In persistent rat hypothalamic slices thyreostilnulating hormone activates only the oxytocinergic cells of the supraoptic and paraventricular nuclei. This effect manifests itself in increased volume of nucleoli in oxytocinergic cells and in markedly increased content of c-Fos-immunoreactive cells in both nuclei.
Key Words: thyreostimulating hormone; vasopressin; oxytocin; paraventricular and supraoptic nuclei of the hypothalamusThe interactions between the nonapeptidergic neurosecretory system of the hypothalamus and the hypothalamus-hypophysis-thyroid gland system, which produces thyroliberin, thyreostimulating hormone (TSH), and the thyroid gland hormones, have been extensively investigated [1,5,13]. It was demonstrated that vasopressin stimulates the thyroid gland both in vivo and in vitro. There is evidence that thyroid hormones modify the activity of nonapeptidergic cells [6]. The effects of thyroliberin on the function of neurosecretory cells in the supraoptic (SON) and paraventricular (PVN) nuclei of rat hypothalalnus were studied [2][3][4]11,17].The interactions between the nonapeptidergic neurosecretory system of the hypothalamus and TSH-cells of the adenohypophysis have not been studied in sufficient detail. Nevertheless, it is known that vasopressin and oxytocin affect TSH secretion [12,14]. It remains unclear whether TSH has any effect on the activity on nonapeptidergic cells. In the in vivo experiments TSH increased blood concentration of nonapeptide hormones and it was impossible to distinguish between its effects and Laboratory of Neuroendocrinology, M. I. Setchenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, St. Pete~bur9 those of the thyroid gland hormones. We managed to demonstrate a direct effect of TSH on vasopressin-and oxytocinergic cells in experiments on hypothalamic slices.
MATERIALS AND METHODSExperiments were performed oll adult male Wistar rats weighing 120-140 g. The animals were mahltahmd under the standard vivarium conditions. All the experiments were started at 12:00-13:00. The rats were decapitated, the brain was rapidly isolated under stenle conditions, and hypothalalnic slices (400-g lhick) containing SON and/or PVN were prepared. Tlle slices were preincubated for 90 rain at 37~ in Earle's growth medium or in medium 199 with Hanks' balanced salts saturated with carbogen (95% O~+5% CO2). The cells were then transferred to the culture medium containing 50x10 -~ U/ml TSH and incubated for 30 or 60 min under the same conditions.After the incubation the slices were fixed in Bouin's fluid and processed according to the standard histological techniques.Parallel hypothalamic sections were incubated with unlabeled antivasopressin or antioxytocin antibodies and the peroxidase-antiperoxidase complex, using 3,3'-diaminobenzidine for visualization of the 0007-4888/98/0010-0977520.00 9Kluwer Aceademic/Ptenum Puhtishers