scholarly journals A comprehensive effect of acephate on cauda epididymis and accessory sex organs of male rats

2013 ◽  
Vol 7 (23) ◽  
pp. 1560-1567 ◽  
Author(s):  
Dut Jasuja
1983 ◽  
Vol 96 (2) ◽  
pp. 321-327 ◽  
Author(s):  
N. M. Biswas ◽  
P. K. Ghosh ◽  
K. K. Ghosh ◽  
O. W. Neuhaus

Adult male rats were given injections of oestradiol-17β (50 μg/100 g body wt per day) for 7 days. When they were killed 14 days after the last injection, serum levels of gonadotrophins and testosterone and weights of accessory sex organs were less, testicular 17β-hydroxysteroid dehydrogenase 17β-HSD activity was suppressed and spermatogenesis was inhibited. Administration of α2u-globulin (1·5 mg/day) for 14 days to oestrogen-treated rats and for 10 days to control rats resulted in increased concentrations of gonadotrophins and testosterone in the serum. Accessory sex organ weight and spermatogenesis appeared to be normal while 17β-HSD activity increased in oestrogen-treated rats after treatment with α2u-globulin. It was concluded that α2u-globulin has an effect on testicular function in oestrogenized rats by inducing gonadotrophin and testosterone synthesis.


1966 ◽  
Vol 34 (1) ◽  
pp. 117-123 ◽  
Author(s):  
R. L. MORRISON ◽  
D. C. JOHNSON

SUMMARY Male rats were castrated on the day of birth and 5 days later half were given 2·5 mg. testosterone propionate (TP) subcutaneously (androgenization). When 30 days old, single animals were treated with graded doses of TP for 10 days. At the same time 57 males were united in parabiosis with normal intact males, and treated for 10 days with androgen. Androgenization resulted in increased sensitivity of the accessory sex organs to subsequent treatment with TP. Also, the excessive secretion of gonadotrophin by the castrated animals, as measured by androgen production in intact parabiotic partners, was more effectively inhibited by TP in androgenized than in non-androgenized males. The results are consistent with the interpretation that early androgen treatment sensitizes both the male target organs and the hypothalamo-hypophysial system to androgen.


1954 ◽  
Vol 10 (4) ◽  
pp. 291-301 ◽  
Author(s):  
R. W. BRIMBLECOMBE ◽  
I. D. K. HALKERSTON ◽  
M. REISS

SUMMARY ACTH extracts showing inhibition of the stimulatory action of PMS on follicular maturation in infantile female rats and slight stimulation of the growth of the testes and accessory sex organs in infantile male rats and day-old chicks have been investigated. The action of these extracts on the gonads was found to be independent of the adrenal ascorbic acid depleting principle, as ACTH fractions free from inhibitory or stimulatory influence on the gonads could be prepared. The nature of the factor described is discussed.


1987 ◽  
Vol 113 (1) ◽  
pp. 51-55 ◽  
Author(s):  
F. T. A. Fitzpatrick ◽  
B. D. Greenstein

ABSTRACT The effects of several steroids on the regenerating thymus in ageing male rats have been studied. Rats aged from 12 to 15 months were orchidectomized and 7 days later implanted s.c. with silicone elastomer tubing containing 25 mg testosterone, 5α-dihydrotestosterone (DHT), oestradiol, progesterone or corticosterone. One group of rats received an empty implant. Thirty days later the rats were killed and the thymus, spleen, ventral prostate and seminal vesicles weighed and retained for histology. Whole blood was taken for total and differential white cell counts; plasma was prepared for radioimmunoassay of testosterone, oestradiol, progesterone and corticosterone. After orchidectomy only, a multilobular thymus was present, and histologically the tissue appeared healthy. In testosterone- and oestradiol-treated rats, thymus weight was reduced to about 50% of that in untreated animals. Histologically, much of the thymus taken at autopsy was fat and what remained was poorly organized and contained a much lower density of thymocytes. The total white cell count was significantly reduced in these animals, the effect appearing to be predominantly on lymphocytes. Although treatment with DHT also resulted in a lower mean thymus weight than that of orchidectomized animals, histologically the tissue appeared similar to that of the untreated castrated animals. In rats treated with DHT, the total white cell count was significantly higher than in testosterone-implanted rats. Both progesterone and corticosterone implants resulted in significantly smaller mean thymus weights, although these steroids were not as potent as testosterone or oestradiol. Corticosterone, but not progesterone, appeared to cause a significant reduction in circulating lymphocytes. Dihydrotestosterone possessed only half the potency of testosterone in restoring the weights of the accessory sex organs. Serum concentrations of testosterone in orchidectomized old rats were 0·33 ± 0·02 nmol/l and in testosterone-implanted rats 4·8 ± 0·4 nmol/l. These results raise the possibility that testosterone and oestradiol may have caused atrophy of the thymus, while DHT may have retarded regeneration of the thymus without any atrophic effect. It remains to be seen whether the different responses between testosterone and DHT, in both the thymus and accessory sex organs, are due to differences in intrinsic action or differences in the metabolism of the steroids. J. Endocr. (1987) 113, 51–55


1970 ◽  
Vol 65 (1) ◽  
pp. 103-110 ◽  
Author(s):  
Kjell J. Tveter

ABSTRACT [6,7-3H] 17β-Oestradiol with a specific activity of 42.4 Ci/mmole was injected intramuscularly into three to four month old male rats, castrated three days previously. The radioactivity in liver, skeletal muscle, blood, the anterior pituitary gland, the seminal vesicles and in the different prostatic lobes was measured by liquid scintillation counting at different intervals after the administration. A high and prolonged uptake of radioactivity was found in the anterior pituitary gland. The uptake by the accessory sex organs was much lower, but significantly higher than that by skeletal muscle. The uptake by the prostate and the seminal vesicles in castrated animals was similar to that in non-castrated animals. The pattern of radioactivity uptake in the anterior pituitary gland of castrated male rats given [3H] testosterone was distinctly different from that after administration of [3H] 17β-oestradiol. There was a rapid elimination of radioactivity from the adenohypophysis after the administration of [3H] testosterone.


