- Open Access
Copulation or sensory cues from the female augment Fos expression in arginine vasopressin neurons of the posterodorsal medial amygdala of male rats
© Hari Dass and Vyas; licensee BioMed Central Ltd. 2014
- Received: 5 January 2014
- Accepted: 22 May 2014
- Published: 2 June 2014
The posterodorsal part of the medial amygdala is essential for processing reproductively salient sensory information in rodents. This is the initial brain structure where information from olfactory system and male hormones intersect. The neurochemical identity of the neurons participating in the sensory processing in medial amygdala remains presently undetermined. Many neurons in this brain structure express arginine vasopressin in a testosterone-dependent manner, suggesting that this neuropeptide is maintained by the androgenic milieu.
Here we use Fos, a protein expressed by recently active neurons, to quantify activation of arginine vasopressin neurons after exposure to odor from physically inaccessible female. We compare it to mating with accessible female and to reproductively innocuous odor.
We show that inaccessible female activate arginine vasopressin neurons in the male posterodorsal medial amygdala. The magnitude of activation is not further enhanced when physical access with resultant mating is granted, even though it remains undetermined if same population of AVP neurons is activated by both inaccessible female and copulation. We also show that arginine vasopressin activation cannot be fully accounted for by mere increase in the number of Fos and AVP neurons.
These observations posit a role for the medial amygdala arginine vasopressin in reproductive behaviors, suggesting that these neurons serve as integrative node between the hormonal status of the animal and the availability of reproductive opportunities.
- Sexual behavior
- Social behavior
The medial amygdala (MeA) plays an important role during male reproductive behavior in the rodents . Lesions of the MeA reduce reproductive behavior in hamsters , rats  and gerbils . In hamsters, the anterior MeA is involved in discrimination of conspecific odor from same-sex versus opposite-sex donors, while the posterodorsal MeA is selectively activated by opposite-sex conspecifics . Fiber-sparing lesions of anterior MeA in this species reduce number of Fos immunoreactive cells in the posterodorsal MeA and efferent forebrain regions , suggesting a unidirectional flow of chemosensory information through anterior MeA to its downstream targets. In male rats, MeA lesions drastically reduce penile erections in response to an inaccessible estrous female . Interestingly, such lesions do not affect reflexive erections in response to penile sheath retraction. These observations suggest that MeA involvement in male reproductive behavior is restricted to motivation and not to the downstream initiation of mating in this species.
MeA is a sexually dimorphic structure (reviewed in ), characterized by more neurons and larger neuronal soma in males compared to females [9, 10]. Important from the perspective of this report, male MeA also contains sunstantial number of extra-hypothalamic parvocellular population of arginine vasopressin (AVP) neurons . Testosterone is required for sexual dimorphism of the MeA neurons  and also for AVP expression in the MeA [12, 13]. The essential nature of testosterone is further supported by the observations that antagonism of androgen receptors in the MeA inhibits penile erection in male rats in presence of estrus females ; an effect reversed by testosterone implants within the MeA of castrates [15, 16].
Further evidence suggests that the contribution of the MeA to reproductive behavior is anchored in its ability to integrate pheromonal information with hormonal milieu. Soiled bedding from females increases MeA-Fos in male mice with or without aromatase  and in testosterone-primed gonadectomized rats [18, 19]. Since Fos is regarded as a proxy for recent neuronal activity , this observation suggests that pheromones enhance the activity of MeA neurons. Similarly, female vaginal fluid increases Fos expression in the MeA of mandarin voles . These observations provide correlational support for activation of the MeA in pheromonal processing. Experiments in Syrian hamster further strengthen this. Mating in this species requires intact ability to smell female pheromones and presence of testicular testosterone; absence of either countermands copulation. Interestingly, implantation of testosterone in the MeA of castrates can reinitiate copulatory behavior . Yet, the ability of the testosterone to rescue effects of the castration is dependent on olfactory inputs, such that surgical removal of olfactory bulbs renders testosterone implants ineffective [22, 23]. Since both olfactory inputs afferent to MeA and testosterone within MeA are required for the rescue, it suggests that MeA integrates information from sensory environment and internal androgenic milieu.
