Biomedical subjects

C A Dudley

Publications and source records attributed to C A Dudley.

At least 19 recordsLinked to original sources

PubMed1999

Functional dichotomy within the vomeronasal system: distinct zones of neuronal activity in the accessory olfactory bulb correlate with sex-specific behaviors.

Chemosensory neurons in the vomeronasal organ (VNO) detect pheromones that elicit social and reproductive behaviors in most terrestrial vertebrates. Vomeronasal receptor neurons are chemoarchitecturally divided into two populations based on their position in the VNO, the type of G-protein subunit expressed, the family of putative pheromone receptor expressed, and termination site of their axons in the accessory olfactory bulb (AOB). To investigate the functional implications of these two segregated VNO-AOB pathways, we stimulated mice with pheromonal cues associated with different behavioral contexts and examined cellular activation patterns in the AOB. Exposure of ICR male mice to BALB/c males resulted in aggressive behavior, accompanied by a VNO-dependent increase in c-fos immunoreactivity in a cluster of cells located almost exclusively in the caudal AOB in both strains. This caudal cluster of activated cells did not appear to require the overt display of aggressive behavior because it was present in both the dominant and submissive males and could be evoked when the stimulus animal was anesthetized. In contrast, exposure of an ICR male to an ICR female in diestrus resulted in activation of cells located predominantly in the rostral AOB. Our findings indicate that male-to-male interactions involving interstrain recognition activate a separate population of vomeronasal receptor neurons than chemosensory cues detected in a sexual context. The results suggest that the dichotomy in the peripheral vomeronasal system serves to separate pheromones based on the behaviors they drive. As such, the results provide a bioassay for identifying pheromone molecules.

Aggression↗

PubMed1999

Activation of an anatomically distinct subpopulation of accessory olfactory bulb neurons by chemosensory stimulation.

Chemosensory cues known as pheromones play a key role in rodent reproductive physiology and social interactions. Pheromone molecules are detected by receptor cells located in the vomeronasal organ and conveyed exclusively to the accessory olfactory bulb, and then to limbic and hypothalamic sites for integration with other factors modulating reproductive physiology. We report here that chemosensory cues from the female mouse selectively activate a subpopulation of cells located in the anterior part of the accessory olfactory bulb of the male mouse. Exposure of male mice to female-soiled bedding resulted in a massive induction of c-fos expression, which was primarily confined to neurons located in the anterior part of the accessory olfactory bulb and was eliminated by removal of the vomeronasal organ. Exposure of the male to soiled bedding from a different stain of male mice also elevated c-fos expression, but immunoreactive cells were more evenly distributed along the anterior-posterior axis of the accessory olfactory bulb. No treatment effects were observed in the main olfactory bulb. Previous studies have indicated that vomeronasal receptor neurons are divided into two populations based on location within the organ, site of termination in the accessory olfactory bulb, second messenger content and putative pheromone receptor expression. The present study suggests that the two populations of vomeronasal receptor neurons detect different chemosensory stimuli. Since male mouse- and female mouse-specific urinary substances modulate different aspects of male mouse behavior, the present results suggest that anatomically segregated populations of vomeronasal organ receptor cells modulate distinct behavioral patterns.

Animals↗

PubMed1996

Sequential anaerobic-aerobic biodegradation of PCBs in soil slurry microcosms.

Many industrial locations have identified the need for treatment of polychlorinated biphenyl (PCB) wastes and remediation of PCB-contaminated sites. Biodegradation of PCBs is a potentially effective technology for treatment of PCB-contaminated soils and sludges; however, a practicable remediation technology has not yet been demonstrated. In laboratory experiments, soil slurry microcosms inoculated with microorganisms extracted from PCB-contaminated Hudson River sediments have been used for anaerobic dechlorination of weathered Aroclor 1248 in contaminated soil with a low organic carbon content. Anaerobic incubation was then followed by exposure to air, addition of biphenyl, and inoculation with Pseudomonas sp. LB400, an aerobic PCB degrader. The sequential anaerobic-aerobic treatment constituted an improvement compared to anaerobic or aerobic treatment alone by reducing the total amount of PCBs remaining and decreasing the tendency for end products to accumulate in humans. A 70% reduction of PCBs was observed during sequential treatment with products containing fewer chlorines and having a shorter half-life in humans than the original PCBs. The aerobic treatment alone was also quite effective as a stand-alone treatment reducing the PCBs by 67%. The results represent a case in which anaerobic river sediment organisms have been successfully transferred to a matrix free of river or lake sediments.

