Summary: Cardiovascular Disease (CVD) remains the leading cause of death worldwide and is linked to a variety of co- morbidities including Type 2 Diabetes Mellitus (T2DM), and Obesity. Work over the last 20 years by our group and others have identified the Angiotensin II Type 2 Receptor (AT2R) as a key player in the development and pathogenesis of cardiac and vascular structural damage. Clinically, in men, loss of Agtr2 expression is associated with increased arterial stiffness, impaired kidney function, and increased pulse pressure. Literature shows that female-specific increase in AT2R expression protects murine female models from vascular injury. Healthy female (ZL-F) rats have higher cardiac expression of the X-linked Agtr2 compared to male (ZL-M) rats; but T2DM suppressed cardiac Agtr2 expression only in ZDF-F (female), not in ZDF-M (male). We posit that increasing Agtr2 expression in ZDF-F rat heart will render protection from cardiomyocyte loss and scarring and this treatment will be of particular benefit to women suffering from CVD. However, there are no AT2R agonists that can increase Agtr2 expression. We observed that NP-6A4, a novel peptide agonist of AT2R, could increase Agtr2 expression in rat and human CV cells and mitigate cardiac hypertrophy, fibrosis and capillary rarefaction in male Zucker obese rats. Our conceptually novel central hypothesis is based on these observations and states that NP-6A4-AT2R-signaling offers a new therapeutic approach to mitigate sex differences in CVD by increasing Agtr2 gene expression. We discovered two new cross-talks induced by NP- 6A4-AT2R; first is activation of ALK2-ALK1 pathway that mitigates capillary rarefaction, and the second is suppression of the mineralocorticoid receptor (MR) involved in pathological CV remodeling. In Aim 1, we will validate our hypothesis that NP-6A4 improves structural and functional cardiac and vascular parameters in rat models with chronic CVD induced by T2DM via increasing Agtr2 expression and signaling. We will use our new methods of detecting subclinical damage and subsequent protective remodeling via speckle tracking echocardiography (STE) in combination with histopathology, and extensive molecular signaling approaches. In Aim 2, we will investigate if NP-6A4 mitigates cardiac and vascular structural damage caused by acute mechanical- and drug-induced injury. We will also investigate a) the role of cross-talk between NP-6A4-AT2R and the Activin-like kinases (ALK2-ALK1 pathway) in improving capillary density, and b) the significance of the cross-talk between NP-6A4-AT2R and MR in mitigating pathological cardiovascular remodeling. Collectively, positive results of this study will have high clinical relevance since they validate a) the efficacy of NP-6A4 as a novel therapeutic for acute and chronic CVD, and for mitigating sex differences in CVD, and b) the efficacy of STE-based diagnosis of the progression and mitigation of T2DM-induced subclinical cardiovascular da...