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1.
Article in English | MEDLINE | ID: mdl-34649923

ABSTRACT

The apparent virilization of the female spotted hyena raises questions about sex differences in behavior and morphology. We review these sex differences to find a mosaic of dimorphic traits, some of which conform to mammalian norms. These include space-use, dispersal behavior, sexual behavior, and parental behavior. By contrast, sex differences are reversed from mammalian norms in the hyena's aggressive behavior, social dominance, and territory defense. Androgen exposure early in development appears to enhance aggressiveness in female hyenas. Weapons, hunting behavior, and neonatal body mass do not differ between males and females, but females are slightly larger than males as adults. Sex differences in the hyena's nervous system are relatively subtle. Overall, it appears that the "masculinized" behavioral traits in female spotted hyenas are those, such as aggression, that are essential to ensuring consistent access to food; food critically limits female reproductive success in this species because female spotted hyenas have the highest energetic investment per litter of any mammalian carnivore. Evidently, natural selection has acted to modify traits related to food access, but has left intact those traits that are unrelated to acquiring food, such that they conform to patterns of sexual dimorphism in other mammals.


Subject(s)
Carnivora , Hyaenidae , Androgens , Animals , Female , Hyaenidae/anatomy & histology , Hyaenidae/physiology , Male , Sex Characteristics
2.
Brain Behav Evol ; 92(1-2): 82-95, 2018.
Article in English | MEDLINE | ID: mdl-30415261

ABSTRACT

The relationship between brain size and body size across species "from mouse to elephant" is described by a function of positive slope. Almost uniformly, the relationship between brain size and body size within a species has a positive slope, though this is less steep than across species. The spotted hyena, Crocuta crocuta, differs from most other mammals in a number of ways including the fact that, on average, adult females weigh more than adult males and occasionally display greater body lengths. Brains of 5 female and 4 male hyenas were weighed in the field near Moyale in Northern Kenya, and body weights and body lengths were obtained from the same animals. When our analyses of brain/body relationships in these animals revealed an unanticipated negative relationship between brain size and body length, we extended our measurements to include intracranial volume in 19 skulls (8 females and 11 males) from the collection at the Museum of Vertebrate Zoology, University of California Berkeley; body weights and lengths were also available. A third dataset was formed by measuring intracranial volumes in 60 spotted hyena skulls (27 females and 33 males) in the Natural History Museum, London, UK; body lengths and intracranial volumes were available. Brain/body size slopes, in general, were not significantly different from zero except in 3 cases: brain weight/body length for Moyale males alone and males and females together, and cranial volume/body weight for Museum of Vertebrate Zoology males and females together. Although most of the slopes were not significantly different from zero, they were all negative, and a statistical test which combined probabilities from the 3 datasets supports the conclusion that there is a negative relationship between brain size and body size in spotted hyenas. Possible explanations for the negative slopes are discussed, including costs and benefits of large brains and large bodies and physiological mechanisms.


Subject(s)
Body Size , Brain/anatomy & histology , Hyaenidae/anatomy & histology , Animals , Female , Male , Organ Size , Sex Characteristics
3.
Anat Rec (Hoboken) ; 299(3): 385-99, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26694958

ABSTRACT

Anatomy of male and female external genitalia of adult mice (Mus musculus) and broad-footed moles (Scapanus latimanus) was re-examined to provide more meaningful anatomical terminology. In the past the perineal appendage of male broad-footed moles has been called the penis, while the female perineal appendage has been given several terms (e.g. clitoris, penile clitoris, peniform clitoris and others). Histological examination demonstrates that perineal appendages of male and female broad-footed moles are the prepuce, which in both sexes are covered externally with a hair-bearing epidermis and lacks erectile bodies. The inner preputial epithelium is non-hair-bearing and defines the preputial space in both sexes. The penis of broad-footed moles lies deep within the preputial space, is an "internal organ" in the resting state and contains the penile urethra, os penis, and erectile bodies. The clitoris of broad-footed moles is defined by a U-shaped clitoral epithelial lamina. Residing within clitoral stroma encompassed by the clitoral epithelial lamina is the corpus cavernosum, blood-filled spaces and the urethra. External genitalia of male and female mice are anatomically similar to that of broad-footed moles with the exception that in female mice the clitoris contains a small os clitoridis and lacks defined erectile bodies, while male mice have an os penis and a prominent distal cartilaginous structure within the male urogenital mating protuberance (MUMP). Clitori of female broad-footed moles lack an os clitoridis but contain defined erectile bodies, while male moles have an os penis similar to the mouse but lack the distal cartilaginous structure.


