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1.
J Appl Toxicol ; 41(10): 1649-1659, 2021 10.
Artigo em Inglês | MEDLINE | ID: mdl-33629778

RESUMO

Tebuconazole is a widely used fungicide in agriculture, and it may easily enter in the human food chain. In addition, tebuconzaol skin permeation coefficient (Log Kp) is -5.55 cm/s and it does not violate Lipinski's rule. It may mimic as a ligand for various endocrine and reproductive receptor leading to toxicological response or disease manifestation. We studied interactive potential of tebuconazole with thyroid and sex hormone-binding globulin. The main methods for this in silico analyses are molecular docking and molecular dynamic (MD) simulation. This paper explores how agriculture fungicide tebuconzaol exposure can be a risk for endocrine and reprotoxicity due to its stable interactive potency with thyroid and sex hormone-binding globulin (2CEO and 1D2S). Thyroid impairment is one of the most common endocrine issues in human health. In molecular docking analyses, tebuconazole exhibited binding potency of -6.28 kcal/mol with 2CEO compared to its native ligand thyroxin and inhibitor propylthiouracil which had the binding potency of -9.9 and -4.49 kcal/mol, respectively. The binding score of tebuconzaol with 1D2S was found to be -7.54 kcal/mol compared to native ligand dihydrotestosteron and inhibitor aminoglutethimide which exhibited the binding score of -6.84 and -11.41 kcal/mol, respectively. Therefore, each complex was subjected to MD simulation for comparative assessment of physical movement. The root mean square deviation (RMSD), root mean square fluctuation (RMSF), Radius of Gyration and hydrogen bonding exhibited that fluconazole had stable binding pattern with 2CEO and 1D2S which was almost similar to native ligand and its inhibitor. Study revealed that tebuconazole may lead to potent endocrine and reproductive disruptions.


Assuntos
Disruptores Endócrinos/toxicidade , Fungicidas Industriais/toxicidade , Simulação de Acoplamento Molecular , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Globulina de Ligação a Hormônio Sexual/efeitos dos fármacos , Glândula Tireoide/efeitos dos fármacos , Triazóis/toxicidade , Adulto , Disruptores Endócrinos/química , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Globulina de Ligação a Hormônio Sexual/química , Glândula Tireoide/química , Triazóis/química
2.
J Appl Toxicol ; 40(7): 947-964, 2020 07.
Artigo em Inglês | MEDLINE | ID: mdl-32072669

RESUMO

Many obese patients are exposed to hypolipidemic and serotonin-norepinephrine reuptake inhibitor (SNRI) drugs. Statins are one of the most marketed drugs in the world to treat dyslipidemia, while sibutramine, a SNRI drug, is prescribed in some countries to treat obesity and is detected as an additive in many adulterated weight loss supplements marketed worldwide. Previous studies reported adverse effects of isolated exposure to these drugs on male rat reproductive parameters. In the present work, we further investigated male reproductive toxicity of these drugs, administered in isolation or combination in adult rats for a longer period of treatment. Adult male rats (90 days) were treated (gavage) for 70 days with saline and dimethyl sulfoxide (control), sibutramine (10 mg/kg), rosuvastatin (5 mg/kg), or rosuvastatin combined with sibutramine. Sibutramine alone or with rosuvastatin, promoted a reduction in food intake and body weight gain, weight of the epididymis, ventral prostate and seminal vesicle; as well as decreased sperm reserves and transit time through the epididymis; androgen depletion; and increased index of cytoplasmic droplet. The rosuvastatin-treated group showed reduced frequency of ejaculation. Exposure to this drug alone or combined with sibutramine impaired epididymal morphology. Co-exposed rats had altered epididymal morphometry, and seminal vesicle and testis weights. The rats also showed decreased fertility after natural mating and a trend toward a delay in ejaculation, suggesting a small synergistic effect of these drugs. Given the greater reproductive efficiency of rodents, the results obtained in the present study raise concern regarding possible fertility impairment in men taking statins and SNRI drugs.


Assuntos
Ciclobutanos/toxicidade , Ciclobutanos/uso terapêutico , Obesidade/tratamento farmacológico , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Rosuvastatina Cálcica/toxicidade , Rosuvastatina Cálcica/uso terapêutico , Testículo/efeitos dos fármacos , Adulto , Animais , Humanos , Masculino , Modelos Animais , Ratos , Ratos Wistar
3.
Neuro Endocrinol Lett ; 39(6): 427-433, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-30796792

