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1.
Childs Nerv Syst ; 33(3): 407-417, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28062893

RESUMO

PURPOSE: Alcohol consumption in pregnancy may cause fetal alcohol syndrome (FAS) in the infant. This study aims to investigate prenatal alcohol exposure related neuroapoptosis on the cerebral cortex tissues of newborn rats and possible neuroprotective effects of betaine, folic acid, and combined therapy. METHODS: Pregnant rats were divided into five experimental groups: control, ethanol, ethanol + betaine, ethanol + folic acid, and ethanol + betaine + folic acid combined therapy groups. We measured cytochrome c release, caspase-3, calpain and cathepsin B and L. enzyme activities. In order to observe apoptotic cells in the early stages, TUNEL method was chosen together with histologic methods such as assessing the diameters of the apoptotic cells, their distribution in unit volume and volume proportion of cortical intact neuron nuclei. RESULTS: Calpain, caspase-3 activities, and cytochrome c levels were significantly increased in alcohol group while cathepsin B and L. activities were also found to be elevated albeit not statistically significant. These increases were significantly reversed by folic acid and betaine + folic acid treatments. While ethanol increased the number of apoptotic cells, this increase was prevented in ethanol + betaine and ethanol + betaine + folic acid groups. Morphometric examination showed that the mean diameter of apoptotic cells was increased with ethanol administration while this increase was reduced by betaine and betaine + folic acid treatments. CONCLUSION: We observed that ethanol is capable of triggering apoptotic cell death in the newborn rat brains. Furthermore, folic acid, betaine, and combined therapy of these supplements may reduce neuroapoptosis related to prenatal alcohol consumption, and might be effective on preventing fetal alcohol syndrome in infants.


Assuntos
Apoptose/efeitos dos fármacos , Betaína/uso terapêutico , Córtex Cerebral/patologia , Etanol/toxicidade , Ácido Fólico/uso terapêutico , Fármacos Neuroprotetores/uso terapêutico , Efeitos Tardios da Exposição Pré-Natal , Animais , Animais Recém-Nascidos , Apoptose/fisiologia , Concentração Alcoólica no Sangue , Calpaína/metabolismo , Caspase 3/metabolismo , Catepsina B/metabolismo , Catepsina L/metabolismo , Depressores do Sistema Nervoso Central/toxicidade , Citocromos c/metabolismo , Modelos Animais de Doenças , Feminino , Gravidez , Efeitos Tardios da Exposição Pré-Natal/induzido quimicamente , Efeitos Tardios da Exposição Pré-Natal/tratamento farmacológico , Efeitos Tardios da Exposição Pré-Natal/patologia , Ratos , Ratos Sprague-Dawley
2.
Int J Med Mushrooms ; 18(4): 301-11, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27481296

RESUMO

In this article we report the healing effects of a Phellinus linteus fruiting body hot water extract (PLE) in streptozotocin (STZ)-induced diabetic rats. PLE was given before and after STZ. The preprotective, protective, and postprotective effects of PLE on STZ-induced oxidative stress were studied using biochemical (caspase 3 activity, cytosolic-to-lysosomal ratio of cathepsin B and L, DNA fragmentation levels), ordinary histological and immuno-histochemical investigation parameters. Following oral administration of PLE after STZ application, the serum glucose concentration significantly decreased up to 41.13% compared with the control group (P < 0.05). The hypoglycemic potential of the PLE was further supported by an increase of insulin secretion in the islets of Langerhans. In addition, the number of cells in Langerhans islets increased by 45.89% when PLE was given after STZ application. On the other hand, the use of PLE before oxidative stress could not prevent the onset of diabetes. This is, to our knowledge, the first study of the effect of application time of orally administered Ph. Linteus hot water extract on STZ-induced diabetes.


