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砷作为砷化镓免疫抑制成分的证据。

Evidence for arsenic as the immunosuppressive component of gallium arsenide.

作者信息

Burns L A, Sikorski E E, Saady J J, Munson A E

机构信息

Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.

出版信息

Toxicol Appl Pharmacol. 1991 Aug;110(1):157-69. doi: 10.1016/0041-008x(91)90298-s.

Abstract

Gallium arsenide (GaAs) has been shown previously to suppress the in vivo antibody-forming cell (AFC) response to sheep erythrocytes (SRBC) when administered intratracheally at concentrations between 50 and 200 mg/kg. In the present studies, direct addition of GaAs to in vitro-generated antibody cultures resulted in dose-dependent suppression of the primary antibody response, and was only seen when GaAs was added within 36 hr following immunization. Using atomic absorption spectrophotometry on tissue samples from mice exposed to 200 mg/kg GaAs, arsenic concentrations were found to peak in the spleen at 24 hr and decline, whereas gallium concentrations continue to rise through 14 days. Concentrations of each metal in the spleen at 24 hr are comparable to the concentrations achieved for each metal when GaAs is added at 25 microM to the in vitro model system. The 24 hr time point was chosen for comparison because all in vivo-in vitro studies were conducted using spleens from mice 24 hr after GaAs exposure. NaAsO2 and Ga(NO3)3 suppressed the AFC response dose-dependently, and in a time-dependent manner similar to GaAs when added to the in vitro system. However, based on IC50 values for each salt, the role of the gallium component in the immunosuppression appears weak. Oxalic acid (OA) and meso-2,3-dimercaptosuccinic acid (DMSA), chelators of gallium and arsenic respectively, were added to cultures with GaAs to confirm that arsenic was the primary immunosuppressive component. DMSA dose-dependently blocked GaAs-induced immunosuppression in vitro, while OA had no effect. The metal-binding compounds were determined to be specific for the metals used in these studies and did not cross-react with one another. DMSA was evaluated for its ability to prevent suppression of the AFC response in splenocytes from GaAs-exposed mice and was able to block GaAs-induced suppression of the AFC response when given sc every 4 hr beginning 1 hr prior to GaAs exposure. These data indicate that the arsenic component of GaAs is the major contributor to the GaAs-induced immunosuppression and that this effect occurs within the first 36 hr of the 5-day culture period in a concentration-dependent manner.

摘要

先前已表明,当以50至200毫克/千克的浓度经气管内给药时,砷化镓(GaAs)可抑制体内对绵羊红细胞(SRBC)的抗体形成细胞(AFC)反应。在本研究中,将GaAs直接添加到体外产生抗体的培养物中会导致对初次抗体反应的剂量依赖性抑制,并且仅在免疫后36小时内添加GaAs时才会出现这种情况。使用原子吸收分光光度法对暴露于200毫克/千克GaAs的小鼠的组织样本进行检测,发现砷浓度在24小时时在脾脏中达到峰值,然后下降,而镓浓度在14天内持续上升。在24小时时脾脏中每种金属的浓度与将GaAs以25微摩尔添加到体外模型系统中时每种金属所达到的浓度相当。选择24小时这个时间点进行比较是因为所有体内-体外研究都是使用GaAs暴露后24小时的小鼠脾脏进行的。亚砷酸钠(NaAsO2)和硝酸镓(Ga(NO3)3)以剂量依赖性方式抑制AFC反应,并且当添加到体外系统中时,其抑制方式与GaAs类似,呈时间依赖性。然而,根据每种盐的半数抑制浓度(IC50)值,镓成分在免疫抑制中的作用似乎较弱。分别将草酸(OA)和中-2,3-二巯基丁二酸(DMSA)(镓和砷的螯合剂)添加到含有GaAs的培养物中,以确认砷是主要的免疫抑制成分。DMSA在体外剂量依赖性地阻断了GaAs诱导的免疫抑制,而OA没有效果。已确定这些金属结合化合物对本研究中使用的金属具有特异性,并且彼此之间不会发生交叉反应。对DMSA预防GaAs暴露小鼠脾细胞中AFC反应抑制的能力进行了评估,结果发现,从GaAs暴露前1小时开始每4小时皮下注射一次DMSA,能够阻断GaAs诱导的AFC反应抑制。这些数据表明,GaAs中的砷成分是GaAs诱导免疫抑制的主要因素,并且这种效应在5天培养期的前36小时内以浓度依赖性方式发生。

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