Hormonal Control of Sexual Differentiation of the Hypothalamus in the Neonatal Female Rat

• Published in: Differentiation (London) Vol. 2; no. 5; pp. 275 - 285
• Main Authors: Doughty, Cynthia, McDonald, P.G.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Elsevier B.V 01.10.1974; Blackwell Publishing Ltd
• Subjects: Age Factors; Animals; Animals, Newborn; Diethylamines - pharmacology; Estrogen Antagonists; Ethanol - analogs & derivatives; Ethanol - pharmacology; Female; Genitalia, Female - growth & development; Hypothalamus - physiology; Organ Size; Ovary - anatomy & histology; Phenyl Ethers - pharmacology; Rats; Sex Characteristics; Sex Determination Analysis; Sexual Behavior, Animal; Testosterone - pharmacology
• ISSN: 0301-4681; 1432-0436
• DOI: 10.1111/j.1432-0436.1974.tb00362.x

Groups of female rats were treated either on the day of birth or at 5 days of age with oil, testosterone propionate (TP), MER-25 (an oestrogen antagonist) or TP plus MER-25. Treatment with oil and MER-25 alone on day 1 or 5 did not prevent the development of cyclic repro ductive activity in any of the females. Administration of TP on the day of birth inhibited vaginal opening and prevented cyclic ovarian activity. Treatment with TP on day 5 significantly advanced the time of vaginal opening but prevented both vaginal and ovarian cyclicity. Treatment on the day of birth with a combination of MER-25 and TP did not significantly prevent the masculinizing action of TP. In most cases vaginal opening failed to occur; the ovaries were small and devoid of corpora lutea. Sexual receptivity was not significantly affected by treatment on the day of birth with oil, TP or MER-25 alone. When MER-25 was given before the TP, however, receptivity was significantly enhanced compared with oil treatment. At 5 days of age treatment with MER-25 plus TP prevented the masculinizing action of TP. Most of the animals had normal ovarian weights, and ovaries which contained both follicles and corpora lutea. The most effective treatment for preventing the action of TP was administration of MER-25 6 h before the injection of androgen. After treatment at 5 days of age, sexual receptivity was significantly reduced in all groups compared with the oil-treated animals. Administration of MER-25 plus TP did not enhance sexual receptivity above that found in the animals receiving TP alone. The results are discussed in terms of the possible role of oestrogen in controlling hypothalamic differentiation in the neonatal female rat.