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1.
Braz. j. biol ; 83: 1-9, 2023. tab
Article in English | LILACS, VETINDEX | ID: biblio-1468869

ABSTRACT

The present study was conducted to evaluate the chemical composition, antioxidant activity and hypoglycemic effects of whole kumquat (Ku) powder in diabetic rats fed a high-fat-high-cholesterol (HFHC) diet. The antioxidant activities were evaluated using stable 1,1-diphenyl 2-picrylhydrazyl (DPPH) free radical scavenging method, 2,2'-azinobis (3-ethyl benzo thiazoline-6-sulphonic acid) radical cation (ABTS) and Ferric reducing antioxidant power (FRAP). Total phenolic content was (51.85 mg GAE/g) and total flavonoid content was (0.24 mg Cateachin Equivalent, CE/g). DPPH and ABTS values were 3.32 and 3.98 mg Trolox equivalent (TE)/g where FRAP value was 3.00 mM Fe²+/kg dry material. A total of 90 albino rats were used in the present study. Rats group were as follows: normal diet; normal treated (2, 4, and 6% Ku.), diabetic rats (non-treated), diabetic + HFHC diet (non-treated), HFHC (non-treated), Diabetic (treated), HFHC (treated) and Diabetic + HFHC (treated). The diets were followed for 8 weeks. Blood samples were collected at the end of the experiment. Serum glucose was recorded and thyroid hormones (T4, Thyroxine and T3, Triiodothyronine) were conducted. Diet supplemented with Kumquat at different concentrations have a hypoglycemic effect and improve the thyroid hormones of both diabetic rats and HFHC diabetic rats.


O presente estudo foi conduzido para avaliar a composição química, a atividade antioxidante e os efeitos hipoglicêmicos do pó de kumquat (Ku) em ratos diabéticos alimentados com uma dieta rica em gordura e colesterol (HFHC). As atividades antioxidantes foram avaliadas usando o método de eliminação de radicais livres de 1,1-difenil 2-picrilhidrazil (DPPH), 2,2'-azinobis (ácido 3-etilbenzotiazolina-6-sulfônico) radical cátion (ABTS) e antioxidante redutor férrico potência (FRAP). O conteúdo fenólico total foi (51,85 mg GAE / g) e o conteúdo total de flavonoides foi (0,24 mg Cateachin Equivalent, CE / g). Os valores de DPPH e ABTS foram 3,32 e 3,98 mg equivalente de Trolox (TE) / g, em que o valor de FRAP foi de 3,00 mM Fe²+ / kg de material seco. Um total de 90 ratos albinos foi usado no presente estudo. O grupo dos ratos foi o seguinte: dieta normal: tratados normais (2, 4 e 6% Ku.), ratos diabéticos (não tratados), diabéticos + dieta HFHC (não tratados), HFHC (não tratados), diabéticos (tratados), HFHC (tratados) e diabéticos + HFHC (tratados). As dietas foram seguidas por 8 semanas. Amostras de sangue foram coletadas ao final do experimento. A glicose sérica foi registrada e os hormônios tireoidianos (T4, Tiroxina e T3, Triiodotironina) foram conduzidos. A dieta suplementada com kumquat em diferentes concentrações tem um efeito hipoglicêmico e melhora os hormônios tireoidianos tanto de ratos diabéticos quanto de ratos diabéticos com HFHC.


Subject(s)
Animals , Rats , Antioxidants/analysis , Diabetes Mellitus/drug therapy , Hypoglycemic Agents/analysis , Thyroid Hormones/pharmacology , Rats/metabolism , Rats/blood , Rutaceae/chemistry
2.
Acta sci., Biol. sci ; 40: 40040-40040, 20180000. ilus, graf
Article in English | LILACS, VETINDEX | ID: biblio-1460810

ABSTRACT

The liver is an essential organ for body energy homeostasis, controlling the biosynthesis, uptake and the disposal of carbohydrates and lipids. The hepatic steatosis is a common condition frequently associated with metabolic diseases and is characterized by the excessive accumulation of triglycerides in the liver. In recent years, many efforts have been devoted to prevent and treat the hepatic steatosis, but it remains being pointed out as the major cause for chronic hepatic diseases in Western countries. A considerable part of the knowledge about the physiopathology of hepatic steatosis, the effects of diets and drugs on the metabolic capacity of the liver to metabolize fatty acids, as well as the potential therapeutic approaches for hepatic steatosis derived from experimental animal models using rodents. Here, in this article, we present the details of some of the most common techniques used to evaluate fatty acid metabolism in liver of rats, including quantification of total lipid content, measurement of fatty acid oxidation in isolated subcellular fractions and procedures to measure the activities of important lipogenic enzymes. Classical protocols previously described to be performed using samples from other tissues were adapted to liver samples and different techniques with equivalent aims were compared. The principles and the advantages in terms of reliability and costs were discussed and the procedures here described can be applied for a low-cost broad evaluation of the fatty acid metabolism in liver of rats submitted to different experimental conditions.


