Literature DB >> 20688369

Sperm treatment affects capacitation parameters and penetration ability of ejaculated and epididymal boar spermatozoa.

C Matás1, M Sansegundo, S Ruiz, F A García-Vázquez, J Gadea, R Romar, P Coy.   

Abstract

This work was designed to study how this ability is affected by different sperm treatments routinely used for in vitro fertilization (IVF) assay. In this study, boar sperm samples from epididymal or ejaculated origin were processed by three different methods: left unwashed (NW group), washed in Dulbecco's phosphate-buffered saline supplemented with 0.1% BSA (BSA group), and washed on a Percoll(®) gradient (PERCOLL group). After preparation of semen samples, changes in motility patterns were studied by CASA, calcium uptake by spectrofluorimetry, and ROS generation, spontaneous acrosome reaction, and lipid disorder by means of flow cytometry. Finally IVF assays were also performed with the different semen samples and penetrability results evaluated at 2 and 4 h post insemination (hpi). Independently of the sperm treatment, epididymal spermatozoa showed higher values of progressive motility, percentage of live cells with low lipid disorder, and penetration ability at 4 hpi than the corresponding ejaculated spermatozoa. Ejaculated spermatozoa showed higher levels of calcium uptake, ROS generation and percentage of spontaneous acrosome reaction than epididymal sperm. Regarding sperm treatments, PERCOLL group showed the highest values for some motility parameters (linearity of the curvilinear trajectory, straightness, and average path velocity/curvilinear velocity), ROS generation and penetration ability at 2 and 4 hpi; however this same group showed the lowest values for sperm curvilinear velocity and lateral head displacement. From all experimental groups, ejaculated-PERCOLL-treated spermatozoa showed the highest fertilization ability after 2 hpi. Results suggest that capacitation pathways can be regulated by suitable treatments making the ejaculated sperm able to reach capacitation and fertilize oocytes in similar levels than epididymal spermatozoa, although most of the studied capacitation-associated changes do not correlate with this ability.
Copyright © 2010 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20688369     DOI: 10.1016/j.theriogenology.2010.06.002

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  9 in total

1.  Morphological study of boar sperm during their passage through the female genital tract.

Authors:  Francisco Alberto García-Vázquez; Iván Hernández-Caravaca; Carmen Matás; Cristina Soriano-Úbeda; Silvia Abril-Sánchez; María José Izquierdo-Rico
Journal:  J Reprod Dev       Date:  2015-06-26       Impact factor: 2.214

2.  Oviductal epithelial cells selected boar sperm according to their functional characteristics.

Authors:  Rebeca López-Úbeda; Francisco A García-Vázquez; Joaquín Gadea; Carmen Matás
Journal:  Asian J Androl       Date:  2017 Jul-Aug       Impact factor: 3.285

3.  Manipulation of bicarbonate concentration in sperm capacitation media improvesin vitro fertilisation output in porcine species.

Authors:  Cristina Soriano-Úbeda; Jon Romero-Aguirregomezcorta; Carmen Matás; Pablo E Visconti; Francisco A García-Vázquez
Journal:  J Anim Sci Biotechnol       Date:  2019-03-11

4.  Comparative Analysis of Mitochondrial Proteome Reveals the Mechanism of Enhanced Ram Sperm Motility Induced by Carbon Ion Radiation After In Vitro Liquid Storage.

Authors:  Yuxuan He; Hongyan Li; Yong Zhang; Junjie Hu; Yulong Shen; Jin Feng; Xingxu Zhao
Journal:  Dose Response       Date:  2019-01-10       Impact factor: 2.658

5.  Bovine epididymal spermatozoa treatment for in vitro fertilization: Heparin accelerates fertilization and enables a reduction in coincubation time.

Authors:  Andrielle T M Cunha; José O Carvalho; Ana L S Guimarães; Ligiane O Leme; Felippe M Caixeta; João H M Viana; Margot A N Dode
Journal:  PLoS One       Date:  2019-01-07       Impact factor: 3.240

6.  Elucidating the Role of K+ Channels during In Vitro Capacitation of Boar Spermatozoa: Do SLO1 Channels Play a Crucial Role?

Authors:  Marc Yeste; Marc Llavanera; Guillermo Pérez; Fabiana Scornik; Josep Puig-Parri; Ramon Brugada; Sergi Bonet; Elisabeth Pinart
Journal:  Int J Mol Sci       Date:  2019-12-15       Impact factor: 5.923

7.  Relationship between the Length of Sperm Tail Mitochondrial Sheath and Fertility Traits in Boars Used for Artificial Insemination.

Authors:  Karl Kerns; Jennifer Jankovitz; Julie Robinson; Amanda Minton; Chris Kuster; Peter Sutovsky
Journal:  Antioxidants (Basel)       Date:  2020-10-23

8.  Replacement of Albumin by Preovulatory Oviductal Fluid in Swim-Up Sperm Preparation Method Modifies Boar Sperm Parameters and Improves In Vitro Penetration of Oocytes.

Authors:  Sergio Navarro-Serna; Evelyne París-Oller; Ondrej Simonik; Raquel Romar; Joaquín Gadea
Journal:  Animals (Basel)       Date:  2021-04-22       Impact factor: 2.752

9.  Potential fertilizer of spermatozoa in porcine epididymal tail post-orchiectomy.

Authors:  Mariela Adriana Ydiaquez-Miranda; José Antonio Herrera-Barragán; Miguel González-Lozano; Alejandro Ávalos-Rodríguez
Journal:  Vet Res Forum       Date:  2021-09-15       Impact factor: 0.950

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.