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1.
Biol Trace Elem Res ; 202(4): 1644-1655, 2024 Apr.
Article in English | MEDLINE | ID: mdl-37495827

ABSTRACT

This study evaluated the effect of prepubertal arsenic exposure in the liver and kidney of pubescent rats and their reversibility 30 days after arsenic withdrawal. Male pups of Wistar rats (21 days old) were divided into two groups (n = 20/group): control animals received filtered water, and exposed rats received 10 mg L-1 arsenic from postnatal day (PND) 21 to PND 51. The liver and kidney of 52 days old rats (n = 10/group) were examined to investigate the effects of arsenic on micromineral content, antioxidant enzyme activity, histology, and biochemistry parameters. The other animals were kept alive under free arsenic conditions until 82 days old and further analyzed by the same parameters. Our results revealed that 52-day-old rats increased arsenic content in their liver and arsenic and manganese in their kidney. In those animals, glycogen and zinc content and catalase activity were reduced in the liver, and the selenium content decreased in the kidney. Thirty days later, arsenic reduced the manganese and iron content and SOD and CAT activity in the liver of 82-day-old rats previously exposed to arsenic, while glycogen and selenium content decreased in their kidney. In contrast, PND 82 rats exhibited higher retention of copper in the liver, an increase in iron and copper content, and CAT and GST activity in the kidney. Significant histological alterations of liver and kidney tissues were not observed in rats of both ages. We conclude that arsenic-induced toxicity could alter differently the oxidative status and balance of trace elements in pubertal and adult rats, demonstrating that the metalloid can cause effects in adulthood.


Subject(s)
Arsenic , Selenium , Rats , Male , Animals , Arsenic/metabolism , Copper/pharmacology , Rats, Wistar , Selenium/pharmacology , Selenium/metabolism , Manganese/pharmacology , Catalase/metabolism , Antioxidants/metabolism , Liver/metabolism , Kidney/metabolism , Iron/metabolism , Oxidative Stress , Glycogen/metabolism
2.
Microsc Microanal ; 29(2): 635-648, 2023 04 05.
Article in English | MEDLINE | ID: mdl-37749728

ABSTRACT

Pulmonary arterial hypertension (PAH) is characterized by elevated arterial pressure and vascular resistance. PAH may cause alterations in the microcirculation of several organs, including the kidney, liver, brain, and testes. However, it remains unclear whether monocrotaline-induced PAH exerts detrimental effects on animal testes. Thus, we analyzed the impact of PAH on testicular morphology and function. Additionally, we investigated the effect of resistance exercise training (RT) on testicular parameters in PAH rats. Eight healthy Wistar rats and eight PAH rats were subjected to RT training for 30 days; the other PAH and healthy rats (n = 8/group) did not exercise. PAH rats had lower reproductive organ weight, serum testosterone levels, testicular glucose, and nitric oxide (NO) levels, Leydig cell parameters, tubular morphometry, germ cell counts, and daily sperm production than healthy animals did. The practice of RT attenuated the negative impact of PAH on the relative weights of the testes and epididymides, Leydig cell number, nuclear volume, testicular NO levels, and seminiferous epithelium architecture. Moreover, RT positively influenced testosterone levels in PAH animals. We conclude that PAH exerts deleterious effects on testicular histology and function. However, RT can be beneficial to the PAH-affected testicular parameters.


Subject(s)
Pulmonary Arterial Hypertension , Resistance Training , Male , Rats , Animals , Humans , Rats, Wistar , Testis , Semen , Testosterone
3.
Theriogenology ; 198: 305-316, 2023 Mar 01.
Article in English | MEDLINE | ID: mdl-36634444

ABSTRACT

Due to environmental contamination, the environment constantly receives pollutants from various anthropic actions. These pollutants put ecological health at risk due to contamination and accumulation in living organisms, including wild animals and humans. Exposure can cause physiological, morphological, and behavioral changes in living beings. In this context, laboratory studies have frequently investigated how environmental contaminants affect the male reproductive system and gametes. However, few studies have examined how these contaminants affect male reproduction in naturally exposed animals. To better understand this topic, we conducted a systematic review of the effects of exposing male vertebrate animals to polluted environments on their reproductive functions. After an extensive search using the PubMed/MEDLINE, Scopus, and Web of Science databases, 39 studies met our inclusion criteria and were eligible for this review. This study showed that reproductive damages were frequent in fishes, amphibians, reptiles, birds, and mammals exposed to contaminated environments. Wild animals are exposed mainly to endocrine-disrupting compounds (EDCs), toxic metals, and radiation. Exposure to pollutants causes a reduction in androgen levels, impaired spermatogenesis, morphological damage to reproductive organs, and decreased sperm quality, leading to reduced fertility and population decline. Although several species have been studied, the number of studies is limited for some groups of vertebrates. Wildlife has proven valuable to our understanding of the potential effects of environmental contaminants on human and ecosystem health. Thus, some recommendations for future investigations are provided. This review also creates a baseline for the understanding state of the art in reproductive toxicology studies.


