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1.
牛促黄体素(bLH)同源放射免疫分析法的建立   总被引:2,自引:2,他引:0  
本实验用兔抗牛LH血清、~(125)I-标记的牛LH建立牛LH的放射免疫分析法。本方法灵敏度为0.12ng USDA-bLH-B-5/ml,与NIH-bTSH-S_(10),USDA-bFSH-BP_3和oPRL的交叉反应分别小于1.0%,0.1%和0。牛血浆添加USDA-bLH-B-5的回收率为100.8±4.7%,标准曲线的范围为0.019-1.25ng USDA-bLH-B-5。组内变异系数为3.4%(n=20)、组间变异系数为5.2%(n=7)。垂体兴奋试验表明本方法能灵敏、特异地测定出牛血液中LH的变化。  相似文献   

2.
本试验以假孕大鼠卵巢组织匀浆作 LH/HCG受体建立了 bLH/HCG放射受体分析法(RRA)。bLH和HCG的剂量反应曲线平行,灵敏度分别为0.1ng/管和0.03ng/管。用本方法测定牛血浆LH水平时,不需要对血浆进行处理,供测血浆量可取10-40μl。方法的重复性较好,组内变异系数为8.89%,组间变异系数为14.69%;无LH牛血浆添加bLH和HCG的回收率分别为98.98±11.94%和102.8±5.81%。 研究了无LH牛血浆和BSA对标准曲线的影响。与前人对人血浆的研究结果比较,发现牛血浆和人血浆对RRA的干扰特性不同,推论血浆RRA干扰因子存在着种属特异性。  相似文献   

3.
用放射免疫分析法(RIA)测定了10头白香猪发情周期外周血清孕酮(P4)、17β-雌二醇(E2)和促黄体素(LH)含量的变化。血清孕酮的含量,在发情周期的第2d逐渐升高,峰值为21.25ng/ml±2.00ng/ml;E2含量的变化较特殊,在发情当天出现一个峰值,但最高值却出现在发情周期的第11d~13d,为79.48pg/ml±10.77pg/ml;促黄体素的含量在发情当日达到最高值以后逐渐下降。  相似文献   

4.
LRH—A3对全奶母牦牛的诱导发情效果和作用机理初探   总被引:5,自引:2,他引:3  
《中国畜牧杂志》2002,38(1):14-15
本研究初步探讨了促性腺素释放激素类似物(LRH-A3)对全奶母牦牛(在当年4~6月份产犊的泌乳母牦牛)的诱导发情排卵效果及机理.1998年7月对试验组(n=20)母牦牛注射LRH-A3(300μg/头),对照组(n=42)未作任何处理.9月15日前用普通牛公牛配种,9月15日后用公牦牛补配.1999年产犊率为试验组50.0%(10/20),对照组28.6%(20/42),试验组和对照组差异极显著(P<0.01).对5头母牦牛在注射LRH-A3前30min及注射后30,45和60min血清中促黄体素(LH)浓度测定以进一步探明全奶母牦牛诱导发情第一情期受胎率低的原因.结果发现,虽然注射LRH-A3后60min全奶母牦牛血清中LH浓度显著升高(P<0.05),但该峰值(3.34±0.67ng/ml,n=5)未达到自然发情排卵的LH峰值(17.1829±2.1174ng/ml).  相似文献   

5.
LRH-A_3对全奶母牦牛的诱导发情效果和作用机理初探   总被引:1,自引:1,他引:0  
本研究初步探讨了促性腺素释放激素类似物 (LRH A3 )对全奶母牦牛 (在当年 4~ 6月份产犊的泌乳母牦牛 )的诱导发情排卵效果及机理。 1998年 7月对试验组 (n =2 0 )母牦牛注射LRH A3 (30 0 μg/头 ) ,对照组 (n =42 )未作任何处理。9月 15日前用普通牛公牛配种 ,9月 15日后用公牦牛补配。 1999年产犊率为试验组 5 0 .0 % (10 / 2 0 ) ,对照组 2 8.6 %(2 0 / 42 ) ,试验组和对照组差异极显著 (P <0 .0 1)。对 5头母牦牛在注射LRH A3 前 30min及注射后 30 ,45和 6 0min血清中促黄体素 (LH)浓度测定以进一步探明全奶母牦牛诱导发情第一情期受胎率低的原因。结果发现 ,虽然注射LRH A3后 6 0min全奶母牦牛血清中LH浓度显著升高 (P <0 .0 5 ) ,但该峰值 (3.34± 0 .6 7ng/ml,n =5 )未达到自然发情排卵的LH峰值 (17.182 9± 2 .1174ng/ml)。  相似文献   