Aerobiosis↗

PubMed1996

Signal processing in the vomeronasal system: modulation of sexual behavior in the female rat.

Chemosensory cues detected by the vomeronasal (VN) organ modulate a variety of social interactions in many species. In particular, activation of the VN system by pheromones regulates sexual behavior in the rodent. Although the exact nature of stimulus access to the organ is not clearly defined, the neuroanatomical pathway connecting the VN organ to hypothalamic centers controlling reproductive function is well established and relatively straightforward. Electrophysiological techniques have provided insight into the signal transduction process throughout the VN system. Combining behavioral studies with immunocytochemical detection of immediate early genes and neuropeptides reveals that gonadotropin hormone releasing hormone (GnRH)-containing neurons are specifically activated by stimulation of the VN organ. Furthermore, some of the activated GnRH neurons project to the ventromedial hypothalamus where they are hypothesized to induce sexual responsiveness. Early anecdotal evidence of an influence of the VN organ on human reproductive events has been substantiated by more recent anatomical, behavioral, and electrophysiological studies. Thus, further deciphering of the signal transduction process within the VN system of the rodent may yield unique insights into behaviors associated with human reproduction.

Amygdala↗

PubMed1995

Electrophysiological evidence for glutamate as a vomeronasal receptor cell neurotransmitter.

Bipolar receptor cells in the vomeronasal organ send axonal projections to the accessory olfactory bulb where they synapse with mitral cell dendrites. Although the nature of the synapse is thought to be excitatory, the neurotransmitter(s) involved has not yet been identified. Electrophysiological recordings of single neurons in the mitral cell layer of the AOB in response to vomeronasal nerve stimulation were conducted to characterize the synaptic response and the underlying neurotransmitter substance. Extracellular activity was recorded in vivo (whole animal) and in vitro (AOB slice) from female rats. In vivo, the predominant response to stimulation of the VNO was excitation. In many instances in the whole animal preparation, the excitation was followed by an inhibitory response. Attempts to block the excitatory response by ejecting kynurenic acid in close proximity to the mitral cell being recorded were not successful. Since this failure may have been due to inability of the antagonist to reach its presumed site of action at the dendrite, further recordings were carried out in vitro. In the AOB slice preparation, the predominant response to stimulation of the VN nerve endings was excitation. Superfusion of the non-NMDA antagonist, CNQX, into the medium resulted in a reduction of the orthodromic excitation in 5 of 8 cells. The NMDA antagonist, AP-5, was found to blunt orthodromic excitation in 1 of 4 cells. These results suggest that the excitatory response evoked in mitral cells followng stimulation of the VN nerve is mediated by glutamate.

2-Amino-5-phosphonovalerate↗

PubMed1994

Lesions of the accessory olfactory bulb decrease lordotic responsiveness and reduce mating-induced c-fos expression in the accessory olfactory system.

The effect of bilateral lesion of the accessory olfactory bulb (AOB) on the mating-induced enhancement of sexual receptivity was investigated in ovariectomized (OVX) female rats. Lesions of the AOB significantly reduced the lordosis-to-mount (L/M) ratio in mating tests conducted 20 to 50 days after the lesion but L/M ratios at earlier (10 days) and later (51-90 days) time periods were not affected. The decrease in L/M was accompanied by a reduction in the number of c-fos immunopositive cells in the medial amygdala (mAMYG) and bed nucleus of the stria terminalis (BNST) measured after 3 h of repetitive mating. In the mAMYG, the reduction in c-fos immunoreactivity was correlated to the L/M ratio as well as to the number of intromissions received during the mating tests. The results suggest that information processed from the AOB to the mAMYG and the BNST is important for facilitation of lordosis behavior, and that the mAMYG may integrate information from the AOB with ascending input activated during copulatory behavior to regulate receptivity.

Amygdala↗

PubMed1993

Influence of male rats on the luteinizing hormone-releasing hormone neuronal system in female rats: role of the vomeronasal organ.

