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1.
Environ Sci Pollut Res Int ; 29(36): 54827-54841, 2022 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-35312919

RESUMO

The current study was conducted to assess the beneficial effect of selenium (Se) on maneb-induced cardiotoxicity and fatty acid alterations in adult mice. Swiss albino male mice were assigned into four experimental groups. The first group consisted of negative controls. The second group represented the positive controls where mice received daily, via the diet, sodium selenite at a dose of 0.2 mg/kg. For the third group, mice were subjected to intraperitoneal injections of maneb (30 mg/kg BW). The fourth group (MB+Se) received daily the same dose of maneb as group 3 along with sodium selenite at the same dose as group 2. Mice exposure to maneb caused cardiotoxicity as indicated by an increase in malondialdehyde, hydrogen peroxide, and protein carbonyl levels, and an alteration of the antioxidant defense system (catalase, glutathione peroxidase, superoxide dismutase, glutathione, and vitamin C). Plasma lactate dehydrogenase activity and total cholesterol, triglyceride, and low-density lipoprotein cholesterol levels increased, while high-density lipoprotein cholesterol level decreased. Results showed also a decrease in the amount of n-3 PUFA, docosahexaenoic, docosapentaenoic, and eicosapentaenoic acids. However, an increase in the levels of MUFA, cis-vaccenic, and palmitoleic acids was observed. Co-administration of Se restored the parameters indicated above to near control values. The histopathological findings confirmed the biochemical results. Selenium could be a useful and efficient agent against maneb-induced cardiotoxicity.


Assuntos
Antioxidantes , Cardiotoxicidade , Maneb , Selênio , Animais , Antioxidantes/farmacologia , Colesterol , Peroxidação de Lipídeos , Maneb/toxicidade , Camundongos , Estresse Oxidativo , Selênio/farmacologia , Selenito de Sódio , Superóxido Dismutase/metabolismo
2.
Biomed Res Int ; 2020: 1315202, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-31998777

RESUMO

Oleuropein and hydroxytyrosol, as major compounds of olive leaves, have been reported to exert numerous pharmacological properties, including anticancer, antidiabetic, and anti-inflammatory activities. The purpose of this study is to evaluate and compare the protective effect of oleuropein- and hydroxytyrosol-rich extracts, derived from olive leaves, on high-fat diet-induced lipid metabolism disturbance and liver injury in rats. In this respect, four groups of male rats (8 per group) were used: control group (Control), group treated with high-fat diet (HFD), group treated with HFD and oleuropein (HFD + OLE), and group treated with HFD and hydroxytyrosol (HFD + HYD). The current research showed that the treatment with the HFD increased the body weight and adipose tissue mass in male rats. Moreover, the plasma levels of triglycerides, total cholesterol, LDL-cholesterol, AST, ALT, LDH, and TNF-α were also raised. The hepatic immunohistochemical analysis revealed a significant increase in the expression of inflammatory genes (COX-2, NF-κB, and TNF-α). Equally, it showed a rise of the apoptotic markers (a decrease in the expression of the Bcl-2 and an increase of the P53). In addition, the oral administration of oleuropein- and hydroxytyrosol-rich olive leaf extracts at 16 mg/kg similarly reduced the body weight and adipose tissue mass and improved the lipid profile. Moreover, these extracts, mainly the hydroxytyrosol-rich extract, reduced the elevated liver enzymes, enhanced the antioxidant status, and attenuated the liver inflammation and apoptosis. These findings suggest that the oleuropein- and hydroxytyrosol-rich olive leaf extracts possessed hypolipidemic and hepatoprotective effects against the HFD-induced metabolic disorders by enhancing the antioxidative defense system and blocking the expression of the proteins involved in inflammation and liver damage.


