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Gregory F Ball

Publications and source records attributed to Gregory F Ball.

43 records · Page 3Linked to original sources

Seasonal changes in the densities of alpha(2) noradrenergic receptors are inversely related to changes in testosterone and the volumes of song control nuclei in male European starlings.

The functions of song and the contextual cues that elicit song change seasonally in parallel with testosterone (T) concentrations in male European starlings. T is high in spring when at least one function of male song is that of immediate mate attraction, and low outside the context of breeding, when starlings primarily use song for dominance or flock maintenance. Several brain nuclei that control song contain high densities of alpha(2)adrenergic receptors. T can regulate the density of alpha(2)adrenergic receptors in the avian brain, indicating that the density of alpha(2) adrenergic receptors within the song system might change seasonally. Although the function of seasonal brain variation is not entirely clear, in many songbirds the volumes of song nuclei are largest when T is high and males sing most. Male starlings, however, sing both when T is high and when T is low. Therefore, exploring seasonal changes in T and the volumes of song nuclei could provide insight into the function of these changes. The present study was performed to explore the relationships among T, the volumes of song nuclei, and the densities of alpha(2) adrenergic receptors within the song system of male starlings. Song nuclei (the high vocal center [HVc], robust nucleus of the archistriatum [RA], and Area X) were largest, T was highest, and the density of alpha(2) adrenergic receptors (within HVc and RA) was lowest during the breeding season. The reverse pattern was observed outside of the breeding season. These results suggest that changes in T, volumes of song nuclei, and alpha(2) receptor densities might regulate seasonal changes in song behavior or the context that will elicit song in male starlings.

Adrenergic alpha-Antagonists↗

Neuroendocrinology of song behavior and avian brain plasticity: multiple sites of action of sex steroid hormones.

Seasonal changes in the brain of songbirds are one of the most dramatic examples of naturally occurring neuroplasticity that have been described in any vertebrate species. In males of temperate-zone songbird species, the volumes of several telencephalic nuclei that control song behavior are significantly larger in the spring than in the fall. These increases in volume are correlated with high rates of singing and high concentrations of testosterone in the plasma. Several song nuclei express either androgen receptors or estrogen receptors, therefore it is possible that testosterone acting via estrogenic or androgenic metabolites regulates song behavior by seasonally modulating the morphology of these song control nuclei. However, the causal links among these variables have not been established. Dissociations among high concentrations of testosterone, enlarged song nuclei, and high rates of singing behavior have been observed. Singing behavior itself can promote cellular changes associated with increases in the volume of the song control nuclei. Also, testosterone may stimulate song behavior by acting in brain regions outside of the song control system such as in the preoptic area or in catecholamine cell groups in the brainstem. Thus testosterone effects on neuroplasticity in the song system may be indirect in that behavioral activity stimulated by testosterone acting in sites that promote male sexual behavior could in turn promote morphological changes in the song system.

Androgens↗

Sex differences in the densities of alpha 2-adrenergic receptors in the song control system, but not the medial preoptic nucleus in zebra finches.

In songbirds, song is regulated by a specialized group of brain nuclei known as the song system. Other aspects of courtship, such as male sexual interest in a female, are likely regulated by the medial preoptic nucleus (POM). The song control system and the POM are rich in norepinephrine, which appears to regulate courtship behaviors, including song. Zebra finches (Taeniopygia guttata) exhibit an extreme sexual dimorphism in song behavior; males sing, primarily to attract or maintain mates, and females do not. We explored possible sex differences in the distribution and density of the alpha(2)-adrenergic receptors in the song system and POM of zebra finches. Receptors were labeled with the selective ligand, [(3)H] RX821002, via autoradiographic procedures. In males, dense alpha(2)-receptors were observed in the song system (Area X, the high vocal center (HVc), the lateral portion of the magnocellular nucleus of the anterior neostriatum, and the robust nucleus of the archistriatum). In contrast, in females neither the lateral portion of the magnocellular nucleus of the anterior neostriatum nor the HVc could be identified based on alpha(2)-receptor binding. Females lack Area X and indeed differential alpha(2)-binding was not observed within the female lobus parolfactorius. The robust nucleus of the archistriatum contained less dense alpha(2)-binding in females compared to males. Alpha(2)-binding in the POM was similar in males and females. The dimorphism in alpha(2)-binding in nuclei of the song system likely relates to the dimorphism in song behavior observed in male and female zebra finches.

Animals↗

Interactions between aromatase (estrogen synthase) and dopamine in the control of male sexual behavior in quail.