Subject(s)
Genitalia, Female/anatomy & histology , Genitalia, Male/anatomy & histology , Moles/anatomy & histology , Animals , Female , Male , Mice , Rats
4.
Differentiation ; 87(1-2): 4-22, 2014.
Article in English | MEDLINE | ID: mdl-24582573

ABSTRACT

This review/research paper summarizes data on development of the external genitalia of the spotted hyena, a fascinating mammal noted for extreme masculinization of the female external genitalia. The female spotted hyena is the only extant mammal that mates and gives birth through a pendulous penis-like clitoris. Our studies indicate that early formation of the phallus in both males and females is independent of androgens; indeed the phallus forms before the fetal testes or ovaries are capable of synthesizing androgens. Likewise, pre- and postnatal growth in length of the penis and clitoris is minimally affected by "androgen status". Nonetheless, several internal morphologies, as well as external surface features of the phallus, are androgen-dependent and thus account for dimorphism between the penis and clitoris. Finally, estrogens play a critical role in penile and clitoral development, specifying the position of the urethral orifice, determining elasticity of the urethral meatus, and facilitating epithelial-epithelial fusion events required for proper formation of the distal urethra/urogenital sinus and prepuce. Accordingly, prenatal inhibition of estrogen synthesis via administration of letrozole (an aromatase inhibitor) leads to malformations of the glans as well as the prepuce (hypospadias). The effects of prenatal androgens, anti-androgens and impaired estrogen synthesis correlated with the tissue expression of androgen and estrogen receptors.


Subject(s)
Androgens/metabolism , Estrogens/metabolism , Genitalia, Female/growth & development , Hyaenidae/growth & development , Animals , Clitoris/growth & development , Female , Hyaenidae/genetics , Male , Ovary/growth & development , Penis/growth & development , Testis/growth & development
5.
Endocrinology ; 153(3): 1435-43, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22253421

ABSTRACT

Exposures to sex steroids during fetal development are thought to contribute to the unique urogenital anatomy and social dominance of the female spotted hyena: overt phenotypes not shared by other hyenids (i.e. striped hyena, brown hyena, and aardwolf). Because both androgens and estrogens influence development of genitalia and behavior, and because plasma SHBG regulates their access to tissues, we compared the Shbg gene sequences, structures, and steroid-binding properties in the four extant hyenids. We found the hyenid Shbg genes (>95% identical) and mature protein sequences (98% identical) are highly conserved. As in other mammals, the hyenid SHBG all bind 5α-dihydrotestosterone with high affinity (K(d) = 0.62-1.47 nm), but they also bind estrone and dehydroepiandrosterone with similarly high affinity, and this unusual property was attributed to specific amino acids within their SHBG steroid-binding sites. Phylogenetic comparisons also indicated that the spotted hyena SHBG precursor uniquely lacks two leucine residues and has a L15W substitution within its secretion signal polypeptide, the reduced size and hydrophobicity of which markedly decreases the production of SHBG and may therefore explain why serum SHBG concentrations in male and female spotted hyenas are approximately five times lower than in other hyenids. This is important because low plasma SHBG concentrations in spotted hyenas will increase exposure to biologically active androgens and estrogen as well as to their precursors (dehydroepiandrosterone and estrone), which may contribute to the masculinized external genitalia of female spotted hyenas and to female social dominance over males.


