The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships
ISSN: |
0015-6264
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Source: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
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Topics: |
Medicine
Process Engineering, Biotechnology, Nutrition Technology
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Type of Medium: |
Electronic Resource
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URL: |
_version_ | 1798292463252668416 |
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autor | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. |
autorsonst | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. |
book_url | http://dx.doi.org/10.1016/S0015-6264(69)80463-3 |
datenlieferant | nat_lic_papers |
fussnote | The relative abilities of substituted phenols to induce drug-metabolizing enzymes were measured either 24 hr after a single dose or after 6-10 daily doses. The phenols carried various combinations of the substituents, methyl, ethyl, isopropyl, tert-butyl, tert-amyl, phenyl, benzyl, methoxy, methoxymethyl, hydroxymethyl, dimethylaminomethyl and nitro. When the effect was measured 24 hr after a single dose, a close relationship was found between the induction of drug-metabolizing enzymes and the lipid-water partition coefficient of the test compound. When the effect was measured after six daily doses this relationship was less distinct; further dosing could lead either to an accentuation or to a diminution of the effect. One compound which provided less evidence of induction after six doses than after a single dose was 2,6-di-tert-butyl-4-methoxymethylphenol. This regression of enzyme activity on repeated dosing was not related to any histological change or to the amount or distribution of histochemically-demonstrable glucose 6-phosphatase in the liver. Many of the substituted phenols also induced uridine diphosphate glucose dehydrogenase, an effect apparently unrelated either to the lipid-water partition coefficient or to the induction of drug-metabolizing enzymes. Liver enlargement was not invariably related to the induction of either drug-metabolizingactivities or uridine diphosphate glucose dehydrogenase. |
hauptsatz | hsatz_simple |
identnr | NLZ177139889 |
issn | 0015-6264 |
journal_name | Food and Cosmetics Toxicology |
materialart | 1 |
package_name | Elsevier |
publikationsort | Amsterdam |
publisher | Elsevier |
reference | 7 (1969), S. 603-619 |
search_space | articles |
shingle_author_1 | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. |
shingle_author_2 | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. |
shingle_author_3 | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. |
shingle_author_4 | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. |
shingle_catch_all_1 | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships 0015-6264 00156264 Elsevier |
shingle_catch_all_2 | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships 0015-6264 00156264 Elsevier |
shingle_catch_all_3 | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships 0015-6264 00156264 Elsevier |
shingle_catch_all_4 | Gilbert, D. Martin, A.D. Gangolli, S.D. Abraham, R. Golberg, L. The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships 0015-6264 00156264 Elsevier |
shingle_title_1 | The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships |
shingle_title_2 | The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships |
shingle_title_3 | The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships |
shingle_title_4 | The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships |
sigel_instance_filter | dkfz geomar wilbert ipn albert fhp |
source_archive | Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
timestamp | 2024-05-06T08:48:55.120Z |
titel | The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships |
titel_suche | The effect of substituted phenols on liver weights and liver enzymes in the rat: Structure-activity relationships The relative abilities of substituted phenols to induce drug-metabolizing enzymes were measured either 24 hr after a single dose or after 6-10 daily doses. The phenols carried various combinations of the substituents, methyl, ethyl, isopropyl, tert-butyl, tert-amyl, phenyl, benzyl, methoxy, methoxymethyl, hydroxymethyl, dimethylaminomethyl and nitro. When the effect was measured 24 hr after a single dose, a close relationship was found between the induction of drug-metabolizing enzymes and the lipid-water partition coefficient of the test compound. When the effect was measured after six daily doses this relationship was less distinct; further dosing could lead either to an accentuation or to a diminution of the effect. One compound which provided less evidence of induction after six doses than after a single dose was 2,6-di-tert-butyl-4-methoxymethylphenol. This regression of enzyme activity on repeated dosing was not related to any histological change or to the amount or distribution of histochemically-demonstrable glucose 6-phosphatase in the liver. Many of the substituted phenols also induced uridine diphosphate glucose dehydrogenase, an effect apparently unrelated either to the lipid-water partition coefficient or to the induction of drug-metabolizing enzymes. Liver enlargement was not invariably related to the induction of either drug-metabolizingactivities or uridine diphosphate glucose dehydrogenase. |
topic | WW-YZ ZM |
uid | nat_lic_papers_NLZ177139889 |