In male quail, like in other vertebrates including rodents, testosterone acting especially through its estrogenic metabolites is necessary for the activation of male sexual behavior. Also, the administration of dopamine agonists and antagonists profoundly influences male sexual behavior. How the steroid-sensitive neural network and dopamine interact physiologically, remains largely unknown. It is often implicitly assumed that testosterone or its metabolite estradiol, stimulates male sexual behavior via the modification of dopaminergic transmission. We have now identified in quail two possible ways in which dopamine could potentially affect sexual behavior by modulating the aromatization of testosterone into an estrogen. One is a long-acting mechanism that presumably involves the modification of dopaminergic transmission followed by the alteration of the genomic expression of aromatase. The other is a more rapid mechanism that does not appear to be dopamine receptor-mediated and may involve a direct interaction of dopamine with aromatase (possibly via substrate competition). We review here the experimental data supporting the existence of these controls of aromatase activity by dopamine and discuss the possible contribution of these controls to the activation of male sexual behavior.

Animals↗

Effects of lesions of nucleus taeniae on appetitive and consummatory aspects of male sexual behavior in Japanese quail.

Neurochemical, hodological and functional criteria suggest that the nucleus taeniae and parts of the adjacent archistriatum represent the avian homologue of parts of the mammalian amygdaloid complex. It has been proposed in particular that the nucleus taeniae is the homologue of the mammalian medial amygdala. In male quail, relatively large lesions to the posterior/medial archistriatum selectively decrease the expression of appetitive sexual behavior in a manner reminiscent of similar manipulations involving the medial amygdala in mammals. We investigated the effects of discrete lesions restricted to nucleus taeniae and of lesions to an adjacent part of the archistriatum (pars intermedium ventralis, AIv) on the expression of appetitive (ASB) and consummatory (CSB) aspects of male sexual behavior. ASB was measured by a learned social proximity response (after copulation a male quail stands in front of a window providing visual access to a female) and by the frequency of rhythmic cloacal sphincter movements. CSB was assessed by the frequency of mount attempts (MA) and cloacal contact movements (CCM). Lesions confined to nucleus taeniae and to AIv did not influence the acquisition or the maintenance of the two responses indicative of ASB. In contrast, lesions of nucleus taeniae significantly increased the occurrence frequencies of MA and CCM when administered before the beginning of behavior testing and increased the frequency of MA only when performed on sexually experienced subjects. No effect of AIv lesions could be detected. The discrepancy between these results and previous experiments in quail might reflect procedural differences, but more probably differences in locations of the lesions that were restricted in the current study to the anterior part of taeniae. Those in the Thompson study were in the posterior part of this nucleus. These findings indicate that there is a larger degree of functional heterogeneity in the nucleus taeniae than previously thought. The effects of taeniae lesions suggest that this nucleus, similar to the medial amygdala in mammals, might be implicated in the control of sexual satiety.

Amygdala↗

Steroid receptor coactivator SRC-1 exhibits high expression in steroid-sensitive brain areas regulating reproductive behaviors in the quail brain.

The steroid receptor coactivator SRC-1 modulates ligand-dependent transactivation of several nuclear receptors, including the receptors for sex steroid hormones. Reducing the expression of SRC-1 by injection of specific antisense oligonucleotides markedly inhibits the effects of estrogens of the sexual differentiation of brain and behavior in rats and inhibits the activation of female sexual behavior in adult female rats. SRC-1 thus appears to be involved in both the development and activation of sexual behavior. In the Japanese quail brain, we amplified by RT-PCR a 3,411-bp fragment extending from the HLH domain to the activating domain-2 of the protein. The quail SRC-1 is closely related to the mammalian (m) SRC-1 and contains a high proportion of GC nucleotides (62.5%). Its amino acid sequence presents 70% identity with mammalian SRC-1 and contains the three conserved LXXLL boxes involved in the interaction with nuclear receptors. In both males and females, RT-PCR demonstrates a similarly high level of expression in the telencephalon, diencephalon, optic lobes, brain stem, spinal cord, pituitary, liver, kidney, adrenal gland, heart, lung, gonads and gonoducts. Males express significantly higher levels of SRC-1 in the preoptic area-hypothalamus than females. In both sexes, lower levels of expression are observed in the cerebellum and muscles. In situ hybridization utilizing a mixture of four digoxigenin-labeled oligonucleotides confirms at the cellular level the widespread distribution of SRC-1 mRNA in the brain and a particularly dense expression in steroid-sensitive areas that play a key role in the control of male sexual behavior. These data confirm the presence and describe for the first time the SRC-1 distribution in the brain of an avian species. They confirm its broad, nearly ubiquitous, distribution in the entire body including the brain as could be expected for a coactivator that regulates to the action of many nuclear receptors. However this distribution is heterogeneous in the brain and sexually differentiated in at least some areas. The very dense expression of SRC-1 in limbic and mesencephalic nuclei that are associated with the control of male sexual behavior is consistent with the notion that this coactivator plays a significant role in the activation of this behavior.

Adrenal Glands↗