Fiala Sandra Mara, Pimentel Cláudio Alves, Mattos Ana Luiza Gelpi, Gregory Ricardo Macedo, Mattos Rodrigo Costa
Reprolab-Departamento de Medicina Animal, Faculdade de Veterinária, UFRGS, Caixa Postal 15039, 91501-970 Porto Alegre, RS, Brazil.
Theriogenology. 2007 Feb;67(3):556-62. doi: 10.1016/j.theriogenology.2006.09.005. Epub 2006 Oct 10.
Our objective was to determine whether the concentration of cooled sperm inseminated influenced sperm transport and intensity of the uterine inflammatory reaction 2, 4 and 24h after insemination. Experimental subjects were 189 estrous mares with a dominant follicle > or =35 mm in diameter and no bacterial growth or neutrophils detected in uterine smears. Each mare was randomly assigned to receive one of the following intrauterine treatments (volume, 20 mL): insemination with 5x10(6) mL(-1) or 25x10(6) mL(-1) or 50x10(6) mL(-1) sperm diluted in 3 mL seminal plasma (SP) and 17 mL skim milk; seminal plasma or skim milk extender. Mares in a control group received no intrauterine treatment. Mares were slaughtered 2, 4 or 24h after insemination or infusion. Oviducts were separated from the uterus, and uterus and oviducts were then flushed with phosphate-buffered saline (PBS). After flushing, an endometrial sample was collected for further histopathological examination. The grade of uterine fibrosis and the amount of neutrophils in the stratum compactum were evaluated. A sample of each tubal flushing was examined for sperm count, and a sample of each uterine flushing was examined for PMN count. It was concluded that compounds in the insemination dose provoked a uterine inflammatory response, which was more rapid and intense as sperm concentration increased. In contrast, sperm transport through 4h after insemination was not influenced by sperm concentration.
我们的目的是确定授精时输入的冷冻精液浓度是否会影响授精后2小时、4小时和24小时的精子运输以及子宫炎症反应的强度。实验对象为189匹处于发情期的母马,其优势卵泡直径≥35毫米,子宫涂片未检测到细菌生长或中性粒细胞。每匹母马随机接受以下子宫内处理之一(体积为20毫升):用5×10⁶毫升⁻¹或25×10⁶毫升⁻¹或50×10⁶毫升⁻¹的精子在3毫升精浆(SP)和17毫升脱脂乳中稀释后进行授精;精浆或脱脂乳稀释液。对照组的母马不进行子宫内处理。母马在授精或灌注后2小时、4小时或24小时被屠宰。将输卵管与子宫分离,然后用磷酸盐缓冲盐水(PBS)冲洗子宫和输卵管。冲洗后,采集子宫内膜样本进行进一步的组织病理学检查。评估子宫纤维化程度和致密层中的中性粒细胞数量。对每个输卵管冲洗样本进行精子计数检查,对每个子宫冲洗样本进行PMN计数检查。得出的结论是,授精剂量中的化合物引发了子宫炎症反应,随着精子浓度的增加,炎症反应更快、更强烈。相比之下,授精后4小时内的精子运输不受精子浓度的影响。