Effect of prenatal exposure to bisphenol A on the serum testosterone concentration of rats at birth

2006 ◽  
Vol 25 (7) ◽  
pp. 369-373 ◽  
Author(s):  
M Tanaka ◽  
S Nakaya ◽  
M Katayama ◽  
H Leffers ◽  
S Nozawa ◽  
...  
Keyword(s):  
Bisphenol A ◽  
Sexual Differentiation ◽  
Neonatal Period ◽  
Serum Testosterone ◽  
In Utero ◽  
Female Rats ◽  
Male Rats ◽  
Testosterone Concentration ◽  
Fetal Serum ◽  
And Control

In the rat, testosterone (T) in the neonatal period plays an important role in sexual differentiation and there is a serum T surge in male rats 2 hours after birth. Pregnant female rats were exposed to various doses of bisphenol A (BPA) from gestational day 1 (GD1) through 2 hours after parturition. About half of the BPA-exposed and control dams were subjected to cesarean section on GD22. The male fetuses on GD22 were immediately sacrificed and blood was collected. The other half of the BPA-treated and control dams delivered at GD23 (parturition day). The male pups were sacrificed 2 hours after birth. Serum T concentration was determined by radioimmunoassay (RIA). The BPA concentration in the fetal serum on GD22 increased inversely to the T levels in the serum. The T concentration in the pups' serum 2 hours after birth decreased inversely to the BPA concentration in the serum. However, there were no differences in the serum T concentration among the various doses of BPA. These results suggest that exposure to BPA in utero inhibits the T surge in the neonatal period and we speculate that exposure to BPA in utero disrupts the endocrine environment in the neonatal male.

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.

Effect of neonatal allylestrenol treatment (hormonal imprinting) on the serum testosterone and progesterone concentration in adult rat

1995 ◽  
Vol 7 (5) ◽  
pp. 1249 ◽  
Author(s):  
E Pap ◽  
G Csaba
Keyword(s):  
Serum Testosterone ◽  
Female Rats ◽  
Male Rats ◽  
Hormone Concentration ◽  
Progesterone Concentration ◽  
Serum Progesterone ◽  
Testosterone Concentration ◽  
Hormonal Imprinting ◽  
Adult Rat ◽  
Serum Hormone

Serum testosterone concentration was significantly elevated in adult male rats by a single perinatal allylestrenol administration. One week after a second allylestrenol treatment in adulthood the hormone concentration dropped below the control values. Serum progesterone concentration was significantly lowered in adult female rats by a single perinatal allylestrenol administration. Following a second allylestrenol treatment in adulthood the hormone concentration reached the control values. These experiments demonstrate that the hormonal imprinting caused by allylestrenol (a steroid used in the treatment of endangered pregnancy) not only acts at receptor level and produces changes in sexual behaviour, but also induces modifications in serum hormone concentrations.

PARTIAL FEMINIZATION OF HEPATIC STEROID METABOLISM IN MALE RATS AFTER NEONATAL ADMINISTRATION OF CYPROTERONE ACETATE

1975 ◽  
Vol 64 (2) ◽  
pp. 267-275 ◽  
Author(s):  
JAN-ÅKE GUSTAFSSON ◽  
MAGNUS INGELMAN-SUNDBERG ◽  
ÅKE STENBERG ◽  
FRIEDMUND NEUMANN
Keyword(s):  
Sexual Differentiation ◽  
Enzyme Activities ◽  
Cyproterone Acetate ◽  
Microsomal Fraction ◽  
Neonatal Period ◽  
Female Rats ◽  
Male Rats ◽  
Supernatant Fraction ◽  
Male And Female Rats ◽  
Neonatal Administration

SUMMARY The metabolism of [4-14C]4-androstene-3, 17-dione, [4-14C]5α-androstane-3α, 17β-diol and 1,2-3H]5α-androstane-3α, 17β-diol 3,17-disulphate was studied using the microsomal fraction and the metabolism of [4-14C]4-androstene-3, 17-dione was studied using the 105 000 g supernatant fraction of liver from male and female rats aged 5 months that had been treated with cyproterone acetate before (from day 13 of pregnancy) and after birth (until 3 weeks of age). Nearly all sex-dependent enzyme activities in the treated male rats were changed in a direction characteristic of female rats: 5α-reductase active on 4-androstene-3, 17-dione increased in activity whereas 3β- and 17α-hydroxysteroid reductases and 6β- and 16α-hydroxylases active on 4-androstene-3, 17-dione and 2α-, 2β- and 18-hydroxylases active on 5α-androstane-3α, 17β-diol decreased in activity. Enzyme activities not under gonadal control, i.e. 3α- and 17β-hydroxysteroid reductases active on 4-androstene-3, 17-dione and 7α-hydroxylase active on both 4-androstene-3, 17-dione and 5α-androstane-3α, 17β-diol, were not affected by cyproterone acetate. The liver enzyme activities in treated female rats were generally not affected although significant effects were noted in two cases; in one of these (17α-hydroxysteroid reductase) a testosterone-like effect was observed. The results obtained are probably best explained in the following way: treatment with the anti-androgen during the neonatal period results in less efficient imprinting of the hypothalamo-hypophysial system leading to less pronounced masculine setting of sex-dependent enzyme levels and also to a relative androgen unresponsiveness. It is suggested that the biochemical methods used in the present investigation may be used for more exact estimation of the degree of neonatal sexual differentiation of the hypothalamo-hypophysial system than biological and psychological methods previously available.