Despite the role of the MeA in processing of reproductively salient sensory cues, the neurochemical identity of the pertinent cell groups is yet undetermined. As mentioned before, many MeA neurons also express AVP in a testosterone dependent manner. This is important because the AVP mediates several social and sexual behaviors, e.g. monogamy in voles  and social recognition of juveniles in male rats . Moreover, AVP neurons are activated during copulation in bed nucleus of stria terminalis , a brain region with significant neuro-architectural similarity to the MeA.
In view of androgen-dependent expression of the MeA-AVP and the role of the testosterone in the pheromonal processing, we hypothesized that sensory cues from females selectively activate AVP producing neurons in the MeA. We tested this hypothesis by quantifying co-labeling of AVP and Fos, an immediate early gene product that marks recently activated neurons, post-exposure to rabbit odor or inaccessible estrus female or copulation. Posteroventral and posterodorsal sub-nuclei of MeA were quantified separately in view of their disparate neurochemistry and differential involvement in processing of olfactory signals .
Reproductive stimuli suppressed number of Fos-ir neurons in the MePV, but increased it in the MePD
We utilized repeated measure ANOVA to compare number of Fos-ir neurons in MePV and MePD across experimental treatments. Main effect of the experimental treatments reached statistical significance (F(2,14) = 4.44; p =0.032). ANOVA revealed significant differences for the main effect of the sub-nuclei (MePD > MePV, 59.2% change in marginal means; F(1,14) = 35.46; p < 0.001) and the interaction (F(2,14) = 29.21; p < 0.001).
In contrast to the MePV, the number of Fos-ir neurons in the MePD exhibited significant increase after copulation, compared to rabbit odor (Figure 2B, 57% increase; p < 0.05). Exposure to an estrous female did not result in a significant increase (p = 0.259). The number of Fos-ir neurons was greater in the MePD compared to the MePV when animals were treated with reproductive stimuli (post-hoc paired t-test: p < 0.05) and not statistically different during control stimulus (|t5| = 2.35, p = 0.066).
MePD contained greater number of AVP-ir neurons
Reproductive stimuli increased number of colabeled neurons in MePD, but not in MePV
ANOVA revealed significant main effects of experimental treatments (F(2,14) = 27.28; p < 0.001) and of sub-nuclei (F(1,14) = 373.72; p < 0.0001). Interaction between treatments and sub-nuclei was also highly significant (F(2,14) = 73.10; p < 0.001).
In the MePD, exposure to estrus females robustly increased number of colabeled neurons compared to the control stimuli (Figure 4B, 233% increase; post-hoc LSD test: p < 0.00001). Similarly, mating with females also increased number of colabeled neurons in the male MePD (300% increase; p < 0.00001).
