1.Erratum to "Aloe-Emodin Protects RIN-5F (Pancreatic β-cell) Cell from Glucotoxicity via Regulation of Pro-Inflammatory Cytokine and Downregulation of Bax and Caspase 3".
Ali A ALSHATWI ; P SUBASH-BABU
Biomolecules & Therapeutics 2016;24(3):346-346
The authors request to change the corresponding author's name as Ali A Alshatwi* from P. Subash-Babu in author list.
2.Erratum to “Marine Sponges as a Drug Treasure” Biomol.Ther. 24 (2016) 347–362.
Komal ANJUM ; Syed Qamar ABBAS ; Sayed Asmat Ali SHAH ; Najeeb AKHTER ; Sundas BATOOL ; Syed Shams ul HASSAN
Biomolecules & Therapeutics 2016;24(5):559-559
The authors request to correct the title of Table 3.
3.Aloe-Emodin Protects RIN-5F (Pancreatic beta-cell) Cell from Glucotoxicity via Regulation of Pro-Inflammatory Cytokine and Downregulation of Bax and Caspase 3.
Ali A ALSHATWI ; P SUBASH-BABU
Biomolecules & Therapeutics 2016;24(1):49-56
To determine the protective effect of aloe-emodin (AE) from high glucose induced toxicity in RIN-5F (pancreatic beta-cell) cell and restoration of its function was analyzed. RIN-5F cells have been cultured in high glucose (25 mM glucose) condition, with and without AE treatment. RIN-5F cells cultured in high glucose decreased cell viability and increased ROS levels after 48 hr compared with standard medium (5.5 mM glucose). Glucotoxicity was confirmed by significantly increased ROS production, increased pro-inflammatory (IFN-gamma, IL-1beta,) & decreased anti-inflammatory (IL-6&IL-10) cytokine levels, increased DNA fragmentation. In addition, we found increased Bax, caspase 3, Fadd, and Fas and significantly reduced Bcl-2 expression after 48 hr. RIN-5F treated with both high glucose and AE (20 muM) decreased ROS generation and prevent RIN-5F cell from glucotoxicity. In addition, AE treated cells cultured in high glucose were transferred to standard medium, normal responsiveness to glucose was restored within 8hr and normal basal insulin release within 24 hr was achieved when compared to high glucose.
Apoptosis
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Caspase 3*
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Cell Survival
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DNA Fragmentation
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Down-Regulation*
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Glucose
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Insulin
4.Antinociceptive, Immunomodulatory and Antipyretic Activity of Nymphayol Isolated from Nymphaea stellata (Willd.) Flowers.
Subash Babu PANDURANGAN ; Antony Samy PAUL ; Ignacimuthu SAVARIMUTHU ; Alshatwi A ALI
Biomolecules & Therapeutics 2013;21(5):391-397
In the present study, we aimed to analyze the antinociceptive, immunomodulatory and antipyretic activities of nymphayol were investigated in wistar rats and mice. Antinociceptive effect was evaluated by acetic acid induced writhing, formalin induced paw licking and hot-plate tests. Immunomodulatory activity was assessed by neutrophil adhesion test, humoral response to sheep red blood cells, delayed-type hypersensitivity, phagocytic activity and cyclophosphamide induced myelosuppression. Antipyretic activity was evaluated by yeast induced hyperthermia in rats. Nymphayol produced significant (p<0.05) antinociceptive activity in acetic acid induced writhing response and late phase of the formalin induced paw licking response. Pre-treatment with nymphayol (50 mg/kg, oral) evoked a significant increase in neutrophil adhesion to nylon fibres. The augmentation of humoral immune response to sheep red blood cells by nymphayol (50 mg/kg) was evidenced by increase in antibody titres in rats. Oral administration of nymphayol (50 mg/kg) to rats potentiated the delayed-type hypersensitivity reaction induced by sheep red blood cells. Treatment with nymphayol showed a significant (p<0.05) reduction in pyrexia in rats. The results suggest that nymphayol possesses potent anti-nociceptive, immunomodulatory and antipyretic activities.
Acetic Acid
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Administration, Oral
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Animals
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Cyclophosphamide
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Erythrocytes
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Fever
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Flowers*
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Formaldehyde
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Hypersensitivity
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Hyperthermia, Induced
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Immunity, Humoral
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Mice
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Neutrophils
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Nylons
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Nymphaea*
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Rats
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Rats, Wistar
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Sheep
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Yeasts