RESUMO

OBJECTIVES: This work assessed sexual and neurobehavioral parameters after ovarian treatment with autologous PRP. DESIGN: Questionnaire study. MATERIAL AND METHODS: Patients receiving ovarian PRP injection (n=80) due to low ovarian reserve and/or at least 1 prior failed IVF cycle were sampled. Pre- and post-treatment levels in self-reported daily energy, sleep quality, skin tone/hair thickness/nail growth, cognitive clarity, menstrual pattern, cervical mucus/vaginal lubrication, libido, sexual activity, ability to achieve orgasm, and overall sexual experience were measured. RESULTS: Mean±SD age and baseline BMI among patients were 45.5±6yrs and 25±5.1kg/m2, respectively. Average weight loss after ovarian PRP was 1kg (p=0.056). After ovarian PRP, superior nail growth, skin tone, and hair thickness was observed by 46.3% of patients [95%CI=35%,57.8%]; the same ratio experienced increased "clarity of thinking" following the procedure. Irregular or absent menses affected 56.3% of patients at enrollment, and menses returned or cyclicity improved in 24.4% after treatment [95%CI=12.9%,39.5%]. Increased post-treatment vaginal lubrication/cervical mucus production was reported by 51.3% of women [95%CI=39.8%, 62.6%] accompanied by increased libido in 55% [95%CI=43.5%,66.2%]. More frequent sexual activity after ovarian PRP was noted from 46.3% of subjects [95%CI=35%, 57.8%] coinciding with a 45% improvement in overall sexual experience before vs. after ovarian PRP [95%CI=33.9%, 56.5%]. CONCLUSION: This investigation is the first to document responses across neurobehavioral and metabolic parameters after ovarian PRP. Injection of PRP-derived growth factors directly into ovarian tissue seems to enable a local signaling milieu favoring development of hormonally active ovarian elements, thus "re-potentiating" low or absent reserve.


Assuntos
Peptídeos e Proteínas de Sinalização Intercelular/administração & dosagem , Reserva Ovariana/efeitos dos fármacos , Plasma Rico em Plaquetas , Medicina Regenerativa/métodos , Adulto , Feminino , Humanos , Pessoa de Meia-Idade , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Estudos Retrospectivos
4.
Reprod Toxicol ; 84: 75-92, 2019 03.
Artigo em Inglês | MEDLINE | ID: mdl-30503857

RESUMO

In an OECD Test Guideline 416 multigenerational study, groups of 24 male and 24 female Sprague-Dawley rats were administered sodium molybdate dihydrate at 0, 5, 17, or 40 mg molybdenum (Mo)/kg bw/day in the drinking water or 40 mg Mo/kg bw/day in the diet over two generations to assess reproductive toxicity. No adverse effect on reproductive function was observed at any dose level in either generation as indicated by no significant dose-related effect on estrus cycles, sperm parameters, mating, fertility, gestation, litter size, pup survival, growth or postnatal development. Systemic toxicity, including decreased body weight, food consumption (males only) and water consumption, was observed among both sexes given 40 mg Mo/kg bw/day in the diet. Serum levels of Mo and copper were increased in a dose-related manner. The No Observed Adverse Effect Levels (NOAEL) are 17 mg Mo/kg bw/day for systemic toxicity and 40 mg Mo/kg bw/day for reproductive toxicity.


Assuntos
Molibdênio/toxicidade , Animais , Peso Corporal/efeitos dos fármacos , Dieta , Água Potável , Ingestão de Alimentos/efeitos dos fármacos , Feminino , Masculino , Molibdênio/sangue , Molibdênio/farmacocinética , Molibdênio/urina , Nível de Efeito Adverso não Observado , Gravidez , Ratos Sprague-Dawley , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos
5.
J Steroid Biochem Mol Biol ; 185: 237-247, 2019 01.
Artigo em Inglês | MEDLINE | ID: mdl-30253226

RESUMO

The study was undertaken to explore the molecular mechanism of eurycomanone, a major compound of Eurycoma longifolia plant in increasing the reproductive processes in the male fish model. Chitosan-nanoconjugated eurycomanone nanoparticles with a significant particle size [130 nm (CED1); 144.1 nm (CED2)] and stable zeta potentials (+49.1 mV and +30 mV) were synthesized and evaluated against naked eurycomanone (ED1 and ED2). In present study, short-term and long-term experiments were conducted to evaluate the effect of nano-formulation on expression of endocrine-related genes, circulating hormone concentrations (Follicle stimulating hormone, FSH; luteinizing hormone, LH; progesterone, testosterone and 17-ß estradiol) and reproductive capacity of male Clarias magur. In short-term experiment, the sampling of tissues was done on hourly basis after injection of eurycomanone either alone or with chitosan and long-term experiment was carried for 21 days and in this the injection was repeated after 7 days and 14 days. Treatments CED1 and CED2 showed controlled and sustained surge of the transcript level of selected genes (except aromatase) and serum hormones (except 17ß-estradiol) compared to ED1 and ED2 groups. The transcript levels of aromatase and serum 17ß-estradiol hormone showed the declining trend in the chitosan conjugated groups. The gonadosomatic index (GSI), reproductive capacity, intracellular calcium and selenium and cellular structure of testes were improved in CED1 and CED2 groups compared to other treatments. Furthermore, the effect of chitosan conjugated eurycomanone was evaluated in primary testicular cells and an increase in the mRNA expression level of endocrine-related genes was detected. This is the first report of the use of chitosan conjugated eurycomanone and present study elucidates the molecular mechanism of eurycomanone in increasing the reproductive output in animals.


