Abstract

The effects of the herbicides paraquat, dinoseb and 2,4-D on intracellular Ca2+ levels and on vasopressin-induced Ca2+ mobilization were investigated in intact isolated hepatocytes. Incubation of rat hepatocytes with paraquat (5 mM for 60 min) and dinoseb (10 microM) resulted in a time-dependent loss of viability by approximately 25%. Viability of cells treated with 2,4-D decreased significantly, dropping to about 20% at 10 mM and 60 min incubation. Exposure of hepatocytes to paraquat (1-10 mM) for 60 min had no effect on the basal level of [Ca2+]i. Additionally, exposure to paraquat had no effect on the magnitude and on the duration of the [Ca2+]i response to vasopressin. In the presence of 2,4-D (1-10 mM), basal [Ca2+]i increases as a function of herbicide concentration. The magnitude of the delta[Ca2+]i response decreases from 256 +/- 8 nM in control to 220 +/- 5 nM, at 10 mM 2,4-D. Exposure of hepatocytes to dinoseb (1-10 microM) had no effect on the basal level of [Ca2+]i. However, a strong concentration-dependent decrease in the magnitude of delta[Ca2+]i in response to vasopressin was noticed at 60 min incubation. Dinoseb markedly inhibited the stimulation of the production of inositol phosphates by vasopressin stimulus. The present study demonstrates that paraquat, 2,4-D and dinoseb cause cell death in hepatocytes by mechanisms not related to an early increase in [Ca2+]i. Additionally, it has been shown for the first time that dinoseb disturbs the transduction mechanism promoted by vasopressin by inhibiting the formation of IP3.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.