M. Sugiura et al., CROCIN (CROCETIN DI-GENTIOBIOSE ESTER) PREVENTS THE INHIBITORY EFFECTOF ETHANOL ON LONG-TERM POTENTIATION IN THE DENTATE GYRUS IN-VIVO, The Journal of pharmacology and experimental therapeutics, 271(2), 1994, pp. 703-707
The effects of crocin (crocetin di-gentiobiose ester) and its analogs
on long-term potentiation (LTP) of evoked potential in the dentate gyr
us were investigated by using anesthetized rats. Intracerebroventricul
ar injection of crocin (51.2 nmol) alone did not affect the synaptic p
otential evoked by single stimulation of the medial perforant path, an
d neither inhibited nor facilitated the LTP induced by strong (30 puls
es at 60 Hz) or weak (20 pulses at 60 Hz) tetanus. Administration of e
thanol (30 v/v%, 2 ml/kg i.v.) blocked the LTP induced by application
of tetanus (30 pulses at 60 Hz), but the LTP-blocking effect of ethano
l was prevented by preadministration of crocin (51.2 nmol i.c.v.). Cro
cetin gentiobiose glucose ester also antagonized the LTP-blocking effe
ct of ethanol, but it required a higher dose (102.5 nmol i.c.v.) to ex
hibit a more significant effect than crocin. Crocetin di-glucose ester
at a dose up to 102.5 nmol (i.c.v.) did not significantly affect the
LTP-blocking effect of ethanol. Neither gentiobiose alone (102.5 nmol
i.c.v.) nor glucose alone (204.9 nmol i.c.v.) mimicked the activity of
crocin. These results suggest that crocin can prevent the ethanol-ind
uced impairment of hippocampal synaptic plasticity in vivo and that ge
ntiobioses attached to the fatty acid chain are important for crocin t
o exert the biological activity.