Reproductively salient stimuli specifically activated AVP-ir neurons in the MePD
Mean ± SeM values pertaining to co-labeled AVP-ir and Fos-ir cells
Mean ± SeM
Rabbit (n = 6)
Estrous (n = 5)
Copulation (n = 6)
Percentage of Fos-ir cells that were also AVP-ir
23.6 ± 3.9
23.4 ± 6.3
19.2 ± 2.3
5.5 ± 1.0
45.6 ± 2.8*#
47.0 ± 3.6*#
Percentage of AVP-ir cells that were also Fos-ir
11.8 ± 1.8
28.2 ± 5.7*
27.2 ± 4.1*
24.3 ± 3.9 #
64.5 ± 4.3*#
58.4 ± 1.6*#
Amongst the various nuclei of the extended amygdala, the MeA is especially important for the appetitive aspects of the reproduction because it is the initial site during pheromonal processing where main and accessory olfactory information intersects [5, 28, 29]. It robustly expresses androgen receptors and is sexually dimorphic in the structure [30–32]. The androgen responsiveness suggests that the MEA has access to and can plausibly integrate both the internal hormonal milieu and external pheromonal environment. Lesions of this structure ablate penile erections in male rats in response to an inaccessible female , while leaving reflexive erections intact . Importance of MeA efferents for mating can be ascertained by the observation that simultaneous unilateral MeA lesion coupled with contralateral medial preoptic lesion ablates mating behavior . The MeA also shares bidirectional innervation with bed nucleus of stria terminalis (BNST). For example, in male hamsters after exposure to a female odor, greater number of MePD neurons colabeled with Fos and a retrograde tracer injected in the BNST . This demonstrates that female odors increases activity in BNST-projecting neurons of the MePD, compared to an odor from male conspecifics. The greater communication between MePD and the BNST is consistent with the ontological and hodological similarities between these brain regions .
Despite the importance of neurons in the MeA in the processing of reproductively salient cues, neurochemical identity of the activated neurons is still undetermined. Data presented in this report shows that the exposure to a physically inaccessible female rat can selectively activate AVP neurons in the MePD, in contrast to the MePV or in contrast to reproductively innocuous rabbit urine. Moreover, the extent of AVP neurons being activated cannot be explained by arithmetic changes in AVP or Fos neurons, thus suggesting that AVP neurons are activated in a non-random manner. While the present report examined two sub-nuclei of the MeA, it is possible that other MeA sub-nuclei or other parts of the social brain network are also activated during exposure to the reproductively salient stimuli.
We demonstrate a rapid increase in the density of Fos neurons in the MePD after exposure to an inaccessible female or post-copulation. This suggests that Fos in the MePD is dynamically regulated by the presence of sensory cues. Yet, this increase in Fos density is not sufficient to explain the full extent of MePD-AVP activation. This is substantiated by the fact that a greater number of active neurons express AVP and a greater fraction of the AVP neurons become active. Thus, AVP neurons are activated during exposure to sexually salient environmental signals. This is consistent with the prior observations in desert finches expressing vasotocin, a neuropeptide homologous to the AVP. This bird is an opportunistic breeder similar to the rat. In this species co-housing with females enhances activation of the pre-existing vasotocin neurons in the bed nucleus of stria terminalis of the males, compared to the unisexual group of males .
The extent of MePD-AVP activation does not seem to be affected by presence or absence of the physical contact or mating itself. In other words, sensory signals of a physically inaccessible female and the actual mating induce equivalent amount of AVP activation. It should be however noted that experiments described in this report cannot differentiate if same or different population of MePD-AVP neurons are activated by inaccessible female and copulation. Localized manipulations in MeA does increase reproductive motivation of the males even when females are inaccessible or even when soiled bedding or vaginal fluids are used instead of the females . Testosterone implants in the MeA rescue the effects of castration on appetitive aspects of the reproductive behavior. It is not clear if testosterone in these cases directly activates androgen receptor and/or is aromatized to estradiol and subsequently binds to estrogen receptors. Mice lacking aromatase gene exhibit MeA-Fos activation comparable to the wild-type individuals when exposed to female odors , suggesting direct role for the androgen receptors. These observations and data in present report suggest, but do not prove, that MePD is involved in processing of information with no additional role in mating. It should be noted that, contrary to the suggestion of non-additional role of the MeA testosterone in consummatory reproductive behavior, androgen receptor occupancy in MeA does facilitate intromission and ejaculation if simultaneous estrogen receptor binding is available throughout the brain and the periphery .
