Temperature and photoperiod interact to affect reproduction and GnRH synthesis in male prairie voles

Prairie voles (Microtus ochrogaster), like most rodent species, exhibit a phenotypic polymorphism in reproductive response to winter conditions or to short day lengths in the laboratory. Laboratory studies on seasonally breeding species have traditionally focused on the role of photoperiod in modulating reproduction and other seasonal adaptions. However, because animals use proximate environmental factors in addition to photoperiod to phase seasonal adaptions with the appropriate time of year, the present study investigated the interaction of photoperiod and temperature on reproductive function and the gonadotropin-releasing hormone (GnRH) neuronal system. Male prairie voles were housed in either long (LD 16:8) or short (LD 8:16) photoperiods. Voles in each photoperiodic condition were also exposed to either mild (20 degrees C) or low (8 degrees C) temperatures. After 10 weeks, voles were killed and their brains were processed using in situ hybridization for mRNA for proGnRH. The results suggest that GnRH synthesis is not affected by exposure to a single inhibitory proximate factor (i.e. short days or low temperatures alone), even when reproduction is inhibited, whereas a combination of inhibitory proximate factors leads to a decrease in GnRH synthesis (i.e. fewer neurones staining for mRNA for proGnRH). These data suggest that the neuroendocrine mechanisms regulating seasonal alterations in reproductive function are likely to differ between harsh and mild winters.     

Organization of sensory neocortex in prairie voles (Microtus ochrogaster)

In the current investigation, the functional organization of visual, auditory, and somatosensory cortex was examined in prairie voles (Microtus ochrogaster) by using electrophysiological recording techniques. Functional boundaries of cortical fields were directly related to myeloarchitectonic boundaries. Our results demonstrated that most of the neocortex is occupied by the visual, auditory, and somatosensory areas. Specifically, a small area 17, or primary visual area (V1), was located on the caudomedial pole of the neocortex; a large auditory cortex (AC), which contains the primary auditory area (A1) and other auditory fields, encompassed almost the entire temporal pole; and a large area 3b, or primary somatosensory area (S1), contained a complete representation of the contralateral body surface. Furthermore, these areas were coextensive with distinct myeloarchitectonic appearances. We also observed that the AC appeared to be disproportionately large in the prairie vole compared with other rodents. In addition, we found that both primary and nonprimary areas contained neurons that responded to auditory stimulation. Finally, we observed within S1 a disproportionate amount of cortex that was devoted to representing the perioral hairs and the snout and also that neurons within this representation had very small receptive fields. We discuss the expanded auditory domain and the enlarged representation of perioral hairs as they relate to the specialized life style of the prairie vole.     

Lesions of the vomeronasal organ disrupt mating-induced pair bonding in female prairie voles (Microtus ochrogaster)

The prairie vole (Microtus ochrogaster) is a highly social, monogamous species and displays pair bonding that can be assessed by the presence of selective affiliation with the familiar partner versus a conspecific stranger. In female prairie voles, exposure to a male or to male sensory cues is essential for estrus induction, and the subsequent mating facilitates pair bond formation. In the present study, we examined the role of the vomeronasal organ (VNO) in estrus induction and pair bonding in female prairie voles. VNO lesions did not alter olfaction mediated by the main olfactory system, but did prevent male-induced estrus induction. We by-passed the necessity of the VNO for estrus induction by estrogen priming the females. Despite the fact that all subjects displayed similar levels of mating, social contact and locomotor activities, VNO lesioned females failed to show mating-induced pair bonding whereas intact and sham-lesioned females displayed a robust preference for the familiar partner. Our data not only support previous findings that the VNO is important for estrus induction but also indicate that this structure is crucial for mating-induced pair bonding, suggesting an important role for the VNO in reproductive success in prairie voles.     