O fígado é um órgão essencial para a homeostase energética, controlando a biossíntese, a captação e a eliminação de carboidratos e lipídios. A esteatose hepática é uma condição frequentemente associada a doenças metabólicas e é caracterizada pelo acúmulo excessivo de triacilgliceróis no fígado. Nos últimos anos, muitos esforços têm sido dedicados para prevenir e tratar a esteatose hepática, mas essa condição continua sendo apontada como a principal causa de doenças hepáticas crônicas em países ocidentais. Uma parte considerável do conhecimento sobre a fisiopatologia da esteatose hepática, sobre os efeitos de dietas e drogas na capacidade metabólica do fígado em metabolizar ácidos graxos, bem como sobre as possíveis abordagens terapêuticas para a esteatose hepática, derivam de estudos com modelos animais experimentais usando roedores. Neste artigo, apresentamos os detalhes de algumas das técnicas que podem ser usadas para avaliar o metabolismo de ácidos graxos no fígado de ratos, incluindo a quantificação do conteúdo lipídico total, medida da oxidação de ácidos graxos em frações subcelulares isoladas e procedimentos para medir as atividades de importantes enzimas lipogênicas. Protocolos clássicos previamente descritos para serem realizados utilizando amostras de outros tecidos foram adaptados para amostras de fígado e diferentes técnicas com objetivos equivalentes foram comparadas. Os princípios e as vantagens em termos de confiabilidade e custos foram discutidos e os procedimentos aqui descritos podem ser aplicados para uma avaliação ampla e de baixo custo do metabolismo de ácidos graxos no fígado de ratos submetidos a diferentes condições experimentais.


Subject(s)
Animals , Rats , Fatty Liver/veterinary , Laboratory and Fieldwork Analytical Methods/analysis , Rats/metabolism , Fatty Acids/analysis , Fatty Acids/metabolism
3.
J. venom. anim. toxins incl. trop. dis ; 20: 1-9, 04/02/2014. ilus, tab, graf
Article in English | LILACS, VETINDEX | ID: biblio-1484568

ABSTRACT

Scorpion envenoming is a public health problem in Brazil, where Tityus serrulatus and T. bahiensis are considered the most dangerous scorpions. They are well adapted to urbanized environments, and there is an increasing probability of human exposure to these venoms, including during pregnancy. Not much is known about the effects of prenatal exposure to the venom, and no information is available to aid in the rational treatment of victims stung during pregnancy. Thus, this study aimed to investigate whether venom from the scorpion T. bahiensis administered once to pregnant female rats at a dose that causes a moderate envenomation may lead to deleterious effects on the reproductive performance of the dams and on the development of their offspring. This is the first work demonstrating that T. bahiensis venom, when administered experimentally to rats, alters maternal reproductive performance and the morphological development of fetuses. The venom was given to dams on the 5th (GD5) or on the 10th (GD10) gestational day. After laparotomy, on GD21, fetuses and placentas were counted, weighed and externally analyzed. The corpora lutea were counted. The sex and vitality of fetuses were evaluated, and each litter was then randomly divided for visceral or skeletal analyses. Data were analyzed by ANOVA followed by the Tukey-Kramer test and Fisher's exact test. The significance level for all tests was set at p < 0.05.


Subject(s)
Animals , Pregnancy, Animal/immunology , Rats/metabolism , Scorpion Venoms/analysis , Scorpions/classification
4.
Article in English | LILACS | ID: lil-724679

ABSTRACT

Scorpion envenoming is a public health problem in Brazil, where Tityus serrulatus and T. bahiensis are considered the most dangerous scorpions. They are well adapted to urbanized environments, and there is an increasing probability of human exposure to these venoms, including during pregnancy. Not much is known about the effects of prenatal exposure to the venom, and no information is available to aid in the rational treatment of victims stung during pregnancy. Thus, this study aimed to investigate whether venom from the scorpion T. bahiensis administered once to pregnant female rats at a dose that causes a moderate envenomation may lead to deleterious effects on the reproductive performance of the dams and on the development of their offspring. This is the first work demonstrating that T. bahiensis venom, when administered experimentally to rats, alters maternal reproductive performance and the morphological development of fetuses. The venom was given to dams on the 5th (GD5) or on the 10th (GD10) gestational day. After laparotomy, on GD21, fetuses and placentas were counted, weighed and externally analyzed. The corpora lutea were counted. The sex and vitality of fetuses were evaluated, and each litter was then randomly divided for visceral or skeletal analyses. Data were analyzed by ANOVA followed by the Tukey-Kramer test and Fisher's exact test. The significance level for all tests was set at p < 0.05.


Subject(s)
Animals , Pregnancy, Animal/immunology , Rats/metabolism , Scorpion Venoms/analysis , Scorpions/classification
5.
Int. j. morphol ; 29(3): 754-761, Sept. 2011. ilus
Article in Spanish | LILACS | ID: lil-608654

ABSTRACT

En el presente estudio se evaluó el efecto del propóleos sobre el metabolismo de la glucosa en ratones C57/BL-6 con diabetes mellitus tipo 2 inducida por dieta alta en grasa. Se midieron los cambios en las concentraciones séricas de lípidos, glucosa e insulina, y el efecto sobre la captación de 2-deoxi-[2,6-3H]-D-glucosa, síntesis de [14C]-glicógeno y descarboxilación de [U-14C]-D-glucosa inducida por insulina en músculo aislado. Los resultados muestran que en ratones diabéticos, el tratamiento con propóleos (150 mg/kg/día) reduce los niveles de insulina e índice HOMA (P<0.05). También disminuyó la obesidad abdominal de estos animales (P<0.05). Por otro lado, no modificó las concentraciones plasmáticas de glucosa, colesterol total y triglicéridos. Se observó también que la captación de 2-deoxi-[2,6-3H]-D-glucosa, síntesis de [14C]-glicógeno y descarboxilación de [U-14C]-D-glucosa inducida por insulina en músculo sóleo de ratones tratados con propóleos fue significativamente superior al grupo control (P<0.05). En resumen, nuestros datos confirman que el propóleos es capaz de modular el metabolismo de glucosa en ratones C57/BL-6 con diabetes mellitus tipo 2 inducida por dieta alta en grasa. Los datos obtenidos constituyen un importante antecedente que avala el posible uso del propóleos como fuente de polifenoles con actividad antidiabetogénica.


