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Kisspeptin receptor agonist (FTM080) increased plasma concentrations of luteinizing hormone in anestrous ewes

机译:Kisspeptin受体激动剂(FTM080)增加了发情母羊血浆黄体生成素的浓度

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摘要

Kisspeptin receptor (KISS1R) agonists with increased half-life and similar efficacy to kisspeptin in vitro may provide beneficial applications in breeding management of many species. However, many of these agonists have not been tested in vivo. These studies were designed to test and compare the effects of a KISS1R agonist (FTM080) and kisspeptin on luteinizing hormone (LH) in vivo. In experiment 1 (pilot study), sheep were treated with FTM080 (500 pmol/kg BW) or sterile water (VEH) intravenosuly. Blood was collected every 15 min before (1 h) and after (1 h) treatment. In experiment 2, sheep were treated with KP-10 (human Metastin 45-54; 500 pmol/kg BW), one of three dosages of FTM080 (500 (FTM080:500), 2500 (FTM080:2500), or 5000 (FTM080:5000) pmol/kg BW), or VEH intravenously. Blood was collected every 15 min before (1 h) and after (4 h) treatment. In experiment 1, FTM080:500 increased (P < 0.05) plasma LH concentrations when compared to VEH. The area under the curve (AUC) of LH following FTM080:500 treatment was also increased (P < 0.05). In experiment 2, plasma LH concentrations increased (P < 0.05) following treatment with KP-10 and FTM080:5000 when compared to VEH and FTM080:500. The AUC of LH following KP-10 was greater than (P < 0.05) all other treatments and the AUC of LH following FTM080:5000 was greater than (P < 0.05) all treatments except KP-10. These data provide evidence to suggest that FTM080 stimulates the gonadotropic axis of ruminants in vivo. Any increased half-life and comparable efficacy of FTM080 to KP-10 in vitro does not appear to translate to in vivo in sheep.
机译:具有增加的半衰期和与kisseptin体外相似的功效的kisseptin受体(KISS1R)激动剂可能在许多物种的育种管理中提供有益的应用。然而,许多这些激动剂尚未在体内进行测试。这些研究旨在测试和比较KISS1R激动剂(FTM080)和Kisspeptin对体内黄体生成素(LH)的作用。在实验1(试点研究)中,绵羊经FTM080(500 pmol / kg体重)或静脉注射无菌水(VEH)处理。在治疗前(1小时)和治疗后(1小时)每15分钟收集一次血液。在实验2中,用KP-10(人Metastin 45-54; 500 pmol / kg体重),三种剂量的FTM080(500(FTM080:500),2500(FTM080:2500)或5000(FTM080) :5000)pmol / kg BW)或静脉注射VEH。在治疗前(1小时)和之后(4小时)每15分钟收集一次血液。在实验1中,与VEH相比,FTM080:500增加了(P <0.05)血浆LH浓度。 FTM080:500处理后LH的曲线下面积(AUC)也增加了(P <0.05)。在实验2中,与VEH和FTM080:500相比,用KP-10和FTM080:5000处理后血浆LH浓度增加(P <0.05)。 KP-10后LH的AUC大于所有其他治疗(P <0.05),FTM080:5000后LH的AUC大于除KP-10之外的所有治疗(P <0.05)。这些数据提供证据表明FTM080在体内刺激了反刍动物的促性腺轴。 FTM080与KP-10在体外的任何半衰期延长和可比的功效在绵羊中似乎都无法转化为体内。

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