Subject(s)
Ecosystem , Environmental Pollutants , Animals , Male , Humans , Semen , Vertebrates , Animals, Wild , Environmental Pollutants/toxicity , Environmental Pollution , Mammals , Genitalia, Male , Reproduction
4.
Toxicology ; 460: 152886, 2021 08.
Article in English | MEDLINE | ID: mdl-34352348

ABSTRACT

Arsenic intoxication affects male reproductive parameters of prepubertal rats. Besides, morphological and functional alterations in their testis and epididymis may remain after withdrawal of arsenic insult, causing potential impairment in male fertility during adulthood. In this study, we aimed at analyzing the effect of prepubertal arsenic exposure on the fecundity of epididymal sperm from sexually mature Wistar rats, assessing fertility indexes, sperm parameters, and sperm phosphoproteins content. Male pups on postnatal day (PND) 21 received filtered water (controls, n = 10) and 10 mg L-1 arsenite (n = 10) daily for 30 days. From PND52 to PND81, rats from both groups received filtered water. During this period, the males mated with non-exposed females between PND72 and PND75. Our results showed that sexually mature rats presented low sperm production, epididymal sperm count, motility, and quality after prepubertal arsenic exposure. These findings possibly contributed to the low fertility potential and high preimplantation loss. Epididymal sperm proteome detected 268 proteins, which 170 were found in animals from both control and arsenic groups, 27 proteins were detected only in control animals and 71 proteins only in arsenic-exposed rats. In these animals, SPATA 18 and other five proteins were upregulated, whereas keratin type II cytoskeletal 1 was downregulated (q < 0.1). The results of KEGG pathway analysis demonstrated an enrichment of pathways related to dopaminergic response, adrenergic signaling, protein degradation, and oocyte meiosis in arsenic-exposed animals. Moreover, 26 proteins were identified by phosphoproteomic with different phosphorylation pattern in animals from both groups, but SPATA18 was phosphorylated only in arsenic-exposed animals. We concluded that prepubertal exposure to arsenic is deleterious to sperm quality and male fertility, altering the sperm phosphoproteins profile.


Subject(s)
Arsenic/toxicity , Epididymis/metabolism , Fertility/physiology , Phosphoproteins/metabolism , Sexual Maturation/physiology , Spermatozoa/metabolism , Animals , Arsenic/administration & dosage , Cattle , Epididymis/drug effects , Epididymis/pathology , Fertility/drug effects , Humans , Male , Mice , Rats , Rats, Wistar , Reproduction/drug effects , Reproduction/physiology , Sexual Maturation/drug effects , Spermatozoa/drug effects , Spermatozoa/pathology
5.
Microsc Microanal ; : 1-13, 2021 Jun 29.
Article in English | MEDLINE | ID: mdl-34184626

ABSTRACT

Green tea is a popular drink used for therapeutic purposes to mitigate the consequences of diabetes. In this study, we aimed at evaluating the potential of green tea infusion to ameliorate structural and enzymatic damages caused by hyperglycemia in the testis and epididymis of Wistar rats. For that, nondiabetic and streptozotocin-induced diabetic rats (negative control and diabetes control, respectively) received 0.6 mL of water by gavage. Another set of diabetic animals received 100 mg/kg of green tea infusion diluted in 0.6 mL of water/gavage (diabetes + green tea) daily. After 42 days of treatment, the testes and epididymides were removed and processed for histopathological analysis, micromineral determination, and enzymatic assays. The results showed that treatment with green tea infusion preserved the testicular and epididymal histoarchitecture, improving the seminiferous epithelium and the sperm production previously affected by diabetes. Treatment with green tea reduced tissue damages caused by this metabolic condition. Given the severity of hyperglycemia, there was no efficacy of the green tea infusion in maintaining the testosterone levels, antioxidant enzyme activity, and microminerals content. Thus, our findings indicate a protective effect of this infusion on histological parameters, with possible use as a complementary therapy for diabetes.

