种公马的 GnRH 免疫和随后使用 GnRH 激动剂对睾丸功能进行早期再刺激所引起的内分泌变化。

IF 2.1
Camille Gautier, Jörg Aurich, Maria Melchert, Lisa-Hélène Wagner, Martim Kaps, Carolina T C Okada, Reinhard Ertl, Ingrid Walter, Christine Aurich
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引用次数: 0

摘要

背景:目的:本研究评估了促性腺激素释放激素(GnRH)免疫后睾丸功能恢复情况因动物个体而异,有些种公马要经过很长时间才能恢复生育能力。我们假设,GnRH 激动剂治疗可促进接种过 GnRH 疫苗的种公马恢复正常的内分泌功能:方法:将设得兰种公马分为实验组和对照组(各 6 头)。实验组种公马接种两次 GnRH 疫苗,每次间隔 4 周。当睾酮浓度下降到 0.3ng/mL 以下时,每头实验种公马与年龄匹配的对照组动物一起进行血睾。三周后,开始每天使用 GnRH 激动剂丁螺环酮(4μg/天,持续 4 周,之后为 8μg/天)。当接种疫苗的种公马体内睾酮浓度超过 0.5ng/mL 时,切除剩余的睾丸。采集血液进行LH、FSH、雌二醇和抗苗勒氏管激素(AMH)分析,保留睾丸和附睾组织进行实时qPCR和组织学分析:主要结果:GnRH疫苗接种降低了血液中LH和FSH的浓度,导致睾丸组织结构退化和精子发生中断。持续约60天的每日丁螺环酮治疗部分恢复了促性腺激素分泌,并促使睾丸组织的功能组织恢复,精子发生有效:结论:通过每天使用低剂量的丁螺环酮治疗,GnRH 疫苗接种过的种公马的睾丸内分泌功能可以得到恢复。在剂量、间隔时间和持续时间方面,丁螺环酮治疗方案可能会有所改进:建议对睾丸功能长期受抑制的GnRH疫苗种公马进行每日丁螺环酮治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endocrine changes induced by GnRH immunisation and subsequent early re-stimulation of testicular function with a GnRH agonist in stallions.

Context: Resumption of testicular function after gonadotrophin-releasing hormone (GnRH) immunisation varies among individual animals and some stallions regain fertility only after a prolonged time.

Aims: This study evaluated endocrine effects of GnRH immunisation and early subsequent re-stimulation with a GnRH agonist. We hypothesised that GnRH agonist treatment advances resumption of normal endocrine function in GnRH-vaccinated stallions.

Methods: Shetland stallions were assigned to an experimental and a control group (n =6 each). Experimental stallions were GnRH-immunised twice, 4weeks apart. Each experimental stallion was hemicastrated together with an age-matched control animal when testosterone concentration decreased below 0.3ng/mL. Three weeks later, daily treatment with the GnRH agonist buserelin was initiated (4μg/day for 4weeks followed by 8μg/day). The remaining testicle was removed when testosterone concentration exceeded 0.5ng/mL in vaccinated stallions. Blood was collected for LH, FSH, oestradiol and anti-müllerian hormone (AMH) analyses, and testicular and epididymal tissue were conserved for real-time qPCR and histology.

Key results: GnRH vaccination reduced blood concentrations of LH and FSH, with a structural deterioration of testicular tissue and disruption of spermatogenesis. Daily buserelin treatment for approximately 60days partially restored gonadotropin secretion and induced a recovery of the functional organisation of the testicular tissue with effective spermatogenesis.

Conclusions: Endocrine testicular function can be restored in GnRH-vaccinated stallions by daily low-dose buserelin treatment. The buserelin treatment protocol may potentially be improved regarding the dose, interval and duration.

Implications: Daily buserelin treatment can be recommended for treatment of GnRH-vaccinated stallions with prolonged inhibition of testicular function.

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