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This Article Full Text Full Text (PDF) Supplemental Figure All Versions of this Article: JME-08-0050v1 41/3/117    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Google Scholar Articles by Chalmers, J. A Articles by Belsham, D. D PubMed PubMed Citation Articles by Chalmers, J. A Articles by Belsham, D. D

Departments of¹ , Physiology² Medicine, Obstetrics/Gynaecology, University of Toronto, Medical Sciences Building 3247A, 1 King's College Circle, Toronto, Ontario, M5S 1A8 Canada³ Heart and Stroke/Richard Lewar Centre of Excellence for Cardiovascular Research and Toronto General Hospital Research Institute, Toronto, Canada⁴ Institute of Circulatory and Respiratory Health, Canadian Institutes of Health Research, Ottawa, Canada

(Correspondence should be addressed to D D Belsham; Email: d.belsham{at}utoronto.ca)

^* *J A Chalmers and S-Y J Lin contributed equally to this work

Neuroendocrine peptides express biologic activity relevant to the cardiovascular system, including regulating heart rate and blood pressure, though little is known about the mechanisms involved. Here, we investigated neuroendocrine gene expression underlying diurnal physiology of the heart. We first used microarray and RT-PCR analysis and demonstrate the simultaneous expression of neuroendocrine genes in normal murine heart, including POMC, GnRH, neuropeptide Y, leptin receptor, GH-releasing hormone, cocaine- and amphetamine-regulated transcript, proglucagon, and galanin. We examined diurnal gene expression profiles, with cosinar bioinformatics to evaluate statistically significant rhythms. The POMC gene exhibits a day/night, circadian or diurnal, pattern of expression in heart, and we postulated that this may be important to cardiac growth and renewal. POMC diurnal gene rhythmicity is altered in pressure-overload cardiac hypertrophy, when compared with control heart, and levels increased at the dark-to-light transition times. These findings are also consistent with the proposal that neuropeptides mediate adverse remodeling processes, such as occur in pathologic hypertrophy. To investigate cellular responses, we screened three cell lines representing fibroblasts, cardiac myocytes, and vascular smooth muscle cells (NIH3T3, heart line 1, and mouse vascular smooth muscle cell line 1 (Movas-1) respectively). POMC mRNA expression is the most notable in Movas-1 cells and, furthermore, exhibits rhythmicity with culture synchronization. Taken together, these results highlight the diverse neuroendocrine mRNA expression profiles in cardiovasculature, and provide a novel model vascular culture system to research the role these neuropeptides play in organ health, integrity, and disease.