Heavy metals in green mussels (Perna viridis) from the Gulf of Thailand.

Concentrations of seven heavy metals were determined in green mussels (Perna viridis) collected between April and June 1995 from eight locations along the costal area of the Gulf of Thailand. The average concentrations (n = 96) of the heavy metals detected in mussel samples, on the basis of dry weight, were 1.20 mg kg-1 cadmium, 0.78 mg kg-1 for chromium, 9.85 mg kg-1 for copper, 1.09 mg kg-1 for lead 2.78 mg kg-1 for manganese, 1.54 mg kg-1 for nickel, and 94,48 mg kg-1 for zinc. The levels of cadmium, chromium, nickel, and lead found in green mussels from four locations in the Upper Gulf were significantly (P < 0.05) higher than those detected in mussels from four locations in the Lower Gulf, while the levels of copper, manganese, and zinc did not differ significantly (P > 0.05) between the Upper and Lower Gulf. Comparison with earlier studies revealed that the concentrations of some metals in the mussels collected from the Upper Gulf are increasing. The concentrations of heavy metals in green mussels from the Gulf of Thailand were within acceptable levels for human consumption.

Comparison of the adrenalytic activity of mitotane and a methylated homolog on normal adrenal cortex and adrenal cortical carcinoma.

Mitotane is an important adrenalytic drug for the treatment of adrenal cancer whose use is limited by toxicity. Reports from another laboratory indicated that a methylated homolog of Mitotane (Mitometh) tested in guinea pigs possessed comparable adrenalytic activity but was less toxic than Mitotane. This observation prompted us to undertake a comparative study of these two drugs on the basis that Mitometh may be a superior agent for the treatment of adrenal cancer. Preliminary studies in guinea pigs failed to show a significant adrenalytic effect for either Mitotane or Mitometh. Thus, we extended the study to 13 mongrel dogs weighing 12-15 kg that were treated daily with Mitometh or Mitotane (50-100 mg/kg) for 6 or 12 days. Cortisol decreased to undetectable levels and adrenocorticotropic hormone (ACTH) rose to 10 times the baseline levels within 72 h in Mitotane-treated animals. Despite the achievement of similar drug levels, Mitometh treatment in dogs failed to suppress cortisol or increase ACTH. To determine whether these differences were due to differences in bioavailability, we measured the relative concentration of Mitotane and Mitometh in homogenates of adrenal cortex obtained from Mitotane- and Mitometh-treated dogs. The adrenal concentration of Mitometh determined in Mitometh-treated dogs was 5 times higher than the concentration of Mitotane measured in Mitotane-treated animals. Whereas the adrenal glands of Mitotane-treated dogs showed hemorrhage and necrosis, the Mitometh-treated animals showed no adrenal damage. Despite the lack of adrenalytic activity, Mitometh maintained its toxicity as demonstrated by microscopic evidence of hepatic necrosis and an increase in hepatic enzymes. The adrenalytic effects of both agents was also studied in vitro using a human functioning adrenal cortical carcinoma cell line, NCI-H295. Whereas Mitotane strongly suppressed cell growth, Mitometh had a weaker effect. We conclude that Mitometh is not likely to be effective in the therapy of adrenal cancer. Moreover, the results of this study are supportive of the view that metabolic transformation of Mitotane is in some way linked to its adrenalytic action.