Specific binding of 11-ketotestosterone in an androgen target organ,the kidney of the male three-spined stickleback,Gasterosteus aculeatus |
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Authors: | Staffan Jakobsson Ian Mayer Rüdiger W. Schulz Marinus A. Blankenstein Bertil Borg |
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Affiliation: | (1) Department of Zoology, University of Stockholm, S-106 91 Stockholm, Sweden;(2) Department of Experimental Zoology, University of Utrecht, Padualaan 8, 3584 CH Utrecht, The Netherlands;(3) Department of Endocrinology, Academic Hospital Utrecht, 3584 CX Utrecht, The Netherlands |
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Abstract: | The kidney of male three-spined stickleback,Gasterosteus aculeatus, hypertrophies during the breeding season and produces a glue which is used in the building of the nest. This hypertrophy is androgen dependent, with 11-ketotestosterone (11KT) being more effective than other tested steroids in stimulating this secondary sexual character. In the present study kidneys were excised from stickleback males that had been castrated two days earlier. The purpose of this gonadectomy was to reduce the endogenous levels of androgens without allowing time for the kidney to regress. Tissue fragments were incubated with tritiated 11KT with and without unlabelled steroids at increasing concentrations. Displaceable specific 11KT binding was found in kidney tissue fragments whereas only non-specific binding was observed when liver and muscle were investigated in a similar way. Unlabelled 11KT displaced specifically bound, tritiated 11KT with an ED50-value (50% of displaceable binding) of 28 nM. Similar ED50 values were found for 17-hydroxy-5 -androstane-3,11-dione (29 nM) and 5 -dihydrotestosterone (20 nM), whereas higher ED50 concentrations were estimated for testosterone (T; 203 nM) and progesterone (69 nM). No displacement of tritiated 11KT was found for the other investigated substances tested; estradiol, 17 ,20 -dihydroxy-4-pregnen-3-one, flutamide or cyproterone acetate. No specific binding to kidney tissue fragments could be detected when labelled T was used instead of labelled 11KT. Specific binding of 11KT or T was not found either in the kidney cytosol or nuclear extracts. However, using the kidney membrane fraction a displacement of tritiated 11KT with unlabelled 11KT (10–6M) was observed. In conclusion there is a specific binding of 11KT in the stickleback kidney. The absence of binding in liver and muscle, the ED50 value observed and the displacement with some, but not all steroids are consistent with a receptor function. The presence of binding in membrane fractions, but not in cytosol or nuclear extracts suggests that the binding is not related to classic steroid receptors. |
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Keywords: | three-spined stickleback secondary sexual character kidney hypertrophy 11-ketotestosterone testosterone specific binding displacement |
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