LUTEINIZATION OF OVARIAN GRAFTS IN RATS RELATED TO TREATMENT WITH TESTOSTERONE IN THE NEONATAL PERIOD

1969 ◽  
Vol 43 (2) ◽  
pp. 253-NP ◽  
Author(s):  
W. LADOSKY ◽  
J. G. L. NORONHA ◽  
I. F. GAZIRI
Keyword(s):  
Wistar Rats ◽  
Testosterone Propionate ◽  
Neonatal Period ◽  
Central Mechanism ◽  
Female Rats ◽  
Corpora Lutea ◽  
Male Wistar Rats

SUMMARY Male Wistar rats were castrated on the day of birth and divided into two groups; the first was injected with 0·1 mg. testosterone propionate (TP), on the day of castration and the second with 0·5 mg. TP after day 10. When 45 days old, all were grafted with an ovary in the kidney. Animals in the first group showed ovaries with ripening follicles without corpora lutea; those in the second group had corpora lutea at different stages of maturation. Ovaries grafted into female rats spayed on the day of birth developed luteinization even when injected with 0·5 mg. TP after the 10th day of life, but not if the hormone was injected earlier. Since the hypothalamus is sensitive to androgens only before the 10th day of life even in gonadectomized rats, it can be argued that the female pattern of gonadotrophin control does not correspond to the undifferentiated hypothalamus but depends on some active central mechanism. The period during which the hypothalamus is still sensitive to androgens would correspond to the undifferentiated equipotential stage.

Leptin administration during lactation leads to different nutritional, biometric, hemodynamic, and cardiac outcomes in prepubertal and adult female Wistar rats

2021 ◽  
pp. 1-6
Author(s):  
Karyne Pollo de Souza ◽  
Samuel de Sousa Pedro ◽  
Nazareth Novaes Rocha ◽  
Emiliana Barbosa Marques ◽  
Christianne Bretas Vieira Scaramello
Keyword(s):  
Left Ventricle ◽  
Test Performance ◽  
Wistar Rats ◽  
Female Rats ◽  
Internal Diameter ◽  
Critical Periods ◽  
Adult Age ◽  
Cardiac Outcomes ◽  
Male Wistar Rats ◽  
Echocardiographic Parameters

Abstract Literature reports that insults, such as hormonal disturbances, during critical periods of development may modulate organism physiology and metabolism favoring cardiovascular diseases (CVDs) later in life. Studies show that leptin administration during lactation leads to cardiovascular dysfunction in young and adult male Wistar rats. However, there are sex differences regarding CVD. Thus, the present work aimed to investigate neonatal leptin administration’s consequences on different outcomes in female rats at prepubertal and adult age. Newborn Wistar female rats were divided into two groups, Leptin and Control, receiving daily subcutaneous injections of this adipokine (8 μg/100 g) or saline for the first 10 of 21 d of lactation. Nutritional, biometric, hemodynamic, and echocardiographic parameters, as well as maximal effort ergometer performance, were determined at postnatal days (PND) 30 and 150. Leptin group presented lower food intake (p = 0.0003) and higher feed efficiency (p = 0.0058) between PND 21 and 30. Differences concerning echocardiographic parameters revealed higher left ventricle internal diameter (LVID) in systole (p = 0.0051), as well as lower left ventricle ejection fraction (LVEF) (p = 0.0111) and fractional shortening (FS) (p = 0.0405) for this group at PND 30. Older rats treated with leptin during lactation presented only higher LVID in systole (p = 0.0270). Systolic blood pressure and maximum effort ergometer test performance was similar between groups at both ages. These data suggest that nutritional, biometric, and cardiac outcomes due to neonatal leptin administration in female rats are age-dependent.

scholarly journals Effects of a new thyrotropic drug isolated from Potentilla alba on the male reproductive system of rats and offspring development

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Lubov V. Krepkova ◽  
Valentina V. Bortnikova ◽  
Aleksandra N. Babenko ◽  
Praskovya G. Mizina ◽  
Vladimir A. Mkhitarov ◽  
...  
Keyword(s):  
Animal Study ◽  
Male Fertility ◽  
Wistar Rats ◽  
Medical Condition ◽  
Adverse Outcomes ◽  
Female Rats ◽  
Childbearing Age ◽  
Offspring Development ◽  
Male Wistar Rats ◽  
And Control

