LESIONS OF THE SUPRACHIASMATIC NUCLEI AND THE SEROTONIN-DEPENDENT PHASIC RELEASE OF LUTEINIZING HORMONE IN THE RAT: EFFECTS ON DRINKING RHYTHMICITY AND ON THE CONSEQUENCES OF PREOPTIC AREA STIMULATION

1980 ◽  
Vol 84 (2) ◽  
pp. 231-236 ◽  
Author(s):  
C. W. COEN ◽  
P. C. B. MacKINNON

Ovariectomized rats in which <7% of the suprachiasmatic nuclei had been spared by bilateral radiofrequency lesions were distinguishable from those with >40% of the nuclei by their consistent failure to show the oestrogen-induced daily surge of LH, either with or without pharmacological manipulations of serotonin (5-HT), and also by their loss of the normal rhythmicity of drinking. Minor damage to structures adjacent to the suprachiasmatic nuclei was similar in both groups. The identical facility with which electrical stimulation of the preoptic area induced LH release in the two groups of animals suggested that they were not characterized by different degrees of damage to the preopticotuberal pathway. These results are considered in relation to evidence indicating that the suprachiasmatic nuclei represent the densest concentration of 5-HT terminals in the forebrain and also the site of a mechanism involved in the generation of circadian rhythms.

1972 ◽  
Vol 54 (2) ◽  
pp. 227-237 ◽  
Author(s):  
H. G. BURGER ◽  
G. FINK ◽  
V. W. K. LEE

SUMMARY The presence of luteinizing hormone releasing factor (LH-RF) activity was investigated in pituitary stalk and systemic blood collected from rats ovariectomized at least 3 weeks previously, and in stalk blood from male rats in which electrodes had been implanted in the medial preoptic area of the brain. Most of the assayable luteinizing hormone (LH) present in the blood samples was eliminated by acid-ethanol extraction followed by ultrafiltration. The ultrafiltrates were injected into ovariectomized rats treated with oestrogen and progesterone, and increments in the concentration of LH in the sera of these animals, estimated by radioimmunoassay, were taken as an indication that the filtrate was able to release LH from the anterior pituitary gland. The ultrafiltrates of both the stalk and systemic plasma from the ovariectomized rats exhibited LH-RF activity as did the ultrafiltrates of blood collected from the pituitary stalk of the male rats during electrical stimulation of the preoptic area; stalk blood collected from these animals before the current was applied appeared to be inactive. The LH-RF activity of the ultrafiltrates of systemic and pituitary stalk plasma taken from ovariectomized rats was similar, and, therefore, the possibility is raised that the response of the pituitary glands in ovariectomized rats treated with oestrogen and progesterone is of an all or none type. The presence of appreciable quantities of LH-RF in the systemic plasma of ovariectomized rats may explain the discrepancy between bioassay and immunoassay estimates of LH in the plasma of these animals. The rapid increase in the concentration of serum LH and in the LH-RF activity of pituitary stalk plasma which followed stimulation of the preoptic area suggests that this region of the brain may be important in the control of the secretion of LH in the male as well as in the female animal.


1973 ◽  
Vol 58 (2) ◽  
pp. 163-176 ◽  
Author(s):  
M. E. VELASCO ◽  
I. ROTHCHILD

SUMMARY Factors affecting luteinizing hormone (LH) secretion in response to stimulation of the preoptic area (POA) of the forebrain in rats were explored by determining serum LH levels after electrochemical stimulation of the POA. In rats made anovulatory by exposure to constant light (CLA rats), peak concentrations of LH in serum were found 2 h after stimulation with 5–15 mC, and 1 h after stimulation with 0·5–1 mC. The peak levels increased with increasing doses between 0·5 and 15 mC. The incidence of rats ovulating and the mean number of ovulations/rat were roughly proportional to the stimulating dose, but a plateau was reached between 5 and 10 mC. A threshold level of serum LH seemed to be necessary for ovulation, and the incidence of ovulations of six ova or more/rat increased with the increase in peak serum LH level. Preoptic-roof section, which cuts dorsal afferents to the POA, enhanced the increase in serum LH in response to POA stimulation in CLA rats, while sodium pentobarbitone anaesthesia decreased the response. In both cases, the incidence of ovulation and the number of ovulations/rat were not different from values found in POA-stimulated control CLA rats showing the same peak serum LH level. In normal cyclic rats the response of serum LH to stimulation was much greater on the morning of pro-oestrus than on that of oestrus; at prooestrus a second rise occurred between 17.00 and 19.00 h. Three days after ovariectomy the basal level of LH increased; these ovariectomized rats showed a small increase in response to a dose of 5 mC. Treatment with 20 μg oestradiol benzoate at the time of ovariectomy, however, resulted in a lowered basal LH level, but the peak response to 5 mC was almost as great as that found in similarly stimulated intact CLA rats. In intact males and in neonatally androgen-treated females the peak levels of serum LH in response to doses of 5 or 15 mC were equivalent to those in CLA females in response to doses of only 1–5 mC.