Olfactory information processed by the vomeronasal system is reported to influence reproductive functions in a variety of mammals. The present studies were designed to determine if male-associated cues affect the luteinizing hormone-releasing hormone (LHRH) neuronal system, and, if so, to determine the extent to which these cues are processed by the vomeronasal organ (VNO). Ovariectomized rats underwent VNO removal (VNX) or sham surgery (VN-Sham). Forty-eight hours after estrogen priming (5 micrograms), they were subjected to one of the following treatments: repeated mating, repeated exposure to male-soiled bedding or repeated exposure to clean bedding. In animals treated for 180 min, coronal brain sections were double labelled for Fos protein and LHRH. An intense Fos immunoreactivity was induced following mating in the majority of LHRH neurons in the VN-Sham females, whereas removal of the VNO significantly suppressed the mating-induced Fos staining. Exposure of female rats to male-soiled bedding or clean bedding did not induce appreciable Fos immunoreactivity in LHRH neurons. Following 90 min of mating or exposure to bedding, blood samples were assayed for luteinizing hormone (LH). Mating stimulated the release of LH in VN-Sham females, while the removal of the VNO significantly suppressed the mating-induced LH release. Exposure of the females to male-soiled bedding or clean bedding did not induce an LH surge. The present results demonstrate that male-originating sensory cues (i.e. repeated mating) can influence the LHRH neuronal system, as evidenced by the presence of Fos immunoreactivity in LHRH cell bodies, and indicate that this effect is mediated through the VNO to a certain extent.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1992

LHRH neurons in the medial septal-diagonal band-preoptic area do not project directly to the hippocampus: a double-labeling immunohistochemical study.

While neurons containing immunoreactive luteinizing hormone-releasing hormone (LHRH) are scattered primarily in the medial septal-diagonal band of Broca-medial preoptic area (mS-dbB-PO) complex, autoradiographic studies have demonstrated dense concentrations of LHRH receptors in the hippocampus. The route by which LHRH is transported to its hippocampal receptors is unknown. The present study was designed to test the hypothesis that LHRH-containing neurons in the mS-dbB-PO complex project to hippocampal sites containing LHRH receptors, thereby serving as a source of innervation to these receptors. Large (0.10 microliters) or small (0.02 microliters) volumes of the retrograde tracer wheat germ agglutinin (WGA) were injected unilaterally into four separate hippocampal locations in six ovariectomized female rats. In an additional five females, a 0.15 microliter volume of the retrograde tracer fluorogold (FG) was similarly injected. After a five day survival period, the animals were sacrificed. Vibratome sections of the brain were stained for both WGA and LHRH with a dual immunohistochemical technique. Since FG is a fluorescent chromagen, brains of animals injected with FG only required processing for LHRH immunofluorescence. As a positive control, some sections containing retrogradely labeled cells filled with either WGA or FG were processed for choline acetyltransferase (CHAT) immunoreactivity. The WGA and FG injections covered targeted hippocampal sites and neurons containing retrogradely transported WGA or FG were found in abundance in the mS-dbB-PO complex. In accord with previous reports, many CHAT-positive and fewer LHRH-positive neurons were found in this complex. Approximately 5-10% of the CHAT-positive neurons also contained WGA or FG; however, no neurons were found to co-localize LHRH and either of the retrograde tracers. The results indicate that LHRH neurons in the mS-dbB-PO complex do not project directly to hippocampal sites containing LHRH receptors.

Animals↗

PubMed1991

Role of the ventromedial nucleus of hypothalamus in the male-induced enhancement of lordosis in female rats.

The involvement of the ventromedial nucleus of the hypothalamus (VMH) in the mating-induced enhancement of lordosis in ovariectomized estrogen-primed rats was investigated. In the first experiment, females with bilateral VMH or sham lesions were primed with 2 micrograms estradiol benzoate, and 48 h later they were subjected to repeated-mating tests. The VMH-lesioned rats failed to exhibit lordosis during the tests; however, the sham-operated females exhibited a gradual increase in lordosis quotient (LQ) with repetitive matings. In the second experiment, ovariectomized females were bilaterally implanted with estradiol (E2) or cholesterol (C) in the VMH, 48 h prior to behavioral testing. Repeated-mating-induced elevation in LQ was observed in the females when they were bilaterally implanted with E2 in the VMH; C was ineffective. To exclude the possibility of the spread of E2 to areas adjacent to VMH, plasma-luteinizing hormone (LH) was measured. Elevation in the circulating LH levels following ovariectomy was not suppressed in the females following bilateral E2 implants in the VMH, suggesting that the effect of estrogen is localized within or immediately around the VMH. The results suggest that the integrity of the VMH is critical for the potentiation of lordosis behavior in ovariectomized estrogen-primed females by male-originating sensory cues, and that selective priming of the VMH with estrogen is sufficient for the male-induced enhancement of lordosis.

