ABSTRACT
Olanzapine (OLZ) is an antipsychotic medication used to treat postpartum psychiatric symptoms. It aimed to evaluate the effects of administering OLZ to lactating rats on testicular parameters of adult Wistar rats. Mothers received 2.5, 5 or 10 mg/kg until weaning. Adult male rats showed decrease in body weight, weight of testes, epididymis, prostate, seminal gland and gonadosomatic index when higher doses of OLZ were administered. Testicular volumetric parameters, as well as the length of seminiferous tubules, were also reduced in animals treated with the highest doses of OLZ. The diameter of the seminiferous tubules and the height of the seminiferous epithelium were reduced. There was also a relevant decrease in the population of Sertoli cells and a relevant reduction in the volume of individual Leydig cells. Histopathological analysis of the testes showed lesions compatible with testicular degeneration in rats treated with the highest dose of OLZ. There was a significant reduction in plasma testosterone levels in all treatments. It is noted, therefore, that the adverse impact on the testes of the highest doses of the drug during the neonatal period persisted into adulthood, with the dose of 2.5 mg/kg of OLZ proving to be safer than the others.
Subject(s)
Antipsychotic Agents , Benzodiazepines , Lactation , Olanzapine , Rats, Wistar , Testis , Testosterone , Animals , Male , Testis/drug effects , Lactation/drug effects , Female , Olanzapine/administration & dosage , Antipsychotic Agents/pharmacology , Antipsychotic Agents/administration & dosage , Benzodiazepines/pharmacology , Benzodiazepines/administration & dosage , Testosterone/blood , Rats , Organ Size/drug effects , Body Weight/drug effectsABSTRACT
The effects of systemic insulin administration at different concentrations on the testicular tissue of diabetic adult rats, induced by streptozotocin, are evaluated by the morphological analysis of spermatogenic process. Twenty-four adult male rats were divided into 1) Control Group: they received citrate buffer, by intraperitoneal injection; 2) Diabetic Group: induced by intraperitoneal injection of streptozotocin (60 mg. kg-1 of body weight); 3) Insulin 50%: induced diabetes treated with half of standard dosage of insulin; 4) Insulin 100%: induced diabetes treated with standard dose of insulin. After eight weeks, animals were weighted and anesthetized; testicles were removed and processed in resin. Body and testicular weight of diabetic rats decreased when compared to that of control. Parameters increased with insulin therapy. Testosterone levels were low in diabetic animals but rates recovered after insulin therapy. Nuclear diameter and volume of Leydig cells decreased in diabetic rats although they significantly increased after insulin therapy. Results showed that the administration of insulin in diabetic rats promoted a protective effect of testicular parenchyma, enhancing efficient recovery on testosterone levels and increase in daily sperm production.
Subject(s)
Seminiferous Tubules , Testis , Convulsive Therapy , Diabetes Mellitus , Leydig CellsABSTRACT
OBJECTIVES: The purpose of this study was to evaluate the correlation between clinical aspects and urethral lesions with reproductive status and age at neutering in obstructed male cats. METHODS: All cats with compatible signs of urethral obstruction (UO) treated at the Veterinary Hospital of the Federal Rural University of Pernambuco from 2019 to 2021 were divided into three groups according to their reproductive status: intact; prepubertal neutered; and post-pubertal neutered. Cats with compatible signs of UO were selected for further analysis. Age, clinical signs, age at neutering and age of the first obstructive event were documented. Cats with recurrent obstructive urinary signs or urethral trauma that made catheterization impossible were referred for perineal urethrostomy. The morphology of the excised penises was assessed by histopathological analysis. RESULTS: Of 84 cats with signs of UO included in this study, 28.6% were classified as intact, 28.6% as prepubertal neutered and 42.8% as post-pubertal neutered. Intact cats had a significantly earlier onset of UO compared with prepubertal and post-pubertal neutered cats, as seen by the age at obstruction (3.6 vs 5.7 and 5.5 years, respectively). Similar clinical signs and histopathological lesions were observed in all groups. The main clinical signs observed were stranguria, hematuria and pollakiuria. All cats had some degree of injury in the penile urethra. The most common lesions were hemorrhage, fibrosis and congestion. CONCLUSIONS AND RELEVANCE: It appears that intact cats had an earlier onset of UO than neutered cats, regardless of age at neutering. Urethral histopathological lesions and clinical signs were similar in both groups. Pediatric neutering represents a useful tool in the control of abandoned and stray animals and the consequent dissemination of zoonoses, thus having a positive impact on public health.
Subject(s)
Cat Diseases , Orchiectomy , Urethral Obstruction , Animals , Cats , Male , Cat Diseases/pathology , Cat Diseases/surgery , Urethral Obstruction/pathology , Urethral Obstruction/surgery , Urethral Obstruction/veterinary , Orchiectomy/veterinaryABSTRACT
The aim of the present study was to analyze the effects of melatonin treatment on diabetic rat testes. Fifty albino rats were divided into the following groups: CG: control group; GD: placebo-induced and placebo-treated mice; GDI: insulin-induced and post-confirmation diabetes-induced rats; GDM: diabetes-induced and melatonin-treated post-confirmation mice and GDMS: diabetes-induced and melatonin-treated mice simultaneously. Melatonin was administered at a dose of 10â¯mg/kg in drinking water every day for 20 days at night. Diabetes was induced by streptozotocin (60â¯mg/kg) and confirmed after the fifth day of induction. Insulin was administered at 5 IU (international units)/day at different times of the day for 20 days. The testes were submitted to histopathological, morphometric, immunohistochemical and oxidative stress analysis. Melatonin moderately decreased glycemic levels, protected weight loss and morphometric changes in the testicles, increased antioxidant enzyme levels and stabilized plasma testosterone and androgen receptor levels and decreased inflammatory markers in the testicles. Showing its potential to mitigate diabetes effects.
