EFFECT OF A SINGLE INJECTION OF CHLORPROMAZINE INTO INFANT MALE RATS ON SUBSEQUENT GONADOTROPHIN SECRETION

1970 ◽  
Vol 48 (2) ◽  
pp. 151-NP ◽  
Author(s):  
W. LADOSKY ◽  
W. M. KESIKOWSKI ◽  
I. F. GAZIRI

SUMMARY A single injection of 20 μg chlorpromazine/g body weight into male rats 10 days after birth accelerated spermatogenesis when the animals were 45 days old; this was not observed in rats injected on days 1, 5, 8, 12 or 15 of life. When half an ovary was grafted into the eye of rats treated on day 10, they showed a higher incidence of luteinization than ovarian grafts in rats treated at any other age. Compared with animals surgically castrated at the same age, chlorpromazine did not act as by 'pharmacological castration', but induced some alteration in the brain which promoted higher secretion of luteinizing hormone, characteristic of the female pattern of gonadotrophin control, as demonstrated by accelerated spermatogenesis and a higher degree of luteinization. These results suggest that the sexual differentiation of the brain occurs on about the 10th day of postnatal life and can be blocked by chlorpromazine.

1968 ◽  
Vol 46 (4) ◽  
pp. 697-700 ◽  
Author(s):  
K. Brown-Grant

The changes observed in the metabolism of radioiodide and radiophosphorus by the thyroid gland of intact adult male rats following a single injection of estradiol benzoate (4 μg/100 g body weight) are consistent with the suggestion (F. Labrie, G. Pelletier, and C. Fortier. Federation Proc. 26, 484 (1967). Abstr.) that at this dose level estrogen causes a hypersecretion of TSH in such animals.


2020 ◽  
Vol 2 (2) ◽  
pp. 113-116
Author(s):  
Indah Permata Sari ◽  
Muhammad Ichwan ◽  
Yahwardiah Siregar

D-galactose is aldohexose which occurs naturally in the body, including in the brain which is found in lactose disaccharides in honey, beets and milk products. Needed in the body for lactose formation during the process of lactogenesis. Provision of large amounts of D-galactose can cause oxidative damage to various tissues and organs. The purpose was to see changes in body weight in male rats after being given a D-galactose injection. Samples using male mice aged 8 weeks with a weight of ± 30 grams, the number of samples was 6 mice swiss webster strain. intra-peritoneal injection of D-galactose is given for 6 weeks every day (150 mg / kg / bb). The results of this study indicate that the statistical analysis is significant p <0.05 (p = 0.016). The conclusion after being given injection of D-galactose for 6 weeks every day intra peritoneally was found D-galactose had an effect on the weight gain of male mice.


1982 ◽  
Vol 100 (2) ◽  
pp. 168-176 ◽  
Author(s):  
K. M. Pirke ◽  
B. Spyra

Abstract. The effect of starvation was studied in male Wistar rats. After only 2 days of food deprivation, LH concentrations in serum are greatly suppressed, while a significant increase in plasma corticosterone occurs after 5 days' starvation. The noradrenaline and dopamine turnover in the basal hypothalamus is decreased after 2 days. The catecholamine turnover is also reduced in the preoptic area, and in the median eminence. Injection of the catecholamine precursor l-dopa (100 mg/kg) can prevent the increase of plasma corticosterone, but not the decrease of LH. The α-agonist clonidine (150 μg/kg), but neither the β-agonist salbutamol (0.5 mg/kg), nor the dopamine agonist apomorphine (1.0 mg/kg) can prevent the starvation induced corticosterone increase. The decrease of plasma LH is not influenced by the dopamine or noradrenaline agonists. From these data, it appears that a decreased activity of noradrenergic neurons may be responsible for the corticosterone increase in the plasma of starved rats.