AVP neurons mediate social and sexual behaviors in a variety of species and paradigms. Relevant examples include social recognition in rats [38–40] and development of pair bonding in monogamous voles . Homologous neuropeptides are involved in flocking and territoriality in birds ; and in mate recognition and mating in nematode Caenorhabditis elegans. AVP neurons in medial bed nucleus of stria terminalis are also activated during copulation in mice [26, 43]. While these strands of evidences suggest a pervasive role for the AVP in a variety of social and sexual behaviors, it is currently unknown if the sexual sensory cues themselves activate AVP neurons. In this backdrop, we show that exposure to inaccessible females is able to activate AVP neurons in MePD, the actual act of copulation not being obligatory. This is consistent with the prior observations that testosterone acting within the MeA promotes sexual arousal to the odor of female rats, without any apparent effect on mating behavior itself.
Reproductive investment and testosterone levels in animals are frequently calibrated to incipient metabolic conditions and mating opportunities [44, 45]. It is plausible that AVP within the MePD serves as integrative node between reproductive status of the animal (signaled by testosterone mediated expression of AVP) and availability of reproductive opportunities (signaled by activation of AVP neurons by sexual pheromones). Related to this, social isolation after weaning reduces the volume of MeA and blunts the sexual behavior in rats . Similarly, ageing reduces MeA-AVP and AVP innervation to brain regions efferent to the MeA .
In conclusion, data presented here show that AVP neurons in MePD are activated during the processing of reproductive cues. It is likely that these neurons play critical role in the mediation of pheromone-directed reproductive behaviors. In addition this report provides support to the role of extra-hypothalamic AVP neurons in reproductive and affiliative behaviors.
Wistar rats (47–50 days old) were obtained from the vivarium at National University of Singapore. Animals (housed 2/cage) were maintained on 12 hour light–dark cycle with ad libitum food and water (lights on at 0700 hours). The Nanyang Technological University institutional animal care and use committee reviewed and approved all procedures. These procedures are compliant with the NIH guidelines. All the male and female subjects used in this paper were sexually naïve at the start of the experiment.
Exposure to reproductive stimuli
Males were habituated for ten successive days ((ten minutes each day, between 1100 and 1400 hours) in a rectangular arena, in which they would eventually receive the stimuli (46 × 9 cm; 15 cm high). On the day of exposure males were shifted into the procedure room just before the beginning of the light phase (7 AM). After a four hour rest period they were exposed to either a physically inaccessible estrus female behind translucent perforated plastic partition (N = 5) or allowed to mate with an accessible receptive female (N = 6). Females were allowed to explore the entire arena for two hours before the start of the trial, during which time they placed urine marks in the arena. To control for novelty of the odor, a third group of males was exposed to rabbit urine on an inaccessible towel (N = 6). All animals were sacrificed two hour after the onset of stimulus exposure.
Naturally cycling females were used as the stimulus. Estrus phase was determined using examination of vaginal lavage, obtained by gentle flushing of cells from vaginal lining using 20 μl buffered saline (between 1030 and 1100 hours). Unstained lavages were examined on a glass slide using 20× magnification. Females in estrus were identified by presence of cornified cells and absence of nucleated cells.
Animals were deeply anaesthetized and transcardially perfused with 4% paraformaldehyde. Free floating brain sections (40 μm thick) were incubated in a cocktail of primary antibodies for 72 hours at 4°C (guinea pig anti-AVP, 1:500, Bachem; and, rabbit anti-Fos, 1:100, Santa Cruz Biotenchology). This was followed by incubation with secondary antibodies at room temperature for 2 hours (biotinylated anti guinea pig; 1: 200 + anti rabbit-DyLight 549;1:200; obtained from Vector Laboratories). The biotinylated antibody signal was developed using Vectastain elite ABC kit (Vector Laboratories) and tyramide signal amplification system (Perkin Elmer). Sections were counter stained with DAPI for 1 minute.
Brain sections between Bregma levels −2.76 mm and −3.24 mm (Interaural 7.28 to 7.08) were selected for analysis. Sections were imaged at 40× magnification and 1.2× digital zoom using a confocal microscope (optically sliced at 4 μm, three set of stacks per animal, Carl Zeiss LSM 710). Neurons positive for DAPI, Fos and AVP were counted. Scores were cumulated per animal.
