Literature DB >> 207725

Nonlinear (amplified) relationship between nuclear occupancy by triiodothyronine and the appearance rate of hepatic alpha-glycerophosphate dehydrogenase and malic enzyme in the rat.

J H Oppenheimer, P Coulombe, H L Schwartz, N W Gutfeld.   

Abstract

Three separate approaches were applied to examine the general relationship between R, the rate of induction of specific enzymes (mitochondrial alpha-glycero-phosphate dehydrogenase and cytosolic malic enzyme) and q, the fractional nuclear occupancy by triiodothyronine in male Sprague-Dawley rats. Daily 200-microgram injections of triiodothyronine per 10u g body wt for 7 days resulted in saturation of the hepatic nuclear sites and the achievement of an apparent new steady state of enzyme levels. The increase achieved over base-line hypothyroid levels was then compared with the increment over hypothyroid base line characteristic of intact euthyroid animals with 47% of nuclear sites occupied. The maximal theoretical reate of steady-state enzyme induction could be protected on the basis of the observed maximal increase in enzyme activity observed 1 day after the injection of graded doses of hormone and lambda, the known fractional rate of enzyme dissipation. The 24-h dose-response studies were used to generate R as a continuous function of q, both in hypothyroid as well as in euthyroid animals. This approach involved the numerical solution of an ordinary differential equation describing the rate of change of enzyme as a function of R, which was assumed to be uniquely related to q. Results of these analyses indicated that the ratio of the maximal rate of induction of enzyme at full occupancy to the rate of induction under euthyroid conditions assumes a value between 9.0 and 19.5, depending on the precise analytic and experimental approach applied. This value is far in excess of the theoretical ratio 2.13 which on would anticipate if R were linearly related to q and 47% of the nuclear sites occupied under physiological conditions. Thus, the signal for enzyme induction appears to undergo progressjive amplification with increasing nuclear occupancy. Moreover, the curve describing the relationship between R and q appears highly nonlinear throughout (concave upwards). Although the molecular mechanism responsible for amplification is unknown, recognition of this phenomenon may be helpful in understanding tissue effects of thyroid hormone excess. Moreover, the analytic technique for determining R as a function of q may be of general applicability in studying hormonal response systems under nonsteady-state conditions.

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Year:  1978        PMID: 207725      PMCID: PMC372617          DOI: 10.1172/JCI109024

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  32 in total

1.  INFLUENCE OF THYROID HORMONES ON L-ALPHA-GLYCEROPHOSPHATE DEHYDROGENASES AND OTHER DEHYDROGENASES IN VARIOUS ORGANS OF THE RAT.

Authors:  Y P LEE; H A LARDY
Journal:  J Biol Chem       Date:  1965-03       Impact factor: 5.157

2.  Partial purification of the triiodothyronine receptor from rat liver nuclei. Differences in the chromatographic mobility of occupied and unoccupied sites.

Authors:  E S Silva; H Astier; U Thakare; H L Schwartz; J H Oppenheimer
Journal:  J Biol Chem       Date:  1977-10-10       Impact factor: 5.157

3.  Regulation of growth hormone messenger RNA by thyroid and glucocorticoid hormones.

Authors:  J A Martial; J D Baxter; H M Goodman; P H Seeburg
Journal:  Proc Natl Acad Sci U S A       Date:  1977-05       Impact factor: 11.205

4.  Apparent positive cooperative effects in cyclic AMP and corticosterone production by isolated adrenal cells in response to ACTH analogues.

Authors:  D Rodbard
Journal:  Endocrinology       Date:  1974-05       Impact factor: 4.736

5.  Thyroid hormone induction of alpha-glycerophosphate dehydrogenase in rats of different ages.

Authors:  S Shapiro; C J Percin
Journal:  Endocrinology       Date:  1966-12       Impact factor: 4.736

6.  Specificity of the alpha-glycerophosphate dehydrogenase and malic enzyme response to thyroxine.

Authors:  W R Ruegamer; G H Newman; D A Richert; W W Westerfeld
Journal:  Endocrinology       Date:  1965-10       Impact factor: 4.736

7.  Dose-dependent depletion of nuclear receptors by L-triiodothyronine: evidence for a role in induction of growth hormone synthesis in cultured GH1 cells.

