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d-柠檬烯在α2u-球蛋白转基因小鼠中诱发了透明滴状肾病。

d-Limonene induced hyaline droplet nephropathy in alpha 2u-globulin transgenic mice.

作者信息

Lehman-McKeeman L D, Caudill D

机构信息

Miami Valley Laboratories, Procter & Gamble Company, Cincinnati, Ohio 45239-8707.

出版信息

Fundam Appl Toxicol. 1994 Nov;23(4):562-8. doi: 10.1006/faat.1994.1141.

Abstract

d-Limonene is a hyaline droplet inducing agent and produces nephrotoxicity in male rats when the 1,2-epoxide metabolite binds to alpha 2u-globulin. Mice, which do not synthesize alpha 2u-globulin, are resistant to hyaline droplet nephropathy. In this study, the ability of d-limonene to cause hyaline droplet nephropathy in a transgenic mouse engineered to express alpha 2u-globulin was evaluated. The C57BL/6-derived mice excreted 0.4 +/- 0.1 mg alpha 2u-globulin/day, or approximately 16 mg alpha 2u-globulin/kg body wt. This represents about 30% of the amount excreted by adult male rats (11.9 +/- 1.1 mg/day or approximately 48 mg/kg). Transgenic mice excreted less mouse urinary protein (9.3 +/- 1.2 mg/day) than normal mice (15.1 +/- 1.6 mg/day). Unlike normal male rats, untreated transgenic mice did not show significant spontaneous hyaline droplet formation. Liver microsomes from naive transgenic mice oxidized d-limonene to the cis- and transisomers of the 1,2-epoxide, and following oral treatment with [14C]d-limonene reversible binding of d-limonene equivalents to renal cytosolic proteins was observed. Furthermore, with d-limonene treatment, hyaline droplets were observed in the transgenic mouse kidneys. These droplets, however, were much smaller in size than those seen in d-limonene-treated male rats. The accumulation of alpha 2u-globulin in the kidneys of transgenic mice and normal male rats before and after d-limonene treatment was analyzed by Western blotting. These results indicated that alpha 2u-globulin was present in the kidneys of the control transgenic mice, despite the lack of spontaneous hyaline droplet formation. After d-limonene treatment, approximately a three-fold increase in alpha 2u-globulin in the transgenic mouse kidney was observed, a response similar in magnitude to that seen in d-limonene-treated male rats. These results indicate that expression of alpha 2u-globulin in a species that does not normally develop hyaline droplet nephropathy is necessary and sufficient to render that species sensitive to this renal toxicity.

摘要

d-苎烯是一种可诱导透明滴形成的物质,当1,2-环氧化物代谢产物与α2u-球蛋白结合时,会在雄性大鼠中产生肾毒性。不合成α2u-球蛋白的小鼠对透明滴肾病具有抗性。在本研究中,评估了d-苎烯在经基因工程改造以表达α2u-球蛋白的转基因小鼠中引发透明滴肾病的能力。源自C57BL/6的小鼠每天排泄0.4±0.1毫克α2u-球蛋白,即约16毫克α2u-球蛋白/千克体重。这约为成年雄性大鼠排泄量(11.9±1.1毫克/天或约48毫克/千克)的30%。转基因小鼠排泄的小鼠尿蛋白(9.3±1.2毫克/天)比正常小鼠(15.1±1.6毫克/天)少。与正常雄性大鼠不同,未经处理的转基因小鼠未显示出明显的自发性透明滴形成。来自未接触过d-苎烯的转基因小鼠的肝微粒体将d-苎烯氧化为1,2-环氧化物的顺式和反式异构体,并且在用[14C]d-苎烯口服处理后,观察到d-苎烯等效物与肾细胞溶质蛋白的可逆结合。此外,经d-苎烯处理后,在转基因小鼠肾脏中观察到透明滴。然而,这些滴的尺寸比在经d-苎烯处理的雄性大鼠中看到的要小得多。通过蛋白质免疫印迹法分析了d-苎烯处理前后转基因小鼠和正常雄性大鼠肾脏中α2u-球蛋白的积累情况。这些结果表明,尽管缺乏自发性透明滴形成,但α2u-球蛋白仍存在于对照转基因小鼠的肾脏中。经d-苎烯处理后,观察到转基因小鼠肾脏中α2u-球蛋白增加了约三倍,这一反应的幅度与在经d-苎烯处理的雄性大鼠中看到的相似。这些结果表明,在通常不会发生透明滴肾病的物种中表达α2u-球蛋白对于使该物种对这种肾毒性敏感是必要且充分的。

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