Calculation of observed and expected frequencies
We calculated the expected probability of encountering colabeled neurons by multiplying individual probabilities of AVP-ir and Fos-ir neurons. Individual probabilities for AVP-ir were calculated by division of number of AVP-ir neurons with total number of DAPI positive neurons counted (i.e. probability that a particular DAPI positive neuron will be also be AVP-ir). Individual probabilities for Fos-ir were also counted in the similar manner. A product of these probabilities defines the baseline expectation of colabeling by mere chance and assuming biological independence between Fos and AVP activation. The observed numbers of the colabeled cells were compared to the expected baseline, with null hypothesis of colabeling being a mere mathematical coincidence (adapted from ).
Repeated measures analysis of variance (ANOVA) was used to quantify statistical significance for main effects and interactions. In case of within-subject comparisons, paired Student’s t-test was employed for post-hoc significance testing. In case of between-subject comparisons, LSD test was used. Values reported are mean ± SEM.
Funded by Nanyang Technological University and Ministry of Education, Singapore.
- Greco B, Edwards DA, Michael RP, Clancy AN: Androgen receptors and estrogen receptors are colocalized in male rat hypothalamic and limbic neurons that express Fos immunoreactivity induced by mating. Neuroendocrinology. 1998, 67: 18-28. 10.1159/000054294.PubMedView ArticleGoogle Scholar
- Lehman MN, Winans SS, Powers JB: Medial nucleus of the amygdala mediates chemosensory control of male hamster sexual behavior. Science. 1980, 210: 557-60. 10.1126/science.7423209.PubMedView ArticleGoogle Scholar
- Kondo Y: Lesions of the medial amygdala produce severe impairment of copulatory behavior in sexually inexperienced male rats. Physiol Behav. 1992, 51: 939-43. 10.1016/0031-9384(92)90074-C.PubMedView ArticleGoogle Scholar
- Heeb MM, Yahr P: Cell-body lesions of the posterodorsal preoptic nucleus or posterodorsal medial amygdala, but not the parvicellular subparafascicular thalamus, disrupt mating in male gerbils. Physiol Behav. 2000, 68: 317-31. 10.1016/S0031-9384(99)00182-1.PubMedView ArticleGoogle Scholar
- Maras PM, Petrulis A: Chemosensory and steroid-responsive regions of the medial amygdala regulate distinct aspects of opposite-sex odor preference in male Syrian hamsters. Eur J Neurosci. 2006, 24: 3541-52. 10.1111/j.1460-9568.2006.05216.x.PubMedView ArticleGoogle Scholar
- Maras PM, Petrulis A: The anterior medial amygdala transmits sexual odor information to the posterior medial amygdala and related forebrain nuclei. Eur J Neurosci. 2010, 32: 469-82. 10.1111/j.1460-9568.2010.07289.x.PubMedView ArticleGoogle Scholar
- Kondo Y, Sachs BD, Sakuma Y: Importance of the medial amygdala in rat penile erection evoked by remote stimuli from estrous females. Behav Brain Res. 1998, 91: 215-22.PubMedGoogle Scholar
- Cooke BM: Steroid-dependent plasticity in the medial amygdala. Neuroscience. 2006, 138: 997-1005. 10.1016/j.neuroscience.2005.06.018.PubMedView ArticleGoogle Scholar