Assuntos
Gorduras na Dieta/efeitos adversos , Iridoides/farmacologia , Hepatopatias , Fígado , Olea/química , Álcool Feniletílico/análogos & derivados , Extratos Vegetais/farmacologia , Folhas de Planta/química , Animais , Gorduras na Dieta/farmacologia , Glucosídeos Iridoides , Iridoides/química , Metabolismo dos Lipídeos , Fígado/lesões , Fígado/metabolismo , Fígado/patologia , Hepatopatias/tratamento farmacológico , Hepatopatias/metabolismo , Hepatopatias/patologia , Masculino , Álcool Feniletílico/química , Álcool Feniletílico/farmacologia , Extratos Vegetais/química , Ratos
3.
Environ Sci Pollut Res Int ; 27(8): 8091-8102, 2020 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-31897980

RESUMO

Zinc is one of the important essential trace minerals to human health due to its antioxidant properties. The present study was conducted to elucidate its potential protective role against maneb-induced nephrotoxicity. For this purpose, animals were randomly divided into four groups of six each. Mice of group I (negative controls) have received daily 0.5 ml of distilled water, a solvent of maneb. Mice of group II (MB) have received 30 mg/kg bw of maneb daily by intraperitoneal way. Mice of group III (MB + Zn) have received the same dose of maneb as group II, along with ZnSO4 (30 mg/kg bw) daily. Mice of group IV (Zn), considered as positive controls, have received the same dose of ZnSO4 as group III daily. Our results revealed that ZnSO4 co-administration to maneb-treated mice decreased kidney levels of malondialdehyde, hydrogen peroxide, protein carbonyls, and advanced oxidation protein products; the levels of non-enzymatic antioxidants like vitamin C, glutathione, and metallothionein. It recovered the alteration of antioxidant enzyme activities (catalase, superoxide dismutase, and glutathione peroxidase) and attenuated DNA fragmentation. Furthermore, this essential trace element was also able to alleviate kidney biomarkers' alterations by lowering plasma levels of creatinine, urea, uric acid, and lactate dehydrogenase. In addition, the histopathological changes induced by maneb were improved following zinc administration. Our results indicated that zinc might be beneficial against maneb-induced renal oxidative damage in mice.


Assuntos
Glutationa Peroxidase , Glutationa , Rim , Maneb , Superóxido Dismutase , Zinco , Animais , Camundongos , Antioxidantes , Dano ao DNA , Glutationa/química , Glutationa Peroxidase/química , Glutationa Peroxidase/metabolismo , Rim/fisiopatologia , Estresse Oxidativo , Distribuição Aleatória , Superóxido Dismutase/química , Zinco/química
4.
Food Funct ; 9(6): 3220-3234, 2018 Jun 20.
Artigo em Inglês | MEDLINE | ID: mdl-29781491

RESUMO

In the present study, we investigated the protective effects of oleuropein- and hydroxytyrosol-rich extracts obtained from olive leaves against bisphenol A (BPA)-induced hyperlipidemia and liver injury in male rats. For this purpose, four groups of male rats (8 per group) were used: control group (Control), rats treated with BPA, rats treated with both BPA and oleuropein (OLE-BPA), and rats treated with both BPA and hydroxytyrosol (HYT-BPA). After 60 days of treatment, the results obtained using the DXA technique showed that treatment with BPA (10 mg per kg b.w.) increased the body weight and adipose tissue mass in male rats. Moreover, plasma levels of triglycerides, total cholesterol, LDL-cholesterol, AST, ALT, LDH, and TNF-α increased. The immunohistochemical analysis revealed a significant increase in the expression of COX-2 and p53 and a decrease in the expression of Bcl-2 related to liver inflammation. Oral administration of oleuropein and hydroxytyrosol-rich extracts obtained from olive leaves at 16 mg kg-1 reduced both the body weight and adipose tissue mass. These extracts were able to ameliorate liver damage and improve the elevated levels of TG and liver enzymes of BPA-treated rats possibly through enhancing CAT and SOD activities. Western blot results revealed that administration of the abovementioned extracts decreased the protein expression of NF-κB and TNF-α through the p38 signaling pathway. Overall, the findings suggest that the olive leaf extracts possess hypolipidemic and hepatoprotective effects against BPA-induced metabolic disorders through enhancing the antioxidative defense system and regulating the important signaling pathway activities.


