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Comparison of Kinetic Study and Protective Effects of Biological Dipeptide and Two Porphyrin Derivatives on Metal Cytotoxicity Toward Human Lymphocytes
In this research, dipeptide (his-β-alanine) and porphyrin derivatives were choosen for comparing chelating ability of toxic metals such as Al(3+), Cu(2+), Hg(2+) and Pb(2)(+ )in-vitro. The reason for choosing these two compounds is that both of them are naturally present in biological systems and co...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shaheed Beheshti University of Medical Sciences
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610760/ https://www.ncbi.nlm.nih.gov/pubmed/29201094 |
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author | Khosravi, Maryam Rahimi, Rahmatollah pourahmad, Jalal Zarei, Mohammad Hadi Rabbani, Mahboubeh |
author_facet | Khosravi, Maryam Rahimi, Rahmatollah pourahmad, Jalal Zarei, Mohammad Hadi Rabbani, Mahboubeh |
author_sort | Khosravi, Maryam |
collection | PubMed |
description | In this research, dipeptide (his-β-alanine) and porphyrin derivatives were choosen for comparing chelating ability of toxic metals such as Al(3+), Cu(2+), Hg(2+) and Pb(2)(+ )in-vitro. The reason for choosing these two compounds is that both of them are naturally present in biological systems and comparison of chelating ability of these two compounds has not yet been done. Synthesis and comparison of kinetic study of dipeptide (his-β-alanine), meso-tetrakis(4-trimethylanilinium) porphyrin (TAPP) and Tetrakis(4-sulfonatophenyl)porphyrin (TPPS(4)) were carried out by our team. In addition, cytotoxicity assays of metals and chelators were also performed using methylthiazoletetrazolium (MTT) test. Furthermore we investigated the protective effect of chelators against cytotoxicity, induced by differenrt toxic metals such as Al(3+), Cu(2+), Hg(2+) and Pb(2+ )on human lymphocytes. EC(50) values on human lymphocytes obtained after 12 h. incubation for Al(3+), Cu(2+) and Hg(2+ )were 30, 51, 3 µM respectively and for Pb(2+) no cytotoxicity was observed on human lymphocyte up to 1000 µM concentration. EC(50) obtained for chelators dipeptide, TPPS(4) and TAPP were 948, 472 and 175 µM respectively. Pretreatment of human lymphocyte with subtoxic concentations of chelators reduced toxicity of the metals against human blood lymphocytes. |
format | Online Article Text |
id | pubmed-5610760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Shaheed Beheshti University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-56107602017-12-01 Comparison of Kinetic Study and Protective Effects of Biological Dipeptide and Two Porphyrin Derivatives on Metal Cytotoxicity Toward Human Lymphocytes Khosravi, Maryam Rahimi, Rahmatollah pourahmad, Jalal Zarei, Mohammad Hadi Rabbani, Mahboubeh Iran J Pharm Res Original Article In this research, dipeptide (his-β-alanine) and porphyrin derivatives were choosen for comparing chelating ability of toxic metals such as Al(3+), Cu(2+), Hg(2+) and Pb(2)(+ )in-vitro. The reason for choosing these two compounds is that both of them are naturally present in biological systems and comparison of chelating ability of these two compounds has not yet been done. Synthesis and comparison of kinetic study of dipeptide (his-β-alanine), meso-tetrakis(4-trimethylanilinium) porphyrin (TAPP) and Tetrakis(4-sulfonatophenyl)porphyrin (TPPS(4)) were carried out by our team. In addition, cytotoxicity assays of metals and chelators were also performed using methylthiazoletetrazolium (MTT) test. Furthermore we investigated the protective effect of chelators against cytotoxicity, induced by differenrt toxic metals such as Al(3+), Cu(2+), Hg(2+) and Pb(2+ )on human lymphocytes. EC(50) values on human lymphocytes obtained after 12 h. incubation for Al(3+), Cu(2+) and Hg(2+ )were 30, 51, 3 µM respectively and for Pb(2+) no cytotoxicity was observed on human lymphocyte up to 1000 µM concentration. EC(50) obtained for chelators dipeptide, TPPS(4) and TAPP were 948, 472 and 175 µM respectively. Pretreatment of human lymphocyte with subtoxic concentations of chelators reduced toxicity of the metals against human blood lymphocytes. Shaheed Beheshti University of Medical Sciences 2017 /pmc/articles/PMC5610760/ /pubmed/29201094 Text en © 2017 by School of Pharmacy, Shaheed Beheshti University of Medical Sciences and Health Services This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Khosravi, Maryam Rahimi, Rahmatollah pourahmad, Jalal Zarei, Mohammad Hadi Rabbani, Mahboubeh Comparison of Kinetic Study and Protective Effects of Biological Dipeptide and Two Porphyrin Derivatives on Metal Cytotoxicity Toward Human Lymphocytes |
title | Comparison of Kinetic Study and Protective Effects of Biological Dipeptide and Two Porphyrin Derivatives on Metal Cytotoxicity Toward Human Lymphocytes |
title_full | Comparison of Kinetic Study and Protective Effects of Biological Dipeptide and Two Porphyrin Derivatives on Metal Cytotoxicity Toward Human Lymphocytes |
title_fullStr | Comparison of Kinetic Study and Protective Effects of Biological Dipeptide and Two Porphyrin Derivatives on Metal Cytotoxicity Toward Human Lymphocytes |
title_full_unstemmed | Comparison of Kinetic Study and Protective Effects of Biological Dipeptide and Two Porphyrin Derivatives on Metal Cytotoxicity Toward Human Lymphocytes |
title_short | Comparison of Kinetic Study and Protective Effects of Biological Dipeptide and Two Porphyrin Derivatives on Metal Cytotoxicity Toward Human Lymphocytes |
title_sort | comparison of kinetic study and protective effects of biological dipeptide and two porphyrin derivatives on metal cytotoxicity toward human lymphocytes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610760/ https://www.ncbi.nlm.nih.gov/pubmed/29201094 |
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