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首页> 外文期刊>The Journal of Reproduction and Development >In Vitro Assessment of Progesterone and Prostaglandin E-2 Production by the Corpus Luteum in Cattle Following Pharmacological Synchronization of Estrus
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In Vitro Assessment of Progesterone and Prostaglandin E-2 Production by the Corpus Luteum in Cattle Following Pharmacological Synchronization of Estrus

机译:发情期药理学同步后,黄体中牛黄体对孕激素和前列腺素E-2产生的体外评估

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We studied the secretory function of the corpus luteum (CL) in cows following different estrus synchronization protocols. Estrus was synchronized using one (n=4) or two injections (n=5) of prostaglandin F-2 alpha (PGF(2 alpha); dinoprost), two injections of different analogues of PGF(2 alpha) (aPGF(2 alpha)), luprostiol (n=5) and cloprostenol (n=5), at eleven-day intervals, a gestagen implant (norgestomet, n=5, for 10 days) or norgestomet together with a subsequent dinoprost injection on the day of implant removal (n=5). CL samples were collected by ovariectomy on Day 7-8 of the estrous cycle. Luteal strips were stimulated with LH (100 ng/ml) or prostaglandin E-2 (PGE(2), 10(-6)M) for 24 h in culture media. The progesterone (P-4) and PGE(2) concentrations in the media were measured by enzyme immunoassay. In the control CL (spontaneous estrus; n=5), LH and PGE(2) stimulated P-4 and PGE(2) (P<0.001). The effects of both factors on P-4 were reduced in the CL following dinoprost- and cloprostenol-synchronized estrus (P<0.05) and were absent in the luprostiol-synchronized CL (P>0.05). In the norgestomet-synchronized CL, the stimulatory effects of LH and PGE(2) were higher compared with the CL synchronized by aPGF(2 alpha) (P<0.05). Pharmacological manipulation of the estrous cycle using aPGF(2 alpha) may cause lower P-4 secretion. Estrus synchronization inhibited CL sensitivity to luteotropic factors. Therefore, attention should be focused on the estrous synchronization method in both in vivo and in vitro studies of CL functions in cattle.
机译:我们研究了遵循不同发情同步协议的牛黄体(CL)的分泌功能。使用一(n = 4)或两次注射(n = 5)前列腺素F-2 alpha(PGF(2 alpha);地诺前列素),两次注射PGF(2 alpha)的不同类似物(aPGF(2 alpha) )),以每11天一次的间隔注射Luprostiol(n = 5)和Cloprostenol(n = 5),孕激素植入剂(norgestomet,n = 5,持续10天)或Norgestomet并在植入当天进行随后的地诺前列素注射去除(n = 5)。在发情周期的第7-8天通过卵巢切除术收集CL样品。黄体带用LH(100 ng / ml)或前列腺素E-2(PGE(2),10(-6)M)在培养基中刺激24 h。通过酶免疫法测定培养基中的孕酮(P-4)和PGE(2)浓度。在对照CL(自发发情; n = 5)中,LH和PGE(2)刺激了P-4和PGE(2)(P <0.001)。在狄诺前列素和氯前列腺素同步发情后,CL中两种因子对P-4的影响均降低(P <0.05),而在与前列腺素同步化的CL中则不存在(P> 0.05)。在norgestomet同步的CL,与aPGF(2 alpha)同步的CL相比,LH和PGE(2)的刺激作用更高(P <0.05)。使用aPGF(2 alpha)的发情周期的药理学操作可能会导致P-4分泌降低。发情同步抑制了CL对嗜水因子的敏感性。因此,在牛体内CL功能的体内和体外研究中,应将注意力集中在发情同步方法上。

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