1985
DOI: 10.1002/jat.2550050606
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Effects of phthalic acid esters on drug metabolizing enzymes of rat liver

Abstract: Di(2-ethylhexyl)phthalate (DEHP) inhibited UDP-glucuronyltransferase activity of rat liver in vitro and in vivo. Diethyl phthalate and dimethoxyethyl phthalate also inhibited this enzyme in vitro. On the other hand, DEHP did not inhibit the activity of the cytosolic enzyme N-acetyltransferase; it also did not alter the levels of rat liver microsomal cytochrome P-450 in vitro. It is suggested that DEHP may alter the composition of microsomal phospholipids.

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Cited by 9 publications
(6 citation statements)
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“…Although there have been no observations of clinical problems attributable to the use of those compounds, there is experimental evidence of subtle toxicity [10], [26]. The cytotoxicity test using the method of cell culture is considered to be a preliminary test to evaluate the biocompatibility of a material.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Although there have been no observations of clinical problems attributable to the use of those compounds, there is experimental evidence of subtle toxicity [10], [26]. The cytotoxicity test using the method of cell culture is considered to be a preliminary test to evaluate the biocompatibility of a material.…”
Section: Discussionmentioning
confidence: 99%
“…The addition of phthalates is aimed at increasing flexibility, extensibility and to enhance working properties [6][9]. Although low or no toxicity related to these compounds has been reported, they possess phthalates, potentially toxic compounds which may promote undesirable biological effects [10] such as reducing male fertility [11], functioning as xenoestrogens [12][13] inducing hormonal tumors, and causing fetal malformations [14][15].…”
Section: Introductionmentioning
confidence: 99%
“…Chronically administered, DEHP and MEHP have multiple effects on the liver, testis, kidney, lung and heart at much lower doses. In the liver, enzyme systems involving oxygen radical metabolism are stimulated (8)(9)(10), and the phase I and II enzymes for the biotransformation of xenobiotics are altered (11)(12)(13)(14). Among the morphological changes, there is a strong peroxisome proliferation that is especially evident in rats but also occurs in humans (6).…”
Section: Introductionmentioning
confidence: 99%
“…Chronically administered, DEHP and MEHP develop multiple effects on liver, kidney, lung, heart and testis at much lower doses. In the liver, enzyme systems of the oxygen radical metabolization are stimulated (10)(11)(12) and the phase I and II enzymes of biotransformation of xenobiotics (13)(14)(15)(16) are altered. Among the morphologic changes is a strong peroxisome proliferation especially in rats but in humans as well (8).…”
Section: Introductionmentioning
confidence: 99%