The microcystins (Mcyst) are cyclic peptide hepatotoxins produced by cyanobacteria. They are chemically very stable and represent a public health threat when they occur in water bodies used for human consumption. Mice injected ip with Mcyst (LD50 50-100 mu g/kg) accumulate Mcyst in the liver and die within 2-4 hr with massive intrahepatic hemorrhage, Pretreatment of mice with cyclosporin A (CP), rifamycin (Rif), trypan blue (TB), and trypan red (TR) protected the animals from a lethal dose of the toxin. The studies reported here using the freshly isolated rat hepatocyte model were undertaken in order (1) to evaluate the contribution of Mcyst transport in hepatocytes to the mechanism of chemoprotection for Mcyst in vivo toxicity by CP, Rif, TB, and TR and (2) to better characterize the hepatic Mcyst transporter in this model and determine its relationship to other bile acid/organic anion transporters that have already been fully described. Incubations with I-125-Mcyst were used to measure Mcyst uptake and accumulation in hepatocytes, It has been shown that at the cellular level Mcyst binds to and inhibits protein phosphatases 1 and 2A (PP) at nanomolar concentrations. Lethal doses of Mcyst in mice resulted in rapid profound inhibition of hepatic PP activity, PP activity was also inhibited in hepatocytes incubated with 100-500 nM Mcyst, PP inhibition in these studies was used as a marker of metabolic effects of the toxin. The chemoprotectants CP (5 mu M), Rif(50 mu M), TR (20 mu M), and TB (20 mu M) decreased accumulation of Mcyst (320 nM, a toxic concentration) after 30 min incubation to 37, 26, 30, and 66%, respectively, of that of cells treated with Mcyst only. Inhibition of PP activity in these cells was decreased, Inhibition of PP activity in hepatocytes was also decreased by known inhibitors of Mcyst transport: 50 mu M of the bile acids cholate and taurocholate (TC) and 50 mu M sulfobromophthalein. For all compounds tested the amount of Mcyst accumulated in the hepatocytes correlated qualitatively with the extent of PP inhibition, From these results it can be concluded that inhibition of Mcyst uptake by hepatocytes is the most likely mechanism of chemoprotection for Mcyst in vivo toxicity for TR, TB, CP, and Rif. Uptake of Mcyst was unaffected by changes in the ionic composition of the uptake buffer but was significantly decreased when PP activity of hepatocytes was inhibited by preincubation with Mcyst, This effect resulted directly from PP inhibition since preincubation with calyculin A (a cell permeant PP inhibitor, chemically unrelated to Mcyst) also led to inhibition of Mcyst uptake, In contrast, alanine and TC uptake were unaffected in cells with PP activity fully inhibited, indicating that the activities of these latter transporters, unlike that for Mcyst, are probably not controlled by serine/threonine phosphorylation. The pattern of inhibition, the lack of sodium or chloride dependency, and the sensitivity to PP inhibition indicate that the hepatic transport of Mcyst is unlikely to be via one of the already fully characterized sinusoidal bile salt organic anion transporters. (C) 1995 Academic Press, Inc.
