Gonadotrophic, prolactin, corticosterone, and gonadal hormones levels over 15 months in Giant Amazon River Turtles - Podocnemis expansa (Schweigger, 1812) (Testudines: Podocnemididae), in captive conditions

Gonadotrofinas, prolactina, corticosterona, e as hormonas sexuais durante 15 meses de Tartarugas da Amazônia - Podocnemis expansa (Schweigger, 1812) (Testudines: Podocnemididae), em condições de cativeiro

Abstract

In order to achieve successful captive breeding the Podocnemis expansa, it is necessary to study their reproductive endocrinology. The purpose of this research was to evaluate and characterize plasma concentrations in gonadotrophic, gonadic, corticosterone and prolactin hormones from Giant Amazon Turtles under captive conditions. Blood samples were collected over a 15 month period. The samples were assayed by the use of radioimmunoassay, prolactin, corticosterone, LH, FSH, testosterone, 17β-estradiol and progesterone. We verified significant seasonal pattern increase in 17β-estradiol levels and decrease in progesterone levels in the course of a year, which indicates vitellogenesis. This is related to normal ovarian cycles and possibly to the functional integrity of the hypothalamus-pituitary-gonad axis of captive females. There were negative correlations between testosterone and corticosterone in the male samples, suggestive of stress (management stress) on the reproductive system. The plasma concentrations of gonadotrophic, gonadic, prolactin and corticosterone hormones may be used as a reference for further research and possible therapeutic approaches. The data collected during this research are unprecedented for this species and may serve as a reference for future research regarding the reproductive cycle of this turtle, also allowing reproductive management while in captivity. Information about these hormones must be gathered from wild populations during different periods of the year for better clarification of the reproductive physiology of this species.

Keywords:  Podocnemis expansa; LH; FSH; progesterone; testosterone; 17β-estradiol; corticosterone; prolactin; seasonality; reproduction

Resumo

Com o objetivo de obter reprodução em cativeiro de Podocnemis expansa, é necessário reunir o conhecimento a respeito de sua endocrinologia reprodutiva. O objetivo deste trabalho foi avaliar e caracterizar as concentrações plasmáticas de hormônios gonadotróficos, gonadais, corticosterona e prolactina em Tartarugas da Amazônia em condições de cativeiro. Amostras de sangue foram coletadas durante 15 meses. As amostras foram ensaiadas pelo uso de um radioimunoensáio, prolactina, corticosterona, LH, FSH, testosterona, 17β-estradiol e progesterona. Verificou-se aumento de padrão sazonal significativo nos níveis de 17β-estradiol e diminuição dos níveis de progesterona ao longo do ano, o que indica o recrutamento folicular. Isto está relacionado com ciclos ovarianos normais e possivelmente para a integridade funcional do eixo hipotálamo-hipófise-gônadas de fêmeas em cativeiro. Houve correlação negativa entre testosterona e corticosterona nas amostras do sexo masculino, sugestivos de efeito do estresse de manejo sobre o sistema reprodutivo. As concentrações plasmáticas de hormônios gonadotrofinas, gonadais, prolactina e hormônios corticosterona pode ser usado como referência para futuras pesquisas e possíveis abordagens terapêuticas. Os dados médios coletados durante a pesquisa são inéditos para a espécie e pode servir como referência para futuras pesquisas sobre o sistema reprodutivo da tartaruga, também permitindo manejo reprodutivo em cativeiro. Informações sobre esses hormônios devem ser recolhidas a partir de natureza selvagem em diferentes períodos do ano para melhor esclarecimento da fisiologia da reprodução desta espécie.

Palavras-chave:  Podocnemis expansa; LH; FSH; progesterona; testosterona; 17β-estradiol; corticosterona; prolactina; sazonalidade; reprodução

1. Introduction

The Giant Amazon River Turtle (Podocnemis expansa, Schweigger, 1812b) South America’s largest freshwater turtle, has considerable data published concerning clutch size, hatching and nesting behavior and ecology (Vanzolini, 2003; Ferreira Junior and Castro, 2010). Recently, there has been a great interest in the commercialization of Podocnemis expansa, to alleviate the over collection of wild caught turtles. For this purpose, the research on size at sexual maturity is important once it is considered a potential tool through the study of chronology by carcass morphology; besides, it could answer questions regarding longevity, sexual maturity and population age structure (Chinsamy and Valenzuela, 2008).