Abstract Background The dysfunction of the thyroid gland is a common medical condition. Nowadays, patients frequently use medicinal herbs as complementary or alternative options to conventional drug treatments. These patients may benefit from treatment of thyroid dysfunctions with Potentilla alba L. preparations. While it has been reported that Potentilla alba preparations have low toxicity, nothing is known about their ability to affect reproductive functions in patients of childbearing age. Methods Male Wistar rats were orally treated with a thyrotrophic botanical drug, standardized Potentilla alba Dry Extract (PADE), at doses 8 and 40 times higher than the median therapeutic dose recommended for the clinical trials, for 60 consecutive days. Male Wistar rats receiving water (H2O) were used as controls. After completing treatment, half of the PADE-treated and control males were used to determine PADE gonadotoxicity, and the remaining half of PADE-treated and control males were mated with intact females. Two female rats were housed with one male for two estrus cycles. PADE effects on fertility and fetal/offspring development were evaluated. Results Herein, we report that oral treatment of male Wistar rats with PADE before mating with intact females instigated marked effects on male reproductive organs. Treatment significantly decreased the motility of the sperm and increased the number of pathological forms of spermatozoa. Additionally, a dose-dependent effect on Leydig cells was observed. However, these PADE effects did not significantly affect male fertility nor fetal and offspring development when PADE-treated males were mated with intact females. Conclusions PADE treatment of male rates negatively affected sperm and testicular Leydig cell morphology. However, these changes did not affect male fertility and offspring development. It is currently not known whether PADE treatment may affect human male fertility and offspring development. Therefore, these results from an animal study need to be confirmed in humans. Results from this animal study can be used to model the exposure-response relationship and adverse outcomes in humans.

scholarly journals Commercial Formulation of Chlorpyrifos Alters Neurological Behaviors and Fertility

Biology ◽  
2020 ◽  
Vol 9 (3) ◽  
pp. 49
Author(s):  
Enoka P. Kudavidanage ◽  
D. M. I. Dissanayake ◽  
W. L. Rangi Keerthirathna ◽  
N. Lasni Wathima Nishshanke ◽  
L. Dinithi C. Peiris
Keyword(s):  
Wistar Rats ◽  
Serum Testosterone ◽  
Female Rats ◽  
Male Rats ◽  
Risk Minimization ◽  
Commercial Formulation ◽  
Male Wistar Rats ◽  
Neurological Alterations ◽  
Implantation Sites ◽  
Androgen Levels

Pesticides are known to result in toxic insult. We aimed to evaluate Judo 40, the commercial formulation of chlorpyrifos on the neurological activities, fertility, and hormone levels of male rats. Male Wistar rats were treated orally with 1 mL of 20 or 50 mg/kg Judo 40. The doses were administered four times, twice a day. Sexual and exploratory behavior indices, fertility indices, serum androgen levels, blood acetylcholinesterase (BChE) levels, and neurological and muscular effects were evaluated. Serum testosterone and luteinizing hormone were significantly reduced in the rats receiving 50 mg/kg Judo 40. A reduction in viable implantation sites and live pups born were evident in the female rats mated with the male rats treated with the highest dose. Similarly, in the rats treated with the highest dose of Judo 40, a significant reduction in plasma BChE enzyme was observed. According to the results, prolonged Judo 40 exposure can cause impairment of the neurological alterations and sex hormones leading to impaired fertility. Therefore, chemical handlers should be educated on protection and risk minimization.

PREVENTION OF CENTRAL DEFEMINIZATION BUT NOT MASCULINIZATION IN MALE RATS BY INHIBITION NEONATALLY OF OESTROGEN BIOSYNTHESIS

1977 ◽  
Vol 74 (3) ◽  
pp. 375-382 ◽  
Author(s):  
J. T. M. VREEBURG ◽  
PAULA D. M. VAN DER VAART ◽  
P. VAN DER SCHOOT
Keyword(s):  
Sexual Function ◽  
Ovarian Function ◽  
Testosterone Propionate ◽  
Neonatal Period ◽  
Female Rats ◽  
Male Rats ◽  
Normal Male ◽  
Male And Female ◽  
Male And Female Rats ◽  
Copulatory Behaviour