Assuntos
Compostos Benzidrílicos/efeitos adversos , Iridoides/administração & dosagem , Metabolismo dos Lipídeos/efeitos dos fármacos , Hepatopatias/tratamento farmacológico , Olea/química , Fenóis/efeitos adversos , Álcool Feniletílico/análogos & derivados , Extratos Vegetais/administração & dosagem , Animais , Antioxidantes/administração & dosagem , Humanos , Glucosídeos Iridoides , Hepatopatias/etiologia , Hepatopatias/metabolismo , Masculino , Álcool Feniletílico/administração & dosagem , Folhas de Planta/química , Ratos
5.
Food Chem Toxicol ; 106(Pt A): 455-465, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28595958

RESUMO

The purpose of this study was to evaluate the protective effect of ethanolic olive fruit extract (OFE) and its phenolic compound, oleuropein (OLE), against hepato-renal toxicity induced by deltamethrin (DEM), a synthetic pyrethroid, in Wistar rats. The kidney and liver tissues were collected after 30 days of treatment for subsequent investigation. Rats that were given DEM had a highly significant elevation in the serum biomarkers as well as hepatic and renal levels of lipid peroxidation (MDA). Additionally, a significant reduction in the total antioxidant capacity (ABTS+), superoxide dismutase (SOD) and catalase (CAT) activities was noted. This toxic effect was confirmed by histological studies and the expression levels of inflammatory (cox-2) and apoptotic genes (bcl-2 and p53). The findings for the OFE and OLEtreated groups highlighted the efficacy of olive fruit phenolic compounds as hepatic and renal-protectant in DEM-induced hepato-renal toxicity through improving the oxidative status as well as suppressing inflammation and apoptosis. Therefore, they may be used as protective natural compounds against DEM-induced hepato-renal toxicity.


Assuntos
Inseticidas/toxicidade , Rim/efeitos dos fármacos , Fígado/efeitos dos fármacos , Nitrilas/toxicidade , Olea/química , Estresse Oxidativo/efeitos dos fármacos , Fenóis/administração & dosagem , Extratos Vegetais/administração & dosagem , Substâncias Protetoras/administração & dosagem , Piretrinas/toxicidade , Animais , Apoptose/efeitos dos fármacos , Catalase/metabolismo , Rim/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Fígado/metabolismo , Masculino , Ratos , Ratos Wistar , Superóxido Dismutase/metabolismo
6.
J Food Sci Technol ; 54(2): 313-325, 2017 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-28242930

RESUMO

This study investigated the potential effects of fermented sardinelle protein hydrolysates (FSPHs) obtained by two proteolytic bacteria, Bacillus subtilis A26 (FSPH-A26) and Bacillus amyloliquefaciens An6 (FSPH-An6), on hypercaloric diet (HCD) induced hyperglycemia and oxidative stress in rats. Effects of FSPHs on blood glucose level, glucose tolerance, α-amylase activity and hepatic glycogen content were investigated, as well as their effect on the oxidative stress state. Biochemical findings revealed that, while undigested sardinelle proteins did not exhibit hypoglycemic activity, oral administration of FSPHs to HCD-fed rats reduced significantly α-amylase activity as well as glycemia and hepatic glycogen levels. Further, the treatment with FSPHs improved the redox status by decreasing the levels of lipid peroxidation products and increasing the activities of the antioxidant enzymes (superoxide dismutase, glutathione peroxidase and catalase) and the level of glutathione in the liver and kidneys, as compared to those of HCD-fed rats. FSPHs were also found to exert significant protective effects on liver and kidney functions, evidenced by a marked decrease in alkaline phosphatase activity and a modulation of creatinine and uric acid contents. These results indicated the beneficial effect of FSPHs on the prevention from hyperglycemia and oxidative stress.

