1. Volume 78, Issue 9, Pages 883-894 (November 2010)
CCR2 antagonism improves insulin resistance, lipid metabolism, and diabetic nephropathy in type 2 diabetic mice 
Young Sun Kang, Mi Hwa Lee, Hye Kyoung Song, Gang Jee Ko, Oh Sung Kwon, Tae Kyung Lim, Sung Hwan Kim, Sang Youb Han, Kum Hyun Han, Ji Eun Lee, Jee Young Han, Hyoung Kyu Kim, Dae Ryong Cha 
Kidney International 
Volume 78, Issue 9, Pages (November 2010)
DOI: /ki
Copyright © 2010 International Society of Nephrology Terms and Conditions

2. Figure 1
Effects of RS on 24-h urinary albumin excretion in experimental animals. Twenty-four-hour urine was collected at monthly intervals after RS administration. Data shown are means±s.e.m.; *P<0.05 and **P<0.01, control vs RS
Kidney International  , DOI: ( /ki )
Copyright © 2010 International Society of Nephrology Terms and Conditions

3. Figure 2
Effects of RS on insulin resistance, glucose intolerance, and metabolic parameters in experimental animals. (a) Insulin tolerance test, (b) glucose tolerance test (GTT), (c) plasma lipid concentrations, (d) plasma insulin concentrations, and (e) HOMA-IR. Data in GTT were expressed as percentage of basal glucose levels due to high basal glucose levels. Data shown are means±s.e.m. HOMA-IR, the homeostasis model assessment index, was calculated using the equation fasting glucose (mmol/l) × fasting insulin (mUnits/l)/22.5. Comparisons were performed between control groups and the RS treatment group at the same time points; *P<0.05, control vs RS504393; **P<0.01, control vs RS HOMA-IR, homeostasis model assessment-insulin resistance.
Kidney International  , DOI: ( /ki )
Copyright © 2010 International Society of Nephrology Terms and Conditions

4. Figure 3
Representative renal histological findings in experimental animals. (a1–a2) PAS stain; (b1–b2) MT stain; (c) mesangial expansion score; (panels a1, b1) control db/db mice; (panels a2, b2) db/db mice treated with RS504393; short arrows show (panel a1) typical mesangial expansion area and (panel b1) MT (+) sclerotic area. Data shown are means±s.e.m.; **P<0.01, control vs RS Original magnification × 400. MT, Masson's trichrome; PAS, periodic acid-Schiff.
Kidney International  , DOI: ( /ki )
Copyright © 2010 International Society of Nephrology Terms and Conditions

5. Figure 4
Representative histological findings of various organs in experimental animals. (a1–a2) Pancreas, PAS stain, (b1–b2) liver, HE stain, (c1–c2) aorta, HE stain, (d1–d2) fat, HE stain, (e1–e2) heart, MT stain. (f–h) Quantitative analysis of (panel f) islet cell mass, (panel g) lipid content in the liver, (panel h) aorta intimal/medial ratio, and (panel i) adipocyte size. (Panels a1–e1) control db/db mice; (panels a2–e2) db/db mice treated with RS Islet cell mass, adipocyte size, and aorta intimal/medial ratio are expressed as percentage value relative to control group; short arrows show (panel a1) enlarged islet cell mass, (panel b1) typical fat accumulation, (panel c1) medial thickness area, and (panel d1) enlarged adipocyte. Data are shown as means±s.e.m.; *P<0.05, control vs RS504393; **P<0.01, control vs RS Original magnification × 400. HE, hematoxylin and eosin; MT, Masson's trichrome; PAS, periodic acid-Schiff.
Kidney International  , DOI: ( /ki )
Copyright © 2010 International Society of Nephrology Terms and Conditions

6. Figure 5
Effects of RS on mRNA expression for proinflammatory and profibrotic cytokines in the renal and adipose tissues in experimental animals. (a) Gene expression in the renal cortical tissues. (b) Gene expression in the adipose tissues. Data are shown as means±s.e.m. *P<0.05, control vs RS504393; **P<0.01, control vs RS504393; ***P<0.001, control vs RS MCP-1; monocyte chemoattractant protein-1; PAI-1; plasminogen activator inhibitor-1; PPARγ, peroxisome proliferator-activated receptor-γ; TGF-β1, transforming growth factor-β1.
Kidney International  , DOI: ( /ki )
Copyright © 2010 International Society of Nephrology Terms and Conditions

7. Figure 6
Representative renal immunohistochemical staining findings in experimental animals. (a1–a2) PAI-1, (b1–b2) type IV collagen, (c1–c2) TGF-β1, (d1–d2) CD68; (e–f) immunohistochemical staining score; (panels a1–d1) control db/db mice; (panels a2–d2) db/db mice treated with RS Short arrows show (panel a1) typical PAI-1-positive area, (panel b1) type IV collagen-positive area, (panel c1) TGF-β1-positive area, and (panel d1) CD68-positive area. Data are shown as means±s.e.m. *P<0.05, control vs RS504393; **P<0.01, control vs RS Original magnification × 400. PAI-1; plasminogen activator inhibitor-1; TGF-β1, transforming growth factor-β1.
Kidney International  , DOI: ( /ki )
Copyright © 2010 International Society of Nephrology Terms and Conditions

8. Figure 7
Effects of RS on lipid metabolism in experimental animals. (a) mRNA expression for renal lipid metabolism in the renal cortical tissues. (b–c) Cholesterol and triglyceride contents in the kidney. (d–e) Cholesterol and triglyceride contents in the adipose tissue. (f) Representative immunoblot from renal cortical tissues for SREBP-1: arrow shows 68-kDa band of the active cleaved site of SREBP-1. Data are shown as means±s.e.m. *P<0.05, control vs RS504393; ***P<0.001, control vs RS ABCA1, ATP-binding cassette transporter-1; FXR, farnesoid X receptor; HMG-CoA reductase, 3-hydroxy-3-methylglutaryl-coenzyme A; SREBP-1c, sterol regulatory element-binding protein-1c.
Kidney International  , DOI: ( /ki )
Copyright © 2010 International Society of Nephrology Terms and Conditions

9. Figure 8
Effects of RS on lipid peroxidation and oxidative stress in experimental animals. (a–b) Tissue content of lipid hydroperoxides (LPOs) in the renal cortical tissues and adipose tissues. (c–d) Plasma and 24-h urinary levels of 8-isoprostane; urinary excretion of 8-isoprostane was corrected by urinary creatinine. Data are shown as means±s.e.m. *P<0.05, control vs RS504393; **P<0.01, control vs RS504393; ***P<0.001, control vs RS
Kidney International  , DOI: ( /ki )
Copyright © 2010 International Society of Nephrology Terms and Conditions

10. Figure 9
Effect of RS on adipocyte differentiation and 2-deoxy-D-glucose (2-DOG) uptake in cultured adipocytes. (a) Oil-red O stain. Adipocytes were cultured without RS (A) or with RS (B) at a concentration of 100 nmol/l (b) 2-DOG uptake assay. Differentiated adipocytes were stimulated with 10 nmol/l of insulin with or without 100 nmol/l of RS The radioactivity was normalized for total protein concentration in each condition and 2-DOG uptake was expressed as % change over control. Data are shown as means±s.e.m. ***P<0.01 vs control, #P<0.05 vs insulin.
Kidney International  , DOI: ( /ki )
Copyright © 2010 International Society of Nephrology Terms and Conditions