IX-X of both males and females. The male n.IX-X neuron is a more complex and hypertrophied version of the female n.IX-X cell. The number of primary dendrites is the same for both sexes, but males have more total dendritic segments. The overall dendritic length of male n.IX-X neurons is two to three times that of the female. Males have longer dendritic segments between all branch points. Male and female frogs differ in levels of circulating androgens; neurons of n.IX-X are targets for androgenic steroids. To determine if androgen can affect dendritic morphology in adult females, we examined Golgi-impregnated cells in n.IX-X from ovariectomized females treated with testosterone for 1 month. The total number of dendritic segments was reduced by androgen treatment due to reduction in the number of higher order dendritic segments; the number of primary dendritic segments was unchanged. Androgen treatment may induce resorption of higher order dendritic branches. The overall dendritic length of androgen-treated female n.IX-X neurons was unchanged, and dendritic segments were longer. Thus, although androgen can alter dendrites of n.IX-X cells in adult females, this short-term treatment does not produce a masculine dendritic architecture.

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Year:  1988        PMID: 3392529     DOI: 10.1002/neu.480190503

Source DB:  PubMed          Journal:  J Neurobiol        ISSN: 0022-3034


  6 in total

1.  Courtship and copulation in the adult male green anole: effects of season, hormone and female contact on reproductive behavior and morphology.

Authors:  Jennifer K Neal; Juli Wade
Journal:  Behav Brain Res       Date:  2006-12-15       Impact factor: 3.332

2.  Behavioural display systems across nine Anolis lizard species: sexual dimorphisms in structure and function.

Authors:  Michele A Johnson; Juli Wade
Journal:  Proc Biol Sci       Date:  2010-02-03       Impact factor: 5.349

3.  Electrophysiology and dye-coupling are sexually dimorphic characteristics of individual laryngeal muscle fibers in Xenopus laevis.

Authors:  M L Tobias; D B Kelley
Journal:  J Neurosci       Date:  1988-07       Impact factor: 6.167

Review 4.  Androgen receptors and muscle: a key mechanism underlying life history trade-offs.

Authors:  D Ashley Monks; Melissa M Holmes
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2017-10-23       Impact factor: 1.836

5.  Xenopus vocalizations are controlled by a sexually differentiated hindbrain central pattern generator.

Authors:  Heather J Rhodes; Heather J Yu; Ayako Yamaguchi
Journal:  J Neurosci       Date:  2007-02-07       Impact factor: 6.167

Review 6.  Sexually differentiated central pattern generators in Xenopus laevis.

Authors:  Erik Zornik; Ayako Yamaguchi
Journal:  Trends Neurosci       Date:  2008-05-09       Impact factor: 13.837

  6 in total

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