6.
Life Sci ; 276: 119450, 2021 Jul 01.
Article in English | MEDLINE | ID: mdl-33798548

ABSTRACT

AIMS: Although excessive fat and caffeine intake are independent risk factors for bone microstructural and functional disturbances, their association remains overlooked. Thus, we investigated the impact of high-fat diet (HFD) and caffeine alone and combined on serum lipid profile, bone microstructure, micromineral distribution and biomechanical properties. METHODS: Forty female C57BL/6 mice were randomized into 4 groups daily treated for seventeen weeks with standard diet (SD) or HFD (cafeteria diet) alone or combined with 50 mg/kg caffeine. KEY FINDINGS: The association between HFD and caffeine reduced the weight gain compared to animals receiving HFD alone. Caffeine alone or combined with HFD increases total and HDL cholesterol circulating levels. HFD also reduced calcium, phosphorus and magnesium bone levels compared to the groups receiving SD, and this reduction was aggravated by caffeine coadministration. From biomechanical assays, HFD combined with caffeine increased bending strength and stiffness of tibia, a finding aligned with the marked microstructural remodeling of the cortical and cancellous bone in animals receiving this combination. SIGNIFICANCE: Our findings indicated that HFD and caffeine interact to induce metabolic changes and bone microstructural remodeling, which are potentially related to bone biomechanical adaptations in response to HFD and caffeine coadministration.


Subject(s)
Body Weight , Bone and Bones/physiopathology , Caffeine/administration & dosage , Central Nervous System Stimulants/administration & dosage , Diet, High-Fat/adverse effects , Animals , Biomechanical Phenomena , Bone and Bones/drug effects , Cholesterol/blood , Female , Mice , Mice, Inbred C57BL
7.
Chem Biol Interact ; 333: 109314, 2021 Jan 05.
Article in English | MEDLINE | ID: mdl-33171135

ABSTRACT

Arsenic is a pollutant widely found in the environment due to natural and anthropogenic sources. Exposure to arsenic forms in drinking water has been related with male reproductive dysfunctions in humans and experimental animals at adult age. However, the impact of this pollutant on postnatal reproductive development of male offspring exposed in utero to arsenic is still unknown. Therefore, this study aimed to investigate the effects of prenatal arsenic exposure on the postnatal development of the testes and epididymides of rats, during prepuberty. For this purpose, pregnant female Wistar rats were provided drinking water containing 0 or 10 mg/L sodium arsenite (AsNaO2) from gestational day 1 (GD 1) until GD 21 and the male offspring was evaluated in different periods of prepuberty. Our results showed that prenatal arsenic exposure affected the initial sexual development of male pups, reducing their body weight and relative anogenital distance at postnatal day 1. At different periods of prepuberty, male pups from arsenic exposed dams showed a reduction of body and reproductive organs weights, testosterone levels and testis morphometric parameters. Moreover, these pups presented changes in the expression of SOD1, SOD2, CAT and GSTK1 genes and in the activity of superoxide dismutase, catalase and glutathione s-transferase in the testes and epididymides during prepuberty. Taken together, our results show that prenatal arsenic exposure provoked reproductive disorders in prepubertal male rats, probably due to reproductive reprograming and oxidative stress induced by this pollutant.


Subject(s)
Arsenic/toxicity , Epididymis/drug effects , Prenatal Exposure Delayed Effects/metabolism , Testis/drug effects , Animals , Antioxidants/metabolism , Body Weight/drug effects , Epididymis/metabolism , Epididymis/pathology , Female , Gene Expression Regulation, Enzymologic/drug effects , Male , Organ Size/drug effects , Pregnancy , Prenatal Exposure Delayed Effects/enzymology , Prenatal Exposure Delayed Effects/pathology , Puberty , Rats , Rats, Wistar , Testis/metabolism , Testis/pathology
8.
J. Phys. Educ. ; 32: e3249, 2021. tab, graf
Article in Portuguese | LILACS-Express | LILACS | ID: biblio-1356377

ABSTRACT

RESUMO Este artigo teve como objetivo analisar se, e em que medida, o marcador de gênero conforma diferentes perspectivas, oportunidades e incentivos que homens e mulheres na carreira esportiva no futsal, bem como para a reconversão para outra carreira vocacional. Para isso, descrevemos o perfil de atletas homens e mulheres sob o ponto de vista da trajetória esportiva e da dupla carreira. Utilizamos um questionário com 95 homens e 87 mulheres, participantes dos campeonatos adultos de futsal paulista. Nossos resultados apontam que a dupla carreira é predominante tanto para homens quanto para mulheres. Para elas, a dupla carreira com os estudos vai da adolescência até a idade adulta, quando os clubes as concedem bolsa universitária e salário. Após o ensino superior, as chances de permanência no futsal diminuem para mulheres, o que pode indicar a reconversão para outra carreira vocacional e chance de mobilidade social, já que elas são a primeira geração da família a atingir esse nível de ensino. Para os homens, a dupla carreira se estabelece mais precocemente, na infância e se torna, na idade adulta, conciliação com o trabalho, pois, com exceção de uma pequena parcela, a maioria não é remunerada para jogar. Essas diferenças demonstram a desigualdade de desenvolvimento do futsal entre os gêneros.


