Search Results

You are looking at 1 - 10 of 16 items for

  • Author: P. S. BROWN x
Clear All Modify Search
Free access

P. S. Brown

Sundberg, Fawcett, Illner & McCann (1975) have shown that high concentrations of indomethacin (1 and 2·7 mM) can increase the release of LH and FSH from rat pituitary tissue in vitro. Such concentrations, however, have other actions in addition to the inhibition of prostaglandin (PG) synthetase for which the drug is commonly used experimentally (Flower, 1974). The effects of lower concentrations of indomethacin have therefore been tested.

Free access

P. S. BROWN

Summary.

The pituitary content of fsh was equivalent to approximately 50 μg nih. fsh sl/gland in female hamsters aged 26 days and fell to 12 μg/gland by 40 days. Male hamsters had similar levels at 26 days but the hormone content rose to 105 μg/gland by 40 days. This contrast between males and females is similar to that found in rats during sexual maturation. In guinea-pigs, pituitary fsh fell in both males and females from means of 45 and 40 μg/gland at 18 days to 15 and 12 μg/gland at 88 days. Testosterone treatment of female rats on the 5th day of life reduced pituitary fsh to 65% of normal at 28 days of age but caused no significant changes at 22, 25, 34 or 40 days.

Free access

P. S. BROWN and LINDA FAWKE

Summary.

Drugs were injected on experimental Days 2 to 5 into mature male rats that were (1) intact, (2) castrated on Day 1, or (3) castrated on Day 1 and treated with testosterone. The animals were killed on Day 7 and the pituitary fsh content compared with that of controls. Methallibure prevented the rise in fsh content caused by testosterone in the third group and reduced pituitary fsh in intact rats: this may have resulted from inhibition of fsh synthesis. Methallibure increased pituitary fsh in castrated rats, probably by inhibiting its secretion. Reserpine increased fsh content in each type of animal and p-chlorophenylalanine increased it in all but intact rats: these drugs probably inhibit fsh secretion. The fsh content was reduced by α-methyltyrosine in testosterone-treated castrated rats while thymoxamine increased it in such animals and in intact rats. These findings do not clarify the rôle of catecholamines in fsh secretion. The similarity of the effects of reserpine and p-chlorophenylalanine supports the suggestion that 5-hydroxytryptamine plays an excitatory rôle in fsh secretion.

Free access

LINDA FAWKE and P. S. BROWN

Summary.

The follicle-stimulating hormone (fsh) content of the pituitary gland of immature female rats was equivalent to 240 μg nih-fsh-sl at the age of 22 days but had fallen to 19 μg at 40 days. In rats approaching sexual maturity, it was sometimes possible to show a significant fall in fsh between 12.00 and 18.00 hours on the same day. In adults with regular 4-day oestrous cycles, there was a significant rise in pituitary fsh content from the morning of pro-oestrus (26 μg) to the morning of oestrus (41 μg). No fall in fsh content was found during the afternoon of pro-oestrus. An Appendix describes experiments in which various methods of killing rats and storing pituitary material are compared.

Free access

P. S. Brown and P. J. O'Shaughnessy

Summary. Male rats, aged 19 days, were injected with 1 mg cyproterone acetate, an antiandrogen, and killed 24 h later. In 9 out of 10 experiments this increased the apparent FSH-binding capacity by testicular tissue in vitro. In 4 out of 5 similar experiments, injection of 500 μg testosterone propionate caused a significant reduction in FSH binding. Observed changes were small but this does not preclude the possibility that androgens contribute to the physiological control of FSH receptor numbers.

Free access

LINDA FAWKE, AUDREY MORRIS and P. S. BROWN

Summary.

Compensatory hypertrophy of the remaining testis was not detected in mice hemicastrated at ages varying from 3 to 18 weeks, and killed 1, 2 or 3 weeks later. The response of hemicastrated mice to drugs and sex steroids was tested to see whether these animals were useful in studying the effects of antigonadotrophic substances. Seminal vesicle weight was significantly reduced by oestradiol, progesterone, methallibure and reserpine (though small doses of reserpine caused unexpected increases). Increase in testis weight was significantly reduced by oestradiol, methallibure, chlorpromazine and reserpine. Correction of seminal vesicle and increase in testis weight for initial body weight was found to be valid and useful. Hemicastrated mice were used to test drugs which inhibit the synthesis of biogenic monoamines: p-chlorophenylalanine reduced seminal vesicle weight but α-methyltyrosine was without effect.

Free access

BARBARA R. PEARCE and P. S. BROWN

Data on the pituitary content of follicle-stimulating hormone (fsh) in immature female rats have been published (Kragt & Ganong, 1968; Goldman & Mahesh, 1968; Fawke & Brown, 1970), but there seems to be little comparable information about the male. The following results have been obtained in males from our colony of Porton rats: the experiments were under conditions similar to those used in a previous investigation of the females (Fawke & Brown, 1970). Three series of measurements were made (see Table 1). Results are strictly comparable within each series as they were obtained from animals born on the same day. In Series B and C, rats were randomized individually; in Series A, which involved unweaned rats, whole litters were killed together and only the allocation of litters was random. The animals
Free access

S. A. R. CHOUDHURY, R. M. SHARPE and P. S. BROWN

Summary.

Injection of pimozide reduced compensatory ovarian hypertrophy and raised pituitary LH content in hemispayed cyclic and androgenized female rats. Pimozide inhibited spontaneous and induced ovulation and markedly reduced the rise in serum LH during the afternoon of pro-oestrus. Pimozide failed to reduce serum LH in male rats and caused no apparent delay in sexual maturation in males or females. The results suggest that the drug suppresses the ovulatory release of LH, presumably by antagonizing hypothalamic dopamine. The drug appears to have less striking effects on the tonic secretion of FSH and LH.

Free access

M. WELLS, P. S. BROWN and F. J. CUNNINGHAM

Urinary gonadotrophins have frequently been measured during the menstrual cycle (see Evans & Simpson, 1950; Loraine & Schmidt-Elmendorff, 1963). The most commonly applied method of assay has been that depending on the uterine response in immature mice, which measures both follicle-stimulating hormone (fsh) and luteinizing hormone (lh) (Brown & Billewicz, 1962), and this might explain why some workers have found that it fails to provide evidence of a meaningful relationship between pituitary and ovarian function (Loraine & Schmidt-Elmendorff, 1963). Preliminary experiments (Brown, Wells & Cunningham, 1964) have suggested that the method of Cunningham (1962) might be useful in demonstrating significant changes in pituitary gonadotrophic function if such occur. The method depends on the induction of ovulation in immature mice, and
Free access

P. E. Mattner, B. W. Brown and J. R. S. Hales

Summary. Vessels with histological features characteristic of arterio–venous anastomoses were found in the stroma but not in CL. In 5 conscious ewes at the mid-luteal stage of the oestrous cycle, ovarian blood flow was significantly greater (P < 0·025) with microspheres of 50 than of 15 μm diameter in ovaries without CL (0·23 ± 0·04 (s.e.m.) and 0·11 ± 0·02 ml/min, respectively), but not in ovaries with CL (4·42 ± 0·86 and 3·73 ± 0·70 ml/min, respectively). In 5 similar but anaesthetized ewes, the portion of each ovarian artery within the ovarian vascular pedicle was bypassed with re-entrant catheters through which microspheres were perfused. A greater proportion (P < 0·01) of 50 than of 15 μm microspheres was retained in ovaries with (90 and 79%) or without (82 and 45%) a CL.

It is concluded that functional arterio–venous anastomoses are present in sheep ovaries.