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spelling todo:paper_00062952_v39_n5_p817_KleimanDePisarev2023-10-03T14:04:16Z Thyroid function and thyroxine metabolism in hexachlorobenzene-induced porphyria Kleiman De Pisarev, D.L. Del Carmen Rios De Molina, M. San Martin De Viale, L.C. 5 aminolevulinate synthase hexachlorobenzene propylthiouracil radioisotope thyroxine animal experiment article female liothyronine blood level liver weight nonhuman porphyria priority journal protein bound iodine rat thyroid function thyrotropin blood level thyroxine blood level thyroxine metabolism 5-Aminolevulinate Synthetase Animal Body Weight Chlorobenzenes Dose-Response Relationship, Drug Female Hexachlorobenzene Iodine Radioisotopes Liver Organ Weight Porphyria Porphyrins Rats Rats, Inbred Strains Support, Non-U.S. Gov't Thyroid Gland Thyroxine Triiodothyronine The effects of hexachlorobenzene (HCB) administration on the development of porphyria and on changes in thyroid function and thyroid hormone metabolism were examined. Female Wistar rats were treated with HCB for 1 or 8 weeks. At both treatment times liver weight was notably increased with a slight change in thyroid weight at 8 weeks. Serum thyroxine (T4) levels were depressed, whereas levels of triiodothyronine (T3) were not depressed significantly at both treatment times. One or eight weeks of HCB treatment did not alter the incorporation and distribution of [125I] into intrathyroidal aminoacids. A 50% reduction in protein bound iodine (PB[125I]) was seen in both groups of animals. HCB altered [125I]T4 metabolism in rat liver slices, increasing T4 dehalogenation. HCB administration for 1 week did not affect urinary excretion of porphyrins or their precursors, or hepatic porphyrin content. The activity of aminolaevulinate synthase was not affected, but there was a 25% and 51% inhibition in porphyrinogen carboxy-lyase (PCL) activity for the uroporphyrinogen disappearance or the coproporphyrinogen formation respectively. After 8 weeks of HCB administration the rats showed a characteristic porphyria. Our results show that HCB treatment increased hepatic thyroxine metabolism, without alterations in thyroid hormone synthesis. Serum T4 and PCL activity behaved differently in both time- and dose-dependent studies, with serum T4 being the more sensitive parameter which responded at earlier times and lower doses. © 1990. Fil:Kleiman De Pisarev, D.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Del Carmen Rios De Molina, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:San Martin De Viale, L.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00062952_v39_n5_p817_KleimanDePisarev
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 5 aminolevulinate synthase
hexachlorobenzene
propylthiouracil
radioisotope
thyroxine
animal experiment
article
female
liothyronine blood level
liver weight
nonhuman
porphyria
priority journal
protein bound iodine
rat
thyroid function
thyrotropin blood level
thyroxine blood level
thyroxine metabolism
5-Aminolevulinate Synthetase
Animal
Body Weight
Chlorobenzenes
Dose-Response Relationship, Drug
Female
Hexachlorobenzene
Iodine Radioisotopes
Liver
Organ Weight
Porphyria
Porphyrins
Rats
Rats, Inbred Strains
Support, Non-U.S. Gov't
Thyroid Gland
Thyroxine
Triiodothyronine
spellingShingle 5 aminolevulinate synthase
hexachlorobenzene
propylthiouracil
radioisotope
thyroxine
animal experiment
article
female
liothyronine blood level
liver weight
nonhuman
porphyria
priority journal
protein bound iodine
rat
thyroid function
thyrotropin blood level
thyroxine blood level
thyroxine metabolism
5-Aminolevulinate Synthetase
Animal
Body Weight
Chlorobenzenes
Dose-Response Relationship, Drug
Female
Hexachlorobenzene
Iodine Radioisotopes
Liver
Organ Weight
Porphyria
Porphyrins
Rats
Rats, Inbred Strains
Support, Non-U.S. Gov't
Thyroid Gland
Thyroxine
Triiodothyronine
Kleiman De Pisarev, D.L.
