Role of the natriuretic peptide system in lipogenesis/lipolysis

被引:50
作者
Dessi-Fulgheri, P [1 ]
Sarzani, R [1 ]
Rappelli, A [1 ]
机构
[1] Univ Ancona, Clin Med Interna S, Ancona, Italy
关键词
natriuretic peptides; natriuretic peptide receptors; obesity; adipose tissue; lipolysis; hypertension;
D O I
10.1016/S0939-4753(03)80018-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: There is recent evidence that the natriuretic peptide (NP) system promotes adipose tissue lipolysis in primates. This effect is mediated by the interaction of NP with its active receptors through guanylyl cyclase activation and cGMP production. This review will briefly focus on the new aspects of NP pathophysiology in man. Data synthesis: NP receptors have been described in rodent adipocytes, and the expression of their mRNA is found in human adipose tissue together with high level of ANP binding sites. In isolated fat cells, atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) were able to stimulate lipolysis as much as isoproterenol, a nonselective P-adrenergic receptor agonist, whereas C-type natriuretic peptide (CNP) had the lowest lipolytic effect. The potent lipolytic effect of NP has also been confirmed in samples of abdominal adipose tissue from healthy subjects. The potency order of the lipolytic effect (ANP > BNP > CNP) and ANP-induced cGMP production supported the presence of type A natriuretic peptide receptor in human fat cells. The effect of NP on lipid metabolism is confirmed by the fact that intravenous ANP infusion is followed by plasma NEFA and glycerol concentration increase (reflecting lipid mobilisation). Conclusions: The NP system seems to play an important role in lipid metabolism, possibly affecting the pathophysiology of obesity and obesity-related disorders, such hypertension. Further studies, however, are needed to completely establish the mechanisms involved in NP-induced lipolysis and the real relevance of this new pathway specific of primates. (C)2003, Medikal Press.
引用
收藏
页码:244 / 249
页数:6
相关论文
共 21 条
[1]   In situ assessment of the role of the beta(1)-, beta(2)- and beta(3)-adrenoceptors in the control of lipolysis and nutritive blood flow in human subcutaneous adipose tissue [J].
Barbe, P ;
Millet, L ;
Galitzky, J ;
Lafontan, M ;
Berlan, M .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 117 (05) :907-913
[2]  
COPPACK SW, 1994, J LIPID RES, V35, P177
[3]   A RAPID AND POTENT NATRIURETIC RESPONSE TO INTRAVENOUS-INJECTION OF ATRIAL MYOCARDIAL EXTRACT IN RATS [J].
DEBOLD, AJ ;
BORENSTEIN, HB ;
VERESS, AT ;
SONNENBERG, H .
LIFE SCIENCES, 1981, 28 (01) :89-94
[4]   Structure, localization, and regulation of cGMP-inhibited phosphodiesterase (PDE3) [J].
Degerman, E ;
Belfrage, P ;
Manganiello, VC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (11) :6823-6826
[5]   Plasma atrial natriuretic peptide and natriuretic peptide receptor gene expression in adipose tissue of normotensive and hypertensive obese patients [J].
Dessì-Fulgheri, P ;
Sarzani, R ;
Tamburrini, P ;
Moraca, A ;
Espinosa, E ;
Cola, G ;
Giantomassi, L ;
Rappelli, A .
JOURNAL OF HYPERTENSION, 1997, 15 (12) :1695-1699
[6]   Low calorie diet enhances renal, hemodynamic, and humoral effects of exogenous atrial natriuretic peptide in obese hypertensives [J].
Dessì-Fulgheri, P ;
Sarzani, R ;
Serenelli, M ;
Tamburrini, P ;
Spagnolo, D ;
Giantomassi, L ;
Espinosa, E ;
Rappelli, A .
HYPERTENSION, 1999, 33 (02) :658-662
[7]  
Galitzky J, 2001, J LIPID RES, V42, P536
[8]   ATRIAL NATRIURETIC POLYPEPTIDE INHIBITS HYPERTROPHY OF VASCULAR SMOOTH-MUSCLE CELLS [J].
ITOH, H ;
PRATT, RE ;
DZAU, VJ .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (05) :1690-1697
[9]   Regulation of lipolysis: natriuretic peptides and the development of cachexia [J].
Kalra, PR ;
Tigas, S .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2002, 85 (01) :125-132
[10]   MOLECULAR-BIOLOGY OF THE NATRIURETIC PEPTIDES AND THEIR RECEPTORS [J].
KOLLER, KJ ;
GOEDDEL, DV .
CIRCULATION, 1992, 86 (04) :1081-1088