Assuntos
Peixes-Gato/fisiologia , Quitosana/farmacologia , Infertilidade Masculina/tratamento farmacológico , Extratos Vegetais/farmacologia , Quassinas/farmacologia , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Testículo/fisiologia , Animais , Células Cultivadas , Estradiol/sangue , Eurycoma/química , Hormônio Foliculoestimulante/sangue , Hormônio Luteinizante/sangue , Masculino , Nanopartículas/química , Progesterona/sangue , Testosterona/sangue
6.
Arch Ital Urol Androl ; 90(1): 54-58, 2018 Mar 31.
Artigo em Inglês | MEDLINE | ID: mdl-29633799

RESUMO

OBJECTIVE: Vegetable oils have an important place in our daily diet. This study starts from this point to investigate the effects of canola oil and hazelnut oil in the male reproductive system in rats. MATERIAL AND METHODS: 30 male rats were used in this 16-week study. The animals were divided into three groups: the animals in group I served as the control group, while the animals in group II and group III were fed with hazelnut and canola oil, respectively. The testes of all rats were excised for histopathologic evaluation and immunohistochemical (IHC) evaluation with a standard method. Blood samples were obtained for determination of serum hormone levels. RESULTS: No significant differences were noted with respect to behavior or weight among the three groups. Rats in the canola oil group (group III) had higher luteinizing hormone (LH) and higher testosterone levels than rats in the control group. Rats who received hazelnut oil (group II) exhibited similar findings, with these levels being higher than they were in the control group. No statistical differences were shown for histopathology or IHC testosterone antibody levels across all treatment groups. Conclussion: Canola oil was shown to have a greater effect on serum LH and testosterone compared to the control group and the group fed with hazelnut oil. Further investigation is required into how these oils affect serum hormone and sperm activity.


Assuntos
Corylus/química , Óleos de Plantas/farmacologia , Óleo de Brassica napus/farmacologia , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Animais , Peso Corporal/efeitos dos fármacos , Hormônios Esteroides Gonadais/sangue , Imuno-Histoquímica , Hormônio Luteinizante/sangue , Masculino , Ratos , Ratos Sprague-Dawley , Testículo/anatomia & histologia , Testículo/efeitos dos fármacos , Testosterona/sangue
7.
Regul Toxicol Pharmacol ; 95: 385-394, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29678769

RESUMO

This study aimed to investigate the effects of beta-cypermethrin (ß-CYP) on female reproductive function and examine the morphology of the uterine endometrium and follicular development. The results found that the rate of successful pregnancy in the ß-CYP-treated groups significantly decreased. The levels of serum E2 and FSH were significantly increased in the ß-CYP-treated groups. The concentrations of serum P and LH were significantly decreased in the ß-CYP-treated groups. The uterine endometrium was damaged and the endometrial pinopode was markedly inhibited. In addition, the total number of follicles of all types was significantly lower in the medium- and high-dose ß-CYP-treated groups. These results suggest that ß-CYP significantly affected the reproductive function of female mice. ß-CYP may have significantly decreased the fertility of female mice by disturbing the reproductive hormone concentrations and inhibiting the development of the endometrium and the endometrial pinopode.


Assuntos
Inseticidas/toxicidade , Piretrinas/toxicidade , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Animais , Endométrio/efeitos dos fármacos , Endométrio/patologia , Estrogênios/sangue , Feminino , Hormônio Foliculoestimulante/sangue , Hormônio Luteinizante/sangue , Masculino , Camundongos , Gravidez , Progesterona/sangue
8.
Braz. J. Vet. Res. Anim. Sci. (Online) ; 55(1): 1-16, 2 abr. 2018. ilus, graf
Artigo em Inglês | LILACS, VETINDEX | ID: biblio-912690

RESUMO

Human-wildlife conflicts, a growing and sad reality worldwide, makes population control of wildlife and feral animals one of the biggest challenges in wildlife management, especially due to the rapidly expanding human population, and consequently the ever-diminishing natural habitats of animals. Human activities and the destruction of nature forcing wildlife to move inevitably into urban and agricultural areas, causing "conflicts", such as the risk of zoonosis and traffic accidents, as well as damage to crops in the search for food, whose losses reach millions of dollars. For decades, science has been engaged in extensive efforts to develop methods of "humane" population control methods, and many techniques are being employed in order to control wildlife population. In this article, we present an overview of applied contraceptive methods with simplified graphic demonstrations of their interactions with reproductive physiology, furthermore relating pro and contra of utilized antifertility agents. These are being compared to a set of desired characteristics for free-ranging wildlife for in-field applications, with emphasis on reversible immunocontraception ­ concluding, therefore, the reasons why this concept is becoming the most appropriate and promising for free-ranging wildlife.(AU)


