Probe ultrasonification of egg yolk plasma forms low-density lipoprotein nanoparticles that efficiently protect canine semen during cryofreezing
Around the world, many couples have turned to in vitro fertilization as a viable solution to fertility issues. Low-density lipoprotein (LDL) is a protein best known for transporting fat molecules throughout the body, but it has also been shown to protect sperm cells during cryopreservation due to it...
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Published in | The Journal of biological chemistry Vol. 298; no. 7; p. 101975 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.07.2022
American Society for Biochemistry and Molecular Biology |
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Abstract | Around the world, many couples have turned to in vitro fertilization as a viable solution to fertility issues. Low-density lipoprotein (LDL) is a protein best known for transporting fat molecules throughout the body, but it has also been shown to protect sperm cells during cryopreservation due to its micellar structure. In the present study, we aimed to evaluate different protocols for the preparation of nanoparticles from egg yolk plasma (EYP) containing LDL to improve the viability of cryopreserved canine semen. EYP was subjected to three distinct treatments: ultrasonification in an ultrasound bath at 40 kHz for 30 min (LDL-B); ultrasonification via an ultrasound probe at 50% amplitude for 30 min (LDL-P); and high-pressure homogenization at 10,000 PSI for six cycles (LDL-H). Sperm quality was assessed after thawing using computer-assisted sperm analysis and flow cytometry. The results revealed that compared to the EYP control, the LDL-P formulation presented significantly higher efficiency (p < 0.05) in maintaining total and progressive sperm motility, sperm membrane integrity and fluidity, and levels of intracellular reactive oxygen species. The LDL-P nanoparticles had an average size of approximately 250 nm, a polydispersity index value of 0.3, and −1.15 mV of zeta potential, which are very important because it is an indicator of the stability of a colloidal dispersion. Therefore, we conclude that ultrasonication of EYP using a probe is an efficient method for the preparation of LDL nanoparticles that would enhance the cryoprotection of semen during freezing. |
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AbstractList | Around the world, many couples have turned to
in vitro
fertilization as a viable solution to fertility issues. Low-density lipoprotein (LDL) is a protein best known for transporting fat molecules throughout the body, but it has also been shown to protect sperm cells during cryopreservation due to its micellar structure. In the present study, we aimed to evaluate different protocols for the preparation of nanoparticles from egg yolk plasma (EYP) containing LDL to improve the viability of cryopreserved canine semen. EYP was subjected to three distinct treatments: ultrasonification in an ultrasound bath at 40 kHz for 30 min (LDL-B); ultrasonification
via
an ultrasound probe at 50% amplitude for 30 min (LDL-P); and high-pressure homogenization at 10,000 PSI for six cycles (LDL-H). Sperm quality was assessed after thawing using computer-assisted sperm analysis and flow cytometry. The results revealed that compared to the EYP control, the LDL-P formulation presented significantly higher efficiency (
p
< 0.05) in maintaining total and progressive sperm motility, sperm membrane integrity and fluidity, and levels of intracellular reactive oxygen species. The LDL-P nanoparticles had an average size of approximately 250 nm, a PDI value of 0.3, and −1.15 mV of zeta potential, which are very important because it is an indicator of the stability of a colloidal dispersion. Therefore, we conclude that ultrasonication of EYP using a probe is an efficient method for the preparation of LDL nanoparticles that would enhance the cryoprotection of semen during freezing. Around the world, many couples have turned to in vitro fertilization as a viable solution to fertility issues. Low-density lipoprotein (LDL) is a protein best known for transporting fat molecules throughout the body, but it has also been shown to protect sperm cells during cryopreservation due to its micellar structure. In the present study, we aimed to evaluate different protocols for the preparation of nanoparticles from egg yolk plasma (EYP) containing LDL to improve the viability of cryopreserved canine semen. EYP was subjected to three distinct treatments: ultrasonification in an ultrasound bath at 40 kHz for 30 min (LDL-B); ultrasonification via an ultrasound probe at 50% amplitude for 30 min (LDL-P); and high-pressure homogenization at 10,000 PSI for six cycles (LDL-H). Sperm quality was assessed after thawing using computer-assisted sperm analysis (CASA) and flow cytometry. The results revealed that compared to the EYP control, the LDL-P formulation presented significantly higher efficiency (p < 0.05) in maintaining total and progressive sperm motility, sperm membrane integrity and fluidity, and levels of intracellular reactive oxygen species (ROS). The LDL-P nanoparticles had an average size of approximately 250 nm, a polydispersity index value of 0.3, and -1.15 mV of zeta potential, very important