Follicular and oviductal fluids have shown modulatory effects on sperm capa
citation of boar spermatozoa in vitro, implicating glycosaminoglycans (GAGs
) in the process. Capacitation in pigs is believed to occur in vivo during
storage in the sperm reservoir, where spermatozoa maintain viability and me
mbrane stability awaiting ovulation. Exposure to the nonsulphated GAG hyalu
ronan induces capacitation in vitro (chlortetracycline-monitored) without e
liciting acrosome exocytosis, indicating that it exerts a protective role o
n sperm viability. Oviductal fluids (isthmus and ampulla) of cycling sows w
ere collected in vivo to disclose temporal changes in concentrations of bot
h sulphated and nonsulphated GAGs between late prooestrus and meta-oestrus.
Further, heparan-sulphate and hyaluronan were immunohistochemically locali
zed in the oviductal tissues of uninseminated and inseminated sows, around
the period of ovulation. Concentrations of sulphated GAGs were two-fold hig
her than hyaluronan. All tubal GAGs increased significantly from late pro-o
estrus and were highest during the pre-ovulatory period before beginning to
decrease postovulation, the exception being the ampullar hyaluronan, whose
levels remained high towards meta-oestrus. Heparan sulphate (syndecans) an
d hyaluronan were both immunohistochemically detected in the endosalpinx. S
yndecan-immunolabelling was present in the epithelium and stroma along the
tube, whereas hyaluronan was always localized in the lamina propria and mos
t of the lining epithelium was negative, during the stages studied. The onl
y exception was the sperm reservoir (deep crypts and furrows of the Utero-t
ubal Junction (UTJ)/isthmus) where sperm clusters were seen close to the ep
ithelial HA-immunolabelling in the inseminated sows, but only pre-ovulatory
. The presence of GAGs in the tubal fluid and the conspicuous location of h
yaluronan suggest they play a role in the formation and function of the spe
rm reservoir.