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分泌促黄体生成素释放激素的乳腺癌Walker256/S导致的绝经后样骨质流失。

Postmenopause-like bone loss by mammary carcinoma Walker256/S which secretes luteinizing hormone-releasing hormone.

作者信息

Waki Y, Miyamoto K, Yamamoto S, Saitoh Y, Kasugai S, Ohya K

机构信息

Department of Pharmacology and Pharmaceutics, Graduate School of Natural Science and Technology, Kanazawa University, Japan.

出版信息

Jpn J Pharmacol. 1999 Jun;80(2):119-25. doi: 10.1254/jjp.80.119.

Abstract

When Walker 256/S carcinosarcoma (W256/S) was subcutaneously inoculated into the back of mature female Wistar Imamichi rats (10-week-old), the tumor grew rapidly and caused increases in the urinary excretions of calcium and hydroxyproline, without changes in the serum concentrations of calcium and inorganic phosphorus. Furthermore, osteoporosis-like changes in the femurs and decrease in uterus weight were observed, as previously reported for W256/S-bearing young rats. In the healthy mature female rats, the estrus cycle passed through four stages (proestrus, estrus, metestrus and diestrus) within 4 to 5 days, with a peak of serum estradiol and progesterone levels in the proestrus stage. On the other hand, after subcutaneous inoculation of W256/S into the rats, the estrus cycle tended to pause upon the metestrus or diestrus stage, accompanied with significantly low estradiol and progesterone levels in serum. W256/S tumor produced and secreted luteinizing hormone-releasing hormone (LH-RH). In conclusion, it seems that the ectopical secretion of LH-RH from the tumor resulted in the decrease in the secretion of gonadotropic hormones, following low level of sex hormones and stopping the estrus cycle. Therefore, W256/S-bearing rats may be a model for osteoporosis of hypoovarianism or postmenopause.

摘要

将Walker 256/S癌肉瘤(W256/S)皮下接种到成熟雌性Wistar Imamichi大鼠(10周龄)的背部时,肿瘤生长迅速,导致尿钙和羟脯氨酸排泄增加,而血清钙和无机磷浓度无变化。此外,观察到股骨出现类似骨质疏松的变化,子宫重量减轻,这与之前报道的携带W256/S的幼年大鼠情况相同。在健康的成熟雌性大鼠中,发情周期在4至5天内经历四个阶段(动情前期、动情期、动情后期和动情间期),动情前期血清雌二醇和孕酮水平达到峰值。另一方面,将W256/S皮下接种到大鼠体内后,发情周期往往在动情后期或动情间期暂停,同时血清中雌二醇和孕酮水平显著降低。W256/S肿瘤产生并分泌促黄体生成激素释放激素(LH-RH)。总之,肿瘤异位分泌LH-RH似乎导致促性腺激素分泌减少,随后性激素水平降低并使发情周期停止。因此,携带W256/S的大鼠可能是卵巢功能减退或绝经后骨质疏松的模型。

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