Influence of gonadal hormones on the development of parental behavior in adult virgin prairie voles (Microtus ochrogaster)

Prairie voles (Microtus ochrogaster) are a socially monogamous species and both sexes are parental after the birth of pups. In contrast, sexually inexperienced adult prairie voles differ in their behavior towards pups such that virgin males are paternal whereas virgin females are often infanticidal. To test whether there exists a discrete perinatal 'sensitive period' during which gonadal hormones influence this behavior, and to distinguish between the relative contributions of estrogenic and androgenic mechanisms to this influence, prairie voles were exposed to testosterone propionate (TP), the anti-androgen flutamide, or the aromatase inhibitor 1,4,6-androstatriene-3,17-doine (ATD) either prenatally via their pregnant dam for the last 15-19 days of the 22-day gestational period or postnatally on days 1-7. None of the treatments altered the high paternal responsiveness of males or the high infanticide rate in females when compared with controls. Females exposed prenatally to ATD, however, had levels of parental behavior that were significantly higher than the lowest levels observed in prenatally TP-treated females. These results suggest that sex differences in the parental behavior of adult virgin prairie voles are not generated exclusively by androgenic or estrogenic mechanisms during a restricted prenatal or early postnatal 'sensitive period' and that the parental behavior of virgin females may be more susceptible to any influence of gonadal hormones during development than males.     

Early postnatal gene expression in the developing neocortex of prairie voles (Microtus ochrogaster) is related to parental rearing style

The earliest and most prevalent sensory experience includes tactile, thermal, and olfactory stimulation delivered to the young via contact with the mother, and in some mammals, the father. Prairie voles (Microtus ochrogaster), like humans, are biparental and serve as a model for understanding the impact of parent/offspring interactions on the developing brain. Prairie voles also exhibit natural variation in the level of tactile stimulation delivered by the parents to the offspring, and this has been well documented and quantified. Previous studies revealed that adult prairie vole offspring who received either high (HC) or low (LC) tactile contact from their parents have differences in the size of cortical fields and the connections of somatosensory cortex. In the current investigation, we examined gene expression, intraneocortical connectivity, and cortical thickness in newborn voles to appreciate when differences in HC and LC offspring begin to emerge. We observed differences in developmentally regulated genes, as well as variation in prelimbic and anterior cingulate cortical thickness at postnatal Day 1 (P1) in HC and LC voles. Results from this study suggest that parenting styles, such as those involving high or low physical contact, impact the developing neocortex via very early sensory experience as well as differences in epigenetic modifications that may emerge in HC and LC voles.     

Sexual dimorphism and hormone responsiveness in the spinal cord of the socially monogamous prairie vole (Microtus ochrogaster)

Prairie voles (Microtus ochrogaster) are exceptional among rodents in that many aspects of their brain and behavior are not masculinized by exogenous aromatizable androgens. However, the sexually differentiated endpoints studied to date rely on estrogenic mechanisms in other mammals. We examined whether sexual differentiation of an androgen receptor‐dependent sex difference would be similarly distinct in prairie voles. Male mammals have more and larger motoneurons projecting to perineal muscles than do females. This sex difference normally arises from males' perinatal androgen exposure and can be eliminated by treating developing females with androgens. Gross dissection revealed bulbospongiosus muscles in adult male, but not female, prairie voles. Retrograde tracing from males' bulbocavernosus muscles and the external anal sphincter from both sexes revealed sexually dimorphic populations of labeled motoneurons in the ventral horn of the lumbar spinal cord. Similar to other rodents, males had twice as many motoneurons as females, although no sex difference in motoneuron size was detected. Unexpectedly, prenatal or early postnatal exposure to testosterone propionate had no effect on adult females' motoneuron number or size. In adulthood, gonadectomy alone or followed by chronic testosterone treatment also had no effect on females' motoneuron size or number, although castration reduced motoneuron size in males. Comparing gonadally intact weanlings confirmed that the sex difference in motoneuron number exists before adulthood. As with some other sexually dimorphic traits, and perhaps related to their unique social organization, sexual differentiation of the prairie vole spinal cord differs from that found in most other laboratory rodents. J. Comp. Neurol. 516:117–124, 2009. © 2009 Wiley‐Liss, Inc.     

Biosynthesis of gonadotropin releasing hormone (GnRH): present status

Although the mechanism of GnRH synthesis has not yet been elucidated, many experimental data argue in favour of a ribosomal pathway resulting in the biosynthesis of a precursor with a size larger than the decapeptide. The existence of high mol. wt (HMW) immunoreactive forms of GnRH in hypothalamic extracts has been reported but without any evidence that they are precursors of the hypothalamic hormone. Some results obtained with immunocytological methods also suggest that at least a part of immunoreactive GnRH in perikarya might be extended on one or both its terminal ends. In our laboratory, we first investigated the process of GnRH biosynthesis in vivo by infusing tritiated amino acids into the third ventricle of rats. The results, along with the demonstration of the existence of HMW GnRH, support a ribosomal mechanism of GnRH synthesis. Also, preliminary data from our laboratory demonstrate that poly (A+) enriched RNA preparations from rat hypothalami contain compounds capable of hybridizing to a synthetic oligodeoxynucleotide probe which is complementary to a part of the GnRH sequence.     