SUMMARY An inhibitor of aromatization, androsta-1,4,6-triene-3,17-dione (ATD), was administered to newborn male and female rats and various parameters of gonadal and sexual function were examined in adulthood. Males injected with 1 mg ATD on the day of birth (day 1) and on days 3, 5, 10 and 15 postnatally, subsequently (day 55) showed normal male and female copulatory behaviour, but were not able to maintain cyclicity in ovarian transplants. When the ATD was administered by Silastic implants, however, cyclicity in ovarian transplants did occur. Neither form of treatment brought about significant changes in neonatal plasma or testicular testosterone concentrations. Female rats implanted on day 3 of life with Silastic capsules containing ATD and then given an injection of 0·25 mg testosterone propionate on day 5 subsequently showed normal ovarian function, whereas the controls receiving only testosterone propionate showed persistent vaginal cornification, anovulation and polyfollicular ovaries. The results support the view that the central conversion of testicular androgens to oestrogens during the neonatal period is necessary to abolish cyclic gonadotrophin release and to suppress female copulatory behaviour.

scholarly journals Stimulation of the corpora lutea of the rat by means of progesterone and testosterone

1937 ◽  
Vol 124 (836) ◽  
pp. 362-368 ◽  
Keyword(s):  
Guinea Pigs ◽  
Rhesus Monkeys ◽  
Testosterone Propionate ◽  
Female Rats ◽  
Corpora Lutea ◽  
Normal Female ◽  
Once Daily ◽  
Black And White ◽  
White Rats ◽  
Stimulation Of

The administration of progestin or progesterone inhibits oestrus in normal female experimental animals and leads to the cessation of follicular growth (Papanicolaou 1926, working on guinea-pigs; Gley 1928, on rats; Corner 1935, on monkeys). Active testicular extracts or testosterone have a similar effect (Ihrke and D’Amour 1931; Lendle 1931; and Robson 1936, working on rats; Zuckerman 1937, on rhesus monkeys). There is evidence that a phase of luteal activity occurs whenever the ripening of follicles is inhibited (see Evans 1928; Weichert 1930, amongst others), and it was therefore of interest to enquire whether or not luteinization of the ovaries is also an effect of the administration of progesterone and testosterone to normally cyclic female rats. Previous reports on this question are negative. Papanicolaou (1926) observed degenerative changes in the ovaries of guinea-pigs in which several successive oestrous cycles had been suppressed by means of progestin. Selye, Browne and Collip (1936) injected six rats with 4 mg. of progesterone for 12 days, and at the close of the experiment found that neither recent corpora lutea nor mature follicles were present in the ovaries. Albino and black and white rats were used. All injections were given once daily and subcutaneously. Oestrone was administered in aqueous solution, and both progesterone and testosterone propionate in oil. At the end of each experiment the uterus and one of the ovaries were fixed in Bouin’s fluid, and after sectioning, stained with haematoxylin and eosin, the ovary being sectioned serially. The second ovary of each animal was fixed in Flemming’s chrome-osmium fluid with acetic acid, and prepared to show osmicated fats according to the technique described by Deanesly (1930). In certain cases, noted below, the uterus was traumatized by the method of Shelesnyak (1933α) (a modification of that of Long and Evans), in order to produce deciduomata.

SERUM GONADOTROPHIN LEVELS DURING DEVELOPMENT IN MALE, FEMALE AND ANDROGENIZED FEMALE RATS AND THE EFFECT OF GENERAL DISTURBANCE ON HIGH LUTEINIZING HORMONE LEVELS

1976 ◽  
Vol 70 (3) ◽  
pp. 361-371 ◽  
Author(s):  
P. C. B. MACKINNON ◽  
J. M. MATTOCK ◽  
M. B. TER HARR
Keyword(s):  
Wistar Rats ◽  
High Serum ◽  
Female Rats ◽  
Serum Prolactin ◽  
Adult Males ◽  
Serum Lh ◽  
Male Wistar Rats ◽  
Serial Blood Sampling ◽  
Lh Release ◽  
Very High