ANDROGEN CONCENTRATIONS IN PLASMA AND TESTIS OF DEVELOPING RATS

1968 ◽  
Vol 40 (4) ◽  
pp. 485-491 ◽  
Author(s):  
J. A. RESKO ◽  
H. H. FEDER ◽  
R. W. GOY
Keyword(s):  
Sexual Differentiation ◽  
Critical Period ◽  
Neonatal Period ◽  
Testicular Tissue ◽  
Postnatal Period ◽  
Male Rats ◽  
Electron Capture Detection ◽  
Gas Liquid Chromatography ◽  
Testosterone Concentration ◽  
Peripheral Plasma

SUMMARY Testosterone and androstenedione levels in plasma and testicular tissue of developing rats were measured using gas—liquid chromatography with electron capture detection. The major androgen of both the adult and early postnatal period of development was testosterone. Pooled plasma from 230 one-day-old male rats contained 0·027 μg. testosterone/100 ml. The concentration of testosterone in the testes at this age was 0·328 μg./g. wet tissue. With increasing age there was a decline in testosterone concentration in plasma as well as in gonadal tissue which lasted until about the age of 30 days. The period from 40 to 60 days was characterized by an increasing concentration of testosterone in the plasma and gonads. During adulthood, testosterone reached concentrations as high as 0·202 μg./100 ml. peripheral plasma. Androstenedione could not be detected in the circulation during the critical period of neonatal neural sexual differentiation, but it was present in the testes at this stage. In the pubertal and adult stages androstenedione was found in the plasma and testes. Its concentration, particularly in adulthood, was not as great as that of testosterone. These results indicate that testosterone is present in plasma and testicular tissue of the rat during the neonatal period when behavioural and physiological sexual differentiation is presumed to occur.

Short-Term and Long-Term Effects of Bisphenol A (BPA) Exposure During Breastfeeding on the Biochemical and Endocrine Profiles in Rats

2018 ◽  
Vol 50 (06) ◽  
pp. 491-503 ◽  
Author(s):  
Ana Santos-Silva ◽  
Egberto de Moura ◽  
Cintia Pinheiro ◽  
Elaine Oliveira ◽  
Patricia Lisboa
Keyword(s):  
Bisphenol A ◽  
Female Rats ◽  
Male Rats ◽  
Control Group ◽  
High Dose ◽  
Long Term Effects ◽  
Adult Rat ◽  
Endocrine Profiles ◽  
And Control

AbstractNeonates can be exposed to bisphenol A (BPA) through placenta and milk, and BPA is associated with disorders such as precocious puberty and obesity. We evaluated the effects of BPA exposure during breastfeeding on the biochemical and endocrine profiles in young and adult rat progeny. From postnatal day (PND) 3 to 15 dams were divided into low-dose BPA treatment [50 μg/kg/day s.c. (BPA-LD)], high-dose BPA treatment [5 mg/kg/day s.c. (BPA-HD)], and Control (vehicle) groups. Milk was collected at PND15 and 21, which represents the end of exposure and 6 days after withdrawal, respectively. Dams were euthanized at weaning. Offspring of both genders were euthanized at PND15, 21, and 180. Milk estradiol levels were lower in the BPA-HD group than in the control group at PND 15; however, they were higher at PND21. Female rats whose mothers were BPA-exposed showed more significant differences from those in the control group, including better glycemic control and lipid profiles and higher food intake without higher adiposity, in adulthood than in the weaning period, when they presented with higher adiposity and hyperestrogenism. Conversely, male rats showed more abnormalities after BPA exposure compared to control rats, including insulin, leptin, testosterone, and thyroid hormone changes, when young but exhibited fewer alterations in adulthood, with increase only in LDLc in the BPA-HD rats. Taken together, the present findings suggest that exposure to BPA exclusively through milk affects adiposity, metabolism, and/or hormones of offspring in the short and long term, possibly compromising normal development in both sexes.

Toxicological evaluation of hydroethanol leaf extract of Pupalia lappacea (Linn.) Juss. (Amaranthaceae) in rodents

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Murtala Akanji Abdullahi ◽  
Elijah Oladapo Oyinloye ◽  
Akinyinka Alabi ◽  
Aderonke Adeyinka Aderinola ◽  
Luqman Opeyemi Ogunjimi ◽  
...  
Keyword(s):  
Leaf Extract ◽  
Density Lipoprotein ◽  
Serum Testosterone ◽  
Female Rats ◽  
Male Rats ◽  
Laboratory Animals ◽  
Serum Testosterone Level ◽  
Control Group ◽  
Toxicological Evaluation ◽  
Liver And Kidney