Assuntos
Basidiomycota/química , Diabetes Mellitus Experimental/tratamento farmacológico , Hipoglicemiantes/farmacologia , Extratos Vegetais/farmacologia , Polissacarídeos/farmacologia , Administração Oral , Animais , Diabetes Mellitus Experimental/induzido quimicamente , Modelos Animais de Doenças , Carpóforos/química , Humanos , Insulina/metabolismo , Secreção de Insulina , Ilhotas Pancreáticas/efeitos dos fármacos , Masculino , Phellinus , Ratos , Ratos Sprague-Dawley , Estreptozocina/efeitos adversos
3.
Exp Ther Med ; 9(3): 1023-1027, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25667671

RESUMO

To the best of our knowledge, this is the first study concerning the effect of boric acid (BA) administration on fetal alcohol syndrome (FAS). In this study, the aim was to investigate prenatal alcohol-induced oxidative stress on the cerebral cortex of newborn rat pups and assess the protective and beneficial effects of BA supplementation on rats with FAS. Pregnant rats were divided into three groups, namely the control, alcohol and alcohol + boric acid groups. As markers of alcohol-induced oxidative stress in the cerebral cortex of the newborn pups, malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) levels were measured. Although the MDA levels in the alcohol group were significantly increased compared with those in the control group (P<0.05), the MDA level in the alcohol + boric acid group was shown to be significantly decreased compared with that in the alcohol group (P<0.01). The CAT activity of the alcohol + boric acid group was significantly higher than that in the alcohol group (P<0.05). The GPx activity in the alcohol group was decreased compared with that in the control group (P<0.05). These results demonstrate that alcohol is capable of triggering damage to membranes of the cerebral cortex of rat pups and BA could be influential in antioxidant mechanisms against oxidative stress resulting from prenatal alcohol exposure.

4.
Mol Biol Rep ; 41(10): 6743-53, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-24996291

RESUMO

Excessive alcohol consumption and alcoholism cause medical problems with high mortality and morbidity rates. In this study we aimed to decrease the alcohol related tissue damage by inhibiting calpain activation which plays an important role in apoptosis and necrosis, in rats with cardiomyopathy induced by acute alcohol consumption. Male Sprague-Dawley rats were separated into four groups (control, vehicle, alcohol and alcohol + inhibitor) with 10 rats in each. Control group received isocaloric maltose while vehicle group received isocaloric maltose with DMSO, and alcohol group received 8 g/kg absolute ethanol by gavage. Inhibitor group received 20 mg/kg calpain inhibitor 1 intraperitonally prior to alcohol administration. Calpain activities, cathepsin L levels and cytochrome c release rates were significantly increased in alcohol group compared to control group (p < 0.05). Serum CK MB and BNP levels of alcohol group were excessively increased compared to control group (respectively p < 0.001 and p < 0.01). Serum BNP levels of alcohol + inhibitor group were significantly (p < 0.05) decreased compared to alcohol group. In addition to these, histological evaluation of light microscope images and the results of DNA fragmentation and immunohistochemical caspase-3 activity results showed significant improvement of these parameters in alcohol + inhibitor group compared to alcohol group. Results of our biochemical and histological evaluation results revealed that the calpain inhibitor N-acetyl-leu-leu-norleucinal may have an ameliorating effect on acute alcohol consumption related cardiac tissue damage due to its effects on cell death pathways.


Assuntos
Consumo Excessivo de Bebidas Alcoólicas/complicações , Calpaína/antagonistas & inibidores , Cardiomiopatias/etiologia , Cardiomiopatias/prevenção & controle , Inibidores de Cisteína Proteinase/farmacologia , Leupeptinas/farmacologia , Animais , Calpaína/metabolismo , Cardiomiopatias/metabolismo , Cardiomiopatias/patologia , Caspase 3/metabolismo , Catepsina B/metabolismo , Catepsina L/metabolismo , Creatina Quinase Forma MB/sangue , Inibidores de Cisteína Proteinase/administração & dosagem , Citocromos c/metabolismo , Modelos Animais de Doenças , Humanos , Imuno-Histoquímica , Leupeptinas/administração & dosagem , Masculino , Miocárdio/metabolismo , Miocárdio/patologia , Proteínas do Tecido Nervoso/sangue
5.
Pharm Biol ; 52(8): 994-1002, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24597653

