Previous studies from this laboratory have demonstrated that dietary consumption of omega-3 fatty acids (FAs) can modulate arteiorlar resistance in normal rats and rats with renal ablation. Preliminary data is presented suggesting that omega-3 FAs modulate arteriolar tone by limiting the synthesis of TXA2, by altering the hydrolysis of phosphatidylinositol, or by modulating the expression of PKC-alpha. This proposal will elucidate the cellular basis of altered arteriolar tone by utilizing cultured glomerular muscle cells to study excitation-contraction coupling. As a basis for these studies, they have recently demonstrated decreased Angiotensin II (Ang II)-stimulated phosphorylation of the 20 kDa light chain (LC20) of myosin in mesangial cells enriched with eicospentaenoic acid (EPA). These findings were coupled with a parallel decrease in cell TXA2 synthesis.
In aim #1, they will define the role of TXA2 in promoting Ang II-stimulated LC20 phosphorylation by using single test agents to selecting inhibit or excite TXA2 mediated LC20 phosphorylation. Since PKC-alpha may also be involved in Ang II stimulated LC20 phosphorylation and EPA appears to modulate its expression in vivo, they will also define the role of PCK-alpha in mediating Ang-II stimulated LC20 phosphorylation in aim #2. To elucidate PKC-alpha mediated responses from other events involved in excitation-contraction coupling, they have developed a mutant, catalytically inactive PKC-alpha (dominant-negative activity) and have successfully expressed the mutant enzyme in COS-7 and mesangial cells. Significant inhibition of PKC-alpha wild-type activity was attained. Two dimensional peptide mapping will complement these studies to explore site-specific alterations in phosphorylation, e.g., serine -1, 2 versus serine -19. Parallel experiments in kinase dead cells enriched with EPA will be performed to differentiate PKC-alpha independent versus dependent effects of EPA on excitation-contraction coupling. These studies will provide novel insights into the mechanisms which regulate excitation-contraction coupling in muscle cells and may provide a clue to the pathogenesis of altered arteriolar tone in hypertension, atherosclerosis and progressive renal disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK052039-01A1
Application #
2467468
Study Section
Cardiovascular and Renal Study Section (CVB)
Project Start
1998-01-01
Project End
2001-12-31
Budget Start
1998-01-01
Budget End
1998-12-31
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Saint Louis University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Saint Louis
State
MO
Country
United States
Zip Code
63103
Schmitz, Paul G; Antony, Karthikapallil A (2002) Omega-3 fatty acids in ESRD: should patients with ESRD eat more fish? Nephrol Dial Transplant 17:11-4
Schmitz, Paul G; McCloud, Linda K; Reikes, Sanford T et al. (2002) Prophylaxis of hemodialysis graft thrombosis with fish oil: double-blind, randomized, prospective trial. J Am Soc Nephrol 13:184-90
Schmitz, P G; Zhang, K; Dalal, R (2000) Eicosapentaenoic acid suppresses PDGF-induced DNA synthesis in rat mesangial cells: involvement of thromboxane A2. Kidney Int 57:1041-51
Lane, P H; Tyler, L D; Schmitz, P G (1998) Chronic administration of furosemide augments renal weight and glomerular capillary pressure in normal rats. Am J Physiol 275:F230-4