Department of Veterinary Biomedical Sciences, University of Saskatchewan, Saskatoon, Canada.
Reprod Biol Endocrinol. 2010 May 12;8:44. doi: 10.1186/1477-7827-8-44.
Previously, we documented the presence of ovulation-inducing factor (OIF) in the seminal plasma of llamas and alpacas. The purpose of the study was to define the biochemical characteristics of the molecule(s) in seminal plasma responsible for inducing ovulation.
In Experiment 1, llama seminal plasma was centrifuged using filtration devices with nominal molecular mass cut-offs of 30, 10 and 5 kDa. Female llamas (n = 9 per group) were treated i.m. with whole seminal plasma (positive control), phosphate-buffered saline (negative control), or the fraction of seminal plasma equal or higher than 30 kDa, 10 to 30 kDa, 5 to 10 kDa, or < 5 kDa. In Experiment 2, female llamas (n = 7 per group) were given an i.m. dose of seminal plasma treated previously by: 1) enzymatic digestion with proteinase-K, 2) incubation with charcoal-dextran, 3) heating to 65 degrees C, or 4) untreated (control). In Experiment 3, female llamas (n = 10 per group) were given an i.m. dose of pronase-treated or non-treated (control) seminal plasma. In all experiments, llamas were examined by transrectal ultrasonography to detect ovulation and CL formation. Ovulation rate was compared among groups by Fisher's exact test and follicle and CL diameters were compared among groups by analyses of variance or student's t-tests.
In Experiment 1, all llamas in the equal or higher than 30 kDa and positive control groups ovulated (9/9 in each), but none ovulated in the other groups (P < 0.001). In Experiment 2, ovulations were detected in all llamas in each treatment group; i.e., respective treatments of seminal plasma failed to inactivate the ovulation-inducing factor. In Experiment 3, ovulations were detected in 0/10 llamas given pronase-treated seminal plasma and in 9/10 controls (P < 0.01).
We conclude that ovulation-inducing factor (OIF) in llama seminal plasma is a protein molecule that is resistant to heat and enzymatic digestion with proteinase K, and has a molecular mass of approximately equal or higher than 30 kDa.
此前,我们曾在美洲驼精液中发现排卵诱导因子(OIF)。本研究旨在确定精液中诱导排卵的分子的生化特性。
在实验 1 中,使用截留分子量分别为 30、10 和 5 kDa 的过滤装置对美洲驼精液进行离心。9 只雌性美洲驼(每组 9 只)分别肌肉注射全精液(阳性对照)、磷酸盐缓冲液(阴性对照)或截留分子量大于 30 kDa、10-30 kDa、5-10 kDa 或小于 5 kDa 的精液部分。在实验 2 中,7 只雌性美洲驼(每组 7 只)接受了经以下处理的精液:1)蛋白酶 K 酶消化,2)用活性炭-葡聚糖孵育,3)加热至 65°C,或 4)未经处理(对照)。在实验 3 中,10 只雌性美洲驼(每组 10 只)接受了蛋白酶处理或未经处理(对照)的精液的肌内注射剂量。在所有实验中,通过直肠超声检查来检测排卵和黄体形成。通过 Fisher 精确检验比较各组的排卵率,通过方差分析或学生 t 检验比较各组的卵泡和黄体直径。
在实验 1 中,所有截留分子量大于等于 30 kDa 和阳性对照组的美洲驼都排卵(每组 9 只),但其他组无一排卵(P < 0.001)。在实验 2 中,所有处理组的美洲驼都发生了排卵,即精液的处理未能使排卵诱导因子失活。在实验 3 中,10 只接受蛋白酶处理的精液的美洲驼无一排卵,而 10 只对照的美洲驼均排卵(P < 0.01)。
我们得出结论,美洲驼精液中的排卵诱导因子(OIF)是一种对热和蛋白酶 K 酶消化具有抗性的蛋白质分子,其分子量约等于或大于 30 kDa。