Os conflitos Humanos-Animais Selvagens são uma realidade crescente e triste no mundo inteiro, tornando o controle populacional da fauna silvestre e animais ferais o maior desafio, principalmente diante do crescimento da população humana e, consequentemente, da diminuição dos habitats naturais dos animais. As atividades humanas e a destruição da natureza, forçam os animais de vida livre a se dirigirem para áreas urbanas e agrícolas, inevitavelmente, causando conflitos, como o risco de zoonoses, acidentes de trânsito, bem como danos às plantações, quando em busca de alimentos, cujo prejuízo chega a milhões de dólares. Durante décadas, a ciência esteve empenhada em esforços extensivos para desenvolver métodos de controle populacional "humano"; e muitas técnicas foram utilizadas, a fim de se realizar um controle populacional destes animais silvestres. Neste artigo será apresentada uma visão geral dos métodos anticoncepcionais aplicados, com demonstrações gráficas simplificadas de suas interações com a fisiologia reprodutiva, bem como relacionando os prós e os contras dos agentes antifertilidade empregados; também serão comparados com um conjunto de características desejadas para as aplicações em fauna a campo, com ênfase em imunocontracepção reversível, concluindo assim, com as razões do porque este conceito torna-se o mais apropriado e promissor para animais silvestres de vida livre.(AU)


Assuntos
Animais , Animais Selvagens/fisiologia , Anticoncepção/veterinária , Controle da População/métodos , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Desequilíbrio Ecológico/prevenção & controle
9.
Med Pr ; 66(5): 725-37, 2015.
Artigo em Polonês | MEDLINE | ID: mdl-26647990

RESUMO

Both ethylene and propylene glycol alkyl ethers (EGAEs and PGAEs, respectively) are widely used, mainly as solvents, in industrial and household products. Some EGAEs demonstrate gonadotoxic, embriotoxic, fetotoxic and teratogenic effects in both humans and experimental animals. Due to the noxious impact of these ethers on reproduction and development of organisms EGAEs are replaced for considerably less toxic PGAEs. The data on the mechanisms of testicular, embriotoxic, fetotoxic and teratogenic effects of EGAEs are presented in this paper. Our particular attention was focused on the metabolism of some EGAEs and their organ-specific toxicities, apoptosis of spermatocytes associated with changes in the expression of various genes that code for oxidative stress factors, protein kinases and nuclear hormone receptors.


Assuntos
Éteres/efeitos adversos , Etilenoglicol/efeitos adversos , Desenvolvimento Humano/efeitos dos fármacos , Propilenoglicol/efeitos adversos , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Solventes/efeitos adversos , Humanos
10.
Reprod Toxicol ; 55: 114-23, 2015 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-25656794

RESUMO

There is a great need for rapid testing strategies for reproductive toxicity testing, avoiding animal use. The EU Framework program 7 project ChemScreen aimed to fill this gap in a pragmatic manner preferably using validated existing tools and place them in an innovative alternative testing strategy. In our approach we combined knowledge on critical processes affected by reproductive toxicants with knowledge on the mechanistic basis of such effects. We used in silico methods for prescreening chemicals for relevant toxic effects aiming at reduced testing needs. For those chemicals that need testing we have set up an in vitro screening panel that includes mechanistic high throughput methods and lower throughput assays that measure more integrative endpoints. In silico pharmacokinetic modules were developed for rapid exposure predictions via diverse exposure routes. These modules to match in vitro and in vivo exposure levels greatly improved predictivity of the in vitro tests. As a further step, we have generated examples how to predict reproductive toxicity of chemicals using available data. We have executed formal validations of panel constituents and also used more innovative manners to validate the test panel using mechanistic approaches. We are actively engaged in promoting regulatory acceptance of the tools developed as an essential step towards practical application, including case studies for read-across purposes. With this approach, a significant saving in animal use and associated costs seems very feasible.