ABSTRACT This article analyzed whether, and to what extent, gender shapes different perspectives, opportunities and incentives to the athletic career in Brazilian futsal for men and women, as well to another vocational career. For this, we describe the profile of male and female athletes from their sporting trajectory and dual career. We used a questionnaire with 95 men and 87 women, participating in the adult futsal championships in São Paulo Our results show that dual careers are predominant for both men and women. For the latter, dual career with studies lasts from adolescence to adulthood, when clubs grant them a university scholarship and salary. After higher education, the chances of staying in futsal decrease for women, which may indicate the conversion to another vocational career and the chance of social mobility, since they are the first generation of their family to reach this level of education. For men, dual career is established earlier, in childhood and becomes, in adulthood, coping with work, since most are unpaid to play, with the exception of a small portion. These differences demonstrate the inequality of futsal development between genders.

9.
Toxicol Appl Pharmacol ; 409: 115304, 2020 12 15.
Article in English | MEDLINE | ID: mdl-33127376

ABSTRACT

Arsenic induces reproductive disorders in pubertal males after prepubertal exposure. However, it is unclear the extent to which those effects remain in testis and epididymis of sexually mature rats after arsenic insult. This study evaluated the effects of prepubertal arsenic exposure in male organs of pubertal rats, and their reversibility in adult rats. Male pups of Wistar rats on postnatal day (PND) 21 were divided into two groups (n = 20/group): Control animals received filtered water and exposed rats received 10 mg L--1 arsenic from PND 21 to PND 51. At PND 52, testis and epididymis of ten animals per group were examined for toxic effects under morphological, functional, and molecular approaches. The other animals were kept alive under free arsenic conditions until PND 82, and further analyzed for the same parameters. Pubertal rats overexpressed mRNA levels of SOD1, SOD2, CAT, GSTK1, and MT1 in their testis and SOD1, CAT, and GSTK1 in their epididymis. In those organs, catalase activity was altered, generating byproducts of oxidative stress. The antioxidant gene expression was unchanged in adult rats in contrast to the altered activity of antioxidant enzymes. Histological alterations of testis and epididymis tissues were observed in pubertal and adult rats. Interestingly, only adult rats exhibited a remarkable decrease in serum testosterone levels. Prepubertal exposure to arsenic caused morphological and functional alterations in male reproductive organs of pubertal rats. In adult rats, these damages disappeared, remained, get worsened, or recovered depending on the parameter analyzed, indicating potential male fertility disorders during adulthood.


Subject(s)
Arsenic/toxicity , Reproduction/drug effects , Animals , Animals, Newborn , Antioxidants/metabolism , Epididymis/drug effects , Epididymis/metabolism , Male , Organ Size/drug effects , Oxidative Stress/drug effects , RNA, Messenger/metabolism , Rats , Rats, Wistar , Testis/drug effects , Testis/metabolism , Testosterone/metabolism
10.
Life Sci ; 257: 118132, 2020 Sep 15.
Article in English | MEDLINE | ID: mdl-32710949

ABSTRACT

AIM: Arsenic, an environmental contaminant, represents a public health problem worldwide. Studies have shown its association with molecular mechanisms related to cardiomyocytes redox balance. However, the microstructure and ultrastructure of cardiac tissue, as well as the activity of its antioxidant defenses front of disturbances in the mineral bioavailability induced by arsenic are still scarce. Thus, the aim of this study was to evaluate if arsenic exposure might induce structural and ultrastructural damages in cardiac tissue, including pathological remodeling of the parenchyma and stroma. Moreover, its impact on micromineral distribution and antioxidant enzymes activity in heart tissue was also evaluated. MAIN METHODS: Adult male Wistar rats were divided into three groups that received 0, 1 and 10 mg/L sodium arsenite in drinking water for eight weeks. The hearts were collected and subjected to structural and ultrastructural analysis, mineral microanalysis and antioxidant enzymes quantification. Functional markers of cardiac damages were evaluated using serum samples. KEY FINDINGS: Arsenic exposure induced dose-dependent structural and ultrastructural remodeling of cardiac tissue, with parenchyma loss, increase of stroma components, collagen deposition, and pathological damages such as inflammation, sarcomere disorganization, mitochondria degeneration and myofilament dissociation. Moreover, this metalloid was bioaccumulated in the tissue affecting its micromineral content, which resulted in antioxidant imbalance and increased levels of oxidative stress and cardiac markers. SIGNIFICANCE: Taken together, our findings indicate that the heart is a potential target to arsenic toxicity, and long-term exposure to this metalloid must be avoided, once it might induce several cardiac tissue pathologies.


