Jewgenow K, Naidenko S V, Goeritz F, Vargas A, Dehnhard M
Leibniz-Institute for Zoo Biology and Wildlife Research, PF 601103, Berlin, Germany.
Gen Comp Endocrinol. 2006 Nov;149(2):151-8. doi: 10.1016/j.ygcen.2006.05.015. Epub 2006 Jul 14.
The aim of the present study was to identify relevant fecal testosterone metabolites in the Eurasian lynx (Lynx lynx) using HPLC analysis and to evaluate the specificity of two testosterone immunoassays against these fecal metabolites. Finally, fecal hormone analysis was used to characterize seasonal reproductive activity of captive male Eurasian and Iberian (Lynx pardinus) lynx. Fecal samples from a male Eurasian lynx who received an i.v. injection of [3H]testosterone were subjected to HPLC analysis. All HPLC fractions were analyzed for radioactivity and androgen content by two testosterone immune assays (EIA and Testosterone-Immulite kits, DPC Biermann, Germany). Furthermore, fecal samples from four Eurasian lynx males (n=174) and three Iberian lynx (n=52) were collected throughout the year and fecal testosterone metabolites were determined with Testosterone-Immulite assay. HPLC separation of radiolabeled Eurasian lynx fecal extract indicated that the majority of testosterone metabolites are substances with a higher polarity than testosterone. Only minor proportion of radioactivity co-eluted with authentic testosterone and dihydrotestosterone. Enzymatic hydrolysis and solvolysis of the fecal extract were insufficient to liberate testosterone. After solvolysis relatively more activity was eluated the position of DHT, but the majority of metabolites remained unaffected. The EIA measured substantial amount of immunoreactivity, which corresponded with two radioactive peaks. Additionally, both immunoassays recognized two metabolites, which were only minor components according to their radioactivity. The Immulite assay was able to recognize a metabolite at the position of dihydrotestosterone. HPLC separation of Iberian lynx feces extracts revealed a similar metabolite pattern determined by EIA that were typical for Eurasian lynx fecal extracts. Simultaneous analyses of fecal samples with both testosterone assays provided comparative results for both lynx species (Eurasian lynx, r2=0.488; p<0.001; Iberian lynx, r2=0.85, p<0.0001). Thus, seasonal reproductive activity of male Eurasian lynx was demonstrated also by Immulite -assay, confirming high testosterone levels during breeding season in March/April as previously documented with EIA. Preliminary results on testosterone measurements in Iberian lynx feces confirmed the suitability of the applied Immulite test in this highly endangered species.
本研究的目的是利用高效液相色谱(HPLC)分析鉴定欧亚猞猁(Lynx lynx)粪便中的相关睾酮代谢物,并评估两种睾酮免疫测定法对这些粪便代谢物的特异性。最后,采用粪便激素分析来描述圈养雄性欧亚猞猁和伊比利亚猞猁(Lynx pardinus)的季节性繁殖活动。对一只接受静脉注射[3H]睾酮的雄性欧亚猞猁的粪便样本进行HPLC分析。通过两种睾酮免疫测定法(酶免疫分析(EIA)和睾酮免疫发光试剂盒,德国DPC Biermann公司)对所有HPLC馏分的放射性和雄激素含量进行分析。此外,全年收集了四只雄性欧亚猞猁(n = 174)和三只伊比利亚猞猁(n = 52)的粪便样本,并用睾酮免疫发光测定法测定粪便中的睾酮代谢物。对放射性标记的欧亚猞猁粪便提取物进行HPLC分离表明,大多数睾酮代谢物是极性高于睾酮的物质。只有一小部分放射性与纯睾酮和二氢睾酮共洗脱。粪便提取物的酶促水解和溶剂解不足以释放睾酮。溶剂解后,在二氢睾酮位置洗脱的活性相对较多,但大多数代谢物仍未受影响。EIA检测到大量免疫反应性,这与两个放射性峰相对应。此外,两种免疫测定法都识别出两种代谢物,根据其放射性,它们只是次要成分。免疫发光测定法能够识别二氢睾酮位置的一种代谢物。对伊比利亚猞猁粪便提取物进行HPLC分离,发现其代谢物模式与EIA测定的欧亚猞猁粪便提取物典型模式相似。同时用两种睾酮测定法对粪便样本进行分析,为两种猞猁(欧亚猞猁,r2 = 0.488;p < 0.001;伊比利亚猞猁,r2 = 0.85,p < 0.0001)提供了比较结果。因此,免疫发光测定法也证明了雄性欧亚猞猁的季节性繁殖活动,证实了3月/4月繁殖季节期间睾酮水平较高,这与之前EIA记录的情况一致。伊比利亚猞猁粪便中睾酮测量的初步结果证实了所应用的免疫发光检测法适用于这种高度濒危物种。