Research characterizing the gonadic and hormonal variation levels related to reproduction, throughout one or more cycles, would help in the study of the reproductive process and could give feedback on the optimization of captive breeding. The pattern observed could be altered in favor of the captive environment (management stress). It is as necessary to clarify aspects of the reproductive life in nature and captivity, generating results that favor the reproductive management of the species in controlled environments as well as in nature.

The most studied reproductive pattern of the Giant Amazon River turtle is the process of nesting (Alho and Padua, 1982; Gomes and Ferreira Junior, 2011; Alves-Junior et al., 2012).

No research on plasma concentration of different gonadotrophic and reproductive hormones have been reported for Giant Amazon River turtles. In this study, we aimed to better understand the reproductive cycle of Giant Amazon River turtles in captivity and observe the integrity of the hypothalamic--pituitary--gonadal axis. To do so, we measured and monitored hormones in both sexes (LH, FSH, 17β-estradiol, progesterone, testosterone and corticosterone), during a 15-month period. Knowing the reproductive physiology and endocrinology is necessary to manage reproduction of Podocnemis expansa in captivity.

2. Material and Methods

This research consisted of a retrospective formal review by the IACUC-UFG (nº 041/13), and was conducted in the Experimental Pisciculture Sector of Universidade Federal of Goiás, Goiania City, Goiás State, located at 16° 40’ 22” latitude south and 49° 15’ 29” longitude west, presenting an average height of 730m. The region’s climate is of the B2WB’4a’ type. In this location, mean temperature reach 21.9 °C (maximum 29.4 °C minimum 15.2 °C), relative humidity 71.5%, annual precipitation 1487.2 mm and total insulation 2645.7h. A total of 45 turtles (22 males and 23 females) were transferred from the Brazilian Institute of Environment and Renewable Natural Resources (IBAMA) base, located in Neropolis. The procedures and management of animals were reviewed and approved by IBAMA.

The animals were kept in reservoirs of 30, 10 and 1.5 meters of length, width and height, respectively. The reservoirs were enclosed with a 16mm steel fence, 1.30 meters tall and 1 meter away from the river margin. A 10 m³, 5 meters wide, sandbank was built to be used by the animals to sunbathe. The animals were fed with commercial rations for fish¹ (9mm) twice a day during the hottest periods of the day, with guaranteed humidity (max) 8%, crude protein (min) 28%, ether extract (min) 5%, fibrous matter (max) 7%, mineral matter (max) 10%, calcium (max) 1.2%, and phosphorous (min) 0.6%. The quantity was regulated by animal consumption, and it was reduced during cloudy days.

The turtles used in this experiment had the carapace size as measured by Bataus (1998). These strands refer to wild animals that present a reproductive behavior of aggregation considered able to reproduce. We determined two carapace length groups of females (Group 1 – 51.51 ± 6.37 cm; N=16; and Group 2 – 63.26 ± 4.66 cm; N=7, and three groups of males (Group 1 – 40.27 ± 1.13 cm; N=7; Group 2 – 44.96 ± 1.72 cm; N=6; Group 3 – 53.33 ± 9.23 cm; N=9. During the experimental period the water levels of the reservoirs were kept at the maximum. The water quantity was reduced only during blood collection, in order to note the production and secretion patterns without interference of water decline.

Blood samples were collected by veterinarians in the following periods during 15 months: July, August, September, October, November and February, March, May, June, July and September sequentially. The blood was collected from the occipital sinus or the vertebral sinus and the tail, through vein puncture with the use of 5mL syringes with 14G needles. The blood was centrifuged, packed in 2mL Eppendorf tubes and stored in a freezer at 20 °C until defrosting.

