The processing and storage of ram semen reduce the motility and disrup
t the membrane integrity of spermatozoa. It is generally assumed that
these changes are detrimental and are associated with a loss of fertil
ising capacity. Despite many years of empirical research that has esta
blished a variety of methods for the processing, storage and inseminat
ion of spermatozoa, fertility is generally lower after cervical insemi
nation with stored than fresh semen, The components of the sperm cell
responsible for this low fertility are not clearly understood, However
, recent evidence suggests that while many spermatozoa remain motile a
fter storage, the membranes of the motile cells are destabilised to th
e point where they may not survive Further ageing in the female tract
after cervical insemination. These membrane changes are similar to the
capacitation and acrosome reaction of spermatozoa, Thus, stored sperm
atozoa may require less capacitation time in the female tract, and may
readily fertilise oocytes if placed in their immediate vicinity, as w
ith in vitro fertilisation, tubal or even intrauterine insemination. I
t may be possible to prevent or reverse some of these membrane changes
, for example using antioxidants, and thus improve fertility following
cervical insemination of sheep.