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Effect of chronic lead intoxication on the distribution and elimination of amoxicillin in goats
A study of amoxicillin pharmacokinetics was conducted in healthy goats and goats with chronic lead intoxication. The intoxicated goats had increased serum concentrations of liver enzymes (alanine aminotransferase and γ-glutamyl transferase), blood urea nitrogen, and reactivated δ-aminolevulinic acid...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Veterinary Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885732/ https://www.ncbi.nlm.nih.gov/pubmed/23820209 http://dx.doi.org/10.4142/jvs.2013.14.4.395 |
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author | Soliman, Ahmed M. Abu-Basha, Ehab A. Youssef, Salah A. H. Amer, Aziza M. Murphy, Patricia A. Hauck, Catherine C. Gehring, Ronette Hsu, Walter H. |
author_facet | Soliman, Ahmed M. Abu-Basha, Ehab A. Youssef, Salah A. H. Amer, Aziza M. Murphy, Patricia A. Hauck, Catherine C. Gehring, Ronette Hsu, Walter H. |
author_sort | Soliman, Ahmed M. |
collection | PubMed |
description | A study of amoxicillin pharmacokinetics was conducted in healthy goats and goats with chronic lead intoxication. The intoxicated goats had increased serum concentrations of liver enzymes (alanine aminotransferase and γ-glutamyl transferase), blood urea nitrogen, and reactivated δ-aminolevulinic acid dehydratase compared to the controls. Following intravenous amoxicillin (10 mg/kg bw) in control and lead-intoxicated goats, elimination half-lives were 4.14 and 1.26 h, respectively. The volumes of distribution based on the terminal phase were 1.19 and 0.38 L/kg, respectively, and those at steady-state were 0.54 and 0.18 L/kg, respectively. After intramuscular (IM) amoxicillin (10 mg/kg bw) in lead-intoxicated goats and control animals, the absorption, distribution, and elimination of the drug were more rapid in lead-intoxicated goats than the controls. Peak serum concentrations of 21.89 and 12.19 µg/mL were achieved at 1 h and 2 h, respectively, in lead-intoxicated and control goats. Amoxicillin bioavailability in the lead-intoxicated goats decreased 20% compared to the controls. After amoxicillin, more of the drug was excreted in the urine from lead-intoxicated goats than the controls. Our results suggested that lead intoxication in goats increases the rate of amoxicillin absorption after IM administration and distribution and elimination. Thus, lead intoxication may impair the therapeutic effectiveness of amoxicillin. |
format | Online Article Text |
id | pubmed-3885732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Korean Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38857322014-01-13 Effect of chronic lead intoxication on the distribution and elimination of amoxicillin in goats Soliman, Ahmed M. Abu-Basha, Ehab A. Youssef, Salah A. H. Amer, Aziza M. Murphy, Patricia A. Hauck, Catherine C. Gehring, Ronette Hsu, Walter H. J Vet Sci Original Article A study of amoxicillin pharmacokinetics was conducted in healthy goats and goats with chronic lead intoxication. The intoxicated goats had increased serum concentrations of liver enzymes (alanine aminotransferase and γ-glutamyl transferase), blood urea nitrogen, and reactivated δ-aminolevulinic acid dehydratase compared to the controls. Following intravenous amoxicillin (10 mg/kg bw) in control and lead-intoxicated goats, elimination half-lives were 4.14 and 1.26 h, respectively. The volumes of distribution based on the terminal phase were 1.19 and 0.38 L/kg, respectively, and those at steady-state were 0.54 and 0.18 L/kg, respectively. After intramuscular (IM) amoxicillin (10 mg/kg bw) in lead-intoxicated goats and control animals, the absorption, distribution, and elimination of the drug were more rapid in lead-intoxicated goats than the controls. Peak serum concentrations of 21.89 and 12.19 µg/mL were achieved at 1 h and 2 h, respectively, in lead-intoxicated and control goats. Amoxicillin bioavailability in the lead-intoxicated goats decreased 20% compared to the controls. After amoxicillin, more of the drug was excreted in the urine from lead-intoxicated goats than the controls. Our results suggested that lead intoxication in goats increases the rate of amoxicillin absorption after IM administration and distribution and elimination. Thus, lead intoxication may impair the therapeutic effectiveness of amoxicillin. The Korean Society of Veterinary Science 2013-12 2013-12-19 /pmc/articles/PMC3885732/ /pubmed/23820209 http://dx.doi.org/10.4142/jvs.2013.14.4.395 Text en © 2013 The Korean Society of Veterinary Science. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Soliman, Ahmed M. Abu-Basha, Ehab A. Youssef, Salah A. H. Amer, Aziza M. Murphy, Patricia A. Hauck, Catherine C. Gehring, Ronette Hsu, Walter H. Effect of chronic lead intoxication on the distribution and elimination of amoxicillin in goats |
title | Effect of chronic lead intoxication on the distribution and elimination of amoxicillin in goats |
title_full | Effect of chronic lead intoxication on the distribution and elimination of amoxicillin in goats |
title_fullStr | Effect of chronic lead intoxication on the distribution and elimination of amoxicillin in goats |
title_full_unstemmed | Effect of chronic lead intoxication on the distribution and elimination of amoxicillin in goats |
title_short | Effect of chronic lead intoxication on the distribution and elimination of amoxicillin in goats |
title_sort | effect of chronic lead intoxication on the distribution and elimination of amoxicillin in goats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885732/ https://www.ncbi.nlm.nih.gov/pubmed/23820209 http://dx.doi.org/10.4142/jvs.2013.14.4.395 |
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