Ventral striatopallidal oxytocin and vasopressin V1a receptors in the monogamous prairie vole (Microtus ochrogaster)

Oxytocin receptors (OTR) and vasopressin V1a receptors (V1aR) in the ventral forebrain play critical roles in the formation of pair bonds in the monogamous prairie vole. Previous reports have been inconsistent in the identification of the specific brain regions in the ventral forebrain that express these receptors. To delineate more clearly the neuroanatomical boundaries of the OTR and V1aR fields in this species, we compared OTR and V1aR binding in adjacent brain sections and also with markers that delineate neuroanatomical boundaries in the ventral forebrain. OTR binding displayed an overlapping distribution with substance P mRNA and preproenkephalin mRNA, both markers for the shell and core of the nucleus accumbens. V1aR binding was nonoverlapping with each of these markers but colocalized with iron accumulation as shown by Perls' iron stain as well as leucine-enkephalin immunoreactivity, both markers for the ventral pallidum. OTR and V1aR mRNA were also restricted within the nucleus accumbens and ventral pallidum, respectively. Furthermore, destruction of ventral striatal dopaminergic terminals with 6-hydroxydopamine infusions into the nucleus accumbens did not alter OTR binding. Immunocytochemical analysis of oxytocin and vasopressin in the ventral forebrain demonstrated the presence of oxytocin-immunoreactive fibers in the nucleus accumbens and vasopressin-immunoreactive fibers in the ventral pallidum, with males showing a greater density of vasopressin fibers than females, but there was no such sex difference in the oxytocin system. Based on these results, we discuss potential neural mechanisms by which receptors in these brain regions mediate pair bond formation in this monogamous species. J. Comp. Neurol. 468:555-570, 2004.     

The luteinizing hormone releasing hormone (LHRH) neuronal networks of the guinea pig brain. III. The regulation of cyclic gonadotropin secretion

The effects of selected CNS lesions on the ovulatory cycle as well as the distribution of LHRH terminals in the median eminence of the female guinea pig were examined. Radiofrequency lesions were placed in the medial preoptic area (MPOA) or suprachiasmatic nucleus (SCN). Animals were studied for varying lengths of time (1–5 months) following lesion placement. The occurrence of at least two ovulatory cycles was determined by cyclicity in vaginal opening, the presence of viable corpora lutea and measurements of luteal phase elevations in serum progesterone. The distribution of LHRH immunoreactivity was determined by immunocytochemical procedures on Bouin's fixed, paraffin-embedded brain sections. Lesions of the MPOA or SCN resulted in different degrees of loss of LHRH fibers in the zona externa of the ventral and lateral aspects of the infundibular stalk as well as complete loss of terminals throughout the zona interna. Despite depletion of LHRH fibers, all animals with SCN (n= 8) and the majority with MPOA (4/6) lesions showed regular ovulatory cycles. Two females with MPOA lesions presented two different anovulatory syndromes. Anovulation appeared unrelated to the size or site of the lesions or the degree of depletion of LHRH fibers in the infundibulum. It would appear that these brain areas and their LHRH projections are not essential for cyclic gonadotropic release.     

Increase in brain and pituitary radioimmunoassayable gonadotropin releasing hormone (GnRH) in the European silver eel treated with sexual steroid or human chorionic gonadotropin

In the female silver eel, a single estradiol 17 β (E₂) injection significantly increased radioimmunoassayable GnRH (IRGnRH) in the di- and mesencephalon and also in the telencephalon and olfactory lobes, during the first following days; after a chronic estradiol treatment, the pituitary IRGnRH was doubled. In the male silver eel, a single injection of human chorionic gonadotropin (hCG), which is able to induce a progressive testicular development and a durable increase in androgens production, produced a long-term effect on IRGnRH: IRGnRH was significantly increased in the same brain areas as in E₂-treated females; a more important rise (10-fold) was observed for pituitary IRGnRH, probably reflecting the accumulation of GnRH in the axonal endings which directly innervate the pituitary in teleosts. These results suggest a positive effect of sexual steroids on GnRH synthesis but not release in the silver eel.     

