2020
DOI: 10.1016/j.repbio.2020.01.002
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Cholesterol-loaded cyclodextrin is efficient in preserving sperm quality of cryopreserved ram semen with low freezability

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Cited by 18 publications
(11 citation statements)
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“…This treatment improves sperm membrane stability after incorporating exogenous cholesterol to the plasma membrane, which in turn enhances sperm cryosurvival, motility, mitochondrial activity and the number of sperm attached to zona pellucida, reducing at the same time cryo-capacitation and premature tyrosine phosphorylation [133][134][135][136]. The beneficial effects of CLC seem to be greater in those ejaculates with low freezability, at least in ram sperm [137]. Moreover, the addition of CLC to the extender attenuated in gazelle sperm the degradation of three proteins related to energy metabolism and cytoskeletal organization (CAPZB, HSP90A, PAGM2) during the freezing-thawing process compared to untreated sperm, which may explain the increased motility observed in CLC treated sperm [38].…”
Section: Molecular Aspects Of Those Novel Strategies To Reduce Sperm mentioning
confidence: 99%
“…This treatment improves sperm membrane stability after incorporating exogenous cholesterol to the plasma membrane, which in turn enhances sperm cryosurvival, motility, mitochondrial activity and the number of sperm attached to zona pellucida, reducing at the same time cryo-capacitation and premature tyrosine phosphorylation [133][134][135][136]. The beneficial effects of CLC seem to be greater in those ejaculates with low freezability, at least in ram sperm [137]. Moreover, the addition of CLC to the extender attenuated in gazelle sperm the degradation of three proteins related to energy metabolism and cytoskeletal organization (CAPZB, HSP90A, PAGM2) during the freezing-thawing process compared to untreated sperm, which may explain the increased motility observed in CLC treated sperm [38].…”
Section: Molecular Aspects Of Those Novel Strategies To Reduce Sperm mentioning
confidence: 99%
“…Para avaliar a integridade da membrana plasmática e do potencial acrossômico e de membrana mitocondrial, as sondas fluorescentes utilizadas foram: iodeto de propídio (PI), aglutinina Pisum sativum conjugada com isotiocianato de fluoresceína (FITC-PSA) e 5,5',6,6'tetracloro-1,1, iodeto de 3,3'tetraetilbenzimidazolilcarbocianina (JC-1), respectivamente (adaptado Pavaneli et al, 2020) (17) . Para a análise da peroxidação lipídica foram utilizados 4,4-Difluoro-5-(4-fenil-1,3-butadienil)-4-bora-3a, 4a-diaza-sindaceno ácido-3-undecanoico (C11-BODIPY581 / 591) (18) e dihidroetídio (DHE) (19) . Essas análises foram realizadas usando uma citometria de fluxo (BD Accuri™ C6).…”
Section: Análises Pós Criopreservaçãounclassified
“…To evaluate integrity of plasma membrane and acrosome and mitochondrial membrane potential, the fluorescent probes used were: propidium iodide (PI), fluorescein isothiocyanate-conjugated Pisum sativum agglutinin (FITC-PSA) and 5.5',6.6'-tetrachloro-1,1,3,3'tetraethylbenzimidazolylcarbocyanine iodide (JC-1), respectively (adapted from Pavaneli et al, 2020) (17) . For the analysis of lipid peroxidation, we used 4,4-difluoro-5-(4-phenyl-1,3-butadienyl)-4-bora-3a, 4a-diaza-sindacene acid-3-undecanoic (C11-BODIPY581/591) (18) and dihydroethidium (DHE) (19) . These analyses were performed using a flow cytometer (BD Accuri™ C6).…”
Section: Post-cryopreservation Semen Analysismentioning
confidence: 99%