SUMMARY Serum LH, FSH and prolactin levels were measured in blood samples which were obtained by decapitation from groups of female, neonatally androgenized female and male Wistar rats at 2-day intervals from birth to maturity. An increase in serum FSH levels was observed between 4 and 24 days of age in both the female and androgenized female groups, while a much later increase, between 28 and 44 days of age, occurred in the males. Serum prolactin levels increased gradually from birth in all three groups until adult levels were attained. In contrast, serum LH levels were in general low in all three groups of animals, although very high levels (> 7 ng/ml) were recorded in 22 out of 168 females and 8 out of 192 males between 4 and 28 days of age, as well as in adult males; occasional high LH levels were also seen in the androgenized females. The nature of the high serum LH levels was investigated in anaesthetized and unanaesthetized immature females by serial blood sampling using a number of techniques. Unexpectedly, only three out of 58 animals had high LH levels: two of these showed an episodic form of LH release during which levels increased to peak values and then declined within a period of about 30 min. On investigation it was found that general disturbance within the 45 min before decapitation could inhibit high LH levels in females aged between 23 and 30 days.

scholarly journals Androgen responsiveness of the liver of the developing rat

1974 ◽  
Vol 144 (2) ◽  
pp. 225-229 ◽  
Author(s):  
J-Å Gustafsson
Keyword(s):  
Testosterone Propionate ◽  
Neonatal Period ◽  
Female Rats ◽  
Male Rats ◽  
Second Phase ◽  
Final Phase ◽  
Male And Female ◽  
Androgen Treatment ◽  
Male And Female Rats ◽  
Developing Rat

The activities of the hepatic microsomal 2α-, 2β-, 7α- and 18-hydroxylase systems active on 5α-[4-14C]androstane-3α,17β-diol were studied in male and female rats which had been castrated at birth and at the age of 7, 13, 21, 27, 34, 43 and 55 days, treated for 5 days with 2mg of testosterone propionate/kg body weight and killed 6 days after castration. The 7α-hydroxylase system was affected very little by androgen treatment at all stages during development. On the other hand it was found that the rat liver passed through three phases during development with respect to androgen responsiveness as judged by changes in the activities of the 2α, 2β- and 18-hydroxylase systems: a first phase (from the neonatal period up to about 19 days of age) with a relative androgen unresponsiveness in both male and female rats, a second phase (from about 27 to about 33 days of age) when male and female rats responded equally well to androgens and a final phase (from about 40 days of age) with a successively decreasing androgen responsiveness in female rats but with a retained responsiveness in male rats. The hypothesis is presented that neonatal imprinting of the liver by testicular androgen(s) determines the development and degree of androgen responsiveness of liver tissue in the rat.

Mechanisms of action of testosterone propionate on LH and FSH release by the pituitary gland in cyclic female rats

1980 ◽  
Vol 95 (2) ◽  
pp. 158-165 ◽  
Author(s):  
J. Roos ◽  
S. Plas-Roser ◽  
Cl. Aron
Keyword(s):  
Pituitary Gland ◽  
Sharp Increase ◽  
Testosterone Propionate ◽  
Sharp Decrease ◽  
Mechanisms Of Action ◽  
The Other ◽  
Female Rats ◽  
Corpora Lutea ◽  
Other Hand ◽  
Lh Release

Abstract. The aim of this work was to determine whether changes in pituitary responsiveness to LRH could account for the effect of testosterone propionate (TP) on the gonadotrophic function of the pituitary in 4-day cyclic female rats. Doses of 250, 500 and 1000 ng LRH were injected ip on pro-oestrus at 15.30 h in rats either pre-treated with 5 mg TP on dioestrus II at 10.00 h or injected with 30 mg/kg pentobarbital (PB) at 13.00 h. LH release induced within 30 min by LRH was higher in PB than in TP-treated rats. Even by using 250 ng LRH full ovulation was observed on the morning of oestrus in PB-treated rats. On the other hand, only partial ovulation occurred whatever the dose of LRH used in TP-treated rats; a great number of luteinized follicles was shown to be constantly associated with post-ovulatory corpora lutea. While LRH caused a significant FSH release (30 min later) in TP-treated rats, no FSH release could be shown in PB-treated rats. The pituitary FSH content appeared to be decreased and the pituitary LH content remained unchanged while a sharp increase in both blood FSH and LH concentrations occurred following injection of 1000 ng LRH in TP-treated rats. Concomitantly a sharp decrease in the number of pituitary gonadotrophs (AB-PAS+) was observed. A significant decrease in the number of the small roundshaped PAS positive cells was also observed. The mechanisms whereby TP influences the function of the pituitary-ovarian axis are discussed in the light of these results.

