Use este identificador para citar ou linkar para este item: https://repositorio.inpa.gov.br/handle/1/18413
Título: Noninvasive monitoring of androgens in male amazonian manatee (Trichechus Inunguis): Biologic validation
Autor: Amaral, Rodrigo S.
Weber Rosas, Fernando Cesar
Viau, Priscila
D'Affonsêca Neto, José Anselmo
Silva, Vera Maria Ferreira da
Oliveira, Cláudio Alvarenga de
Palavras-chave: Androgen
Gonadorelin
Animals
Blood
Chemistry
Feces
Lacrimal Apparatus
Male
Metabolism
Physiology
Reproduction
Saliva
Trichechus Inunguis
Urine
Androgens
Animal
Feces
Gonadotropin-releasing Hormone
Lacrimal Apparatus
Male
Reproduction
Saliva
Trichechus Inunguis
Urine
Animalsia
Bovinae
Sirenia
Trichechidae
Trichechus Inunguis
Data do documento: 2009
Revista: Journal of Zoo and Wildlife Medicine
É parte de: Volume 40, Número 3, Pags. 458-465
Abstract: The Amazonian manatee (Trichechus inunguis) is endemic in the Amazonian basin and is the only exclusively fresh water sirenian. Historically hunted on a large scale, this species is now considered endangered, and studies on the reproductive physiology are critical for the improvement of reproductive management of captive and wild populations of manatees. The aim of this study was to verify the viability of androgen measurement in saliva, lacrimal, urine, and fecal samples of the Amazonian manatee by conducting a hormone challenge. Two adult male manatees (A-l and A-2) were submitted to an experimentation protocol of 12 day (Dl to D10). On DO, the animals received an intramuscular injection of gonadotropin-releasing hormone (GnRH)- analogue. Salivary, lacrimal, urinary, and fecal samples were collected daily (between 0800 hours and 0900 hours) and frozen at -20° C until assayed. Fecal samples were lyophilized, extracted with 80% methanol, and diluted in buffer before the radioimmunoassay (RIA). Urine samples underwent acid hydrolysis and were diluted in depleted bovine serum. Salivary and lacrimal samples were assayed without the extraction step. Hormonal assays were conducted with a commercial testosterone RIA kit. An androgen peak (>median + 2 interquartile range [IQR]) was observed in all matrices of both animals, although it was less prominent in the lacrimal samples of A- 2. However, the fecal androgen peak (A-l peak = 293.78 ng/g dry feces, median [IQR] = 143.58 [32.38] ng/g dry feces; A-2 peak = 686.72 ng/g dry feces, median [IQR] = 243.82 [193.16] ng/g dry feces) occurred later than urinary (A-l peak = 648.16 ng/mg creatinine [Cr], median [IQR] = 23.88 [30.44] ng/mg Cr; A-2 peak = 370.44 ng/mg Cr, median [IQR] = 113.87 [117.73] ng/mg Cr) and salivary (A-l peak = 678.89 pg/ml, median [IQR] = 103.69 [119.86] pg/ml; A-2 peak = 733.71 pg/ml, median [IQR] = 262.92 [211.44] pg/ml) androgen peaks. These intervals appear to be correlated with the long digesta passage time in this species. The salivary and urinary peaks were closely associated. These results demonstrate that androgen concentrations in saliva, urine, or feces samples reflect reliably physiologic events and are a powerful tool for noninvasive reproductive monitoring of Amazonian manatees. Copyright 2009 by American Association of Zoo Veterinarians.
DOI: 10.1638/2008-0111.1
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