Upregulation of the alpha sub(1)-adrenoceptor-induced phosphoinositide and inotropic response in hypothyroid rat heart

In this study, we examined changes in the biochemical and inotropic events of the alpha sub(1)-adrenoceptor signaling pathway in hypothyroid rat hearts. Hypothyroidism was induced by treating experimental animals with 0.05% 6-n-propyl-2-thiouracil (PTU) in drinking water for 7 weeks. A significant d...

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Published inMolecular and cellular biochemistry Vol. 283; no. 1-2; pp. 93 - 100
Main Authors Jalali, Shahrzad, Durston, Melanie, Panagia, Vincenzo, Mesaeli, Nasrin
Format Journal Article
LanguageEnglish
Published 01.02.2006
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Summary:In this study, we examined changes in the biochemical and inotropic events of the alpha sub(1)-adrenoceptor signaling pathway in hypothyroid rat hearts. Hypothyroidism was induced by treating experimental animals with 0.05% 6-n-propyl-2-thiouracil (PTU) in drinking water for 7 weeks. A significant decrease of beta - and an increase in alpha sub(1)-adrenoceptor density as well as an increase in the basal activity of the phosphoinositide (4,5) bisphosphate hydrolyzing phospholipase C was observed in sarcolemmal membranes purified from hypothyroid hearts as compared to age-matched euthyroid controls. Following stimulation with 10 mu M phenylephrine (in the presence of 10 mu M atenolol), the increase of contractile parameters over baseline values was significantly higher in hypo- than euthyroid hearts, while the opposite occurred under beta -stimulation with 0.1 mu M isoproterenol. Interestingly, the increase in phenylephrine-mediated positive inotropy was accompanied by a significant increase in the sarcolemmal phospholipase C activity and in the inositol 1,4,5-trisphosphate content in hypothyroid as compared to euthyroid controls. Our results suggest that cardiac alpha sub(1)-adrenoceptor and its associated phosphoinositide signaling pathway may act as a reserve for catecholamine inotropic response in hypothyroidism, where the beta -adrenoceptors are compromised.
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ISSN:0300-8177
1573-4919
DOI:10.1007/s11010-006-2348-9