We have examined the effectiveness of the in vitro rat hippocampal slice pr
eparation as a means of rapidly and specifically detecting the marine algal
toxins saxitoxin, brevetoxin, and domoic acid and have identified toxin-sp
ecific electrophysiological signatures for each. Brevetoxin (PbTX3, 50-200
nM) produced a significant reduction in orthodromic population spike amplit
ude which was quick to reverse during a 50 min wash-out, while antidromic p
opulation spikes and field EPSPs exhibited only slight reductions, and fibr
e spiof orthodrokes showed no change at all. Domoic acid (100 nM) produced
a robust, reversible increase in amplitude mic spikes, and the appearance o
f multiple spikes (i.e., epileptiform activity) within minutes of toxin was
h-in. Other notable features of the domoic acid signature included a signif
icant decrease in amplitude of the field EPSPs, and a complete absence of e
ffect on either antidromic or fibre spikes. Fifty nanomolar saxitoxin (PSP)
abolished all responses in all slices. Only antidromic spikes showed any r
ecovery during wash-out. Field EPSP and fiber spike analysis further demons
trated that the preparation is capable of reliably detecting saxitoxin in a
linearly responsive fashion at toxin concentrations of 25-200 nM, and test
s of naturally contaminated shellfish confirmed the utility of this assay a
s a screening method for PSP. Our findings suggest that the in vitro hippoc
ampal slice preparation has potential in the detection and analysis of thre
e marine algal toxins important to the shellfish industry. (C) 1999 Elsevie
r Science Ltd. All rights reserved.