Opposite Effects of 2,2′,4,4′,5,5′-Hexachlorobiphenyl and 2,3,7,8-Tetrachlorodibenzo-p-dioxin on the Antibody Response to Sheep Erythrocytes in Mice

R.J. Smialowicz , M.J. Devito, M.M. Riddle, W.C. Williams, L.S. Birnbaum
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Abstract

The effect that cotreatment with 2,2′,4,4′,5,5′-hexachlorobiphenyl (PCB153) and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) has on the antibody plaque-forming cell (PFC) response to sheep red blood cells (SRBCs) was determined in female B6C3F1 mice. Groups of eight mice per group were given a single oral dose of PCB153 alone (0, 3.58, 35.8, or 358 mg/kg), TCDD alone (0, 0.1, 1, or 10 μg/kg), and all possible combinations of these doses in corn oil 7 days prior to immunization with SRBCs. Separate groups of mice were given phenobarbital (PB) parenterally by intraperitoneal injection at a dosage of 160 mg/kg/day for 3 days. Four days after intravenous immunization, body, spleen, thymus, and liver weights and the PFC response to SRBCs were determined. Exposure to TCDD alone resulted in a dose-related suppression of the PFC response, with significant suppression at 1 and 10 μg/kg. In contrast, exposure to PCB153 alone resulted in the enhancement of the PFC response at 358 mg/kg. Combined exposure to 358 mg/kg PCB153 and TCDD resulted in no change (PCB153 + 0.1 μg/kg TCDD) or suppression (PCB153 + 1 or 10 μg/kg TCDD) of the PFC response relative to PCB153 alone; however, the PFC response was enhanced (PCB153 + 0.1 μg/kg TCDD), unaffected (PCB153 + 1 μg/kg TCDD), or suppressed (PCB153 + 10 μg/kg TCDD) relative to corn oil controls. PB did not affect the PFC response to SRBCs, despite a 13-fold induction of hepatic pentoxyresorufinO-dealkylase (PROD) activity. These results suggest that PCB153 enhancement of the PFC response is not related to PROD induction and that it acts as a functional antagonist rather than an aryl hydrocarbon receptor or dispositional antagonist. By enhancing the PFC response to SRBCs, PCB153 raises the “setpoint” response level. Consequently, cotreatment with an immunosuppressive dose of TCDD fails to suppress the PFC response relative to corn oil controls, while clearly suppressing it relative to the appropriate control, PCB153 alone.

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2,2 ',4,4 ',5,5 ' -六氯联苯和2,3,7,8-四氯二苯并-对二恶英对小鼠绵羊红细胞抗体反应的相反作用
研究了2,2 ',4,4 ',5,5 ' -六氯联苯(PCB153)和2,3,7,8-四氯二苯并-对二恶英(TCDD)共处理对雌性B6C3F1小鼠抗体斑块形成细胞(PFC)对绵羊红细胞(srbc)反应的影响。每组8只小鼠在srbc免疫前7天分别口服单剂量PCB153(0、3.58、35.8或358 mg/kg)、TCDD(0、0.1、1或10 μg/kg)以及玉米油中所有可能的剂量组合。各组小鼠腹腔注射苯巴比妥(PB),剂量为160 mg/kg/d,连续3 d。静脉免疫4天后,测定体、脾、胸腺和肝脏的重量以及PFC对红细胞的反应。单独暴露于TCDD导致PFC反应的剂量相关抑制,在1和10 μg/kg时抑制显著。相比之下,单独暴露于PCB153会导致PFC反应在358 mg/kg时增强。与单独暴露于PCB153相比,联合暴露于358 mg/kg PCB153和TCDD对PFC反应没有改变(PCB153 + 0.1 μg/kg TCDD)或抑制(PCB153 + 1或10 μg/kg TCDD);然而,与玉米油对照相比,PFC反应增强(PCB153 + 0.1 μg/kg TCDD)、未受影响(PCB153 + 1 μg/kg TCDD)或抑制(PCB153 + 10 μg/kg TCDD)。PB不影响PFC对srbc的反应,尽管肝脏戊氧基间苯二酚脱烷基酶(PROD)活性可诱导13倍。这些结果表明PCB153对PFC反应的增强与PROD诱导无关,它是一种功能性拮抗剂,而不是芳烃受体或排位拮抗剂。通过增强PFC对srbc的响应,PCB153提高了“设定值”响应水平。因此,与玉米油对照相比,与免疫抑制剂量的TCDD共处理不能抑制PFC反应,而与单独使用PCB153的适当对照相比,却明显抑制了PFC反应。
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