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Thyroid hormone metabolism and nuclear binding in Gunn rats

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Abstract

We examined the serum concentrations of total, free thyroid hormones and TSH, activity of hepatic T45′-deiodinase, and T3 binding to hepatic nuclei in homozygous (j/j) and heterozygous (j/+) Gunn rats. Both total T3 and free T3 (FT3) concentrations in sera from j/j rats were significantly lower than those of j/+ rats on 5–10, 15–20, and 25–30 days after birth. Both total T4 and free T4 (FT4) concentrations in j/j and j/+ rat sera were not significantly different on 5–10 days. However, in j/j rats they were significantly higher than those of j/+ rats on days 15–20 and 25–30. Serum reverse T3 (rT3) concentrations were higher in j/j than in j/+ rats on days 5–10, 15–20, and 25–30. Serum TSH concentration in j/j and j/+ rats on 15 days post-natal were 1.42±1.28 and 1.65±1.24 µg/l (mean±SD), respectively, wich were not significantly different from each other. T3 formation from T4 in hepatic microsomal fractions obtained 15 days after birth was significantly lower in homozygotes than in heterozygotes (4.89±1.18 vs 11.15±2.38 pmol/mg protein/min, p < 0.005). Binding constants (Ka) as well as maximal binding capacities (MBC) for T3 of hepatic nuclei from 15 day-old j/j and j/+ rats were similar (ka; 3.58×109 vs3.15×109 M−1, MBC; 0.316 vs0.380 pmol/mg DNA). From these results we suggest that decreased conversion from T4 to T3 is one of the major reasons for high serum levels of T4 and rT3, and low levels of T3 in j/j rats, and that nuclear T3 binding and pituitary TSH secretion are unaltered in j/j rats.

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References

  1. Gunn C.H. Hereditary acholuric jaundice in a new mutant strain of rats. J. Hered. 29/137, 1938.

    Google Scholar 

  2. Carbone J.V., Grodsky G.M. Constitutional nonhemolytic hyperbilirubinemia in the rat: Defect of bilirubin conjugation. Proc. Soc. Exp. Biol. Med. 94: 461, 1957.

    Article  CAS  PubMed  Google Scholar 

  3. Schmid R., Axelrod J., Hammaker L., Swarm R.L. Congenital jaundice in rats, due to a defect in glucuronide formation. J. Clin. Invest. 37: 1123, 1958.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  4. Nagai F., Homma H., Tanase H., Matsui M. Studies on the genetic linkage of bilirubin and androstene UDP-glucuronyltransferases by crossbreeding of two mutant rat strains. Biochem. J. 252: 897, 1988.

    CAS  PubMed Central  PubMed  Google Scholar 

  5. Gomba S.Z., Gautier A., Lemarchand-Beraud T.H., Gardiol D. Pigmentation and dysfunction of Gunn rat thyroid. Correlation between morphological and biochemical data. Virchows Arch. [B.] 20: 41, 1976.

    CAS  Google Scholar 

  6. Japundzic M., Bastomsky C.H., Nadler N.J., Japundic I. Observations sur le pigment thyroidien chez les rats de Gunn. Bull. Assoc. Anat. (Nancy) 59: 427, 1975.

    CAS  Google Scholar 

  7. Lüders D. Einfluss von Phenobarbital auf die Schilddrüsenfunktion bei Wistar- und Gunnratten: Versuche mit 1251-Thyroxin. Z. Kinderheilk. 113: 129, 1972.

    Article  PubMed  Google Scholar 

  8. Benathan M., Lemarchand-Beraud T.H., Berthier C., Gautier A., Gardiol D. Thyroid function in Gunn rats with genetically altered thyroid hormone catabolism. Acta. Endocrinol (Copenh.) 102: 71, 1983.

    CAS  Google Scholar 

  9. Flock E.V., Bollman J.L., Owen C.A. Jr., Zollman P.E. Conjugation of thyroid hormones and analogs by the Gunn rat. Endocrinology 77: 303, 1965.

    Article  CAS  PubMed  Google Scholar 

  10. Bastomsky C.H. The biliary excretion of thyroxine and its glucuronic acid conjugate in normal and Gunn rats. Endocrinology 92: 35, 1973.

    Article  CAS  PubMed  Google Scholar 

  11. Saltzman J.R., Clark D.W., Utiger, R.D. Diminished hepatic triiodothyronine production in Gunn rats. Acta Endocrinol (Copenh.) 113: 281, 1986.