Subject(s)
Arsenic/toxicity , Heart/drug effects , Myocardium/pathology , Ventricular Remodeling/drug effects , Animals , Arsenic/administration & dosage , Arsenic/analysis , Catalase/metabolism , Dose-Response Relationship, Drug , Glutathione Transferase/metabolism , Male , Myocardium/chemistry , Myocardium/ultrastructure , Rats , Rats, Wistar , Superoxide Dismutase/metabolism
11.
Biomed Pharmacother ; 126: 110097, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32203891

ABSTRACT

AIMS: In this work, we aimed to evaluate the effects of the Leishmania infantum chagasi infection on the liver of vaccinated mice, considering parameters of tissue damage and the inflammatory response elicited by vaccination. MAIN METHODS: We used recombinant LPG3 protein (rLPG3) as immunogen in BALB/c mice before challenge with promastigote forms of L. infantum chagasi. The animals were separated into five groups: NI: non-infected animals; NV: non-vaccinated; SAP: treated with saponin; rLPG3: immunized with rLPG3; rLPG3 + SAP: immunized with rLPG3 plus SAP. The experiment was conducted in replicate, and the vaccination protocol consisted of three subcutaneous doses of rLPG3 (40 µg + two boosters of 20 µg). The mice were challenged two weeks after the last immunization. KEY FINDINGS: Our results showed that rLPG3 + SAP immunization decreased the parasite burden in 99 %, conferring immunological protection in the liver of the infected animals. Moreover, the immunization improved the antioxidant defenses, increasing CAT and GST activity, while reducing the levels of oxidative stress markers, such as H2O2 and NO3/NO2, and carbonyl protein in the organ. As a consequence, rLPG3 + SAP immunization preserved tissue integrity and reduced the granuloma formation, inflammatory infiltrate and serum levels of AST, ALT, and ALP. SIGNIFICANCE: Taken together, these results showed that rLPG3 vaccine confers liver protection against L. infantum chagasi in mice, while maintaining the liver tissue protected against the harmful inflammatory effects caused by the vaccine followed by the infection.


Subject(s)
Glycosphingolipids/immunology , Leishmania infantum/immunology , Leishmaniasis/prevention & control , Leishmaniasis/parasitology , Liver Diseases, Parasitic/prevention & control , Liver Diseases, Parasitic/parasitology , Protozoan Vaccines/immunology , Recombinant Proteins/immunology , Animals , Antibodies, Protozoan , Antioxidants , Disease Models, Animal , Immunization , Leishmaniasis/pathology , Liver Diseases, Parasitic/pathology , Mice , Oxidative Stress , Parasite Load , Reactive Nitrogen Species/metabolism , Reactive Oxygen Species/metabolism
12.
J Appl Toxicol ; 40(2): 214-223, 2020 02.
Article in English | MEDLINE | ID: mdl-31429093

ABSTRACT

Arsenic is a metalloid widely found in the environment in organic and inorganic forms. Exposure to inorganic arsenic forms via drinking water has been associated with an increased incidence of negative health effects, including reproductive disorders and dysfunction of the endocrine system. However, the impact of arsenic exposure on female reproductive development is still unclear. Therefore, in the present study, we evaluated the effects of prenatal exposure to arsenic on the initial sexual development and puberty onset, and in the morphology of the female reproductive organs, estrous cycle regularity and fertility parameters during adulthood. To do that, pregnant female Wistar rats were exposed to 10 mg/L sodium arsenite via drinking water from gestational day (GD) 1 until GD 21 and the female offspring was evaluated in different postnatal days. Our results showed that prenatal arsenic exposure induced a decrease of litter weight and morphological masculinization in females at postnatal day 1. Moreover, these females had a delay in the age of puberty onset and alteration in estrous cycle number and length. During adulthood, females from the sodium arsenite group showed an increase in endometrium, myometrium and perimetrium areas, and an imbalance in uterine antioxidant enzyme activity. These animals also presented an increase in post-implantation loss and reabsorption number, leading to reduced viable fetus number. In conclusion, prenatal arsenic exposure in rats was able to promote female masculinization, alter sexual development and impair reproductive performance.


Subject(s)
Arsenites/toxicity , Estrous Cycle/drug effects , Maternal Exposure/adverse effects , Prenatal Exposure Delayed Effects , Puberty/drug effects , Reproduction/drug effects , Sodium Compounds/toxicity , Animals , Body Weight/drug effects , Female , Fertility/drug effects , Models, Animal , Pregnancy , Rats , Rats, Wistar
13.
Rev. bras. ciênc. esporte ; 42: e2023, 2020.
Article in Portuguese | LILACS-Express | LILACS | ID: biblio-1137371

ABSTRACT

RESUMO Na busca de possíveis articulações didáticas, objetivamos analisar se o modelo de educação esportiva é capaz de produzir o protagonismo e a autonomia dos estudantes, coadunar com a inovação pedagógica na educação física escolar. Para tanto, fizemos um estudo de caso em uma escola, durante um semestre letivo, combinamos observação, entrevista com a professora e grupo focal com os alunos. O modelo ajudou a inovar na abordagem do esporte, promoveu maior e diversificada participação discente, autonomia e corresponsabilidade. Permanece ainda como limitante o legado do modelo tradicional de aula, de modo que inovar é um desafio não só didático, mas também cultural.


