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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抗绵羊红细胞抗体反应的相反作用。

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.

作者信息

Smialowicz R J, DeVito M J, Riddle M M, Williams W C, Birnbaum L S

机构信息

National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA.

出版信息

Fundam Appl Toxicol. 1997 Jun;37(2):141-9. doi: 10.1006/faat.1997.2323.

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 micrograms/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 micrograms/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 microgram/ kg TCDD) or suppression (PCB153 + 1 or 10 micrograms/kg TCDD) of the PFC response relative to PCB153 alone; however, the PFC response was enhanced (PCB153 + 0.1 microgram/kg TCDD), unaffected (PCB153 + 1 microgram/kg TCDD), or suppressed (PCB153 + 10 micrograms/kg TCDD) relative to corn oil controls. PB did not affect the PFC response to SRBCs, despite a 13-fold induction of hepatic pentoxyresorufin O-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.

摘要

在雌性B6C3F1小鼠中,测定了2,2',4,4',5,5'-六氯联苯(PCB153)与2,3,7,8-四氯二苯并对二恶英(TCDD)联合处理对针对绵羊红细胞(SRBC)的抗体空斑形成细胞(PFC)反应的影响。每组八只小鼠,在以SRBC免疫前7天,经口单独给予单一剂量的PCB153(0、3.58、35.8或358 mg/kg)、单独给予TCDD(0、0.1、1或10 μg/kg),以及这些剂量在玉米油中的所有可能组合。另外几组小鼠通过腹腔注射以160 mg/kg/天的剂量经肠胃外给予苯巴比妥(PB),持续3天。静脉免疫后4天,测定体重、脾脏、胸腺和肝脏重量以及对SRBC的PFC反应。单独暴露于TCDD导致PFC反应出现剂量相关的抑制,在1和10 μg/kg时出现显著抑制。相比之下,单独暴露于PCB153在剂量为358 mg/kg时导致PFC反应增强。相对于单独的PCB153,联合暴露于358 mg/kg PCB153和TCDD导致PFC反应无变化(PCB153 + 0.1 μg/kg TCDD)或受到抑制(PCB153 + 1或10 μg/kg TCDD);然而,相对于玉米油对照,PFC反应增强(PCB153 + 0.1 μg/kg TCDD)、未受影响(PCB153 + 1 μg/kg TCDD)或受到抑制(PCB153 + 10 μg/kg TCDD)。尽管肝脏戊氧基瑞香素O-脱烷基酶(PROD)活性诱导了13倍,但PB并未影响对SRBC的PFC反应。这些结果表明,PCB153对PFC反应的增强与PROD诱导无关,并且它作为一种功能性拮抗剂而非芳烃受体或处置拮抗剂发挥作用。通过增强对SRBC的PFC反应,PCB153提高了“设定点”反应水平。因此,相对于玉米油对照,用免疫抑制剂量的TCDD联合处理未能抑制PFC反应,而相对于适当的对照,即单独的PCB153,则明显抑制了PFC反应。

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