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Utilization of fluorescent probe association for simultaneous assessment of plasmatic, acrosomal, and mitochondrial membranes of rooster spermatozoa
Celeghini, ECC; Arruda, RP; Albuquerque, R; Silva, FHA; Faria, DE; Andrade, AFC; Nascimento, J; Raphael, CF.
Afiliação
  • Celeghini, ECC; Universidade de São Paulo Faculdade de Medicina Veterinária e Zootecnia Departamento de Reprodução Animal.
  • Arruda, RP; Universidade de São Paulo Faculdade de Medicina Veterinária e Zootecnia Departamento de Reprodução Animal.
  • Albuquerque, R; USP FMVZ Departamento de Nutrição e Produção Animal.
  • Silva, FHA; USP Faculdade de Zootecnia e Engenharia de Alimentos Departamento de Zootecnia.
  • Faria, DE; USP Faculdade de Zootecnia e Engenharia de Alimentos Departamento de Zootecnia.
  • Andrade, AFC; Universidade de São Paulo Faculdade de Medicina Veterinária e Zootecnia Departamento de Reprodução Animal.
  • Nascimento, J; Universidade de São Paulo Faculdade de Medicina Veterinária e Zootecnia Departamento de Reprodução Animal.
  • Raphael, CF; Universidade de São Paulo Faculdade de Medicina Veterinária e Zootecnia Departamento de Reprodução Animal.
Article em En | VETINDEX | ID: vti-717796
Biblioteca responsável: BR68.1
ABSTRACT
This experiment was designed with the objective of developing a simple, practical, and high repeatability technique for the simultaneous evaluation of the integrity of the plasmatic and acrosomal membranes, as well as funcional mitochondria of domestic fowl spermatozoa using an association of fluorescent probes. Four ejaculates (motility > 80% and abnormal morphology 10%) from each of six Ross male broiler breeder (n=24) were diluted in TALP sperm medium (25x10(6) spermatozoa/mL) and split into two aliquots, and one of these aliquots was flash frozen in liquid nitrogen and thawed to damage all cellular membranes. Three treatments were prepared from these aliquots, with the following ratios of Fresh semenFlash frozen semen 1000 (T100), 5050 (T50), and 0100 (T0). A 150-µL aliquot of diluted semen was placed in a microcentrifuge tube with the addition of 2-µL PI, 2-µL MITO, and 50-µL FITC-PSA, and incubated at 38.5º C/8 min in the dark. An 8-µL sample was placed on a slide, coverslipped, and examined by epifluorescence microscopy. Each sample had 200 cells counted and classified based on the fluorescence emitted by each probe. By regression analysis, plasma membrane integrity, as detected by PI, was determined as v=4.17+0.82X (R²=0.95). Acrosome integrity, as detected by FITC-PSA, generated the equation v=4.19+0.84X (R²=0.96). Functional mitochondria was estimated by the equation v=3.20+0.83X (R²=0.96). This is an efficient technique to simultaneously evaluate plasmatic, acrosomal, and mitochondrial membranes in fowl sperm. It is suggested that its application in flow cytometry systems allows this methodology to be applied in large scale.
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Texto completo: 1 Base de dados: VETINDEX Idioma: En Revista: R. bras. Ci. avíc. / Rev. bras. ciênc. avic Ano de publicação: 2007 Tipo de documento: Article
Texto completo: 1 Base de dados: VETINDEX Idioma: En Revista: R. bras. Ci. avíc. / Rev. bras. ciênc. avic Ano de publicação: 2007 Tipo de documento: Article