6 research outputs found
INTRACELLULAR REGULATION OF ATRIAL EXCITATION CONTRACTION COUPLING IN NORMAL AND ARRHYTHMOGENIC HEARTS
Atrial fibrillation (AF) is the most common arrhythmia with a prevalence of 1-2% of the US population and it is the most important single risk factor for an ischemic stroke. Despite decades of research, successful termination of the arrhythmia remains difficult. The challenge is in part due to our incomplete understanding of atrial myocyte Ca2+ signaling and underlying disease mechanisms. In the atria, like all cardiac tissue, the conducted action potential (AP) underlies triggering of the [Ca2+]i transient, which is responsible for activating contraction. The process that links electrical activity to Ca2+ signaling and contraction is known as excitation-contraction coupling (ECC).
The objective of this dissertation is to understand the mechanism of excitation contraction coupling in atrial myocytes. To achieve this goal, we (1) developed tools to specifically study atrial cell biology, (2) we studied the role of altered Ca2+ buffering on ionic membrane currents and Ca2+ signaling, (3) we investigated the role that reactive oxygen species (ROS) plays in altered Ca2+ signaling and the morphology of the AP and (4) we measured intracellular sodium concentration ([Na+]i ) and studied Na+ and Ca2+ signaling in a transgenic murine model of AF. This work includes mathematical modeling of atrial cell electrical and Ca2+ signaling to define our quantitative understanding of the processes involved.
Our results indicate that increased Ca2+ buffering plays a major role in speeding the inactivation of the L type Ca2+ current (ICa,L ). This work also shows that low concentrations of H2O2 for a brief period increases atrial Ca2+ spark rate, changes spark characteristics and decreases the duration of the AP. We quantified for the first time the [Na+]i in murine atrial cells both at rest and during field stimulation in control and transgenic mice. Our results indicate that [Na+]i is significantly lower in atrial myocytes in comparison to their ventricular counterparts, which reveal important differences in how [Na+]i is regulated in atrial cells. Moreover, our work demonstrates that [Na+]i and [Ca2+]i homeostasis are profoundly affected during AF. The results further our understanding of mechanisms that modulate excitation-contraction coupling in atrial myocytes in normal and pathophysiological conditions
Modeling the Structure and Function of L-Type Calcium Channel (Cav1.2) to Understand its Effect in Cardiac Propagation
Region of slowed conduction acts as core for spiral wave reentry in cardiac cell monolayers
The Significance of autonomy and autonomy support in psychological development and psychopathology
This chapter, in keeping with the spirit of the field of developmental psychopathology, examines both the developmental underpinnings of healthy autonomy and the processes involved in its disruption and manifestation as pathology. It critically examines the interface between normal and impaired development. The chapter sets forth a definition of autonomy that is informed by both philosophical and clinical analyses and that differentiates autonomy from closely related constructs such as free will, independence, individualism, and detachment. Then, it explores how autonomy is intertwined with the developmental processes of intrinsic motivation, internalization, attachment, and emotional integration, paying particular attention to how conditions in the social context either support the motivational and emotional bases of normal development or, undermine these bases, leading to psychopathology. Finally, the chapter discusses the experience and dynamics of autonomy with regard to varied psychological disorder