Subject(s)
Antioxidants/pharmacology , Diabetes Mellitus, Experimental/drug therapy , Melatonin/pharmacology , Testis/drug effects , Animals , Body Weight/drug effects , Diabetes Mellitus, Experimental/blood , Lipid Peroxidation/drug effects , Male , Oxidative Stress/drug effects , Rats, Wistar , Streptozocin/pharmacologyABSTRACT
The objective of this study was to evaluate the toxic effects of progesterone (P4F) and estradiol (E2F) and the effect of these steroid hormones complexed into cyclodextrins, commercially available drugs, such as micronized progesterone (P4M) and transdermal estradiol (E2T), and evaluate them as endocrine disruptors through biological parameters of Danio rerio. An acute toxicity test was performed with hormones using D. rerio embryos according to OECD 236 guidelines. The heart rate, mortality, and teratogenic effects were evaluated. In addition, a chronic toxicity test was assayed with adult animals for evaluation of animal behavior, reproductive capacity, and electrophysiological responses of the retina. Analysis of the results of the acute toxicity test with embryos exposed to progestins and estrogens showed that free hormones caused a higher percentage of teratogenic effects such as pericardial edema, yolk sac edema, and spinal deformation. Behavioral evaluation (30-60 days) of adult animals exposed to P4M, E2F, and E2T demonstrated higher frequencies of aggressive behaviors such as Chase away, Persecution, Escape, and Attack. Analysis of reproductive capacity did not show significant differences in the number of viable eggs, and no significant changes were observed in the electrophysiological responses of the retina. According to these results, there is a higher toxicity effect of hormones in the free form when compared to the commercial forms and inclusion complexes. This indicates that complexation into cyclodextrin reduced the toxicity of the hormones according to the parameters studied.
Subject(s)
Cyclodextrins , Hormones/toxicity , Steroids/toxicity , Zebrafish/growth & development , Animals , Biological Products , Drug-Related Side Effects and Adverse Reactions , Embryo, Nonmammalian/drug effects , Endocrine Disruptors/pharmacology , Pharmaceutical Preparations , Progesterone/pharmacology , Progestins/pharmacology , Reproduction/drug effects , Toxicity Tests , Zebrafish/physiologyABSTRACT
ABSTRACT: The aim of the present study was to investigate the correlations among chronic inflammatory reaction, immunostaining and parasite load in the genital system of female dogs naturally infected with Leishmania infantum . Animals (n = 10) used in this study were from the Department of Vector Control and Animal Surveillance of the municipality of Caruaru, state of Pernambuco, Brazil. Fragments of the vulva, vagina, cervix, uterine body, uterine horns and ovaries were submitted to histopathological analysis, immunohistochemistry (IHC) and DNA detection of amastigotes by qPCR. Correlations were found between the IHC findings and chronic inflammatory infiltrate related to L. Infantum only in the vulva and vagina; whereas, the same inflammatory reactions without immunostaining were observed in all organs, except the ovaries. L. Infantum DNA was detected in all organs of genital system, with no difference in parasite load observed among the different organs. No correlation was reported between parasite load and inflammatory lesions in the organs evaluated, except for the uterine body, in which an inverse correlation was detected. In conclusion, the vulva and vagina were the major sites of lesions and immunostaining for L. Infantum amastigotes in the genital system of female dogs. Moreover, parasite load exerted no influence on the intensity of the lesions in the organs evaluated.
RESUMO: Considerando a falta de estudos sobre lesões nos órgãos genitais de cadelas naturalmente infectadas por Leishmania infantum , o objetivo do presente estudo foi investigar a correlação entre reação inflamatória crônica, imunomarcação e carga parasitária, no sistema genital. Dez animais foram fornecidos pelo Departamento de Controle de Vetores e Vigilância Animal do município de Caruaru, Estado de Pernambuco, Brasil. Fragmentos de vulva, vagina, cérvix, corpo do útero, corno do útero e ovários foram avaliados por descrição histopatológica, imuno-histoquímica (IHQ) e detecção de DNA de formas amastigotas por qPCR. A relação entre IHQ e infiltrado inflamatório crônico relacionado com L. infantum foi observada apenas na vulva e vagina, enquanto as mesmas reações sem imunomarcação foram observadas em todos os órgãos, exceto nos ovários. DNA de L. infantum foi detectado em todos os órgãos do sistema genital, porém, sem diferença de carga parasitária entre eles. Não houve correlação entre a carga parasitária e lesões inflamatórias nos órgãos avaliados, com exceção do corpo do útero, em que foi encontrada uma correlação inversa. Em conclusão, a vulva e a vagina foram os principais locais de lesões e imunomarcação para formas amastigotas L. infantum no sistema genital de cadelas. A carga parasitária não influenciou a intensidade das lesões nos órgãos avaliados.
