Differential changes of neuroactive amino acids in samples obtained from discrete rat brain regions after systemic administration of saxitoxin.

Aspartic acid, glutamic acid, gamma-amino-n-butyric acid (GABA) and 2-aminoethanesulfonic acid are neuroactive amino acids. They are found in the central rat nervous system. Here, we have studied if a relationship exists between the presence of saxitoxin (STX) a paralytic poisoning shellfish (PSP) and the neuroactive amino acids. Samples of striatum (S), hypothalamus (H), mid brain (MB), frontal cortex (FC), brain stem (BS), right hemisphere (RH) and left hemisphere (LH) of rat brain were collected and analyzed for neuroactive amino acids (AAn(t)) by Aswad method (1984). Experiments, consisting of intraperitoneal injection of SXT (5 and 10microgkg(-1) body weight) to young male rats, evoked significant changes in AAn(t) above basal values. Aspartic and glutamic acid significantly increased for RH and LH (after 30min the increased was 116% and 210%, P< or =0.001 over basal values, respectively). On the other hand, aspartic, glutamic, taurine and GABA significantly decreased for S (after 30min the decreased was 77.4%; 84%; 93.8% and 95.3%, P< or =0.001 over basal values, respectively). These results suggest that STX alters AAn(t). It is produced at least in part, because STX blocks voltage-gated sodium channels and this blockade could decrease AAn(t) release by exocytotic dependent mechanism of depolarization.

Application of precolumn oxidation HPLC method with fluorescence detection to evaluate saxitoxin levels in discrete brain regions of rats.

Saxitoxin (STX) is one of several related toxins that cause paralytic shellfish poisoning (PSP). This toxin blocks neuronal transmission by binding to the voltage-gated Na+ channel and for this reason, it has been widely used in the study of Na+ channel. The aim of this study was to analyze STX distribution in different rat brain regions after its acute intraperitoneal (i.p.) administration. Male rats (150-200 g) were injected i.p. with STX (5 and 10 microg/kg of body weight). After three time intervals of 30, 60, and 120 min (for 5 microg/kg STX dose) and 30 min (for 10 microg/kg STX dose) animals were sacrificed by cervical dislocation. Brains were removed and dissected in seven regions. STX concentration was measured using a precolumn oxidation high-performance liquid chromatographic method with fluorescence detection (HPLC/FLD). STX was found in all the regions evaluated at ppm levels meaning that STX peripherical administered across the blood-brain barrier and is distributed along the whole brain.