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Testosterone in a Cyclodextrin-Containing Formulation: Behavioral and Physiological Effects of Episode-like Pulses in Rats

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Abstract

Testosterone, administered in the form of an inclusion complex with 2-hydroxypropyl-β-cyclodextrin by subcutaneous injection, enters the circulation in a manner markedly similar to the natural episodic release by the testes. The effects of a regimen of once-a-day administration of complexed testosterone to adult (castrated or intact) rats and to senescent (intact) rats were investigated. Although this procedure left the castrated animals with concentrations of circulatory hormone far below physiological levels for much of the day, a significant improvement in androgen-sensitive behavior and physiology was obtained. Furthermore, the testosterone effects were more pronounced when high doses were used periodically rather than when the same total amount of testosterone was equally divided among doses. The same supplementation to intact rats intensified androgen-sensitive behavior and physiology over normal levels. In senescent rats uniform pulses of the testosterone complex also improved behavior and physiology. Specifically, spermatogenesis was stimulated and, notably, the treatment increased muscle weight without substantial enlargement of the prostate. Since the testosterone–cyclodextrin complex also can be effectively administered as a sublingual tablet, the data suggest that similar regimens may be recommended for elderly men suffering from decreases in muscle mass.

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REFERENCES

  1. F. E. Yates. Biol. Reprod. 24:73 (1981).

    Google Scholar 

  2. G. B. Ellis and C. Desjardins. Endocrinology 110:1618–1627 (1982).

    Google Scholar 

  3. J. D. Veldhuis, M. L. Carlson, and M. L. Johnson. Proc. Natl. Acad. Sci. USA 84:7686–7690 (1987).

    Google Scholar 

  4. C. Desjardins. Biol. Reprod. 24:1–21 (1981).

    Google Scholar 

  5. J. M. Graham and C. Desjardins. Science 210:1039–1041 (1980).

    Google Scholar 

  6. J. Brotherton. Sex Hormone Pharmacology, Academic Press, New York, 1976.

    Google Scholar 

  7. D. P. DeKlerk, D. S. Coffey, L. L. Ewing, I. R. McDermott, W. G. Reiner, C. H. Robinson, W. W. Scott, J. D. Strandberg, P. Talalay, P. C. Walsh, L. G. Wheaton, and B. R. Zirkin. J. Clin. Invest. 64:842–849 (1979).

    Google Scholar 

  8. W. E. Berndtson, C. Desjardins, and L. L. Ewing. J. Endocrinol. 62:125–135 (1974).

    Google Scholar 

  9. G. T. Taylor, J. Weiss, and J. Haller. Anat. Rec. 211:304–310 (1985).

    Google Scholar 

  10. G. T. Taylor, J. Weiss, and T. Frechmann, J. Reprod. Fertil. 77:419–423 (1986).

    Google Scholar 

  11. K. Hirano and H. Yamada. Chem. Pharm. Bull. Jap. 29:1410–1415 (1981).

    Google Scholar 

  12. J. Pitha, S. M. Harman, and M. E. Michel. J. Pharm. Sci. 75:165–167 (1986).

    Google Scholar 

  13. T. O. Carpenter, J. M. Pettifor, R. M. Russell, J. Pitha, S. Mobarhan, M. S. Ossip, S. Wainer, and C. S. Anast. J. Pediat. 111:507–512 (1987).

    Google Scholar 

  14. G. B. Ellis and C. Desjardins. Biol. Reprod. 30:619–627 (1984).

    Google Scholar 

  15. N. B. Schwartz and S. N. Justo. Endocrinology 100:1550–1556 (1977).

    Google Scholar 

  16. L. W. Kaler and W. B. Neaves. Endocrinology 108:712–719 (1981).

    Google Scholar 

  17. A. Coquelin and C. Desjardins. Am. J. Physiol. 243:E257–E263 (1982).

    Google Scholar 

  18. C. H. Phoenix and K. C. Chambers. Proc. Soc. Exp. Biol. Med. 183:151–162 (1986).

    Google Scholar 

  19. R. A. Steiner, W. J. Bremner, D. K. Clifton, and D. M. Dorsa. Biol. Reprod. 31:251–258 (1984).

    Google Scholar 

  20. E. Nieschlag. In R. J. Santen and R. S. Swordloff (eds.), Male Reproductive Dysfunction, Marcel Dekker, New York, 1986, p. 199.

    Google Scholar 

  21. G. T. Taylor, J. Weiss, and R. Rupich. Physiol. Behav. 35:735–739 (1985).

    Google Scholar 

  22. E. C. Grant. Behavior 21:260–281 (1963).

    Google Scholar 

  23. G. T. Taylor, D. Regan, and J. Haller. J. Endocrinol. 96:143–152 (1983).

    Google Scholar 

  24. FDA. FDA Drug Bulletin, Oct. 1987, pp. 27–28.

  25. J. D. Wilson and J. E. Griffin. Metabolism 29:1278–1295 (1980).

    Google Scholar 

  26. L. L. Ewing, C. Desjardins, and L. G. Stratton. In J. Urquhart and F. E. Yates (eds.), Temporal Aspects of Therapeutics, Plenum Press, New York, 1973, p. 165.

    Google Scholar 

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Taylor, G.T., Weiss, J. & Pitha, J. Testosterone in a Cyclodextrin-Containing Formulation: Behavioral and Physiological Effects of Episode-like Pulses in Rats. Pharm Res 6, 641–646 (1989). https://doi.org/10.1023/A:1015922019038

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  • DOI: https://doi.org/10.1023/A:1015922019038

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