ABSTRACT
ABSTRACT: Canine visceral leishmaniasisis an important disease caused by the protozoon Leishmania infantum which affects several organs and systems, including the genital tract. The L. infantum tropism to the male genital system and correlation among parasite load, immunohistochemistry detection and structural changes in these organs is controversy. Therefore, the aim of this study was to evaluate this correlation in the genital organs of the male dogs naturally infected with L. infantum. Samples from testicles, epididymis, prostate, glans penis, prepuce and scrotum were collected from 19 positive adult dogs. Structural changes were observed in the testicles (5.2%), epididymis (2.6%), prepuce (5.2%) and scrotum (5.2%) of the samples positive at immunohistochemistry examination. Conversely, similar structural changes were observed in all tissues negative at immunohistochemistry analysis. Moreover, L. infantum DNA was detected in all organs with the highest parasite load found in testicles, epididymis, and prostate gland. , Testicles had the highest parasite load but the lowest number of inflammatory lesions. These inflammatory lesions were observed in all organs of reproductive system of dogs; however, no correlation was observed between the parasite load and inflammatory lesions of dogs naturally infected with L. infantum.
RESUMO: A Leishmaniose Visceral Canina é uma importante enfermidade causada pelo protozoário Leishmania infantum que afeta diversos órgãos e sistemas, incluindo o trato genital. No entanto, o tropismo da L. infantum pelo sistema genital masculino e a correlação entre carga parasitária, detecção imunohistoquímica e alterações estruturais nesses órgãos ainda é uma questão controversa. Sendo assim, o objetivo deste estudo foi avaliar essa correlação em órgãos genitais de cães naturalmente infectados por L. infantum. Para tal, amostras de testículos, epidídimos, próstata, glande, prepúcio e escroto foram coletadas de 19 cães adultos positivos. Lesões microscópicas associadas com imunomarcação de formas amastigotas do parasito foram observadas nos testículos (5,2%), epidídimos (2,6%), prepúcio (5,2%) e escroto (5,2%). Por outro lado, alterações estruturais sem imunomarcação foram observadas em todos os órgãos. Além disso, o DNA de L. infantum foi encontrado em todos os órgãos com maior carga parasitária nos testículos, epidídimos e próstata. Curiosamente, os testículos apresentaram a maior carga parasitária, porém apresentaram o menor grau de lesões inflamatórias. Essas lesões inflamatórias foram observadas em todos os órgãos do sistema reprodutor de cães com L. infantum. Entretanto, não houve correlação entre carga parasitária e lesões inflamatórias nestes órgãos.
ABSTRACT
Visceral leishmaniasis (VL) is a chronic disease caused by
A leishmaniose visceral (LV) é uma doença crônica causada pelo protozoário
ABSTRACT
Teratogenicity and developmental abnormalities in the offspring of female rats that ingested ethanol extract of Neem plants during pregnancy and lactation period were assessed. Twenty-four female Wistar rats were randomly distributed in control group and in three experimental groups and treated during the 4th, 5th, and 6th day of pregnancy. After birth, the lactating females received, by gavage, 65, 135 and 200 mg kg-1 of Neem ethanol extract, during 15 days. Results show, there was no significant difference in body mass index of neonatal rats in the 4 groups evaluated, whereas mean rate of offspring survival was 79.4%. Hair growth, incisor teeth eruption, ear detachment, eyelid opening, and spontaneous ambulation were similar for all groups. Likewise, physical development and development of motor activity, ambulation, and postural reflexes were similar for all groups. The administration of Neem ethanol extract did not cause any reproductive or systemic toxicity in animals. Results show that, Neem ethanol extract safe at doses 65, 135 and 200 mg kg-1 in pregnant or lactating rats.
Teratogenicidade e anormalidades no desenvolvimento de proles de ratas que ingeriram o extrato etanólico de folhas de nim durante a gestação e lactação foram avaliadas. Vinte e quatro ratas Wistar foram distribuídas aleatoriamente em um grupo controle e três grupos experimentais tratados no quarto, quinto e sexto dias de gestação. Após o nascimento, as fêmeas lactantes receberam através de gavagem, o extrato etanólico de nim nas doses de 65, 135 e 200 mg kg-1 durante 15 dias. Nenhuma diferença significativa foi observada em relação ao índice de massa corpórea das fêmeas em lactação nos grupos em todos os momentos e a taxa média de sobrevivência dos filhotes foi de 79,4%. O tempo de crescimento piloso, erupção dos dentes incisivos, descolamento de orelha, abertura palpebral e deambulação espontânea foram semelhantes em todos os grupos. O desenvolvimento físico e da atividade motora, deambulação e reflexos posturais foram semelhantes em todos os grupos. A administração não resultou em toxicidade reprodutiva ou sistêmica. Os resultados mostraram que o extrato etanólico do nim é seguro para uso nas doses de 65, 135 e 200mg kg-1 em ratas prenhes ou em lactação.
Subject(s)
Rats , Azadirachta , Plants, Medicinal , Reproduction , TeratogensABSTRACT
Current study investigates the effects of maternal protein restriction during pregnancy and lactation on the testis of immature rats. Female Wistar rats were mated and, after confirming pregnancy, they were divided into two groups: undernourished group (UG) fed on a diet with casein 8%, and control group (CG) fed on a diet with casein 17 %, during pregnancy and lactation. After weaning, male offspring from the two experimental groups were fed on normal diet up to 35 days old when they were euthanized. Body and testicular weights decreased in UG when compared to those in CG. Volumetric density of seminiferous tubules was higher in CG whilst intertubular space increased in UG. The number of lumenated seminiferous tubules was higher in CG than in UG. Tubular diameter, seminiferous epithelium height and total length of seminiferous tubules were lower in UG. Round spermatids were frequently found in seminiferous tubules cross-section of CG. On the other hand, spermatocytes I in prophases was the germ cell commonly found in seminiferous tubules cross-sections of UG. Undernutrition during pregnancy and lactation period of the male Wistar rats altered the morphometric testicular parameters related to tubular compartment and delayed the onset of spermatogenesis.