In the current study, we investigated the effect of propolis on diabetic mice undergoing propolis treatment (150 mg/kg/day) for a 6 week period. We also evaluated serum lipids, glucose, insulin levels and the effect on glucose uptake of 2-deoxy-D-[2,6-3H] glucose, [14C]-glycogen synthesis and [U-14C]-D-glucose decarboxylation induced by insulin in muscle tissue. Our results show that treatment with propolis (150 mg/kg/day) reduced insulin and HOMA index (P<0.05). Propolis also lowered abdominal obesity (P<0.05). No effects over serum glucose, total cholesterol and triglycerides levels were observed. We also observed that uptake of 2-deoxy-D-[2,6-3H] glucose, [14C]-glycogen synthesis and [U-14C]-D-glucose decarboxylation induced by insulin in soleus muscle of mice treated with propolis were significantly greater than control group (P<0.05). In summary, our data establishes that propolis modulates glucose metabolism. This result constitutes important data indicating that propolis can be used as a polyphenols source with antidiabetogenic activity.


Subject(s)
Rats , /chemically induced , /metabolism , Propolis/administration & dosage , Propolis/metabolism , Glucose/antagonists & inhibitors , Rats/metabolism
6.
Rev. Inst. Nac. Hig ; 42(2): 50-55, jul. 2011. tab
Article in Spanish | LILACS, LIVECS | ID: lil-631804

ABSTRACT

Introducción: El nimesulide es un analgésico antiinflamatorio no esteroideo, asociado en reportes de casos clínicos con hepatotoxicidad. Sin embargo, se han publicado pocos estudios controlados en animales. Objetivo: Determinar si la administración de dosis terapéuticas de nimesulide, durante diferentes periodos, altera el funcionalismo hepático en ratas Wistar machos y hembras. Materiales y métodos: Cuarenta ratas Wistar fueron distribuidas en 4 grupos de 10 cada uno (5 hembras y 5 machos). Grupo I (control): recibió 0.1 mL de solución salina durante 7 días, los animales de los grupos II, III y IV fueron tratados con nimesulide (3 mg/kg) durante 7, 21 y 35 días, respectivamente. Se determinaron niveles séricos de bilirrubina, fosfatasa alcalina y transaminasas. Resultados: La actividad de la enzima alanino-amino-transferasa (ALT) aumentó en machos (p< 0.01) y hembras (p < 0.02) de los grupos III y IV respecto a los controles. En los machos de los grupos II y IV aumentó la fosfatasa alcalina en comparación con las hembras de los mismos grupos (p < 0.05). Las bilirrubinas di - recta y total disminuyeron en las hembras del grupo IV respecto al control (p < 0.03). Conclusiones: Los resultados sugieren que a dosis terapéuticas el nimesulide altera el funcionalismo hepático en ratas Wistar.


Introduction: Nimesulide is a non-steroidal antiinfflamatory drug associated with hepatotoxicity. Nevertheless, there have few published controlled studies with animals. Objec - tive: Determine whether the administration of therapeutic doses of nimesulide during differents periods alters hepatic function in male and female rats. Materials and me - thods: Forty Wistar rats were classified into 4 groups of 10 rats each. Group I received 0,1 ml of saline for 7 days, whe reas the animals from groups II, III and IV were treated with Ni mesulide (3 mg/kg) during 7, 21 and 35 days, respectively. It has determined serum levels of bilirubin, alkaline phos pha tase and transaminases. Results: Alanino-amino-transferase (ALT) enzyme was increased in males (p<0.01) and females (p<0.02) from groups III and IV in com parison with the control group. Alkalin phosphate increased in males from groups II and IV in comparison with the females from these same groups (p< 0.05). Direct and total bilirubins decreased in group IV females (p< 0.03) in comparison with the control group. Conclusions: The administration of therapeutic doses of nimesulide affects hepatic function on Wistar rats.


Subject(s)
Humans , Animals , Male , Female , Rats , Pharmaceutical Preparations/classification , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Liver Function Tests/methods , Anti-Inflammatory Agents/analysis , Rats/metabolism , Public Health
7.
São Paulo; s.n; 2010. 110 p.
Thesis in Portuguese | LILACS | ID: lil-594071

ABSTRACT

Introdução As doenças cardiovasculares estão entre as principais causas de morte no Brasil e no mundo. Evidências epidemiológicas e clínicas estabelecem associação entre dieta, dislipidemia e aumento do risco de morte. O consumo de proteína isolada de amaranto tem efeito hipocolesterolemizante e por isso pode reduzir, de modo significativo, os fatores de risco das doenças cardiovasculares. Objetivo Avaliar o efeito da ingestão do isolado protéico de amaranto, no perfil de lipoproteínas plasmáticas e na expressão de proteínas relacionadas à modulação da síntese do colesterol hepático. Métodos Vinte e oito ratos Wistar (Ratus novergicus) foram distribuidos em quatro grupos e receberam dietas diferenciadas pela fonte protéica. Os grupos experimentais (I e Icol) receberam dieta com 20por cento de proteína de amaranto e os grupos controle (C e Ccol) receberam dieta com 20por cento de caseína. As dietas col apresentavam 1por cento de colesterol. Ao grupo controle foi fornecida a média da quantidade de ração ingerida pelos grupos experimentais I e Icol (controle pair feeding). Para determinar o efeito da ingestão das dietas no metabolismo do colesterol, foram avaliadas as concentrações plasmáticas de triacilgliceróis, colesterol total e HDL-c, e as concentrações hepáticas de colesterol e lipídios totais. O efeito da ingestão da proteína de amaranto na regulação das vias de síntese do colesterol hepático foi investigado pela avaliação da expressão das proteínas nucleares:receptor X hepático alfa (LXR alfa), receptor ativado por proliferadores de peroxissoma alfa (PPAR alfa) e proteína ligadora do elemento regulado por esterol 2 (SREBP-2). Resultados A dieta Icol promoveu menor concentração plasmática de colesterol total e triacilgliceróis (36por cento e 47por cento , respectivamente) em comparação ao grupo Ccol...


