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Antiurolithiatic and antioxidant activity of Mimusops elengi on ethylene glycol-induced urolithiasis in rats

OBJECTIVE: To evaluate the potential of Mimusops elengi in the treatment of renal calculi. MATERIALS AND METHODS: Petroleum ether, chloroform, and alcohol extracts of Mimusops elengi bark were evaluated for antiurolithiatic and antioxidant activity in male albino Wistar rats. Ethylene glycol (0.75%)...

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Autores principales: Ashok, Purnima, Koti, Basavaraj C., Vishwanathswamy, A.H.M.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991697/
https://www.ncbi.nlm.nih.gov/pubmed/21189910
http://dx.doi.org/10.4103/0253-7613.71925
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author Ashok, Purnima
Koti, Basavaraj C.
Vishwanathswamy, A.H.M.
author_facet Ashok, Purnima
Koti, Basavaraj C.
Vishwanathswamy, A.H.M.
author_sort Ashok, Purnima
collection PubMed
description OBJECTIVE: To evaluate the potential of Mimusops elengi in the treatment of renal calculi. MATERIALS AND METHODS: Petroleum ether, chloroform, and alcohol extracts of Mimusops elengi bark were evaluated for antiurolithiatic and antioxidant activity in male albino Wistar rats. Ethylene glycol (0.75%) in drinking water was fed to all the groups (Groups II–IX) except normal control (Group I) for 28 days to induce urolithiasis for curative (CR) and preventive (PR) regimen. Groups IV, V, and VI served as CR, and groups VII, VIII, and IX as PR were treated with different extracts of M. elengi bark. Groups I, II, and III served as normal control, positive control (hyperurolithiatic), and standard (cystone 750 mg/kg), respectively. Oxalate, calcium, and phosphate were monitored in the urine and kidney. Serum BUN, creatinine, and uric acid were also recorded. In vivo antioxidant parameters such as lipid peroxidation (MDA), glutathione (GSH), superoxide dismutase (SOD), and catalase (CAT) were also monitored. RESULTS: All the extracts of M. elengi were safe orally and exhibited no gross behavioral changes in the rats. In hypercalculi animals, the oxalate, calcium, and phosphate excretion grossly increased. However, the increased deposition of stone forming constituents in the kidneys of calculogenic rats were significantly (P < 0.001) lowered by curative and preventive treatment with alcohol extract (AlE) of M. elengi. It was also observed that alcoholic extract of M. elengi produced significant (P < 0.001) decrease in MDA, and increased GSH, SOD, and CAT. These results confirm that AlE of M. elengi possess potent antiurolithiatic activity. CONCLUSION: The results obtained suggest potential usefulness of the AlE of M. elengi bark as an antiurolithiatic agent.
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spelling pubmed-29916972010-12-28 Antiurolithiatic and antioxidant activity of Mimusops elengi on ethylene glycol-induced urolithiasis in rats Ashok, Purnima Koti, Basavaraj C. Vishwanathswamy, A.H.M. Indian J Pharmacol Research Article OBJECTIVE: To evaluate the potential of Mimusops elengi in the treatment of renal calculi. MATERIALS AND METHODS: Petroleum ether, chloroform, and alcohol extracts of Mimusops elengi bark were evaluated for antiurolithiatic and antioxidant activity in male albino Wistar rats. Ethylene glycol (0.75%) in drinking water was fed to all the groups (Groups II–IX) except normal control (Group I) for 28 days to induce urolithiasis for curative (CR) and preventive (PR) regimen. Groups IV, V, and VI served as CR, and groups VII, VIII, and IX as PR were treated with different extracts of M. elengi bark. Groups I, II, and III served as normal control, positive control (hyperurolithiatic), and standard (cystone 750 mg/kg), respectively. Oxalate, calcium, and phosphate were monitored in the urine and kidney. Serum BUN, creatinine, and uric acid were also recorded. In vivo antioxidant parameters such as lipid peroxidation (MDA), glutathione (GSH), superoxide dismutase (SOD), and catalase (CAT) were also monitored. RESULTS: All the extracts of M. elengi were safe orally and exhibited no gross behavioral changes in the rats. In hypercalculi animals, the oxalate, calcium, and phosphate excretion grossly increased. However, the increased deposition of stone forming constituents in the kidneys of calculogenic rats were significantly (P < 0.001) lowered by curative and preventive treatment with alcohol extract (AlE) of M. elengi. It was also observed that alcoholic extract of M. elengi produced significant (P < 0.001) decrease in MDA, and increased GSH, SOD, and CAT. These results confirm that AlE of M. elengi possess potent antiurolithiatic activity. CONCLUSION: The results obtained suggest potential usefulness of the AlE of M. elengi bark as an antiurolithiatic agent. Medknow Publications 2010-12 /pmc/articles/PMC2991697/ /pubmed/21189910 http://dx.doi.org/10.4103/0253-7613.71925 Text en © Indian Journal of Pharmacology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ashok, Purnima
Koti, Basavaraj C.
Vishwanathswamy, A.H.M.
Antiurolithiatic and antioxidant activity of Mimusops elengi on ethylene glycol-induced urolithiasis in rats
title Antiurolithiatic and antioxidant activity of Mimusops elengi on ethylene glycol-induced urolithiasis in rats
title_full Antiurolithiatic and antioxidant activity of Mimusops elengi on ethylene glycol-induced urolithiasis in rats
title_fullStr Antiurolithiatic and antioxidant activity of Mimusops elengi on ethylene glycol-induced urolithiasis in rats
title_full_unstemmed Antiurolithiatic and antioxidant activity of Mimusops elengi on ethylene glycol-induced urolithiasis in rats
title_short Antiurolithiatic and antioxidant activity of Mimusops elengi on ethylene glycol-induced urolithiasis in rats
title_sort antiurolithiatic and antioxidant activity of mimusops elengi on ethylene glycol-induced urolithiasis in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991697/
https://www.ncbi.nlm.nih.gov/pubmed/21189910
http://dx.doi.org/10.4103/0253-7613.71925
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