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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 274 (1972), S. 229-237 
    ISSN: 1432-1912
    Keywords: Rat Folic Acid Reductase ; Pregnancy ; Fetus ; Newborns ; Trimethoprim
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The folic acid reductase activity in various organs of adult rats was studied in comparison to pregnant females (20th day of gestation) and fetal rats. The enzyme activities in the tissues of pregnant rats were in general about 30% higher than in normal adults. Fetal rats also possess the ability to catalyze the reduction of dihydrofolic acid, but it is evident that the liver and kidney have a considerably reduced capacity to form tetrahydrofolate. The folic acid reductase activity in liver and kidney rises for 10 days after birth and then declines to normal enzyme levels by the 4th week of life. Further studies concerning the interaction between trimethoprim and folic acid reductase in adult rats demonstrate that an oral dose of 5 or 50 mg/kg results in about a 30% increase of folic acid reductase activity in liver and kidney. The experiments suggest that there is a stimulation of enzyme synthesis following trimethoprim administration; because, the trimethoprim induced increase of the reductase activity is blocked by the administration of either puromycin or actinomycin D.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 272 (1972), S. 369-377 
    ISSN: 1432-1912
    Keywords: Trimethoprim ; Placental Transfer ; Distribution ; Elimination ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary After a single i.v. administration of 50 mg/kg of Trimethoprim (TM) to rats in late pregnancy, a diffusion equilibrium of the folic acid inhibitor in the foetal organs is reached after 30–60 min. The TM levels in maternal as well as in foetal organs can have an inhibitory effect on folic acid reductase activity. The elimination of TM is lower in pregnant than in non-pregnant animals. The TM elimination of the foeti is dependent on the elimination capacity of the mother. Three-days-old rats eliminate TM some four times slower than mature animals owing to their reduced kidney development.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 278 (1973), S. 227-230 
    ISSN: 1432-1912
    Keywords: Trimethoprim ; Rat Folic Acid Reductase ; Pregnancy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The increased level of folic acid reductase activity in rats during the perinatal period is inhibited following the oral administration of 5 or 50 mg/kg Trimethoprim. When the enzyme activity was tested in vitro, the highest sensitivity to the antimetabolite was displayed by the liver reductase isolated from rats the 20th day of pregnancy, the lowest was observed in the foetal liver extract. It is proposed that the stimulated reductase activity during the pregnancy is caused by a newly synthesized, Trimethoprim-sensitive enzyme form. The results of the in vitro experiments could contribute to the suggested hypothesis.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-136X
    Keywords: Gonadotropic hormone ; Sex steroids ; Reproductive cycle ; Testis ; Rainbow trout, Oncorhynchus mykiss
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Male rainbow trout were treated with salmon gonadotropic hormone (GTH) at different stages of the circannual reproductive cycle; spawning fish were also treated with an antiserum against salmon GTH. Injection of GTH led to a several-fold increase of plasma sex steroid levels during spermatogenesis and in the spawning season but was without effect at early stages of testicular development. GTH neutralization during the spawning season was followed by a several-fold decrease of plasma sex steroid levels. During spermatogenesis and in the spawning season, both treatment regimes resulted in an increased sensitivity of testicular explants in response to a subsequent stimulation of steroid secretion in vitro. This up-regulatory response may facilitate and maintain the high sex steroid plasma levels observed during the spawning season. It may also be necessary to allow for concomitant peak values of plasma GTH and sex steroids in the spawning season, a situation difficult to understand within the negative feedback concept. The adaptive capacities of the testicular steroidogenic system indicate that it is not only an effector site for GTH but also an active part of the endocrine system controling reproduction.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-136X
    Keywords: Sex steroids ; Blood levels ; Testicular in vitro secretion ; Pubertal development ; African catfish (Clarias gariepinus)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Blood serum and testicular tissue samples were collected from 3 to 13-month-old African catfish (groups A-G) in order to study their pubertal development. The sampling covered the period from before the beginning of spermatogenesis until full maturity. Testes of fish in group A contained spermatogonia alone. In testes of group B, spermatogonia, spermatocytes and spermatids were present. Spermatozoa were first observed in group C and became predominant as the fish attained full maturity (group G). Several sex steroids were determined in the blood samples. Testosterone was the quantitatively dominating androgen in the blood serum (3–5 ng·ml-1) in groups B and C (fish in group A were too small to collect blood samples). In group D, the concentrations of 11-ketotestosterone and 11β-hydroxyandrostenedione increased to levels similar to those of testosterone. Androstenedione that was undetectable before (below 0.4 ng·ml serum-1), also increased to 3–5 ng·ml-1 in group D. The levels of androgens kept increasing until the fish attained full maturity (group G). In order to monitor the responsiveness to gonadotropic hormone and the steroid secretion capacity, the in vitro secretion of two steroids (11β-hydroxyandrostenedione and 17α,20β-dihydroxy-4-pregnen-3-one) by testicular tissue was quantified at the different stages of development. Testicular maturation was accompanied by changes of both the steroid secretion capacities and of the sensitivity to gonadotropic hormone. The most important changes occurred just after the initiation of spermatogenesis, as spermatocyte/spermatid formation was associated with a drop of the secretory capacity (amount of steroid secreted per milligram of tissue incubated) and with a reduced sensitivity to gonadotropic hormone. At later stages, when the testicular weight substantially increased concurrently with the formation of numerous spermatozoa, both the secretory capacity and the responsiveness to gonadotropic hormone increased again to reach the levels typical of adult fish. The blood levels of androgens appeared to be positively related to the increasing testicular weight in the later phases of development.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-0878
    Keywords: Key words Teleost fish ; Puberty ; Testes ; Sex steroids ; Ultrastructure ; Steroidogenesis ; Clarias gariepinus (Teleostei)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract  The present report focuses on the mechanism(s) involved in the steroid-induced decrease of androgen production in immature African catfish testes that was observed in previous studies. Juvenile animals were implanted with Silastic pellets containing different 11-oxygenated androgens (11-ketotestosterone, KT; 11β- hydroxyandrostenedione, OHA; 11-ketoandrostenedione, KA), testosterone (T) or estradiol-17β (E2). Control groups received steroid-free pellets. Two weeks later, testis tissue fragments were either incubated with increasing concentrations of catfish luteinizing hormone (LH), or incubated with [3H]-pregnenolone ([3H]-P5) or [3H]-androstenedione ([3H]-A). Tissue fragments were also prepared for the quantitative assessment of Leydig cell morphology. Most of the parameters studied were not affected significantly by implantation of E2. Implantation of all androgens inhibited both the basal and the LH-stimulated androgen secretory capacity in vitro. This was associated with a reduced size of the Leydig cells and loss of half of their mitochondria. The studies on the metabolism of tritiated steroid hormones indicated that steroidogenic steps prior to 11β-hydroxylation, probably C17–20 lyase activity, were affected by all androgens. Although the effects of 11-oxygenated androgens and T on Leydig cells were mostly similar, previous work showed that only the 11-oxygenated androgens stimulated spermatogenesis, suggesting that distinct mechanisms of action are used by 11-oxygenated androgens and T. These mechanisms, however, seem to merge on the same target(s) to impair Leydig cell androgen production. Such a negative feedback mechanism may be of relevance in the context of the decline in androgen secretion per milligram testis tissue that accompanies the first wave of spermatogenesis in pubertal African catfish.
    Type of Medium: Electronic Resource
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