Subject(s)
Animals , Rats , Amaranthus , Cholesterol/metabolism , Eating , Proteins/isolation & purification , Rats/metabolism
8.
Int. j. morphol ; 27(3): 719-725, sept. 2009. ilus
Article in English | LILACS | ID: lil-598928

ABSTRACT

This study was undertaken to evaluate the relationship and effects of diabetes on liver morphology, architecture and function. The hepatic effects of diabetes were evaluated in vivo using streptozotocin (STZ)-induced diabetic rats as an experimental model. The degree of hepatic dysfunction was measured by using biochemical parameters like serum transaminases (ALT and AST), alkaline phosphatase (ALP)and pseudocholinesterase (PChE) while the histopathological studies were carried out to support the enzymic Parameters. The aim of the study was to investigate the association between diabetic hepatic complications and liver enzyme alterations. This study was performed in the Department of Anatomy; Institute of Pharmaceutical Sciences and Institute of Diabetology and endocrinology of Baqai Medical University, Karachi. Diabetes was induced by a single dose of STZ (45 mg/kg, b.w.) given intraperitoneally in sodium citrate buffer at pH 4.5. Eighty albino rats were divided into five groups: control (A) and STZ treated (B, C, D, and E) which were sacrificed 2, 4, 6 and 8 weeks post treatment respectively. Histopathological examination of liver showed accumulation of lipid droplets, lymphocytic infiltration, increased fibrous content, dilatation and congestion of portal vessels and proliferation of bile ducts. Increased levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), ALP and PChE were observed in the liver. It seems that the diabetic complications in the liver like hepatocyte destruction etc. are likely to be due to alterations in enzyme levels.


Este estudio se realizó para evaluar la relación y los efectos de la diabetes sobre la morfología, arquitectura y la función del hígado. Los efectos hepáticos de la diabetes se evaluaron in vivo utilizando estreptozotocina (STZ) para inducir diabetes en ratas como un modelo experimental. El grado de disfunción hepática se midió mediante el uso de parámetros bioquímicos, como las transaminasas séricas (ALT y AST), fosfatasa alcalina (ALP) y pseudocolinesterasa (PChE), mientras que los estudios histopatológicos se llevaron a cabo para apoyar los parámetros enzimáticos. El objetivo del estudio fue investigar la asociación entre las complicaciones hepáticas diabéticas y la alteración de enzimas hepáticas. Este estudio se realizó en el Departamento de Anatomía, Instituto de Ciencias Farmacéuticas y el Instituto de Diabetología y Endocrinología de la Baqai Medical University, Karachi. La diabetes fue inducida por una dosis única de STZ (45 mg/kg de peso corporal) administrada por vía intraperitoneal en tampón citrato de sodio a pH 4,5. Ochenta ratas albinas se dividieron en cinco grupos: control (A) y tratados con STZ (B, C, D y E), las que se sacrificaron a las 2, 4, 6 y 8 semanas después del tratamiento. El examen histopatológico de hígado mostró acumulación de gotitas de lípidos, infiltración linfocítica, aumento del contenido de fibras, dilatación y congestión de los vasos portales, y la proliferación de conductos biliares. Aumento de los niveles de aspartato aminotransferasa (AST), alanina aminotransferasa (ALT), ALP y PChE fueron observados en el hígado. Parece que las complicaciones de la diabetes en el hígado como la destrucción de los hepatocitos etc., son probablemente debido a alteraciones en los niveles de las enzimas.


Subject(s)
Animals , Mice , Diabetes Mellitus, Experimental/chemically induced , Diabetes Mellitus, Experimental/metabolism , Streptozocin/adverse effects , Streptozocin/metabolism , Liver , Rats/physiology , Rats/metabolism
9.
Int. j. morphol ; 27(3): 783-790, sept. 2009. ilus
Article in English | LILACS | ID: lil-598937

ABSTRACT

We studied the effects of streptozotocin (STZ)-induced diabetes on kidney morphology, anatomy, architecture and on the activities of aminotransferases (AST and ALT), alkaline phosphatase (ALP) and pseudocholinesterase (PChE) in albino rats. The aim of the study was to investigate the association between diabetic kidney complications and kidney enzyme alterations. This study was performed in the Department of Anatomy and Institute of Pharmaceutical Sciences, Baqai Medical University, Karachi and Pathology department of College of Physicians & Surgeons (CPSP) Pakistan in 2007-08. Diabetes was induced by a single dose of STZ (45 mg/kg, b.w.) given intraperitoneally in sodium citrate buffer at pH 4.5. Eighty (80) albino rats were divided into five groups: control (A) and STZ treated (B, C, D, and E) which were sacrificed 2, 4, 6 and 8 weeks post treatment respectively. Histopathology of kidney showed lesions similar to human glomerulosclerosis, glomerular membrane thickening, arteriolar hyalinization and tubular necrosis. Increased levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP) and pseudocholinesterase (PChE) were observed in the kidney. It seems that the diabetic complications in the kidney are likely to be associated with alterations in enzyme levels.