O objetivo deste estudo foi investigar o efeito da restrição proteica materna durante prenhez e lactação no testículo de ratos imaturos. Fêmeas de ratos Wistar foram acasaladas e, uma vez confirmada a gestação, foram divididas em dois grupos e alimentadas durante a prenhez e a lactação: grupo desnutrido (GD), dieta com caseína 8%, e grupo controle (GC), dieta com caseína 17%. Após o desmame, os machos de ambas as proles receberam a dieta normal até os 35 dias de idade, quando ocorreu a eutanásia. O peso corporal e o peso testicular diminuíram no GD com relação ao GC. A densidade volumétrica dos túbulos seminíferos foi maior no GC, assim como o espaço intertubular aumentou no GD. O número de túbulos seminíferos luminados foi maior no GC comparado ao GD. Diâmetro tubular, altura do epitélio seminífero e comprimento total dos túbulos seminíferos diminuíram no GD. Espermátides arredondadas foram frequentemente encontradas nas seções transversais do GC. Por outro lado, espermatócitos I em prófase foram o tipo celular mais frequentemente encontrado no GD. A desnutrição durante a gestação e a lactação em ratos Wistar machos alteraram parâmetros morfométricos testiculares relacionados ao compartimento tubular e atrasou o início da espermatogênese.
Subject(s)
Rats , Malnutrition , Seminiferous Tubules , TestisABSTRACT
The goal of present study was to evaluate the effects of diabetes on quantitative parameters of Leydig cells. Twelve adults Wistar rats were divided in: 1) Diabetic Group (DG), which was induced by a single intraperitoneal injection of streptozotocin (60 mg kg-1 of body weight); and 2) Control Group (CG), which received citrate buffer intraperitoneal. After eight weeks of diabetic induction, the animals were weighted, anesthetized and testicles were removed and routinely processed to paraffin embedded. Body weight (40%) and testicular weight (18%) of diabetic rats were significantly lower than control group. Diabetic rats showed an increase in interstitial compartment but the tubular compartment did not differ. The individual volume of Leydig cells and nuclear diameter were lower in DG. However, the population of these cells was increased. In conclusion, diabetes induced by streptozotocin in adult rats promoted alterations in testicular compartments and changes on volume, nuclear diameter and population of Leydig cells, compromising the testicular function.
O objetivo do presente estudo foi avaliar os efeitos do 'diabetes' nos parâmetros quantitativos de células de Leydig. Doze ratos machos adultos foram divididos em: 1) Grupo Diabético (GD) induzidos por injeção intraperitoneal única de estreptozotocina (60 mg kg-1 de peso corporal); e 2) Grupo Controle (GC) receberam tampão citrato, via intraperitoneal. Após oito semanas da indução, os animais foram pesados, anestesiados, os testículos foram removidos e processados rotineiramente em parafina. O peso corporal (40%) e testicular (18%) dos ratos diabéticos reduziu significativamente em relação ao grupo controle. Ratos diabéticos mostraram aumento no compartimento intersticial, mas o compartimento tubular não apresentou diferença significativa. O volume individual e o diâmetro nuclear de células de Leydig reduziram em GD. No entanto, a população dessas células aumentou. Em conclusão, o 'diabetes' induzido por estreptozotocina, em ratos adultos, promoveu alterações nos compartimentos testiculares e mudanças no volume, diâmetro nuclear e população das células de Leydig, comprometendo a função testicular.
Subject(s)
Rats , Connective Tissue Cells , Streptozocin , TestisABSTRACT
OBJECTIVE To evaluate the larvicidal activity of Azadirachta indica, Melaleuca alternifolia, carapa guianensis essential oils and fermented extract of Carica papaya against Aedes aegypti (Linnaeus, 1762) (Diptera: Culicidae). METHODS The larvicide test was performed in triplicate with 300 larvae for each experimental group using the third larval stage, which were exposed for 24h. The groups were: positive control with industrial larvicide (BTI) in concentrations of 0.37 ppm (PC1) and 0.06 ppm (PC2); treated with compounds of essential oils and fermented extract, 50.0% concentration (G1); treated with compounds of essential oils and fermented extract, 25.0% concentration (G2); treated with compounds of essential oils and fermented extract, 12.5% concentration (G3); and negative control group using water (NC1) and using dimethyl (NC2). The larvae were monitored every 60 min using direct visualization. RESULTS No mortality occurred in experimental groups NC1 and NC2 in the 24h exposure period, whereas there was 100% mortality in the PC1 and PC2 groups compared to NC1 and NC2. Mortality rates of 65.0%, 50.0% and 78.0% were observed in the groups G1, G2 and G3 respectively, compared with NC1 and NC2. CONCLUSIONS The association between three essential oils from Azadirachta indica, Melaleuca alternifolia, Carapa guianensis and fermented extract of Carica papaya was efficient at all concentrations. Therefore, it can be used in Aedes aegypti Liverpool third larvae stage control programs.