- Mizukami S, Nishizuki M, Arai Y: Sexual difference in nuclear volume and its ontogeny in the rat amygdala. Exp Neurol. 1983, 79: 569-75. 10.1016/0014-4886(83)90235-2.PubMedView ArticleGoogle Scholar
- Cooke BM, Tabibnia G, Breedlove SM: A brain sexual dimorphism controlled by adult circulating androgens. Proc Natl Acad Sci U S A. 1999, 96: 7538-40. 10.1073/pnas.96.13.7538.PubMedPubMed CentralView ArticleGoogle Scholar
- Wang Z, De Vries GJ: Androgen and estrogen effects on vasopressin messenger RNA expression in the medial amygdaloid nucleus in male and female rats. J Neuroendocrinol. 1995, 7: 827-31. 10.1111/j.1365-2826.1995.tb00722.x.PubMedView ArticleGoogle Scholar
- DeVries GJ, Buijs RM, Van Leeuwen FW, Caffe AR, Swaab DF: The vasopressinergic innervation of the brain in normal and castrated rats. J Comp Neurol. 1985, 233: 236-54. 10.1002/cne.902330206.PubMedView ArticleGoogle Scholar
- Auger CJ, Coss D, Auger AP, Forbes-Lorman RM: Epigenetic control of vasopressin expression is maintained by steroid hormones in the adult male rat brain. Proc Natl Acad Sci. 2011, 108: 4242-7. 10.1073/pnas.1100314108.PubMedPubMed CentralView ArticleGoogle Scholar
- Bialy M, Nikolaev-Diak A, Kalata U, Nikolaev E: Blockade of androgen receptor in the medial amygdala inhibits noncontact erections in male rats. Physiol Behav. 2011, 103: 295-301. 10.1016/j.physbeh.2011.02.003.PubMedView ArticleGoogle Scholar
- Bialy M, Sachs BD: Androgen implants in medial amygdala briefly maintain noncontact erection in castrated male rats. Horm Behav. 2002, 42: 345-55. 10.1006/hbeh.2002.1821.PubMedView ArticleGoogle Scholar
- Cooke BM, Breedlove SM, Jordan CL: Both estrogen receptors and androgen receptors contribute to testosterone-induced changes in the morphology of the medial amygdala and sexual arousal in male rats. Horm Behav. 2003, 43: 336-46. 10.1016/S0018-506X(02)00047-8.PubMedView ArticleGoogle Scholar
- Aste N, Honda S, Harada N: Forebrain Fos responses to reproductively related chemosensory cues in aromatase knockout mice. Brain Res Bull. 2003, 60: 191-200. 10.1016/S0361-9230(03)00035-2.PubMedView ArticleGoogle Scholar
- Bressler SC, Baum MJ: Sex comparison of neuronal Fos immunoreactivity in the rat vomeronasal projection circuit after chemosensory stimulation. Neuroscience. 1996, 71: 1063-72. 10.1016/0306-4522(95)00493-9.PubMedView ArticleGoogle Scholar
- Paredes RG, Lopez ME, Baum MJ: Testosterone augments neuronal Fos responses to estrous odors throughout the vomeronasal projection pathway of gonadectomized male and female rats. Horm Behav. 1998, 33: 48-57. 10.1006/hbeh.1998.1435.PubMedView ArticleGoogle Scholar
- Hoffman GE, Smith MS, Verbalis JG: c-Fos and related immediate early gene products as markers of activity in neuroendocrine systems. Front Neuroendocrinol. 1993, 14: 173-213. 10.1006/frne.1993.1006.PubMedView ArticleGoogle Scholar
- He F, Wu R, Yu P: Study of Fos, androgen receptor and testosterone expression in the sub-regions of medial amygdala, bed nucleus of stria terminalis and medial preoptic area in male mandarin voles in response to chemosensory stimulation. Behav Brain Res. 2014, 258: 65-74.PubMedView ArticleGoogle Scholar
- Wood RI, Coolen LM: Integration of chemosensory and hormonal cues is essential for sexual behaviour in the male Syrian hamster: role of the medial amygdaloid nucleus. Neuroscience. 1997, 78: 1027-35. 10.1016/S0306-4522(96)00629-X.PubMedView ArticleGoogle Scholar