Del Carmen Rios De Molina, M.
San Martin De Viale, L.C.
Thyroid function and thyroxine metabolism in hexachlorobenzene-induced porphyria
topic_facet 5 aminolevulinate synthase
hexachlorobenzene
propylthiouracil
radioisotope
thyroxine
animal experiment
article
female
liothyronine blood level
liver weight
nonhuman
porphyria
priority journal
protein bound iodine
rat
thyroid function
thyrotropin blood level
thyroxine blood level
thyroxine metabolism
5-Aminolevulinate Synthetase
Animal
Body Weight
Chlorobenzenes
Dose-Response Relationship, Drug
Female
Hexachlorobenzene
Iodine Radioisotopes
Liver
Organ Weight
Porphyria
Porphyrins
Rats
Rats, Inbred Strains
Support, Non-U.S. Gov't
Thyroid Gland
Thyroxine
Triiodothyronine
description The effects of hexachlorobenzene (HCB) administration on the development of porphyria and on changes in thyroid function and thyroid hormone metabolism were examined. Female Wistar rats were treated with HCB for 1 or 8 weeks. At both treatment times liver weight was notably increased with a slight change in thyroid weight at 8 weeks. Serum thyroxine (T4) levels were depressed, whereas levels of triiodothyronine (T3) were not depressed significantly at both treatment times. One or eight weeks of HCB treatment did not alter the incorporation and distribution of [125I] into intrathyroidal aminoacids. A 50% reduction in protein bound iodine (PB[125I]) was seen in both groups of animals. HCB altered [125I]T4 metabolism in rat liver slices, increasing T4 dehalogenation. HCB administration for 1 week did not affect urinary excretion of porphyrins or their precursors, or hepatic porphyrin content. The activity of aminolaevulinate synthase was not affected, but there was a 25% and 51% inhibition in porphyrinogen carboxy-lyase (PCL) activity for the uroporphyrinogen disappearance or the coproporphyrinogen formation respectively. After 8 weeks of HCB administration the rats showed a characteristic porphyria. Our results show that HCB treatment increased hepatic thyroxine metabolism, without alterations in thyroid hormone synthesis. Serum T4 and PCL activity behaved differently in both time- and dose-dependent studies, with serum T4 being the more sensitive parameter which responded at earlier times and lower doses. © 1990.
format JOUR
author Kleiman De Pisarev, D.L.
Del Carmen Rios De Molina, M.
San Martin De Viale, L.C.
author_facet Kleiman De Pisarev, D.L.
Del Carmen Rios De Molina, M.
San Martin De Viale, L.C.
author_sort Kleiman De Pisarev, D.L.
title Thyroid function and thyroxine metabolism in hexachlorobenzene-induced porphyria
title_short Thyroid function and thyroxine metabolism in hexachlorobenzene-induced porphyria
title_full Thyroid function and thyroxine metabolism in hexachlorobenzene-induced porphyria
title_fullStr Thyroid function and thyroxine metabolism in hexachlorobenzene-induced porphyria
title_full_unstemmed Thyroid function and thyroxine metabolism in hexachlorobenzene-induced porphyria
title_sort thyroid function and thyroxine metabolism in hexachlorobenzene-induced porphyria
url http://hdl.handle.net/20.500.12110/paper_00062952_v39_n5_p817_KleimanDePisarev
work_keys_str_mv AT kleimandepisarevdl thyroidfunctionandthyroxinemetabolisminhexachlorobenzeneinducedporphyria
AT delcarmenriosdemolinam thyroidfunctionandthyroxinemetabolisminhexachlorobenzeneinducedporphyria
AT sanmartindevialelc thyroidfunctionandthyroxinemetabolisminhexachlorobenzeneinducedporphyria
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