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在斯普拉格-道利大鼠乳腺肿瘤诱导过程中,7,12-二甲基苯并(a)蒽对雌二醇-17β分泌的刺激作用。

Stimulation of estradiol-17 beta secretion by 7,12-dimethylbenz (a) anthracene during mammary tumor induction in Sprague-Dawley rats.

作者信息

el Abed A, Kerdelhue B, Castanier M, Scholler R

出版信息

J Steroid Biochem. 1987 Jun;26(6):733-8. doi: 10.1016/0022-4731(87)91047-8.

Abstract

Testosterone, androstenedione, progesterone, 17-hydroxyprogesterone, estrone and estradiol-17 beta serum levels were measured at given times after dimethylbenz (a) anthracene (DMBA) treatment of a sensitive rat strain Sprague-Dawley (S-D) and a resistant strain Wistar (W). Tumors appeared with a 100% incidence around the 14th to 15th estrous cycle after DMBA treatment in in Sprague-Dawley rats. Hormonal determinations were made, during the 5th or 6th estrous cycle after DMBA treatment, in groups of 4-day cycling rats of both strains which were given DMBA or the carrier solution (sesame oil) when they were about 55-days old. In Sprague-Dawley female rats, DMBA treatment significantly stimulated estradiol-17 beta and estrone preovulatory surge on proestrous days. No such stimulation was found for any other steroid at any time of the estrous cycle. On the other hand, the resistant Wistar rats did not show any disturbed preovulatory or basal steroid hormone release after the carcinogen treatment. These results complete and explain previous findings concerning the hypothalamo-pituitary activity after DMBA treatment of S-D rats: an early and persistent alteration in the centers involved in the hormonal cyclicity of the hypothalamo-pituitary-ovarian axis must be a result of the DMBA treatment. This deregulation could probably account for the distant and selective production of tumors in the mammary gland induced by a single gastric administration of DMBA.

摘要

在用二甲基苯并(a)蒽(DMBA)处理敏感大鼠品系斯普拉格-道利(S-D)和抗性品系威斯塔(W)后的特定时间,测定血清睾酮、雄烯二酮、孕酮、17-羟孕酮、雌酮和雌二醇-17β水平。在DMBA处理后的第14至15个动情周期左右,斯普拉格-道利大鼠的肿瘤发生率达100%。在DMBA处理后的第5或6个动情周期,对两品系4天一个动情周期的大鼠进行激素测定,这些大鼠在约55日龄时给予DMBA或载体溶液(芝麻油)。在斯普拉格-道利雌性大鼠中,DMBA处理显著刺激了动情前期雌二醇-17β和雌酮的排卵前激增。在动情周期的任何时间,未发现其他类固醇有此类刺激。另一方面,抗性威斯塔大鼠在致癌物处理后未表现出任何排卵前或基础类固醇激素释放紊乱。这些结果完善并解释了先前关于DMBA处理S-D大鼠后下丘脑-垂体活动的研究结果:参与下丘脑-垂体-卵巢轴激素周期性的中枢早期和持续改变必定是DMBA处理的结果。这种失调可能是单次胃内给予DMBA诱导乳腺远处和选择性肿瘤产生的原因。

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