2018
DOI: 10.1016/j.androl.2017.02.002
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Association of open field behavior with blood and semen characteristics in roosters: an alternative animal model

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Cited by 10 publications
(10 citation statements)
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“…In bulls, no correlation was found between serum T levels and sperm indices (Gábor et al ., ). No significant correlation was found between blood T and seminal characteristics in Iranian indigenous‏ ‏roosters (Ommati et al ., )‎. Zeman et al .…”
Section: Discussionmentioning
confidence: 98%
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“…In bulls, no correlation was found between serum T levels and sperm indices (Gábor et al ., ). No significant correlation was found between blood T and seminal characteristics in Iranian indigenous‏ ‏roosters (Ommati et al ., )‎. Zeman et al .…”
Section: Discussionmentioning
confidence: 98%
“…Epididymal sperm concentration was determined using a Neubauer hemocytometer under a light microscope at 200× magnification. Sperm viability and abnormality were evaluated in duplicate (200 sperm per slide) after eosin–nigrosin staining (Seed et al ., ; Ommati et al ., ). Spermatozoa without tail or head or with protoplasmic droplets were considered as abnormal.…”
Section: Methodsmentioning
confidence: 97%
“…Sperm concentration was measured by transferring a portion of diluted epididymal fluid (10 µL) onto a Neubauer chamber and observing the cells under a light microscope (200 × magnification). The hypo-osmotic swelling (HOS) test, as a valid index of membrane integrity, was performed by mixing 10 µL of sperm suspension with 50 µL of hypo-osmotic solution (50-mOsm NaCl) for 10 min at 37 • C and calculating the percentages of spermatozoa (in at last 200 sperm per slide) with a swollen "bubble" around the curled flagellum, using light microscopy (1,000 × magnification) (31,56). Sperm abnormality and viability were measured in duplicate (200 sperm per sample) after eosin-nigrosin staining (20,31).…”
Section: Sperm Quality Evaluationmentioning
confidence: 99%
“…The hypo-osmotic swelling (HOS) test, as a valid index of membrane integrity, was performed by mixing 10 µL of sperm suspension with 50 µL of hypo-osmotic solution (50-mOsm NaCl) for 10 min at 37 • C and calculating the percentages of spermatozoa (in at last 200 sperm per slide) with a swollen "bubble" around the curled flagellum, using light microscopy (1,000 × magnification) (31,56). Sperm abnormality and viability were measured in duplicate (200 sperm per sample) after eosin-nigrosin staining (20,31). Spermatozoa with protoplasmic droplets, ab-axial tails, malformed heads, double tails, coiled tails, bent tails, and without tail or head were recorded as abnormal under a phase-contrast microscope (Olympus BX41; Olympus Optical Co. Ltd, Japan) (28,57).…”
Section: Sperm Quality Evaluationmentioning
confidence: 99%
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