Abstract Objectives Several studies have established the ethnobotanical benefits of Pupalia lappacea (PL) in laboratory animals without extensive toxicological evaluation of its safety profiles. Thus, an extensive toxicological investigation of sub-chronic oral administration of the hydroethanol leaf extract of P. lappacea in rodents was carried out in this study. Methods Different groups of rats were treated orally with the extract (10, 50 and 250 mg/kg) daily for 90 consecutive days. The control group received distilled water (10 mL/kg). After 90 days, some rats were left for additional 30 days without treatment for reversibility study. Blood and organs samples were collected for different evaluations at the end of study periods. Results The extract decreased the bodyweights, feeding and water intakes in female rats. PL increased the weights of the liver and kidney in male rats. PL increased the red blood cell (RBC), packed cell volume (PCV), hemoglobin (Hb), triglycerides (TRIG), cholesterol and high density lipoprotein (HDL) contents in rats. PL (250 mg/kg) significantly reduced the sperm motility and serum testosterone level. Cyto-architectural distortions of the testes, liver and spleen were visible. Conclusions The findings showed that P. lappacea is relatively safe at lower doses but cautions should be taken at higher dose.

The development of the hypothalamo–pituitary axis in the neonatal rat: sexual maturation in male and female rats as assessed by hypothalamic LHRH and pituitary and serum LH and FSH concentrations

1977 ◽  
Vol 55 (5) ◽  
pp. 1091-1097 ◽  
Author(s):  
J. H. Dussault ◽  
P. Walker ◽  
J. D. Dubois ◽  
F. Labrie
Keyword(s):  
Developmental Process ◽  
Neonatal Period ◽  
Neonatal Rat ◽  
Female Rats ◽  
Human Foetus ◽  
Marked Rise ◽  
Male And Female Rats ◽  
Specific Radioimmunoassay ◽  
Serum Lh ◽  
And Control

Using specific radioimmunoassay techniques, we have measured hypothalamic LHRH concentration and pituitary and serum LH and FSH concentrations in neonatal rats from 0 to 60 days after birth. There were no sex differences demonstrable for hypothalamic LHRH concentration, which rose from minimal values at 2 days to peak concentrations at 22–28 days and declined significantly with the approach of puberty. Pituitary LH concentration in the two sexes rose to peak values at 19–25 days, with significantly higher values observed in females (p < 0.01). Serum LH concentration was high in both sexes at birth, the values in females being significantly higher than those observed in males (p < 0.01). While the serum LH concentration remained relatively stable throughout the study period in males, it declined rapidly to a nadir at 28 days in females. Pituitary FSH concentration was low at birth in both sexes. Females demonstrated a marked rise to peak concentrations at 16 days while males achieved significantly lower peak prepuberal values (p < 0.01) at 28 days. Serum FSH concentration was significantly higher in females (p < 0.01) at birth and rose further to peak values at 16 days. Males attained peak serum FSH concentrations at 35 days. These data demonstrate that the maturation of the hypothalamo–pituitary–gonadal axis develops in the neonatal period in the rat and confirm the presence of significant differences in hypothalamic sexual differentiation and control. The possibility of this developmental process in the neonatal rat as a model for the study of the midgestational hypothalamic maturation of the human foetus is discussed.

Investigation of the effects of bisphenol-A exposure on lymphoid system in prenatal stage

2020 ◽  
Vol 36 (7) ◽  
pp. 502-513
Author(s):  
Işil Aydemir ◽  
Caner Özbey ◽  
Oktay Özkan ◽  
Şadiye Kum ◽  
Mehmet İbrahim Tuğlu
Keyword(s):  
Lymph Node ◽  
Bisphenol A ◽  
Tissue Damage ◽  
Corn Oil ◽  
Histopathological Examination ◽  
Female Rats ◽  
Male Rats ◽  
High Dose ◽  
Organ Function ◽  
Pregnant Rats

Bisphenol-A (BPA) used in the production of plastic materials is a temperature-soluble agent. It also has a steroid hormone-like activity; therefore, it poses a danger to human health. In our study, we aimed to investigate the effects of BPA on lymph node and spleen in male rats exposed to this agent during prenatal stage. The pregnant female rats were divided into four groups: control, sham, low dose (300 µg/kg BPA), and high dose (900 µg/kg BPA). BPA was dissolved in 1 mL of corn oil and administered to the pregnant rats every day during pregnancy. On the 21st and 45th day after the birth, male rats’ lymph node and spleen samples were taken and histopathological examination was performed. Samples were stained with hematoxylin and eosin to determine the general histological appearance, and with CD3 and CD20 immunohistochemically. The results of staining were evaluated by H-score, and statistical analysis was performed. In the samples, BPA applications were not found to cause significant tissue damage. But there was a significant decrease in the immunoreactivities of CD3 and CD20 after BPA applications in both 21st and 45th day samples. After high dose BPA administration, decreased CD3 immunoreactivity was statistically significant. It is thought that BPA does not cause histologically significant tissue damage, but it may impair organ function at cellular level. The investigation of molecules involved in organ function will be useful in revealing the mechanisms that will cause dysfunction.

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.

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