Expression and subcellular localization of the mu-opioid receptor in equine spermatozoa: evidence for its functional role

The development of fertilizing ability in sperm cells is associated with changes in the plasma membrane. However, to date the exact nature of sequentially activated primary receptors and channels and the signal transduction pathways derived from these remains elusive. We analyzed the expression and localization of the m-opioid receptor in equine spermatozoa. A transcript corresponding to the third extracellular loop that selectively binds m agonists was amplified, sequenced and compared with the known sequences in humans, rats and cattle. The amplification product showed a high degree of nucleotide conservation. By immunofluorescence, m-opioid receptor labeling was found on the sperm head and on the tail and disappeared in the acrosomal region of acrosome-reacted sperm cells. Immunoblotting revealed two bands of 50 and 65 kDa. Effects of the opioid antagonist naloxone on motility and on viability and capacitation/acrosome reaction were investigated by computer assisted sperm analysis and Hoechst 33258/chlortetracycline (H258/CTC) staining. Progressive motility was significantly reduced after 3 h incubation in 1023M naloxone (P < 0.05), whereas it increased significantly after 5 h in 1028M naloxone (P < 0.05). Sperm velocity at 5 h was significantly reduced by the addition of 1023M naloxone (P < 0.05), but increased significantly in the presence of 1028M (P < 0.001). Curvilinear velocity and amplitude of lateral head displacement in spermatozoa incubated in the presence of naloxone were not indicative of hyperactivation. H258/CTC staining showed that 1028M naloxone significantly stimulated capacitation (P < 0.01) after 3 h. However, it had no effect on sperm cell viability and acrosomal status. Overall, this study provides the first evidence that the m-opioid receptor is expressed in equine spermatozoa and that naloxone significantly affects motility and capacitation.