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用环磷酰胺和/或促性腺激素释放激素激动剂处理的雌性大鼠的生殖性能。

Reproductive performance of female rats treated with cyclophosphamide and/or LHRH agonist.

作者信息

Ataya K, Ramahi-Ataya A

机构信息

Department of Obstetrics and Gynecology, MetroHealth Medical Center/Case Western Reserve University, Cleveland, Ohio 44109-1998.

出版信息

Reprod Toxicol. 1993 May-Jun;7(3):229-35. doi: 10.1016/0890-6238(93)90229-z.

Abstract

Previous studies addressing the ovarian protective effects of luteinizing hormone releasing hormone agonists (LHRHa) against adverse effects of chemotherapy have examined histologic and/or hormonal parameters without evaluating reproductive performance. In this report, we initially established a model for chronic treatment of female rats with cyclophosphamide (CTX) that allowed long term survival. In a second experiment, thirty seven female cycling rats (age: 70 days) were divided into 4 treatment groups. They were given either CTX (4 mg/kg/day, 5 days/week) for a total of 76 days (217 mg/kg) and/or the LHRHa leuprolide (Lupron) 5 micrograms/day by subcutaneous minipump (Alza) for 98 days. LHRHa was started 10 days before CTX and ended 12 days after the last CTX injection. All LHRHa-treated rats entered persistent diestrus. At the end of treatment, most rats treated with CTX only were in persistent estrus. Breeding was started at 218 days of age. A laparotomy to count implantation sites was performed 15 to 16 days after vaginal plug/sperm was demonstrated. All nonpregnant rats were remated. Chi square and ANOVA were used for statistical analysis. The data presented demonstrate that: 1. LHRHa given before and after CTX increased the pregnancy rate/mating (from 4/11 to 9/10; P < 0.05), the number of implantations/mated rat (from 2.5 +/- 1.4 to 13.7 +/- 1.7; P < 0.01), and reduced the need for remating (from 7/11 to 1/10; P < 0.05); 2. LHRHa-treated rats performed better than controls. We conclude that LHRHa protects against chemotherapy-induced fertility reduction in female rats.

摘要

以往关于促黄体生成素释放激素激动剂(LHRHa)对化疗不良反应的卵巢保护作用的研究,仅检测了组织学和/或激素参数,而未评估生殖性能。在本报告中,我们首先建立了一个用环磷酰胺(CTX)长期治疗雌性大鼠的模型,该模型能使大鼠长期存活。在第二个实验中,37只处于发情周期的雌性大鼠(年龄:70天)被分为4个治疗组。它们分别接受CTX(4毫克/千克/天,每周5天),共76天(217毫克/千克),和/或通过皮下微型泵(阿尔扎公司)给予LHRHa亮丙瑞林(抑那通)5微克/天,持续98天。LHRHa在CTX治疗前10天开始给药,并在最后一次CTX注射后12天结束。所有接受LHRHa治疗的大鼠都进入了持续的间情期。治疗结束时,大多数仅接受CTX治疗的大鼠处于持续发情期。在218日龄时开始繁殖。在确认出现阴道栓/精子后的15至16天进行剖腹手术以计数着床点。所有未怀孕的大鼠再次交配。采用卡方检验和方差分析进行统计分析。所呈现的数据表明:1. 在CTX治疗前后给予LHRHa可提高妊娠率/交配率(从4/11提高到9/10;P<0.05),每只交配大鼠的着床数(从2.5±1.4提高到13.7±1.7;P<0.01),并减少再次交配的需求(从7/11减少到1/10;P<0.05);2. 接受LHRHa治疗的大鼠比对照组表现更好。我们得出结论,LHRHa可预防化疗引起的雌性大鼠生育力下降。

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