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1.
Zygote ; 26(4): 333-335, 2018 Aug.
Article in English | MEDLINE | ID: mdl-30277454

ABSTRACT

SummaryThe aim of this study was to evaluate the effect of incubating semen for different periods (90, 270 or 450 min) with or without Trolox® (100 or 150 µM) on the quality of sperm from Saimiri collinsi. Sperm motility, vigour, and plasma membrane integrity (PMI) were evaluated in both fresh semen and semen incubated for different time periods, i.e. 90, 270 or 450 min of incubation. Supplementation of semen extender with Trolox® 100 µM improved sperm motility, vigour and PMI for up to 270 min of incubation.


Subject(s)
Chromans/pharmacology , Cryopreservation/veterinary , Cryoprotective Agents/pharmacology , Saimiri/physiology , Semen Preservation/veterinary , Spermatozoa/physiology , Animals , Antioxidants/pharmacology , Cell Membrane , Male , Semen Analysis , Sperm Motility/drug effects , Spermatozoa/drug effects
2.
Theriogenology ; 84(5): 743-9.e1, 2015 Sep 15.
Article in English | MEDLINE | ID: mdl-26047706

ABSTRACT

The Neotropical nonhuman primate squirrel monkey (Saimiri sp.) is one of the most commonly used species in research in several areas of knowledge. However, little progress has been reported in respect to techniques for preservation of their gametes. Thus, the main objectives of this study were (1) to describe testicular and seminal aspects of a new species, Saimiri collinsi, (2) to preserve semen of this species by cooling or freezing using ACP-118 (powdered coconut water), and (3) to test two glycerol (GLY) concentrations (1.5% or 3%) for semen freezing in the presence of ACP-118. The experimental group started with 14 captive males, but only 11 were suitable to collect ejaculates containing sperm. After anesthesia, both testes were evaluated: length, width, height, and testicular circumference. Semen was collected by electroejaculation and evaluated, followed by dilution, cooling, and freezing. Seminal parameters and sperm motility, vigor, plasma membrane integrity, and normal morphology were evaluated after each step; functionality was also checked in fresh and frozen-thawed sperm. Sperm motility, plasma membrane integrity, and normal sperm in cooled semen (n = 11) were 44.1 ± 34.0, 63.1 ± 15.6, and 73.8 ± 19.8, respectively, with vigor ranging of 2 to 3. Sperm motility, plasma membrane integrity, normal and functional sperm in frozen semen (n = 5) were 0.6 ± 1.3 (1.5% and 3% GLY); 4.4 ± 4.9 (1.5% GLY) and 6.6 ± 7.2 (3% GLY); 86.8 ± 3.0 (1.5% GLY) and 88.8 ± 5.1 (3% GLY); 13.3 ± 11.9 (1.5% GLY) and 14.3 ± 13.5 (3% GLY), respectively, and vigor 0 for both 1.5% and 3% GLY. No significant difference between GLY concentrations was observed. We concluded that electroejaculation was efficient for semen collection of S collinsi and tested the cooling protocol that allowed to recover a satisfactory percentage (63%) of membrane intact sperm. However, the freezing protocol was not appropriate to sperm preservation.


Subject(s)
Saimiri/physiology , Semen Preservation/veterinary , Spermatozoa/physiology , Animals , Cryopreservation/methods , Cryopreservation/veterinary , Male , Semen Analysis/veterinary , Semen Preservation/methods
3.
Anim Reprod Sci ; 134(3-4): 210-5, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22959640

ABSTRACT

The experiment described the morphological and morphometrical characteristics as well as estimate the population of primordial, primary and secondary ovarian follicles from common squirrel monkey (Saimiri sciureus). Ovaries (n=10) from five senile squirrel monkeys were collected after natural death and processed for classical histology. The mean ovarian population was estimated as 915.04 ± 78.83, 230.46 ± 20.82 and 115.88 ± 15.72 primordial, primary and secondary follicles per ovary, respectively. 73.30% were classified as primordial, 18.62% as primary, and 8.09% as secondary follicles. From all these developmental stages, the mean diameters of follicles, oocytes, oocytes nuclei and the mean number of granulosa cells were described. The number of granulosa cells surrounding normal primordial follicles (5.65 ± 0.001) was lower (P<0.05) than the number of granulosa cells (13.17 ± 0.02) surrounding the primary follicles. Secondary follicles presented the highest (P<0.001) number of granulosa cells surrounding each oocyte (273.73 ± 20.80). We have estimated the follicular population, as well as described the morphometric and morphological characteristics of preantral follicles from senile squirrel monkeys, which may be a valuable animal model for female ovarian aging studies.


Subject(s)
Aging/physiology , Ovarian Follicle/anatomy & histology , Ovarian Follicle/cytology , Saimiri , Animals , Cell Count , Cell Nucleus/physiology , Cell Nucleus/ultrastructure , Cell Size , Female , Granulosa Cells/cytology , Granulosa Cells/ultrastructure , Oocytes/cytology , Oocytes/ultrastructure , Organ Size , Ovarian Follicle/ultrastructure , Saimiri/anatomy & histology , Saimiri/physiology , Statistics as Topic
4.
Comp Biochem Physiol B Biochem Mol Biol ; 149(1): 209-14, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17931920

ABSTRACT

Growth hormone overexpression increases growth and consequently increases the metabolic rate in fishes. Therefore, the objective of this study was to evaluate the effects of growth hormone overexpression in zebrafish Danio rerio in terms of growth, oxygen consumption, reactive oxygen species production, lipid hydroperoxide content, antioxidant enzyme activity and glutamate-cysteine ligase catalytic subunit gene expression. The employed models were wild type and transgenic (hemizygous and homozygous) zebrafish expressing the Odonthestes argentinensis growth hormone gene directed by the Cyprinus carpio beta-actin promoter. Higher growth parameters were observed in the hemizygous group. The homozygous group possessed higher oxygen consumption and reactive oxygen species production. Growth hormone transgenesis causes a decrease in glutamate-cysteine ligase catalytic subunit expression, an enzyme responsible for glutathione synthesis. Although the lipid hydroperoxide content was similar between groups, we demonstrate that growth hormone overexpression has the potential to generate oxidative stress in fishes.


Subject(s)
Glutamate-Cysteine Ligase/biosynthesis , Growth Hormone/biosynthesis , Lipid Peroxidation/genetics , Oxygen Consumption/genetics , Reactive Oxygen Species/metabolism , Zebrafish Proteins/biosynthesis , Actins/genetics , Actins/metabolism , Animals , Animals, Genetically Modified/genetics , Animals, Genetically Modified/metabolism , Antioxidants/metabolism , Catalytic Domain/genetics , Glutamate-Cysteine Ligase/genetics , Glutathione/biosynthesis , Glutathione/genetics , Growth Hormone/genetics , Promoter Regions, Genetic/genetics , Zebrafish , Zebrafish Proteins/genetics
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