Moving sperm forward
Objective: The purpose of this study was to investigate a manual sperm sorting method (Swim-up) and a non-invasive microfluidics method (Zymot microfluidics) with emphasis on formation of reactive oxygen species (ROS) and DNA fragmentation as objective measurements of spermatozoa quality. Standard p...
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UiT Norges arktiske universitet
2023
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ftunivtroemsoe:oai:munin.uit.no:10037/33614 2024-06-23T07:55:24+00:00 Moving sperm forward Hellsten, Benjamin 2023-05-26 https://hdl.handle.net/10037/33614 eng eng UiT Norges arktiske universitet UiT The Arctic University of Norway https://hdl.handle.net/10037/33614 Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Copyright 2023 The Author(s) https://creativecommons.org/licenses/by-nc-sa/4.0 :Andre helsefag: 829 Other health science disciplines: 829 MBI-3911 Mastergradsoppgave Master thesis 2023 ftunivtroemsoe 2024-05-29T00:47:55Z Objective: The purpose of this study was to investigate a manual sperm sorting method (Swim-up) and a non-invasive microfluidics method (Zymot microfluidics) with emphasis on formation of reactive oxygen species (ROS) and DNA fragmentation as objective measurements of spermatozoa quality. Standard phase contrast imaging of spermatozoa was compared with quantitative phase contrast microscopy (QPM) imaging. Study design: Anonymized spermatozoa samples (n=9) from healthy men in North Norway were sorted with the Swim-up method and Zymot microfluidics (Zymot; Gaithersburg Maryland, USA). Analysis of ROS was done with an Oxisperm II kit (Halotech; Madrid, Spain) and by measuring MDA levels (Sigma-Aldrich; St. Louis USA) of spermatozoa. DNA fragmentation was visualized with spermatozoa chromatin staining using a Halosperm G2 kit (Halotech; Madrid, Spain) in conjunction with a Nikon ECLIPSE E 200 phase microscope (Nikon; Tokyo, Japan). QPM analysis was done with an in-house microscope and software. An un-paired T-test and ROUT test was completed to identify P-values and outliers. The software used for this was GraphPad Prism 9 version 9.0.0 (GraphPad; San Diego, California, USA) Results: Native sperm and sperm plasma fractions had lower ROS levels in Swim-up samples compared to un-differentiated samples as analyzed with Oxisperm II, resulting in (P=0.0001). MDA-analysis showed that Swim-up and Zymot samples had lower ROS than Raw samples, showing a 0.05- and 0.7-fold difference respectively, resulting in P-value 0.0011 for Swim-up and P-value 0.0014 for Zymot. There was no significant difference in MDA levels between Swim-up and Zymot samples (P-value 0.6193). Swim-up and Zymot samples had a lower spermatozoa/ml than Raw samples, with the mean of Zymot and Swim-up being 460 and 877.7-fold lower. The resulting P-values were 0.001 for Zymot samples and <0.0001 for Swim-up samples. When comparing Swim-up and Zymot sample concentration, no difference was found as their datapoints were close to each other’s mean value ... Master Thesis North Norway University of Tromsø: Munin Open Research Archive Norway St. Louis ENVELOPE(-67.496,-67.496,-67.132,-67.132) Aldrich ENVELOPE(158.217,158.217,-80.117,-80.117) |
institution |
Open Polar |
collection |
University of Tromsø: Munin Open Research Archive |
op_collection_id |
ftunivtroemsoe |
language |
English |
topic |
:Andre helsefag: 829 Other health science disciplines: 829 MBI-3911 |
spellingShingle |
:Andre helsefag: 829 Other health science disciplines: 829 MBI-3911 Hellsten, Benjamin Moving sperm forward |
topic_facet |
:Andre helsefag: 829 Other health science disciplines: 829 MBI-3911 |
description |
Objective: The purpose of this study was to investigate a manual sperm sorting method (Swim-up) and a non-invasive microfluidics method (Zymot microfluidics) with emphasis on formation of reactive oxygen species (ROS) and DNA fragmentation as objective measurements of spermatozoa quality. Standard phase contrast imaging of spermatozoa was compared with quantitative phase contrast microscopy (QPM) imaging. Study design: Anonymized spermatozoa samples (n=9) from healthy men in North Norway were sorted with the Swim-up method and Zymot microfluidics (Zymot; Gaithersburg Maryland, USA). Analysis of ROS was done with an Oxisperm II kit (Halotech; Madrid, Spain) and by measuring MDA levels (Sigma-Aldrich; St. Louis USA) of spermatozoa. DNA fragmentation was visualized with spermatozoa chromatin staining using a Halosperm G2 kit (Halotech; Madrid, Spain) in conjunction with a Nikon ECLIPSE E 200 phase microscope (Nikon; Tokyo, Japan). QPM analysis was done with an in-house microscope and software. An un-paired T-test and ROUT test was completed to identify P-values and outliers. The software used for this was GraphPad Prism 9 version 9.0.0 (GraphPad; San Diego, California, USA) Results: Native sperm and sperm plasma fractions had lower ROS levels in Swim-up samples compared to un-differentiated samples as analyzed with Oxisperm II, resulting in (P=0.0001). MDA-analysis showed that Swim-up and Zymot samples had lower ROS than Raw samples, showing a 0.05- and 0.7-fold difference respectively, resulting in P-value 0.0011 for Swim-up and P-value 0.0014 for Zymot. There was no significant difference in MDA levels between Swim-up and Zymot samples (P-value 0.6193). Swim-up and Zymot samples had a lower spermatozoa/ml than Raw samples, with the mean of Zymot and Swim-up being 460 and 877.7-fold lower. The resulting P-values were 0.001 for Zymot samples and <0.0001 for Swim-up samples. When comparing Swim-up and Zymot sample concentration, no difference was found as their datapoints were close to each other’s mean value ... |
format |
Master Thesis |
author |
Hellsten, Benjamin |
author_facet |
Hellsten, Benjamin |
author_sort |
Hellsten, Benjamin |
title |
Moving sperm forward |
title_short |
Moving sperm forward |
title_full |
Moving sperm forward |
title_fullStr |
Moving sperm forward |
title_full_unstemmed |
Moving sperm forward |
title_sort |
moving sperm forward |
publisher |
UiT Norges arktiske universitet |
publishDate |
2023 |
url |
https://hdl.handle.net/10037/33614 |
long_lat |
ENVELOPE(-67.496,-67.496,-67.132,-67.132) ENVELOPE(158.217,158.217,-80.117,-80.117) |
geographic |
Norway St. Louis Aldrich |
geographic_facet |
Norway St. Louis Aldrich |
genre |
North Norway |
genre_facet |
North Norway |
op_relation |
https://hdl.handle.net/10037/33614 |
op_rights |
Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Copyright 2023 The Author(s) https://creativecommons.org/licenses/by-nc-sa/4.0 |
_version_ |
1802647991684694016 |