ToxSci Advance Access originally published online on December 1, 2004
Toxicological Sciences 2005 84(1):149-156; doi:10.1093/toxsci/kfi046
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Toxicological Sciences vol. 84 no. 1 © Society of Toxicology 2005; all rights reserved.
Dietary Exposure to Aroclor 1254 Alters Central and Peripheral Vasopressin Release in Response to Dehydration in the Rat
* Environmental Toxicology Program and Department of Cell Biology & Neuroscience, University of California at Riverside, Riverside, California 92521
Received September 21, 2004; accepted November 3, 2004
Central vasopressin (VP) release from magnocellular neuroendocrine cells (MNCs) in the supraoptic nucleus (SON) occurs from their somata and dendrites within the SON several hours after acute dehydration, and is an important autoregulatory mechanism influencing the systemic release of VP from MNC terminals in the posterior pituitary. To begin to explore the impact of polychlorinated biphenyls (PCBs) on brain mechanisms of body fluid regulation, both central and systemic VP release in response to acute dehydration were assessed in adult male rats fed the commercial PCB mixture Aroclor 1254 (30 mg/kg/day) for 15 days. Water intake and body weight were recorded daily, and on day 15 rats were dehydrated by intraperitoneal injection of 3.5 M saline (controls received physiological saline) and sacrificed 4–6 h later. Intranuclear VP release was measured in SON tissue punches in vitro, and systemic VP release was measured in the same rats. SON prepared from dehydrated PCB-naive rats released significantly more VP than did SON from control rats (4.9 ± 0.8 vs. 2.7 ± 0.4 pg/ml/µg). In contrast, while Aroclor 1254 exposure had no effect on baseline water intake, weight gain, or plasma osmolality responses to dehydration in PCB-fed rats, the SON failed to respond with increased VP release during dehydration. Consistent with previous studies showing an inhibitory effect of central VP on plasma VP output, dehydrated PCB-fed rats had an exaggerated 863% increase in plasma VP over basal levels, compared to a 241% increase in PCB-naïve rats, suggesting that the MNC system is subtly disrupted.
Key Words: osmoregulation; magnocellular neuroendocrine cells; polychlorinated biphenyls; somatodendritic release; supraoptic nucleus.
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