Animals↗

PubMed1991

Facilitation of sexual receptivity in the female rat by C-terminal fragments of LHRH.

Ovariectomized female rats implanted with cannulae directed bilaterally towards the ventromedial nucleus of the hypothalamus (VMH) were primed with estrogen (2 micrograms) and tested for sexual receptivity before and after infusion of the C-terminal LHRH fragment, Ac-LHRH5-10. Animals responsive to the Ac-LHRH5-10 fragment were tested at two-week intervals for responsiveness to other LHRH fragments modified in the C-terminal or saline in the following order: LHRH5-10, des-Gly6LHRH, LHRH5-9OH, saline, and LHRH7-9OH. The lordosis-to-mount (L/M) ratio was used as an index of sexual receptivity. The quality of lordotic posturing and the number of proceptive and resistive behaviors were also recorded for each test. A one-way ANOVA performed on the difference in L/M between pre- and postinfusion tests revealed a significant overall treatment effect. The nonacetylated LHRH5-10 fragment and the LHRH5-9OH fragment were effective in enhancing the L/M ratio, whereas des-Gly6LHRH and LHRH7-9OH were not. The enhancement of sexual behavior by C-terminal fragments of LHRH was associated with a lack of proceptive behavior and moderate levels of resistive behavior. The results indicate that several C-terminal fragments of LHRH are capable of elevating the L/M ratio and suggest that amino acids in positions 6 through 9 may be important for this effect.

Amino Acid Sequence↗

PubMed1990

Electrophysiological identification of a pathway from the septal area to the medial amygdala: sensitivity to estrogen and luteinizing hormone-releasing hormone.

Medial amygdala neurons responsive to electrical stimulation of the medial septal area were electrophysiologically identified in ovariectomized, urethane-anesthetized female rats. Peristimulus time histograms were collected and used to define the orthodromic response. The action of iontophoretically applied luteinizing hormone-releasing hormone (LHRH) and an LHRH fragment, Ac-LHRH5-10, on the activity of orthodromically responsive neurons was tested. Of a total of 187 neurons recorded, 119 were identified as orthodromically responsive. Three types of orthodromic responses were observed: excitatory, inhibitory, and complex. Priming the animals with 5 micrograms estradiol benzoate (EB) 48 hr prior to recording had no effect on the overall number of neurons responding to septal area stimulation, but EB priming did significantly reduce the percentage of orthodromically excited neurons. The firing rate of the majority of amygdala neurons responsive to septal area stimulation was not affected by iontophoretically applied LHRH (59 of 76) or LHRH fragment (41 of 65). In some cases, application of LHRH (10 of 76) or Ac-LHRH5-10 (12 of 55) produced a change in neuronal firing that was similar in direction to the orthodromically evoked response. When applied during the collection of peristimulus time histograms, both peptides were also able to modulate the orthodromically evoked response (five of 18 cells tested with LHRH and three of 14 cells tested with Ac-LHRH5-10). The results demonstrate a large projection from the septal area to the amygdala, one component of which is altered by estrogen priming.(ABSTRACT TRUNCATED AT 250 WORDS)

Amygdala↗

PubMed1990

Differential effects of a luteinizing-hormone-releasing hormone (LHRH) antagonist analogue on lordosis behavior induced by LHRH and the LHRH fragment Ac-LHRH5-10.

Both the luteinizing-hormone-releasing hormone (LHRH) decapeptide and an LHRH fragment consisting of the last 6 amino acids of the decapeptide, Ac-LHRH, have been shown to enhance lordosis behavior in ovariectomized, estradiol-benzoate treated female rats. Although the behavioral efficacy of the 2 peptides is similar, several lines of research suggest that the fragment and the decapeptide may act via different mechanisms. The present study attempted to differentiate the behavioral action of the 2 peptides by administering a long-acting LHRH antagonist analogue prior to infusion of either Ac-LHRH or LHRH. Without antagonist administration, the decapeptide and the fragment were equally effective in elevating lordotic posturing 90 min after bilateral infusion through cannulae positioned in the ventromedial nucleus of the hypothalamus (VMH). Infusion of a potent LHRH antagonist analogue [Ac-dehydro, Pro, pCl, D-Phe, DTrp]-LHRH, into the VMH significantly reduced the lordosis-to-mount ratio in animals subsequently treated with the LHRH decapeptide, but had no significant effect on lordotic behavior when the animals were subsequently infused with the Ac-LHRH fragment. The results indicate that LHRH enhancement of mating behavior is a receptor-mediated event and suggest that the Ac-LHRH fragment enhances lordotic behavior via a mechanism that is distinct from that of the LHRH decapeptide.

