scholarly journals Thyroid hormone analogue 3,5‐diiodothyropropionic acid (DITPA) promotes healthy vasculature in the adult myocardium independent of thyroid metabolic effects

2009 ◽  
Vol 23 (S1) ◽  
Author(s):  
Yingheng Liu ◽  
Dajun Wang ◽  
Rebecca Redetzke ◽  
Anthony Martin Gerdes
Thyroid ◽  
2004 ◽  
Vol 14 (5) ◽  
pp. 345-353 ◽  
Author(s):  
Parviz Yazdanparast ◽  
Bo Carlsson ◽  
Aarne Oikarinen ◽  
Juha Risteli ◽  
Jan Faergemann

2005 ◽  
Vol 185 (3) ◽  
pp. 393-399 ◽  
Author(s):  
G M Ledda-Columbano ◽  
A Perra ◽  
M Pibiri ◽  
F Molotzu ◽  
A Columbano

Thyroid hormone is known to elicit diverse cellular and metabolic effects in various organs, including mitogenesis in the rat liver. In the present study, experiments were carried out to determine whether thyroid hormone is able to stimulate cell proliferation in another quiescent organ such as the pancreas. 3,5,3′-l-tri-iodothyronine (T3) added to the diet at a concentration of 4 mg/kg caused a striking increase in nuclear bromodeoxyuridine (BrdU) incorporation of rat acinar cells 7 days after treatment (the labeling index was 46.7% in T3-treated rats vs 7.1% in controls). BrdU incorporation was limited to the acinar cells, with duct cells and islet cells being essentially negative. The increase in DNA synthesis was accompanied by the presence of several mitotic figures. Histological examination of the pancreas did not exhibit any sign of T3-induced toxicity. Determination of the apoptotic index, measurement of the serum levels of α-amylase and lipase, and glycemia determination did not show any increase over control values, suggesting that the enhanced proliferation of acinar cells was a direct effect induced by T3 and not a regenerative response consequent to acinar or β-cell injury. Additional experiments showed that DNA synthesis was induced as early as 2 days after T3 treatment (the labeling index was 9.4 vs 1.9% in controls) and was associated with increased protein levels of cyclin D1, cyclin A and proliferating cell nuclear antigen, with no substantial differences in the expression of the cyclin-dependent kinase inhibitor p27. The mitogenic effect of T3 on the pancreas was not limited to the rat, since extensive acinar cell proliferation was also observed in the pancreas of mice treated with T3 for 1 week (the labeling index was 28% in T3-treated mice vs 1.8% in controls). Treatment with three other ligands of nuclear receptors, ciprofibrate, all-trans retinoic acid and 1,4-bis[2-(3,5-dichloropyridyloxy)]benzene, induced little or no pancreatic cell proliferation. These results demonstrated that T3 is a powerful inducer of cell proliferation in the pancreas and suggested that pancreatic acinar cell proliferation by selected agents may have potential for therapeutic use.


Biology ◽  
2019 ◽  
Vol 8 (3) ◽  
pp. 57 ◽  
Author(s):  
Kevin J. Phillips

While it is now understood that the proper expansion of adipose tissue is critically important for metabolic homeostasis, it is also appreciated that adipose tissues perform far more functions than simply maintaining energy balance. Adipose tissue performs endocrine functions, secreting hormones or adipokines that affect the regulation of extra-adipose tissues, and, under certain conditions, can also be major contributors to energy expenditure and the systemic metabolic rate via the activation of thermogenesis. Adipose thermogenesis takes place in brown and beige adipocytes. While brown adipocytes have been relatively well studied, the study of beige adipocytes has only recently become an area of considerable exploration. Numerous suggestions have been made that beige adipocytes can elicit beneficial metabolic effects on body weight, insulin sensitivity, and lipid levels. However, the potential impact of beige adipocyte thermogenesis on systemic metabolism is not yet clear and an understanding of beige adipocyte development and regulation is also limited. This review will highlight our current understanding of beige adipocytes and select factors that have been reported to elicit the development and activation of thermogenesis in beige cells, with a focus on factors that may represent a link between exercise and ‘beiging’, as well as the role that thyroid hormone signaling plays in beige adipocyte regulation.


2010 ◽  
Vol 65 (8) ◽  
pp. 512-513
Author(s):  
Paul W. Ladenson ◽  
Jens D. Kristensen ◽  
E. Chester Ridgway ◽  
Anders G. Olsson ◽  
Bo Carlsson ◽  
...  

Thyroid ◽  
2002 ◽  
Vol 12 (6) ◽  
pp. 527-533 ◽  
Author(s):  
Eugene Morkin ◽  
Gregory D. Pennock ◽  
Peter H. Spooner ◽  
Joseph J. Bahl ◽  
Steven Goldman

2014 ◽  
Vol 171 (14) ◽  
pp. 3476-3484 ◽  
Author(s):  
Claudia Musilli ◽  
Gaetano De Siena ◽  
Maria Elena Manni ◽  
Andrea Logli ◽  
Elisa Landucci ◽  
...  

Thyroid ◽  
2006 ◽  
Vol 16 (11) ◽  
pp. 1157-1162 ◽  
Author(s):  
Parviz Yazdanparast ◽  
Bo Carlsson ◽  
Aarne Oikarinen ◽  
Juha Risteli ◽  
Thomas Lavin ◽  
...  

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