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Functional and histological bladder damage in mice after photodynamic therapy: the influence of sensitiser dose and time of administration.

The bladders of anaesthetised mice were illuminated with red laser light (630 nm) at intervals of 1 day to 4 weeks after i.p. administration of Photofrin. Light was delivered intravesically by inserting a fibre optic, with a diffusing bulb tip, into the centre of fluid filled bladders. A single ligh...

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Autores principales: Stewart, F. A., Oussoren, Y.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968612/
https://www.ncbi.nlm.nih.gov/pubmed/8398691
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author Stewart, F. A.
Oussoren, Y.
author_facet Stewart, F. A.
Oussoren, Y.
author_sort Stewart, F. A.
collection PubMed
description The bladders of anaesthetised mice were illuminated with red laser light (630 nm) at intervals of 1 day to 4 weeks after i.p. administration of Photofrin. Light was delivered intravesically by inserting a fibre optic, with a diffusing bulb tip, into the centre of fluid filled bladders. A single light dose of 11.3 J cm-2 applies 1 day after 10 mg kg-1 Photofrin caused a severe acute response, with increased urination frequency (five to seven times control) and hematuria. Recovery was good, however, and by 10 weeks only a mild (approximately two-fold) increase in frequency remained. There was no reduction in the amount of acute bladder damage or in the rate of healing when the interval between Photofrin and light was increased from 1 to 7 days but a 2 to 3 week interval lead to a significant reduction in damage. For an interval of 4 weeks there was only a mild (less than two-fold) increase in urination frequency during the first week. A drug dose of 2.5 mg kg-1 given 1 day before illumination caused transient haematuria but no increase in urination frequency. Doses of 5, 7.5 or 10 mg kg-1 all caused photosensitisation and the amount of bladder damage was drug dose dependent. The bladder seems to be well able to recover from severe acute damage induced by PDT. Occasional incidences of pyelonephritis were seen, however, suggesting that urinary tract infection during the acute period may lead to permanent renal damage. IMAGES:
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spelling pubmed-19686122009-09-10 Functional and histological bladder damage in mice after photodynamic therapy: the influence of sensitiser dose and time of administration. Stewart, F. A. Oussoren, Y. Br J Cancer Research Article The bladders of anaesthetised mice were illuminated with red laser light (630 nm) at intervals of 1 day to 4 weeks after i.p. administration of Photofrin. Light was delivered intravesically by inserting a fibre optic, with a diffusing bulb tip, into the centre of fluid filled bladders. A single light dose of 11.3 J cm-2 applies 1 day after 10 mg kg-1 Photofrin caused a severe acute response, with increased urination frequency (five to seven times control) and hematuria. Recovery was good, however, and by 10 weeks only a mild (approximately two-fold) increase in frequency remained. There was no reduction in the amount of acute bladder damage or in the rate of healing when the interval between Photofrin and light was increased from 1 to 7 days but a 2 to 3 week interval lead to a significant reduction in damage. For an interval of 4 weeks there was only a mild (less than two-fold) increase in urination frequency during the first week. A drug dose of 2.5 mg kg-1 given 1 day before illumination caused transient haematuria but no increase in urination frequency. Doses of 5, 7.5 or 10 mg kg-1 all caused photosensitisation and the amount of bladder damage was drug dose dependent. The bladder seems to be well able to recover from severe acute damage induced by PDT. Occasional incidences of pyelonephritis were seen, however, suggesting that urinary tract infection during the acute period may lead to permanent renal damage. IMAGES: Nature Publishing Group 1993-10 /pmc/articles/PMC1968612/ /pubmed/8398691 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Stewart, F. A.
Oussoren, Y.
Functional and histological bladder damage in mice after photodynamic therapy: the influence of sensitiser dose and time of administration.
title Functional and histological bladder damage in mice after photodynamic therapy: the influence of sensitiser dose and time of administration.
title_full Functional and histological bladder damage in mice after photodynamic therapy: the influence of sensitiser dose and time of administration.
title_fullStr Functional and histological bladder damage in mice after photodynamic therapy: the influence of sensitiser dose and time of administration.
title_full_unstemmed Functional and histological bladder damage in mice after photodynamic therapy: the influence of sensitiser dose and time of administration.
title_short Functional and histological bladder damage in mice after photodynamic therapy: the influence of sensitiser dose and time of administration.
title_sort functional and histological bladder damage in mice after photodynamic therapy: the influence of sensitiser dose and time of administration.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968612/
https://www.ncbi.nlm.nih.gov/pubmed/8398691
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