Animals↗

PubMed1990

Role of the vomeronasal organ in the male-induced enhancement of sexual receptivity in female rats.

The role of the vomeronasal organ (VNO) in the male-induced enhancement of sexual receptivity in ovariectomized estrogen-primed rats was investigated. Removal of the VNO significantly reduced the enhancement of sexual receptivity following mating, as compared with the sham-operated controls. The sham-operated females exhibited a surge of luteinizing hormone (LH) following mating; however, LH release induced by pairing with males was less manifested in the VNO-removed females. This suggests that in female rats, VNO removal impairs the male-induced release of LH-releasing hormone (LHRH). Since LHRH enhances sexual receptivity in ovariectomized estrogen-primed rats, the present results suggest that the increase in sexual receptivity in female rats following mating probably results from a VNO-mediated LHRH release.

Animals↗

PubMed1989

Re-evaluation of the effects of norepinephrine on the single-unit activity of paraventricular neurosecretory neurons.

Electrical stimulation of the A1 noradrenergic region elicited predominantly an excitatory orthodromic response from paraventricular neurosecretory neurons recorded in urethane-anesthetized male rats. In a majority of cases, locally applied norepinephrine (NE) as well as A1 region stimulation excited paraventricular neurosecretory neurons. However, in some neurons including a subpopulation of putative vasopressin neurons, iontophoresed NE was inhibitory. Both excitatory and inhibitory effects of NE were selectively blocked by the alpha-antagonist, phentolamine, but not by the beta-antagonist, timolol. In general, the results support the notion that the A1 noradrenergic input to paraventricular neurosecretory neurons is excitatory. Nevertheless, the results do not exclude the possibility that NE exerts a specific, alpha-receptor-mediated, inhibitory effect on a subpopulation of paraventricular neurons.

Action Potentials↗

PubMed1989

Inhibitory effect of norepinephrine on the single-unit activity of caudally projecting paraventricular neurons.

The role of norepinephrine (NE) in controlling the single-unit activity of paraventricular (PVN) neurons projecting to or passing through the caudal ventrolateral medulla (CVLM) was investigated in adult male rats anesthetized with urethane. Of 72 PVN neurons studied, 19 were antidromically activated by CVLM stimulation (Group I) and 48 were antidromically activated by posterior pituitary (PP) stimulation (Group II). The remaining 5 neurons were antidromically driven by both CVLM and PP stimulation (Group III). In 14 of the 19 Group I neurons and in all the 5 Group III neurons, iontophoretically applied NE was demonstrated to be inhibitory to the single-unit activity. No excitatory effect of NE was observed. In contrast, both excitatory and inhibitory actions of NE were observed in the Group II neurons. Of 37 Group II neurons tested, 28 were excited and 7 were inhibited by NE. The inhibitory effect of NE in Group I and Group III neurons was selectively blocked by the alpha antagonist, phentolamine, that was coiontophoresed with NE, but not by the beta antagonist, timolol (n = 9). The unit activity of Group I neurons that were inhibited by NE was not altered by an increase in arterial blood pressure (n = 3), whereas the unit activity of one NE-insensitive Group I neuron was decreased by an increase in blood pressure. Taken together, the results suggest that NE plays an alpha-adrenoreceptor-mediated inhibitory role in controlling the single-unit activity of caudally projecting PVN neurons. These neurons include a subpopulation of PVN neurons that project caudally as well as to the PP. The possible function associated with the NE-sensitive, caudally projecting PVN neurons may be other than the regulation of blood pressure.

Animals↗

PubMed1988

Facilitation of lordosis in female rats by CNS-site specific infusions of an LH-RH fragment, Ac-LH-RH-(5-10).