RESUMO

CONTEXT: Excess use of alcohol is known to be associated with liver diseases such as fatty liver, alcoholic hepatitis, and cirrhosis. Various practices may be applied to prevent or treat the damage caused by chronic alcoholism. Coprinus comatus (O.F. Müll.) Pers. (Agaricaceae) is a macrofungus that has been reported to aid the recovery of murine livers damaged by benzopyrene. OBJECTIVE: In this study, the possible therapeutic effects of three different doses (50, 100, and 150 mg/kg) of C. comatus polysaccharide (PS) extract were studied in rats subjected to an alcoholic diet. The histological and biochemical results were compared between the control and experimental groups. MATERIALS AND METHODS: Modified Lieber-Decarli's calorie-adjusted liquid alcohol diet was given orally for 60 d. In addition to histopathology, alanine transaminase (ALT), aspartate transaminase (AST), mitochondrial membrane integrity, total cytochrome-c oxidase activity (TotalStCox), total mitochondrial cytochrome-c oxidase activity (TotalMtStCox), and caspase-3 values were used as liver parameters, and liver sections from all experimental groups were examined by electron microscopy. RESULTS: Using histopathological assessment, it was observed that there was a decline in liver hepatocyte vacuolization in the treatment group fed 50 mg PS/kg. The TotalStCox and TotalMtStCox values of this group differed from the EtOH control group (p < 0.05). DISCUSSION AND CONCLUSION: Daily administration of 50 mg/kg of C. comatus PS extract considerably reduced the negative effects of alcohol on liver structure and function.


Assuntos
Coprinus , Etanol/toxicidade , Hepatopatias Alcoólicas/tratamento farmacológico , Extratos Vegetais/administração & dosagem , Polissacarídeos/administração & dosagem , Recuperação de Função Fisiológica/efeitos dos fármacos , Animais , Hepatopatias Alcoólicas/fisiopatologia , Masculino , Extratos Vegetais/isolamento & purificação , Polissacarídeos/isolamento & purificação , Distribuição Aleatória , Ratos , Ratos Sprague-Dawley , Recuperação de Função Fisiológica/fisiologia
6.
Int J Food Sci Nutr ; 65(4): 482-8, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24392995

RESUMO

In the present study, the curative effects of crude polysaccharides (PSs) from mushrooms on the symptoms of alcoholic liver injury were investigated. PSs from Agaricus bisporus, Agaricus brasiliensis, and Phellinus linteus fruiting bodies were administered by gavage at levels of 100 mg per kg body weight per day for 7 d after the onset of the disease. The caspase-3 activity, mitochondrial membrane potential, mitochondrial outer membrane integrity of the liver tissues of sacrificed rats, and the serum alanine aminotransferase (ALT) levels were determined. In addition, light and transmission electron microscope (TEM) studies were performed for histopathological and cytological evaluations on liver sections. PSs from A. brasiliensis decreased ALT level and mitochondrial membrane potential and increased the outer membrane integrity; microscopic examinations also revealed normal hepatocytes and tissue. On the basis of our data, it can be argued that crude PSs from Agaricus brasiliensis have therapeutic potential for alcoholic liver injury.


Assuntos
Agaricus/química , Basidiomycota/química , Descoberta de Drogas , Fígado Gorduroso Alcoólico/tratamento farmacológico , Carpóforos/química , Polissacarídeos Fúngicos/uso terapêutico , Fígado/efeitos dos fármacos , Animais , Caspase 3/metabolismo , Etnofarmacologia , Fígado Gorduroso Alcoólico/metabolismo , Fígado Gorduroso Alcoólico/patologia , Fígado Gorduroso Alcoólico/fisiopatologia , Polissacarídeos Fúngicos/isolamento & purificação , Fígado/metabolismo , Fígado/fisiopatologia , Fígado/ultraestrutura , Masculino , Medicina Tradicional , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Microscopia Eletrônica de Transmissão , Membranas Mitocondriais/efeitos dos fármacos , Membranas Mitocondriais/metabolismo , Infiltração de Neutrófilos/efeitos dos fármacos , Distribuição Aleatória , Ratos Sprague-Dawley
7.
Clin Exp Hypertens ; 36(1): 1-8, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-23631764