Se estudiaron los efectos de la diabetes inducida por estreptozotocin (STZ) sobre la morfología, anatomía, arquitectura y sobre las actividades de aminotransferasas (ALT y AST), fosfatasa alcalina (ALP) y pseudocolinesterasa (PChE) en los riñones de ratas albinas. El objetivo del estudio fue investigar la asociación entre las complicaciones renales diabéticas y la alteración de las enzimas renales. Este estudio se realizó en el Departamento de Anatomía y el Instituto de Ciencias Farmacéuticas, Universidad de Medicina Baqai, Karachi y el departamento de Patología de Colegio de Médicos y Cirujanos (CPSP) Pakistán entre el 2007-2008. La diabetes fue inducida por una dosis única de STZ (45 mg / kg de peso corporal) administrada por vía intraperitoneal en tampón de citrato de sodio a pH 4.5. Ochenta (80) ratas albinas fueron divididas en cinco grupos: control (A) y STZ tratados (B, C, D y E), que se sacrificaron a las 2, 4, 6 y 8 semanas después del tratamiento, respectivamente. La histopatología del riñón mostró lesiones similares a la glomeruloesclerosis en humanos, engrosamiento de la membrana glomerular, hialinización arteriolar y necrosis tubular. Aumento de los niveles de aspartato aminotransferasa (AST), alanina aminotransferasa (ALT), fosfatasa alcalina (ALP) y pseudocolinesterasa (PChE) fueron observados en el riñón. Parece que las complicaciones de la diabetes en el riñón están directamente asociadas con alteraciones en los niveles de las enzimas.


Subject(s)
Animals , Male , Adult , Mice , Diabetes Mellitus, Experimental/physiopathology , Diabetes Mellitus, Experimental/metabolism , Diabetes Mellitus, Experimental/blood , Streptozocin/adverse effects , Streptozocin/pharmacology , Streptozocin/toxicity , Kidney/anatomy & histology , Kidney/injuries , Kidney/metabolism , Kidney Diseases/chemically induced , Kidney Diseases/metabolism , Kidney Diseases/veterinary , Rats , Rats/anatomy & histology , Rats/metabolism
10.
Rev. para. med ; 23(2)abr.-jun. 2009. tab
Article in Portuguese | LILACS | ID: lil-589438

ABSTRACT

Objetivo: revisar na literatura os efeitos da desnutrição e etanol na morfologia de rins de ratos. Método: Foi realizada uma revisão sistemática com busca de artigos na base de dados PubMed, SciELO e LILACS. Foram excluídos artigos contendo estudos com seres humanos e que não avaliassem os efeitos da desnutrição e do etanol nos rins e que não pesquisassem a morfologia renal. Resultados: para os efeitos da desnutrição, não foram encontrados artigos na base PubMed, porém foram encontrados 46 na LILACS e 2 na SciELO, totalizando 48 artigos, sendo descartados 46 artigos. Para os efeitos do etanol, foram encontrados 373 artigos na base PubMed, 13 na LILACS e 3 na SciELO, totalizando 389 artigos, sendo descartados 386 artigos. O total geral de artigos analisados foram de 437, sendo 5 selecionados para esta revisão. Conclusão: tanto a desnutrição, quanto o etanol provocam alterações na morfologia dos rins de ratos, porém ainda são bastante escassos esses estudos na literatura.


Objective: To review - in specialized literature - the effects of malnutrition and ethanol in the morphology of kidneys of rats. Methodology: A systematic review was held by searching articles in the PubMed, SciELO and LILACS database. Articles which contained studies with human beings, or did not evaluate the effects of malnutrition and ethanol in the kidneys, and those which did not research the renal morphology were excluded. Results: For the effects of malnutrition, no PubMed based articles were found; however, 46 LILACS and 2 SciELO based ones were found, which adds up to 48 articles; 46 of them were not considered. For the effects of ethanol, 373 PubMed based articles, 13 LILACS and 3 SciELO based ones were found, which adds up to 389 articles; 386 of them were not considered. The total amount of 437 articles was analyzed and 5 of them were selected for this review. Conclusion: Not only the malnutrition, but also the ethanol lead to alterations in the morphology of kidneys of rats, however, these studies are still scarce in specialized literature.


Subject(s)
Animals , Rats , Malnutrition/metabolism , Ethanol/pharmacokinetics , Kidney/metabolism , Rats/metabolism , Kidney/pathology , Fetal Nutrition Disorders/metabolism
11.
J. bras. nefrol ; 30(2): 99-104, abr.-jun. 2008. tab
Article in Portuguese | LILACS | ID: lil-601720

ABSTRACT

Introdução: A Vitis vinifera L. é um antioxidante natural extraído das sementes de uva, seus componentes ativos constituem flavonóides e proantocianidinas, que, além de atuarem como seqüestradores de radicais livres, promovem a vasodilatação, inibem fosfolipases, ciclooxigenases e lipoxogenases, bem como reduzem a peroxidação lipídica. Este estudo visou avaliar o efeito renoprotetor da Vitis vinifera sobre a função renal de ratos com lesão renal aguda isquêmica (LRAi). Métodos: Foram utilizados ratos Wistar, machos, adultos, submetidos à isquemia, procedimento que se constituiu no clampeamento bilateral dos pedículos renais por 40 minutos. Os ratos foram distribuídos em grupos que receberam ou não o pré-tratamento com Vitisvinifera (3,0mg/kg, VO, uma vez ao dia, durante cinco dias antes do procedimento cirúrgico). Foram avaliados a função renal, por meio da depuração de creatinina, e o perfil oxidativo, por meio da mensuração de peróxidos urinários, através do método FOX – 2. Resultados: O grupo submetido ao tratamento com Vitis vinifera apresentou melhora significativa da função renal, atenuando a redução da depuração de creatinina e fluxo urinário, além do menor incremento dos níveis de peróxidos urinários. Conclusão: A utilização da Vitis vinifera como agente antioxidante promoveu proteção funcional nos animais com LRA isquêmica, com melhora significativa de função renal e diminuição da excreção de peróxidos urinários, em relação ao grupo controle.