    CAS  Google Scholar 

  12. Nakagawa T., Matsumura K., Takeda K., Shinoda N., Matsuda A., Matsushita T., Tagami T. Effect of stripping thyroxin from thyroxin-binding globulin on the measurement of free thyroxin in serum by equilibrium dialysis and by radioimmunoassay. Clin. Chem. 36: 313, 1990.

    CAS  PubMed  Google Scholar 

  13. Hogeboom G.H. Fractionation of cell components of animal tissues. Method Enzymol. 1: 16, 1955.

    Article  CAS  Google Scholar 

  14. Visser T.J. Mechanism of inhibition of iodothyronine-5′ -deiodinase by thioureylenes and sulfite. Biochim. Biophys. Acta. 611: 371, 1980.

    Article  CAS  PubMed  Google Scholar 

  15. Kamikubo K., Nakamura S., Horike S., Sakata S., Yasuda K. Kinetics of hepatic thyroxine 5′-deiodinase. Acta Endocrinol (Copenh.) 103: 558, 1983.

    CAS  Google Scholar 

  16. Hamada S., Nakamura H., Nanno M. Triiodothyronine-induced increase in rat nuclear thyroid-hormone receptors associated with increased mitochondrial α-glycerophosphate dehydrogenase activity. Biochem. J. 162: 371, 1979.

    Google Scholar 

  17. Schneider W.C. Phosphorus compounds in animal tissues. I. Extraction and estimation of desoxypentose nucleic acid and of pentose nucleic acid. J. Biol. Chem. 161: 293, 1945.

    CAS  PubMed  Google Scholar 

  18. Kaplan M.M., Utiger R.D. Iodothyronine metabolism in rat liver homogenate. J. Clin. Invest. 61: 459, 1978.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  19. Larsen P.R., Silva J.E., Kaplan M.M. Relationship between circulating and intracellular thyroid hormones: Physiological and clinical implications. Endocr. Rev. 2: 87, 1981.

    Article  CAS  PubMed  Google Scholar 

  20. Inada M., Kasagi K., Kurata S., Kazama Y., Takayama H., Torizuka K., Fukase M., Soma T. Estimation of thyroxine and triiodothyronine distribution and of the conversion rate of thyroxine to triiodothyronine in man. J. Clin. Invest. 55: 1337, 1975.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  21. Chopra I.J. An assessment of dairy production and significance of thyroidal secretion of 3, 3′, 5′ -triiodothyronine (reverse T3) in man. J. Clin. Invest. 56: 32, 1976.

    Article  Google Scholar 

  22. Chowdhury J.R., Chowdhury N.R., Moscioni A.D., Tukey R., Tephly T., Arias I.M. Differential regulation by triiodothyronine of substrate-specific uridinediphosphoglucuronate glucuronosyl transferases in rat liver. Biochim. Biophys. Acta 761: 58, 1983.

    Article  CAS  PubMed  Google Scholar 

  23. Moscioni A.D., Gartner L.M. Thyroid hormone and hepatic UDP-glucuronosyl transferase activity: contrary effects in rat and mouse. Res. Commun. Chem. Pathol. Pharmacol. 39: 445, 1983.

    CAS  PubMed  Google Scholar 

  24. Van Steenbergen W., Fevery J., DeGroot J. Thyroid hormones and the hepatic handling of bilirubin; II. Effects of hypothyroidism and hyperthyroidism on the apparent maximal biliary secretion of bilirubin in the Wistar rat. J. Hepatol. 7: 229, 1988.

    Article  PubMed  Google Scholar 

  25. Eerson C.H., Lew R., Braverman L.E., DeVito W.J. Serum thyrotropin concentration are more highly correlated with serum triiodothyronine concentrations than with serum thyroxine concentrations in thyroid hormone-infused thyroidectomized rats. Endocrinology 124: 2415, 1989.

    Article  Google Scholar 

  26. Chopra I.J., Solomon D.H., Chopra U., Young R.T., Chua Teco G.N. Alterations in circulating thyroid hormones and thyrotropin in hepatic cirrhosis; evidence for euthyroidism despite subnormal serum triiodothyronine. J. Clin. Endocrinol. Metab. 39: 501, 1974.

    Article  CAS  PubMed  Google Scholar 

  27. Hepner G.W., Chopra I.J. Serum thyroid hormone levels in patients with liver diseases. Arch. Intern. Med. 139: 1117, 1979.

    Article  CAS  PubMed  Google Scholar 

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Komaki, T., Sakata, S., Kamikubo, K. et al. Thyroid hormone metabolism and nuclear binding in Gunn rats. J Endocrinol Invest 14, 409–415 (1991). https://doi.org/10.1007/BF03349091

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