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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 />

15

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