6.
放射免疫法测定枫泾(FJ)和长白(L)青年母猪(各4头)首次发情周期内外周血清中促卵泡素(FSH)、促黄体素(LH)、17β-雌二醇(E_2)、孕酮(P_4)、和睾酮(T)的含量。测定结果,初情期开始日龄FJ猪平均为104.3±11.50天,L猪为235.0±1.95天。两猪种首次发情周期内外周血清中同种生殖激素有相似的变化趋势。在首次情期内,FJ和L猪的FSH平均含量分别波动在28.6±8.6~49.4±6.0ng/ml和16.8±2.5~38.9±0ng/ml之间;FSH总平均含量FJ猪组(37.8±2.7)显著高于L猪(27.0±3.1ng/ml)P<0.05;FJ猪发情0~2小时的FSH平均含量(34.4±2.1ng/ml)极显著地高于L猪(22.2±1.7ng/ml)P<0.001。排卵前LH峰均值FJ猪组(5.31±0.75ng/ml)显著高于L猪组(1.83±0.75ng/ml)P<0.05。发情当天(0天)E_2达峰值,FJ和L猪组分别是30.5±3.9和20.4±5.3pg/ml,两者无显著差异(P>0.05)。FJ和L猪组各自的P_4(ng/ml)和T(pg/ml)分泌呈显著正相关,相关系数依次为γ_F=0.71,P<0.05,γ_L=0.95,P<0.01。LH、FSH的含量高很可能是FJ猪高排卵率的重要因素之一。  相似文献   

7.
本试验采用放射免疫法测定了卵巢囊肿奶牛外周血浆中促黄体素、孕酮、雌二醇和睾酮水平。测定结果,促黄体素水平卵泡囊肿为0.84±0.25ng/ml(n=12),黄体囊肿为0.83±0.23ng/ml(n=5);孕酮水平卵泡囊肿为0.56±0.30ng/ml(n=12),黄体囊肿为2.85±0.64ng/ml(n=5);雌二醇水平卵泡囊肿为28.44±22.47pg/ml(n=12),黄体囊肿为8.14±0.88pg/ml(n=5);睾酮水平卵泡囊肿为84.67±40.40pg/ml(n=12),黄体囊肿为51.98±7.77pg/ml(n=5)。认为卵巢囊肿奶牛外周血浆中促黄体素水平低于正常期奶牛的水平;卵泡囊肿奶牛血浆中孕酮水平低于1ng/ml,黄体囊肿奶牛血浆中孕酮水平高于1ng/ml;卵泡囊肿奶牛血浆中雌二醇水平较高;卵泡囊肿奶牛公牛相与体内高水平睾酮有关。  相似文献   

8.
用放射免疫法测定并研究了在初情期间24小时内和交配过程中的3头枫泾公猪外周血清促黄体素(LH)、睾酮(T)和皮质醇(F)的含量及分泌范型。3头公猪平均于102日具有射精能力,开始进入初情期。初情期前(76~88日龄)T和LH含量较低,其平均值分别为1.28±0.44和1.57±0.09ng/ml。102日龄后,T含量迅速升高,平均为8.43±0.87ng/ml,与初情期前比较,差异极显著,(P<0.01);LH也随之升高,平均为2.04±0.15ng/ml,但前、后差异不明显(P>0.05)。初情期间24小时内,LH含量波动在1.04±0.40~2.25±0.87ng/ml之间,总平均为1.64±0.28ng/ml;T和F均呈突发性分泌方式,总平均值分别为4.32±1.49和14.79±9.61ng/ml,二者的分泌呈极显著正相关(r=0.88)。T和F的含量早上显著高于夜间(24点)。3头公猪在106日龄分别与发情母猪交配过程中,三种激素均处于较高水平,射精阶段T值显著高于爬下后5~6分钟的值,而LH和F值无显著变化。综上所述,初步揭示枫泾公猪平均于108日龄已建立睾酮、促黄体素和皮质醇性成熟的分泌范型。  相似文献   