Hormonal analysis was carried out through radioimmunoassay (RIA) (Yalow and Berson, 1960). All of the samples from each experiment were assayed using the same RIA to avoid inter-assay variation. Plasma concentrations of luteinizing hormone (LH), follicle-stimulating hormone (FSH), prolactin (PRL) and corticosterone (CT) were measured for both sexes; 17-β estradiol (E₂) and progesterone (P₄) for females; testosterone (T) for males. The validation for each assay was determined using unknow samples in different volumes to evaluate the paralelism with standard curves and the intra-assay coefficients of variation were calculated (Grotjan and Keel, 1996). Plasma concentrations of LH, FSH and PRL were determined by double-antibody RIA using peptide for iodination (rLH-I₉, rFSH-I₇ and rPRL-I₆), standard reference (rLH-RP₃, rFSH-RP₂ and rPRL-RP₃), and specific antibodies (rLH-S₁₀, rFSH-S₁₁ and rPRL-S₉) provided by the National Hormone and Peptide Program (NIDDK, Baltimore,MD-USA / Harbor-UCLA Medical Center, CA-USA). Dr. Franci's Laboratory produced the iodinated hormones by chloramine-T method (Hunter and Greenwood, 1962) and the secondary antibody in sheep. The intra-assay coefficients of variation for LH, FSH and PRL were 3%, 3% and 5.8%, respectively. The lower limits of detection were 0.05 ng/ml for LH, 0.2 ng/ml for FSH and 0.09 ng/ml for PRL. Plasma CT measure required previous extraction in ethanol. The RIA used specific antibody and standard from Sigma (St. Louis, MO-USA) and H₃-corticosterone from NEN Life Sciences Products (Boston, M- USA). The lower limit of detection and the intra-assay coefficient for CT were 1.0 ng/ml and 2.5%, respectively. Plasma concentrations of 17-β estradiol, progesterone and testosterone were determined by double antibody radioimmunoassay using specific kits provided by Maia (BioChem ImmunoSystems, Itália S.P.A). The intra-assay coefficients of variation for 17-β estradiol, progesterone and testosterone were 2.5%, 3.2% and 5.4%, respectively. The lower limits of detection were 1.2 pg/ml for 17-β estradiol, 0.3ng/ml for progesterone, and 0.3 ng/ml for testosterone. The data were analyzed by SAS Institute (1997). Descriptive analyses were presented to the hormone levels (means, deviation standards and range). The hormonal levels data were transformed to logarithm scale in order to analyze it by the Fisher correlations, variance analyses utilizing Duncan test, and relationship between months and plasma levels of 17-β estradiol, progesterone in females.

3. Results and Discussion

The carapace size groups did not show hormone level differences, therefore we compare sex groups.

Table 1 presents the plasma levels of 17β-estradiol, evaluated during 15 months. We observed an increase in 17β-estradiol concentrations during the period between July and May, which is the rainy season. We verified a decrease in the plasma levels of the 17β-estradiol of the following year and a subsequent increase in September. This pattern is likely to represent a seasonal behavior, even though these animals were in captivity. As for progesterone plasma levels (Table 1), we observed a seasonal pattern, increased during the months of the dry season (July to October), whereas it decreased during the rainy season (November to May). The period between August and September is the nesting season in the Araguaia River region.

Table 1
Means of plasma levels of the gonadotrophic, gonadal, prolactin and corticosterone hormones from collections made throughout 15 months in female Podocnemis expansa in captivity.

