首页> 外文期刊>General and comparative endocrinology >Prolactin in the brushtail possum (Trichosurus vulpecula): Development of homologous radioimmunoassay using recombinant possum prolactin.
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Prolactin in the brushtail possum (Trichosurus vulpecula): Development of homologous radioimmunoassay using recombinant possum prolactin.

机译:牛尾负鼠(Trichosurus vulpecula)中的催乳激素:使用重组负鼠泌乳素开发同源放射免疫分析法。

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摘要

We report the production of recombinant possum prolactin (posPrl), and its use in the development and validation of a highly specific homologous radioimmunoassay for the measurement of prolactin (Prl) in brushtail possums. This enabled the subsequent investigation of some basic mechanisms involved in the regulation of Prl secretion in this species. Recombinant posPrl spanning the entire coding region was expressed in Escherichia coli, resulting in a 199 amino acid protein with a molecular weight approximately 23kDa. The potency of posPrl was 45.3+/-4.8% that of ovine Prl in a radioreceptor assay using possum mammary gland receptors and induced a 3.4+/-0.8-fold increase in progesterone secretion in primary possum granulosa cells. Antiserum (G27) was raised against recombinant posPrl and was highly specific for possum Prl ( approximately 30% binding at 1:60,000 final dilution), and exhibited negligible cross-reactivity (<0.0001%) with possum growth hormone. Serial dilutions of pituitary gland extracts, and plasma samples from male and female possums gave parallel inhibition curves to recombinant posPrl standards in the assay. Biological validation of the RIA included treating possums with drugs known to alter Prl secretion in other mammals. In seasonally anoestrous female possums, administration of 20mug thyrotropin-releasing hormone (TRH) resulted in a 15-fold increase (P<0.01) in plasma Prl concentrations. In mid-late lactating female possums, a bolus of cabergoline (dopamine agonist; 75mug) reduced (P<0.05) plasma Prl levels to baseline for 24h, while repeated administration (6x75mug at 12h intervals) suppressed (P<0.01) plasma Prl concentrations until 24h after the last injection. Prolonged inhibition of Prl levels subsequently caused marked (P<0.01) attenuation in rate of bodyweight increase of pouch young. The amplitude of the Prl surge in response to a bolus of TRH (15mug) was 5-fold lower in cabergoline-treated, compared to control mid-late lactating possums. In conclusion, we report the developmentand validation of a robust and sensitive RIA for measuring Prl concentrations in the plasma of brushtail possums.
机译:我们报告了重组负鼠催乳素(posPrl)的生产,及其在开发和验证高度特异性的同源放射免疫分析法以用于测量燕尾负鼠中催乳素(Prl)中的用途。这使得能够随后研究参与调节该物种中Prl分泌的一些基本机制。跨越整个编码区的重组posPr1在大肠杆菌中表达,得到199个氨基酸的蛋白质,分子量约为23kDa。在使用负鼠乳腺受体的放射受体测定中,posPrl的效力是绵羊Prl的45.3 +/- 4.8%,并诱导原代负鼠颗粒细胞中孕激素分泌增加3.4 +/- 0.8倍。产生了针对重组posPrl的抗血清(G27),并且对负鼠Prl具有高度特异性(最终稀释度为1:60,000时约30%结合),并且与负鼠生长激素的交叉反应性可忽略不计(<0.0001%)。垂体提取物的连续稀释液以及雄性和雌性负鼠的血浆样品在测定中与重组posPrl标准品具有平行的抑制曲线。 RIA的生物学验证包括用已知能改变其他哺乳动物Prl分泌的药物治疗负鼠。在季节性食道的女性负鼠中,施用20杯的促甲状腺激素释放激素(TRH)可使血浆Prl浓度增加15倍(P <0.01)。在哺乳期中后期的女性负鼠中,卡麦角林(多巴胺激动剂; 75杯)推注可降低(P <0.05)血浆Prl水平至基线24小时,而重复给药(6x75杯,间隔12h)可抑制(P <0.01)血浆Prl浓度直到最后一次注射后24小时。长期抑制Prl水平会导致幼仔体重增加速率显着(P <0.01)下降。与对照中后期泌乳负鼠相比,在卡麦角林治疗中,响应TRH推注(15杯)的Prl激增幅度要低5倍。总而言之,我们报告了一种健壮而灵敏的RIA的开发和验证,该RIA用于测量刷状负鼠血浆中的Prl浓度。

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