Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2192436 | Journal of Molecular and Cellular Cardiology | 2006 | 10 Pages |
Vitamin D3 deficiency enhances cardiac contraction in experimental studies, yet paradoxically this deficiency is linked to congestive heart failure in humans. Activated vitamin D3 (1α,25-dihydroxyvitamin D3) or calcitriol, decreases peak force and activates protein kinase C (PKC) in isolated perfused hearts. However, the direct influence of this hormone on adult cardiac myocyte contractile function is not well understood. Our aim is to investigate whether 1α,25-dihydroxyvitamin D3 acutely modulates contractile function via PKC activation in adult rat cardiac myocytes. Sarcomere shortening and re-lengthening were measured in electrically stimulated myocytes isolated from adult rat hearts, and the vitamin D3 response (10−10 to 10−7 M) was compared to shortening observed under basal conditions. Maximum changes in sarcomere shortening and relaxation were observed with 10−9 M 1α,25-dihydroxyvitamin D3. This dose decreased peak shortening, and accelerated contraction and relaxation rates within 5 min of administration, and changes in the Ca2+ transient contributed to the peak shortening and relaxation effects. The PKC inhibitor, bis-indolylmaleimide (500 nM) largely blocked the acute influence of the most potent dose (10−9 M) on contractile function. While peak shortening and shortening rate returned to baseline within 30 min, there was a sustained acceleration of relaxation that continued over 60 min. Phosphorylation of the Ca2+ regulatory proteins, phospholamban, and cardiac troponin I correlated with the accelerated relaxation observed in response to acute application of 1α,25-dihydroxyvitamin D3. Accelerated relaxation continued to be observed after chronic addition of 1α,25-dihydroxyvitamin D3 (e.g. 2 days), yet this sustained increase in relaxation was not associated with increased phosphorylation of phospholamban or troponin I. These results provide evidence that 1α,25-dihydroxyvitamin D3 directly modulates adult myocyte contractile function, and protein kinase C plays an important signaling role in the acute response. Phosphorylation of key Ca2+ regulatory proteins by this kinase contributes to the enhanced relaxation observed in response to acute, but not chronic calcitriol.