1964 ◽  
Vol 46 (1) ◽  
pp. 12-24 ◽  
Author(s):  
Dorothy E. Woolley ◽  
Paola S. Timiras

ABSTRACT Ovariectomy, hypophysectomy and administration of oestradiol, progesterone, testosterone or methylandrostenediol altered water or electrolyte concentrations in plasma, liver, cerebral cortex, brain stem and cerebellum in the rat. High daily doses of the steroids (500 μg/100 g body weight) increased plasma sodium levels. Oestradiol, followed by progesterone, then testosterone and methylandrostenediol, was most effective in producing hypernatraemia. Lower doses of oestradiol (10–200 μg/100 g body weight) did not change plasma sodium concentrations. Plasma potassium was increased by ovariectomy and decreased by low doses of oestradiol in ovariectomized, but not in hypophysectomized, rats. All doses of oestradiol lowered per cent plasma water in intact adult male rats and ovariectomized adult females, but not in hypophysectomized rats. High doses of the steroids, especially of oestradiol plus progesterone, raised concentrations of water, sodium, potassium and chloride in the liver, whereas water, sodium and potassium concentrations remained constant in brain. Each of the steroids elevated brain chloride concentrations. Of the brain areas analyzed, the cerebral cortex most consistently showed increased chloride after injections. Testosterone and progesterone, followed by oestradiol and then methylandrostenediol, were most potent in increasing brain chloride concentrations. Because the sex hormones have previously been shown to alter brain excitability, it is postulated that some of these alterations may be correlated with concomitant changes in brain anionic concentrations.


2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. A56-A57
Author(s):  
Nicole A Teaney ◽  
Nicole E Cyr

Abstract The nutrient-sensor protein Sirtuin 1 (Sirt1; silent mating type information regulation 2 homolog 1) has been shown to have significant and opposing effects on insulin resistance, leptin resistance, and body weight in the periphery and the brain. In the hypothalamic arcuate nucleus (ARC) of the brain, Sirt1 increases in the obese state and acts to promote weight gain as well as insulin and leptin resistance by increasing the orexigenic neuropeptides Agouti-related protein (AgRP) and neuropeptide Y (NPY), and in a distinct set of ARC neurons, by decreasing POMC and thus its anorexigenic derivative alpha-melanocyte stimulating hormone (alpha-MSH) (1). Sirt1’s actions on these neuropeptides are mediated at least in part by the deacetylation of the transcription factor forkhead box O1 (FOXO1). Another mechanism by which Sirt1 regulates body weight appears to be through mediating changes in the synapses of these neuropeptide-producing ARC neurons. For example, a previous study demonstrated that Sirt1 inhibition with the specific Sirt1 inhibitor, Ex-527, decreased AgRP-NPY inhibitory synaptic input on POMC neurons, which suggests that the obesity-induced increase in ARC Sirt1 would increase AgRP-NPY inhibition of POMC neurons thus promoting weight gain (2). The present study investigated how Sirt1 regulates synapses specifically in POMC-producing N43-5 neurons. Results reveal that inhibition of Sirt1 with Ex-527 significantly increased the presynaptic marker Synapsin 1 (Syn1) in N43-5 neurons. Furthermore, we investigated whether the Sirt1 target, FOXO1, mediates these synaptic changes. FOXO1 overexpression significantly decreased Syn1 and transfection of mutant FOXO1 significantly increased Syn1. Overall, our results suggest that Sirt1 regulates synapses of POMC neurons and does so in a manner that differs from Sirt1’s regulation of AgRP-NPY neuronal synapses. Future work will elucidate the mechanisms and consequences of Sirt1 and FOXO1 regulation of POMC neuron synapses under different nutritional conditions in vitro and in vivo. (1) Cyr, N. E., Steger, J. S., Toorie, A. M., Yang, J. Z., Stuart, R., Nillni, E. A. (2014). Central Sirt1 Regulates Body Weight and Energy Expenditure Along With the POMC-Derived Peptide α-MSH and the Processing Enzyme CPE Production in Diet-Induced Obese Male Rats, Endocrinology, 155(7), 2423–2435. (2) Dietrich, M. O., Antunes, C., Geliang, G., Liu, Z., Borok, E., Nie, Y., . . . Horvath, T. L. (2010). Agrp neurons mediate Sirt1’s action on the melanocortin system and energy balance: Roles for Sirt1 in neuronal firing and synaptic plasticity. The Journal of Neuroscience, 30(35), 11815–11825.


2002 ◽  
Vol 95 (3) ◽  
pp. 897-900 ◽  
Author(s):  
M. A. Persinger ◽  
L. S. St-Pierre

Male rats were seized with lithium and pilocarpine and then injected within 30 min. with either acepromazine or ketamine. These rats as well as age-matched normal rats were observed daily for one year. The rats which had received the ketamine after the seizures were significantly heavier than either the normal rats or the other group of seized rats. The bulk of this increased weight was due to the marked increase in white, extremely dense adipose tissue. Compared to the acepromazine-treated rats, the ketamine-treated rats did not exhibit spontaneous seizures and exhibited cerebral widths comparable to normal rats. These results suggest that the multifocal, graded neuronal loss associated with this seizure model may allow other “configurations” to emerge that can support normal behaviors as well as new characteristics.


