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Comparision of uroprotective activity of reduced glutathione with Mesna in Ifosfamide induced hemorrhagic cystitis in rats

BACKGROUND: Ifosfamide (IFO) is widely used DNA-alkylating agents in cancer chemotherapy for management of solid tumors and hematological malignancies. However, hemorrhagic cystitis limits the use of IFO. OBJECTIVES: To compare the efficiency of reduced glutathione with 2-Mesna in reducing Ifosfamid...

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Autores principales: Ali, Syed Amir, Danda, Sandeep Kumar, Basha, Syed Abdul Azeez, Rasheed, Asif, Ahmed, Osman, Ahmed, M. Muqtedar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912792/
https://www.ncbi.nlm.nih.gov/pubmed/24550594
http://dx.doi.org/10.4103/0253-7613.125188
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author Ali, Syed Amir
Danda, Sandeep Kumar
Basha, Syed Abdul Azeez
Rasheed, Asif
Ahmed, Osman
Ahmed, M. Muqtedar
author_facet Ali, Syed Amir
Danda, Sandeep Kumar
Basha, Syed Abdul Azeez
Rasheed, Asif
Ahmed, Osman
Ahmed, M. Muqtedar
author_sort Ali, Syed Amir
collection PubMed
description BACKGROUND: Ifosfamide (IFO) is widely used DNA-alkylating agents in cancer chemotherapy for management of solid tumors and hematological malignancies. However, hemorrhagic cystitis limits the use of IFO. OBJECTIVES: To compare the efficiency of reduced glutathione with 2-Mesna in reducing Ifosfamide (IFO) induced hemorrhagic cystitis (HC) in wistar rats. MATERIALS AND METHODS: Ifosfamide and 2-Mesna were dissolved in sterile water for injection and administered to wistar rats of albino strains. The rats were randomly assigned to one of the four groups of 6 rats each: Group I: Vehicle control; Group II: 120 mg/kg of IFO alone by intraperitoneal injection (i.p); Group III: 40 mg/kg Mesna i.p., at the same time and at 4 and 8 h after IFO administration; Group IV: 500 mg/kg of glutathione i.p., 30 min prior to IFO as above. The animals were observed for 5 days. On 6(th) day, rats were sacrificed by dissecting the intrajugular vein. The bladders were macroscopically and histopathologically evaluated. RESULTS: Control animals had normal bladders with assigned scores of ‘0’ for the three parameters of edema, hemorrhage and histopathological changes. All the animals receiving IFO (group II) had evidence of HC as evidenced by alterations of edema and hemorrhages. These alterations were almost abolished (P < 0.001) by the glutathione (group III) or Mesna (group IV) in IFO-treated animals. CONCLUSION: Glutathione could be as useful as Mesna in the preventive management of IFO-induced HC.
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spelling pubmed-39127922014-02-18 Comparision of uroprotective activity of reduced glutathione with Mesna in Ifosfamide induced hemorrhagic cystitis in rats Ali, Syed Amir Danda, Sandeep Kumar Basha, Syed Abdul Azeez Rasheed, Asif Ahmed, Osman Ahmed, M. Muqtedar Indian J Pharmacol Research Article BACKGROUND: Ifosfamide (IFO) is widely used DNA-alkylating agents in cancer chemotherapy for management of solid tumors and hematological malignancies. However, hemorrhagic cystitis limits the use of IFO. OBJECTIVES: To compare the efficiency of reduced glutathione with 2-Mesna in reducing Ifosfamide (IFO) induced hemorrhagic cystitis (HC) in wistar rats. MATERIALS AND METHODS: Ifosfamide and 2-Mesna were dissolved in sterile water for injection and administered to wistar rats of albino strains. The rats were randomly assigned to one of the four groups of 6 rats each: Group I: Vehicle control; Group II: 120 mg/kg of IFO alone by intraperitoneal injection (i.p); Group III: 40 mg/kg Mesna i.p., at the same time and at 4 and 8 h after IFO administration; Group IV: 500 mg/kg of glutathione i.p., 30 min prior to IFO as above. The animals were observed for 5 days. On 6(th) day, rats were sacrificed by dissecting the intrajugular vein. The bladders were macroscopically and histopathologically evaluated. RESULTS: Control animals had normal bladders with assigned scores of ‘0’ for the three parameters of edema, hemorrhage and histopathological changes. All the animals receiving IFO (group II) had evidence of HC as evidenced by alterations of edema and hemorrhages. These alterations were almost abolished (P < 0.001) by the glutathione (group III) or Mesna (group IV) in IFO-treated animals. CONCLUSION: Glutathione could be as useful as Mesna in the preventive management of IFO-induced HC. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC3912792/ /pubmed/24550594 http://dx.doi.org/10.4103/0253-7613.125188 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ali, Syed Amir
Danda, Sandeep Kumar
Basha, Syed Abdul Azeez
Rasheed, Asif
Ahmed, Osman
Ahmed, M. Muqtedar
Comparision of uroprotective activity of reduced glutathione with Mesna in Ifosfamide induced hemorrhagic cystitis in rats
title Comparision of uroprotective activity of reduced glutathione with Mesna in Ifosfamide induced hemorrhagic cystitis in rats
title_full Comparision of uroprotective activity of reduced glutathione with Mesna in Ifosfamide induced hemorrhagic cystitis in rats
title_fullStr Comparision of uroprotective activity of reduced glutathione with Mesna in Ifosfamide induced hemorrhagic cystitis in rats
title_full_unstemmed Comparision of uroprotective activity of reduced glutathione with Mesna in Ifosfamide induced hemorrhagic cystitis in rats
title_short Comparision of uroprotective activity of reduced glutathione with Mesna in Ifosfamide induced hemorrhagic cystitis in rats
title_sort comparision of uroprotective activity of reduced glutathione with mesna in ifosfamide induced hemorrhagic cystitis in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912792/
https://www.ncbi.nlm.nih.gov/pubmed/24550594
http://dx.doi.org/10.4103/0253-7613.125188
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