	Corticosterone ng/ml									Prolactin ng/ml									FSH ng/ml									LH ng/ml
Month/Year	n	mean		± sd			range			n	mean		± sd			range			n	mean		± sd			range			n	mean		± sd			range
Jul-01	4	3.30	±	0.95	bac		2.00	↔	4.00	4	1.05	±	0.34	ba		0.76	↔	1.45	3	0.38	±	0.15	a		0.23	↔	0.52	2	0.07	±	0.01	b		0.06	↔	0.08
Aug-01	8	3.41	±	2.05	bac		0.90	↔	6.70	6	0.57	±	0.29	b		0.12	↔	0.90	6	0.61	±	0.45	a		0.33	↔	1.52	5	0.32	±	0.16	a		0.18	↔	0.59
Sep-01	16	7.65	±	1.96	bc		2.30	↔	9.90	14	0.85	±	0.50	ba		0.22	↔	2.08	12	0.61	±	0.52	a		0.11	↔	1.90	11	0.21	±	0.12	ba		0.10	↔	0.47
Oct-01	6	4.68	±	1.23	c		3.40	↔	6.60	6	1.25	±	0.63	a		0.59	↔	2.26	4	0.69	±	0.62	a		0.20	↔	1.58	6	0.27	±	0.23	a		0.08	↔	0.68
Nov-01	6	9.13	±	8.61	bac		3.10	↔	26.20	4	0.78	±	0.87	ba		0.31	↔	2.08										3	0.34	±	0.12	a		0.23	↔	0.47
Feb-02	6	4.88	±	4.09	ba		1.40	↔	12.80	6	1.12	±	1.12	ba		0.39	↔	3.37	6	0.42	±	0.14	a		0.23	↔	0.54	6	0.23	±	0.10	a		0.08	↔	0.40
Mar-02	6	4.62	±	2.16	a		2.80	↔	8.70	6	0.74	±	0.64	ba		0.31	↔	2.02	5	0.74	±	0.73	a		0.14	↔	1.73
May-02	16	5.71	±	2.54	bac		1.30	↔	9.50	13	0.69	±	0.34	ba		0.16	↔	1.45	10	0.73	±	0.45	a		0.27	↔	1.82	11	0.22	±	0.21	ba		0.04	↔	0.84
Jun-02	15	3.25	±	2.15	bac		0.90	↔	7.00	13	0.75	±	0.39	ba		0.21	↔	1.71	12	0.47	±	0.27	a		0.14	↔	1.07	10	0.32	±	0.28	a		0.06	↔	0.92
Jul-02	15	4.33	±	2.82	ba		0.80	↔	9.30	13	0.92	±	0.49	ba		0.28	↔	1.81	11	0.66	±	0.56	a		0.07	↔	1.66	10	0.22	±	0.08	a		0.14	↔	0.33
Sep-02	19	7.08	±	5.80	bac		0.70	↔	20.30	17	0.63	±	0.33	ba		0.19	↔	1.18	17	0.61	±	0.32	a		0.07	↔	1.25	14	0.25	±	0.31	ba		0.09	↔	1.28
		Progesterone ng/ml								Estradiol pg/ml
Month/Year	n	mean		± sd			range			n	mean		± sd			range
Jul-01	4	0.67	±	0.07	a		0.58	↔	0.76	4	8.88	±	1.58	d		7.28	↔	10.77
Aug-01	8	0.60	±	0.22	a		0.27	↔	0.85	8	13.68	±	5.84	dc		7.77	↔	24.11
Sep-01	16	1.10	±	1.47	a		0.21	↔	6.37	16	23.05	±	6.43	bac		15.83	↔	35.02
Oct-01	6	0.71	±	0.31	a		0.29	↔	1.03	6	27.66	±	6.14	ba		20.71	↔	38.07
Nov-01	4	0.25	±	0.14	bc		0.08	↔	0.41	5	23.79	±	18.57	bc		7.28	↔	52.88
Feb-02	6	0.48	±	0.72	bc		0.08	↔	1.93	6	30.99	±	17.63	ba		11.17	↔	62.97
Mar-02	4	0.45	±	0.22	ba		0.18	↔	0.69	6	29.71	±	14.11	ba		11.35	↔	51.55
May-02	11	0.54	±	0.42	ba		0.11	↔	1.60	16	40.79	±	24.63	ba		8.91	↔	95.91
Jun-02	13	0.25	±	0.17	bc		0.08	↔	0.55	13	47.10	±	61.70	bac		7.52	↔	198.95
Jul-02	15	0.19	±	0.11	c		0.08	↔	0.47	14	33.34	±	12.64	ba		10.42	↔	63.62
Sep-02	14	0.30	±	0.17	bc		0.13	↔	0.60	19	47.70	±	23.37	a		19.42	↔	100.77

• Different letters in the column (P<0.05).