Subject(s)
Aedes/drug effects , Plant Oils/pharmacology , Animals , Azadirachta/chemistry , Carica/chemistry , Larva/drug effects , Melaleuca/chemistry , Meliaceae/chemistry , Plant Oils/isolation & purification , Time FactorsABSTRACT
OBJECTIVE To evaluate the larvicidal activity of Azadirachta indica, Melaleuca alternifolia, carapa guianensis essential oils and fermented extract of Carica papaya against Aedes aegypti (Linnaeus, 1762) (Diptera: Culicidae). METHODS The larvicide test was performed in triplicate with 300 larvae for each experimental group using the third larval stage, which were exposed for 24h. The groups were: positive control with industrial larvicide (BTI) in concentrations of 0.37 ppm (PC1) and 0.06 ppm (PC2); treated with compounds of essential oils and fermented extract, 50.0% concentration (G1); treated with compounds of essential oils and fermented extract, 25.0% concentration (G2); treated with compounds of essential oils and fermented extract, 12.5% concentration (G3); and negative control group using water (NC1) and using dimethyl (NC2). The larvae were monitored every 60 min using direct visualization. RESULTS No mortality occurred in experimental groups NC1 and NC2 in the 24h exposure period, whereas there was 100% mortality in the PC1 and PC2 groups compared to NC1 and NC2. Mortality rates of 65.0%, 50.0% and 78.0% were observed in the groups G1, G2 and G3 respectively, compared with NC1 and NC2. CONCLUSIONS The association between three essential oils from Azadirachta indica, Melaleuca alternifolia, Carapa guianensis and fermented extract of Carica papaya was efficient at all concentrations. Therefore, it can be used in Aedes aegypti Liverpool third larvae stage control programs. .
OBJETIVO Avaliar a eficácia de composto de óleos essenciais de Azadirachta indica, Melaleuca alternifolia, Carapa guianensis e extrato fermentado de Carica papaya sobre larvas de Aedes aegypti (Linnaeus, 1762) (Diptera: Culicidae). MÉTODOS O ensaio larvicida foi realizado em triplicata com 300 larvas para cada grupo experimental utilizando larvas de terceiro estádio, as quais foram expostas por 24h, em 2013. Os grupos foram: controles positivos com larvicida industrial (BTI) nas concentrações de 0,37 ppm (CP1) e 0,06 ppm (CP2); tratado com composto de óleos essenciais e extrato fermentado na concentração de 50,0% (G1); tratado composto e óleos essenciais e extrato fermentado na concentração de 25,0% (G2); tratado com composto de óleos essenciais e um extrato fermentado na concentração de 12,5% (G3); controle negativo com água (CN1) e controle dimetil sulfóxido (CN2). As larvas foram monitoradas a cada 60 min através de visualização direta. RESULTADOS Larvas dos grupos CN1 e CN2 não tiveram mortalidade durante o período de 24h de exposição, mas os grupos CP1 e CP2 apresentaram taxa de mortalidade de 100% em relação a CN1 e CN2. Os tratamentos G1, G2 e G3 exerceram atividade larvicida de 65,0%, 50,0% e 78,0%, respectivamente, quando comparados a CN1 e CN2. CONCLUSÕES A associação entre os três óleos essenciais de Azadirachta indica, Melaleuca alternifolia, Carapa guianensis e extrato fermentado de Carica papaya foi eficiente em todas as concentrações testadas, podendo ser utilizado no controle de larvas de terceiro estádio de A. aegypti linhagem Liverpool. .
Subject(s)
Animals , Aedes/drug effects , Plant Oils/pharmacology , Azadirachta/chemistry , Carica/chemistry , Larva/drug effects , Melaleuca/chemistry , Meliaceae/chemistry , Plant Oils/isolation & purification , Time FactorsABSTRACT
In current assay the serotoninergic system in newly-born Wistar rats underwent pharmacological modification by fluoxetine, a selective serotonin reuptake inhibitor (SSRI), to investigate its repercussion on testicular parameters in adult animals. Thirty animals were distributed according to treatment: control animals (n = 6), animals treated with 1 mg kg-1 (n = 6), 5 mg kg-1 (n = 6), 10 mg kg-1 (n = 6) and 20 mg kg-1 (n = 6) of fluoxetine (IP). When 150 days old, the animals were anesthetized and perfused intra-cardiacally with fixative solution. Testes were routinely processed for inclusion in plastic resin (methacrylate glycol). Further, 4 µm-thick histological sections were stained with toluidine blue/sodium borate 1% and analyzed histometrically. Pharmacological intervention on the serotoninergic system during the postnatal period of the testes development in Wistar rats with fluoxetine chlorohydrate reduced parameters, such as testicular weight, testis liquid weight and seminiferous tubules diameter. However, testicular parameters, such as daily sperm production (DSP), spermatogenesis efficiency (DSP/g/testis) and cell population in stage VII of adult animals, were not influenced by fluoxetine chlorohydrate usage during neonatal period. Results show that administration of fluoxetine during 21 days after birth may induce adverse changes in the spermatogenesis of adult rats.
No presente trabalho, o sistema serotoninérgico de ratos Wistar recém-nascidos foi farmacologicamente modificado por um inibidor seletivo de recaptação da serotonina, fluoxetina, com o objetivo de observar sua repercussão nos parâmetros testiculares em ratos adultos. Trinta animais foram distribuídos de acordo com o tratamento: controle (n = 6), tratado com 1 mg kg-1 (n = 6), 5 mg kg-1 (n = 6), 10 mg kg-1 (n = 6) e 20 mg kg-1 (n = 6) de fluoxetina. Aos 150 dias de vida, os animais foram anestesiados e perfundidos intracardiacamente com solução fixadora. Os testículos foram removidos e processados para inclusão em resina plástica (glicol metacrilato). Cortes histológicos com 4 µm de espessura foram corados por azul de toluidina/borato de sódio 1% e analisados histometricamente. O tratamento com fluoxetina reduziu nos parâmetros de peso testicular líquido e bruto, bem como no diâmetro dos túbulos seminíferos. Entretanto, os parâmetros testiculares de produção espermática diária (PED), eficiência espermática (PED/g/testículo) e população de células germinativas no estágio VII não estavam alteradas pelo tratamento com fluoxetina. Em conclusão, a administração de fluoxetina durante 21 dias após o nascimento pode induzir efeitos adversos na espermatogênese de ratos adultos.