- Wood RI, Newman SW: Integration of chemosensory and hormonal cues is essential for mating in the male Syrian hamster. J Neurosci. 1995, 15: 7261-9.PubMedGoogle Scholar
- Lim MM, Hammock EA, Young LJ: The role of vasopressin in the genetic and neural regulation of monogamy. J Neuroendocrinol. 2004, 16: 325-32. 10.1111/j.0953-8194.2004.01162.x.PubMedView ArticleGoogle Scholar
- Bluthe RM, Schoenen J, Dantzer R: Androgen-dependent vasopressinergic neurons are involved in social recognition in rats. Brain Res. 1990, 519: 150-7. 10.1016/0006-8993(90)90073-K.PubMedView ArticleGoogle Scholar
- Ho JM, Murray JH, Demas GE, Goodson JL: Vasopressin cell groups exhibit strongly divergent responses to copulation and male-male interactions in mice. Horm Behav. 2010, 58: 368-77. 10.1016/j.yhbeh.2010.03.021.PubMedPubMed CentralView ArticleGoogle Scholar
- Choi GB, Dong H-w, Murphy AJ, Valenzuela DM, Yancopoulos GD, Swanson LW, Anderson DJ: Lhx6 delineates a pathway mediating innate reproductive behaviors from the amygdala to the hypothalamus. Neuron. 2005, 46: 647-60. 10.1016/j.neuron.2005.04.011.PubMedView ArticleGoogle Scholar
- Samuelsen CL, Meredith M: The vomeronasal organ is required for the male mouse medial amygdala response to chemical-communication signals, as assessed by immediate early gene expression. Neuroscience. 2009, 164: 1468-76. 10.1016/j.neuroscience.2009.09.030.PubMedPubMed CentralView ArticleGoogle Scholar
- Meredith M: Vomeronasal, olfactory, hormonal convergence in the brain. cooperation or coincidence?. Ann N Y Acad Sci. 1998, 855: 349-61. 10.1111/j.1749-6632.1998.tb10593.x.PubMedView ArticleGoogle Scholar
- Morris JA, Jordan CL, King ZA, Northcutt KV, Breedlove SM: Sexual dimorphism and steroid responsiveness of the posterodorsal medial amygdala in adult mice. Brain Res. 2008, 1190: 115-21.PubMedPubMed CentralView ArticleGoogle Scholar
- Blake CB, Meredith M: Change in number and activation of androgen receptor-immunoreactive cells in the medial amygdala in response to chemosensory input. Neuroscience. 2011, 190: 228-38.PubMedPubMed CentralView ArticleGoogle Scholar
- Zhou L, Blaustein JD, De Vries GJ: Distribution of androgen receptor immunoreactivity in vasopressin- and oxytocin-immunoreactive neurons in the male rat brain. Endocrinology. 1994, 134: 2622-7.PubMedGoogle Scholar
- Kondo Y, Arai Y: Functional association between the medial amygdala and the medial preoptic area in regulation of mating behavior in the male rat. Physiol Behav. 1995, 57: 69-73. 10.1016/0031-9384(94)00205-J.PubMedView ArticleGoogle Scholar
- Been LE, Petrulis A: Chemosensory and hormone information are relayed directly between the medial amygdala, posterior bed nucleus of the stria terminalis, and medial preoptic area in male Syrian hamsters. Horm Behav. 2011, 59: 536-48. 10.1016/j.yhbeh.2011.02.005.PubMedPubMed CentralView ArticleGoogle Scholar
- Johnston JB: Further contributions to the study of the evolution of the forebrain. J Comp Neurol. 1923, 35: 337-481. 10.1002/cne.900350502.View ArticleGoogle Scholar
