AI Article Synopsis

  • Incubation of boar spermatozoa with oligomycin A leads to immediate immobilization and impairs their ability to undergo in vitro capacitation (IVC) and acrosome exocytosis (IVAE).
  • Oligomycin A does not affect oxygen consumption, ATP levels, or mitochondrial membrane potential (MMP), suggesting its inhibitory effects are independent of overall energy maintenance.
  • The study indicates that the activity of mitochondrial ATP synthase, sensitive to oligomycin A, is crucial for proper sperm motility and the successful processes of IVC and IVAE.

Article Abstract

Incubation of boar spermatozoa in a capacitation medium with oligomycin A, a specific inhibitor of the F0 component of the mitochondrial ATP synthase, induced an immediate and almost complete immobilisation of cells. Oligomycin A also inhibited the ability of spermatozoa to achieve feasible in vitro capacitation (IVC), as measured through IVC-compatible changes in motility patterns, tyrosine phosphorylation levels of the acrosomal p32 protein, membrane fluidity and the ability of spermatozoa to achieve subsequent, progesterone-induced in vitro acrosome exocytosis (IVAE). Both inhibitory effects were caused without changes in the rhythm of O2 consumption, intracellular ATP levels or mitochondrial membrane potential (MMP). IVAE was accompanied by a fast and intense peak in O2 consumption and ATP levels in control spermatozoa. Oligomycin A also inhibited progesterone-induced IVAE as well as the concomitant peaks of O2 consumption and ATP levels. The effect of oligomycin on IVAE was also accompanied by concomitant alterations in the IVAE-induced changes on intracellular Ca(2+) levels and MMP. Our results suggest that the oligomycin A-sensitive mitochondrial ATP-synthase activity is instrumental in the achievement of an adequate boar sperm motion pattern, IVC and IVAE. However, this effect seems not to be linked to changes in the overall maintenance of adequate energy levels in stages other than IVAE.

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Source
http://dx.doi.org/10.1071/RD13145DOI Listing

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