Effect of Follicle Size and Follicle-Stimulating Hormone on Ovulation Induction and Embryo Recovery in the Mare     

T.J. CoxE.L. Squires  PhD  honDACT  E.M. Carnevale 《Journal of Equine Veterinary Science》2009

The timing of ovulation is an important component to many equine breeding strategies. The action of luteinizing hormone on ovulation induction has been recognized; however, potential effects of follicle-stimulating hormone (FSH) have been less defined. Objectives of this study were to determine whether (1) mares could be induced to ovulate follicles ≤30 mm; (2) equine FSH (eFSH) has a positive effect on ovulation induction, and (3) ovulation of small follicles would affect embryo recovery. Light-horse mares (n = 12) between 4 and 10 years of age were assigned to treatments when they had a dominant growing follicle with a mean diameter of 24, 28, or 35 ± 2 mm and endometrial edema. Treatments were (1) H35, human chorionic gonadotropin (hCG) at 35 ± 2 mm; (2) F35, eFSH at 35 ± 2 mm; (3) H28, hCG at 28 ± 2 mm; (4) FH28, eFSH and hCG at 28 ± 2 mm; (5) D28, deslorelin (gonadotropin-releasing hormone [GnRH] analog) at 28 ± 2 mm; (6) FH24/H24, hCG or eFSH and hCG at 24 ± 2 mm. Mares’ reproductive tracts were scanned at 24 ± 2-hour intervals after treatment to detect ovulation. Mares were inseminated, and embryos were collected. Numbers of mares that ovulated within 48 ± 2 hours after treatment were: H35, 8/8 (100%); F35, 8/14 (57%); H28, 7/12 (58%); FH28, 9/12 (75%); D28, 3/7 (43%) and FH/H24, 4/14 (29%). The number of mares that ovulated in 48 ± 2 hours for H35 was not different from that for FH28 but was higher (P < .05) than all other groups. Embryo recovery rates, diameters, developmental stages, and morphology scores were not different for mares ovulating 48 hours or less versus more than 48 hours after treatment or among treatment groups. Results of this study demonstrate that follicles ≤30 mm can be induced to ovulate with no effect on embryo recovery or quality, as assessed by stereomicroscopy.  相似文献   

Cortisol disrupts the ability of estradiol-17β to induce the LH surge in ovariectomized ewes     

B.N. Pierce  I.J. Clarke  A.I. Turner  E.T.A. Rivalland  A.J. Tilbrook   《Domestic animal endocrinology》2009,36(4):202-208

Stress disrupts the preovulatory luteinizing hormone (LH) surge in females, but the mechanisms are unknown. We tested the hypothesis that cortisol compromises the ability of estrogen to induce a preovulatory-like LH surge in ovariectomized ewes in both the breeding and nonbreeding season. Luteinizing hormone surges were induced in ovariectomized ewes by treatment with progesterone followed by a surge-inducing estradiol-17β (E2) stimulus using a crossover design. The experiment was replicated in the breeding and nonbreeding seasons. Cortisol reduced the incidence of LH surges irrespective of season. Cortisol increased the latency from E2 stimulus to the onset of the surge in the breeding season only and suppressed the LH surge amplitude during both seasons (P < 0.01). We conclude that cortisol can interfere with the LH surge in several ways: delay, blunt, and in extreme cases prevent the E2-induced LH surge. Furthermore, the effect of cortisol to delay the E2-induced LH surge is more pronounced in the breeding season. These results show that cortisol disrupts the positive feedback effect of E2 to trigger an LH surge and suggest the involvement of multiple mechanisms.  相似文献   

Effects of GnRH treatment on initiation of pulses of LH,LH release,and subsequent concentrations of progesterone     

S.D. Fields  B.L. PerryG.A. Perry 《Domestic animal endocrinology》2009

Progesterone is essential for establishment and maintenance of pregnancy. One proposed method to increase progesterone is administering GnRH at insemination. However, this method has resulted in conflicting results. Therefore, 2 experiments were conducted to evaluate how administering GnRH at insemination affected pulses of luteinizing hormone (LH) and subsequent progesterone. In Experiment 1, cows were allotted to 2 treatments: (1) GnRH (100 μg) given approximately 12 h after initiation of estrus (n = 5); and (2) Control (n = 5). Blood samples were collected at 15-min intervals for 6 h at 12 (blood sampling period 1), 26 (blood sampling period 2), 40 (blood sampling period 3), 54 (blood sampling period 4), and 68 (blood sampling period 5) h after onset of estrus. Daily blood samples were collected for 17 d. In Experiment 2, cows were allotted into 2 treatments: GnRH administered 10 to 11 h (n = 10) or 14 to 15 h (n = 10) after onset of estrus. Daily blood samples were collected for 17 d. Cows treated with GnRH tended (P ≤ 0.075) to have greater LH release during blood sampling period 1, tended (P = 0.095) to have fewer pulses during blood sampling period 2, tended (P = 0.067) to have greater concentrations of progesterone, and had an earlier (P = 0.05) increase in progesterone than control cows. Cows treated with GnRH 10 to 11 h after onset of estrus had greater (P = 0.01) progesterone and an earlier (P = 0.04) increase in progesterone than cows treated 14 to 15 h. In conclusion, timing of GnRH treatment following onset of estrus influenced pulses of LH and subsequent progesterone.  相似文献   