Introduction: Vitis vinifera L. is an antioxidant agent extracted from grape seeds, and composed of flavonoids and proanthocyanidins. It has been shown to reduce free radicals, induce vasodilation, inhibit phospholipase, cyclooxygenase and lipooxygenase, and reduce the total lipid peroxidation index. The aim of this study was to evaluate the protective renal effect of the Vitis vinifera on renal function in rats with acute renal ischemic injury (ARIi). Methods: Male, adult, Wistar rats underwent renal ischemia for 40 minutes. They were distributed into groups that received or not Vitis vinifera (3.0mg/kg, P.O., once a day, during the 5 days prior to surgery). Renal function was evaluated by creatinine clearance, and the oxidative profile (urinary peroxide) was measured by the FOX – 2 assay. Results: The group submitted to treatment with Vitis vinifera showed a significantly lower degree of renal injury, with almost no reduction in creatinine clearance and in urinary output, along with a reduction in the level of urinary peroxide promoted by the ischemic maneuver. Conclusion: The use of the Vitis vinifera, an antioxidant agent, promoted functional renal protection in the animals with ischemia ARIi.


Subject(s)
Animals , Antioxidants/analysis , Ischemia/diagnosis , Rats/metabolism
12.
Salvador; s.n; 2008. 57 p. graf.
Thesis in Portuguese | LILACS | ID: lil-540655

ABSTRACT

A regulação do equilíbrio hidroelétrico é desempenhada por um conjunto de mecanismos viscerais e comportamentais, nos quais se incluem a ingestão de água e sal controlados por diversos neurotransmissores e áreas cerebrais. Estudos sugerem a participação de mecanismos Serotoninérgicos na indução das respostas fisiológicas relacionadas com a regulação da ingestão de água e sal. No presente estudo analisamos o envolvimento dos receptores 5-HT³ Serotoninérgicos localizados na ASM sobre a ingestão de água e sal em ratos sódio-depletados. Verificamos que a estimulação farmacológica específica dos receptores Serotoninérgicos 5-HT³ localizados na ASM, pelo agonista 5-HT³ seletivo m-CPBG, aumenta a ingestão de sal em ratos sódio-depletados. A especificidade deste efeito parece assegurada pelo fato de que o pré-tratamento com Ondansetrona, antagonista dos receptores Serotoninérgicos 5-HT³, aboliu completamente a elevação na ingestão de sal produzida pela administração do m-CPBG na ASM. Esse efeito Natriorexigênio parece não ser dependente de alterações na pressão arterial, visto que a micro-injeção na ASM do m-CPBG não foi capaz de modificar este parâmetro. Além disso, constatamos que a administração isolada do antagonista Ondasterona é incapaz de produzir efeito significativo sobre a ingestão de água e sal em ratos sódio-depletados. Tomando em conjunto os achados acima mencionados sugere-se que os receptores Serotoninérgicos do subtipo 5-HT³ localizados na ASM quando ativados farmacologicamente são capazes de ativar mecanismos centrais envolvidos com a procura e a ingestão de sódio.


Subject(s)
Animals , Rats , Sodium Chloride/analysis , Rats/metabolism , Receptors, Serotonin/metabolism , Septal Nuclei , Septum of Brain/metabolism , Water-Electrolyte Balance , Animal Experimentation , Drinking Behavior , Satiety Response
13.
Int. j. morphol ; 24(3): 417-422, sept. 2006. ilus
Article in Spanish | LILACS | ID: lil-474606

ABSTRACT

El metotrexato es ampliamente usado en la terapia de varias enfermedades malignas. El presente trabajo fue diseñado para investigar los cambios histológicos e histoquímicos del hígado de rata albina, después de administrar dicho fármaco. Se usaron 15 ratas albinas, machos, adultas, que fueron divididas en 3 grupos: El grupo I no tuvo tratamiento correspondiendo al control. A los grupos II y III se les administró, por vía intraperitoneal, una solución salina normal y metotrexato, respectivamente, con una dosificación de 0,5 mg por Kg de peso, dos veces por semana, con una duración total de 3, 6 y 9 semanas. Las ratas fueron sacrificadas y los hígados extraídos y procesados para los estudios histológico e histoquímico. El examen de los hígados del grupo III mostró infiltración celular mononuclear y un incremento en la cantidad de fibras colágenas en la vía portal. Hubo áreas focales de necrosis de células hepáticas con distorsión de la arquitectura hepática normal. Además, hubo un gradual y progresivo decrecimiento del contenido de glicógeno en los hepatocitos. La actividad de deshidrogenasa succínica y fosfatas alcalinas también disminuyó, pero sí hubo un aumento de la actividad de las fosfatasas ácidas en las áreas degeneradas y pérdida de actividades en áreas de necrosis celular masiva. En conclusión, inyecciones repetidas de metotrexato causan daño hepático de maginitud definida. Esta hepatotoxicidad progresó a medida que las dosis se fueron acumulando. El presente estudio muestra evidencias claras de la potencia citotóxica de este medicamento.


