Rodrigo A. Carrasco
Marcelo H. Ratto
Gregg P. Adams1*- 1Department of Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK, Canada
- 2Department of Animal Science, Universidad Austral de Chile, Valdivia, Chile
Introduction
Based on the mechanism of ovulation, mammals may be classified as spontaneous (i.e., pig, cattle, sheep, goats) or induced ovulators (i.e., rabbit, ferret, cat, koala, llama, camel, alpaca). High or increasing concentrations of estradiol exert a positive feedback on the hypothalamus triggering an LH surge and ovulation in spontaneous ovulators, while ovulation is triggered by mating in induced ovulators. South American camelids are classified as induced ovulators but the ovulatory response is triggered by semen (1); copulation itself plays a minor role (2). Originally dubbed ovulation-inducingi factor, the factor responsible for eliciting ovulation in camelids is the protein nerve growth factor [NGF; (3–5)]. A highly conserved molecule, NGF is concentrated in camelid semen (and semen of many species), and systemic absorption from intrauterine seminal deposition has been implicated as the inciting cause of the preovulatory surge in circulating concentrations of LH after mating or parenteral administration of nerve growth factor (1, 6). Although the mechanistic pathway of NGF-induced ovulation is unknown, it is thought to be mediated at the hypothalamus instead of the pituitary gland (7). Nerve growth factor may act by binding to neurons that possess one or both NGF receptors (TrkA and P75) in the hypothalamus of llamas or by interacting with third-ventricular tanycytes, a group of cells derived from modified ependyma that possess the P75 receptor (8). A recent study using nasal placodes from mouse embryo (a source of GnRH neurons) showed that the activation of P75 signaling pathways triggered an increase in depolarization events in GnRH neurons (9), suggesting that NGF in semen may be acting at the median eminence to trigger ovulation during mating.
In a recent report (10), the effects of estradiol-17β administration on ovulation and luteal development in llamas were examined. Administration of increasing concentrations of estradiol-17β (0.6, 1, and 1.6 mg/llama) increased the ovulatory rate in an incremental manner (0/4, 1/4, and 6/6, respectively). Although LH concentrations were not reported, the ovulatory response, corpus luteum development, and plasma progesterone profile were consistent with the idea that estradiol triggers ovulation in this species. In an earlier study (11), results showed that ovariectomized llamas had an impaired response to NGF-induced LH surge, which was partially recovered by pre-treatment with estradiol. Thus, it was suggested that estradiol promotes the fullness of the pre-ovulatory LH surge induced by NGF. The report from Bianchi et al. (10), however, is the first to directly test the effects of estradiol on ovulation in llamas.
Discussion
The results of Bianchi et al. (10) are consistent with previous studies in other induced ovulators. In rabbits, administration of a combination of estrogen and progesterone daily for 2 days, but not estrogen or progesterone independently, led to ovulation in 40% of synchronized does (12). In California voles, administration of estradiol-17β or estradiol benzoate caused ovulation in up to 28% of treated females (13). In these studies, however, assessment of the ovulatory response was based on single examinations (laparotomy or post-mortem), while Bianchi et al. (10) used a non-invasive approach (ultrasonography and blood sampling) that allowed clear characterization of corpus luteum form and function. Despite the limited information available in scientific literature, results point out the possibility that camelids, and other induced ovulators, may elicit an LH surge in response to both estradiol and NGF. How NGF and estradiol induce ovulation in camelids remains unknown, but we hypothesize that the routes involved are different between the molecules based on differences in chemical composition (steroid vs. polypeptide), cellular mechanism of action (nuclear vs. transmembrane receptors), and receptor distribution (Figure 1).
Figure 1. Proposed mechanistic pathways followed by estradiol and NGF in the hypothalamus of llamas to trigger ovulation. Estradiol, through neuronal populations (i.e., kisspeptin; kiss) expressing its nuclear receptor (black), may be influencing GnRH neurons (green) to trigger an LH surge. In contrast, the effects of NGF on GnRH neurons may be triggered by activation of NGF receptors (TrkA and P75) in hypothalamic neurons that act as afferents to GnRH neurons. Alternatively, blood borne NGF may be activating P75 receptor in tanycytes (yellow), which are in close association to GnRH nerve terminals at the portal vessels in the median eminence (ME). CHO, choroid plexus.
