Response of hepatic mitochondrial α-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

J. M. Tibaldi, N. Sahnoun, Martin I. Surks

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Abstract

To characterize the hepatic response to L-triiodothyronine (T3) in an experimental nonthyroidal disease, we determined the activity of hepatic mitochondrial α-glycerophosphate dehydrogenase (α-GPD) and cytosol malic enzyme (ME) as a function of the saturation of the nuclear T3 receptor during constant T3 infusions in rats bearing the Walker 256 carcinoma. Groups of control and tumor-bearing rats were infused by minipumps (Alza Corp., Palo Alto, CA) with vehicle, 1.2 or 4.5 μg T3/100 body wt per day for 3 d. The range for serum T3 was 47.2 ± 4.1 to 165 ± 17.3 ng/dl for the control rats and 13.2 ± 1.3 to 135 ± 14.3 ng/dl for the tumor-bearing rats. Nuclear T3 receptor concentration was between 0.41 ± 0.66 and 0.47 ± 0.02 ng/mg DNA in control rats and was decreased in tumor-bearing rats to between 0.23 ± 0.03 and 0.26 ± 0.03 ng/mg DNA. Nuclear T3 receptor concentrations were not influenced by the T3 infusions. Specifically bound nuclear T3, determined by radioimmunoassay of extracts of isolated nuclei, was decreased nearly 50% in the tumor-bearing rats. However, the calculated percentage saturation of the T3 nuclear receptor remained similar in control and tumor-bearing rats at each level of T3 infusion. Dose-response curves for α-GPD and ME were curvilinear and showed an exponential increase in enzyme activity with progressive receptor saturation. In tumor-bearing rats, the activity curves or calculated appearance rate curves for α-GPD were shifted significantly upward and to the left, indicating greater sensitivity to T3, and those of ME were shifted downward and to the right, indicating decreased responsiveness to T3. Our findings suggest that cellular factors result in postreceptor amplification of the α-GPD response and diminution of the ME response to T3 in tumor-bearing rats. Augmentation of the α-GPD response may be a prototype for other hormonal responses that may enable the tumor-bearing rat to maintain an apparent euthyroid state in association with decreased serum T3.

Original languageEnglish (US)
Pages (from-to)705-714
Number of pages10
JournalJournal of Clinical Investigation
Volume74
Issue number3
StatePublished - 1984

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Walker Carcinoma 256
Glycerolphosphate Dehydrogenase
Triiodothyronine
Thyroid Hormones
Liver
Enzymes
Thyroid Hormone Receptors
Cytoplasmic and Nuclear Receptors
Neoplasms
DNA
Serum
Cytosol
Radioimmunoassay

ASJC Scopus subject areas

  • Medicine(all)

Cite this

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title = "Response of hepatic mitochondrial α-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",
abstract = "To characterize the hepatic response to L-triiodothyronine (T3) in an experimental nonthyroidal disease, we determined the activity of hepatic mitochondrial α-glycerophosphate dehydrogenase (α-GPD) and cytosol malic enzyme (ME) as a function of the saturation of the nuclear T3 receptor during constant T3 infusions in rats bearing the Walker 256 carcinoma. Groups of control and tumor-bearing rats were infused by minipumps (Alza Corp., Palo Alto, CA) with vehicle, 1.2 or 4.5 μg T3/100 body wt per day for 3 d. The range for serum T3 was 47.2 ± 4.1 to 165 ± 17.3 ng/dl for the control rats and 13.2 ± 1.3 to 135 ± 14.3 ng/dl for the tumor-bearing rats. Nuclear T3 receptor concentration was between 0.41 ± 0.66 and 0.47 ± 0.02 ng/mg DNA in control rats and was decreased in tumor-bearing rats to between 0.23 ± 0.03 and 0.26 ± 0.03 ng/mg DNA. Nuclear T3 receptor concentrations were not influenced by the T3 infusions. Specifically bound nuclear T3, determined by radioimmunoassay of extracts of isolated nuclei, was decreased nearly 50{\%} in the tumor-bearing rats. However, the calculated percentage saturation of the T3 nuclear receptor remained similar in control and tumor-bearing rats at each level of T3 infusion. Dose-response curves for α-GPD and ME were curvilinear and showed an exponential increase in enzyme activity with progressive receptor saturation. In tumor-bearing rats, the activity curves or calculated appearance rate curves for α-GPD were shifted significantly upward and to the left, indicating greater sensitivity to T3, and those of ME were shifted downward and to the right, indicating decreased responsiveness to T3. Our findings suggest that cellular factors result in postreceptor amplification of the α-GPD response and diminution of the ME response to T3 in tumor-bearing rats. Augmentation of the α-GPD response may be a prototype for other hormonal responses that may enable the tumor-bearing rat to maintain an apparent euthyroid state in association with decreased serum T3.",
author = "Tibaldi, {J. M.} and N. Sahnoun and Surks, {Martin I.}",
year = "1984",
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pages = "705--714",
journal = "Journal of Clinical Investigation",
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AU - Tibaldi, J. M.