EFFECTS OF DIHYDROTESTOSTERONE AND OESTRADIOL ON SEXUAL DIFFERENTIATION IN MALE RATS

1980 ◽  
Vol 84 (3) ◽  
pp. 397-407 ◽  
Author(s):  
P. VAN DER SCHOOT
Keyword(s):  
Sexual Differentiation ◽  
Testosterone Propionate ◽  
Neonatal Period ◽  
Combined Treatment ◽  
Female Rats ◽  
Male Rats ◽  
Normal Male ◽  
Oestradiol Benzoate ◽  
The Brain ◽  
Copulatory Behaviour

Adult male rats which had been castrated at birth and treated with the non-aromatizable androgen dihydrotestosterone propionate (DHTP) showed incomplete copulatory behaviour. When tested with oestrous female rats during treatment with testosterone propionate (TP) they readily mounted these females and showed frequent penile intromissions but rarely ejaculated. In a long series of observations the proportion of ejaculating rats in tests of 30 min did not exceed 50%. Neonatally castrated rats treated with DHTP during infancy thus seemed to be capable of ejaculation in adulthood during treatment with TP, but the threshold for the occurrence of the ejaculatory reflex seemed to be higher than in normal male rats. By replacing treatment in adulthood with TP by a combined treatment with DHTP and oestradiol benzoate (OB), the frequency of ejaculation was not increased. It was concluded that the incomplete copulatory behaviour was not due to reduced efficiency of aromatization of androgen within the brain of these rats. The addition of OB to DHTP during the neonatal period of treatment enhanced the frequency of ejaculation in adulthood. The combined treatment of 0·1 mg DHTP on days 1, 3 and 5 with 0·01 mg OB on day 1 made adult copulatory behaviour during treatment with TP indistinguishable from that of rats castrated on day 10 or rats castrated at birth and treated with TP during infancy. It was concluded that the masculine organization of systems and structures involved in the display of male copulatory behaviour occurs under the influence of both non-aromatizable androgen and oestrogen, oestrogen being most likely the substance required to 'organize' the central nervous aspects of the regulation of this behaviour. The absence neonatally of nonaromatizable androgen and/or oestrogen results in specific deficiencies in adult copulatory behaviour as compared with the behaviour of normal male rats.

scholarly journals Freshly isolated hepatocyte transplantation in acetaminophen-induced hepatotoxicity model in rats

2012 ◽  
Vol 49 (4) ◽  
pp. 291-295 ◽  
Author(s):  
Daniela Rodrigues ◽  
Themis Reverbel Da Silveira ◽  
Ursula Matte
Keyword(s):  
Portal Vein ◽  
Wistar Rats ◽  
Hepatocyte Transplantation ◽  
Female Rats ◽  
Therapeutic Modality ◽  
Rat Hepatocyte ◽  
Male Wistar Rats ◽  
Phosphate Buffered Saline ◽  
Isolated Rat ◽  
Time Point

CONTEXT: Hepatocyte transplantation is an attractive therapeutic modality for liver disease as an alternative for orthotopic liver transplantation. OBJECTIVE: The aim of the current study was to investigate the feasibility of freshly isolated rat hepatocyte transplantation in acetaminophen-induced hepatotoxicity model. METHODS: Hepatocytes were isolated from male Wistar rats and transplanted 24 hours after acetaminophen administration in female recipients. Female rats received either 1x10(7) hepatocytes or phosphate buffered saline through the portal vein or into the spleen and were sacrificed after 48 hours. RESULTS: Alanine aminotransferase levels measured within the experiment did not differ between groups at any time point. Molecular analysis and histology showed presence of hepatocytes in liver of transplanted animals injected either through portal vein or spleen. CONCLUSION: These data demonstrate the feasibility and efficacy of hepatocyte transplantation in the liver or spleen in a mild acetaminophen-induced hepatotoxicity model.

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