A. Gorodinsky et al., DYNORPHIN-B INHIBITS THYMIDINE INCORPORATION INTO DNA IN FETAL-RAT AND GUINEA-PIG BRAIN-CELL AGGREGATES, Regulatory peptides, 54(1), 1994, pp. 109-110
Numerous studies suggest that opioids have a modulatory role in the re
gulation of neural cell proliferation (1). We have found that mu opioi
d receptor agonists inhibit thymidine incorporation into DNA of neural
cells in rat fetal brain cell aggregates (2). This inhibition is cult
ure age-dependent. Moreover, morphine inhibited glial cell proliferati
on in a concentration dependent manner (3). In contrast, U50488, a kap
pa opioid receptor agonist, exerted either an inhibitory or stimulator
y action on thymidine incorporation depending on the culture duration
(4). Here we addressed the question of the effect of the endogenous ka
ppa-selective opioid peptide, Dynorphin B, on thymidine incorporation
in rat or guinea pig aggregates expressing more than 50% of mu (rat) o
r kappa (guinea pig) receptors. In both cultures Dynorphin B inhibited
DNA synthesis by 30-40%.