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J Am Assoc Lab Anim Sci. 2020 May 1;59(3):282-287. doi: 10.30802/AALAS-JAALAS-19-000112. Epub 2020 Apr 2.
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本文引用的文献

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Vaginal Cytology of the Laboratory Rat and Mouse: Review and Criteria for the Staging of the Estrous Cycle Using Stained Vaginal Smears.实验大鼠和小鼠的阴道细胞学:使用染色阴道涂片对发情周期进行分期的综述及标准
Toxicol Pathol. 2015 Aug;43(6):776-93. doi: 10.1177/0192623315570339. Epub 2015 Mar 3.
2
Policy: NIH to balance sex in cell and animal studies.政策:NIH 将在细胞和动物研究中平衡性别。
Nature. 2014 May 15;509(7500):282-3. doi: 10.1038/509282a.
3
Administration of luteinizing hormone releasing hormone agonist for synchronization of estrus and generation of pseudopregnancy for embryo transfer in rats.使用促黄体生成素释放激素激动剂使大鼠发情同步并诱导假孕以用于胚胎移植。
J Am Assoc Lab Anim Sci. 2014 May;53(3):232-7.
4
Female mice liberated for inclusion in neuroscience and biomedical research.被释放用于神经科学和生物医学研究的雌性小鼠。
Neurosci Biobehav Rev. 2014 Mar;40:1-5. doi: 10.1016/j.neubiorev.2014.01.001. Epub 2014 Jan 20.
5
Estrus cycle status defined by vaginal cytology does not correspond to fluctuations of circulating estrogens in female mice.阴道细胞学定义的发情周期状态与雌性小鼠循环雌激素的波动不对应。
Shock. 2014 Feb;41(2):145-53. doi: 10.1097/SHK.0000000000000070.
6
Gene-manipulated embryonic stem cells for rat transgenesis.基因修饰的胚胎干细胞用于大鼠转基因。
Cell Mol Life Sci. 2011 Jun;68(11):1911-5. doi: 10.1007/s00018-011-0669-7. Epub 2011 Mar 25.
7
Sex bias in neuroscience and biomedical research.神经科学和生物医学研究中的性别偏见。
Neurosci Biobehav Rev. 2011 Jan;35(3):565-72. doi: 10.1016/j.neubiorev.2010.07.002. Epub 2010 Jul 8.
8
The female rat reproductive cycle: a practical histological guide to staging.雌性大鼠生殖周期:分期的实用组织学指南。
Toxicol Pathol. 2008 Apr;36(3):375-84. doi: 10.1177/0192623308315665. Epub 2008 Apr 25.
9
The rodent estrous cycle: characterization of vaginal cytology and its utility in toxicological studies.啮齿动物的发情周期:阴道细胞学特征及其在毒理学研究中的应用。
Birth Defects Res B Dev Reprod Toxicol. 2007 Apr;80(2):84-97. doi: 10.1002/bdrb.20106.
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Synchronization of ovulation in dairy cows using PGF2alpha and GnRH.使用前列腺素F2α和促性腺激素释放激素同步奶牛排卵
Theriogenology. 1995 Nov;44(7):915-23. doi: 10.1016/0093-691x(95)00279-h.

应用阴道阻抗测量法鉴定给予促黄体激素释放激素(LHRH)激动剂的大鼠动情前期。

Using Vaginal Impedance Measurement to Identify Proestrus in Rats Given Luteinizing Hormone Releasing Hormone (LHRH) Agonist.

机构信息

Comparative Medicine Program, University of Missouri, Columbia, Missouri; Department of Veterinary Pathobiology, University of Missouri, Columbia, Missouri.

Veterinary Research Scholars Program, University of Missouri, Columbia, Missouri.

出版信息

J Am Assoc Lab Anim Sci. 2020 May 1;59(3):282-287. doi: 10.30802/AALAS-JAALAS-19-000112. Epub 2020 Apr 2.

DOI:10.30802/AALAS-JAALAS-19-000112
PMID:32241334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7210735/
Abstract

Vaginal cytology is the most common method of monitoring the estrous cycle in rats; however, this test requires specific technical training and can be subject to interpretation. Vaginal impedance offers a quicker and less technically challenging alternative and has been used successfully to identify estrus in normally cycling breeder rats. We hypothesize that vaginal impedance can also be used to stage the estrous cycle in rats that have been given luteinizing hormone releasing hormone (LHRH) for timed mating. Vaginal impedance measurements and vaginal cytology were performed in LHRH-primed female rats ( = 36) at the expected peak of proestrus and paired with proven stud males. Breeding success was determined by gross necropsy to detect embryo implantation sites in the female rats. We found that the predictive rates of vaginal cytology and impedance measurement for proestrus were similar; however, both methods resulted in high proportions of false positive and false negative determinations (28% and 31%, respectively). We further hypothesized that females respond to LHRH at variable rates, resulting in variable times of peak proestrus. To test this, vaginal impedance measurements were performed multiple times throughout the expected day of proestrus in LHRH-primed female rats ( = 36). Females were either paired with a male 24 h after reaching the proestrus threshold ( = 18) or paired according to our standard protocol at 1300 h on the day after the expected proestrus ( = 18). Sequential measurements reduced false positive and negative rates (14% and 8%, respectively). Pregnancy rates did not differ based on the time of pairing during expected estrus. Overall, we determined vaginal impedance can be more successful than vaginal cytology at identifying proestrus in the rat, but only if multiple measurements are taken.

摘要

阴道细胞学是监测大鼠发情周期最常用的方法;然而,这种测试需要特定的技术培训,并且可能存在解释上的差异。阴道阻抗提供了一种更快、技术要求更低的替代方法,并已成功用于识别正常发情的繁殖大鼠的发情期。我们假设阴道阻抗也可用于对已给予促黄体激素释放激素 (LHRH) 进行定时交配的大鼠进行发情期分期。在预期发情前期高峰时,对接受 LHRH 刺激的雌性大鼠 (n = 36) 进行阴道阻抗测量和阴道细胞学检查,并与已证明的雄性大鼠配对。通过大体解剖检查雌性大鼠以检测胚胎植入部位来确定繁殖成功率。我们发现,阴道细胞学和阻抗测量预测发情前期的准确率相似;然而,这两种方法都导致了高比例的假阳性和假阴性结果(分别为 28%和 31%)。我们进一步假设,雌性对 LHRH 的反应速度不同,导致发情前期高峰的时间不同。为了验证这一点,我们对接受 LHRH 刺激的雌性大鼠 (n = 36) 在预期发情前期的整个期间多次进行阴道阻抗测量。在达到发情前期阈值后 24 小时 (n = 18),或根据我们的标准方案在预期发情前期后的 1300 小时 (n = 18),与雄性大鼠配对。连续测量降低了假阳性和假阴性的比例(分别为 14%和 8%)。根据预期发情期的配对时间,妊娠率没有差异。总体而言,我们确定阴道阻抗比阴道细胞学更能成功地识别大鼠的发情前期,但前提是要进行多次测量。