Assuntos
Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Medição de Risco , Testes de Toxicidade , Antagonistas de Androgênios/toxicidade , Alternativas aos Testes com Animais , Animais , Simulação por Computador , Estrogênios/toxicidade , Ensaios de Triagem em Larga Escala , Humanos , Modelos Biológicos , Mutagênicos/toxicidade , Teratógenos/toxicidade
11.
Nanotoxicology ; 9(1): 64-70, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24533579

RESUMO

As silver nanoparticles (AgNPs) have antimicrobial properties and potentiate the activity of some antibiotics, they are broadly used in both medical and nonmedical applications. In this study, prepubertal male Wistar rats were orally treated with 15 or 30 µg/kg/day AgNPs from postnatal day 23 (PND23) to PND58 and sacrificed at PND102. The acrosome integrity, plasma membrane integrity, mitochondrial activity and morphological alterations of the sperm were analyzed. Sexual partner preference, sexual behavior and the serum concentrations of FSH, LH, testosterone and estradiol were also recorded. The results were evaluated following the appropriate statistical analyses, and differences among the groups were considered significant when p < 0.05. AgNPs reduced the acrosome and plasma membrane integrities, reduced the mitochondrial activity and increased the abnormalities of the sperm in both treatment groups. AgNP exposure also delayed the onset of puberty, although no changes in body growth were observed in either treatment group. The animals did not show changes in sexual behavior or serum hormone concentrations. This study shows for the first time that prepubertal exposure to AgNPs causes alterations in adult sperm parameters. Importantly, the sperm appeared to be more sensitive to the toxic effects of AgNPs and demonstrated adverse effects following exposure to lower doses. Consequently, the effects of AgNPs on sperm should be considered in order to establish safety limits for the use of these particles.


Assuntos
Disruptores Endócrinos/toxicidade , Nanopartículas Metálicas/toxicidade , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Comportamento Sexual Animal/efeitos dos fármacos , Prata/toxicidade , Espermatozoides/efeitos dos fármacos , Animais , Animais Recém-Nascidos , Disruptores Endócrinos/química , Feminino , Hormônios/sangue , Masculino , Nanopartículas Metálicas/química , Distribuição Aleatória , Ratos , Ratos Wistar , Prata/química
12.
Life Sci ; 105(1-2): 48-55, 2014 Jun 06.
Artigo em Inglês | MEDLINE | ID: mdl-24780318

RESUMO

AIMS: Reactive oxygen species play a role in the signal transduction of beta-adrenergic receptors. We investigated whether an antioxidant (tocopherol) can reduce the effect of terbutaline in beta-2-adrenergic receptor (ß2-AR)-regulated smooth muscles. MAIN METHODS: Contractility of the tissues from nonpregnant (trachea) and 22-day-pregnant (myometrium and cervix) rats was investigated in an isolated organ bath. The tracheal and uterine ß2-AR expressions were increased by 17-beta-estradiol valerate (E2) and progesterone (P4), respectively. The accumulation of cyclic-AMP (cAMP), and the total oxidant (TOS) and total antioxidant status (TAS) were also measured. The oxidative stress index (OSI) was defined as the ratio of TOS and TAS. KEY FINDINGS: Terbutaline (10(-10)-10(-5)M) decreased the contractions in the nontreated and the P4-pretreated myometria, but tocopherol (10(-7)M) did not alter these actions. Terbutaline (10(-6)M) increased the cervical resistance both in the nontreated and in the P4-treated samples, while tocopherol reduced this action only in the P4-treated cervices. Terbutaline (10(-9)-10(-4)M) reduced the tracheal tones both in the nontreated and in the E2-treated tissues, while tocopherol reduced these effects. The changes in the intracellular cAMP levels of the tissues were in harmony with the isolated organ results. The OSI was highest in the trachea and lowest in the pregnant myometrium. SIGNIFICANCE: A higher OSI is linked to a higher tocopherol sensitivity of beta-mimetic-induced relaxation. Our results suggest that the antiasthmatic effect of beta-mimetics may worsen, while their tocolytic effect may remain unchanged during parallel tocopherol administration.


Assuntos
Músculo Liso/metabolismo , Estresse Oxidativo/fisiologia , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Sistema Respiratório/efeitos dos fármacos , Terbutalina/antagonistas & inibidores , Tocoferóis/farmacologia , Análise de Variância , Animais , Antioxidantes/metabolismo , Western Blotting , AMP Cíclico/metabolismo , Feminino , Contração Muscular/efeitos dos fármacos , Contração Muscular/fisiologia , Músculo Liso/efeitos dos fármacos , Oxidantes/metabolismo , Estresse Oxidativo/efeitos dos fármacos , Gravidez , Ratos , Ratos Sprague-Dawley , Espécies Reativas de Oxigênio/metabolismo , Reação em Cadeia da Polimerase em Tempo Real , Receptores Adrenérgicos beta 2/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Terbutalina/farmacologia
13.
Curr Drug Saf ; 8(2): 77-97, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23656453