1972 ◽  
Vol 69 (1) ◽  
pp. 153-164 ◽  
Author(s):  
L. Buric ◽  
H. Becker ◽  
C. Petersen ◽  
K. D. Voigt

ABSTRACT Either 0.7 μg [1,2-3H] testosterone* (51 Ci/mm) or 0.8 μg [1,2-3H] 5α-dihydrotestosterone (44 Ci/mm) was administered intravenously to normal adult male rats 3, 7, and 12 days after castration. 30 min after the injection, the animals were sacrificed. Total radioactivity counting was performed on aliquots of extracts of blood, peripheral muscle, prostates and seminal vesicles. In a first TCL the extracts were separated into five fractions. Further purification by acetylation and repeated chromatographic procedures revealed, that fraction C consisted of about 90 % of testosterone, fraction D of varying amounts of 5α- and 5β-DHT, fraction E of androstanedione and androstenedione, and fraction B mainly of androstanediols. The following results should be mentioned: 1. The radioactivity uptake by the accessory sex organs was significantly higher than that of skeletal muscle. The highest values were found on day 3 after castration. 5α-DHT under all conditions produced higher concentrations in the target tissues than testosterone, whereas in skeletal muscle the opposite was found. 2. After testosterone administration testosterone was very efficiently converted to 5α-DHT in target organs. Nevertheless substantial amounts of testosterone and of androstanedione and androstanediols are present. In blood, however, only small amounts of labelled 5α-DHT were found. After 5α-DHT administration, in target organs, 5α-DHT was converted to androstanedione and androstanediols up to about 20%. In blood the bulk of radioactivity was related to the androstanediol fraction. No conclusion therefore can be drawn from the data obtained in blood on the metabolic events occurring in the target organs. 3. The sequence of metabolic events in the target tissues supports the concept of a preferred 17-hydroxy pathway and a lack of 5β-reductase.


1990 ◽  
Vol 126 (3) ◽  
pp. 431-435 ◽  
Author(s):  
H. Mandal ◽  
P. K. Ghosh ◽  
N. M. Biswas

ABSTRACT Adult male rats were given s.c. injections of melatonin (400 μg/100 g body weight per day) for 14 days. On day 15, the weights of the testis and accessory sex organs were less, testicular 17β-hydroxysteroid dehydrogenase (17β-HSD) activity was inhibited, spermatogenesis was suppressed and serum levels of gonadotrophins, testosterone and α2u-globulin were decreased compared with control animals injected with vehicle. In a third group of rats given the same dose of melatonin for 14 days, administration of dihydrotestosterone (DHT) at a dose of 25 μg/100 g body weight per day on days 8–14 resulted in serum levels of α2u-globulin, FSH, LH and testosterone and testicular 17β-HSD activity similar to those seen in vehicle-injected control animals. Weights of the testes and accessory sex organs and spermatogenesis were normal after administration of DHT in melatonintreated rats. In another group of rats, the depressive effects of melatonin treatment on plasma gonadotrophins were reversed by the administration of α2u-globulin on days 8–14. It was concluded that treatment with DHT prevents the depressive action of melatonin on testicular function by inducing the synthesis of α2u-globulin. Journal of Endocrinology (1990) 126, 431–435


1961 ◽  
Vol 23 (3) ◽  
pp. 291-301 ◽  
Author(s):  
P. G. WALL

SUMMARY Male rats were exposed to 400, 800 or 1200 r at varying ages after birth (3–36 days). The subsequent secretory capacity of the testis, as judged by the weight of the accessory sex organs, was markedly impaired following irradiation. The effect of X-irradiation on the secretory interstitial (Leydig) cells depended on both the dose of X-rays used, and the age of the animals at the time of exposure. The reduction in the secretion of androgen was associated with a decrease in the volume of intertubular tissue. The secretory cells became progressively more radio-resistant as the animals neared the age of puberty. The ability of Leydig cells to respond to exogenous gonadotrophin was diminished by irradiation. In contrast, the response of the accessory sex organs to exogenous androgen was not appreciably affected. The results thus clearly demonstrate that the Leydig cells of the pre-pubertal testis are considerably more susceptible to radiation-induced damage than are those of the adult testis.


1974 ◽  
Vol 63 (2) ◽  
pp. 399-NP ◽  
Author(s):  
H. M. FRASER ◽  
A. GUNN ◽  
S. L. JEFFCOATE ◽  
DIANE T. HOLLAND

SUMMARY Autoimmunity to luteinizing hormone releasing hormone (LH-RH) in adult male rats, induced by immunization with LH-RH conjugated to bovine serum albumin, resulted in atrophy of the testes and secondary sex organs and aspermatogenesis. Both immunoreactive luteinizing hormone (LH) and follicle-stimulating hormone (FSH) in serum and the pituitary were reduced to low levels compared with those of control animals. It is suggested that antibodies to LH-RH can inhibit the action of endogenous hormone and that LH-RH is, in fact, the gonadotrophin-releasing hormone in the rat, required for the release of both LH and FSH.


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