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1.
Biomed Res Int ; 2016: 2872708, 2016.
Article in English | MEDLINE | ID: mdl-27990425

ABSTRACT

Due to the development of praziquantel (PZQ) schistosomes resistant strains, the discovery of new antischistosomal agents is of high priority in research. This work reported the in vitro and in vivo effects of the edible and ornamental pomegranate extracts against Schistosoma mansoni. Leaves and stem bark ethanolic extracts of both dried pomegranates were prepared at 100, 300, and 500 µg/mL for in vitro and 600 and 800 mg/kg for in vivo. Adult worms Schistosoma mansoni in RPMI-1640 medium for in vitro and S. mansoni infected mice for in vivo tests were obtained from Theodor Bilharz Research Institute, Cairo, Egypt. In vitro activity was manifested by significant coupled worms separation, reduction of motor activity, lethality, and ultrastructural tegumental alterations in adult worms. In vivo activity was manifested revealed by significant reduction of hepatic granulomas number and diameter, decreased number of bilharzial eggs in liver tissues, lowered liver inflammatory infiltration, decreased hepatic fibrosis, and inducible nitric oxide synthase (iNOS) expression. Ethanolic stem bark extract of edible pomegranate exhibited highest antischistosomal activities both in vitro and in vivo. Therefore, pomegranate showed a good potential to be used as a promising new candidate for the development of new schistosomicidal agents.


Subject(s)
Anthelmintics/pharmacology , Ethanol/chemistry , Lythraceae/chemistry , Plant Extracts/pharmacology , Schistosoma mansoni/drug effects , 3T3 Cells , Administration, Oral , Animals , Anthelmintics/administration & dosage , Bacteria/isolation & purification , Cell Death/drug effects , Endotoxins/biosynthesis , Female , Immunohistochemistry , Liver/drug effects , Liver/enzymology , Liver/pathology , Male , Mice , Nitric Oxide Synthase Type II/metabolism , Plant Extracts/administration & dosage , Plant Leaves/chemistry , Plant Stems/chemistry , Schistosoma mansoni/enzymology , Schistosoma mansoni/ultrastructure
2.
Saudi Med J ; 35(11): 1404-7, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25399222

ABSTRACT

OBJECTIVES: To determine whether exenatide is effective in reducing weight and glycosylated hemoglobin level (HbA1c), and to investigate its efficacy in improving lipid profile, blood pressure, and creatinine levels in the Arab population. METHODS: This study was conducted at the Endocrine Unit, Dubai Hospital, Dubai, United Arab Emirates. We retrospectively collected data from patients with type 2 diabetes started on exenatide between November 2011 and February 2012. Data included demographics, clinical, laboratory results, and medications used. A general linear model adjusted by baseline characteristics (weight, HbA1C, age, use of statins, and duration of diabetes) was used to assess changes between baseline and end of trial in HbA1C, weight, low density lipoprotein cholesterol, total cholesterol, triglycerides, creatinine, and blood pressure. RESULTS: After 6 months of treatment with exenatide, the HbA1c decreased by 0.47% (95% confidence level [CI]: -0.01 - 0.95) (p=0.055). Weight reduction was highly significant; 5.6 kg (95% CI: 3.34 - 7.85) (p<0.001). Those reductions remained significant after adjustment for confounding factors. CONCLUSION: This study showed that weight reduction was highly significant with exenatide. The borderline significance in HbA1c reduction can be attributed to the small sample size. 


Subject(s)
Arabs , Diabetes Mellitus, Type 2/drug therapy , Glycated Hemoglobin/metabolism , Hypoglycemic Agents/therapeutic use , Obesity/metabolism , Peptides/therapeutic use , Venoms/therapeutic use , Weight Loss , Adult , Blood Pressure , Cholesterol, LDL/metabolism , Diabetes Mellitus, Type 2/complications , Diabetes Mellitus, Type 2/metabolism , Exenatide , Female , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Hypercholesterolemia/complications , Hypercholesterolemia/drug therapy , Hypercholesterolemia/metabolism , Male , Middle Aged , Obesity/complications , Retrospective Studies , Triglycerides/metabolism , United Arab Emirates
3.
Fitoterapia ; 83(3): 500-7, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22245081

ABSTRACT

A radical scavenging guided phytochemical study on the stem bark of Tecoma mollis afforded seven active phenylpropanoid glycosides (1-7), including a new one (4), and one iridoid (8). The structures of the isolated compounds were elucidated on the basis of spectroscopic evidences and correlated with known compounds. Compounds (1-7) displayed promising antioxidant activity (DPPH assay) in relation to ascorbic acid (positive control). The antimicrobial activity for compounds (1-8) was evaluated against five bacterial and five fungal strains. The isolated compounds exhibited nonselective weak to moderate antimicrobial activity. The highest antileishmanial activity against Leishmania donovani was observed for compound (7) with an IC50 value of 6.71 µg/ml, using pentamidine and amphotericin B as drug controls. Compound (5) exhibited moderate antimalarial activity (45% inhibition) against chloroquine sensitive (D6) clones of Plasmodium falciparum.


Subject(s)
Anti-Infective Agents/pharmacology , Antioxidants/pharmacology , Antiprotozoal Agents/pharmacology , Bignoniaceae/chemistry , Iridoid Glycosides/pharmacology , Plant Extracts/pharmacology , Propanols/pharmacology , Anti-Infective Agents/isolation & purification , Antimalarials/isolation & purification , Antimalarials/pharmacology , Antioxidants/isolation & purification , Antiprotozoal Agents/isolation & purification , Bacteria/drug effects , Biphenyl Compounds/metabolism , Fungi/drug effects , Iridoid Glycosides/isolation & purification , Leishmania/drug effects , Picrates/metabolism , Plant Bark , Plant Extracts/chemistry , Plant Stems , Plasmodium falciparum/drug effects , Propanols/isolation & purification , Trypanocidal Agents/isolation & purification , Trypanocidal Agents/pharmacology
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