7.
Life Sci ; 176: 54-66, 2017 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-27460865

RESUMO

AIMS: The present study aims to evaluate the antiobesity, hypolipidemic and cardioprotective effects of fermented sardinelle (Sardinella aurita) protein hydrolysates (FSPHs) produced with two proteolytic bacteria, Bacillus subtilis A26 (FSPH-A26) and Bacillus amyloliquefaciens An6 (FSPH-An6). MAIN METHODS: Wistar rats were fed during 10weeks a standard laboratory diet, a high caloric diet (HCD) and a HCD coupled with the oral administration of sardinelle meat flour (SMF) or FSPHs. KEY FINDINGS: HCD caused hyperlipidemia and increased body weight (BW). The daily oral administration of FSPHs or SMF reduced the total cholesterol (TC), triglycerides (TG) and low-density lipoprotein cholesterol (LDL-c) serum levels, and increased the level of high-density lipoprotein cholesterol (HDL-c). Nevertheless, FSPHs were found to be more efficient than SMF. FSPHs also lowered hepatic TC and TG content and decreased the pancreatic lipase activity. Further, the administration of FSPHs or SMF decreased the BW gain, the food intake and the relative epididymal adipose tissue weight. FSPHs exhibited a potent cardioprotective effect against heart attack, which was demonstrated by returning atherogenic indexes to their normal levels and the conservation of standard histological structure of the heart and aorta. SIGNIFICANCE: The overall results indicate that FSPHs contained bioactive peptides which significantly attenuated hyperlipidemia, and might reduce the risk of cardiovascular disease (CVD) in rats fed HCD.


Assuntos
Gorduras na Dieta/efeitos adversos , Farinha de Peixe , Proteínas de Peixes , Frutose/efeitos adversos , Hipolipemiantes , Obesidade , Hidrolisados de Proteína , Animais , Gorduras na Dieta/farmacologia , Proteínas de Peixes/química , Proteínas de Peixes/farmacologia , Frutose/farmacologia , Hipolipemiantes/química , Hipolipemiantes/farmacologia , Lipídeos/sangue , Masculino , Obesidade/sangue , Obesidade/induzido quimicamente , Obesidade/tratamento farmacológico , Obesidade/fisiopatologia , Hidrolisados de Proteína/química , Hidrolisados de Proteína/farmacologia , Ratos , Ratos Wistar
8.
Hum Exp Toxicol ; 36(11): 1146-1157, 2017 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-27941167

RESUMO

Several metals including barium (Ba) known as environmental pollutants provoke deleterious effects on human health. The present work pertains to the potential ability of selenium (Se) and/or vitamin C, used as nutritional supplements, to alleviate the toxic effects induced by barium chloride (BaCl2) in the heart of adult rats. Animals were randomly divided into seven groups of six each: group 1, serving as negative controls, received distilled water; group 2 received in their drinking water BaCl2 (67 ppm); group 3 received both Ba and Se (sodium selenite 0.5 mg kg-1 of diet); group 4 received both Ba and vitamin C (200 mg kg-1 bodyweight) via force feeding; group 5 received Ba, Se, and vitamin C; and groups 6 and 7, serving as positive controls, received either Se or vitamin C for 21 days. The exposure of rats to BaCl2 caused cardiotoxicity as monitored by an increase in malondialdehyde, hydrogen peroxide, and advanced oxidation protein product levels, a decrease in Na+-K+ adenosine triphosphatase (ATPase), Mg2+ ATPase, and acetylcholinesterase activities and in antioxidant defense system (catalase, glutathione peroxidase, superoxide dismutase, glutathione, and nonprotein thiols). Plasma lactate dehydrogenase and creatine kinase activities, total cholesterol, triglyceride, and low-density lipoprotein-cholesterol levels increased, while high-density lipoprotein-cholesterol level decreased. Coadministration of Se and/or vitamin C restored the parameters indicated above to near control values. The histopathological findings confirmed the biochemical results. Se and vitamin C may be a promising therapeutic strategy for Ba-induced heart injury.


Assuntos
Ácido Ascórbico/farmacologia , Compostos de Bário/toxicidade , Cloretos/toxicidade , Cardiopatias/induzido quimicamente , Selênio/farmacologia , Acetilcolinesterase/metabolismo , Adenosina Trifosfatases/metabolismo , Animais , Ácido Ascórbico/administração & dosagem , Dieta , Regulação Enzimológica da Expressão Gênica/efeitos dos fármacos , Coração/efeitos dos fármacos , Cardiopatias/tratamento farmacológico , Peróxido de Hidrogênio , Peroxidação de Lipídeos , Miocárdio/enzimologia , Miocárdio/patologia , Tamanho do Órgão/efeitos dos fármacos , Ratos , Ratos Wistar , Selênio/administração & dosagem , ATPase Trocadora de Sódio-Potássio/metabolismo
9.
Arch Physiol Biochem ; 122(3): 130-40, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26835741

