کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2166798 1091887 2006 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Autonomic regulation of calcium cycling in developing embryonic mouse hearts
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Autonomic regulation of calcium cycling in developing embryonic mouse hearts
چکیده انگلیسی
In the present study, we combined optical Ca2+ imaging with immunocytochemistry studies to characterize autonomic regulation of Ca2+ cycling during early development in isolated embryonic mouse hearts. At embryonic days 9.5-11.5 (E9.5-E11.5), the Ca2+ transient originated in the superior portion of the right atrium, propagated rapidly through both atria, slowly through the atrio-ventricular (AV) ring, and rapidly through both ventricles. Isoproterenol (ISO) significantly increased heart rate, increased Ca2+ transient amplitude, rate of rise (RR) and a rate of decay, and shortened AV conduction time, indicating the presence of functional β-adrenergic receptors. The muscarinic agonist carbachol (CCh) had no effects until 1 day later at E10.5. Both β1-adrenergic and M2 muscarinic receptors were detected in ventricular muscle sections by immunochemistry at E10.5. Growing nerves, labeled using growth-associated protein 43 antibodies, were detected at the E14.5 stage, but not at E10.5, whereas mature sympathetic nerves, detected by tyrosine hydroxylase (TH) labeling, were not yet present at E14.5. These results demonstrate that functional regulation of Ca2+ cycling by β-adrenergic receptors occurs earliest in developing embryonic mouse hearts, followed a day later by muscarinic receptor responsiveness, with autonomic innervation developing later. These results define the functional and structural sequence of autonomic regulation of Ca2+ transient in the embryonic mouse heart.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Cell Calcium - Volume 39, Issue 5, May 2006, Pages 375-385
نویسندگان
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