Cargando…

Theophylline-induced mesenteric periarteritis in F344/N rats

The toxicity and carcinogenic potential of theophylline (an alkaloid bronchodilator drug) was investigated in male and female F344/N rats in 16-day, 14-week, and 2-year gavage and feeding studies. In 16-day studies, rats were fed diets containing 0, 500, 1000, 2000, 4000, and 8000 ppm of theophyllin...

Descripción completa

Detalles Bibliográficos
Autores principales: Nyska, Abraham, Herbert, Ronald A., Chan, Po C., Haseman, Joseph K., Hailey, James R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082802/
https://www.ncbi.nlm.nih.gov/pubmed/9879811
http://dx.doi.org/10.1007/s002040050567
_version_ 1783508418306244608
author Nyska, Abraham
Herbert, Ronald A.
Chan, Po C.
Haseman, Joseph K.
Hailey, James R.
author_facet Nyska, Abraham
Herbert, Ronald A.
Chan, Po C.
Haseman, Joseph K.
Hailey, James R.
author_sort Nyska, Abraham
collection PubMed
description The toxicity and carcinogenic potential of theophylline (an alkaloid bronchodilator drug) was investigated in male and female F344/N rats in 16-day, 14-week, and 2-year gavage and feeding studies. In 16-day studies, rats were fed diets containing 0, 500, 1000, 2000, 4000, and 8000 ppm of theophylline or given 0, 12.5 (twice daily), 25 (once daily), 50 (once daily), 50 (twice daily), 100 (once daily), 200 (once daily), 200 (twice daily), and 400 (once daily) mg theophylline/kg body weight in corn oil by gavage. In 14-week studies, rats were fed diets containing 0, 1000, 2000, and 4000 ppm theophylline or given 0, 37.5, 75, and 150 mg/kg body weight theophylline in corn oil by gavage. In 2-year gavage studies, rats were given 0, 7.5, 25, and 75 mg/kg body weight in corn oil. In 16-day gavage studies, treatment-related periarteritis occurred in arteries of the pancreas and adjacent to the mesenteric lymph nodes of early death male and female rats given 400 mg/kg once daily. In the 14-week studies, treatment-related periarteritis occurred at similar sites and in male rats exposed to 75 and 150 mg/kg, and in all exposed female rats (gavage studies), in females exposed to 1000 ppm, and in both sexes exposed to 2000 and 4000 ppm (feeding studies). In the 2-year study, chronic periarteritis was significantly increased only in the males receiving 75 mg/kg of theophylline. The adventitia, media and intima of medium- and large-sized mesenteric arteries were involved. Similar to other vasodilator chemicals, the pathogenesis of theophylline-induced vascular lesions may be a consequence of hemodynamic changes induced in the vascular wall.
format Online
Article
Text
id pubmed-7082802
institution National Center for Biotechnology Information
language English
publishDate 1998
publisher Springer-Verlag
record_format MEDLINE/PubMed
spelling pubmed-70828022020-03-23 Theophylline-induced mesenteric periarteritis in F344/N rats Nyska, Abraham Herbert, Ronald A. Chan, Po C. Haseman, Joseph K. Hailey, James R. Arch Toxicol Organ Toxicity and Mechanisms The toxicity and carcinogenic potential of theophylline (an alkaloid bronchodilator drug) was investigated in male and female F344/N rats in 16-day, 14-week, and 2-year gavage and feeding studies. In 16-day studies, rats were fed diets containing 0, 500, 1000, 2000, 4000, and 8000 ppm of theophylline or given 0, 12.5 (twice daily), 25 (once daily), 50 (once daily), 50 (twice daily), 100 (once daily), 200 (once daily), 200 (twice daily), and 400 (once daily) mg theophylline/kg body weight in corn oil by gavage. In 14-week studies, rats were fed diets containing 0, 1000, 2000, and 4000 ppm theophylline or given 0, 37.5, 75, and 150 mg/kg body weight theophylline in corn oil by gavage. In 2-year gavage studies, rats were given 0, 7.5, 25, and 75 mg/kg body weight in corn oil. In 16-day gavage studies, treatment-related periarteritis occurred in arteries of the pancreas and adjacent to the mesenteric lymph nodes of early death male and female rats given 400 mg/kg once daily. In the 14-week studies, treatment-related periarteritis occurred at similar sites and in male rats exposed to 75 and 150 mg/kg, and in all exposed female rats (gavage studies), in females exposed to 1000 ppm, and in both sexes exposed to 2000 and 4000 ppm (feeding studies). In the 2-year study, chronic periarteritis was significantly increased only in the males receiving 75 mg/kg of theophylline. The adventitia, media and intima of medium- and large-sized mesenteric arteries were involved. Similar to other vasodilator chemicals, the pathogenesis of theophylline-induced vascular lesions may be a consequence of hemodynamic changes induced in the vascular wall. Springer-Verlag 1998 /pmc/articles/PMC7082802/ /pubmed/9879811 http://dx.doi.org/10.1007/s002040050567 Text en © Springer-Verlag Berlin Heidelberg 1998 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Organ Toxicity and Mechanisms
Nyska, Abraham
Herbert, Ronald A.
Chan, Po C.
Haseman, Joseph K.
Hailey, James R.
Theophylline-induced mesenteric periarteritis in F344/N rats
title Theophylline-induced mesenteric periarteritis in F344/N rats
title_full Theophylline-induced mesenteric periarteritis in F344/N rats
title_fullStr Theophylline-induced mesenteric periarteritis in F344/N rats
title_full_unstemmed Theophylline-induced mesenteric periarteritis in F344/N rats
title_short Theophylline-induced mesenteric periarteritis in F344/N rats
title_sort theophylline-induced mesenteric periarteritis in f344/n rats
topic Organ Toxicity and Mechanisms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082802/
https://www.ncbi.nlm.nih.gov/pubmed/9879811
http://dx.doi.org/10.1007/s002040050567
work_keys_str_mv AT nyskaabraham theophyllineinducedmesentericperiarteritisinf344nrats
AT herbertronalda theophyllineinducedmesentericperiarteritisinf344nrats
AT chanpoc theophyllineinducedmesentericperiarteritisinf344nrats
AT hasemanjosephk theophyllineinducedmesentericperiarteritisinf344nrats
AT haileyjamesr theophyllineinducedmesentericperiarteritisinf344nrats