- Kabelik D, Morrison JA, Goodson JL: Cryptic regulation of vasotocin neuronal activity but not anatomy by sex steroids and social stimuli in opportunistic desert finches. Brain Behav Evol. 2010, 75: 71-84. 10.1159/000297522.PubMedPubMed CentralView ArticleGoogle Scholar
- Baum MJ, Tobet SA, Starr MS, Bradshaw WG: Implantation of dihydrotestosterone propionate into the lateral septum or medial amygdala facilitates copulation in castrated male rats given estradiol systemically. Horm Behav. 1982, 16: 208-23. 10.1016/0018-506X(82)90020-4.PubMedView ArticleGoogle Scholar
- Dluzen DE, Muraoka S, Engelmann M, Landgraf R: The effects of infusion of arginine vasopressin, oxytocin, or their antagonists into the olfactory bulb upon social recognition responses in male rats. Peptides. 1998, 19: 999-1005. 10.1016/S0196-9781(98)00047-3.PubMedView ArticleGoogle Scholar
- Tobin VA, Hashimoto H, Wacker DW, Takayanagi Y, Langnaese K, Caquineau C, Noack J, Landgraf R, Onaka T, Leng G, Meddle SL, Engelmann M, Ludwig M: An intrinsic vasopressin system in the olfactory bulb is involved in social recognition. Nature. 2010, 464: 413-7. 10.1038/nature08826.PubMedPubMed CentralView ArticleGoogle Scholar
- Wacker DW, Ludwig M: Vasopressin, oxytocin, and social odor recognition. Horm Behav. 2012, 61: 259-65. 10.1016/j.yhbeh.2011.08.014.PubMedView ArticleGoogle Scholar
- Goodson JL, Kelly AM, Kingsbury MA: Evolving nonapeptide mechanisms of gregariousness and social diversity in birds. Horm Behav. 2012, 61: 239-50. 10.1016/j.yhbeh.2012.01.005.PubMedPubMed CentralView ArticleGoogle Scholar
- Garrison JL, Macosko EZ, Bernstein S, Pokala N, Albrecht DR, Bargmann CI: Oxytocin/vasopressin-related peptides have an ancient role in reproductive behavior. Science. 2012, 338: 540-3. 10.1126/science.1226201.PubMedPubMed CentralView ArticleGoogle Scholar
- Young LJ, Nilsen R, Waymire KG, MacGregor GR, Insel TR: Increased affiliative response to vasopressin in mice expressing the V1a receptor from a monogamous vole. Nature. 1999, 400: 766-8. 10.1038/23475.PubMedView ArticleGoogle Scholar
- Raab A, Haedenkamp G: Impact of social conflict between mice on testosterone binding in the central nervous system. Neuroendocrinology. 1981, 32: 272-7. 10.1159/000123172.PubMedView ArticleGoogle Scholar
- Blanchard DC, Sakai RR, McEwen B, Weiss SM, Blanchard RJ: Subordination stress: behavioral, brain, and neuroendocrine correlates. Behav Brain Res. 1993, 58: 113-21. 10.1016/0166-4328(93)90096-9.PubMedView ArticleGoogle Scholar
- Cooke BM, Chowanadisai W, Breedlove SM: Post-weaning social isolation of male rats reduces the volume of the medial amygdala and leads to deficits in adult sexual behavior. Behav Brain Res. 2000, 117: 107-13. 10.1016/S0166-4328(00)00301-6.PubMedView ArticleGoogle Scholar
- Van Zwieten EJ, Kos WT, Ravid R, Swaab DF: Decreased number of vasopressin immunoreactive neurons in the medial amygdala and locus coeruleus of the aged rat. Neurobiol Aging. 1993, 14: 245-8. 10.1016/0197-4580(93)90008-Y.PubMedView ArticleGoogle Scholar
- Lin D, Boyle MP, Dollar P, Lee H, Lein ES, Perona P, Anderson DJ: Functional identification of an aggression locus in the mouse hypothalamus. Nature. 2011, 470: 221-6. 10.1038/nature09736.PubMedPubMed CentralView ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.