ABSTRACT Looking forward to didactical articulations, we aimed to analyze if the Sport Education Model can produce protagonism and autonomy within students, in harmony with the pedagogical innovation in physical education. For this purpose, we conducted a case study at a public school during a semester, based on classes observation, an interview with the teacher and a focus group with some students. Sport Education Model helped to innovate in the sport's approach, promoting greater student participation, autonomy and co-responsibility. However, tensioning traditional classes still remains difficult, therefore, achieving innovation is a matter not only didactic but also a cultural challenge.


RESUMEN En la búsqueda de posibles articulaciones didácticas, nuestro objetivo fue analizar si el modelo de educación deportiva es capaz de generar protagonismo y autonomía entre los estudiantes, con la innovación pedagógica en la educación física escolar. Para ello, realizamos un estudio de casos en un colegio durante un semestre lectivo, en que se combinaron observación, entrevista con la profesora y grupo focal con los alumnos. El modelo ayudó a innovar en el abordaje del deporte, lo que promovió una mayor y diversificada participación de los estudiantes, autonomía y corresponsabilidad. Se mantiene todavía como limitante el legado del modelo tradicional de clase, de modo que innovar es un desafío no solo didáctico, sino también cultural.

14.
Environ Sci Pollut Res Int ; 26(12): 12459-12469, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30847815

ABSTRACT

It is known that either arsenic exposure or diabetes can impact renal function. However, it is unclear how these combined factors may influence kidney functions. Therefore, we evaluated morphological, functional, and oxidative parameters in the kidney of diabetic rats exposed to arsenic. Healthy male Wistar rats and streptozotocin-induced diabetic rats were exposed to 0 and 10 mg/L arsenate through drinking water for 40 days. Renal tissue was assessed using morphometry, mitosis and apoptosis markers, mineral proportion, oxidative stress markers, as well as the activity of antioxidant enzymes and membrane-bound adenosine triphosphatases. Arsenate intake altered glucose levels in healthy animals, but it did not reach hyperglycemic conditions. In diabetic animals, arsenate led to a remarkable increase of glycogen nephrosis in distal tubules. In these animals, additionally, the activity of catalase and glutathione S-transferase, besides the proportion of Fe, Cu, and K in renal tissue, was altered. Nevertheless, arsenate did not accumulate in the kidney and did not impact on other parameters previously altered by diabetes, including levels of malondialdehyde, Na, urea, creatinine, and apoptosis and mitosis markers. In conclusion, besides the intensification of glycogen nephrosis, the kidney was able to handle arsenate toxicity at this point, preventing arsenic deposition in the exposed groups and the impairment of renal function.


Subject(s)
Arsenic/toxicity , Glycogen/metabolism , Hazardous Substances/toxicity , Animals , Antioxidants/metabolism , Apoptosis/drug effects , Arsenates , Biomarkers/metabolism , Catalase/metabolism , Creatinine/metabolism , Diabetes Mellitus, Experimental , Kidney/metabolism , Male , Malondialdehyde/metabolism , Nephrosis , Oxidative Stress/drug effects , Rats , Rats, Wistar
15.
PLoS One ; 13(10): e0205023, 2018.
Article in English | MEDLINE | ID: mdl-30332444

ABSTRACT

Reproductive seasonality in Neotropical bats has been assessed to the better understand their reproductive behavior. This knowledge is especially important for the control of Desmodus rotundus population as it is a transmitter of rabies virus. Therefore, we aimed to evaluate the functional activity of testis and epididymis of D. rotundus in dry and rainy seasons under a morphological approach. We observed an increase in tubular diameter and epithelial height of the seminiferous tubules during the rainy season. In the latter, additionally, stereological analysis of the testis showed increased proportion of seminiferous epithelium and reduced percentage of lumen. The sperm number in caput/corpus epididymis increased in rainy season, whereas sperm count and transit time were reduced in cauda region. These alterations were probably related to the recovery of epithelium activities after mating season in dry season. Despite altered nuclear and cytoplasm parameters of Leydig cells between seasons, the volume and number of these cells were constant. Moreover, no change in serum testosterone levels, daily sperm production, and apoptotic index were observed, which indicates that the reproductive pattern in D. rotundus does not change between seasons. Our study offers a baseline for the management of vampire bat population as an attempt to control rabies disease.