Analysis of the relation between logarithm values of 17β-estradiol and progesterone plasma concentrations through time can be represented by the following cubic equations, respectively: LgEstr=0.848+1.379*X-0.257*X²+0.015*X³, R²=0.30, P<0.001 and LgPorg=6.09+0.455*X-1.60*X²+0.011*X³, R² 0.35 P<0.001 (Figure 1). We verified that the plasma levels of 17β-estradiol and progesterone showed an inverse relationship. This cycle was observed throughout the year and coincides with the nesting in the wild, which occurs during the dry season (Bataus, 1998). The occurrence of the nesting season when the river flow is the lowest is the only reproduction pattern known for this species. Therefore, the nesting season may vary from place to place, and according to the occurrence of the dry season. Some of the nesting seasons in different locations in South America are December-January (in Rio Branco, Roraima State, Brazil), February to March (Orinoco River, Venezuela), August to September (Pacaya River, Peru, Madeira and Jaruá, Brazil), October (Trombetas River, Pará State, Brazil), and July to August (Araguaia River, Goiás and Tocatins States, Brazil) (Alho and Pádua, 1982).

Figure 1
Relation between time and logarithm values of plasma levels of progesterone and 17-β-estradiol in female Giant Amazonian river turtles (Podocnemis expansa) in captivity during 15 months.

Previous studies in temperate zone species revealed that progesterone is the main steroid hormone produced by chelonians (Klicka and Mahmoud, 1972, 1973; Chan and Callard, 1974; Callard et al.1978), although its physiological role in chelonian species is still not understood. In ovoviviparous reptiles, progesterone acts as an antigonodal agent by inhibiting ovary growth during gestation. It is possible that, in oviparous turtles, this antigonadal action allows the egg to remain in the reproductive trait until the environment presents favorable conditions for oviposition. In other turtle species, high levels of progesterone usually indicate the presence of the corpus luteum and are related to the ovulation and nesting periods (Callard et al., 1978; Lewis et al., 1979; Sarkar et al., 1996; Mahmoud and Licht, 1997). The antigonadotropic action of progesterone in turtles may inhibit endogenous gonadotrophins and may have an important role in retaining the egg and inhibiting vitellogenesis (Ho et al., 1982; Callard et al., 1991). In this study, we did not observe an inhibiting pattern of progesterone by the gonadotrophins, perhaps because we collected only one sample per month and therefore could not detect this trend. The luteolysis with an increase of 17β-estradiol could be suggestive of a starter of the vitellogenesis process in Giant Amazonian river turtles.

The high plasma levels of 17β-estradiol verified during the pre-vitellogenic phase is directly related to follicle size; therefore, estradiol production co-relates with follicular growth (Lance and Callard, 1978). Plasma detection of either 17β-estradiol or progesterone is considered to be a good indication of a functional reproductive system. For instance, in Trachemys scripta, the pre-ovulatory phase is characterized by a short period during which the plasma levels of both estrogen and progesterone are high, only to rapidly drop after ovulation. Some short peaks of estrogen production also occur due to the production of small follicles in the ovary (Callard et al., 1978). It is possible that animals in captivity have a longer pre-vitellogenic phase, if compared to those in wildlife.

We assessed the plasma concentrations of testosterone in males during the completely experimental period (Table 2) and verified a rise in May and July of the second year. This fact was not observed during the year before, thus could not be considered a seasonal pattern.

Table 2
Means of plasma levels of the gonadotrophic, gonadal, prolactin and corticosterone hormones from collections made throughout 15 months in male Podocnemis expansa in captivity.