9.
本实验以羊参考制剂 NIH—LH—S_(18)为标准品,利用抗羊 LH 血清—放射性碘标记羊 LH 异源放射免疫测定系统(双抗体法)测定了双峰母驼卵泡发育期和精液诱导排卵前后血液中 LH 的水平。对此测定方法的特异性、灵敏度、准确度和精确度均分别进行了相应的检验,证明这一异源放射免疫测定系统可以对双峰驼血液中的 LH 进行测定,为双峰驼排卵机制的研究提供了一种有用的手段。测定时标准曲线的范围为0.125~32.0ng,灵敏度为0.1ng。一次测定内的变异系数为5.84%,测定间的变异系数为17.38%。应用此技术测得两头母驼的4个卵泡发育期中血液内 LH 的基础水平为2.70±1.29ng/ml;两例母驼在人工输精后5~8小时内血液中 LH 的峰值为11.20±4.67ng/ml,约为基础水平的4倍;经直肠检查,在 LH 峰值后40小时左右排卵。  相似文献   

10.
多种动物血清中生物活性LH/CG的放射受体测定法(RRA)   总被引:1,自引:0,他引:1  
利用绵羊卵巢黄体细胞膜作为 LH / CG受体来源 ,以放射性12 5 I- h CG作为示踪标记配体 ,以高纯度的h CG为标准品建立标准曲线 ,建立了一种有效的 LH- RRA测定方法。它能够直接检测多种动物血清中与受体结合的具有生物活性的 LH的动态变化。该法测定程序简单 ,在 2 h内完成并获得可重复性结果。测定方法的灵敏度为 0 .3ng/管 ,批内和批间误差分别为 ( 3.4 1± 3.14 ) %和 ( 8.70± 7.93) %。动物 (牛、兔、猪 )垂体液中 LH含量反应曲线和 h CG标准曲线平行良好。牛、羊、猪、兔、鼠和仓鼠血清中 LH的剂量反应曲线和h CG标准曲线的平行性表明 ,该 LH- RRA可以用来检测不同动物血清中的具有生物活性的 LH变化。回收试验表明 ,在该测定方法中加入 3、10、30 ng h CG时的回收率分别为 ( 10 0 .59± 5.55) %、( 99.55± 9.86 ) %、( 10 4 .2 8± 7.4 5) %,说明测定结果的正确性。该 LH - RRA的测定结果反映了动物正常的生理状态。本试验垂体中有活性的 LH水平远远高于外周循环中的水平 ,雌、雄动物循环血液中的 LH含量不一致。  相似文献   

11.
为了检测山羊迷走神经结状神经节中是否有促黄体生成素受体(LHR)的存在,探讨促黄体生成素(LH)是否能够影响结状神经节内脏感觉神经元的功能活动。本试验采用免疫组织化学SP法观察LHR在结状神经节中的分布特征,利用IPP 6.0图像半定量分析系统分析LHR在结状神经节中阳性神经元和阳性非神经元上的表达量差异。结果显示,LHR主要分布在神经元细胞膜和细胞质中,呈棕黄色为强阳性。在带核的神经元中,神经元细胞核呈圆形空泡状,LHR为阴性反应。神经元群间的神经纤维呈淡黄色,LHR为弱阳性。LHR在神经元胞体上的相对表达量极显著高于节内其他阳性非神经元结构(P0.01)。结果表明,山羊结状神经节内脏感觉神经元是LH作用的主要靶细胞,提示LH有可能通过作用于结状神经节内脏感觉神经元胞体上的LHR参与调节内脏器官感觉信息的传导。  相似文献   

12.
为研究日粮能量水平对塞北乌骨鸡血清促性腺激素分泌的影响,试验选60只30周龄体重相近、来源相同、产蛋性能相似的塞北乌骨鸡,随机分为5组,每组3个重复,每个重复4只鸡。试验1组为对照组,饲喂基础日粮;试验2~5组分别饲喂能量降低5%和10%及提高5%和10%日粮。采用放射免疫分析方法(RIA)测定血浆促卵泡素(FSH)和促黄体素(LH)。结果表明,试验结束时,与试验1组相比,试验2组FSH含量差异极显著(P<0.01);试验2组与试验1、3、4、5组组间LH含量差异极显著(P<0.01)。提示,能量通过促性腺激素分泌影响生殖性能。  相似文献   