because is an indicator of the stability of a colloidal dispersion. Therefore, we conclude that ultrasonication of EYP using a probe is an efficient method for the preparation of LDL nanoparticles that would enhance the cryoprotection of semen during freezing. Around the world, many couples have turned to in vitro fertilization as a viable solution to fertility issues. Low-density lipoprotein (LDL) is a protein best known for transporting fat molecules throughout the body, but it has also been shown to protect sperm cells during cryopreservation due to its micellar structure. In the present study, we aimed to evaluate different protocols for the preparation of nanoparticles from egg yolk plasma (EYP) containing LDL to improve the viability of cryopreserved canine semen. EYP was subjected to three distinct treatments: ultrasonification in an ultrasound bath at 40 kHz for 30 min (LDL-B); ultrasonification via an ultrasound probe at 50% amplitude for 30 min (LDL-P); and high-pressure homogenization at 10,000 PSI for six cycles (LDL-H). Sperm quality was assessed after thawing using computer-assisted sperm analysis and flow cytometry. The results revealed that compared to the EYP control, the LDL-P formulation presented significantly higher efficiency (p < 0.05) in maintaining total and progressive sperm motility, sperm membrane integrity and fluidity, and levels of intracellular reactive oxygen species. The LDL-P nanoparticles had an average size of approximately 250 nm, a polydispersity index value of 0.3, and −1.15 mV of zeta potential, which are very important because it is an indicator of the stability of a colloidal dispersion. Therefore, we conclude that ultrasonication of EYP using a probe is an efficient method for the preparation of LDL nanoparticles that would enhance the cryoprotection of semen during freezing. |
ArticleNumber | 101975 |
Author | Hädrich, Gabriela de Assis Araújo Camelo Junior, Francisco Corcini, Carine Dahl Meneghello Gheller, Stela Mari Dora, Cristiana Lima Anastácio da Silva, Edenara Martins, Diego Varela Junior, Antonio Sergio |
Author_xml | – sequence: 1 givenname: Edenara orcidid: 0000-0001-6965-7797 surname: Anastácio da Silva fullname: Anastácio da Silva, Edenara organization: Faculdade de Veterinária, Universidade Federal de Pelotas, Capão do Leão, Brazil – sequence: 2 givenname: Carine Dahl surname: Corcini fullname: Corcini, Carine Dahl organization: Faculdade de Veterinária, Universidade Federal de Pelotas, Capão do Leão, Brazil – sequence: 3 givenname: Francisco surname: de Assis Araújo Camelo Junior fullname: de Assis Araújo Camelo Junior, Francisco organization: Faculdade de Veterinária, Universidade Federal de Pelotas, Capão do Leão, Brazil – sequence: 4 givenname: Diego surname: Martins fullname: Martins, Diego organization: Faculdade de Veterinária, Universidade Federal de Pelotas, Capão do Leão, Brazil – sequence: 5 givenname: Stela Mari surname: Meneghello Gheller fullname: Meneghello Gheller, Stela Mari organization: Faculdade de Veterinária, Universidade Federal de Pelotas, Capão do Leão, Brazil – sequence: 6 givenname: Gabriela surname: Hädrich fullname: Hädrich, Gabriela organization: Department of Pharmaceutical Technology and Biopharmacy, University of Vienna, Vienna, Austria – sequence: 7 givenname: Cristiana Lima orcidid: 0000-0002-9198-437X surname: Dora fullname: Dora, Cristiana Lima organization: Laboratório de Nanotecnologia Aplicada à Saúde, Universidade Federal do Rio Grande, Rio Grande, Brazil – sequence: 8 givenname: Antonio Sergio orcidid: 0000-0003-4901-5118 surname: Varela Junior fullname: Varela Junior, Antonio Sergio email: varelajras@gmail.com organization: Reprodução Animal Comparada, Instituto de Ciências Biológicas, Universidade Federal do Rio Grande, Rio Grande, Brazil |
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Cites_doi | 10.1021/la010634z 10.1016/S0093-691X(01)00435-6 10.1016/j.anireprosci.2016.02.032 10.1016/S0378-4320(01)00161-0 10.1038/nmat2442 10.1042/BSR20191601 10.1016/j.colsurfb.2004.05.003 10.1111/j.1439-0531.2010.01622.x 10.11648/j.ejb.20170504.12 10.3109/01485019208987691 10.1111/and.12411 10.1016/j.colsurfb.2015.11.034 10.1093/ilar.41.4.187 10.1021/la0355545 10.1016/j.aquaculture.2019.03.015 10.1016/S0304-4157(00)00018-6 10.1095/biolreprod.103.022996 10.1126/science.1125527 10.1016/j.tiv.2016.05.002 10.1016/0011-2240(87)90005-8 |
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Keywords | BCF PDI LDL ACROs ROS MF LPO MI EYP PM CFDA |
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Snippet | Around the world, many couples have turned to in vitro fertilization as a viable solution to fertility issues. Low-density lipoprotein (LDL) is a protein best... Around the world, many couples have turned to in vitro fertilization as a viable solution to fertility issues. Low-density lipoprotein (LDL) is a protein best... Around the world, many couples have turned to in vitro fertilization as a viable solution to fertility issues. Low-density lipoprotein (LDL) is a protein best... |
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Title | Probe ultrasonification of egg yolk plasma forms low-density lipoprotein nanoparticles that efficiently protect canine semen during cryofreezing |
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