Assessment of volumetric sex differences in the song control nuclei HVC and RA in zebra finches by immunocytochemistry for methionine enkephalin and vasoactive intestinal polypeptide

1995 ◽  
Vol 699 (1) ◽  
pp. 83-96 ◽  
Author(s):  
Gregory F. Ball ◽  
Phillipe Absil ◽  
Jacques Balthazart
2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Stuart A Collins ◽  
Ipe Ninan

Abstract The onset of several neuropsychiatric disorders including anxiety disorders coincides with adolescence. Consistently, threat extinction, which plays a key role in the regulation of anxiety-related behaviors, is diminished during adolescence. Furthermore, this attenuated threat extinction during adolescence is associated with an altered synaptic plasticity in the infralimbic medial prefrontal cortex (IL-mPFC), a brain region critical for threat extinction. However, the mechanism underlying the altered plasticity in the IL-mPFC during adolescence is unclear. Given the purported role of vasoactive intestinal polypeptide expressing interneurons (VIPINs) in disinhibition and hence their potential to affect cortical plasticity, we examined whether VIPINs exhibit an adolescence-specific plasticity in the IL-mPFC. We observed an increase in GABAergic transmission and a decrease in excitability in VIPINs during adolescence. Male mice show a significantly higher VIPIN-pyramidal neuron GABAergic transmission compared with female mice. The observed increase in GABAergic transmission and a decrease in membrane excitability in VIPINs during adolescence could play a role in the altered plasticity in the adolescent IL-mPFC. Furthermore, the suppression of VIPIN-mediated GABAergic transmission in females might be relevant to sex differences in anxiety disorders.


2011 ◽  
Vol 106 (4) ◽  
pp. 1747-1765 ◽  
Author(s):  
Lena Veit ◽  
Dmitriy Aronov ◽  
Michale S. Fee

How do animals with learned vocalizations coordinate vocal production with respiration? Songbirds such as the zebra finch learn their songs, beginning with highly variable babbling vocalizations known as subsong. After several weeks of practice, zebra finches are able to produce a precisely timed pattern of syllables and silences, precisely coordinated with expiratory and inspiratory pulses (Franz M, Goller F. J Neurobiol 51: 129–141, 2002). While respiration in adult song is well described, relatively little is known about respiratory patterns in subsong or about the processes by which respiratory and vocal patterns become coordinated. To address these questions, we recorded thoracic air sac pressure in juvenile zebra finches prior to the appearance of any consistent temporal or acoustic structure in their songs. We found that subsong contains brief inspiratory pulses (50 ms) alternating with longer pulses of sustained expiratory pressure (50–500 ms). In striking contrast to adult song, expiratory pulses often contained multiple (0–8) variably timed syllables separated by expiratory gaps and were only partially vocalized. During development, expiratory pulses became shorter and more stereotyped in duration with shorter and fewer nonvocalized parts. These developmental changes eventually resulted in the production of a single syllable per expiratory pulse and a single inspiratory pulse filling each gap, forming a coordinated sequence similar to that of adult song. To examine the role of forebrain song-control nuclei in the development of respiratory patterns, we performed pressure recordings before and after lesions of nucleus HVC (proper name) and found that this manipulation reverses the developmental trends in measures of the respiratory pattern.


1997 ◽  
Vol 50 (5) ◽  
pp. 284-303 ◽  
Author(s):  
Sarah W. Bottjer ◽  
Howard Roselinsky ◽  
Ngoc B. Tran

Behaviour ◽  
1994 ◽  
Vol 131 (3-4) ◽  
pp. 225-259 ◽  
Author(s):  
Gregory F. Ball ◽  
Jacques Balthazart ◽  
Veronique Fiasse ◽  
Phillipe Absil

AbstractNeonatal estradiol injections masculinize both the singing behavior and some morphological aspects of the song control nuclei in female zebra finches (Taeniopygia guttata), but there is to date no physiological evidence that estrogens are responsible for the differentiation of song and the song control nuclei in male zebra finches during normal ontogeny. Injections of estrogen into young males demasculinizes their copulatory behavior, so that it is difficult to understand how the same endocrine environment could simultaneously masculinize song and demasculinize copulation. Attempts to block early estrogen action in males have resulted in a paradoxical hypermasculinization of several aspects of the song control nuclei. In the present experiment, we tried to evaluate the role played by estrogens during zebra finch differentiation by blocking their secretion with the non-steroidal aromatase inhibitor, R76713 or racemic vorozole. Zebra finches received at 2-3 days post-hatch one Silastic implant filled with R76713 or left empty as a control. Implants were left in place until about 45 days of age and birds were then gonadectomized. At the age of 105 days, all birds received a Silastic implant filled with T and, starting two weeks later, they were repeatedly tested for singing and copulatory behavior during a period of 3 weeks. They were then perfused and their brains were analyzed by histological methods to measure the volume of the song control nuclei, HVc, RA, area X and MAN. Treatment with R76713 significantly decreased (± 50%) the number of song bouts produced by the birds but did not affect the copulatory behavior of the males. The behavior of females was not changed by the aromatase inhibitor and, in particular, no increase in mounting behavior was seen in the treated females. The presence of a strong sex dimorphism in the size of all 4 song control nuclei was confirmed but no significant effect of R76713 on these measures could be detected. These data are therefore consistent with the idea that estrogens are implicated in the differentiation of singing behavior in the zebra finch but the small amplitude of the behavioral effect observed and the absence of morphological effect suggest that either other factors also play a major role at this level or that higher doses or longer treatments with the aromatase blocker should be tested.


1997 ◽  
Vol 50 (5) ◽  
pp. 294-303
Author(s):  
Sarah W. Bottjer ◽  
Howard Roselinsky ◽  
Ngoc B. Tran

Sign in / Sign up

Export Citation Format

Share Document