13.
We tested the hypothesis that rapidly expressed inhibitory effects of estradiol (E) on luteinizing hormone (LH) release in the male are attributable, in part, to suppression of luteinizing hormone-releasing hormone (LHRH) release. Hypophyseal-portal cannulated, castrated male sheep were infused with E (15 ng/kg/hr) or vehicle. Portal and jugular blood samples were collected at 10-min intervals for 4 hr before, and for either 12 hr (E, n = 4; vehicle, n = 4) or 24 hr (E, n = 8; vehicle, n = 3) after the start of infusion. In animals sampled for 16 hr, temporal changes in both LHRH and LH were assessed. In animals sampled for 28 hr, only LH data were analyzed. Before either the 12-hr or 24-hr infusion, LHRH and/or LH mean concentrations, pulse amplitude and interpulse interval (IPI) did not differ between E- and vehicle-infused animals. In animals sampled for 16 hr, no effects of time or steroid × time interactions were detected for mean LHRH and LHRH pulse amplitude; however, both were greater (P < 0.01) in vehicle-infused than in E-infused males. LHRH IPI was unaffected by infusion. In contrast, both mean LH and LH pulse amplitude declined (P < 0.01) within 4–8 hr after the start of E infusion, whereas mean LH IPI was unaffected. In animals sampled for 28 hr, an effect of time (P < 0.01) and a steroid × time interaction (P < 0.01) was detected for mean LH, and there was an effect of time (P < 0.01) on LH pulse amplitude. Mean LH IPI was not affected. Our results show that in male sheep E rapidly reduces LH release in the absence of a detectable change in LHRH release.  相似文献   

14.
The present study describes the development and validation of a simple sensitive and specific sandwich enzyme immunoassay (EIA) for the quantification of ovine luteinizing hormone (LH) in plasma. Microtitre plates were coated with the capture antibody 518b7 anti-bovine LH. A second peroxidase-labelled anti-ovine LH antibody was used as tracer. A simple 3-step procedure was used for the sample analysis; (1) incubation of standards and samples with the pre-coated antibody plates for 2 h at 37°C; (2) incubation with the peroxidase-labelled antibody for 1 h at room temperature; and (3) colour development with TMB substrate. A linear dose–response curve was obtained in the range 0–10 ng/ml (r 2 > 0.99). The detection limit was 0.05 ng/ml, and the intra-assay and inter-assay coefficients of variation were 7% and 11.7%, respectively. The theoretical stability of microplates and reagents was calculated, this being greater than one year. Low or undetectable cross-reactivities were recorded for follicle-stimulating hormone, bovine thyroid-stimulating hormone, equine chorionic gonadotrophin and a gonadotrophin-releasing hormone (GnRH) analogue. The EIA was biologically validated by the determination of plasma LH concentrations of nine Rasa Aragonesa ovariectomized and estradiol-implanted ewes after a double GnRH challenge. In conclusion, this enzyme immunoassay provides an efficient, simple and sensitive method for the routine analysis of ovine LH.  相似文献   

15.
Kisspeptin (KP),a neuroendocrine regulator of reproduction,is hypothesized to be an integrator of metabolism and hormones critical to the regulation of reproduction.Lactation is associated with enhanced growth hormone (GH) responsiveness and reduced fertility.Our study was designed to determine the effects of lactation on KP-stimulated GH and luteinizing hormone (LH) secretion.Five nonlactating and five lactating dairy cows were used in the study.Experiments were conducted with lactating cows at weeks 1,5 and 11 after parturition.The experimental treatments (saline and KP [ 100 and 400 pmol/kg body weight] ) were given intravenously and blood was collected and plasma was stored until later assay to determine concentrations of GH,LH,progesterone and non-esterified fatty acids.We found that neither dose of KP stimulated an increase in GH secretion.The low dose of KP increased (P <0.05)LH concentrations only in lactating cows.The higher dose of KP elicited an increase in circulating LH concentrations in both lactating and non-lactating cows.The lower dose of KP increased ( P < 0.05 ) the area under the curve for LH only in cows during week 5 of lactation,and the area under the curve of LH following the highest dose of KP was greater ( P < 0.05 ) in cows during week 5 of lactation than that for the other groups of cows.In summary,lactation status and stage of lactation did not change the sensitivity of the GH system to KP.However,an effect of stage of lactation on KP-stimulated LH secretion was detected in the dairy cows.Study of the KP system during lactation in dairy cows may provide critical insights into the mechanisms for lactation-associated changes in the reproductive axis.  相似文献   