Strategies for Using eFSH for Superovulating Mares   总被引：1，自引：0，他引：1  

Patrick M. McCue DVM  PhD  Melissa Patten BS  David Denniston PhD  Jason E. Bruemmer PhD  Edward L. Squires PhD   《Journal of Equine Veterinary Science》2008,28(2):91-96

The standard treatment for superovulation of mares is to administer equine follicle-stimulating hormone (eFSH) for 4 to 5 days to stimulate multiple follicles and human chorionic gonadotropin (hCG) to induce synchronous ovulations. Objectives of this study were: (1) to determine whether a short-term (3-day) eFSH treatment protocol would result in similar ovulation and embryo recovery rates compared with the standard eFSH protocol; (2) to determine the efficacy of a decreasing dose of eFSH (step-down protocol) on ovulation rate and embryo recovery; (3) to compare the efficacy of hCG and recombinant equine luteinizing hormone (reLH) for inducing ovulation in FSH-treated mares; and (4) to compare embryo recovery rates and embryo size when mares are flushed at 6.5 or 7.0 days after ovulation. Forty light-horse mares were used in 2005 (experiment 1) and 20 different mares were used in 2006 (experiment 2). In experiment 1, mares were randomly assigned to one of three treatment groups: (1) untreated controls, (2) standard eFSH treatment (12.5 mg intramuscularly twice daily), and (3) 3-day eFSH treatment. In experiment 2, mares were randomly assigned to one of four treatments: (1) untreated controls, (2) standard eFSH protocol, (3) 3-day eFSH treatment, and (4) step-down eFSH treatment (12.5 mg twice daily day 1, 8.0 mg twice daily day 2, 4.0 mg twice daily day 3). Within each treatment, mares were given either hCG (2,500 IU) or equine LH (750 mg, EquiPure LH; reLH) to induce synchronized ovulations. Embryo recovery was performed either 6.5 or 7.0 days after ovulation. In experiment 1, numbers of preovulatory follicles and ovulations were less for mares in the 3-day treatment group than the standard group, but were greater than for controls. Embryo recovery per flush was higher in the standard group (2.6) than the 3-day eFSH treatment (0.8) or control groups (0.8). In experiment 2, the number of preovulatory follicles and number of ovulations were greater in the standard and 3-day treatment groups than in control and step-down groups. The percent embryo recovery per ovulation and mean embryo grade were similar for all groups; however, the embryo recovery per flush was higher for mares in the standard treatment than controls (1.3 vs 0.6) but was similar to the 3-day (1.1) and step-down (0.8) treatments. Embryo recovery was similar for flushes performed on days 6.5 and 7.0 post-ovulation. The percentage of control mares ovulating within 48 hours in response to hCG or reLH was similar. In contrast, a higher percentage of eFSH-treated mares ovulated within 48 hours in response to reLH than hCG (92% vs 71%). In both years, the 3-day eFSH treatment protocol resulted in a greater number of preovulatory follicles and a greater number of ovulations than untreated controls. Unfortunately, the increased ovulation rate for mares administered eFSH for 3 days did not result in a greater number of embryos recovered per flush in either year. Use of a step-down eFSH treatment protocol resulted in fewer preovulatory follicles, fewer ovulations, and fewer embryos as compared with the standard eFSH treatment. In conclusion, the standard eFSH treatment resulted in a greater embryo recovery rate per cycle than either the 3-day or step-down treatment protocols. Recombinant equine LH was more effective than hCG in causing ovulation in eFSH-treated mares.  相似文献   

牦牛促黄体素放射受体分析方法的建立     

余四九  黄永明 《甘肃农业大学学报》1992,27(2):99-105

以大鼠睾丸组织匀浆作受体,~(125)I—hCG作放射配体,hCG作参考标准,且在标准曲线各测定管中加入与待测血浆等量的无LH牦牛血浆,籍以排除血浆干扰因子的影响,成功地建立了LH/hCG的放射受体分析方法。试验表明,该法是一种测定牦牛LH的灵敏可靠的方法。  相似文献   

Growth of pot roses and post-harvest rate of water loss as affected by air humidity and temperature variations during growth under continuous light     

Rolf Inge Pettersen  Roar MoeHans Ragnar Gislerød 《Scientia Horticulturae》2007

The effect of diurnal variations in air humidity and temperature under continuous lighting period (LP) on growth, flowering and water loss were studied in two pot-rose cultivars.  相似文献   

