Opioid-mediated Sertoli cells apoptosis is involved in testicular homeostasis and/or reproductive dysfunction

The opioid system may exert positive direct and/or indirect effects on spermatogenesis at multiple
levels including the levels of the central nervous system and at the testes/sperm levels. However, long
term opioid use could be associated with several reproductive complications that place the users at risk of hypogonadism
and even infertility. There is little available information regarding the contribution of opioids and
their apoptotic effects on testis Sertoli cells. Here, the effects of DAMGO (mu opioid receptor’s agonist), DPDPE
(delta opioid receptor’s agonist) and DYN 1-9 (kappa opioid receptor’s agonist) on Sertoli cell viability and
apoptosis were investigated.
METHODS: Cultured Sertoli cells were exposed to each agonist (0.1–100 μM, for 24 or 48 hours) and their
apoptotic effects were investigated.
RESULTS: Cell viability was decreased and apoptosis was increased in the cells exposed to DAMGO in a concentration-
dependent manner, while in the cells exposed to DPDPE, no signifi cant changes were observed. In
cells exposed to DYN 1-9, the viability did not signifi cantly change, however apoptosis increased signifi cantly,
following the exposure to the high concentration of DYN 1-9.
CONCLUSION: These data suggest that mu and Kappa, but not delta receptors mediated apoptosis in Sertoli
cells may be involved, at least in part, in testicular homeostasis and/or reproductive dysfunction (Tab. 1, Fig. 3,
Ref. 52). Text in PDF www.elis.sk