RESUMO

Carcinogenic properties of ulipristal acetate (UPA), a selective progesterone receptor modulator developed for the treatment of benign gynecological conditions such as uterine fibroids, were assessed in a 26-week carcinogenicity study in transgenic TgRasH2 mice and a 104-week study in Sprague Dawley rats. Dose levels used in the mouse study were 15, 45, or 130 mg/kg/day and for the ratstudy the doses used were 1, 3, or 10 mg/kg/day. Vehicle and water controls were part of both studies and a positive control, N-Nitroso-N-methylurea intraperitoneally, was included in the transgenic mouse assay. Survival at all dose levels was similar to vehicle controls in both sexes of both species and there was no evidence of any UPA-induced carcinogenicity in either species. Rats receiving UPA had decreased incidences of fibroadenomas and adenocarcinomas in the mammary gland in all treated groups. UPA exposure [AUC(0-24h)] at the highest dose in rats was 67 times human therapeutic exposure at 10 mg/day. In mice, no tumor of any type increased at UPA exposures up to 313 times of therapeutic exposure. UPA-related findings in mice were limited to organ weight changes in the liver, pituitary, thyroid/parathyroid glands, and epididymis as well as minimal panlobular hepatocellular hypertrophy in male and female mice receiving 130 mg/kg/day. Rats had UPA-related non-neoplastic findings in the reproductive system (mammary gland, ovary, uterus, vagina, seminal vesicle, prostate), endocrine system (adrenal, pituitary), thymus, muscle, liver, pancreas and lungs most of which are considered to be due to exaggerated pharmacological action of the compound.


Assuntos
Norpregnadienos/toxicidade , Receptores de Progesterona/efeitos dos fármacos , Testes de Toxicidade/métodos , Animais , Área Sob a Curva , Relação Dose-Resposta a Droga , Sistema Endócrino/efeitos dos fármacos , Feminino , Masculino , Metilnitrosoureia/farmacologia , Camundongos , Camundongos Transgênicos , Norpregnadienos/administração & dosagem , Norpregnadienos/farmacocinética , Tamanho do Órgão/efeitos dos fármacos , Ratos , Ratos Sprague-Dawley , Receptores de Progesterona/metabolismo , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Especificidade da Espécie
14.
Obstet Gynecol Surv ; 67(6): 357-64, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22713162

RESUMO

Familial Mediterranean fever (FMF) is the most common hereditary recurrent febrile disorder, characterized by the sudden onset of high fever and severe abdominal pain. The implications of this disorder on a woman's health are significant and not well known among obstetrician/gynecologists. The goal of this review is to familiarize providers caring for women on the ramifications of FMF on different aspects of a woman's life, including puberty, fertility, pregnancy, and menopause, as well as to help them to diagnose and manage FMF when these patients become pregnant.


Assuntos
Desenvolvimento Infantil/efeitos dos fármacos , Colchicina , Febre Familiar do Mediterrâneo , Complicações na Gravidez , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Dor Abdominal/etiologia , Dor Abdominal/fisiopatologia , Adolescente , Adulto , Criança , Colchicina/administração & dosagem , Colchicina/efeitos adversos , Anticoncepção/métodos , Gerenciamento Clínico , Febre Familiar do Mediterrâneo/complicações , Febre Familiar do Mediterrâneo/diagnóstico , Febre Familiar do Mediterrâneo/tratamento farmacológico , Febre Familiar do Mediterrâneo/fisiopatologia , Feminino , Febre/etiologia , Febre/fisiopatologia , Humanos , Infertilidade/tratamento farmacológico , Infertilidade/etiologia , Pessoa de Meia-Idade , Osteoporose Pós-Menopausa/etiologia , Gravidez , Complicações na Gravidez/diagnóstico , Complicações na Gravidez/tratamento farmacológico , Complicações na Gravidez/etiologia , Complicações na Gravidez/fisiopatologia , Fatores de Risco , Moduladores de Tubulina/administração & dosagem , Moduladores de Tubulina/efeitos adversos , Saúde da Mulher
15.
Mol Cell Endocrinol ; 355(2): 192-200, 2012 May 22.
Artigo em Inglês | MEDLINE | ID: mdl-22210487

RESUMO

There is growing interest in the potential health threats posed by endocrine-disrupting chemicals (EDCs) to the reproductive system. Soybean is the most important dietary source of isoflavones, an important class of phytoestrogen. While consumption of soy food or phytoestrogen supplements has been frequently associated with beneficial health effects, the potentially adverse effects on development, fertility, and the reproductive and endocrine systems are likely underappreciated. Here we review the available epidemiological, clinical and animal data on the effects of soy and phytoestrogens on the development and function of the male and female reproductive system, and weigh the evidence as to their detrimental impact.


