Comparative analysis of purified Pacific and Caribbean ciguatoxin congeners and related marine toxins using a modified ELISA technique.

The monoclonal antibody to ciguatoxin (CTX) produced from a hybridoma cell line was assayed for the detection of four congeners of CTX: Pacific ciguatoxin-1 (P-CTX-1), Pacific ciguatoxin-2 (P-CTX-2), Pacific ciguatoxin-3 (P-CTX-3), and Caribbean ciguatoxin-1 (C-CTX-1) and related marine toxins, including domoic acid, palytoxin, and okadaic acid, using a modified enzyme-linked immunosorbent assay (ELISA). Lower detection limits were assessed and linearity was statistically established (P<0.05) for P-CTX-1, P-CTX-2, and P-CTX-3 and C-CTX-1 at concentrations ranging from 0 to 5.00 ng, while the other marine toxins showed statistically insignificant cross-reactivities at similar concentrations. Thus, the monoclonal antibody to CTX is able to specifically detect various CTX congeners at levels comparable to those naturally occurring in ciguatoxic fish.

In vitro effects of cortisol on the release and gene expression of prolactin and growth hormone in the tilapia, Oreochromis mossambicus.

Exposure to cortisol inhibits prolactin (PRL) release from the tilapia pituitary within 10-20min through a plasma membrane-associated, non-genomic pathway. In the present study, in vitro effects of cortisol on the release and mRNA levels of two PRLs (PRL(188) and PRL(177)) and growth hormone (GH) were examined in the organ-cultured pituitary of the Mozambique tilapia, Oreochromis mossambicus. The PRL release was significantly greater in hyposmotic (300mOsmolal) than in hyperosmotic (350mOsmolal) medium during the 2-8h of incubation. The mRNA levels of two PRLs, as estimated by RNase protection assay, were increased after 8h in hyposmotic medium. Cortisol (200nM) inhibited the release of two PRLs under hyposmotic conditions within 1h, and the inhibitory effects lasted for 24h. Cortisol also reduced the gene transcription of both PRLs during 2-8h of incubation but not after 24h. No effect of cortisol was observed on PRL release or on its mRNA levels under hyperosmotic condition. There was no significant effect of medium osmolality on the release or mRNA levels of GH during 8h of incubation. However, GH release was significantly stimulated by cortisol after 4h, and the effect lasted for 24h under both hyposmotic and hyperosmotic conditions. Cortisol also caused a significant increase in GH mRNA levels at 8 and 24h. These results suggest that cortisol inhibits PRL release from the tilapia pituitary through non-genomic and also through transcriptional pathways, while stimulating GH release through classical genomically mediated glucocorticoid actions.