RESUMO

Abstract We aim to study the effect of low-dose aspirin and kefir on arterial blood pressure measurements and renal apoptosis in unhypertensive rats with 4 weeks salt diet. Forty adult male Sprague-Dawley rats were divided into five groups: control, high-salt (HS) (8.0% NaCl), HS+aspirin (10 mg/kg), HS+kefir (10.0%w/v), HS+aspirin +kefir. We measured sistolic blood pressure (SBP), mean arterial pressure (MAP), diastolic pressure, pulse pressure in the rats. Cathepsin B, L, DNA fragmentation and caspase-3 activities were determined from rat kidney tissues and rats clearance of creatinine calculated. Although HS diet increased significantly SBP, MAP, diastolic pressure, pulse pressure parameters compared the control values. They were not as high as accepted hypertension levels. When compared to HS groups, kefir groups significantly decrease Cathepsin B and DNA fragmentation levels. Caspase levels were elevated slightly in other groups according to control group. While, we also found that creatinine clearance was higher in HS+kefir and HS+low-dose aspirin than HS group. Thus, using low-dose aspirin had been approximately decreased of renal function damage. Kefir decreased renal function damage playing as Angiotensin-converting enzyme inhibitor. But, low-dose aspirin together with kefir worsened rat renal function damage. Cathepsin B might play role both apoptosis and prorenin-processing enzyme. But not caspase pathway may be involved in the present HS diet induced apoptosis. In conclusion, kefir and low-dose aspirin used independently protect renal function and renal damage induced by HS diet in rats.


Assuntos
Aspirina/administração & dosagem , Pressão Sanguínea/efeitos dos fármacos , Produtos Fermentados do Leite , Rim/efeitos dos fármacos , Cloreto de Sódio na Dieta/administração & dosagem , Cloreto de Sódio na Dieta/efeitos adversos , Inibidores da Enzima Conversora de Angiotensina/administração & dosagem , Animais , Apoptose/efeitos dos fármacos , Caspase 3/metabolismo , Catepsina B/metabolismo , Catepsina L/metabolismo , Produtos Fermentados do Leite/química , Inibidores de Ciclo-Oxigenase/administração & dosagem , Fragmentação do DNA/efeitos dos fármacos , Rim/patologia , Rim/fisiopatologia , Masculino , Ratos , Ratos Sprague-Dawley
8.
Ultrastruct Pathol ; 37(3): 218-26, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23650994

RESUMO

Abstract The authors investigate the curative effects of crude exopolysaccharides (EPS) produced by four Basidomycetes strains on the symptoms of alcoholic liver injury. EPSs were administered to experimental groups at levels of 100 mg per kg body weight per day for 7 days using an oral zonde needle after the onset of the disease. Serum levels of alanine transaminase (ALT), lactate dehydrogenase (LDH), DNA fragmentation, caspase-3 activities, and mitochondrial outer membrane integrity were determined following sacrifice of the rats. Light and transmission electron microscope (TEM) studies were performed on liver sections for histopathological and cytological evaluations. EPS that was obtained from Coprinus comatus OBCC 1014 decreased serum ALT level and increased outer membrane integrity, and allowed for the regaining of histologically and cytologically normal hepatocyte and tissue views. As a result, based on the obtained data, it can be argued that among all studied mushroom strains crude exopolysaccharides from Coprinus comatus OBCC 1014 strain have therapeutic potential for alcoholic liver injury according to control groups.


Assuntos
Basidiomycota/química , Polissacarídeos Fúngicos/farmacologia , Hepatopatias Alcoólicas/prevenção & controle , Fígado/efeitos dos fármacos , Substâncias Protetoras/farmacologia , Alanina Transaminase/sangue , Animais , Biomarcadores/sangue , Caspase 3/metabolismo , Citoproteção , Fragmentação do DNA , Modelos Animais de Doenças , Etanol , Polissacarídeos Fúngicos/isolamento & purificação , L-Lactato Desidrogenase/sangue , Fígado/metabolismo , Fígado/ultraestrutura , Hepatopatias Alcoólicas/sangue , Hepatopatias Alcoólicas/etiologia , Hepatopatias Alcoólicas/patologia , Masculino , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Microscopia Eletrônica de Transmissão , Substâncias Protetoras/isolamento & purificação , Ratos , Ratos Sprague-Dawley , Fatores de Tempo
9.
Cell Biochem Funct ; 31(3): 208-13, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22945768