Photoperiod affects neuronal nitric oxide synthase and aggressive behaviour in male Siberian hamsters (Phodopus sungorus)

Many nontropical animals display physiological and behavioural changes in response to seasonal environmental cues including photoperiod (day length). Male Siberian hamsters (Phodopus sungorus) housed in short photoperiod undergo testicular regression accompanied by reduced circulating testosterone and decreased reproductive behaviour. By contrast to the majority of small mammals studied, aggressive behaviour is elevated in short-day Siberian hamsters when blood testosterone concentrations are not detectable. Because gonadal steroid hormones influence neuronal nitric oxide synthase (nNOS), and this enzyme has been implicated in aggressive behaviour, we hypothesized that nNOS expression would be decreased in short-day male Siberian hamsters and negatively correlated with the display of territorial aggression. Adult male Siberian hamsters were individually housed in either long (LD 16:8 h) or short (LD 8:16 h) photoperiods for 10 weeks. Hamsters were assigned to one of two categories by assessing testicular volume and plasma testosterone values: (i) photoperiodic responsive (i.e. regressed testes and low testosterone concentrations) or (ii) photoperiodic nonresponsive (i.e. testes size and circulating testosterone concentrations equivalent to hamsters maintained in long days). At week 10, aggression was assessed using a resident-intruder test. Latency to initial attack, frequency of attacks and duration of total attacks were recorded during a 10-min aggression trial. Brains were collected immediately after behavioural testing and stained for nNOS expression using immunohistochemistry. All short day-housed hamsters were significantly more aggressive than long-day animals, regardless of gonadal size or testosterone concentrations. Short-day animals, both reproductively responsive and nonresponsive morphs, also had significantly less nNOS-immunoreactive cells in the anterior and basolateral amygdaloid areas and paraventricular nuclei compared to long-day hamsters. Together, these results suggest that seasonal aggression in male Siberian hamsters is regulated by photoperiod, through mechanisms that are likely independent from gonadal steroid hormones.     

Presence of delta opioid receptors on a subset of hypothalamic gonadotropin releasing hormone (GnRH) neurons

Opioid peptides exert an inhibitory effect on hypothalamic gonadotropin releasing hormone (GnRH) secretion mainly by interacting with mu-opioid receptors. Although a direct role for opioids via delta-opioid receptors (DORs) has been suggested, the presence of these receptors on GnRH neurons has never been demonstrated. In the present study, we determined the distribution of DORs in the basal hypothalamus of rat with special focus on their relation to GnRH neurons. Double-labelling immunofluorescence and confocal microscopy revealed that DORs are exclusively present in a subpopulation of GnRH nerve terminals, with the highest density in the external layer of the median eminence. We then studied the functional characteristics of DORs in an immortalized GnRH-secreting neuronal cell line (GT1-1) known to endogenously express this receptor. Here, pertussis toxin pretreatment abolished the delta-agonist (DPDPE) inhibitory effect on cAMP accumulation. We also analyzed the type of G proteins involved in the signal transduced by the DOR and showed that GT1-1 cells express the inhibitory Go and Gi2 alpha-subunits. However, only Go was down-regulated under chronic DPDPE exposure. Finally, since DOR is expressed postnatally in brain, we compared GnRH neuronal cells immortalized at different developmental stages (the more mature GT1-1 and GT1-7 cells, versus the more immature GN11 cells), evidencing that only mature neurons express DOR. In conclusion, our study indicates that a direct control of opioids via delta-receptors occurs on GnRH neurons and validates the use of GT1 cells to further investigate the nature of the DOR present on GnRH neurons.     

Fatherhood reduces the survival of adult‐generated cells and affects various types of behavior in the prairie vole (Microtus ochrogaster )

Motherhood has profound effects on physiology, neuronal plasticity, and behavior. We conducted a series of experiments to test the hypothesis that fatherhood, similarly to motherhood, affects brain plasticity (such as cell proliferation and survival) and various behaviors in the highly social prairie vole (Microtus ochrogaster). In Experiment 1, adult males were housed with their same‐sex cage mate (control), single‐housed (isolation), or housed with a receptive female to mate and produce offspring (father) for 6 weeks. Fatherhood significantly reduced cell survival (assessed by bromodeoxyuridine labeling), but not cell proliferation (assessed by Ki67‐labeling), in the amygdala, dentate gyrus of the hippocampus, and ventromedial hypothalamus, suggesting that fatherhood affects brain plasticity. In Experiment 2, neither acute (20 min) nor chronic (20 min daily for 10 consecutive days) pup exposure altered cell proliferation or survival in the brain, but chronic pup exposure increased circulating corticosterone levels. These data suggest that reduced cell survival in the brain of prairie vole fathers was unlikely to be due to the level of pup exposure and display of paternal behavior, and may not be mediated by circulating corticosterone. The effects of fatherhood on various behaviors (including anxiety‐like, depression‐like, and social behaviors) were examined in Experiment 3. The data indicated that fatherhood increased anxiety‐ and depression‐like behaviors as well as altered aggression and social recognition memory in male prairie voles. These results warrant further investigation of a possible link between brain plasticity and behavioral changes observed due to fatherhood.     