Structural alterations of the luteinizing hormone-releasing hormone (LH-RH) molecule have been performed to yield analogs which are more potent than, or which compete with, the parent hormone to increase the release of LH from the pituitary gland. The effects of these analogs on mating behavior, however, do not always parallel their effects on LH release. The present study tested the effectiveness of a pituitary-inactive fragment of LH-RH, namely Ac-LH-RH-(5-10), in potentiating mating behavior in the ovariectomized, estrogen-primed female rat. This fragment, when infused bilaterally into the medial preoptic area (POA), the ventromedial hypothalamus (VMH), or the midbrain central gray (MCG), significantly enhanced lordosis. Infusion of the fragment into the cerebral cortex was ineffective. Elevated lordotic responding was first apparent in the POA at 15 min postinfusion and was maintained for the duration of the testing session (180 min). Ac-LH-RH-(5-10) infused into the VMH or MCG enhanced lordotic behavior at 90 and 180 min postinfusion. The results indicate that only a portion of the LH-RH molecule may be required for behavioral activity and suggest that degradation of the LH-RH molecule is physiologically relevant.

Animals↗

PubMed1988

A1 noradrenergic action on medial preoptic-medial septal neurons: a neuropharmacological study.

In an attempt to determine whether the excitatory and inhibitory orthodromic responses of single medial preoptic-medial septal (MPO-S) neurons to discrete electrical stimulation of the A1 noradrenergic region were mediated specifically by norepinephrine (NE) and involved different types of adrenoreceptors, a series of electrophysiological and neuropharmacological experiments was conducted. Extracellular single unit recording and local drug application techniques were used in female rats under urethane anesthesia. Chemical lesion of the catecholaminergic nerve terminal plexus in the medial preoptic area with 6-hydroxydopamine abolished both excitatory and inhibitory orthodromic effects of A1 region stimulation on MPO-S neurons, suggesting the noradrenergic nature of the effects. This conclusion was corroborated by the observation that the orthodromic effects were mimicked by locally applied exogenous NE. The excitatory effects were reliably mimicked by a low concentration of NE (0.5 mM; in-barrel concentration) and methoxamine (1.0 mM, an alpha-1 agonist), but not by either low or high concentrations (1 and 100 mM) of clonidine (an alpha-2 agonist) and isoproterenol (a beta agonist). The inhibitory orthodromic effects of A1 region stimulation were reliably mimicked by a high concentration of NE (50 mM), clonidine (100 mM) and isoproterenol (100 mM), but not by a low concentration of NE (0.5 mM), methoxamine (1 mM), clonidine (1 mM) or isoproterenol (1 mM). A high concentration (100 mM) of methoxamine mimicked the inhibitory effects less than 40% of the time. The low concentration (0.5 mM) NE-induced excitation that matched the excitatory orthodromic effect of A1 region stimulation was blocked by phentolamine (100 mM), an alpha blocker, but not by timolol (100 mM), a beta blocker. On the other hand, the high concentration (50 mM) NE-induced inhibition that matched the inhibitory orthodromic effect of A1 region stimulation was blocked by timolol, but not by phentolamine. Taken together, the present results are consistent with the hypotheses that the ascending noradrenergic projections from the A1 region affect the excitability of MPO-S neurons directly through NE and that the excitatory and inhibitory orthodromic effects involve different types of adrenoreceptors, i.e., alpha-1 and beta receptors, respectively.

Action Potentials↗

PubMed1988

Immunocytochemical localization of hypothalamic luteinizing hormone-releasing hormone in male ferrets.

LHRH-containing neurons within the hypothalamus were immunocytochemically identified in adult male ferrets that were either gonadally intact, castrated, or castrated and treated with testosterone. The distribution of LHRH-immunopositive neuron cell bodies was similar in the three treatment groups. The majority of these cells was located mediobasally in the retrochiasmatic area, including some within the ventrolateral aspects of the arcuate nucleus. These soma were associated with a dense basal LHRH fiber plexus which extended to the median eminence. A smaller number of cell bodies was found slightly more dorsal and lateral to the major concentration at the base and midline. Isolated LHRH perikarya were occasionally observed in dorsal areas of the hypothalamus. There were no differences in the mean total number of hypothalamic LHRH cell bodies identified in the three treatment groups. These results indicate that the documented negative feedback effects of testosterone on LH secretion in male ferrets are not the result of an alteration in the absolute number of neurons capable of synthesizing LHRH.

Animals↗