Adiposity and cardiovascular disorders - Disturbance of the regulatory system consisting of humoral and neuronal signals

被引:174
作者
Katagiri, Hideki
Yamada, Tetsuya
Oka, Yoshitomo
机构
[1] Tohoku Univ, Grad Sch Med, Ctr Translat & Adv Anim Res, Div Adv Therapeut Metab Dis,Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Grad Sch Med, Div Mol Metab & Diabet, Sendai, Miyagi 9808575, Japan
关键词
adipocytokines; autonomic nervous system; metabolic syndrome; atherosclerosis; hypertension;
D O I
10.1161/CIRCRESAHA.107.151621
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity, a major healthcare issue, is associated with significant cardiovascular morbidities, including hypertension and atherosclerosis. Numerous intensive studies conducted this decade have revealed that adipose tissue is a major endocrine organ that secretes a variety of bioactive substances, termed adipocytokines. Adipocytokine secretion profiles are altered as obesity develops, which may increase the risk of obesity-related cardiovascular disorders. For instance, leptin is upregulated in obese subjects and plays important roles in the pathophysiology of obesity-related atherogenesis through multiple mechanisms, such as its proliferative, proinflammatory, prothrombotic, and prooxidant actions. In contrast, adiponectin, which is downregulated in obese subjects, has protective effects against cardiovascular disorders at various atherogenic stages. In addition to these factors secreted by adipose tissue, neuronal circuits involving autonomic nerves are now being recognized as an important metabolic regulatory system and have thus attracted considerable attentions. Alterations in fat accumulation in intraabdominal organs, such as visceral adipose tissue and the liver, send afferent neuronal signals to the brain, leading to modulation of sympathetic tonus and thereby affecting the vasculature. Moreover, these humoral and neuronal signaling pathways communicate with each other, resulting in cooperative metabolic regulation among tissues/organs throughout the body. Further elucidation of these regulatory systems is anticipated to lead to new approaches to devising therapeutic strategies for the metabolic syndrome.
引用
收藏
页码:27 / 39
页数:13
相关论文
共 138 条
[71]   Contrasting blood pressure effects of obesity in leptin-deficient ob/ob mice and agouti yellow obese mice [J].
Mark, AL ;
Shaffer, RA ;
Correia, MLG ;
Morgan, DA ;
Sigmund, CD ;
Haynes, WG .
JOURNAL OF HYPERTENSION, 1999, 17 (12) :1949-1953
[72]  
Maruyama I, 2000, ANN NY ACAD SCI, V902, P315
[73]   A transgenic model of visceral obesity and the metabolic syndrome [J].
Masuzaki, H ;
Paterson, J ;
Shinyama, H ;
Morton, NM ;
Mullins, JJ ;
Seckl, JR ;
Flier, JS .
SCIENCE, 2001, 294 (5549) :2166-2170
[74]   Role of adiponectin in preventing vascular stenosis - The missing link of adipo-vascular axis [J].
Matsuda, M ;
Shimomura, I ;
Sata, M ;
Arita, Y ;
Nishida, M ;
Maeda, N ;
Kumada, M ;
Okamoto, Y ;
Nagaretani, H ;
Nishizawa, H ;
Kishida, K ;
Komuro, R ;
Ouchi, N ;
Kihara, S ;
Nagai, R ;
Funahashi, T ;
Matsuzawa, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (40) :37487-37491
[75]   Liver-specific disruption of PPARγ in leptin-deficient mice improves fatty liver but aggravates diabetic phenotypes [J].
Matsusue, K ;
Haluzik, M ;
Lambert, G ;
Yim, SH ;
Gavrilova, O ;
Ward, JM ;
Brewer, B ;
Reitman, ML ;
Gonzalez, FJ .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (05) :737-747
[76]   Adiponectin suppresses proliferation and superoxide generation and enhances eNOS activity in endothelial cells with oxidized LDL [J].
Motoshima, H ;
Wu, XD ;
Mahadev, K ;
Goldstein, BJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 315 (02) :264-271
[77]   Insulin resistance and Type 2 diabetes are not related to resistin expression in human fat cells or skeletal muscle [J].
Nagaev, I ;
Smith, U .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 285 (02) :561-564
[78]   Importance of intra-abdominal visceral fat accumulation to coronary atherosclerosis in heterozygous familial hypercholesterolaemia [J].
Nakamura, T ;
Kobayashi, H ;
Yanagi, K ;
Nakagawa, T ;
Nishida, M ;
Kihara, S ;
Hiraoka, H ;
Nozaki, S ;
Funahashi, T ;
Yamashita, S ;
KamedaTakemura, K ;
Matsuzawa, Y .
INTERNATIONAL JOURNAL OF OBESITY, 1997, 21 (07) :580-586
[79]  
Nakano Y, 1996, J BIOCHEM-TOKYO, V120, P803
[80]   Mice lacking adiponectin show decreased hepatic insulin sensitivity and reduced responsiveness to peroxisome proliferator-activated receptor γ agonists [J].
Nawrocki, AR ;
Rajala, MW ;
Tomas, E ;
Pajvani, UB ;
Saha, AK ;
Trumbauer, ME ;
Pang, Z ;
Chen, AS ;
Ruderman, NB ;
Chen, H ;
Rossetti, L ;
Scherer, PE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (05) :2654-2660