Subject(s)
Sex Hormone-Binding Globulin/metabolism , Animals , Behavior, Animal , CHO Cells , Cloning, Molecular , Cricetinae , Dehydroepiandrosterone/chemistry , Dihydrotestosterone/chemistry , Dose-Response Relationship, Drug , Estrone/chemistry , Female , Humans , Hyaenidae , Kinetics , Male , Models, Biological , Molecular Sequence Data , Phylogeny , Social Behavior , Steroids/metabolism
6.
Gen Comp Endocrinol ; 170(3): 455-9, 2011 Feb 01.
Article in English | MEDLINE | ID: mdl-21036174

ABSTRACT

The androgen receptor blocker flutamide and the 5α-reductase inhibitor finasteride have been used in a variety of species to investigate the ontogeny of sexual dimorphisms by treating pregnant females or neonates at critical periods of sexual differentiation. Likewise, we have used these drugs to study the profound masculinization of the external genitalia in female spotted hyenas. However, a potential pitfall of administering flutamide, either alone or in combination with finasteride, is that it maintains or even raises plasma concentrations of luteinizing hormone (LH) and testosterone (T), because negative feedback of the hypothalamic-pituitary-gonadal axis is disrupted. Contrary to expectations, when pregnant spotted hyenas were treated with flutamide and finasteride (F&F), the concentrations of T during late gestation were suppressed relative to values in untreated dams. Herein, we further investigate the paradoxical effects of F&F treatment on a battery of sex hormones in spotted hyenas. Beyond the effects on T, we found plasma concentrations of LH, estradiol, progesterone and androstenedione (A4) were also significantly lower in F&F-treated pregnant hyenas than in controls. Flutamide and finasteride did not have similar effects on LH, T, and A4 concentrations in male hyenas. The paradoxical effect of F&F treatment on LH and T concentrations in the maternal circulation suggests that negative feedback control of gonadotropin and androgen secretion may be modified in spotted hyenas during pregnancy.


Subject(s)
Androgen Antagonists/pharmacology , Androstenedione/blood , Finasteride/pharmacology , Flutamide/pharmacology , Hyaenidae/physiology , Luteinizing Hormone/blood , Animals , Estradiol/blood , Feedback , Female , Male , Pregnancy , Progesterone/blood , Sex Differentiation/drug effects , Sex Factors , Testosterone/blood
7.
BMC Ecol ; 10: 9, 2010 Mar 30.
Article in English | MEDLINE | ID: mdl-20353550

ABSTRACT

BACKGROUND: Among mammals living in social groups, individuals form communication networks where they signal their identity and social status, facilitating social interaction. In spite of its importance for understanding of mammalian societies, the coding of individual-related information in the vocal signals of non-primate mammals has been relatively neglected. The present study focuses on the spotted hyena Crocuta crocuta, a social carnivore known for its complex female-dominated society. We investigate if and how the well-known hyena's laugh, also known as the giggle call, encodes information about the emitter. RESULTS: By analyzing acoustic structure in both temporal and frequency domains, we show that the hyena's laugh can encode information about age, individual identity and dominant/subordinate status, providing cues to receivers that could enable assessment of the social position of an emitting individual. CONCLUSIONS: The range of messages encoded in the hyena's laugh is likely to play a role during social interactions. This call, together with other vocalizations and other sensory channels, should ensure an array of communication signals that support the complex social system of the spotted hyena. Experimental studies are now needed to decipher precisely the communication network of this species.


Subject(s)
Dominance-Subordination , Hyaenidae/physiology , Sex Characteristics , Vocalization, Animal , Acoustics , Animals , Female , Linear Models , Male , Sound Spectrography
9.
Trends Endocrinol Metab ; 17(9): 349-56, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17010637

ABSTRACT

Female spotted hyenas (Crocuta crocuta) are the only female mammals that lack an external vaginal opening. Mating and birth take place through a urogenital canal that exits at the tip of a hypertrophied clitoris. This 'masculine' phenotype spurred a search for an alternate source of fetal androgens. Although androstenedione from the maternal ovary is readily metabolized to testosterone by the hyena placenta, formation of the penile clitoris and scrotum appear to be largely androgen independent. However, secretions from the fetal testes underlie sex differences in the genitalia and central nervous system that are essential for male reproduction. Naturally circulating androgens, acting prenatally, reduce reproductive success in adult female spotted hyenas. Effects on aggression and dominance might offset these reproductive 'costs' of female androgenization in utero.