Assuntos
Disruptores Endócrinos/farmacologia , Isoflavonas/farmacologia , Fitoestrógenos/farmacologia , Saúde Reprodutiva , Absorção , Animais , Humanos , Isoflavonas/biossíntese , Isoflavonas/metabolismo , Fitoestrógenos/metabolismo , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , /metabolismo
16.
Aquat Toxicol ; 105(3-4): 466-81, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21888872

RESUMO

The objectives of the current study were: (i) to gain a better understanding of the relative importance of water and diet as routes of exposure causing toxicity in fathead minnow (FHM) exposed to metal mining effluents (MME) using a full factorial water/food experimental design (Experiment 1), and (ii) to assess differences in the effects of food quality on toxicity by comparing FHM fed both a live and frozen diet of Chironomus dilutus (Experiment 2). The results showed significant increases in general water quality parameters (e.g., hardness, conductivity) and various metals in the effluent treatment waters compared to control waters, with maximum increase seen in the multi-trophic streams. Metals accumulation (Rb, Al, Se, Sr, Tl, Ce, Co, Cu, Pb) effects of both waterborne and multi-trophic exposures were significant in one or more fathead minnow tissue type (muscle, gonads, liver, larvae) relative to those in the control systems. Condition factor and liver somatic index (LSI) of FHM were also significantly affected in both exposures by one or both routes of exposure (water and/or diet). In addition, cumulative total egg production and cumulative spawning events were significantly affected by both waterborne and dietborne exposures, with maximum effect found in the multi-trophic streams. These results suggest that under environmentally relevant exposure conditions, trophic transfer of metals may lead to greater reproductive effects and increased metal toxicity in fish. It also indicates that metals are assimilated in tissues differently depending on the quality of the food (live vs. frozen). Overall, it appears that the multi-trophic bioassay provides an important link between the laboratory and field, which may allow for a more realistic assessment of the true impact of MME's in the environment.


Assuntos
Constituição Corporal/efeitos dos fármacos , Cyprinidae/fisiologia , Exposição Ambiental/efeitos adversos , Contaminação de Alimentos , Metais Pesados/toxicidade , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Animais , Bioensaio , Carga Corporal (Radioterapia) , Chironomidae/química , Feminino , Larva/efeitos dos fármacos , Masculino , Metais Pesados/farmacocinética , Mineração , Distribuição Aleatória , Testes de Toxicidade Crônica , Poluentes Químicos da Água/farmacocinética , Qualidade da Água
17.
Aquat Toxicol ; 105(3-4): 559-68, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21939616

RESUMO

The presence of endocrine active compounds such as estrogens in treated wastewater effluent and their effects on aquatic life are causing concern among aquatic resource managers. In contrast to 17ß-estradiol (E2), the steroid hormone produced by all vertebrates, the biological effects of estrone (E1), one of its breakdown products are less understood, even though the aquatic concentrations of E1 are often higher than those of E2. The central hypothesis of this study was that at environmental concentrations, E1 has estrogenic effects in fish, with increased vitellogenin concentrations and decreased reproductive success in both male and female fathead minnows, as found with E2. In two replicate experiments, we exposed mature fathead minnows to three concentrations of each estrogen for 21 days in a flow-through exposure system and measured a broad suite of anatomical (body indices, histopathology), physiological (plasma vitellogenin), behavioral (nest defense), and reproductive (fecundity, fertility, hatching) endpoints. These endpoints have previously been associated with adverse effects of estrogenic exposures. While body length and weight parameters were unaltered by exposure, secondary sex characteristics exhibited an exposure concentrated-related decline in male fathead minnows. Interestingly, low concentrations of estrone (≈ 15 ng/L) enhanced the aggressiveness of male fathead minnows in a behavioral assay. Vitellogenin concentrations in male fish increased with higher concentrations of both estrogens, but remained unchanged in all female treatments. A decrease in fecundity was observed at high concentrations of E2 as compared with control minnows. These results suggest that E1, at concentrations previously found in waters receiving wastewater effluent, can have reproductive effects on fish.


Assuntos
Cyprinidae/fisiologia , Estradiol/toxicidade , Estrogênios/toxicidade , Estrona/toxicidade , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Animais , Tamanho Corporal/efeitos dos fármacos , Cyprinidae/sangue , Relação Dose-Resposta a Droga , Feminino , Masculino , Comportamento de Nidação/efeitos dos fármacos , Distribuição Aleatória , Caracteres Sexuais , Vitelogeninas/sangue
18.
Aquat Toxicol ; 105(3-4): 355-60, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21819815

RESUMO

The deleterious effects of tributyltin (TBT) on spermiation in fish have been attributed to its role in inhibiting aromatisation of androgens to estrogens, and the critical role of the latter in sperm development. We test this hypothesis by examining sperm parameters, fertilisation and hatching success in males of two fish species exposed throughout life to doses of Fadrozole, a non-steroidal aromatase inhibitor (AI), provided in their diets. AI-treatment caused 100% male development in zebrafish, but only partial masculinisation in medaka, in both cases supporting previous studies and suggesting different roles of estrogen in sexual differentiation in the two species. Milt volume, initial sperm motility, maximum sperm swimming duration and sperm morphology did not differ significantly between Control and AI-dosed fish in either species, after excluding low milt volumes in sex-changed females in medaka. Fertilisation rates were also unaffected by the aromatase inhibition, but hatching success in medaka was 31% lower than in Control males, suggesting a previously unreported effect of aromatase on sperm quality. The slight effect of aromatase inhibition on sperm parameters in general contrasts with the marked effect of TBT on fish sperm, and suggests that a mechanism other than depressed estrogen levels is involved.


