2020
DOI: 10.1590/1984-3143-ar2020-0533
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Characterization of porcine oocytes stained with Lissamine Green B and their developmental potential in vitro

Abstract: Traditional methods for the evaluation of oocyte quality are based on morphological classification of the follicle, cumulus-oocyte complex, polar body and meiotic spindle. This study is focused on the differences between the morphological assessment of oocyte quality, the assessment based on Lissamine Green B (LB) staining and the analysis of oocytes using a proteomic approach. We evaluated the effectiveness of electrochemical and chemical parthenogenetic activation under our laboratory conditions and evaluate… Show more

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Cited by 2 publications
(2 citation statements)
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“…It has been used previously for the non-invasive morphological assessment of porcine oocyte quality since it enables the detection of oocytes in the pre-apoptotic stage, expressing high levels of TP53, but still with low levels of pro-apoptotic genes [ 18 ]. Moreover, in another study from our group, Bartkova et al [ 17 ] reported LB staining as a non-invasive oocyte selection method that can detect cellular membrane damage in porcine COCs. Although oocyte staining with such stains is considered a non-invasive method, it is still not the optimal approach for oocyte selection, since further treatment and incubation steps need to be incorporated to evaluate the oocytes.…”
Section: Discussionmentioning
confidence: 99%
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“…It has been used previously for the non-invasive morphological assessment of porcine oocyte quality since it enables the detection of oocytes in the pre-apoptotic stage, expressing high levels of TP53, but still with low levels of pro-apoptotic genes [ 18 ]. Moreover, in another study from our group, Bartkova et al [ 17 ] reported LB staining as a non-invasive oocyte selection method that can detect cellular membrane damage in porcine COCs. Although oocyte staining with such stains is considered a non-invasive method, it is still not the optimal approach for oocyte selection, since further treatment and incubation steps need to be incorporated to evaluate the oocytes.…”
Section: Discussionmentioning
confidence: 99%
“…Each COC and its corresponding FF were allocated in separate wells in a 96-well plate. COCs were washed once in PXM-HEPES (HEPES buffered porcine X medium [ 16 ]) and then stained for 15 min at room temperature with 0.5% lissamine green B stain (LB), a vital synthetic stain for determining oocyte quality and competence [ 17 , 18 ]. Each COC was classified separately according to the oocyte stain into high-quality (unstained; HQ) and low-quality (stained; LQ) as presented in Fig.…”
Section: Methodsmentioning
confidence: 99%