Subject(s)
Rats , Fluoxetine , Sertoli Cells , SpermatogenesisABSTRACT
PURPOSE: The pathophysiology of abnormalities associated with myenteric plexus lesions remains imperfectly understood. Such abnormalities have been correlated with subocclusive intestinal conditions in children with Hirschsprung's disease, cases of chronic constipation and, postoperatively, in cases of anorectal anomalies. This study evaluated abnormalities of the myenteric plexus in fetus from female rats that received ethylenethiourea. METHODS: Female rats were exposed to ethylenethiourea on the 11(th) day of pregnancy (experimental group) or to 0.9% physiological solution (control group). Abnormalities were only found in the experimental group. The digestive tract muscle layer was analyzed morphometrically and changes to the frequencies of nerve plexus cells and interstitial cells of Cajal were evaluated, using hematoxylin-eosin, S-100 protein, neuron-specific enolase and C-Kit, respectively. RESULTS: Muscle and skeletal abnormalities were observed in 100%, anorectal anomalies in 86%, absent tail in 71%, short tail in 29%, duodenal atresia in 5%, esophageal atresia in 5% and persistent omphalomesenteric duct in 5%. Histopathological analysis showed a thinner muscle layer associated with lower frequencies of ganglion cells and interstitial cells of Cajal, in all gastrointestinal tract. CONCLUSION: Severe nerve plexus abnormalities associated with muscle layer atrophy were observed throughout the gastrointestinal tract in newborn rats exposed to ethylenethiourea.
Subject(s)
Abnormalities, Drug-Induced/pathology , Digestive System Abnormalities/chemically induced , Ethylenethiourea/toxicity , Muscular Atrophy/chemically induced , Myenteric Plexus/abnormalities , Pregnancy/drug effects , Prenatal Exposure Delayed Effects/chemically induced , Abdominal Muscles/innervation , Animals , Animals, Newborn , Digestive System Abnormalities/classification , Digestive System Abnormalities/pathology , Disease Models, Animal , Female , Fetus/drug effects , Ganglia/cytology , Interstitial Cells of Cajal/cytology , Muscular Atrophy/pathology , Prenatal Exposure Delayed Effects/pathology , Random Allocation , Rats , Rats, Wistar , Staining and Labeling/methods , Statistics, NonparametricABSTRACT
PURPOSE: The pathophysiology of abnormalities associated with myenteric plexus lesions remains imperfectly understood. Such abnormalities have been correlated with subocclusive intestinal conditions in children with Hirschsprung's disease, cases of chronic constipation and, postoperatively, in cases of anorectal anomalies. This study evaluated abnormalities of the myenteric plexus in fetus from female rats that received ethylenethiourea. METHODS: Female rats were exposed to ethylenethiourea on the 11th day of pregnancy (experimental group) or to 0.9 percent physiological solution (control group). Abnormalities were only found in the experimental group. The digestive tract muscle layer was analyzed morphometrically and changes to the frequencies of nerve plexus cells and interstitial cells of Cajal were evaluated, using hematoxylin-eosin, S-100 protein, neuron-specific enolase and C-Kit, respectively. RESULTS: Muscle and skeletal abnormalities were observed in 100 percent, anorectal anomalies in 86 percent, absent tail in 71 percent, short tail in 29 percent, duodenal atresia in 5 percent, esophageal atresia in 5 percent and persistent omphalomesenteric duct in 5 percent. Histopathological analysis showed a thinner muscle layer associated with lower frequencies of ganglion cells and interstitial cells of Cajal, in all gastrointestinal tract. CONCLUSION: Severe nerve plexus abnormalities associated with muscle layer atrophy were observed throughout the gastrointestinal tract in newborn rats exposed to ethylenethiourea.
OBJETIVO: As anomalias associadas a lesões dos plexos mioentéricos permanecem sem plena compreensão da sua fisiopatologia. Alterações nos plexos nervosos têm sido correlacionadas com quadros suboclusivos intestinais em crianças portadoras de doença de Hirschsprung, em constipação crônica e no pós-operatório de anomalias anorretais. Este estudo avaliou as anomalias do plexo mioentérico em fetos de ratos fêmea que ingeriram etilenotioureia (ETU). MÉTODOS: Ratos fêmea foram expostos no 11º dia de gestação a ETU 1 por cento no Grupo Experimento e a solução fisiológica 0,9 por cento no Grupo Controle. Foram observadas anomalias apenas no Grupo experimento, sendo realizada morfometria da camada muscular e avaliadas alterações da frequência celular nos gânglios do plexo mioentérico e nas células intersticiais de Cajal (CIC) utilizando hematoxilina-eosina, P S-100, Enolase Neurônio Específica e C-KIT. RESULTADOS: Foram observadas anomalias musculoesqueléticas (100 por cento), anorretais (86 por cento), ausência de cauda (71 por cento), cauda curta (29 por cento), atresia duodenal (5 por cento), atresia esofágica (5 por cento) e conduto onfalomesentérico persistente (5 por cento). A análise histopatológica mostrou adelgaçamento da camada muscular associada às alterações da frequência das células ganglionares e das CIC em todos os segmentos do trato gastrointestinal. CONCLUSÃO: Foram observadas alterações graves nos plexos nervosos associadas ao adelgaçamento da camada muscular de todo o trato gastrointestinal nos fetos expostos a ETU.