Assuntos
Inibidores da Aromatase/toxicidade , Fadrozol/toxicidade , Oryzias/fisiologia , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Peixe-Zebra/fisiologia , Animais , Feminino , Fertilidade/efeitos dos fármacos , Masculino , Diferenciação Sexual/efeitos dos fármacos , Especificidade da Espécie , Espermatozoides/efeitos dos fármacos , Testes de Toxicidade Crônica
19.
J Chromatogr B Analyt Technol Biomed Life Sci ; 879(29): 3268-76, 2011 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-21531634

RESUMO

We investigated the involvement of D-Aspartic acid (D-Asp) on ovarian and testicular morphology of the green frog, Rana esculenta, and its effect on the testosterone production. The study has been performed throughout the reproductive cycle. In both ovary and testis a substantial amount of D-Asp is endogenously present and its concentration varies as function of reproduction. In the frog, D-Asp content is differently correlated with gonadal and plasmatic levels of testosterone, depending on the sex. In fact, the amount of the D-Asp is inversely linked with that of the testosterone in the ovary, while this correlation directly matched in the testis. In vivo short-term experiments, consisting of a single intra-peritoneal injection of D-Asp (2.0 µmol/g body weight), demonstrated that the enantiomer is significantly accumulated by both the ovary and testis, reaching after 3 h the highest uptake and thereafter decreasing to baseline values within 24 h. Furthermore, D-Asp influences the synthesis and/or the release of testosterone, causing a decrease of its level in the female, and an increase in the male, respectively. In vivo long-term experiments, D-Asp, chronically administered to the frogs of both sexes, enhances the maturation of both gonads, determining in the oocytes an higher accumulation of carbohydrate yolk plates in the ooplasm, and stimulating the spermatogenesis in the testis. Taken altogether, our results show that D-Asp operates differently in female and male frog gonads, indicating that it has different targets in the reproductive machinery depending on the sex.


Assuntos
Ácido D-Aspártico/metabolismo , Ácido D-Aspártico/farmacologia , Rana esculenta/fisiologia , Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Aminoácidos/química , Aminoácidos/metabolismo , Análise de Variância , Animais , Cromatografia Líquida de Alta Pressão , D-Aspartato Oxidase/metabolismo , Ácido D-Aspártico/química , Feminino , Histocitoquímica , Masculino , Ovário/química , Ovário/metabolismo , Testículo/química , Testículo/metabolismo , Testosterona/análise , Testosterona/metabolismo
20.
Reprod Toxicol ; 31(4): 392-401, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21130863

RESUMO

The multi-generation reproductive toxicity study (OECD TG 416 and USEPA 870.3800) has been extensively used internationally to assess the adverse effects of substances on reproduction. Recently the necessity of producing a second generation to assess the potential for human health risks has been questioned. The present standardized retrospective analysis of the impact of the second generation on overall study outcome combines earlier analyses and includes 498 rat multi-generation studies representing 438 different tested substances. Detailed assessment of study reports revealed no critical differences in sensitivities between the generations on the basis of a consideration of all endpoints evaluated. This analysis indicates that the second generation mating and offspring will very rarely provide critical information. These findings are consistent with the conclusions of previous retrospective analyses conducted by RIVM, USEPA and PMRA and support adoption of the proposed OECD extended one-generation reproductive toxicity study protocol in regulatory risk assessment testing strategies.


Assuntos
Fenômenos Reprodutivos Fisiológicos/efeitos dos fármacos , Projetos de Pesquisa , Testes de Toxicidade , Envelhecimento , Animais , Relação Dose-Resposta a Droga , Desenvolvimento Embrionário/efeitos dos fármacos , Determinação de Ponto Final , Feminino , Fertilidade/efeitos dos fármacos , Idade Gestacional , Lactação , Tamanho da Ninhada de Vivíparos/efeitos dos fármacos , Masculino , Exposição Materna , Exposição Paterna , Gravidez , Efeitos Tardios da Exposição Pré-Natal , Ratos , Reprodução/efeitos dos fármacos , Projetos de Pesquisa/normas , Medição de Risco , Testes de Toxicidade/normas
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