Subject(s)
Chiroptera/physiology , Reproduction/physiology , Animals , Chiroptera/growth & development , Epididymis/pathology , Epididymis/physiology , Male , Seasons , Spermatozoa/cytology , Spermatozoa/metabolism , Testis/pathology , Testis/physiology , Testosterone/blood
16.
Life Sci ; 209: 472-480, 2018 Sep 15.
Article in English | MEDLINE | ID: mdl-30144451

ABSTRACT

AIMS: Studies have shown that exposure to either environmental toxicants or hyperglycemia causes hepatic injuries. However, it is unclear the extent to which their combined exposure may influence liver functions. Therefore, we aimed to evaluate morphological and functional hepatic parameters in diabetic rats exposed to arsenic. METHODS: Diabetes was induced in male rats by intraperitoneal streptozotocin injection. While healthy and diabetic animals received saline solution (negative control and diabetes control, respectively), other animals received 10 mg/L sodium arsenate (arsenic control and diabetes + arsenic groups, respectively) for 40 days in drinking water. Liver tissue was subjected to antioxidant enzymes analysis, cytokine assay, arsenic determination, and histopathological evaluation. Functional markers of hepatic damage were analyzed using serum samples. KEY FINDINGS: Arsenate exposure reduced the antioxidant enzymes activity in healthy rats, and it worsened the reduction of GST in diabetic animals. Consequently, arsenate-exposed animals showed increased malondialdehyde and carbonyl protein levels, being this increase worsened in diabetes + arsenic animals. Arsenate-exposed groups also showed hepatic inflammatory process with high number of mast cells and TNF-α production mainly in diabetes + arsenic animals. Vascular alterations, such as congestion, bleeding, and hemosiderin deposition were intensified in diabetes + arsenic animals, whereas glycogen storage reduced in these animals. SIGNIFICANCE: We concluded that arsenate exposure was able to intensify morphological and functional damages in liver tissue of diabetic animals.


Subject(s)
Arsenic/toxicity , Diabetes Mellitus, Experimental/complications , Inflammation/etiology , Liver Diseases/etiology , Oxidative Stress/drug effects , Animals , Inflammation/metabolism , Inflammation/pathology , Inflammation Mediators/metabolism , Lipid Peroxidation/drug effects , Liver Diseases/metabolism , Liver Diseases/pathology , Male , Rats , Rats, Wistar
17.
Reprod Toxicol ; 78: 130-140, 2018 06.
Article in English | MEDLINE | ID: mdl-29702248

ABSTRACT

Arsenic impairs male reproductive functions. However, it is not clear whether different arsenic compounds similarly affect fertility. In this study, we compared the impact of sodium arsenite and arsenate on sperm quality and fertility. After 56 d exposure, male Wistar rats were mated and pregnant females were evaluated by fertility indexes. Clearly, exposure to 10 mg/L arsenite reduced daily sperm production via H2O2 overproduction and germ cells loss. Animals from this group also showed a decrease in epididymal sperm counts and percentage of sperm with intact membranes. Moreover, they presented low fertility potential and high preimplantation loss. In contrast, 10 mg/L arsenate caused oxidative stress in testis, mineral imbalance in epididymis, and sperm membranes damage, with no effects on fertility. Both arsenic compounds at 0.01 mg/L altered reproductive parameters. We concluded that arsenite is more harmful than arsenate to sperm quality and male fertility, with negative influences in early pregnancy.


Subject(s)
Arsenates/toxicity , Arsenites/toxicity , Fertility/drug effects , Sodium Compounds/toxicity , Animals , Catalase/metabolism , Female , Glutathione Transferase/metabolism , Male , Malondialdehyde/metabolism , Rats, Wistar , Sperm Count , Sperm Motility/drug effects , Spermatozoa/drug effects , Testis/drug effects , Testis/metabolism , Testis/pathology , Testosterone/blood
18.
Pensar prát. (Impr.) ; 21(1): 26-39, jan.-mar.2018. tab
Article in Portuguese | LILACS | ID: biblio-914086

ABSTRACT

Este artigo descreve o perfil das atletas e o contexto do futsal feminino, analisando a relação entre o perfil socioeconômico, a formação esportiva e a carreira esportiva destas jogadoras no estado de São Paulo. Para tanto, aplicamos um questionário misto para 87 atletas, abarcando todas as que disputaram o campeonato paulista de 2015. Nossos resultados apontam que a carreira no futsal de mulheres é pouco estruturada, o que ajuda a compreender o motivo pelo qual o perfil das atletas é formado por mulheres de famílias de baixo capital cultural e poder aquisitivo. Para elas, a carreira no futsal constitui um paradoxo, pois não é um projeto de vida em si, mas a fonte de acesso a outro, que pode se consolidar como uma possibilidade de mu-dança social para elas.