Subject(s)
Hyaenidae/embryology , Mammals/embryology , Sex Differentiation/physiology , Androgens/physiology , Animals , Female , Genitalia/physiology , Male , Models, Biological , Urogenital System/anatomy & histology , Virilism/embryology
10.
Horm Behav ; 50(2): 285-92, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16682033

ABSTRACT

In humans and rhesus monkeys, click-evoked otoacoustic emissions (CEOAEs) are stronger in females than in males, and there is considerable circumstantial evidence that this sex difference is attributable to the greater exposure to androgens prenatally in males. Because female spotted hyenas are highly androgenized beginning early in prenatal development, we expected an absence of sexual dimorphism in the CEOAEs of this species. The CEOAEs obtained from 9 male and 7 female spotted hyenas confirmed that expectation. The implication is that the marked androgenization to which female spotted hyenas are exposed masculinizes the cochlear mechanism responsible for CEOAEs. The CEOAEs measured in 3 male and 3 female hyenas that had been treated with anti-androgenic agents during prenatal development were stronger than the CEOAEs of the untreated animals, in accord with the implied inverse relationship between prenatal androgen exposure and the strength of the cochlear mechanisms producing CEOAEs. The CEOAEs of three ovariectomized females and two castrated males were essentially the same as those for the untreated females and males, suggesting that there is little or no activational effect of hormones on CEOAE strength in spotted hyenas. Distortion product OAEs (DPOAEs) also were measured. Those sex differences also were generally small (as they are in humans), and the effects of the anti-androgen agents were inconsistent. Thus, prenatal androgen exposure apparently does affect OAEs, but the effects appear to be greater for the reflection-based cochlear mechanism that underlies CEOAEs than for the nonlinear cochlear mechanism underlying DPOAEs.


Subject(s)
Hyaenidae/physiology , Vocalization, Animal/physiology , Androgen Antagonists/pharmacology , Animals , Cochlea/physiology , Dose-Response Relationship, Drug , Female , Functional Laterality/physiology , Male , Orchiectomy , Ovariectomy , Pregnancy , Prenatal Exposure Delayed Effects , Sex Characteristics
11.
J Urol ; 175(1): 276-83, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16406926

ABSTRACT

PURPOSE: Surgical treatment of the common urogenital sinus phallus has been one of the most challenging areas in pediatric urology. To better understand the neuroanatomy of the common urogenital sinus phallus, we evaluated an animal model naturally having this condition, the spotted hyena, Crocuta crocuta. We compared the neuroanatomy of male and female humans and spotted hyenas using anatomical, immunohistochemical and 3D reconstruction techniques. We also examined the implications of the pattern of clitoral innervation for the unique challenges faced by female spotted hyenas, the only extant species of mammal that mates and gives birth through the clitoris. MATERIALS AND METHODS: Three adult male and 3 female spotted hyenas were studied. With the animals under anesthesia gross anatomical examination was performed before and after artificial erection. Histological analysis was performed on one 95-day fetal male and female spotted hyena specimens, and on 18 human male and female fetal external genitalia specimens using antibodies raised against the neuronal marker S-100. Three-dimensional computer reconstruction using serial sections allowed analysis of the neuroanatomy of the penis, clitoris and common urogenital sinus of the fetal spotted hyena and human. RESULTS: Compared to other mammals, the clitoris and penis of spotted hyenas were remarkably similar in size and configuration in the flaccid and erect states. Male and female hyenas had a single opening on the tip of the glans penis/clitoris. The basic anatomical structures of the corporeal bodies in both sexes of humans and spotted hyenas were similar. As in humans, the dorsal nerve distribution was unique in being devoid of nerves at the 12 o'clock position in the penis and clitoris of the spotted hyena. Dorsal nerves of the penis/clitoris in humans and male spotted hyenas tracked along both sides of the corporeal body to the corpus spongiosum at the 5 and 7 o'clock positions. The dorsal nerves penetrated the corporeal body and distally the glans in the hyena. In female hyenas the dorsal nerves fanned out laterally on the clitoral body. Glans morphology was different in appearance in both sexes, being wide and blunt in the female and tapered in the male. CONCLUSIONS: The neuroanatomy of the male and female external genitalia in the spotted hyena, Crocuta crocuta, although grossly similar, has distinct anatomical and functional characteristics. The clitoris of the spotted hyena is a classic example of a natural animal model of a common urogenital sinus. The neuroanatomical characteristics of the spotted hyena may be a useful model to simulate the anatomy of common urogenital sinus anomaly in humans.