RESUMO

CONTEXT: Pomegranate (Punica granatum L., Punicaceae) is known to possess enormous antioxidant activity. OBJECTIVE: This study investigates the protective effects of pomegranate peel against barium-mediated renal damage. MATERIALS AND METHODS: Rats were exposed during 21 days either to barium (67 ppm), barium + pomegranate peel (5% of diet) or to only pomegranate peel (5% of diet). RESULTS: Exposure rats to barium provoked a significant increase in kidney malondialdehyde (MDA), advanced oxidation protein products (AOPP) and hydrogen peroxide (H2O2) levels. Creatinine, urea and uric acid levels in plasma and urine were also modified. Superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) activities, non protein thiol (NPSH) and reduced glutathione (GSH) levels were decreased. Metallothionein (MT) production was increased and their genes expressions were up-regulated. All these changes were improved by dietary pomegranate peel. Moreover, the distorted histoarchitecture in kidney of barium group was alleviated by pomegranate peel. CONCLUSION: Our data showed, for the first time, the protective effects of pomegranate peel against barium-induced renal oxidative damage.


Assuntos
Compostos de Bário/toxicidade , Cloretos/toxicidade , Nefropatias/prevenção & controle , Lythraceae/química , Extratos Vegetais/farmacologia , Animais , Antioxidantes/metabolismo , Nefropatias/induzido quimicamente , Nefropatias/patologia , Masculino , Oxirredução , Estresse Oxidativo/efeitos dos fármacos , Ratos , Ratos Wistar
10.
Food Funct ; 6(9): 3098-108, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26215160

RESUMO

Oxidative stress generated by an excessive production of free radicals has been linked to the development of several health problems such as cardiovascular diseases. We investigated the protective efficacy of Extra Virgin Olive Oil (EVOO) and its lipophilic fraction (OOLF) and hydrophilic fraction (OOHF) against the cardiotoxicity and DNA damage induced by co-exposure to aluminum (AlCl3) and acrylamide (ACR). Rats were divided into eight groups of six each: controls, AlCl3 (50 mg per kg body weight) administered via drinking water and ACR (20 mg per kg body weight) given by gavage, combined group plus EVOO (300 µl); combined group plus the hydrophilic fraction (1 ml); combined group plus the lipophilic fraction (300 µl); extra virgin olive oil (EVOO) and its fractions were administered daily by gavage for 21 days. Three other groups, considered as positive controls, received either EVOO, OOLF or OOLH. Exposure of rats to both AlCl3 and ACR provoked oxidative stress objectified by an increase in MDA, AOPP and a decrease in GSH, NPSH and vitamin C levels. The activities of CAT, GPx and SOD were also decreased. EVOO and its OOLF fraction exhibited a pronounced enhancement of antioxidant status while a partial recovery in the antioxidant status was obtained with the OOHF fraction. Plasma LDH and CK activities, TC, LDL-C levels, TC/HDL-C and LDL-C/HDL-C ratios were increased, while HDL-C and TG decreased in rats treated with both AlCl3 and ACR. Co-administration of EVOO, OOLF or OOHF to treated rats restored cardiac biomarkers and lipid profile to near-normal values. Histological studies and DNA damage confirmed the biochemical parameters and the beneficial role of EVOO and its two fractions. Our results suggest that extra virgin olive oil and its two fractions can decrease the frequency of cardiac complications and genotoxicity.


Assuntos
Acrilamida/toxicidade , Alumínio/toxicidade , Doenças Cardiovasculares/dietoterapia , Dano ao DNA/efeitos dos fármacos , Miocárdio/metabolismo , Azeite de Oliva/metabolismo , Estresse Oxidativo/efeitos dos fármacos , Animais , Doenças Cardiovasculares/induzido quimicamente , Doenças Cardiovasculares/genética , Doenças Cardiovasculares/metabolismo , Coração/efeitos dos fármacos , Humanos , Masculino , Olea/metabolismo , Azeite de Oliva/química , Ratos
11.
Exp Toxicol Pathol ; 67(7-8): 413-25, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25963946