RESUMO

Gallic acid, a polyphenyl class natural product from gallnut and green tea, is known to be antioxidant, anti-inflammatory and radical scavenger. In this study, we aimed to investigate the possible protective effects of gallic acid on paraoxonase and arylesterase activities in liver exposed to acute alcohol intoxication. Paraoxonase and arylesterase activities in liver tissue and serum aspartate aminotransferase, alanine aminotransferase and lactate dehydrogenase levels were measured. Histological investigations were also made. In our study, we observed a significant increase of serum alanine aminotransferase, aspartate aminotransferase and lactate dehydrogenase activities, which are indicators of liver damage after acute ethanol consumption. Gallic acid therapy has significantly reduced the increase in these biomarkers, indicating a possible hepatoprotective effect of gallic acid. Ethanol consumption caused a significant decrease in liver paraoxonase activity (P < 0.001). Gallic acid treatment partly restored this decreased paraoxonase activity, which resulted from ethanol administration. A gallic acid dose of 100 mg/kg was observed as highest restoring effect for paraoxonase activity (P < 0.05). The activity of arylesterase was decreased in the ethanol group as compared with the control group, but this was not significant. However, 50 mg/kg of gallic acid treatment restored the loss of this activity due to ethanol exposure (P < 0.001). We observed that gallic acid ameliorates the liver damage caused by excessive alcohol consumption in a dose-dependent way. Our results in this study showed that gallic acid might have a protective effect against alcoholic liver disease.


Assuntos
Intoxicação Alcoólica/enzimologia , Arildialquilfosfatase/metabolismo , Hidrolases de Éster Carboxílico/metabolismo , Etanol/toxicidade , Ácido Gálico/farmacologia , Fígado/efeitos dos fármacos , Substâncias Protetoras/farmacologia , Alanina Transaminase/sangue , Intoxicação Alcoólica/metabolismo , Intoxicação Alcoólica/patologia , Animais , Aspartato Aminotransferases/sangue , Feminino , L-Lactato Desidrogenase/sangue , Fígado/enzimologia , Fígado/patologia , Ratos , Ratos Sprague-Dawley
10.
Mol Biol Rep ; 39(12): 10249-55, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23053933

RESUMO

In order to investigate an association between alcohol consumption and lysosomal cysteine protease induced pancreatic injury and preventive effect of gallic acid as dose-dependent, we determined myeloperoxidase and malondialdehyde levels, serum amylase activities and cathepsin B and L activities in the cytosolic and lysosomal fractions of pancreatic tissue in the ethanol (8 g/kg) and ethanol plus gallic acid (at different doses 50, 100 and 200 mg/kg) given rats. Absolute ethanol (8 g/kg) was given by oral gavage. Gallic acid was dissolved in the saline (2 ml/kg) and administered before 30 min the oral administration of ethanol. Pancreatic myeloperoxidase and also malondialdehyde levels and serum amylase activities were measured. Besides, histological investigations were made. Cathepsin B activities in the cytosolic fraction were decreased by gallic acid (200 mg/kg) and increased in ethanol given rats. Cytosolic/lysosomal ratio of cathepsin B and L were found to be low in the all doses of gallic acid as compared to ethanol group. Serum amylase, pancreatic myeloperoxidase activities and malondialdehyde levels in the ethanol group were higher than in the control group. These were not statistically significant for myeloperoxidase and malondialdehyde. Also, our histopathologic results indicated that ethanol administration increased pancreatic tissue injury. Gallic acid especially at 200 mg/kg improved ethanol-mediated pancreatic tissue damage.In conclusion, gallic acid treatments were decreased release of lysosomal cathepsin B and L enzymes into cytoplasmic fraction and prevented alcohol mediated pancreatic tissue injury. Preventive effect of gallic acid might be dose-dependent.


Assuntos
Catepsina B/metabolismo , Catepsina L/metabolismo , Sequestradores de Radicais Livres/administração & dosagem , Ácido Gálico/administração & dosagem , Pancreatite Alcoólica/prevenção & controle , Células Acinares/efeitos dos fármacos , Células Acinares/metabolismo , Células Acinares/patologia , Amilases/sangue , Animais , Citosol/enzimologia , Etanol , Feminino , Sequestradores de Radicais Livres/farmacologia , Ácido Gálico/farmacologia , Lisossomos/enzimologia , Malondialdeído/metabolismo , Pâncreas/efeitos dos fármacos , Pâncreas/enzimologia , Pâncreas/patologia , Pancreatite Alcoólica/sangue , Pancreatite Alcoólica/induzido quimicamente , Pancreatite Alcoólica/enzimologia , Peroxidase/metabolismo , Ratos , Ratos Sprague-Dawley
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