Subject(s)
Clitoris/anatomy & histology , Hyaenidae/anatomy & histology , Penis/anatomy & histology , Animals , Clitoris/innervation , Female , Humans , Male , Penis/innervation , Urogenital Surgical Procedures/methods
12.
Horm Behav ; 48(4): 403-17, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16197946

ABSTRACT

The present review explores sexual differentiation in three non-conventional species: the spotted hyena, the elephant and the tammar wallaby, selected because of the natural challenges they present for contemporary understanding of sexual differentiation. According to the prevailing view of mammalian sexual differentiation, originally proposed by Alfred Jost, secretion of androgen and anti-Mullerian hormone (AMH) by the fetal testes during critical stages of development accounts for the full range of sexually dimorphic urogenital traits observed at birth. Jost's concept was subsequently expanded to encompass sexual differentiation of the brain and behavior. Although the central focus of this review involves urogenital development, we assume that the novel mechanisms described in this article have potentially significant implications for sexual differentiation of brain and behavior, a transposition with precedent in the history of this field. Contrary to the "specific" requirements of Jost's formulation, female spotted hyenas and elephants initially develop male-type external genitalia prior to gonadal differentiation. In addition, the administration of anti-androgens to pregnant female spotted hyenas does not prevent the formation of a scrotum, pseudoscrotum, penis or penile clitoris in the offspring of treated females, although it is not yet clear whether the creation of masculine genitalia involves other steroids or whether there is a genetic mechanism bypassing a hormonal mediator. Wallabies, where sexual differentiation occurs in the pouch after birth, provide the most conclusive evidence for direct genetic control of sexual dimorphism, with the scrotum developing only in males and the pouch and mammary glands only in females, before differentiation of the gonads. The development of the pouch and mammary gland in females and the scrotum in males is controlled by genes on the X chromosome. In keeping with the "expanded" version of Jost's formulation, secretion of androgens by the fetal testes provides the best current account of a broad array of sex differences in reproductive morphology and endocrinology of the spotted hyena, and androgens are essential for development of the prostate and penis of the wallaby. But the essential circulating androgen in the male wallaby is 5alpha androstanediol, locally converted in target tissues to DHT, while in the pregnant female hyena, androstenedione, secreted by the maternal ovary, is converted by the placenta to testosterone (and estradiol) and transferred to the developing fetus. Testicular testosterone certainly seems to be responsible for the behavioral phenomenon of musth in male elephants. Both spotted hyenas and elephants display matrilineal social organization, and, in both species, female genital morphology requires feminine cooperation for successful copulation. We conclude that not all aspects of sexual differentiation have been delegated to testicular hormones in these mammals. In addition, we suggest that research on urogenital development in these non-traditional species directs attention to processes that may well be operating during the sexual differentiation of morphology and behavior in more common laboratory mammals, albeit in less dramatic fashion.


Subject(s)
Androgens/physiology , Elephants/physiology , Hyaenidae/physiology , Macropodidae/physiology , Sex Differentiation/physiology , Urogenital System/physiology , Animals , Elephants/anatomy & histology , Elephants/embryology , Female , Gene Expression Regulation, Developmental/physiology , Genomic Imprinting/physiology , Hyaenidae/anatomy & histology , Hyaenidae/embryology , Macropodidae/anatomy & histology , Macropodidae/embryology , Male , Neurosecretory Systems/physiology , Organogenesis/physiology , Sex Characteristics , Urogenital System/anatomy & histology , Urogenital System/embryology , Urogenital System/growth & development
13.
Biol Reprod ; 73(3): 554-64, 2005 Sep.
Article in English | MEDLINE | ID: mdl-15917348