RESUMO

Bisphenol A (BPA) is a chemical found in hard plastics and the coatings of food and drinks cans which can behave in a similar way to estrogen and other hormones in the human body. This study aimed to evaluate the significance of the treatment with oleuropein and hydroxytyrosol olive leaves rich extracts in reducing functional perturbations and oxidative stress arising from BPA treatment in livers and kidneys of lactating mother rats and their pups'. For this, four groups of lactating mothers were used: controls (group A), treated with bisphenol A (group B), treated with bisphenol A and oleuropein (group C) and with bisphenol A and hydroxytyrosol (group D). As results, we had found, in BPA treated group, either in mothers or in their pups', a significant decrease in morphological parameters, in catalase activity and in total antioxidant capacity associated to an increase in malondialdehyde levels in livers and kidneys. For these rats, the histological aspect showed, also, deep changes. Indeed, we had observed, in livers, hepatocellular necrosis associated to leucocytes infiltration and in kidneys tubular and glomerular necrosis. The co-treatments with BPA and oleuropein (group C) or with BPA and hydroxytyrosol (group D) ameliorate all morphological, biochemical and histological parameters as compared to BPA treated group B. The analysis of BPA and its derivatives with LC-MS/MS showed changes in their localizations between serum, livers or kidneys in all studied groups. In conclusion, the present study demonstrates the hepato-protective and reno-protective effects of oleuropein and hydroxytyrosol olive leaves extracts from BPA and its derivates toxicity.


Assuntos
Antioxidantes/farmacologia , Compostos Benzidrílicos/toxicidade , Iridoides/farmacologia , Fenóis/toxicidade , Álcool Feniletílico/análogos & derivados , Animais , Cromatografia Líquida de Alta Pressão , Feminino , Glucosídeos Iridoides , Rim/efeitos dos fármacos , Lactação , Fígado/efeitos dos fármacos , Mães , Estresse Oxidativo/efeitos dos fármacos , Álcool Feniletílico/farmacologia , Extratos Vegetais/farmacologia , Folhas de Planta , Ratos , Espectrometria de Massas em Tandem
12.
Biomed Environ Sci ; 27(9): 695-706, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25256859

RESUMO

OBJECTIVE: The present study investigated the protective role of Hyparrhenia hirta (H. hirta) against sodium nitrate (NaNO3)-induced hepatoxicity. METHODS: Male Wistar rats were randomly divided into three groups: a control group and two treated groups during 50 d with NaNO3 administered either alone in drinking water or co-administered with H. hirta. RESULTS: NaNO3 treatment induced a significant increase in serum levels of glucose, total cholesterol and triglyceride while serum total protein level decreased significantly. Transaminases and lactate deshydrogenase activities in serum were elevated indicating hepatic cells' damage after treatment with NaNO3. The hyperbilirubinemia and the increased serum gamma glutamyl transferase activities suggested the presence of cholestasis in NaNO3 exposed rats. In parallel, a significant increase in malondialdehyde level along with a concomitant decrease in total glutathione content and superoxide dismutase, catalase and glutathione peroxidase activities were observed in the liver after NaNO3 treatment. Furthermore, nitrate caused a significant induction of DNA fragmentation. These modifications in NaNO3-treated rats corresponded histologically with hepatocellular necrosis and mononuclear cells infiltration. H. hirta supplementation showed a remarkable amelioration of the abnormalities cited above. CONCLUSION: The results concluded that the treatment with H. hirta had a significant role in protecting the animals from nitrate-induced liver dysfunction.


Assuntos
Doença Hepática Induzida por Substâncias e Drogas/prevenção & controle , Fígado/efeitos dos fármacos , Fitoterapia , Extratos Vegetais/uso terapêutico , Poaceae , Animais , Fragmentação do DNA/efeitos dos fármacos , Avaliação Pré-Clínica de Medicamentos , Ingestão de Alimentos/efeitos dos fármacos , Flavonoides/análise , Glutationa/efeitos dos fármacos , Peroxidação de Lipídeos/efeitos dos fármacos , Lipídeos/sangue , Fígado/metabolismo , Fígado/patologia , Masculino , Camundongos , Nitratos , Tamanho do Órgão/efeitos dos fármacos , Extratos Vegetais/farmacologia , Poaceae/química , Distribuição Aleatória , Ratos Wistar
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