This article aimed to describe the profile of the athletes and the context of women futsal play-ers and analyzed the relationship between the socioeconomic profile, the sports training and the athletic career of these players in the state of São Paulo. To achieve this, we applied a sur-vey to all 87 futsal players, who competed in the São Paulo championship of 2015. Our re-sults showed that the career in women's futsal is poorly structured, which points out the rea-son why the profile of athletes is directed to those of families with low cultural capital and purchasing power. For those women, the career in futsal is a paradox, because it is not a pro-ject of life in itself, but the way to access another one, which can be consolidated as a possi-bility of social change for them.


En este artículo se describe el perfil de las atletas y el contexto del futsal femenino, analizan-do la relación entre el perfil socioeconómico, la formación en el deporte y la carrera atlética de esas jugadoras en la ciudad de São Paulo. Para eso, aplicamos un cuestionario mixto a 87 atletas, englobando a todas las que compitieron en el campeonato Paulista de 2015. Nuestros resultados indican que la carrera del futsal femenino es poco estructurada, lo que ayuda a entender por qué el perfil de las atletas está formado por mujeres provenientes de las familias de bajos capital cultural y poder adquisitivo. Para ellas, la carrera del futsal está constituida por una paradoja, ya que no es un proyecto de vida en sí, sino la fuente de acceso a otro, que puede consolidarse como una posibilidad de transformación social para ellas.


Subject(s)
Humans , Female , Soccer , Women , Athletic Performance , Social Change , Brazil , Career Choice
19.
Biol Trace Elem Res ; 183(2): 305-313, 2018 Jun.
Article in English | MEDLINE | ID: mdl-28879625

ABSTRACT

Interactions of arsenic with essential trace elements may result in disturbances on body homeostasis. In the present study, we aimed to investigate the effects of different arsenic compounds on micromineral content and antioxidant enzyme activities in rat liver. Male Wistar rats were randomly divided into five groups and exposed to sodium arsenite and sodium arsenate at 0.01 and 10 mg/L for 8 weeks in drinking water. The concentration of arsenic increased in the liver of all arsenic-exposed animals. The proportion of zinc and copper increased in animals exposed to 0.01 mg/L sodium arsenite. In addition, these animals presented a reduction in magnesium and sodium content. Superoxide dismutase activity decreased mainly in arsenite-exposed animals, whereas catalase activity decreased in animals exposed to 10 mg/L sodium arsenate. Further, exposure to sodium arsenate at 10 mg/L altered copper and magnesium content in the liver, and reduced total protein levels. Overall, both arsenic compounds altered the liver histology, with reduction in the proportion of cytoplasm and hepatocyte, and increased the percentage of sinusoidal capillaries and macrophages. In conclusion, our findings showed that oral exposure to arsenic compounds disturbs the trace elements balance in the liver, especially at low concentration, altering enzymatic and stereological parameters. We concluded that despite the increase in trace elements content, the antioxidant enzyme activities were downregulated and did not prevent morphological alterations in the liver of animals exposed to both arsenic compounds.


Subject(s)
Antioxidants/metabolism , Arsenicals/pharmacology , Liver/drug effects , Liver/metabolism , Animals , Arsenates/pharmacology , Arsenites/pharmacology , Liver/enzymology , Male , Minerals/metabolism , Rats , Rats, Wistar
20.
J Toxicol Environ Health A ; 79(6): 274-86, 2016.
Article in English | MEDLINE | ID: mdl-27029432

ABSTRACT

Arsenic (As), in the form of trivalent arsenite or pentavalent arsenate, is a ubiquitous toxic compound naturally occurring in the environment. This study aimed to evaluate the impact of two different forms of inorganic As on reproductive parameters following oral exposure. Adult Wistar male rats were exposed to sodium arsenite or arsenate at concentrations of 0.01 mg/L or 10 mg/L for 56 d in drinking water. Sodium arsenite at both concentrations and sodium arsenate at 10 mg/L produced reduction in daily sperm production, in number of spermatids in the testis, and in sperm in the epididymal caput/corpus regions. Changes in epididymal morphometry were variable and region specific. Total and progressive sperm motility and sperm morphology did not differ markedly between controls and animals exposed to As. The body and reproductive organs weights, as well as testosterone concentration, remained unchanged among all groups. In conclusion, As exposure in drinking water over 56 d produced damage in male reproductive functions in adult rats, suggesting that fertility problems might occur. Therefore, additional studies need to be undertaken to investigate potential mechanisms underlying sodium arsenite- and arsenate-induced disturbances in fertility and reproductive performance.


Subject(s)
Arsenates/toxicity , Arsenites/toxicity , Fertility/drug effects , Reproduction/drug effects , Animals , Body Weight/drug effects , Drinking Water , Epididymis/pathology , Male , Organ Size/drug effects , Rats , Rats, Wistar , Sperm Count , Sperm Motility/drug effects , Spermatozoa/drug effects , Spermatozoa/ultrastructure , Testosterone/metabolism
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