Authors:  H H Samuels; F Stanley; L E Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  1976-11       Impact factor: 11.205

8.  Thyroid hormone stimulates de novo growth hormone synthesis in cultured GH1 cells: evidence for the accumulation of a rate limiting RNA species in the induction process.

Authors:  H H Samuels; L E Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  1976-10       Impact factor: 11.205

9.  Triiodothyronine stimulates specifically growth hormone mRNA in rat pituitary tumor cells.

Authors:  H Seo; G Vassart; H Brocas; S Refetoff
Journal:  Proc Natl Acad Sci U S A       Date:  1977-05       Impact factor: 11.205

10.  Alpha-amanitin administration results in a temporary inhibition of hepatic enzyme induction by triiodothyronine: further evidence favoring a long-lived mediator of thyroid hormone action.

Authors:  W H Dillmann; H L Schwartz; E Silva; M I Surks; J H Oppenheimer
Journal:  Endocrinology       Date:  1977-06       Impact factor: 4.736

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  16 in total

1.  Sequential changes in rat liver nuclear tri-iodothyronine receptors and mitochondrial alpha-glycerophosphate dehydrogenase activity after administration of tri-iodothyronine.

Authors:  H Nakamura; S Hamada; H Imura
Journal:  Biochem J       Date:  1979-08-15       Impact factor: 3.857

2.  Relationship between the accumulation of pituitary growth hormone and nuclear occupancy by triiodothyronine in the rat.

Authors:  P Coulombe; H L Schwartz; J H Oppenheimer
Journal:  J Clin Invest       Date:  1978-11       Impact factor: 14.808

3.  Stimulation of liver mitochondrial alpha-glycerophosphate dehydrogenase activity by L-thyroxine in thyroidectomized rats: comparison with the suppression of pituitary TSH secretion.

Authors:  G Costante; D Crupi; R Catalfamo; F Trimarchi
Journal:  J Endocrinol Invest       Date:  1990-01       Impact factor: 4.256

Review 4.  The mouse submaxillary gland: a model for the study of hormonally dependent growth factors.

Authors:  P Walker
Journal:  J Endocrinol Invest       Date:  1982 May-Jun       Impact factor: 4.256

5.  Effect of hexachlorobenzene on NADPH-generating lipogenic enzymes and L-glycerol-3-phosphate dehydrogenase in brown adipose tissue.

Authors:  L Alvarez; A Randi; P Alvarez; R Kölliker Frers; D L Kleiman de Pisarev
Journal:  J Endocrinol Invest       Date:  1999-06       Impact factor: 4.256

6.  Thyroid hormone-carbohydrate interaction in the rat: correlation between age-related reductions in the inducibility of hepatic malic enzyme by triiodo-L-thyronine and a high carbohydrate, fat-free diet.

Authors:  M A Forciea; H L Schwartz; H C Towle; C N Mariash; F E Kaiser; J H Oppenheimer
Journal:  J Clin Invest       Date:  1981-06       Impact factor: 14.808

7.  Intracellular conversion of thyroxine to triiodothyronine is required for the optimal thermogenic function of brown adipose tissue.

Authors:  A C Bianco; J E Silva
Journal:  J Clin Invest       Date:  1987-01       Impact factor: 14.808

8.  Response of hepatic mitochondrial alpha-glycerophosphate dehydrogenase and malic enzyme to constant infusions of L-triiodothyronine in rats bearing the Walker 256 carcinoma. Evidence for divergent postreceptor regulation of the thyroid hormone response.

Authors:  J M Tibaldi; N Sahnoun; M I Surks
Journal:  J Clin Invest       Date:  1984-09       Impact factor: 14.808

9.  Thyroid hormone is required for dietary fish oil to induce hypersecretion of biliary cholesterol in the rat.

Authors:  W F Prigge; S R Ketover; R L Gebhard
Journal:  Lipids       Date:  1995-09       Impact factor: 1.880

Review 10.  Association of thyroid hormone receptors with chromatin.

Authors:  D B Jump; J H Oppenheimer
Journal:  Mol Cell Biochem       Date:  1983       Impact factor: 3.396

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