ABSTRACT

Studies were conducted to elucidate the importance of androgen-mediated induction of the extreme masculinization of the external genitalia in female spotted hyenas. Phallic size and shape; androgen receptor (AR) and alpha-actin expression; and sex-specific differences in phallic retractor musculature, erectile tissue, tunica albuginea, and urethra/urogenital sinus were examined in male and female fetuses from Day 30 of gestation to term. Similar outcomes were assessed in fetuses from dams treated with an AR blocker and a 5alpha-reductase inhibitor (antiandrogen treatment). Clitoral and penile development were already advanced at Day 30 of gestation and grossly indistinguishable between male and female fetuses throughout pregnancy. Sex-specific differences in internal phallic organization were evident at Gestational Day 45, coincident with AR expression and testicular differentiation. Antiandrogen treatment inhibited prostatic development in males and effectively feminized internal penile anatomy. We conclude that gross masculinization of phallic size and shape of male and female fetuses is androgen-independent, but that sexual dimorphism of internal phallic structure is dependent on fetal testicular androgens acting via AR in the relevant cells/tissues. Androgens secreted by the maternal ovaries and metabolized by the placenta do not appear to be involved in gross masculinization or in most of the sex differences in internal phallic structure.


Subject(s)
Genitalia, Female/embryology , Genitalia, Male/embryology , Hyaenidae/embryology , Urinary Tract/embryology , Androgen Antagonists/pharmacology , Animals , Enzyme Inhibitors/pharmacology , Female , Fetus/drug effects , Finasteride/pharmacology , Flutamide/pharmacology , Genitalia, Female/drug effects , Genitalia, Male/drug effects , Male , Urinary Tract/drug effects
14.
Dev Psychobiol ; 44(3): 199-207, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15054888

ABSTRACT

Spotted hyena biology suggests mothers and infants will exhibit one of two alternative responses to separation: (a) Due to prolonged dependency, infants will act similarly to Old World monkeys, displaying distress and proximity seeking behaviors; or (b) because mother-infant separations are frequent in the wild, infants will exhibit little distress or change in reunion behavior. Hence, reunion behavior following mother-infant separation was compared to control periods in captive hyena (Crocuta crocuta) mothers and infants at two developmental periods. Significant increases (p < or =.05) in distress (i.e., agitated arousal and increased vocalization) and proximity maintenance (i.e., cub and maternal approaches, and maternal monitoring) as well as a trend towards increased sibling aggression following separation were observed. Responsibility for proximity maintenance, assessed by the Hinde Index, adhered to patterns common to primates---with cubs assuming increased responsibility later in development. Findings are discussed in light of hyena ecology and Attachment Theory.


Subject(s)
Cues , Object Attachment , Animals , Arousal , Behavior, Animal , Carnivora , Female , Male , Maternal Behavior , Videotape Recording , Vocalization, Animal
15.
Adv Exp Med Biol ; 545: 243-53, 2004.
Article in English | MEDLINE | ID: mdl-15086031

ABSTRACT

Although varying degrees of genital masculinization are a reasonably common phenomenon in the world of female mammals, the majority of such variation has not been investigated. In this chapter we have described research on the "masculinized" genitalia of moles and hyenas. Such research raises intriguing possibilities regarding the coordinated role that androgens, estrogens and peptide hormones (e.g., relaxin) might play, at different stages of sexual differentiation and development, in preparing genital tissues for their functional roles in reproduction. Such studies also suggest that non-androgenic mechanisms need to be considered. Arnold (1996) and Carruth et al. (2002) have recently presented the argument for broadening our view of sexual differentiation of brain and behavior, emphasizing direct genetic effects. A similar view has been presented for the Tammar wallaby, where formation of a scrotum, or a pouch, is a direct consequence of the presence/absence of two X chromosomes (Pask and Renfree, 2001). Although our research on moles and hyenas has not yet yielded such definitive results, the research reviewed in this chapter calls attention to processes that could well operate in other mammals, including humans.


Subject(s)
Mammals/physiology , Sex Characteristics , Sex Differentiation/physiology , Animals , Behavior, Animal , Carnivora/physiology , Female , Male , Moles/physiology
16.
Gen Comp Endocrinol ; 135(1): 51-61, 2004 Jan 01.
Article in English | MEDLINE | ID: mdl-14644644