	Corticosterone ng/ml									Prolactin ng/ml									FSH ng/ml										LH ng/ml
Month/Year	n	mean		± sd			range			n	mean		± sd			range			n	mean		± sd			range			n		mean		± sd			range
Jul-01	10	3.09	±	1.45	b		1.40	↔	5.90	9	1.21	±	0.84	ba		0.50	↔	3.20	6	0.62	±	0.19	a		0.33	↔	0.90	5		0.18	±	0.14	bac		0.04	↔	0.38
Aug-01	17	2.42	±	1.12	b		0.80	↔	5.30	13	0.84	±	0.51	ba		0.25	↔	1.80	9	0.42	±	0.30	a		0.11	↔	1.06	11		0.17	±	0.09	bac		0.07	↔	0.36
Sep-01	13	3.17	±	1.76	b		0.80	↔	7.00	8	0.76	±	0.38	ba		0.10	↔	1.44	6	0.80	±	0.44	a		0.30	↔	1.37	7		0.20	±	0.32	bc		0.05	↔	0.91
Oct-01	6	5.90	±	3.56	ba		1.20	↔	8.90	6	1.29	±	0.56	a		0.64	↔	2.07	3	0.31	±	0.12	a		0.17	↔	0.40	4		0.09	±	0.03	c		0.06	↔	0.13
Nov-01	6	5.97	±	7.74	ba		1.50	↔	21.60	5	0.64	±	0.16	ba		0.50	↔	0.81	3	0.48	±	0.32	a		0.11	↔	0.66	4		0.36	±	0.39	bac		0.05	↔	0.91
Feb-02	6	5.27	±	4.42	ba		1.83	↔	14.07	6	1.36	±	1.14	ba		0.32	↔	3.58	6	0.60	±	0.48	a		0.10	↔	1.32	5		0.27	±	0.15	ba		0.10	↔	0.50
Mar-02	6	2.50	±	1.17	b		1.70	↔	4.80	4	1.05	±	0.94	ba		0.50	↔	2.46										3		0.52	±	0.40	a		0.07	↔	0.83
May-02	13	4.42	±	3.01	ba		1.00	↔	9.95	10	1.05	±	0.37	ba		0.50	↔	1.57	6	0.68	±	0.70	a		0.06	↔	1.89	9		0.20	±	0.11	bac		0.07	↔	0.42
Jun-02	13	5.65	±	6.17	ba		0.80	↔	25.20	7	0.67	±	0.46	b		0.21	↔	1.52	5	0.32	±	0.27	a		0.06	↔	0.75	6		0.15	±	0.07	bac		0.09	↔	0.26
Jul-02	13	7.91	±	5.00	a		1.50	↔	19.40	13	0.91	±	0.43	ba		0.35	↔	1.80	8	0.65	±	0.50	a		0.10	↔	1.51	10		0.27	±	0.15	ba		0.09	↔	0.57
Sep-02	18	4.31	±	3.47	b		1.00	↔	11.88	17	1.09	±	0.62	ba		0.36	↔	2.84	15	1.00	±	1.33	a		0.10	↔	5.53	14		0.17	±	0.08	bac		0.08	↔	0.37
	Testosterone ng/ml
Month/Year	n	mean		± sd			range
Jul-01	10	2.58	±	0.73	ba		1.10	↔	3.40
Aug-01	17	2.41	±	0.84	ba		0.80	↔	4.20
Sep-01	12	2.38	±	1.21	ba		0.60	↔	4.50
Oct-01	6	2.12	±	0.75	ba		0.90	↔	3.00
Nov-01	5	2.18	±	0.82	ba		0.90	↔	3.10
Feb-02	6	2.69	±	1.09	ba		1.45	↔	4.50
Mar-02	6	2.58	±	1.80	ba		0.80	↔	4.90
May-02	13	1.61	±	1.28	a		0.09	↔	3.80
Jun-02	13	4.25	±	0.98	c		3.10	↔	6.10
Jul-02	13	3.73	±	1.64	c		2.00	↔	7.90
Sep-02	15	2.38	±	1.78	bc		0.23	↔	5.00

• Different letters in the column (P<0.05).