Subject(s)
Animals , Female , Rats , Abnormalities, Drug-Induced/pathology , Digestive System Abnormalities/chemically induced , Ethylenethiourea/toxicity , Muscular Atrophy/chemically induced , Myenteric Plexus/abnormalities , Pregnancy/drug effects , Prenatal Exposure Delayed Effects/chemically induced , Animals, Newborn , Abdominal Muscles/innervation , Disease Models, Animal , Digestive System Abnormalities/classification , Digestive System Abnormalities/pathology , Fetus/drug effects , Ganglia/cytology , Interstitial Cells of Cajal/cytology , Muscular Atrophy/pathology , Prenatal Exposure Delayed Effects/pathology , Random Allocation , Rats, Wistar , Statistics, Nonparametric , Staining and Labeling/methodsABSTRACT
A exposição da sociedade a Campos Eletromagnéticos (CEM) vem aumentando vertiginosamente em virtude da ampla expansão tecnológica observada nos últimos anos. Tanto a geração, como a distribuição e a utilização de energia elétrica podem gerar Campos Eletromagnéticos de baixa freqüência (50 e 60 Hz). Pesquisas vêm demonstrando que a exposição a estes CEM podem proporcionar alterações fisiológicas significativas, apesar disto, ainda não estão totalmente esclarecidos a extensão destes efeitos, nem os mecanismos de ação que envolve a interação dos CEM com os organismos biológicos. O presente trabalho teve como principal objetivo verificar os efeitos dos CEM (60 Hz e 1 mT) sobre a integridade de DNA e morfologia espermática de ratos sexualmente maduros, que foram expostos ao CEM durante diferentes períodos do seu desenvolvimento. Os resultados obtidos neste trabalho não encontraram indícios de alterações no DNA dos espermatozóides, porém, foram observadas alterações significativas na morfologia dos espermatozoides após a exposição ao CEM. Estas alterações na morfologia espermática podem reduzir o potencial reprodutivo. Portanto, devemos considerar o CEM como um potencial risco a saúde pública, recomendando- se a realização de mais pesquisas buscando estabelecer níveis seguros de exposição aos CEM.
The society's exposure to electromagnetic fields (EMF) has been growing considerable due to the great technological expansion observed in the last few years. Generation as well as distribution and use of electric energy can generate low frequency electromagnetic fields (50 and 60 Hz). Issues have been demonstrating that EMF exposure could provoke significantly physiological changes, however, the extension of EMF effects weren't totally clarified. The major objective of this issue was to evaluate the EMF (60 Hz and 1 mT) effects on DNA integrity and sperm morphology in Wistar rats with mature sexuality that were exposed during different stages of testicular development. According to our results, EMF did not change DNA integrity, but we could observe morphological changes in sperm after exposure to EMF. These changes in sperm morphology may reduce the reproductive potential. Therefore, we should consider the EMF as a potential risk to public health, recommending the implementation of further research seeking to establish safe levels of exposure to EMF.
Subject(s)
Rats , Pathology , Radiation, Nonionizing , Spermatozoa , DNA , Electromagnetic RadiationABSTRACT
PURPOSE: To analyze the action of gangliosides in peripheral nerve regeneration in the sciatic nerve of the rat. METHODS: The sample was composed of 96 male Wistar rats. The animals were anaesthetized and, after identification of the anaesthesic plane, an incision was made in the posterior region of the thigh, followed by skin and muscle divulsion. The right sciatic nerve was isolated and compressed for 2 minutes. Continuous suture of the skin was performed. The animals were randomly divided into two groups: the experimental group (EG), which received subcutaneous injection of gangliosides, and the control group (CG), which received saline solution (0.9 percent) to mimic the effects of drug administration. RESULTS: No differences were observed between the experimental and control groups evaluated on the eighth day of observation. At 15 and 30 days the EG showed an decrease in Schwann cell activity and an apparent improvement in fibre organization; at 60 days, there was a slight presence of Schwann cells in the endoneural space and the fibres were organized, indicating nerve regeneration. At 15 and 30 days, the level of cell reaction in the CG had diminished, but there were many cells with cytoplasm in activity and in mitosis; at 60 days, hyperplastic Schwann cells and mitotic activity were again observed, as well as nerve regeneration, but to a lesser extent than in the EG. CONCLUSION: The administration of exogenous gangliosides seems to improve nerve regeneration.
