chapter 3 - RiuNet
chapter 3 - RiuNet
chapter 3 - RiuNet
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GENERAL INTRODUCTION<br />
spermatozoa kinetic parameters were negatively affected by the depletion<br />
of this ion. Thus, it seems clear that there is a wide interspecific variability<br />
in relation to the presence/absence of extracellular ions and the effect<br />
thereof on the sperm motion parameters, so more studies focusing on this<br />
topic are necessary in order to design optimum species-specific activation<br />
media.<br />
On the other hand, scarce studies regarding the intracellular ion changes<br />
after sperm activation of marine fish have been published (Oda and<br />
Morisawa, 1993; Takai and Morisawa, 1995). Nowadays, the widely<br />
accepted model in marine species suggests that a hyperosmotic shock<br />
causes a spermatozoa membrane depolarization, which in turn results in an<br />
increase in Ca 2+ and K + inside the cell, which is the key factor triggering<br />
sperm motility (Figure 4).<br />
Quiescent sperm<br />
in seminal<br />
plasma<br />
pH increase<br />
Hypothesis?<br />
Initiation of<br />
sperm motitlity<br />
Hyperosmotic<br />
shock<br />
K + increase<br />
Hypothesis?<br />
ATP stores<br />
decreases<br />
Membrane<br />
depolarization<br />
Ca 2+ increase<br />
Hypothesis?<br />
Motility stops<br />
Figure 4. Activation process and signal transduction in marine spermatozoa:<br />
scheme of the interacting processes occurring during the motility period.<br />
However, neither the origin of these ions (from the extracellular medium or<br />
intracellular stores), nor their specific effects on motility and the kinetic<br />
parameters measured by CASA systems have been investigated. In this<br />
respect, new studies involving detailed protocols, channel blockers, etc.<br />
must be carried out in order to find out the specific mechanisms which<br />
occur during motility activation in marine fish sperm.<br />
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