Regulation of progesterone secretion by LH and prolactin during the first half of pregnancy in the mouse.

Pregnant mice were treated with antiserum to LH or bromocriptine to inhibit the activity of LH and prolactin, respectively. Luteal function was monitored by the radioimmunoassay of plasma progesterone. Bromocriptine treatment on Days 2 or 5 of pregnancy produced a rapid decrease in progesterone secretion, but had no effect on luteal function when given on Days 6, 7 or 8 of gestation. Treatment with LH antiserum before implantation did not inhibit progesterone secretion, but luteal function was severely impaired when the antiserum was given on Days 5--9 of pregnancy. These results demonstrate the dynamic nature of luteal dependency on prolactin and LH, and indicate that LH is an essential component of the luetotrophic complex of the mouse.

Urotensin II: a somatostatin-like peptide in the caudal neurosecretory system of fishes.

Urotensin II, a peptide hormone from the caudal neurosecretory system of the teleost, Gillichthys mirabilis, was isolated by using classical chromatographic techniques and high-performance liquid chromatography (HPLC). Direct microtechniques for sequence determination were used to establish its structure. Urotensin II from Gillichthys is a 1363-dalton dodecapeptide with the amino acid sequence Ala-Gly-Thr-Ala-Asp-Cys-Phe-Trp-Lys-Tyr-Cys-Val. This sequence is homologous with somatostatin in positions 1 and 2 and 7-9. The sequence has been verified by the production of a bioactive synthetic urotensin II. The possible chemical and physiological significance of its homology to somatostatin is discussed.

Iontophoretic release of cyclic AMP and dispersion of melanosomes within a single melanophore.

Selective dispersion of melanosomes was often observed after iontophoretic injection of cyclic adenosine monophosphate (AMP) from a glass microelectrode positioned in a target melanophore in frog skin (as viewed from above through a microscope), with other melanophores in the field serving as controls. Because the skin has orderly arrays of several types of closely spaced cells, it is probable that at times the microelectrode also impales cells other than melanophores. When cyclic AMP injection inside a cell resulted in dispersion of melanosomes from a perinuclear position into dendritic processes, the onset of dispersion was relatively rapid, in many cases less than 4 min (mean time of onset, 5.3 +/- 2.9 [SD] min). A much slower dispersion (mean time of onset, 19.0 +/- 5.0 min) of melanosomes was observed when the microelectrode was positioned adjacent to a melanophore, and much larger quantities of cyclic AMP were released. In addition, no changes were observed for injections of 5'-AMP or cyclic guanosine monophosphate (GMP) through electrodes positioned inside or adjacent to melanophores. Potential measurements showed that after impaling a clell, a constant transmembrane potential could often be recorded over many minutes, indicating that the membrane tends to seal around the microelectrode. The results indicate that cyclic AMP acts more rapidly on the inside of a cell than when applied outside a cell and allowed to diffuse through the plasma membrane. This study introduces a model system whereby the properties of the plasma membrane and melanocyte-stimulating hormone (MSH) receptors can be studies within a single target cell.

Plasma testosterone during pregnancy in the mouse.

Levels of plasma testosterone (T) were studied throughout pregnancy and on the day of parturition in selected strains of mice. A dramatic midpregnancy increase in androgen occurred in both strains examined (peak on day 9). A second increase in plasma T was found during the latter half of gestation (days 14-17), at which time plasma estradiol levels were elevated.

Plasma LH levels in the mare during the oestrous cycle.

Plasma levels of LH were determined by heterologous radioimmunoassay utilizing highly purified equine LH as standard. Samples were taken regularly from eleven mares for twenty-six oestrous cycles over a period of 10 weeks. The mean cycle length was 20-5 +/- 3-1 (S.D.) days, and ovulation occurred on average 4-3 +/- 1-6 (S.D.) days from the time heat was first detected. Levels of LH were persistently low from Days 5 to 16 of the cycle (ovulation = Day 0). They then increased slowly over a number of days and continued to rise beyond the levels observed at any time during the immediate preovulatory period or the day of ovulation. A significant decrease from peak levels was not observed until the 3rd day after ovaulation, from which time levels continued to decline toward dioestrous values by an apparent first-order decay process with a half-life of 1-8 days. The pattern of plasma LH in the mare differs from that reported for other species and it is suggested that persistance of high concentrations of LH results from a long half-life of the endogenous LH. This in turn may be responsible for the relatively large number of second ovulations detected in many oestrous cycles.