ABSTRACT

Spotted hyenas (Crocuta crocuta) exhibit an array of behavioral and morphological characteristics that set them apart from other mammals: females are heavier and more aggressive than males, and females have external genitalia that closely resemble those of the male. Because androgenic hormones might mediate the expression of these traits, androgens are of great interest in this species. Past work on circulating androgens in wild hyenas has been limited, in part because of small sample sizes. In this study we validated a non-invasive method of monitoring variation in androgens by measuring total androgen metabolites in the feces of wild and captive spotted hyenas with an enzyme immunoassay. HPLC analysis revealed multiple immunoreactive androgen metabolites in fecal extracts from both males and females. LHRH challenge in three male and two female hyenas in captivity caused an increase in fecal androgens one to three days after LHRH injection. Furthermore, presence of bone in the diet did not affect fecal androgen concentrations in captive female hyenas. In wild spotted hyenas, time of day of fecal deposition, time elapsed between deposition and freezing of the sample, and time elapsed between freezing and extraction did not systematically affect fecal androgen concentrations. Finally, in wild hyenas, fecal androgen patterns mirrored plasma testosterone patterns in that adult immigrant males had higher concentrations than adult natal males, and pregnant females had higher concentrations than lactating females. These methods can therefore be used in future studies addressing relationships among fecal androgens, social status, reproductive state, and behavior in spotted hyenas.


Subject(s)
Androgens/analysis , Feces/chemistry , Gonadotropin-Releasing Hormone/pharmacology , Androgens/blood , Animals , Bone and Bones/chemistry , Carnivora , Diet , Female , Male , Pregnancy
17.
J Morphol ; 256(2): 205-18, 2003 May.
Article in English | MEDLINE | ID: mdl-12635111

ABSTRACT

The unique urogenital anatomy and histology of female spotted hyenas (Crocuta crocuta Erxleben) was reexamined to identify adaptations of "structure" that enable/facilitate urination, mating, and parturition through the clitoris. Unusual features of penile anatomy required for meeting ceremonies and successful mating through a clitoral point of insertion were also examined. As reported previously, the upper urogenital tract of the female spotted hyena is typical of other carnivores and consists of the oviducts, uterine horns, uterine body, and vagina. An anatomically defined cervix is absent, even though a histologically defined transition zone between the uterine body and vagina was demonstrated. Adaptive features of the upper genital tract were a helical-shaped uterine cavity, extensive smooth muscle in the uterus and vagina, and a newly discovered submucosal mucous urogenital gland (SMUG) located immediately caudal to the vagina. The extensive smooth muscle facilitates the expulsion of the large pups at parturition through the recurved birth canal. Secretions of the SMUG provide lubrication and protection for the urogenital mucosa during mating and parturition. Two types of "erections" are suggested by behavioral observations: the common hemodynamic erection required for insertion and thrusting by the male, and phallic "flipping" that commonly occurs earlier in the mating sequence and is sometimes seen during meeting ceremonies. Phallic "flipping" appears to be accomplished by the coordinated contractions of the large ischiocavernosus and retractor muscles acting on the semirigid organ. The extremely thick tunica albuginea and interstitial collagen of the common corporal body of the penis and clitoris gives the flaccid phallus some degree of rigidity even in the resting state in males and nulliparous females. Phallic "flipping" implies a hinge region in which flexibility is the key feature. Such a proximal hinge region of the male and female phallus was defined and was notable for its diminished collagen content. The urogenital sinus traversing the clitoris was specialized for distensibility, thus facilitating receipt of the penis during mating and for passage of the infant to the tip of the glans clitoris, where it emerges at parturition. The morphology of the glans penis is notable for the tapered common corporal body that extends to the distal tip of the glans. This adaptation is suggested to be required for a clitoral (as opposed to a vaginal) point of insertion during mating. Finally, additional segments of erectile tissue devoid of a thick collagenous capsule were demonstrated in the glans penis and glans clitoris, which appear to account for the "partially-locking" of the male into the female during the late stages of a mating sequence. Taken together, it is evident that the unusual sexual behaviors of the male and female spotted hyenas are facilitated by unique structural modifications of the relevant organs.