莱芜黑山羊发情周期中FSH、LH、E2和P的分泌规律   总被引：6，自引：0，他引：6  

侯衍猛  曹洪防  徐云华  钟为  王树迎 《中国兽医学报》2006,26(3):340-343

莱芜黑山羊在发情期和间情期，血浆内的卵泡刺激素（FSH）和黄体生成素（LH）均呈脉冲式分泌，雌激素（E2）和孕嗣（P）为波动式分泌。发情期FSH的脉冲周期较间情期长，两者之间显著差异（P〈0．05）。发情期LH的脉冲周期短于间情期，两者之间差异不显著（P〉0．05）。在整个发情周期中，FSH和LH均先后出现4个分泌峰，FSH和LH的第1个分泌峰分别出现在第7天和第5天，其余3个分泌峰均同时出现（分别为第10、15和20天）。E2和FSH、LH均在发情周期的第20天迭最高峰。P在间情期一直维持在一个较高水平。  相似文献   

促黄体素、肾上腺素对体外家兔赖氏细胞睾酮分泌的影响     

朱宝长  张岳  李震钟 《西北农林科技大学学报(自然科学版)》1987,(2):69-76

采用胰蛋白酶消化法离解家免睾丸细胞,研究赖氏细胞在体外短期培养条件下的内分泌学特性。结果表明,LH/HCG 能够特异性地促进赖氏细胞分泌睾酮(T),而肾上腺素(E)却显著地拮抗 LH/HCG 所致的赖氏细胞 T 生成作用,LRH 对赖氏细胞 T 分泌似无直接作用,茶碱能够有效地提高赖氏细胞对LH 反应的灵敏度。  相似文献   

6种石斑鱼成鱼的性腺发育、脑垂体结构以及垂体中FSHβ和LHβ细胞的免疫识别     

徐文刚  刘立明  王九龙  邹华锋  于文松  征矢野清  唐永政 《上海海洋大学学报》2022,31(1):151-160

以日本海域捕获的宝石石斑鱼(Epinephelus areolatus)、黑边石斑鱼(E.fasciatus)、赤点石斑鱼(E.akaara)、尾纹九棘鲈(Cephalopholis urodeta)、蜂巢石斑鱼(E.merra)和纹波石斑鱼(E.ongus)成鱼为对象,比较其性腺发育和脑垂体结构以及垂体中FSHβ和LHβ免疫信号的分布。结果表明:宝石石斑鱼、黑边石斑鱼、赤点石斑鱼和尾纹九棘鲈性腺发育为未成熟阶段,蜂巢石斑鱼和纹波石斑鱼性腺发育为成熟阶段。6种石斑鱼的脑垂体位于间脑腹面,由神经垂体(NH)和腺垂体(AH)组成。腺垂体从左至右进一步细分为前外侧部(RPD)、中外侧部(PPD)和中间部(PI)。在宝石石斑鱼、赤点石斑鱼和纹波石斑鱼中NH结构被PPD隔开分为上下两部分,而在黑边石斑鱼、尾纹九棘鲈和蜂巢石斑鱼中NH为一个整体。6种石斑鱼脑垂体中FSHβ和LHβ细胞的免疫信号主要分布在PPD和PI区域,且FSHβ信号强度均较LHβ强,推断在石斑鱼性腺发育成熟前后,FSHβ较LHβ重要。为石斑鱼的资源保护及人工繁殖方面提供基础生物学资料和理论依据。  相似文献   

Development of a homologous radioimmunoassay for Mediterranean yellowtail (Seriola dumerilii, Risso 1810) LH     

M. P. García Hernndez  A. García Ayala  B. Agulleiro  A. García  W. van Dijk  R. W. Schulz 《Aquaculture (Amsterdam, Netherlands)》2002,210(1-4):203-218

Purified Mediterranean (M.) yellowtail luteinizing hormone-like gonadotropin (MyLH) and its β-subunit (MyLHβ) served to develop a radioimmunoassay (RIA) for MyLH. The rabbit antisera against MyLH and MyLHβ used for this purpose were tested on pituitary sections by immunocytochemistry. Anti-MyLHβ specifically detected a single type of cells, which were located at the periphery of the proximal pars distalis (PPD) and surrounding the pars intermedia (PI). Anti-MyLH, however, also recognized two other cell types, thyrotropin β-immunoreactive (ir) cells and putative follicle-stimulating hormone-like (MyFSH)-producing cells. Labeling of the two latter cell types was prevented by preabsorption of anti-MyLH with M. yellowtail pituitary glycoprotein -subunit. The standard curve for the RIA was generated using purified MyLH, ¹²⁵I-labeled MyLHβ and anti-MyLHβ at a dilution of 1:70,000, which resulted in the binding of 30% of the tracer added. The standard curve ranged from 0.25 to 50 ng/ml. The midrange of the assay (ED50) was obtained with 5.48–7.87 ng LH/ml. The variation between assays was less than 15%. An average cross-reactivity of FSH in the LH RIA of 8.4% was found. Serial dilutions of M. yellowtail pituitary extracts displaced radiolabelled MyLHβ parallel to the MyLH standard. Application of the LH RIA to blood samples and pituitary cell culture medium provided physiological validation of the assay. Significant increases in LH levels were recorded after salmon GnRH treatments in vivo and in vitro. Serum LH levels from wild fish sampled at the spawning season were significantly higher than those from captive fish sampled in the same period.  相似文献