A clearly defined seasonal pattern in reptiles is well known (Callard et al., 1978) and our findings indicate a seasonal pattern for hormone production in females of Podocnemis expansa in captivity. For instance, in male reptiles, as in mammals, testosterone levels present a cyclic pattern that works according to the occurrence of peaks of hormone releases of GnRH and LH throughout the day (Callard et al., 1976; Lance et al., 1977; Amann and Schanbacher, 1983). Therefore, we expected that a similar pattern could be found in the males living under the same conditions. Analysis of the variation of the average plasma concentrations of testosterone in males through time showed two peaks, one in May and another in July. (Table 2); however, the same testosterone peak was not seen in July in the previous year. Additionally, our study did not start until that month; therefore, we have no information about the testosterone levels in the months prior to July 2001. These turtles had been transferred to the experimental site from an IBAMA station located 25 Km away, in March 2001. Therefore, our data were collected when these animals had just arrived in the new environment. Thus, it is possible that this lack of testosterone peaks in 2001 reflects some of the changes that the animals may have been submitted to when transferred to the new tank (water conditions, nutrition, population density, transport, and other stress-related factors)

The analysis of plasma concentrations of corticosterone (Tables 1 and 2 females and males respectively) showed a weak negative correlation (-0.20, P<0.05), between the levels of testosterone. Previous studies done in several species showed that corticosterone inhibits the production of sexual hormones under stress conditions (Lance and Lauren, 1984; Gregory et al, 1996; Cash et al., 1997).

However, we cannot rule out that the small number of animals used in this research, and our monthly sample collection may have contributed to not detecting the seasonal hormone production during the first year (2001). We observed additional correlations for other hormones in males, such as a positive correlation between prolactin and FSH. In females, we verified a positive, although weak, correlation between corticosteroid and progesterone, whereas we noticed an inverse correlation between both LH (r=-0.20, P<0.10) and 17β-estradiol (r=–19, P<0.07) with progesterone.

It is known that corticosterone levels increase when animals, including reptiles, are manipulated or kept in captivity, reason why this hormone is considered as a stress indicator (Lance and Lauren, 1984; Gregory et al., 1996; Cash et al., 1997). On the other hand, it has been shown in two turtle species (Chelydra serpentina and Chrysemys picta) that a decrease in testosterone levels occurs when these animals are taken to captivity (Licht et al., 1985; Mendonça and Licht, 1986; Mahmoud et al., 1989). This inverse relationship between corticosterone and testoterone levels was also verified in our study (r=–0.20, P<0.03).

Variance analysis of the logarithmic transformation of hormone concentrations in males showed that testosterone concentrations varied significantly throughout the months (lgTest SQM=1.99, F=3.88, P< 0.0002, Rq=0.27, CV=9.35), whereas in females we observed differences in hormone concentrations for 17β-estradiol (lgestr SMQ=1.61, F=4.26, P<0.0001, Rq=0.29, CV=18.8), progesterone (lgprog SQM=3.11, F=7.05, P<0.0001, Rq=0.44, CV=11.39), and corticosterone (lgcort SMQ=1.31, F=2.59, P<0.007, Rq=0.20, CV=8.52).

Despite the fact that the turtles were kept in captivity, and possibly under stress conditions, we detected the production of FSH, both in females (Table 1) and in males (Table 2), throughout the months (July 2001 to September 2002). Contrary from what we expected, no relationship could be established between FSH and any other hormone in both sexes, and no significant production could be detected at any time. However, a weak positive correlation could be detected between FSH and prolactin (r=0.24, P<0.05) in males. Interestingly, a debate exists about the role of prolactin production in males, and some authors suggest that the hormone may be involved with spermatogenesis in mammals (Lincoln et al., 2001).

We observed a similar situation for LH in both sexes, which, like FSH, is another hormone produced by the pituitary (Tables 1 and 2, female and males, respectively), and it is also under control of the hypothalamic GnRH (Lance and Callard, 1978). These findings indicate that the animals, although living in captivity, seem to have a functional pituitary.