Subject(s)
Carnivora/anatomy & histology , Sex Characteristics , Urogenital System/anatomy & histology , Animals , Female , Histocytological Preparation Techniques , Male , Urogenital System/physiology
18.
Biol Reprod ; 67(5): 1405-13, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12390869

ABSTRACT

Prenatal androgen treatment can alter LH secretion in female offspring, often with adverse effects on ovulatory function. However, female spotted hyenas (Crocuta crocuta), renowned for their highly masculinized genitalia, are naturally exposed to high androgen levels in utero. To determine whether LH secretion in spotted hyenas is affected by prenatal androgens, we treated pregnant hyenas with antiandrogens (flutamide and finasteride). Later, adult offspring of the antiandrogen-treated (AA) mothers underwent a GnRH challenge to identify sex differences in the LH response and to assess the effects of prenatal antiandrogen treatment. We further considered the effects of blocking prenatal androgens on plasma sex steroid concentrations. To account for potential differences in the reproductive state of females, we suppressed endogenous hormone levels with a long-acting GnRH agonist (GnRHa) and then measured plasma androgens after an hCG challenge. Plasma concentrations of LH were sexually dimorphic in spotted hyenas, with females displaying higher levels than males. Prenatal antiandrogen treatment also significantly altered the LH response to GnRH. Plasma estradiol concentration was higher in AA-females, whereas testosterone and androstenedione levels tended to be lower. This trend toward lower androgen levels disappeared after GnRHa suppression and hCG challenge. In males, prenatal antiandrogen treatment had long-lasting effects on circulating androgens: AA-males had lower T levels than control males. The sex differences and effects of prenatal antiandrogens on LH secretion suggest that the anterior pituitary gland of the female spotted hyena is partially masculinized by the high androgen levels that normally occur during development, without adverse effects on ovulatory function.


Subject(s)
Androgen Antagonists/pharmacology , Carnivora , Luteinizing Hormone/metabolism , Steroids/blood , Age Factors , Androgens/metabolism , Animals , Chorionic Gonadotropin/pharmacology , Female , Finasteride/pharmacology , Flutamide/pharmacology , Genitalia, Female/drug effects , Genitalia, Female/growth & development , Genitalia, Male/drug effects , Genitalia, Male/growth & development , Gonadotropin-Releasing Hormone/agonists , Gonadotropin-Releasing Hormone/pharmacology , Male , Pregnancy , Prenatal Exposure Delayed Effects , Sex Differentiation/drug effects , Sex Factors , Sexual Maturation/drug effects
19.
J Comp Psychol ; 116(4): 331-41, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12539928

ABSTRACT

Olfaction is crucial to spotted hyenas (Crocuta crocuta), yet there are no controlled studies of their reactions to odors. In Experiment 1, the authors examined responses of captive hyenas to various environmental (prey, nonprey animal, and plant) odors. Subjects approached and sniffed all odors equally but preferentially licked prey odors, scent marked next to odors, and rolled in animal-based odors. In Experiment 2, the authors examined the function of rolling by applying odors to the pelts of captive hyenas. When hyenas wore carrion, they gained positive social attention (increased investigation and allogrooming) from pen mates, but when they wore camphor, the normal social greeting ceremony was curtailed. Thus, olfactory stimuli elicit specific responses, influence where behavior is directed, and can be used to affect social interaction.


Subject(s)
Behavior, Animal/physiology , Environment , Odorants , Smell/physiology , Animals , Arousal/physiology , Carnivora , Choice Behavior/physiology , Discrimination Learning , Female , Male , Random Allocation , Social Behavior
20.
J Comp Psychol ; 116(4): 342-9, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12539929

ABSTRACT

Scent marking in spotted hyenas (Crocuta crocuta) includes the deposition of anal sac secretions, or "paste," and presumably advertises territorial ownership. To test whether captive hyenas classify and discriminate individuals using odor cues in paste, the authors conducted behavioral discrimination bioassays and recorded hyena investigation of paste extracted from various conspecific donors. In Experiment 1, subjects directed most investigative behavior toward scents from unfamiliar hyenas and members of the opposite sex. In Experiment 2, male hyenas discriminated between concurrent presentations of paste from various unfamiliar females in similar reproductive states. Thus, pasted scent marks convey information about the sex, familiarity, and even identity of conspecifics. Aside from territory maintenance, scent marking may also communicate information about individual sexual status.


Subject(s)
Behavior, Animal/physiology , Discrimination Learning , Odorants , Smell/physiology , Animals , Carnivora , Cues , Estrogens/blood , Female , Male , Progesterone/blood
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