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1.
Pharm Biol ; 55(1): 1082-1088, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28193098

ABSTRACT

CONTEXT: Syzygium cumini (L.) Skeels (Myrtaceae) is a medicinal plant widely used in folk medicine for the treatment of diabetes mellitus (DM). However, studies on the use of this plant and of nanoparticle formulations against DM-related fungal infections are scarce. OBJECTIVE: To evaluate the effect of the treatments with aqueous seed extract of S. cumini (ASc) and ASc-loaded polymeric nanoparticles (NPASc) on biochemical parameters in Candida albicans-infected diabetic rats. MATERIALS AND METHODS: Male Wistar rats were divided into eight groups: Control, DM, C. albicans, C. albicans + ASc, C. albicans + NPASc, DM + C. albicans, DM + C. albicans + ASc and DM + C. albicans + NPASc. Rats were daily treated with ASc or NPASc (100 mg/kg) for 21 days. Biochemical parameters in serum and urine, advanced oxidation protein product (AOPP) and TBARS levels in the serum, kidney, liver and pancreas and N-acetyl-ß-d-glucosaminidase (NAG) activities in kidney and urine were evaluated. RESULTS: Biochemical and oxidative stress parameters increased in rats with DM and/or candidiasis. NPASc was more effective than ASc in decreasing glucose (56%), cholesterol (33%) and creatinine (51%) levels; serum (16%) and pancreatic (46%) AOPP and renal (48%) TBARS levels when compared with DM + C. albicans group. In C. albicans group, both treatments decreased NAG activity but did not decrease creatinine levels. CONCLUSIONS: These data suggest that the use of nanotechnology is able to improve plant extract properties such as antioxidant activity that may be useful in diabetes-related complications.


Subject(s)
Antifungal Agents/pharmacology , Antioxidants/pharmacology , Candida albicans/drug effects , Candidiasis/drug therapy , Diabetes Mellitus, Experimental/drug therapy , Diabetes Mellitus, Type 1/drug therapy , Nanoparticles , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Syzygium/chemistry , Animals , Antifungal Agents/chemistry , Antifungal Agents/isolation & purification , Antioxidants/chemistry , Antioxidants/isolation & purification , Biomarkers/blood , Biomarkers/urine , Candidiasis/blood , Candidiasis/microbiology , Candidiasis/urine , Diabetes Mellitus, Experimental/blood , Diabetes Mellitus, Experimental/chemically induced , Diabetes Mellitus, Experimental/urine , Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 1/chemically induced , Diabetes Mellitus, Type 1/urine , Drug Compounding , Kidney/drug effects , Kidney/metabolism , Liver/drug effects , Liver/metabolism , Male , Pancreas/drug effects , Pancreas/metabolism , Phytotherapy , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Plants, Medicinal , Rats, Wistar , Seeds , Solvents/chemistry , Streptozocin
2.
J. physiol. biochem ; 70(2): 321-330, jun. 2014.
Article in English | IBECS | ID: ibc-122954

ABSTRACT

Syzygium cumini (S. cumini) is a plant known for its antidiabetic properties. The aim of this study was to evaluate the effect of Sc aqueous leaf extract (ASc) on adenosine deaminase (ADA) activity in erythrocytes (RBCs) exposed to high glucose concentrations (30 mM) in vitro. We also investigated the effects of the main phenolic compounds found in ASc (gallic acid, rutin, and chlorogenic acid) and the effects of insulin, caffeine, and dipyridamole, which are substances involved in the adenosine metabolism, on ADA activity in vitro. Blood samples were obtained from healthy volunteers and a suspension of RBCs was used for the determination of ADA activity. The results showed that: (1) the effect of ASc on ADA activity was more significant than the combination of phenolic compounds; (2) insulin, caffeine, or dipyridamole prevented high glucose increase of ADA activity at doses as low as 50 μU/mL, 25 μM, and 1 μM, respectively; (3) the inhibitory effect caused by ASc on erythrocyte ADA activity remained practically the same after the combination of the extract with insulin or caffeine; (4) when RBCs were exposed to ASc plus dipyridamole, this chemical attenuated the effect of ASc on ADA activity, suggesting an antagonism or a competition with ASc by the same site of action. Therefore, ASc was more effective in preventing the increase in ADA activity than phenolic compounds, suggesting that ASc may collaborate to improve endothelial dysfunction, antioxidant, anti-inflammatory, and antithrombotic properties of adenosine by affecting its metabolism. The results of this study help to provide evidence of the empirically supported benefits of the use of S. cumini in diabetes


Subject(s)
Humans , Eugenia , Plant Extracts/pharmacokinetics , Phenols/pharmacokinetics , Adenosine Deaminase , Polycythemia/drug therapy , Diabetes Mellitus/drug therapy , Hyperglycemia/prevention & control , Anti-Inflammatory Agents/pharmacokinetics , Fibrinolytic Agents/pharmacokinetics , Antioxidants/pharmacokinetics
3.
J Physiol Biochem ; 70(2): 321-30, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24407852

