| Literature DB >> 32889598 |
Patricia Postingel Quirino1,2, Maira da Silva Rodrigues3, Elis Marina da Silva Cabral3, Diógenes Henrique de Siqueira-Silva4, Ricardo Hideo Mori3, Arno Juliano Butzge5, Rafael Henrique Nóbrega5, Alexandre Ninhaus-Silveira3, Rosicleire Veríssimo-Silveira6.
Abstract
In view of the established climate change scenario and the consequent changes in global temperature, it is essential to study its effects on animal spermatogenesis. Therefore, the aim of this study was to verify the duration of spermatogenesis at different temperatures. For this purpose, 96 male and adult specimens of Astyanax altiparanae were kept in a closed circulation system with water temperature stabilized at 27 °C and 32 °C. Subsequently, the specimens received pulses of BrdU (bromodeoxyuridine) at a concentration of 100 mg/kg/day for 2 consecutive days, and the samples were collected daily for a period of 15 days. Their testes were removed, fixed, processed in historesin, and sectioned in 3 μm, submitted to hematoxylin/eosin staining and to bromodeoxyuridine immunodetection. Partial results of the optimum temperature experiments allowed the classification of A. altiparanae spermatogenic cells in Aund, Adiff, and type B spermatogonia, spermatocytes, spermatids, and spermatozoa. The duration of spermatogenesis was determined as approximately 6 days for animals at a temperature of 27 °C and 1 day for animals at 32 °C. The elevated temperature was also responsible for increasing cell proliferation, resulting in an increase in the number of spermatocytes, spermatids, spermatozoa, and cell death (cell pyknotic). The duration of spermatogenesis in A. altiparanae was directly affected by the elevated water temperature, causing a reduction in the estimated time of spermatogenesis.Entities:
Keywords: Bromodeoxyuridine; Characiformes; Reproduction; Yellow-Tetra
Year: 2020 PMID: 32889598 DOI: 10.1007/s10695-020-00869-7
Source DB: PubMed Journal: Fish Physiol Biochem ISSN: 0920-1742 Impact factor: 2.794