Effect of prostaglandin D2 on the release of luteinizing hormone and prolactin in castrated and intact male rats

1986 ◽  
Vol 112 (2) ◽  
pp. 180-184 ◽  
Author(s):  
Lise Wogensen ◽  
Jørgen Warberg

Abstract. One, 5 or 20 μg of prostaglandin D2 (PGD2) was infused into a lateral ventricle of the brain of anaesthetized intact or castrated male rats, and the response of luteinizing hormone (LH) and prolactin (Prl) was determined. PGD2 stimulated the release of LH in both groups of rats. The greatest LH-response was observed in the castrated rats, where the lowest dose of PGD2 (1 μg) caused the greatest LH response. This dose was ineffective in the non-castrated animals. PGD2 had no effect on the release of Prl neither in intact nor in orchidectomized rats. It is concluded that PGD2 is capable of stimulating the release of LH in male rats and that the stimulating effect is intensified by removal of the gonadal negative feedback effect on the hypothalamo-pituitary unit.

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.


1970 ◽  
Vol 46 (1) ◽  
pp. 1-7 ◽  
Author(s):  
S. TALEISNIK ◽  
M. E. VELASCO ◽  
J. J. ASTRADA

SUMMARY The influence that the interruption of the neural afferents to the hypothalamus exerts on ovulation and on the release of luteinizing hormone (LH) was studied in the rat. Animals with retrochiasmatic sections interrupting the neural connexions between the medial hypothalamus and the preoptic area (POA) showed constant oestrus and failed to ovulate. Animals in which the dorsal neural afferents to the POA were transected had oestrous cycles and ovulated normally. The positive feedback effect of progesterone on LH release in spayed animals primed either with 20 μg. oestradiol benzoate or 2·5 mg. testosterone propionate 3 days before was studied. Transection of the dorsal afferents to the POA favoured an increase in plasma LH, but in animals with retrochiasmatic sections the response was abolished. However, the negative feedback effect of ovarian steroids operated after both types of transection because an increase in plasma LH occurred after ovariectomy. It is concluded that the negative feedback effect of ovarian steroids acts on the medial hypothalamus which can maintain a tonic release of gonadotrophins in the absence of steroids. In contrast, the POA involved in the positive feedback effect of progesterone is concerned with the phasic release of LH.


2018 ◽  
Vol 26 (2) ◽  
pp. 222-228
Author(s):  
Roman Ya. Vlasenko ◽  
Alexander V. Kotov

Aim. To carry out a comparative analysis of characteristics of drinking instrumental activity in rats with different manifestation of risk behavior before and after intracerebral introduction of equally productive dipsogenic doses of angiotensins. Materials and Мethods. The work was conducted on 19 Wistar male rats of 250300 g mass. All manipulations with animals were performed in accordance with the international ethic recommendations on biomedical research with use of animals. All rats were preliminarily scalped under ether anesthesia with removal of soft tissues and periosteum. The cannulae were introduced into rat’s brain through the trephine opening in the lateral ventricle. The length of each cannula was 8 mm, the internal diameter – 0.8 mm. All cannulae had a special restrictor at the distance of about 3.5 mm from the implantable end. Each animal was implanted one cannula into the lateral ventricle of the brain on the right or left side according to the coordinates of stereotaxic atlas for rats (L.D. Pellegrino at al., 1979) (AP = +1.0; L= 2; H= 2.5). Microinjections of substances were made into the brain of nonnarcotized animals using a microsyringe of 5 μL volume («Hamilton», the USA). For intraventricular microinjections, angiotensinII, angiotensinIII and [des – Asp1]angiotensinI («Sigma», the USA) were used. Results. In the article the mechanisms of realization of drinking instrumental activity in rats with different manifestations of risk behavior are described. In view of P.K. Anokhin’s general theory of functional systems, the effects of application of «equally productive» doses of angiotensins on initiation of specific patterns of drinking behavior in rats are discussed. Risk is considered as an independent component of systemic organization of purposive behavior of an individual. It is shown that the «integral pattern of individual behavior» of rats is selectively modulated by angiotensinII and angiotensinIII. This selectivity has a narrow focus and individual manifestations, depending on the background activity of the animals. Conclusion. Depending on the initial level of the intensity of instrumental activity of the animals (with different manifestations of risk behavior), angiotensin II and angiotensin III are involved into initiation of fullscale «integral pattern of individual drinking behavior» or participate in the directed modulation of complex purposive behavior manifested by enhancement of dipsogenic effect. At the same time, [des – Asp1]angiotensinI does not participate in the mechanisms of reproduction of the acquired drinking instrumental habits but induces only mechanisms of initiation of congenital individual forms of drinking behavior.


1971 ◽  
Vol 50 (4) ◽  
pp. 679-683 ◽  
Author(s):  
R. COLLU ◽  
F. FRASCHINI ◽  
L. MARTINI

SUMMARY Melatonin and 5-methoxytryptophol, the two methoxyindoles of pineal origin, were injected into a lateral ventricle of the brain of immature female rats. Treatment was started on the 25th day of age and terminated when the vagina opened. The injection of both methoxyindoles resulted in a statistically significant delay in vaginal opening. Since previous experiments had shown that melatonin specifically inhibits secretion of luteinizing hormone and that 5-methoxytryptophol specifically blocks release of follicle-stimulating hormone, the present results support the hypothesis that the onset of sexual maturation needs a balanced secretion of both gonadotrophins.


1984 ◽  
Vol 62 (9) ◽  
pp. 1231-1233 ◽  
Author(s):  
Gérard Lescoat ◽  
Denise Lescoat ◽  
Danièle Garnier

In 60-day old intact male rats, stress imposed by a strange environment increased the levels of plasma LH and testosterone. Adrenalectomy, performed at 50 days of age, decreased plasma level of testosterone in basal conditions. However, without affecting the plasma level of LH significantly, stress increased plasma testosterone, albeit to a lesser extent, in the adrenalectomized rats. Stimulation of the testicular secretion by the high level of ACTH seems to be the most likely explanation for the observed testosterone peak in the adrenalectomized rat.


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.


1986 ◽  
Vol 26 (3) ◽  
pp. 323-332 ◽  
Author(s):  
M.M. Hinshelwood ◽  
D.J. Dierschke ◽  
E.R. Hauser

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