1984 ◽  
Vol 106 (1) ◽  
pp. 30-37 ◽  
Author(s):  
Lise Wogensen ◽  
Jørgen Warberg

Abstract. Two μg of prostaglandin E2 (PGE2) was infused into a lateral ventricle of the brain of female rats at 09.00 or 13.00 h on the different days of the oestrous cycle and the effect on luteinizing hormone (LH) and prolactin (Prl) release was determined. At 09.00 h PGE2 caused a pronounced release of LH in pro-oestrous, oestrous and metoestrous rats whereas the LH response in dioestrous rats was moderate. The secretion of Prl was only stimulated in rats from the pro-oestrous phase. When infused at 13.00 h PGE2 had a marked stimulatory effect on the release of LH in all groups of rats. The response was almost the same in oestrous, metoestrous and dioestrous rats but pro-oestrous rats a 2-fold higher LH response was observed. On each day of the oestrous cycle it was found that the LH-releasing activity of PGE2 was greater at 13.00 h than at 09.00 h. Thus, the overall greatest responsiveness of LH to PGE2 was noted at 13.00 h on pro-oestrus i.e. at a time which was prior to the onset of the spontaneous LH surge. At 13.00 h – as at 09.00 h – PGE2 was only capable of stimulating Prl release in pro-oestrous rats. Resembling the LH response it was found that PGE2-induced Prl release was greater at 13.00 h than at 09.00 h. In adult male rats the stimulatory effect of PGE2 on LH and Prl release was independent of the time of administration. It is concluded that the neuroendocrine elements of the hypothalamo-pituitary unit in mature female rats exhibit cyclic as well as diurnal alterations in the responsiveness to PGE2.


1980 ◽  
Vol 85 (1) ◽  
pp. 69-74 ◽  
Author(s):  
F. GOGAN ◽  
I. A. BEATTIE ◽  
M. HERY ◽  
E. LAPLANTE ◽  
C. KORDON

SUMMARY Implantation of oestradiol into adult rats of both sexes induced different patterns of LH secretion depending on the time at which gonadectomy or testosterone injection were performed. Castration 2 h after birth allowed an LH peak to occur daily at 18.00 h, but its amplitude was lower than that of adult gonadectomized female rats treated with oestradiol. Castration 24 h after birth elicited two kinds of response; a circadian discharge of LH lower than that of male rats gonadectomized 2 h after birth or a steady low level of LH. The LH rhythmicity induced by implantation of oestradiol was not seen after castration at 8 weeks of age. Neonatal administration of testosterone to female rats prevented the LH peak induced by oestradiol that was seen in adult ovariectomized rats. Neonatal or adult ovariectomy did not interfere with the rhythmical response of LH after implantation of oestradiol. Thus, it is concluded that sexual differentiation of the hypothalamus is primarily of masculine origin.


1985 ◽  
Vol 109 (2) ◽  
pp. 198-203 ◽  
Author(s):  
Rüdiger Schulz ◽  
Annemarie Wilhelm ◽  
Karl Martin Pirke ◽  
Albert Herz

Abstract. Previous studies in male and female immature rats have revealed striking sex differences as concerns endorphinergic and adrenergic control of luteinizing hormone (LH) secretion. The present study examines in 10 days old male and females rats whether these differences result from sexual differentiation of the brain, or acute effects of male and female gonadal hormones. The techniques employed to manipulate these mechanisms were gonadectomy immediately post-partum and androgenization. Androgenization on the 1st and 2nd day of life reduces the ability of naloxone to elevate serum LH levels in females, but failed to modify the LH-elevating effect of clonidine in males. Experiments with castrates showed that testosterone is critical for these sex-related differences. Treatment with testosterone on the 9th day of life of intact or gonadectomized rats revealed the ability of this hormone to modify LH-release acutely. We conclude that sexual differentiation of the brain may be of minor significance for the sex-related LH-control mechanisms in prepubertal rats. Of importance is the acute presence of testosterone, since in its absence male characteristics disappear.


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