Ion channels play a central role as modulators of vascular smooth muscle contractile activity. Of particular relevance in this regard are voltage gated L-type Ca channels (Ca(L)) which control calcium entry into the cell. The activity of Ca(L) channels can be modulated by various kinase cascades that lead either to direct phosphorylation of the channel or phospharylation of some upstream intermediary. In particular, there is convincing evidence that the cAMP/PKA pathway, the cGMP/PKG pathway and the PL/PKC pathway play important roles as modulators of Ca(L) channels. However, the details of how these pathways modulate channel activity are still not clear. The present study investigates kinase regulation of Ca(L) channels in smooth muscle cells of the rabbit portal vein. Experiments are described to investigate the role of G-protein subunits, anchoring proteins, phosphodiesterase activity and phosphatase activity as mediators/modulators of the PKA, PKG and PKC pathways. Whole cell and isolated patch recordings will be undertaken on native vascular myocytes and on Ca(L) channels expressed in mammalian HEK293 cells. The overall hypothesis for these studies is that kinase regulation of Ca(L) channels represents a summation of multiple divergent actions which are set in motion when agonist binds to a receptor. By understanding in greater detail the mechanisms which control calcium entry into vascular smooth muscle cells we may aid in the development of drugs which more selectively modulate vascular Ca(L) channels activity and hence vascular tone. Controlling vascular tone is of central importance in the management of vascular diseases such as high blood pressure and vasospasm which can lead to ischemia, stroke, infarction and ultimately death.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL040399-13
Application #
6389061
Study Section
Experimental Cardiovascular Sciences Study Section (ECS)
Program Officer
Reinlib, Leslie
Project Start
1987-08-01
Project End
2003-06-30
Budget Start
2001-07-01
Budget End
2002-06-30
Support Year
13
Fiscal Year
2001
Total Cost
$197,690
Indirect Cost
Name
University of Nevada Reno
Department
Physiology
Type
Schools of Medicine
DUNS #
146515460
City
Reno
State
NV
Country
United States
Zip Code
89557
Callaghan, Brid; Zhong, Juming; Keef, Kathleen D (2006) Signaling pathway underlying stimulation of L-type Ca2+ channels in rabbit portal vein myocytes by recombinant Gbetagamma subunits. Am J Physiol Heart Circ Physiol 291:H2541-6
Callaghan, B; Koh, S D; Keef, K D (2004) Muscarinic M2 receptor stimulation of Cav1.2b requires phosphatidylinositol 3-kinase, protein kinase C, and c-Src. Circ Res 94:626-33
Eckman, D M; Weinert, J S; Buxton, I L et al. (1994) Cyclic GMP-independent relaxation and hyperpolarization with acetylcholine in guinea-pig coronary artery. Br J Pharmacol 111:1053-60