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滴滴涕的雌激素活性:雌激素受体谱及施用邻,对'-滴滴涕后单个子宫细胞类型的反应。

Estrogenic activity of DDT: estrogen-receptor profiles and the responses of individual uterine cell types following o,p'-DDT administration.

作者信息

Robison A K, Schmidt W A, Stancel G M

出版信息

J Toxicol Environ Health. 1985;16(3-4):493-508. doi: 10.1080/15287398509530758.

Abstract

The administration of o,p'-dichlorodiphenyltrichloroethane (o,p'-DDT) to immature rats stimulates DNA synthesis and cell division in the uterine luminal epithelium (LE), stroma (S), and myometrium (M). The time course of DNA synthesis/cell division in the S and M is similar following administration of o,p'-DDT or 17 beta-estradiol, but the maximum response following pesticide treatment is only 70% of that produced by the hormone. In the LE both compounds yield the same maximum response, but the time course of DNA synthesis/cell division is delayed following o,p'-DDT administration relative to 17 beta-estradiol treatment. The patterns of estrogen receptor retention in uterine nuclei following o,p'-DDT administration are prolonged relative to those observed after 17 beta-estradiol treatment. o,p'-DDT thus produces the uterine hyperplasia characteristic of estrogens, but the magnitude and timing of the response is dependent on the specific cell type observed and is different from that produced by estradiol.

摘要

给未成熟大鼠施用邻,对'-二氯二苯三氯乙烷(o,p'-滴滴涕)可刺激子宫腔上皮(LE)、基质(S)和肌层(M)中的DNA合成和细胞分裂。施用o,p'-滴滴涕或17β-雌二醇后,S和M中DNA合成/细胞分裂的时间进程相似,但农药处理后的最大反应仅为激素产生反应的70%。在LE中,两种化合物产生相同的最大反应,但相对于17β-雌二醇处理,施用o,p'-滴滴涕后DNA合成/细胞分裂的时间进程延迟。相对于17β-雌二醇处理后观察到的情况,施用o,p'-滴滴涕后子宫核中雌激素受体保留的模式延长。因此,o,p'-滴滴涕产生了雌激素特有的子宫增生,但反应的程度和时间取决于所观察的特定细胞类型,并且与雌二醇产生的情况不同。

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