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氯菊酯对大鼠潜在的雌激素和抗雄激素作用。

Potential estrogenic and antiandrogenic effects of permethrin in rats.

作者信息

Kim Soon-Sun, Lee Rhee-Da, Lim Kwon-Jo, Kwack Seung-Jun, Rhee Gyu-Seek, Seok Ji-Hyun, Lee Geun-Shik, An Beum-Soo, Jeung Eui-Bae, Park Kui-Lea

机构信息

National Institute of Toxicological Research, Korea Food and Drug Administration, Seoul, Korea.

出版信息

J Reprod Dev. 2005 Apr;51(2):201-10. doi: 10.1262/jrd.16060. Epub 2004 Dec 15.

Abstract

Many environmental chemicals including pesticides have been reported to possess hormonal activities, and thus are classified as endocrine disruptors. Permethrin, a synthetic pyrethroid insecticide, is used worldwide, which provides potential environmental exposure. However, relatively few studies have reported on hormonal activities, particularly estrogenic and androgenic activities of permethrin, and the results of these studies are in some respects contradictory. Therefore, this study investigated the potential estrogenic and androgenic activities of permethrin in vitro and in vivo. We conducted an uterine Calbindin-D9k (CaBP-9k) gene expression assay and an uterotrophic assay for estrogenic activity, and a Hershberger assay for androgenic activity. The CaBP-9k gene, one of the intracellular calcium binding proteins, is estrogen-responsive in the uterus. The rat uterotrophic and Hershberger assays are generally used as in vivo short-term screening assays for detecting the estrogenic and androgenic activities of chemicals, although these assays are still being validated by the Organization for Economic Cooperation and Development (OECD). Northern blot analysis showed the induction of uterine CaBP-9k mRNA level in response to permethrin as well as co-administration of permethrin with E2. In the uterotrophic assay using 18-day-old female rats, subcutaneous treatments with permethrin (10 to 800 mg/kg) for three days increased relative uterine wet weights, and E2-induced uterine weights. These effects were statistically significant at 800 and 200 mg/kg, respectively. Moreover, permethrin-induced uterine weights were inhibited by the co-administration of ICI 182,780, an antiestrogen. In the Hershberger assay, the administration of permethrin orally to testosterone propionate-treated castrated male rats led to statistically significant reductions in androgen-dependent sex accessory tissue (ventral prostate, seminal vesicles, levator ani and bulbocavernosus muscles, Cowper's gland and glans penis) weights at all doses tested (10, 50 and 100 mg/kg). These results suggest that permethrin might have estrogen-like effects on female rats, but antiandrogen-like effects on males.

摘要

据报道,包括农药在内的许多环境化学物质都具有激素活性,因此被归类为内分泌干扰物。氯菊酯是一种合成拟除虫菊酯类杀虫剂,在全球范围内广泛使用,这增加了潜在的环境暴露风险。然而,关于氯菊酯激素活性的研究相对较少,尤其是其雌激素和雄激素活性,且这些研究结果在某些方面相互矛盾。因此,本研究在体外和体内考察了氯菊酯的潜在雌激素和雄激素活性。我们进行了子宫钙结合蛋白-D9k(CaBP-9k)基因表达试验和子宫增重试验以检测雌激素活性,以及赫什伯格试验以检测雄激素活性。CaBP-9k基因是一种细胞内钙结合蛋白,在子宫中对雌激素有反应。大鼠子宫增重试验和赫什伯格试验通常用作体内短期筛选试验,以检测化学物质的雌激素和雄激素活性,尽管经济合作与发展组织(OECD)仍在对这些试验进行验证。Northern印迹分析表明,氯菊酯以及氯菊酯与E2共同给药均可诱导子宫CaBP-9k mRNA水平升高。在使用18日龄雌性大鼠的子宫增重试验中,皮下注射氯菊酯(10至800 mg/kg)三天可增加相对子宫湿重,并增强E2诱导的子宫重量增加。这些效应在800 mg/kg和200 mg/kg时分别具有统计学意义。此外,ICI 182,780(一种抗雌激素药物)共同给药可抑制氯菊酯诱导的子宫重量增加。在赫什伯格试验中,对丙酸睾酮处理的去势雄性大鼠口服氯菊酯,在所有测试剂量(10、50和100 mg/kg)下均导致雄激素依赖性性附属组织(腹侧前列腺、精囊、提肛肌和球海绵体肌、尿道球腺和阴茎头)重量出现统计学显著降低。这些结果表明,氯菊酯可能对雌性大鼠具有雌激素样作用,但对雄性大鼠具有抗雄激素样作用。

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