Methotrexate (MTX) is widely used in the therapy of various types of malignancy. The present work was designed to investigate the histological and histochemical changes in the liver of albino rat following methotrexate administration. Fifteen adult male albino rats were used in the present work. They were divided into three main groups: Group I was kept without treatment and served as control. Groups II and III were given intraperitoneal injections of normal saline and MTX, respectively, at a dosage of (0.5 mg/Kg) twice weekly for total durations of 3, 6 and 9 weeks. The rats were sacrificed and the livers were excised and processed for histological and histochemical study. Examination of sections of the livers of group III showed mononuclear cell infiltration and an increase in the amount of collagen fibers in the portal tracts. There were focal areas of liver cell necrosis with distortion of the normal hepatic architecture. Moreover, there was a gradual and progressive decrease of glycogen content in the hepatocytes. Furthermore, succinic dehydrogenase and alkaline phosphatase activity were also decreased. In addition there was an increase in acid phosphatase activities in the degenerated areas and loss of activities in areas of massive cellular necrosis. It was concluded that repeated injections of MTX causes hepatic damage of a definite magnitude. This hepatotoxicity progressed with increasing cumulative doses of methotrexate. The present study provided further evidence to the cytotoxic potency of this antifolate.


Subject(s)
Animals , Male , Adult , Rats , Hepatocytes , Hepatocytes/metabolism , Methotrexate/metabolism , Methotrexate/toxicity , Liver/anatomy & histology , Liver/metabolism , Rats/anatomy & histology , Rats/metabolism
14.
Rev. chil. tecnol. méd ; 23(1): 1029-1042, jul. 2003. ilus
Article in Spanish | LILACS | ID: lil-416666

ABSTRACT

El Malatión es un pesticida organofosforado ampliamente utilizado en agricultura, pero que en los mamíferos y el ser humano tiene un efecto altamente tóxico, inhibiendo la acetilcolinesterasa (AChE). Además, tiene la potencialidad de alterar el ciclo celular y de producir distorsiones a nivel de replicación y síntesis del DNA celular. El presente estudio tiene como objetivo describir el efecto de Malatión sobre las células del epitelio intestinal, mediante la detección de micronúcleos o cuerpos cromatínicos, con expresión que se traduce en toxicidad y genotoxicidad celular. Se utilizaron 6 ratas machos de laboratorio Sprague Dowley, las cuales fueron divididas en dos grupos de 3 individuos cada uno: (1) experimental y (2) control. Al grupo experimental se les administró una dosis de 170 mg/kg peso corporal de Malatión, por vía subcutánea, por un período de 13 días. En las preparaciones histológicas de duodeno del grupo control, se observó un epitelio intestinal normal, mientras que en el de las ratas tratadas con Malatión, se encontró la presencia de micronúcleos cromatínicos (MC) o estructuras picnóticas en el citoplasma, aproximadamente en el 80 por ciento de las células. Estos hallazgos permiten concluir que la administración de Malatión altera en forma evidente la histología del epitelio intestinal en las aratas expuestas al pesticida.


Subject(s)
Animals , Male , Rats , Malathion/administration & dosage , Malathion/adverse effects , Malathion/toxicity , Intestinal Mucosa/pathology , Rats/metabolism
15.
Rev. argent. dermatol ; 81(2): 110-7, abr.-jun. 2000. ilus, tab
Article in Spanish | LILACS | ID: lil-278341

ABSTRACT

Spirulina plantesis es una cyanobacteria cuya biomasa posee un alto contenido en proteínas, vitaminas y ácidos grasos que justifica su uso como suplemento en la dieta. El objetivo de este trabajo fue evaluar los efectos de la ingestión de S. platensis sobre el crecimiento, morfología y metabolismo en ratas Sprague-Dawley. 12 ratas hembras de 21 días de edad recibieron diarimente por sonda gástrica 2,0 ml de agua sin (control, N=6) o con 300mg S. platensis seca- pulverizada ( tratadas, N= 6), alimento comercial para roedores y agua ad libitum, durante 50 díaS. Los parámetros evaluados fueron: igesta de alimento comercial/día, peso corporal, ancho de cabeza, largo de la cola (semanalmente). Los animales fueron sacrificados, y se pesaron: hipófisis, hígado, riñones derecho e izquierdo, ciego, ovarios derecho e izquierdo, cuerpo uterino, páncreas, bazo y estómago. Se midio el ancho y largo de los pelos de la región externa de la oreja. La sangre se obtuvo por punción cardíaca; en elksuero se midieron, HDL, LDL y colesterol total, aspartato amino transferasa- GOT (AST), colinesterasa (ChE), y glutamil transferasa (y GT), fosfatasa alcalina, uremia, actividad de la enzima ALA-D y el contenido de pòrfirinas totales en hígado y pelos. Las ratas alimentadas con S. platensis no mostraron diferencias significativas en el crecimiento durante el tratamiento. Semanalmente, el peso corporal, ancho de cabeza y largo de cola no mostraron diferencias entre los tratamientos. El peso del ciego de los tratados (6,6583 +- 0,4209g) fue mayor (p<0,001) que los controles (5,0879 +- 0,9037g). No se observaron diferencias de peso en otros órganos. Los niveles de HDL, LDL y colesteroi total, GOT (AST), ChE, GT y uremia no mostraron diferencias entre tratadas y Control...


Subject(s)
Rats , Dietary Supplements , Rats/growth & development , Rats/metabolism , Cholesterol , Porphyrins
16.
Rev. Soc. Venez. Ciencias Morfol ; 4(1): 40-8, mar. 1998. ilus, tab
Article in Spanish | LILACS | ID: lil-251912

ABSTRACT

Se realizó un estudió ultraestructural y bioquímico sobre los cambios que ocurren en hígado de ratas, así como el efecto de la administración de L y D-cartinina (100 mg/kg/día), despues de ser sometidos a un ayuno parcial, se encontró que las alteraciones afectan principalmente a las mitocondrias, y al retículo endoplasmático rugoso. En las ratas tratadas con L-cartinina, las mitocondrias y el retículo endosplasmático rugoso conservaron la forma y disposición de las muestras controles. En los animales tratados con D-cartinina las alteraciones en el hepatocito fueron drásticas. Los resultados bioquímicos mostraron que los animales que recibieron L-cartinina durante el ayuno, mantuvieron valores de acidos grasos, ATP y L-cartinina muy similares a las muestras controles. Nuestros resultados sugieren que la L-cartinina ejerce un efecto hepatoprotector


