Martinez M F, Kastelic J P, Adams G P, Mapletoft R J
Department of Large Animal Clinical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, 52 Campus Drive, Saskatoon, Sask., S7N 5B4, Canada.
Anim Reprod Sci. 2001 Sep 15;67(3-4):221-9. doi: 10.1016/s0378-4320(01)00128-2.
Two experiments were conducted to compare pregnancy rates when GnRH or estradiol were given to synchronize ovarian follicular wave emergence and ovulation in an MGA-based estrus synchronization program. Crossbred beef cattle were fed melengestrol acetate (MGA, 0.5 mg per day) for 7 days (designated days 0-6, without regard to stage of the estrous cycle) and given cloprostenol (PGF; 500 microg intramuscular (im)) on day 7. In Experiment 1, lactating beef cows (n=140) and pubertal heifers (n=40) were randomly allocated to three groups to receive 100 microg gonadorelin (GnRH), 5 mg estradiol-17beta and 100 mg progesterone (E+P) in canola oil or no treatment (control) on day 0. All cattle were observed for estrus every 12 h from 36 to 96 h after PGF. Cattle in the GnRH group that were detected in estrus 36 or 48 h after PGF were inseminated 12 h later; the remainder were given 100 microg GnRH im 72 h after PGF and concurrently inseminated. Cattle in the E+P group were randomly assigned to receive either 0.5 or 1.0 mg estradiol benzoate (EB) in 2 ml canola oil im 24 h after PGF and were inseminated 30 h later. Cattle in the control group were inseminated 12 h after the first detection of estrus; if not in estrus by 72 h after PGF, they were given 100 microg GnRH im and concurrently inseminated. In the absence of significant differences, all data for heifers and for cows were combined and the 0.5 and 1.0 mg EB groups were combined into a single estradiol group. Estrus rates were 57.6, 57.4 and 60.0% for the GnRH, E+P and control groups, respectively (P=0.95). The mean (+/-S.D.) interval from PGF treatment to estrus was shorter (P<0.001) and less variable (P<0.001) in the E+P group (49.0+/-6.1 h) than in either the GnRH (64.2+/-15.9 h) or control (66.3+/-13.3 h) groups. Overall pregnancy rates were higher (P<0.005) in the GnRH (57.6%) and E+P (55.7%) groups than in the control group (30.0%) as were pregnancy rates to fixed-time AI (47.5, 55.7 and 28.3%, respectively). In Experiment 2, 122 crossbred beef heifers were given either 100 microg GnRH or 2 mg EB and 50 mg progesterone in oil on day 0 and subsequently received either 100 microg GnRH 36 h after PGF and inseminated 14 h later or 1 mg EB im 24 h after PGF and inseminated 28 h later in a 2 x 2 factorial design. Pregnancy rates were not significantly different among groups (41.9, 32.2, 33.3 and 36.7% in GnRH/GnRH, GnRH/EB, EB/GnRH and EB/EB groups, respectively). In conclusion, GnRH or estradiol given to synchronize ovarian follicular wave emergence and ovulation in an MGA-based synchronization regimen resulted in acceptable pregnancy rates to fixed-time insemination.
进行了两项试验,以比较在基于醋酸甲地孕酮(MGA)的发情同步程序中,使用促性腺激素释放激素(GnRH)或雌二醇来同步卵巢卵泡波出现和排卵时的妊娠率。杂种肉牛每天饲喂醋酸甲地孕酮(MGA,0.5毫克),持续7天(指定为第0 - 6天,不考虑发情周期阶段),并在第7天注射氯前列醇(PGF;500微克,肌肉注射)。在试验1中,泌乳母牛(n = 140)和青春期小母牛(n = 40)被随机分为三组,在第0天分别接受100微克促性腺激素释放激素(GnRH)、5毫克17β - 雌二醇和100毫克孕酮(E + P)的菜籽油制剂或不进行处理(对照组)。从PGF处理后36至96小时开始,每隔12小时观察所有牛的发情情况。PGF处理后36或48小时检测到发情的GnRH组牛,在12小时后进行输精;其余牛在PGF处理后72小时肌肉注射100微克GnRH,并同时进行输精。E + P组的牛在PGF处理后24小时被随机分配接受2毫升菜籽油中0.5或1.0毫克苯甲酸雌二醇(EB)的肌肉注射,并在30小时后进行输精。对照组的牛在首次检测到发情后12小时进行输精;如果在PGF处理后72小时仍未发情,则肌肉注射100微克GnRH并同时进行输精。在无显著差异的情况下,将小母牛和母牛的所有数据合并,0.5毫克和1.0毫克EB组合并为一个雌二醇组。GnRH组、E + P组和对照组的发情率分别为57.6%、57.4%和60.0%(P = 0.95)。与GnRH组(64.2±15.9小时)或对照组(66.3±13.3小时)相比,E + P组(49.0±6.1小时)从PGF处理到发情的平均(±标准差)间隔更短(P < 0.001)且变异性更小(P < 0.001)。GnRH组(57.6%)和E + P组(55.7%)的总体妊娠率高于对照组(30.0%),定时输精后的妊娠率也更高(分别为47.5%、55.7%和28.3%)。在试验2中,122头杂种肉牛小母牛在第0天接受100微克GnRH或2毫克EB和50毫克油剂孕酮,随后在PGF处理后36小时接受100微克GnRH并在14小时后输精,或在PGF处理后24小时肌肉注射1毫克EB并在28小时后输精,采用2×2析因设计。各组妊娠率无显著差异(GnRH/GnRH组、GnRH/EB组、EB/GnRH组和EB/EB组分别为41.9%、32.2%、33.3%和36.7%)。总之,在基于MGA的同步方案中,使用GnRH或雌二醇来同步卵巢卵泡波出现和排卵,定时输精后的妊娠率是可以接受的。