OBJETIVO: Avaliar os efeitos de gangliosídeos na regeneração nervosa periférica em nervo isquiático de ratos após axonotmese. MÉTODOS: Foram utilizados 96 ratos machos albinos (Wistar). Os animais foram anestesiados e após constatação do plano anestésico, foi realizada incisão na face posterior da coxa direita do animal. Em seguida, foi realizada a dissecção cirúrgica da pele e do músculo e divulsão dos músculos. O nervo isquiático direito foi isolado e sofreu compressão por 2 minutos. Efetuou-se a sutura contínua da pele. Os animais foram distribuídos aleatoriamente em 2 grupos: experimental (GE) que receberam gangliosídeos pela via sub-cutânea e controle (GC) que receberam soro fisiológico 0,9 por cento com a finalidade de mimetizar os efeitos de administração da droga de estudo. A análise histopatológica foi realizada em 8, 15, 30 e 60 dias. RESULTADOS: Não se evidenciaram diferenças significantes entre os grupos controle e experimental avaliados com 8 dias. Nos grupos experimentais de 15 e 30 dias observou-se uma diminuição da atividade das células de Schwann e aparente melhora na organização das fibras nervosas; com 60 dias havia discreta presença células de Schwann no espaço endoneural e as fibras nervosas estavam organizadas sinalizando a regeneração nervosa. Nos grupos controles de 15 e 30 dias o padrão de reação celular diminuiu, entretanto havia muitas células com citoplasmas em atividade e mistose; com 60 dias observou-se ainda a presença de hiperplasia de células de Schwann, atividade mitótica ainda presente e regeneração nervosa presente, porém em menor grau comparando-se com aquele visto no grupo experimental. CONCLUSÃO: A administração de gangliosídeos exógenos parece incrementar a regeneração nervosa.
Subject(s)
Animals , Chick Embryo , Male , Rats , Gangliosides/therapeutic use , Nerve Regeneration/drug effects , Schwann Cells/pathology , Sciatic Nerve/physiology , Sciatic Neuropathy/drug therapy , Disease Models, Animal , Drug Evaluation, Preclinical , Hyperplasia , Nerve Regeneration/physiology , Random Allocation , Rats, Wistar , Sciatic Neuropathy/pathologyABSTRACT
PURPOSE: To analyze the action of gangliosides in peripheral nerve regeneration in the sciatic nerve of the rat. METHODS: The sample was composed of 96 male Wistar rats. The animals were anaesthetized and, after identification of the anaesthesic plane, an incision was made in the posterior region of the thigh, followed by skin and muscle divulsion. The right sciatic nerve was isolated and compressed for 2 minutes. Continuous suture of the skin was performed. The animals were randomly divided into two groups: the experimental group (EG), which received subcutaneous injection of gangliosides, and the control group (CG), which received saline solution (0.9%) to mimic the effects of drug administration. RESULTS: No differences were observed between the experimental and control groups evaluated on the eighth day of observation. At 15 and 30 days the EG showed an decrease in Schwann cell activity and an apparent improvement in fibre organization; at 60 days, there was a slight presence of Schwann cells in the endoneural space and the fibres were organized, indicating nerve regeneration. At 15 and 30 days, the level of cell reaction in the CG had diminished, but there were many cells with cytoplasm in activity and in mitosis; at 60 days, hyperplastic Schwann cells and mitotic activity were again observed, as well as nerve regeneration, but to a lesser extent than in the EG. CONCLUSION: The administration of exogenous gangliosides seems to improve nerve regeneration.
Subject(s)
Gangliosides/therapeutic use , Nerve Regeneration/drug effects , Schwann Cells/pathology , Sciatic Nerve/physiology , Sciatic Neuropathy/drug therapy , Animals , Chick Embryo , Disease Models, Animal , Drug Evaluation, Preclinical , Hyperplasia , Male , Nerve Regeneration/physiology , Random Allocation , Rats , Rats, Wistar , Sciatic Neuropathy/pathologyABSTRACT
The aim of the present study was to test the hypothesis that the application of fluoxetine a highly selective serotonin reuptake inhibitor (SSRI) ¡ in rats during the suckling period induces changes in testicular development. Groups of newborn male rats were randomly assigned with different doses of fluoxetine 24 hours after birth. Each litter stayed with its respective mother during 21 days. Body weight (BW) was measured daily from the 1st -21st day to calculate daily doses of fluoxetine. 5 mg (T1), 10 mg (T2) 20 mg (T3) or deionized water, were injected intraperitoneally. On the 21st day, animals were heparinized, anesthetized and blood was collected by cardiac puncture to determine by radioimmunoassay the follicle stimulating hormone (FSH) levels. Testis were removed, weighed, and processed for morphometric analysis. Fluoxetine groups presented decreased body and testicular weight when compared with the control group on the 21st day. Our findings show that the manipulation of the serotoninergic system with fluoxetine during the critical period of testicular development alters the Sertoli cell population and all testicular parameters related to this cell.
El propósito del presente estudio fue probar la hipótesis que el uso de fluoxetina - un inhibidor altamente selectivo de la serotonina (SSRI) - induce cambios en el desarrollo testicular de ratas durante el período de amamantamiento. Los grupos de ratas macho recién nacidas fueron asignados aleatoriamente con diversas dosis del fluoxetina, 24 horas después del nacimiento. Cada cría permanecía con su madre respectiva durante 21 días. El peso corporal (BW) fue medido diariamente desde el 21día 1 al 21, para calcular las dosis diarias del fluoxetina. 5 mg (T1), 10 mg (T2) y 20 (T3) o agua desionizada fueron inyectados intraperitonealmente. En el día 21, los animales fueron tratados con heparina, anestesiados y la sangre fue recogida por punción cardiaca para determinar por radioinmunoanálisis los niveles de la hormona folículo-estimulante (FSH). Los testículos fueron retirados, pesados y procesados para el análisis morfométrico. Los grupos tratados con fluoxetina presentaron disminución del tamaño y peso testiculares, en comparación con el grupo control día 21. Los resultados demuestran que la manipulación del sistema serotoninérgico con fluoxetina durante el período crítico del desarrollo testicular, altera la población de células de Sertoli y todos los parámetros testiculares relacionados con este tipo celular.