Young Sun Kang
Korea University · Medicine
About the Lab
Professor Young Sun Kang's research lab focuses on the pathophysiological mechanisms linking metabolic syndrome, obesity, and organ damage, particularly in the kidney and vasculature. The lab investigates the roles of key signaling pathways such as the renin-angiotensin-aldosterone system (RAAS), chemokine systems (e.g., CCL2/CCR2), and growth factors (e.g., VEGF) in mediating inflammation, fibrosis, and vascular dysfunction. A significant portion of the work also explores the use of paramagnetic ions, especially manganese, as contrast agents in proton NMR imaging, emphasizing their biodistribution, relaxivity, and potential for targeted molecular imaging. The lab integrates molecular biology, cell culture models, and in vivo imaging to uncover novel therapeutic targets for metabolic and cardiovascular diseases.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15With excess nutrition, the burden of obesity is a growing problem worldwide. The imbalance between energy intake and expenditure leads to variable disorders as all major risk factors for cardiovascular disease. There are many hypothetical mechanisms to explain obesity-associated hypertension. Activation of the RAAS is a key contributing factor in obesity. Particularly, the RAAS in adipose tissue plays a crucial role in adipose tissue dysfunction and obesity-induced inflammation. The phenotypic c
Angiotensin II (Ang-II) and vascular endothelial growth factor (VEGF) have an important role in the pathogenesis of diabetic nephropathy, but the signaling cascade of VEGF regulation in response to Ang-II in podocytes is largely unknown. In these experiments, we looked at the effect of Ang-II on the production of VEGF, and investigated whether VEGF production depends on the p38 mitogen activated protein kinase (MAPK) pathway in cultured mouse podocytes. Incubation of podocytes with Ang-II induce
Manganese is a powerful paramagnetic material and potential NMR contrast agent. It drastically affects the NMR properties of solutions and tissues and is less toxic than most other transition elements. It also possesses some unusual and advantageous features; it alters T1 and T2 to different degrees, and it can bind to macromolecules to become even more effective at reducing proton relaxation times. The dose dependence of tissue relaxation rate increases has been measured in mice, and proton rel
Some factors affecting the performance of paramagnetic ions as contrast agents for proton NMR imaging have been studied. It is demonstrated that the relaxation rate of an aqueous solution of the ion is not reliably predicted by its magnetic moment, but that significant relaxation enhancement may result when the ion is complexed with large molecules, which increases the dominant correlation time. This enhancement in turn can be altered by factors such as pH and competition for binding. Chelation
Aldosterone receptor antagonism provided additional benefits beyond blockade of the renin-angiotensin system in type II diabetic nephropathy.
There is abundant experimental evidence that the CCL2/CCR2 pathway may be involved in chronic low-grade inflammation of adipose tissue in obesity and related metabolic diseases. Although animal models of diabetes and obesity, as well as human trials, have produced controversial results, there is continued interest in the roles of CCR2 inhibition in metabolic disease. Further identification of the mechanisms for recruitment and activation of phagocytes and determination of the roles of other chem
Dynamic Gd-DTPA-enhanced fast MRI technique can detect acute changes in bone marrow perfusion due to venous occlusion. This technique may have applications in the early detection of nontraumatic AVN.
BACKGROUND: Aliskiren is a direct renin inhibitor (DRI) and provides an organ-protective effect in human and animal experiments. However, there is no current evidence of the effect of DRI on insulin resistance and metabolic abnormalities in type 2 diabetic animals. Methods. We investigated the effects and molecular mechanism of aliskiren in db/db mice and cultured mesangial cells (MCs). RESULTS: Aliskiren treatment for 3 months at a dose of 25 mg/kg/day via an osmotic mini-pump did not induce si
From these results, a more accurate assessment of renal function should be required in a population characterized by older age, male gender and more proteinuria. The MDRD study formula and Cockcroft-Gault formula have greater accuracy and precision with true GFR, and this equation can be applied in subjects with healthy general population.
TLR inhibition by administering GIT27 improved metabolic parameters. GIT27 ameliorates abnormalities of lipid metabolism and may have renoprotective effects on obesity-related kidney disease through its anti-inflammatory properties.
Research Areas
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