Subject(s)
Animals , Rats , Carnitine/administration & dosage , Fasting/adverse effects , Liver/ultrastructure , Protective Agents , Rats/metabolism
17.
Arch. latinoam. nutr ; 44(4): 249-51, dic. 1994. tab
Article in English | LILACS | ID: lil-180960

ABSTRACT

Interactions among vitamin A metabolism and several metals have reported in both normal and pathological situations. In the present report we studied, in rats, the effect of daily injections of 100.000 U.I. of vitamin A during seven days on the content of K, Na, Mg, Fe, Cu, and Zn in the whole liver. The results were compared with the findinds in pair-fed non-treated animals (Control Group). The mean ñ SEM for the concentrations of these elents in the control group were 3.433ñ234 (K), 649ñ19 (Na), 239ñ5 (Mg), 169ñ7 (Fe, 5ñ0,1 (Cu and 31ñ2 (Zn) ug/g wet tisue, respectively. The hypervitaminosis A, confiermed by asignificant increase in tissue concentration of the vitamin, altered the hepatic content of the above mentioned cations. While Na and Zn increased, the other cations decreased its concentrations in the whole liver. Possible mechanisms for these findings are discussed and it is concluded that high doses of vitamin A result in marked changes in the hepatic content of the studied metals


Subject(s)
Rats , Animals , Enzymes/analysis , Liver/metabolism , Metabolism/physiology , Metals/physiology , Rats/metabolism , Vitamin A/metabolism
18.
Alexandria Journal of Veterinary Sciences [AJVS]. 1994; 10 (2): 89-94
in English | IMEMR | ID: emr-31526

ABSTRACT

Experiments were performed to show the effect of long-term administration of fresh and boiled onion extract in dose of 4 ml/day, for one and two months, on some serum constituents. These constituents were insulin, glucose, total lipids, total cholesterol and some enzyme activities. Results indicated that insulin concentration was significantly [P <0.01] increased in rats given fresh onion extract for one and two months and boiled for two months only. Glucose level was significantly [P <0.05] decreased after the 1st month and highly decreased [P <0.01] after the 2nd month in rats administrated both onion extract. AS-T activity was significantly [P <0.01] increased in serum of rats intubated fresh and boiled onion extract whereas, the AL-T activity was significantly [P <0.01] reduced in rats given boiled onion extract. The lactic dehydrogenase activity showed nonsignificant changes during all the experiment. Both onion extract [fresh and boiled] caused significant [P <0.05] decrement in the total lipids and cholesterol values after the first month and highly decreased [P <0.01] after the second month


Subject(s)
Rats/metabolism
19.
Rev. mex. oftalmol ; 67(3): 101-4, mayo-jun. 1993. tab
Article in Spanish | LILACS | ID: lil-124665

ABSTRACT

Varios modelos experimentales reproducen las manifestaciones oculares de la diabetes mellitus, así es el caso del modelo no diabético de suplemento de sacarosa en la rata, el cual es un modelo no diabético que reproduce la nagiopatía diabética, con secreción de insulina normal. Durante seis meses de experimentación, encontramos cambios oculares importantes como cataratas bilaterales, despoblación de las células ganglionares de la retina, así como hipoagregabilidad plaquetaria in vitro. Todo esto, en ausencia de niveles altos de glucosa en la sangre, indica una alta disponibilidad metabólica de la glucosa, lo que determina las lesiones en el cristalino y retina encontradas en este estudio. Este modelo experimental tambien confirma el desarrollo de la hipoagregabilidad plaquetaria in vitro, la cual puede ser atribuída a la estimulación de las plaquetas in vivo.


Subject(s)
Animals , Rats , Sucrose/adverse effects , Sucrose/metabolism , Hyperglycemia/chemically induced , Hyperglycemia/metabolism , Diabetic Retinopathy/physiopathology , Diabetic Retinopathy/metabolism , Rats/metabolism , Vascular Diseases/physiopathology , Vascular Diseases/metabolism , Platelet Activation/physiology , Diabetic Angiopathies/physiopathology , Diabetic Angiopathies/metabolism
20.
J. pneumol ; 18(2): 59-63, jun. 1992. ilus, tab
Article in Portuguese | LILACS | ID: lil-126828

ABSTRACT

A restriçäo protéico-calórica em ratas adultas, durante 21 dias, acarretou queda significante nos pesos corporal e pulmonar desses animais, sem alterar significantemente o conteúdo de água e de DNA de seus pulmöes. A desnutriçäo protéico-calórica provocou, ainda, reduçäo significante no conteúdo pulmonar de RNA, proteína total e das relaçöes RNA/DNA e proteína total/DNA, indicando uma possível diminuiçäo da sintese protéica e do tamanho das células pulmonares respectivamente. As concentraçöes de RNA e proteína total foram semelhantes enquanto a de DNA foi signifivantemente superior nas ratas desnutridas. A desnutriçäo protéico-calórica näo afetou o conteúdo de hidroxiprolina do pulmäo enquanto ocasionou uma elevaçäo significante nas concentraçöes desse aminoácido, sugerindo a ocorrência de maior deposiçäo de colágeno ou a lentidäo de seu "turnover" em relaçäo aos das demais proteínas desse órgäo


Subject(s)
Animals , Female , Rats , Body Weight/physiology , Protein-Energy Malnutrition/veterinary , Organ Size/physiology , Rats/metabolism , Collagen/metabolism , Hydroxyproline/metabolism , Lung/anatomy & histology
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