No relationship could be established between prolactin secretion and progesterone levels in females, or between prolactin and any other hormone in males, except for FSH (r=0.24, P<0.05). No significant differences in prolactin production were observed in any sex, throughout the months. The lack of relation between prolactin and progesterone plasma levels in females was unexpected, as prolactin is a hormone known for its anti-gonadal activity in reptiles (Callard and Zeigler Junior, 1970). Additionally, early studies done in turtles showed that progesterone induces prolactin production (Callard et al., 1975).

Tables 1 and 2 show plasma concentrations of prolactin through time in females and males, respectively. The lack of information about the mating behavior of Podocnemis expansa in captivity makes estimating what would be the standard hormonal patterns very difficult, especially in males.

Table 3 presents the means of plasma concentration levels of the hormones studied during the 15 months in both sexes of the Podocnemis expansa species. Tables 2 and 3 show the values of these hormones for females and males, respectively, for each of the months of collection. These data can be considered the first report for this species.

Table 3
Means of plasma levels of the gonadotrophic, gonadal, prolactin and corticosterone hormones over 15 months in males and females of Podocnemis expansa in captivity.

Gender	Hormones	n	mean	±	sd	range
Females	17b estradiol pg/ml	113	33.63	±	27.85	7.28	↔	198.95
	Progesterone ng/ml	101	0.51	±	0.69	0.08	↔	6.37
	Prolactin ng/ml	102	0.81	±	0.52	0.12	↔	3.37
	LH ng/ml	79	0.25	±	0.21	0.04	↔	1.28
	FSH ng/ml	87	0.60	±	0.43	0.07	↔	1.90
	Cortiscoterone ng/ml	117	5.49	±	3.96	0.70	↔	26.20
Males	Testosterone ng/ml	116	2.68	±	1.43	0.09	↔	7.90
	Prolactin ng/ml	98	0.99	±	0.61	0.10	↔	3.58
	LH ng/ml	78	0.21	±	0.18	0.04	↔	0.91
	FSH ng/ml	68	0.66	±	0.73	0.06	↔	5.53
	Cortiscoterone ng/ml	121	4.48	±	4.03	0.80	↔	25.20

Reproduction is controlled by a complex and delicate endocrine mechanism and it may be affected by biological patterns related to the environment and reproductive strategies of each species. The biological patterns may be incompatible with the current captivity centers, or they may even not be related to the reproductive strategies or the alternation of production rates and hormonal releases during the reproductive process. The impact caused by stress over reproduction could be a great factor regarding the possible failures in captivity breeding.

Knowing the reproductive physiology and endocrinology of Podocnemis expansa may help manage reproduction in captivity. Because the factors related to reproduction in captivity are not sufficiently clear, this research aimed at collecting data that will allow further comprehension of the reproductive physiology of this species, thus allowing better management in captivity.

Our study suggests a seasonal pattern for the levels of 17β-estradiol and the occurrence of a decrease in the levels of progesterone, which indicates follicular recruitment.

In this study we measured the plasma levels of a number of hormones in males and females of Podocnemis expansa in captivity. Our purpose was to better understand the physiology of Podocnemis expansa, due to the lack of reference values available for all the hormones we measured (LH, FSH, progesterone 17β-estradiol, testosterone, prolactin and corticosterone). We present for the first time mean values for these hormones, which can be used and compared for future studies as well as for therapeutic purposes regarding assisted reproduction.

Measurements of these hormones in nature, and in different moments throughout the year, combined with investigations of the hypothalamic-pituitary-gonadal axis of animals in captivity, are necessary to shed light on the reproductive physiology of the Giant Amazon river turtle.

Acknowledgements

This research consisted of a retrospective formal review by the IACUC-UFG (nº 041/13). The authors are grateful to Yeda Bataus from Centro Nacional de Pesquisa e Conservação de Répteis e Anfíbios (RAN) of the Brazilian Institute of Environment and Renewable Natural Resources (IBAMA) for allowing the use of animals and data.

• 1
  Guabi Pirá 28 Tipo: extrusada
• (With 1 figure)

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Publication Dates

• Publication in this collection
  04 May 2017
• Date of issue
  Apr-Jun 2017

History

• Received
  20 Mar 2015
• Accepted
  20 Aug 2015