A local pre-receptor mechanism of hormone stimulus amplification: Focus on angiotensin II in resistance blood vessels
Journal of Hypertension , Volume 24 - Issue 9 p. 1787- 1796
BACKGROUND: The in-vivo correlation between vascular tone and the concentration of free angiotensin (Ang) II at the level of the arterioles, under (patho)physiological conditions, is not known. OBJECTIVE: To examine the in-vivo kinetics of binding of Ang II to Ang II type 1 (AT 1) receptors in vascular tissue. METHODS AND RESULTS: A plane vascular smooth muscle (VSM) sheet containing a single layer of cells, at one side exposed to Ang II, was the starting point for designing a mathematical model based on local receptor density and geometric considerations and on kinetic parameters of Ang II diffusion and Ang II-AT 1 receptor complex formation and internalization. Calculations demonstrate that a diffusing Ang II molecule at short distance from the receptor has an almost 100% chance to be actually bound, so that the apparent binding rate constant (per unit of receptor concentration) is greatly augmented. This pre-receptor stimulus amplification (PRESTAMP) mechanism is sustained by AT 1 receptor-mediated endocytosis and receptor recycling. On the other hand, PRESTAMP also enhances endocytotic receptor downregulation, and calculations predict that steady-state levels of Ang II above threshold have relatively little additional effect. CONCLUSION: The results explain why physiological concentrations of free Ang II far below the equilibrium dissociation constant of its reaction with AT 1 receptors are sufficient to increase vascular resistance, and why a correlation between blood pressure and the concentration of free Ang II is often difficult to demonstrate.
|Andocytosis, Angiotensin II, Angiotensin II type I receptor, Arteriole, Stimulus amplification|
|Journal of Hypertension|
|Organisation||Department of Internal Medicine|
Schalekamp, M.A.D.H. (2006). A local pre-receptor mechanism of hormone stimulus amplification: Focus on angiotensin II in resistance blood vessels. Journal of Hypertension, 24(9), 1787–1796. doi:10.1097/01.hjh.0000242403.91332.70