AbstractThe arachidonate inhibition of the adenylate-cyclase system of cultured pig thyroid cells was not mediated by cyclooxygenase, lipoxygenase or peroxidase metabolites. Indeed ETYA, an inhibitor of cyclooxygenase and lipoxygenase, and methimazole, an inhibitor of peroxidase and iodination were without effect on the arachidonate inhibition. Moreover the effect of arachidonate was amplified by a combination with ETYA. In 32P incorporation experiments we observed a modification of the labelling of individual phospholipids of cultured pig thyroid cells resulting in a decrease into phosphatidylinositol (PI) and an increase into phosphatidate (PA) of arachidonate and ETYA-treated cells. These results may be explained by an inhibition of CDP-...
In a continuous line of rat thyroid cells transformed by the k-ras oncogene (KiKi), the expression o...
In vivo ethylenebisdithiocarbamates and ETU are toxic to the thyroid gland. Since the molecular targ...
Iodide is shown to inhibit the cholinergic stimulation of prostaglandin E2 (PGE2) and F2 alpha (PGF2...
AbstractThe arachidonate inhibition of the adenylate-cyclase system of cultured pig thyroid cells wa...
International audienceThe N-glycan-processing inhibitors swainsonine (Sw) and deoxymannojirimycin (d...
Studies were conducted to define more clearly the site in the thyroid adenylate cyclase complex at w...
Monolayer cultures of thyroid cells lose their iodide organification capacity a few days before the ...
The kinetics and concentration effect on the relationship of thyrotropin (TSH) action on cyclic 3′,5...
2-Iodohexadecanal (IHDA) has been identified as a major thyroid iodolipid which can be formed upon a...
Prostaglandins F1 alpha and F2 alpha, at high concentrations (greater than or equal to 28 microM) en...
The transformation of arachidonic acid by the rat thyroid in vitro has been investigated. At least t...
The action of carbamoylcholine (Cchol), NaF and other agonists on the generation of inositol phospha...
Thyrotrophin (4-256-mu-U/ml) promoted an increase in the rate of release of radioiodine from the org...
4,4'-Di-isothiocyanatostilbene-2,2'-disulfonic acid (DIDS), an inhibitor of several anionic channels...
AbstractThe production of prostaglandin E2 (PGE2) by cultured dog thyroid cells was high in a serum-...
In a continuous line of rat thyroid cells transformed by the k-ras oncogene (KiKi), the expression o...
In vivo ethylenebisdithiocarbamates and ETU are toxic to the thyroid gland. Since the molecular targ...
Iodide is shown to inhibit the cholinergic stimulation of prostaglandin E2 (PGE2) and F2 alpha (PGF2...
AbstractThe arachidonate inhibition of the adenylate-cyclase system of cultured pig thyroid cells wa...
International audienceThe N-glycan-processing inhibitors swainsonine (Sw) and deoxymannojirimycin (d...
Studies were conducted to define more clearly the site in the thyroid adenylate cyclase complex at w...
Monolayer cultures of thyroid cells lose their iodide organification capacity a few days before the ...
The kinetics and concentration effect on the relationship of thyrotropin (TSH) action on cyclic 3′,5...
2-Iodohexadecanal (IHDA) has been identified as a major thyroid iodolipid which can be formed upon a...
Prostaglandins F1 alpha and F2 alpha, at high concentrations (greater than or equal to 28 microM) en...
The transformation of arachidonic acid by the rat thyroid in vitro has been investigated. At least t...
The action of carbamoylcholine (Cchol), NaF and other agonists on the generation of inositol phospha...
Thyrotrophin (4-256-mu-U/ml) promoted an increase in the rate of release of radioiodine from the org...
4,4'-Di-isothiocyanatostilbene-2,2'-disulfonic acid (DIDS), an inhibitor of several anionic channels...
AbstractThe production of prostaglandin E2 (PGE2) by cultured dog thyroid cells was high in a serum-...
In a continuous line of rat thyroid cells transformed by the k-ras oncogene (KiKi), the expression o...
In vivo ethylenebisdithiocarbamates and ETU are toxic to the thyroid gland. Since the molecular targ...
Iodide is shown to inhibit the cholinergic stimulation of prostaglandin E2 (PGE2) and F2 alpha (PGF2...