Anti-inflammatory, Antipruritic and Mast Cell Stabilizing Activity of Aristolochia Indica.
Jessy Elizabeth Mathew, Srinivasan Keloth Kaitheri, Seekarajapuram DinakaranVachala, Magi Jose
Abstract
Jessy Elizabeth Mathew, Srinivasan Keloth Kaitheri, Seekarajapuram DinakaranVachala, Magi Jose
Abstract
OBJECTIVES: Aristolochia indica has been widely used in the traditional medicine for the treatment of a variety of diseases. In the present study different extracts of roots of A. indica were evaluated for their anti-inflammatory, antipruritic and mast cell stabilizing activity. MATERIALS AND METHODS: Anti-inflammatory activity was performed by compound 48/80 induced rat paw edema model and antipruritic activity by examining the incidence of scratching behavior. Mast cell stabilizing activity was performed by compound 48/80 and sheep serum induced mast cell degranulation methods. RESULTS: The ethanol extract (300 mg/kg) and petroleum ether extract (100 mg/kg) were found to inhibit mast cell degranulation significantly equivalent to that of standard drug ketotifen (69%) by compound 48/80 model. In sheep serum model the ethanol extracts (150 and 300 mg/kg) and petroleum ether extract (100 mg/kg) showed good mast cell stabilizing activity (66-67%). Ethanol extract at 150 mg/kg showed 70% reduction of rat paw oedema and also significantly reduced the scratching response. CONCLUSION: Results suggest A. indica has good mast cell stabilizing, anti-inflammatory and antipruritic activity.
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OBJECTIVES: Aristolochia indica has been widely used in the traditional medicine for the treatment of a variety of diseases. In the present study different extracts of roots of A. indica were evaluated for their anti-inflammatory, antipruritic and mast cell stabilizing activity. MATERIALS AND METHODS: Anti-inflammatory activity was performed by compound 48/80 induced rat paw edema model and antipruritic activity by examining the incidence of scratching behavior. Mast cell stabilizing activity was performed by compound 48/80 and sheep serum induced mast cell degranulation methods. RESULTS: The ethanol extract (300 mg/kg) and petroleum ether extract (100 mg/kg) were found to inhibit mast cell degranulation significantly equivalent to that of standard drug ketotifen (69%) by compound 48/80 model. In sheep serum model the ethanol extracts (150 and 300 mg/kg) and petroleum ether extract (100 mg/kg) showed good mast cell stabilizing activity (66-67%). Ethanol extract at 150 mg/kg showed 70% reduction of rat paw oedema and also significantly reduced the scratching response. CONCLUSION: Results suggest A. indica has good mast cell stabilizing, anti-inflammatory and antipruritic activity.
Key concepts: Degranulation, Antipruritic, Mast cell, Petroleum ether, Ketotifen, Pharmacology, Compound 48/80, Traditional medicine