1974 ◽  
Vol 62 (3) ◽  
pp. 589-604 ◽  
Author(s):  
G. FINK ◽  
M. S. AIYER

SUMMARY The responsiveness of the hypothalamo-hypophysial axis to electrical stimulation of the medial preoptic area was tested at various times during the oestrous cycle of the rat. Animals were anaesthetized with sodium pentobarbitone, and glass-insulated bipolar platinum electrodes were stereotaxically implanted in the medial preoptic area. The stimulus consisted of accurately balanced biphasic rectangular pulses, height 500 μA, duration 2 ms and frequency 60 Hz, applied in trains of 30 s intervals. The concentration of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) in blood samples withdrawn from the external jugular vein immediately before and at frequent intervals up to 1 h after application of the stimulus was determined by radioimmunoassay. In all animals the stimulus was applied for a period of 15 min, for it was found that under these conditions the profiles of LH and FSH produced in individual animals were similar to those which followed the i.v. injection of 50 ng synthetic luteinizing hormone releasing factor (LH-RF)/100 g body wt, the minimal ovulatory dose of LH-RF in our laboratory. Both for LH and FSH, the profiles of responsiveness of the hypothalamo-hypophysial axis to electrical stimulation through the oestrous cycle resembled closely the profile of responsiveness of the anterior pituitary gland to LH-RF administered intravenously. There was a relatively gradual increase in pituitary sensitivity, in terms of the mean maximal increments, between the early afternoon of dioestrus and pro-oestrus, followed by an abrupt and marked rise which reached a peak at 18.00 and 21.00 h of pro-oestrus for LH and FSH, respectively. Sensitivity of the hypothalamo-hypophysial axis declined through oestrus and metoestrus reaching a nadir at 13.30 h of dioestrus. While these results do not exclude a change in sensitivity of the neural component of the hypothalamo-hypophysial axis during the oestrus cycle, they do indicate that the timing and magnitude of changes in sensitivity of the anterior pituitary gland to both endogenous and exogenous LH-RF are similar. This raises the possibility that a marked increase in the secretion of LH-RF during the afternoon of pro-oestrus may not be necessary for the occurrence of the surge of LH and FSH, for conceivably the latter could depend on a change in sensitivity of pituitary gonadotrophs to constant or only slightly increased levels of LH-RF in hypophysial portal blood. Our findings are compared with those of workers who have employed electrochemical stimulation of the preoptic area.


1966 ◽  
Vol 51 (2) ◽  
pp. 281-289 ◽  
Author(s):  
J. Moll ◽  
G. H. Zeilmaker

ABSTRACT Castrated young adult inbred male rats bearing ovarian transplants were subjected to electrical stimulation of the hypothalamus. This was done in order to investigate whether discharge of ovulatory amounts of gonadotrophins could be induced in such male animals by this procedure. Bilateral stimulations with unipolar electrodes and a DC current of 1.5 mA applied during 10 seconds induced in the ovarian grafts histological changes indicating the discharge of ovulatory amounts of gonadotrophins. In animals killed one day after stimulation these changes consisted of displacement of the ova towards the centre of the follicles with loosening of the cumulus oophorus. In one animal the ova had left the follicles. In animals killed three days after stimulation numerous young corpora lutea could be observed. These results were obtained with electrode tips either close to the median eminence, or in the preoptic area. Shamstimulations were ineffective. Some of the experimental animals received progesterone pretreatment. This rendered the stimulations ineffective, if continued until the day preceding stimulation, but seemed without effect on the results of stimulation, if two or three days without progesterone preceded the stimulations.


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