16.
为准确掌握雌性黑猩猩排卵时间以利于人工授精,自2008年1月至2009年6月对长春市动植物公园1只成龄雌性黑猩猩发情表现进行观察,记录发情周期天数,并用不孕检测试纸测定促黄体生成素(LH)的分泌情况。结果显示:黑猩猩发情周期平均35.6 d。跟踪测试黑猩猩的3个发情周期尿液中的LH分泌水平,结果为LH峰值在40~60之间,且峰值出现在发情周期的第21天左右。  相似文献   

17.
利用已建立的可测定多种动物血清中促黄体激素 ( LH)生物学活性的 LH-RRA法 ,检测了不同生理状态下的 LH分泌量 ,进一步分析了该 RRA法在实践应用中的可靠性。通过用特异性刺激 LH分泌的 LRH-A3注射动物和诱导体外培养的垂体细胞分泌 LH的试验表明 ,该方法具有很高的特异性和可靠性。结果显示 ,雄兔对于 LRH-A3刺激有特异性反应。 2只兔前后、不同兔同时的对照试验表明 ,该 RRA法可以特异性地检测出 LRH-A3引起的 LH特异性变化。对母猪发情至早期妊娠阶段血清中 LH检测结果表明 ,此 RRA法可有效地测定出猪血清中 LH的动态变化。利用绵羊垂体细胞体外培养模型 ,分别用不同剂量的 LRH-A3( 0、1、1 0、1 0 0、1 0 0 0 ng/孔 )诱导垂体细胞合成和分泌 LH,RRA测定结果表明 ,试验组 LH含量分别比对照组增加 1 .77、1 .78、2 .0 3和 1 .4 6倍 ( P <0 .0 1 ) ,呈现剂量依赖关系。以上结果表明 ,建立的 LH-h CG的 RRA可以替代 RIA和体外生物测定法  相似文献   

18.
为研究发情周期不同阶段牦牛子宫中黄体生成索受体(LHR)的定位及表达变化,笔者利用免疫组织化学SP法分别检测发情期、发情后期、间情期和发情前期牦牛子宫中LHR的表达,并进行光密度值分析.结果表明,LHR免疫阳性产物在牦牛子宫腺上皮细胞、基质细胞、血管内皮细胞、血管平滑肌细胞和肌层平滑肌细胞中均有表达;腺上皮细胞、基质细胞和肌层平滑肌细胞中LHR在发情前期和发情期表达最弱,发情后期表达增加,间情期表达最强(P<0.05);子宫内膜血管平滑肌细胞中LHR的表达在发情期最强,间情期最弱(P<0.05);血管内皮中LHR在发情期和发情前期表达很强,发情后期和间情期显著下降(P<0.05).结果表明LHR参与了发情周期不同阶段牦牛子宫功能变化的调控.  相似文献   

19.
The secretion of luteinizing hormone in ewes of Finnish Landrace during estrus. Acta vet. scand. 1979, 20, 216–223. — Luteinizing hormone immunoreactivity was measured in the venous plasma of four cycling Finnish Landrace sheep during the breeding season in connection with one synchronized estrus and the subsequent one. The ewes were slaughtered after the second estrus to establish the number of ovulations. To determine the LH concentration, a heterologous method of assay was used; this was based on the cross reaction of sheep plasma LH in a human LH radioimmunoassay system.As a result of the investigation, it was found that the peaks of LH were lower during the time of synchronized estrus and that these peaks occurred earlier than in the subsequent estrus. However, the differences were not statistically significant. On account of the limited material, the effect of the occurrence of the LH peak on the number of ovulations could not be established.  相似文献   

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