一种促性腺激素释放激素拮抗剂在圈养沙虎鲨、Carcharias taurus中的应用,以及拮抗剂和生殖类固醇激素的血清水平

IF 0.7 Q4 ZOOLOGY Journal of Zoo and Aquarium Research Pub Date : 2015-07-23 DOI:10.19227/JZAR.V3I3.120
A. Henningsen, B. Whitaker, K. Kight, D. Hess, C. Hadfield, Y. Zohar
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引用次数: 8

摘要

沙虎鲨,Carcharias taurus,通常在世界各地的大型公共水族馆中饲养,但在圈养繁殖方面取得的成功有限。迄今为止,只有四个机构记录了该物种成功的圈养繁殖。在这项研究中,雄性沙虎鲨在服用GnRH拮抗剂(Antide;Bachem, Inc.,托伦斯,CA)。对三条雄性沙虎鲨进行了为期12个月的连续取样。这三只鲨鱼分别接受了0.185和0.225 mg·kg -1剂量的Antide微球注射,间隔69天。通过放射免疫法检测血清样品中类固醇激素17β-雌二醇、孕酮、睾酮、5α-二氢睾酮、皮质酮和GnRH拮抗剂Antide的浓度。获得的结果显示了类固醇谱的周期性模式,并且每次注射后Antide水平分别在33天和27天后达到峰值。最终治疗后8个月仍可检测到循环Antide。然而,与预期的效果相反,所有五种类固醇的浓度在初始施用拮抗剂后立即增加。虽然缺乏对照对象,无法得出关于拮抗剂对类固醇激素水平影响的可靠结论,但在循环Antide水平达到峰值的同时,水平也显著下降。此外,尽管我们不能将其归因于拮抗剂,但在拮抗剂施用后,平均雄激素水平比之前在这组雄性鲨鱼中观察到的水平下降得更快。这是第一次记录使用GnRH拮抗剂在任何软骨鱼。建议进一步研究,包括对照对象,以调查拮抗剂对类固醇激素,生殖周期和行为的影响。
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The use of a gonadotropin releasing hormone antagonist in captive sand tiger sharks, Carcharias taurus, and the serum levels of the antagonist and reproductive steroid hormones
Sand tiger sharks, Carcharias taurus , are commonly maintained in large public aquaria throughout the world, but limited success has been achieved in captive reproduction. Successful captive reproduction in this species has only been documented in four institutions to date. In this investigation, steroid hormone assays in male sand tiger sharks were compared before and after dosing with a GnRH antagonist (Antide; Bachem, Inc., Torrance, CA). Three male sand tiger sharks were sampled serially for 12 months. All three sharks received two microsphere-encapsulated doses of Antide (0.185 and 0.225 mg·kg -1 ), 69 days apart. Serum samples were assayed for concentrations of the steroid hormones 17β-oestradiol, progesterone, testosterone, 5α-dihydrotestosterone, corticosterone, and the GnRH antagonist Antide via radioimmunoassay. The results obtained demonstrate cyclical patterns in the steroid profiles, and that mean Antide level peaked 33 and 27 days following each injection, respectively. Circulating Antide was detectable eight months after the final treatment. Contrary to the anticipated effect, however, concentrations of all five steroids increased immediately following initial administration of the antagonist. Although the lack of control subjects precludes solid conclusions regarding the effects of the antagonist upon steroid hormone levels, notable declines in the levels were observed concurrent with peak circulating Antide levels. Further, although we cannot attribute it to the antagonist, mean androgen levels declined more sharply following antagonist administration than those observed in a previous investigation in this group of male sharks. This is the first documented use of a GnRH antagonist in any chondrichthyan. Further research, including control subjects, is suggested to investigate the effects of the antagonist upon steroid hormones, reproductive cycles and behaviour.
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