Koch A, Hoppen H-O, Dieleman S J, Kooistra H S, Günzel-Apel A-R
Institute for Reproductive Medicine, School of Veterinary Medicine Hannover, Buenteweg 15, D-30559 Hannover, Germany.
Theriogenology. 2006 May;65(8):1666-77. doi: 10.1016/j.theriogenology.2005.09.013. Epub 2005 Nov 9.
In the present study, the pulsatile serum profiles of prolactin, LH and testosterone were investigated in eight clinically healthy fertile male beagles of one to six years of age. Serum hormone concentrations were determined in blood samples collected at 15 min intervals over a period of 6 h before (control) and six days before the end of a four weeks treatment with the dopamine agonist cabergoline (5 microg kg(-1) bodyweight/day). In addition, the effect of cabergoline administration was investigated on thyrotropin-releasing hormone (TRH)-induced changes in the serum concentrations of these hormones. In all eight dogs, the serum prolactin concentrations (mean 3.0 +/- 0.3 ng ml(-1)) were on a relatively constant level not showing any pulsatility, while the secretion patterns of LH and testosterone were characterised by several hormone pulses. Cabergoline administration caused a minor but significant reduction of the mean prolactin concentration (2.9 +/- 0.2 ng ml(-1), p < 0.05) and did not affect the secretion of LH (mean 4.6 +/- 1.3 ng ml(-1) versus 4.4 +/- 1.7 ng ml(-1)) or testosterone (2.5 +/- 0.9 ng ml(-1) versus 2.4 +/- 1.2 ng ml(-1)). Under control conditions, a significant prolactin release was induced by intravenous TRH administration (before TRH: 3.8 +/- 0.9 ng ml(-1), 20 min after TRH: 9.1 +/- 5.9 ng ml(-1)) demonstrating the role of TRH as potent prolactin releasing factor. This prolactin increase was almost completely suppressed under cabergoline medication (before TRH: 3.0 +/- 0.2 ng ml(-1), 20 min after TRH: 3.3 +/- 0.5 ng ml(-1)). The concentrations of LH and testosterone were not affected by TRH administration. The results of these studies suggest that dopamine agonists mainly affect suprabasal secretion of prolactin in the dog.
在本研究中,对8只年龄为1至6岁、临床健康且可育的雄性比格犬的催乳素、促黄体生成素(LH)和睾酮的脉冲式血清水平进行了研究。在使用多巴胺激动剂卡麦角林(5微克/千克体重/天)进行为期四周的治疗结束前6天以及治疗前(对照)6小时内,每隔15分钟采集一次血样,测定血清激素浓度。此外,还研究了卡麦角林给药对促甲状腺激素释放激素(TRH)诱导的这些激素血清浓度变化的影响。在所有8只犬中,血清催乳素浓度(平均3.0±0.3纳克/毫升)处于相对恒定水平,未显示出任何脉冲性,而LH和睾酮的分泌模式则以多个激素脉冲为特征。给予卡麦角林导致平均催乳素浓度略有但显著降低(2.9±0.2纳克/毫升,p<0.05),且不影响LH(平均4.6±1.3纳克/毫升对4.4±1.7纳克/毫升)或睾酮(2.5±0.9纳克/毫升对2.4±1.2纳克/毫升)的分泌。在对照条件下,静脉注射TRH可诱导显著的催乳素释放(TRH注射前:3.8±0.9纳克/毫升,TRH注射后20分钟:9.1±5.9纳克/毫升),证明TRH作为强效催乳素释放因子的作用。在卡麦角林用药情况下,这种催乳素增加几乎完全受到抑制(TRH注射前:3.0±0.2纳克/毫升,TRH注射后20分钟:3.3±0.5纳克/毫升)。LH和睾酮的浓度不受TRH给药的影响。这些研究结果表明,多巴胺激动剂主要影响犬催乳素的基础上分泌。