The results from Bianchi et al. (10) are exciting since estradiol may be stimulating neuronal pathways to trigger a GnRH and LH surge in camelids in addition to providing support for the effects of NGF (11). Based on rabbit studies (14), the principal factor driving hypothalamic discharge of GnRH into the portal vessels in induced ovulators is the conduction of physical coital stimuli via spinal cord transmission of action potentials. That llamas ovulate in response to estradiol and seminal NGF is consistent with the notion that spontaneous and induced ovulation share complimentary mechanistic pathways for generating an LH surge. The notion of complimentary pathways is reflected in observations that the presence of males facilitates the ovulatory response in spontaneous ovulators. For instance, albino rats maintained in a constant light environment were sexually receptive and females responded to mating with an LH surge and ovulation (15). In addition, introduction of rams to ewes stimulates cyclicity and ovulation during the transition from the breeding to non-breeding seasons (16), and clitoral stimulation hastened ovulation in cattle (17). Thus, neuronal systems relevant to spontaneous ovulators may play a role in induced ovulators and vice-versa. Hypothalamic kisspeptin neurons are mediators of the estradiol-induced LH surge in ewes and other spontaneous ovulators (18), and recent studies showed that kisspeptin neurons also participate in surge-release of LH in llamas (19). In llamas, however, the absence of NGF receptor expression in kisspeptin neurons suggests that kisspeptin neurons may not be the direct target of NGF in the hypothalamus (19).
In addition to an influence on gonadotrophin secretion in induced ovulators (1, 20), both estradiol and NGF may modify luteal function. For instance, llamas that ovulated in response to NGF developed a larger corpus luteum and produced more progesterone than llamas treated with GnRH (1), and administration of NGF was associated with an increase in vascularization in the dominant follicle and the consequent corpus luteum (21). In rabbits, estradiol had a luteotrophic effect by preventing apoptosis in luteal cells (22), and, conversely, one of the luteolytic mechanisms of prostaglandin F2alpha may involve blockade of estradiol signaling in luteal cells (23). Although a luteotrophic effect of estradiol was reported in a study in which llamas were treated with high doses of estradiol [10 mg daily for 9 days; (24)], the effect of estradiol on ovarian function in llamas and its relationship with NGF remains to be investigated.
Finally, the findings by Bianchi et al. (10) may provide an explanation for spontaneous ovulation in camelids, a phenomenon that has been reported to occur at a rate of 5–15% in llamas and alpacas (25–27), and 5 and 41.7% in non-lactating and lactating camels, respectively (28). Although circulating concentrations of estradiol were not reported in Bianchi's work and the dose administered of estradiol was relatively high, we infer that a sudden increase in estradiol concentration triggers an LH surge in llamas, as in spontaneous ovulators. Thus, we hypothesize that in camelids the endogenous production of ovarian estradiol does not reach the threshold necessary to trigger an “spontaneous” ovulatory response, and instead, the female camelid relies on seminal NGF to ovulate. Further knowledge is needed regarding the source of estradiol (i.e., gonadal, adrenal, or neural), the effective circulating concentrations of estradiol (or its metabolites) to promote ovulation, and the feedback mechanisms of estradiol on LH secretion in camelids. The findings from Bianchi et al. (10) open a variety of questions regarding the ovulatory process in camelids, and the potential interactions between estradiol and NGF. The llama (and other camelids) is an excellent model to study the differential effects of estradiol (negative and positive feedback) and NGF in the generation of an LH surge.
Classification of species as spontaneous or induced ovulators may be overly strict since the latter can occasionally ovulate spontaneously and ovulation in the former can occasionally be induced or accelerated by coitus. According to Conaway (29), species may be classified as (1) spontaneous ovulators in which ovulation depends on ovarian steroid production with spontaneous occurrence of a luteal phase (pig, cow), (2) spontaneous ovulators in which ovulation depends on ovarian steroid production but a luteal phase is induced by coitus (rat, mouse), or (3) induced ovulators in which coitus induces ovulation with spontaneous occurrence of a luteal phase (rabbit, camels). It is probable that, within species, the mechanism of ovulation is modulated by environmental or social factors and species represent a continuum between the extremes of strictly induced or spontaneous ovulators (30). Silva and Bianchi's work brings that to light. Perhaps the NGF pathway of induced ovulation is an evolutionary strategy for reproductive success that phylogenetically departed from spontaneous ovulation.
Author Contributions
All participated in the conceptualization and writing of this manuscript.
Funding
This research was supported by the Natural Sciences and Engineering Research Council of Canada.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: llama (Lama glama), estradiol, nerve growth factor, ovulation, LH
Citation: Carrasco RA, Ratto MH and Adams GP (2021) Differential Effects of Estradiol on Reproductive Function in Camelids. Front. Vet. Sci. 8:646700. doi: 10.3389/fvets.2021.646700
Received: 27 December 2020; Accepted: 28 January 2021;
Published: 18 February 2021.
Edited by:
Rosa Maria Garcia-Garcia, Complutense University of Madrid, SpainReviewed by:
Margherita Maranesi, University of Perugia, ItalyKhalid El Allali, Agronomic and Veterinary Institute Hassan II, Morocco
Copyright © 2021 Carrasco, Ratto and Adams. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Gregg P. Adams, gpa623@mail.usask.ca