Apoptosis and Bcl-2 Expression in Irradiated Lungs and the Effect of Pentoxifylline

We measured number of bcl-2, apoptotic, neutrophil, and surfactant apoprotein D (SP-D) positive cells in irradiated rat lungs during different time points after the sublethal whole-thorax irradiation of rats. We also investigated the influence of pentoxifylline (PTX) therapy on these markers. Wistar...

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Main Authors: Jan Österreicher, Michal Králik, Leoš Navrátil, Jiřina Vávrová, Jiří Škopek, Jiří Knížek, Aleš Macela
Format: Article
Language:English
Published: Karolinum Press 2001-01-01
Series:Acta Medica
Subjects:
Online Access:https://actamedica.lfhk.cuni.cz/44/4/0125/
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author Jan Österreicher
Michal Králik
Leoš Navrátil
Jiřina Vávrová
Jiří Škopek
Jiří Knížek
Aleš Macela
author_facet Jan Österreicher
Michal Králik
Leoš Navrátil
Jiřina Vávrová
Jiří Škopek
Jiří Knížek
Aleš Macela
author_sort Jan Österreicher
collection DOAJ
description We measured number of bcl-2, apoptotic, neutrophil, and surfactant apoprotein D (SP-D) positive cells in irradiated rat lungs during different time points after the sublethal whole-thorax irradiation of rats. We also investigated the influence of pentoxifylline (PTX) therapy on these markers. Wistar rats were given 15 Gy thoracic irradiation and PTX (35 mg/kg) twice a week. Animals were examined histologically and imunohistochemically at intervals from 1-12 weeks. In non-treated rats compared with treated rats, bcl-2 expression was significantly inhibited from 4 weeks after irradiation. A higher apoptosis presence in non-treated rats from 4 weeks was found and apoptosis development in PTX-treated animals was delayed and started 8 weeks after irradiation. Similar differences were measured during neutrophil granulocytes examination. Neutrophil penetration in non-treated rats was found 5 weeks after irradiation in contrast to the RP onset of PTX-treated animals 8 weeks after irradiation. The number of SP-D positive cells in non-treated rats observed until 5 weeks after irradiation was higher than in the control group. PTX-treated animals expressed higher number of SP-D positive cells during the whole experiment than the control group. We suggest that apoptosis is linked to neutrophil granulocyte actions during the RP onset and that PTX-therapy causes diminished inflammation development.
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spelling doaj.art-018c0303065e4cf1bcf72488846854d42022-12-21T19:55:12ZengKarolinum PressActa Medica1211-42861805-96942001-01-0144412513010.14712/18059694.2019.98Apoptosis and Bcl-2 Expression in Irradiated Lungs and the Effect of PentoxifyllineJan Österreicher0Michal Králik1Leoš Navrátil2Jiřina Vávrová3Jiří Škopek4Jiří Knížek5Aleš Macela6Purkyně Military Medical Academy, Hradec Králové, Department of Radiobiology and Immunology, Hradec Králové, Czech RepublicPurkyně Military Medical Academy, Hradec Králové, Department of Radiobiology and Immunology, Hradec Králové, Czech RepublicCharles University in Prague, 1st Medical Faculty, Department of Biophysics, Prague, Czech RepublicPurkyně Military Medical Academy, Hradec Králové, Department of Radiobiology and Immunology, Hradec Králové, Czech RepublicCharles University in Prague, 1st Medical Faculty, Department of Biophysics, Prague, Czech RepublicPurkyně Military Medical Academy, Hradec Králové, Department of Radiobiology and Immunology, Hradec Králové, Czech RepublicPurkyně Military Medical Academy, Hradec Králové, Department of Radiobiology and Immunology, Hradec Králové, Czech RepublicWe measured number of bcl-2, apoptotic, neutrophil, and surfactant apoprotein D (SP-D) positive cells in irradiated rat lungs during different time points after the sublethal whole-thorax irradiation of rats. We also investigated the influence of pentoxifylline (PTX) therapy on these markers. Wistar rats were given 15 Gy thoracic irradiation and PTX (35 mg/kg) twice a week. Animals were examined histologically and imunohistochemically at intervals from 1-12 weeks. In non-treated rats compared with treated rats, bcl-2 expression was significantly inhibited from 4 weeks after irradiation. A higher apoptosis presence in non-treated rats from 4 weeks was found and apoptosis development in PTX-treated animals was delayed and started 8 weeks after irradiation. Similar differences were measured during neutrophil granulocytes examination. Neutrophil penetration in non-treated rats was found 5 weeks after irradiation in contrast to the RP onset of PTX-treated animals 8 weeks after irradiation. The number of SP-D positive cells in non-treated rats observed until 5 weeks after irradiation was higher than in the control group. PTX-treated animals expressed higher number of SP-D positive cells during the whole experiment than the control group. We suggest that apoptosis is linked to neutrophil granulocyte actions during the RP onset and that PTX-therapy causes diminished inflammation development.https://actamedica.lfhk.cuni.cz/44/4/0125/IrradiationLungPentoxifyllineApoptosisBcl-2
spellingShingle Jan Österreicher
Michal Králik
Leoš Navrátil
Jiřina Vávrová
Jiří Škopek
Jiří Knížek
Aleš Macela
Apoptosis and Bcl-2 Expression in Irradiated Lungs and the Effect of Pentoxifylline
Acta Medica
Irradiation
Lung
Pentoxifylline
Apoptosis
Bcl-2
title Apoptosis and Bcl-2 Expression in Irradiated Lungs and the Effect of Pentoxifylline
title_full Apoptosis and Bcl-2 Expression in Irradiated Lungs and the Effect of Pentoxifylline
title_fullStr Apoptosis and Bcl-2 Expression in Irradiated Lungs and the Effect of Pentoxifylline
title_full_unstemmed Apoptosis and Bcl-2 Expression in Irradiated Lungs and the Effect of Pentoxifylline
title_short Apoptosis and Bcl-2 Expression in Irradiated Lungs and the Effect of Pentoxifylline
title_sort apoptosis and bcl 2 expression in irradiated lungs and the effect of pentoxifylline
topic Irradiation
Lung
Pentoxifylline
Apoptosis
Bcl-2
url https://actamedica.lfhk.cuni.cz/44/4/0125/
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AT jirinavavrova apoptosisandbcl2expressioninirradiatedlungsandtheeffectofpentoxifylline
AT jiriskopek apoptosisandbcl2expressioninirradiatedlungsandtheeffectofpentoxifylline
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