ABSTRACT

Syzygium cumini (S. cumini) is a plant known for its antidiabetic properties. The aim of this study was to evaluate the effect of Sc aqueous leaf extract (ASc) on adenosine deaminase (ADA) activity in erythrocytes (RBCs) exposed to high glucose concentrations (30 mM) in vitro. We also investigated the effects of the main phenolic compounds found in ASc (gallic acid, rutin, and chlorogenic acid) and the effects of insulin, caffeine, and dipyridamole, which are substances involved in the adenosine metabolism, on ADA activity in vitro. Blood samples were obtained from healthy volunteers and a suspension of RBCs was used for the determination of ADA activity. The results showed that: (1) the effect of ASc on ADA activity was more significant than the combination of phenolic compounds; (2) insulin, caffeine, or dipyridamole prevented high glucose increase of ADA activity at doses as low as 50 µU/mL, 25 µM, and 1 µM, respectively; (3) the inhibitory effect caused by ASc on erythrocyte ADA activity remained practically the same after the combination of the extract with insulin or caffeine; (4) when RBCs were exposed to ASc plus dipyridamole, this chemical attenuated the effect of ASc on ADA activity, suggesting an antagonism or a competition with ASc by the same site of action. Therefore, ASc was more effective in preventing the increase in ADA activity than phenolic compounds, suggesting that ASc may collaborate to improve endothelial dysfunction, antioxidant, anti-inflammatory, and antithrombotic properties of adenosine by affecting its metabolism. The results of this study help to provide evidence of the empirically supported benefits of the use of S. cumini in diabetes.


Subject(s)
Adenosine Deaminase/blood , Erythrocytes/drug effects , Hyperglycemia/blood , Phenols/pharmacology , Plant Extracts/pharmacology , Syzygium/chemistry , Chromatography, High Pressure Liquid , Dose-Response Relationship, Drug , Erythrocytes/enzymology , Humans , In Vitro Techniques
4.
Inflammation ; 36(6): 1539-47, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23933911

ABSTRACT

Metabolic syndrome (MetS) leads to changes in enzymatic activities, oxidative and inflammatory parameters. Adenosine deaminase (ADA), dipeptidyl peptidase IV (DPP-IV), butyrylcholinesterase (BuChE) and γ-glutamyltransferase (γ-GT) activities, C-reactive protein (hsCRP) and nitric oxide levels (NOx), as well as oxidative stress markers were analyzed in 39 subjects with MetS and 48 controls. Also, the influence of body mass index (BMI) and anthropometric measurements were evaluated. Disturbances in antioxidant defenses and higher γ-GT and BuChE activities, NOx and hsCRP levels were observed in subjects with MetS. These findings remained associated with MetS after adjustment for BMI, except for hsCRP. ADA was correlated with age, insulin levels and HOMA-IR index in MetS. DPP-IV and total cholesterol (TC), BuChE activity and TC, and VIT C and hsCRP levels also were correlated. The analyzed parameters may reflect the inflammatory state of the MetS, and could contribute to prevention and control of various aspects of this syndrome.


Subject(s)
Butyrylcholinesterase/metabolism , Metabolic Syndrome/enzymology , Metabolic Syndrome/metabolism , Oxidative Stress/immunology , gamma-Glutamyltransferase/metabolism , Adenosine Deaminase/metabolism , Biomarkers/metabolism , Body Mass Index , C-Reactive Protein/metabolism , Cholesterol/blood , Dipeptidyl Peptidase 4/metabolism , Female , Humans , Inflammation/immunology , Male , Middle Aged , Nitric Oxide/metabolism
5.
Clin Biochem ; 45(13-14): 1081-5, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22709933

ABSTRACT

OBJECTIVES: Metabolic syndrome (MetS) is considered a state of chronic inflammation. This study aimed to ascertain selected parameters of purinergic and cholinergic systems related to glucose metabolism and inflammation, as well as (γ)-glutamyltransferase (GGT) and N-acetyl-b-glucosaminidase (NAG) activities and lipoperoxidation in lymphocytes of patients with MetS. DESIGN AND METHODS: The adenosine deaminase (ADA), dipeptidyl peptidase IV (DPP-IV), acetylcholinesterase (AChE), GGT and NAG activities, as well as thiobarbituric acid reactive substances (TBARS) levels were investigated in lymphocytes of patients with MetS (n=38) and healthy volunteers (n=41). We also evaluated the insulin levels, anthropometric measurements and routine biochemical analyses. RESULTS: ADA (p<0.05), DPP-IV and AChE (p<0.0001) activities were higher in patients with MetS when compared to the control group. Furthermore, we observed correlations between ADA and DPP-IV activities (p=0.0002; r=0.5945), TBARS levels and ADA (p=0.0021; r=0.5172) and DPP-IV activities (p=0.0022; r=0.5010). CONCLUSIONS: Our findings showed that MetS might cause tissue distress that disturbed lymphocytic ADA, DPP-IV and AChE activities in response to inflammatory stimuli. These alterations evidence clinical abnormalities, since these enzymatic systems are able to regulate several aspects of adipose tissue function and inflammatory state of MetS and could be used successfully both for preventing and for halting the progression of MetS.


Subject(s)
Lipid Peroxidation , Lymphocytes/enzymology , Metabolic Syndrome/enzymology , Adult , Biomarkers/analysis , Case-Control Studies , Dipeptidyl Peptidase 4/metabolism , Enzyme Activation , Enzyme Assays , Female , Humans , Inflammation/enzymology , Insulin/metabolism , Male , Metabolic Syndrome/diagnosis , Middle Aged , Risk Factors , Thiobarbituric Acid Reactive Substances/metabolism , beta-N-Acetyl-Galactosaminidase/metabolism , gamma-Glutamyltransferase/metabolism
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