The distribution and characterisation of thyrotrophin releasing hormone (TRH) in the human brain

Thyrotrophin releasing hormone-like immunoreactivity (TRHLI) extracted from human hypothalamus was found to be homogeneous and identical to authentic TRH in its chromatographic behaviour on reverse-phase high performance liquid chromatography. The majority of extrahypothalamic TRH also behaved as authentic TRH on HPLC. Study of the regional distribution of TRHLI showed a high concentration in the hypothalamus, periaqueductal grey and amygdala, with lower amounts in the basal ganglia and only trace amounts of TRHLI in the cerebral cortex and cerebellum.     

Reproductive history affects the synaptology of the ageing gonadotropin-releasing hormone system in the male rat

This study is an examination of the density of synaptic input to gonadotropin-releasing hormone (GnRH) neurons in young adult and aged retired breeder male rats. In earlier experiments on aged virgin male rats we observed an increase in synaptic input to this specific neuronal population, ascribable in part to synapses containing flattened vesicles, suggesting GABAergic input. The present study utilized retired breeders in order to dissect the effects of ageing from those associated with reproductive behavioral history. Tissue from the preoptic area was treated for the simultaneous electron microscopic immunocytochemical demonstration of GnRH with tetramethylbenzidine and glutamic acid decarboxylase (the essential enzyme in the production of GABA) using 3,3'-diaminobenzidine. Estimates of the density of synaptic input to the soma of GnRH neurons were made by calculating the percentage of perikaryal membrane with postsynaptic modification. Five GnRH neurons per animal were measured using computerized morpho-metrics and differences in the percent of membrane with synaptic modification between experimental groups were tested using the Mann-Whitney U non-parametric statistic. There was no difference in the total density of synaptic input to GnRH neurons in the young and old animals, or in the proportion of this input that was immunoreactive for glutamic acid decarboxylase. Similar measurements were made on random, non-identified neurons in the same region and a significant decrease with ageing in total synaptic input was found, though the glutamic acid decarboxylase component was unchanged. The present results are in contrast to our earlier findings on virgin males and suggest that reproductive behavioral experience affects the connectivity of GnRH neurons.     

Identification of gonadotropin releasing hormone (GnRH) neurons projecting to the median eminence from third ventricular preoptic area grafts in hypogonadal mice

Functional gonadotropin releasing hormone (GnRH) neurosecretory activity can be restored in genetically hypogonadal (hpg) adult mice with grafts of GnRH-containing fetal or neonatal septal-preoptic area (S/POA) tissue. Neurons implanted into the third ventricle of the host brain survive and send out axons which innervate one of the normal targets of these neurons, the median eminence (ME). Fibers terminate near primary portal vessels where GnRH is available for release into the vasculature, and this axonal outgrowth is essential for the stimulation of gonadotropin secretion, gonadal and accessory sex structure growth, gametogenesis, and fertility. Although it is known that GnRH axons reach their target, it is not known if all such neurons in a graft contribute to the projection. Taking advantage of the fact that axons in the ME, the sole host target, are outside the blood-brain barrier (BBB), long-term grafted animals were injected intraperitoneally with a retrograde tracer, Fluorogold (FG). Normal male mice were injected for comparison. Animals were sacrificed 5 days after injection and brain sections in the area of the graft were stained immunocytochemically for GnRH. In the normal male mice, two-thirds of the GnRH neurons were double-labeled with FG. In grafted individuals which showed increased gonadal growth, the percentage of labeled cells ranged from 17 to 75%. The results indicate that despite tissue injury, ectopic location, and a vastly reduced population, transplanted fetal GnRH neurons recapitulate a pattern seen in normal intact mice where some but not all neurons were capable of capturing a peripherally delivered tracer.