Literature DB >> 2912707

Effect of thyroid hormone and growth hormone on recovery from hypothyroidism of epiphyseal growth plate cartilage and its adjacent bone.

D Lewinson1, Z Harel, P Shenzer, M Silbermann, Z Hochberg.   

Abstract

Hypothyroidism was induced in young female Sprague-Dawley rats by the addition of methimazole (0.67 mg/ml) to drinking water for a period of 7 weeks (7-14 weeks of age). The responses of the articular cartilage, epiphyseal growth plate cartilage, epiphyseal trabecular bone, and metaphyseal trabecular bone in the proximal tibia were assessed by structural parameters. In addition, replacement therapies were introduced for the last 2 weeks of the experimental period. These included 0.7 U/kg BW human GH (hGH), 15 micrograms/kg BW L-T4 (T4), and a combination of hGH and T4 at the same doses. In the hypothyroid rats, the width of epiphyseal growth plate cartilage decreased by 27%, that of articular cartilage by 35%, epiphyseal trabecular bone volume by 30%, and metaphyseal trabecular bone volume by 66% relative to those in age-matched control tissues. T4 treatment led to a full restoration of the epiphyseal trabecular bone and surpassed by 40% the control value. The magnitude of the articular cartilage and the epiphyseal trabecular bone volume returned to control values, while that of metaphyseal trabecular bone was 68% of control values. Treatment with hGH did not improve the epiphyseal growth plate cartilage or articular cartilage. It did restore epiphyseal trabecular bone to almost normal values, but metaphyseal trabecular bone improved to only a small though significant level (45% of control value). The combination of T4 and hGH resulted in an additional enlargement in the width of the epiphyseal growth plate cartilage and an increase in metaphyseal trabecular bone volume compared to those in the T4 group. Qualitative examinations indicated that it was only in the T4 and T4 plus hGH groups that the lowest chondrocytes in the epiphyseal growth plate cartilage resumed their normal hypertrophied size. These results suggest that the change in the hypothyroid state do not rely solely on the lack of pituitary GH synthesis and secretion, as replacement by exogenous GH did not restore normal epiphyseal growth plate cartilage morphology or its remodeling into metaphyseal trabecular bone. Treatment with T4 (which restored endogenous pituitary GH to 30% of control levels) results in full recovery of the epiphyseal growth plate cartilage morphology along with its associated metaphyseal trabecular bone. In addition, it can also be concluded that the decrease in epiphyseal trabecular bone volume observed in the hypothyroid animals was due solely to the GH-deficient state that accompanied hypothyroidism.

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Year:  1989        PMID: 2912707     DOI: 10.1210/endo-124-2-937

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  14 in total

1.  Catch-up growth after prolonged hypothyroidism.

Authors:  B Boersma; B J Otten; G B Stoelinga; J M Wit
Journal:  Eur J Pediatr       Date:  1996-05       Impact factor: 3.183

2.  Thyroid hormone modulation of the hypothalamic growth hormone (GH)-releasing factor-pituitary GH axis in the rat.

Authors:  N Miki; M Ono; N Hizuka; T Aoki; H Demura
Journal:  J Clin Invest       Date:  1992-07       Impact factor: 14.808

3.  Biomechanical performance of diaphyseal shafts and bone tissue of femurs from hypothyroid rats.

Authors:  María I Conti; María P Martínez; María I Olivera; Clarisa Bozzini; Patricia Mandalunis; Carlos E Bozzini; Rosa M Alippi
Journal:  Endocrine       Date:  2009-08-11       Impact factor: 3.633

4.  Mice devoid of all known thyroid hormone receptors are viable but exhibit disorders of the pituitary-thyroid axis, growth, and bone maturation.

Authors:  S Göthe; Z Wang; L Ng; J M Kindblom; A C Barros; C Ohlsson; B Vennström; D Forrest
Journal:  Genes Dev       Date:  1999-05-15       Impact factor: 11.361

5.  Growth hormone involvement in the regulation of tartrate-resistant acid phosphatase-positive cells that are active in cartilage and bone resorption.

Authors:  D Lewinson; P Shenzer; Z Hochberg
Journal:  Calcif Tissue Int       Date:  1993-03       Impact factor: 4.333

6.  Deiodinase-mediated thyroid hormone inactivation minimizes thyroid hormone signaling in the early development of fetal skeleton.

Authors:  Luciane P Capelo; Eduardo H Beber; Stephen A Huang; Telma M T Zorn; Antonio C Bianco; Cecília H A Gouveia
Journal:  Bone       Date:  2008-07-17       Impact factor: 4.398

7.  Growth plate changes associated with Hypothyroidism amongst the pre and postnatal rats.

Authors:  Masood Ahmed Shaikh; Zahid Naeem; Abd Alrahman Alshahat; Farooque Ahmed Shaikh; Shahan Arif
Journal:  Int J Health Sci (Qassim)       Date:  2013-01

8.  Differential effects of insulin-like growth factor I and growth hormone on developmental stages of rat growth plate chondrocytes in vivo.

Authors:  E B Hunziker; J Wagner; J Zapf
Journal:  J Clin Invest       Date:  1994-03       Impact factor: 14.808

9.  Reversible growth failure and complete GH deficiency in a 4-year-old girl with very early Hashimoto's thyroiditis and subsequent hyperplasia of pituitary thyrotroph cells.

Authors:  Laura Gaspari; Françoise Paris; Nicolas Leboucq; Alain Bonafé; Charles Sultan
Journal:  Eur J Pediatr       Date:  2016-02-02       Impact factor: 3.183

Review 10.  Reconciling the effects of inflammatory cytokines on mesenchymal cell osteogenic differentiation.

Authors:  Sagar Deshpande; Aaron W James; Jordan Blough; Alexis Donneys; Stewart C Wang; Paul S Cederna; Steven R Buchman; Benjamin Levi
Journal:  J Surg Res       Date:  2013-08-06       Impact factor: 2.192

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