Possible relationship between adiponectin and renal tubular injury in diabetic nephropathy

被引:59
作者
Fujita, Hlroki [1 ]
Morii, Tsukasa [1 ]
Koshimura, Jun [1 ]
Ishikawa, Motoko [1 ]
Kato, Masako [1 ]
Miura, Takeshi [1 ]
Sasaki, Hiroshi [1 ]
Narita, Takuma [1 ]
Ito, Seiki [1 ]
Kakei, Masafumi [1 ]
机构
[1] Akita Univ, Sch Med, Dept Internal Med, Div Endocrinol Metab & Geriatr Med, Akita 0108543, Japan
关键词
adiponectin; diabetic nephropathy; renal tubular injury; N-acetylglucosaminidase; monocyte chemoattractant protein-1;
D O I
10.1507/endocrj.K06-016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adiponectin is an adipose-derived protein which has anti-inflammatory and anti-atherogenic properties in addition to insulin-sensitizing effects. To date, the role of adiponectin in the pathogenesis of diabetic nephropathy remains unclear. The aim of the present study was to explore the relationship between adiponectin and renal tubular injury in diabetic nephropathy. We determined serum and urinary adiponectin levels in type 2 diabetic patients with normoalbuminuria (n = 19), microalbuminuria (n = 18), and overt diabetic nephropathy (n = 16), and then analyzed the correlations between serum and urinary adiponectin, urinary N-acetylglucosaminidase (NAG) as a clinical marker of renal tubular injury, urinary monocyte chemoattractant protein-1 (MCP-1) as an inflammatory marker in renal tubulointerstitium, and clinical markers of renal disease. Notably, serum and urinary adiponectin levels were significantly increased in patients with overt diabetic nephropathy compared to those with normoalbuminuria and microalbuminuria. In univariate linear regression analysis, serum adiponectin levels were positively correlated with serum creatinine (r = 0.648, P < 0.0001), urinary albumin (r = 0.583, P < 0.0001), urinary NAG (r = 0.406, P < 0.01), urinary MCP-1 (r = 0.514, P < 0.0001). and urinary adiponectin (r = 0.691, P < 0.0001) levels in all diabetic patients. Urinary adiponectin levels were also positively correlated with serum creatinine (r = 0.729, P < 0.0001), urinary albumin (r = 0.799, P < 0.0001), urinary NAG (r = 0.701, P < 0.0001), andurinary MCP-1 (r = 0.801, P < 0.0001) levels in all diabetic patients. Multiple linear regression analysis showed that serum creatinine and urinary adiponectin levels were independently associated with serum adiponectin levels (r(2) = 0.522), and that serum creatinine, urinary NAG, urinary MCP-1, and serum adiponectin levels were independent determinants of urinary adiponectin levels (r(2) = 0.851). These results collectively indicate that renal insufficiency and tubular injury possibly play a contributory role in increases in serum and urinary adiponectin levels in overt diabetic nephropathy. We presume that an increase in circulating adiponectin in overt diabetic nephropathy might be a physiological response to mitigate renal tubular injury and to prevent the further progression of diabetic nephropathy through its anti-inflammatory and anti-atherogenic effects.
引用
收藏
页码:745 / 752
页数:8
相关论文
共 28 条
[1]   Adipocyte-derived plasma protein adiponectin acts as a platelet-derived growth factor-BB-binding protein and regulates growth factor-induced common postreceptor signal in vascular smooth muscle cell [J].
Arita, Y ;
Kihara, S ;
Ouchi, N ;
Maeda, K ;
Kuriyama, H ;
Okamoto, Y ;
Kumada, M ;
Hotta, K ;
Nishida, M ;
Takahashi, M ;
Nakamura, T ;
Shimomura, I ;
Muraguchi, M ;
Ohmoto, Y ;
Funahashi, T ;
Matsuzawa, Y .
CIRCULATION, 2002, 105 (24) :2893-2898
[2]   Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity [J].
Arita, Y ;
Kihara, S ;
Ouchi, N ;
Takahashi, M ;
Maeda, K ;
Miyagawa, J ;
Hotta, K ;
Shimomura, I ;
Nakamura, T ;
Miyaoka, K ;
Kuriyama, H ;
Nishida, M ;
Yamashita, S ;
Okubo, K ;
Matsubara, K ;
Muraguchi, M ;
Ohmoto, Y ;
Funahashi, T ;
Matsuzawa, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (01) :79-83
[3]   The adipocyte-secreted protein Acrp30 enhances hepatic insulin action [J].
Berg, AH ;
Combs, TP ;
Du, XL ;
Brownlee, M ;
Scherer, PE .
NATURE MEDICINE, 2001, 7 (08) :947-953
[4]   Hypoadiponectinemia is associated with ischemic cerebrovascular disease [J].
Chen, MP ;
Tsai, JCR ;
Chung, FM ;
Yang, SS ;
Hsing, LL ;
Shin, SJ ;
Lee, YJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (04) :821-826
[5]   Endogenous glucose production is inhibited by the adipose-derived protein Acrp30 [J].
Combs, TP ;
Berg, AH ;
Obici, S ;
Scherer, PE ;
Rossetti, L .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (12) :1875-1881
[6]   Cardiovascular complications in the diabetic patient with renal disease: an update in 2003 [J].
Dikow, R ;
Ritz, E .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2003, 18 (10) :1993-1998
[7]   Plasma concentrations of a novel, adipose-specific protein, adiponectin, in type 2 diabetic patients [J].
Hotta, K ;
Funahashi, T ;
Arita, Y ;
Takahashi, M ;
Matsuda, M ;
Okamoto, Y ;
Iwahashi, H ;
Kuriyama, H ;
Ouchi, N ;
Maeda, K ;
Nishida, M ;
Kihara, S ;
Sakai, N ;
Nakajima, T ;
Hasegawa, K ;
Muraguchi, M ;
Ohmoto, Y ;
Nakamura, T ;
Yamashita, S ;
Hanafusa, T ;
Matsuzawa, Y .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (06) :1595-1599
[8]   Urinary adiponectin excretion is increased in patients with overt diabetic nephropathy [J].
Koshimura, J ;
Fujita, H ;
Narita, T ;
Shimotomai, T ;
Hosoba, M ;
Yoshioka, N ;
Kakei, M ;
Fujishima, H ;
Ito, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 316 (01) :165-169
[9]   Association of hypoadiponectinemia with coronary artery disease in men [J].
Kumada, M ;
Kihara, S ;
Sumitsuji, S ;
Kawamoto, T ;
Matsumoto, S ;
Ouchi, N ;
Arita, Y ;
Okamoto, Y ;
Shimomura, I ;
Hiraoka, H ;
Nakamura, T ;
Funahashi, T ;
Matsuzawa, Y .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (01) :85-89
[10]   RANTES and monocyte chemoattractant protein-1 (MCP-1) play an important role in the inflammatory phase of crescentic nephritis, but only MCP-1 is involved in crescent formation and interstitial fibrosis [J].
Lloyd, GM ;
Minto, AW ;
Dorf, ME ;
Proudfoot, A ;
Wells, TNC ;
Salant, DJ ;
GutierrezRamos, JC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (07) :1371-1380