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Hemodynamic Effects of the Light Stabilizer Tinuvin 770 in Dogs In Vivo
INTRODUCTION: Tinuvin 770 [bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate, Ciba-Geigy, Basel, Switzerland] is a UV light stabilizer that is a component of many plastic materials used world-wide in the medical and food industries. We report on the acute hemodynamic effects of Tinuvin 770 examined in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Open
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142673/ https://www.ncbi.nlm.nih.gov/pubmed/30288180 http://dx.doi.org/10.2174/1874104501812010088 |
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author | Krepuska, Miklos Hubay, Marta Zima, Endre Kovacs, Aniko Kekesi, Violetta Kalasz, Huba Szilagyi, Brigitta Merkely, Bela Sotonyi, Peter |
author_facet | Krepuska, Miklos Hubay, Marta Zima, Endre Kovacs, Aniko Kekesi, Violetta Kalasz, Huba Szilagyi, Brigitta Merkely, Bela Sotonyi, Peter |
author_sort | Krepuska, Miklos |
collection | PubMed |
description | INTRODUCTION: Tinuvin 770 [bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate, Ciba-Geigy, Basel, Switzerland] is a UV light stabilizer that is a component of many plastic materials used world-wide in the medical and food industries. We report on the acute hemodynamic effects of Tinuvin 770 examined in dogs. MATERIALS AND METHODS: Tinuvin 770 was dissolved in a mixture of saline and ethanol (1:1 v/v) and was administered to 12 intravenously narcotized and respirated dogs in increasing doses (T1-T7: 1, 3.3, 6.6, 10, 33.3, 66.6 and 100 mg, respectively). The doses were given as bolus injections over a three minute period, and the effects were recorded for 12 minutes. The vehicle was used as a control. Hemodynamic parameters (heart rate, blood pressure, end-diastolic pressure, dp/dt, cardiac output) and ECG were monitored continously. RESULTS: At doses T1-T4, systolic and diastolic blood pressures, mean pressure and ventricular contractility were significantly decreased without significant changes in cardiac output, heart rate, or PQ interval. At doses T5 and T6, declines in blood pressure and myocardial contractility were observed. At doses T6 and T7, heart rate and PQ interval decreased substantially. Irreversible circulatory failure occured in one dog after administering dose T6 and in 8 dogs following dose T7. CONCLUSION: Tinuvin 770 induces acute hemodynamic alterations. In lower doses, it causes peripheral vasodilatation, however at higher doses acute cardiac failure occured. Plastics containing Tinuvin 770 should be used with care in medical practice and the laboratory. |
format | Online Article Text |
id | pubmed-6142673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-61426732018-10-04 Hemodynamic Effects of the Light Stabilizer Tinuvin 770 in Dogs In Vivo Krepuska, Miklos Hubay, Marta Zima, Endre Kovacs, Aniko Kekesi, Violetta Kalasz, Huba Szilagyi, Brigitta Merkely, Bela Sotonyi, Peter Open Med Chem J Medicinal Chemistry INTRODUCTION: Tinuvin 770 [bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate, Ciba-Geigy, Basel, Switzerland] is a UV light stabilizer that is a component of many plastic materials used world-wide in the medical and food industries. We report on the acute hemodynamic effects of Tinuvin 770 examined in dogs. MATERIALS AND METHODS: Tinuvin 770 was dissolved in a mixture of saline and ethanol (1:1 v/v) and was administered to 12 intravenously narcotized and respirated dogs in increasing doses (T1-T7: 1, 3.3, 6.6, 10, 33.3, 66.6 and 100 mg, respectively). The doses were given as bolus injections over a three minute period, and the effects were recorded for 12 minutes. The vehicle was used as a control. Hemodynamic parameters (heart rate, blood pressure, end-diastolic pressure, dp/dt, cardiac output) and ECG were monitored continously. RESULTS: At doses T1-T4, systolic and diastolic blood pressures, mean pressure and ventricular contractility were significantly decreased without significant changes in cardiac output, heart rate, or PQ interval. At doses T5 and T6, declines in blood pressure and myocardial contractility were observed. At doses T6 and T7, heart rate and PQ interval decreased substantially. Irreversible circulatory failure occured in one dog after administering dose T6 and in 8 dogs following dose T7. CONCLUSION: Tinuvin 770 induces acute hemodynamic alterations. In lower doses, it causes peripheral vasodilatation, however at higher doses acute cardiac failure occured. Plastics containing Tinuvin 770 should be used with care in medical practice and the laboratory. Bentham Open 2018-08-31 /pmc/articles/PMC6142673/ /pubmed/30288180 http://dx.doi.org/10.2174/1874104501812010088 Text en © 2018 Krepuska et al. https://creativecommons.org/licenses/by/4.0/legalcode This is an open access article distributed under the terms of the Creative Commons Attribution 4. 0 International Public License (CC-BY 4. 0), a copy of which is available at: https://creativecommons. org/licenses/by/4. 0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Medicinal Chemistry Krepuska, Miklos Hubay, Marta Zima, Endre Kovacs, Aniko Kekesi, Violetta Kalasz, Huba Szilagyi, Brigitta Merkely, Bela Sotonyi, Peter Hemodynamic Effects of the Light Stabilizer Tinuvin 770 in Dogs In Vivo |
title | Hemodynamic Effects of the Light Stabilizer Tinuvin 770 in Dogs In Vivo |
title_full | Hemodynamic Effects of the Light Stabilizer Tinuvin 770 in Dogs In Vivo |
title_fullStr | Hemodynamic Effects of the Light Stabilizer Tinuvin 770 in Dogs In Vivo |
title_full_unstemmed | Hemodynamic Effects of the Light Stabilizer Tinuvin 770 in Dogs In Vivo |
title_short | Hemodynamic Effects of the Light Stabilizer Tinuvin 770 in Dogs In Vivo |
title_sort | hemodynamic effects of the light stabilizer tinuvin 770 in dogs in vivo |
topic | Medicinal Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142673/ https://www.ncbi.nlm.nih.gov/pubmed/30288180 http://dx.doi.org/10.2174/1874104501812010088 |
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