Neural regulation of blood pressure by leptin and the related peptides

被引:71
作者
Matsumura, K [1 ]
Tsuchihashi, T [1 ]
Fujii, K [1 ]
Iida, M [1 ]
机构
[1] Kyushu Univ, Dept Med & Clin Sci, Grad Sch Med Sci, Higashi Ku, Fukuoka 8128582, Japan
关键词
appetite; leptin; ghrelin; sympathetic nervous system;
D O I
10.1016/S0167-0115(03)00116-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recent biological advances make it possible to discover new peptides associated with obesity., Leptin, neuropepticle Y, corticotrophin-releasing factor (CRF), alpha-melanocyte stimulating hormone (alpha-MSH), and cocaine- and amphetamine-regulated transcript (CART) peptides are known to participate in appetite and feeding behavior. Various lines of evidence suggest that these peptides participate not only in feeding behavior but also in cardiovascular and sympathetic regulations. Both leptin and ghrelin are secreted from the peripheral tissue; then they reach the brain to modulate sympathetic activity. These two peptides seem to play important roles to transmit peripheral metabolic information to the brain, and to convert it to cardiovascular and sympathetic information. Leptin activates neurons containing alpha-melanocyte stimulating hormone and cocaine- and amphetamine-regulated transcript peptides, resulting in increases in sympathetic activity and blood pressure. Cardiovascular action of a-melanocyte stimulating hormone is mediated through melanocortin-4 receptor, and agouti-related protein (AGRP) plays a role as an endogenous melanocortin-4 receptor antagonist. In contrast, ghrelin and neuropeptide Y in the brain suppress sympathetic activity and decrease blood pressure. Depressor and sympathoinhibitory effects of central neuropeptide Y are inhibited by leptin. Furthermore,. central ghrelin modulates baroreflex control of renal sympathetic nerve activity and heart rate. Thus, leptin and the related peptides, which participate in appetite and feeding behavior, seem to function together to regulate cardiovascular system and sympathetic nerve activity, and may play a key role in the association between obesity and hypertension. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 86
页数:8
相关论文
共 86 条
[1]   Pathophysiological role of leptin in obesity-related hypertension [J].
Aizawa-Abe, M ;
Ogawa, Y ;
Masuzaki, H ;
Ebihara, K ;
Satoh, N ;
Iwai, H ;
Matsuoka, N ;
Hayashi, T ;
Hosoda, K ;
Inoue, G ;
Yoshimasa, Y ;
Nakao, K .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (09) :1243-1252
[2]   BODY-COMPOSITION, BONE METABOLISM, AND HEART STRUCTURE AND FUNCTION IN GROWTH-HORMONE (GH)DEFICIENT ADULTS BEFORE AND AFTER GH REPLACEMENT THERAPY AT LOW-DOSES [J].
AMATO, G ;
CARELLA, C ;
FAZIO, S ;
LAMONTAGNA, G ;
CITTADINI, A ;
SABATINI, D ;
MARCIANOMONE, C ;
SACCA, L ;
BELLASTELLA, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (06) :1671-1676
[3]   EFFECTS OF CORTICOTROPIN-RELEASING FACTOR ON FOOD-INTAKE AND BROWN ADIPOSE-TISSUE THERMOGENESIS IN RATS [J].
ARASE, K ;
YORK, DA ;
SHIMIZU, H ;
SHARGILL, N ;
BRAY, GA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (03) :E255-E259
[4]  
Bailey ART, 2000, J NEUROENDOCRINOL, V12, P191
[5]   Acute cardiovascular and hormonal effects of GH and hexarelin, a synthetic GH-releasing peptide, in humans [J].
Bisi, G ;
Podio, V ;
Valetto, MR ;
Broglio, F ;
Bertuccio, G ;
Del Rio, G ;
Arvat, E ;
Boghen, MF ;
Deghenghi, R ;
Muccioli, G ;
Ong, H ;
Ghigo, E .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1999, 22 (04) :266-272
[6]   Do centrally administered neuropeptides access cognate receptors? An analysis in the central corticotropin-releasing factor system [J].
Bittencourt, JC ;
Sawchenko, PE .
JOURNAL OF NEUROSCIENCE, 2000, 20 (03) :1142-1156
[7]   Pressor effects of orexins injected intracisternally and to rostral ventrolateral medulla of anesthetized rats [J].
Chen, CT ;
Hwang, LL ;
Chang, JK ;
Dun, NJ .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2000, 278 (03) :R692-R697
[8]   THE ANATOMY OF NEUROPEPTIDE-Y-CONTAINING NEURONS IN RAT-BRAIN [J].
CHRONWALL, BM ;
DIMAGGIO, DA ;
MASSARI, VJ ;
PICKEL, VM ;
RUGGIERO, DA ;
ODONOHUE, TL .
NEUROSCIENCE, 1985, 15 (04) :1159-1181
[9]   A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2 [J].
Comuzzie, AG ;
Hixson, JE ;
Almasy, L ;
Mitchell, BD ;
Mahaney, MC ;
Dyer, TD ;
Stern, MP ;
MacCluer, JW ;
Blangero, J .
NATURE GENETICS, 1997, 15 (03) :273-276
[10]   The concept of selective leptin resistance - Evidence from agouti yellow obese mice [J].
Correia, MLG ;
Haynes, WG ;
Rahmouni, K ;
Morgan, DA ;
Sivitz, WI ;
Mark, AL .
DIABETES, 2002, 51 (02) :439-442