AU - Sahnoun, N.

AU - Surks, Martin I.

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N2 - To characterize the hepatic response to L-triiodothyronine (T3) in an experimental nonthyroidal disease, we determined the activity of hepatic mitochondrial α-glycerophosphate dehydrogenase (α-GPD) and cytosol malic enzyme (ME) as a function of the saturation of the nuclear T3 receptor during constant T3 infusions in rats bearing the Walker 256 carcinoma. Groups of control and tumor-bearing rats were infused by minipumps (Alza Corp., Palo Alto, CA) with vehicle, 1.2 or 4.5 μg T3/100 body wt per day for 3 d. The range for serum T3 was 47.2 ± 4.1 to 165 ± 17.3 ng/dl for the control rats and 13.2 ± 1.3 to 135 ± 14.3 ng/dl for the tumor-bearing rats. Nuclear T3 receptor concentration was between 0.41 ± 0.66 and 0.47 ± 0.02 ng/mg DNA in control rats and was decreased in tumor-bearing rats to between 0.23 ± 0.03 and 0.26 ± 0.03 ng/mg DNA. Nuclear T3 receptor concentrations were not influenced by the T3 infusions. Specifically bound nuclear T3, determined by radioimmunoassay of extracts of isolated nuclei, was decreased nearly 50% in the tumor-bearing rats. However, the calculated percentage saturation of the T3 nuclear receptor remained similar in control and tumor-bearing rats at each level of T3 infusion. Dose-response curves for α-GPD and ME were curvilinear and showed an exponential increase in enzyme activity with progressive receptor saturation. In tumor-bearing rats, the activity curves or calculated appearance rate curves for α-GPD were shifted significantly upward and to the left, indicating greater sensitivity to T3, and those of ME were shifted downward and to the right, indicating decreased responsiveness to T3. Our findings suggest that cellular factors result in postreceptor amplification of the α-GPD response and diminution of the ME response to T3 in tumor-bearing rats. Augmentation of the α-GPD response may be a prototype for other hormonal responses that may enable the tumor-bearing rat to maintain an apparent euthyroid state in association with decreased serum T3.

AB - To characterize the hepatic response to L-triiodothyronine (T3) in an experimental nonthyroidal disease, we determined the activity of hepatic mitochondrial α-glycerophosphate dehydrogenase (α-GPD) and cytosol malic enzyme (ME) as a function of the saturation of the nuclear T3 receptor during constant T3 infusions in rats bearing the Walker 256 carcinoma. Groups of control and tumor-bearing rats were infused by minipumps (Alza Corp., Palo Alto, CA) with vehicle, 1.2 or 4.5 μg T3/100 body wt per day for 3 d. The range for serum T3 was 47.2 ± 4.1 to 165 ± 17.3 ng/dl for the control rats and 13.2 ± 1.3 to 135 ± 14.3 ng/dl for the tumor-bearing rats. Nuclear T3 receptor concentration was between 0.41 ± 0.66 and 0.47 ± 0.02 ng/mg DNA in control rats and was decreased in tumor-bearing rats to between 0.23 ± 0.03 and 0.26 ± 0.03 ng/mg DNA. Nuclear T3 receptor concentrations were not influenced by the T3 infusions. Specifically bound nuclear T3, determined by radioimmunoassay of extracts of isolated nuclei, was decreased nearly 50% in the tumor-bearing rats. However, the calculated percentage saturation of the T3 nuclear receptor remained similar in control and tumor-bearing rats at each level of T3 infusion. Dose-response curves for α-GPD and ME were curvilinear and showed an exponential increase in enzyme activity with progressive receptor saturation. In tumor-bearing rats, the activity curves or calculated appearance rate curves for α-GPD were shifted significantly upward and to the left, indicating greater sensitivity to T3, and those of ME were shifted downward and to the right, indicating decreased responsiveness to T3. Our findings suggest that cellular factors result in postreceptor amplification of the α-GPD response and diminution of the ME response to T3 in tumor-bearing rats. Augmentation of the α-GPD response may be a prototype for other hormonal responses that may enable the tumor-bearing rat to maintain an apparent euthyroid state in association with decreased serum T3.

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