Renal effects of leptin in normotensive, hypertensive, and obese rats

被引:77
作者
Villarreal, D
Reams, G
Freeman, RH
Taraben, A
机构
[1] Univ Missouri, Hlth Sci Ctr, Dept Internal Med, Columbia, MO 65212 USA
[2] Univ Missouri, Dept Physiol, Columbia, MO 65212 USA
[3] Harry S Truman Mem Vet Hosp, Columbia, MO 65212 USA
关键词
natriuresis; systemic and renal hemodynamics; plasma renin activity;
D O I
10.1152/ajpregu.1998.275.6.R2056
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The hemodynamic, hormonal, and renal excretory effects of intravenous bolus administration of synthetic murine leptin were examined in groups of anesthetized normotensive (Sprague-Dawley), hypertensive (spontaneously hypertensive), and both lean and obese Zucker rats. In the normotensive animals (n = 8) an intravenous bolus of 400 mu g/kg of leptin produced a significant six- to sevenfold elevation in sodium excretion compared with controls (n = 8). The onset of natriuresis was delayed for similar to 30-45 min. Mean arterial pressure (MAP), creatinine clearance, plasma renin activity (PRA), and plasma aldosterone concentration (PAC) remained unchanged. In contrast, the hypertensive rats were refractory to the natriuretic effects of leptin when infused either with 400 (n = 8) or 1,600 (n = 8) mu g/kg. Also in these animals MAP, creatinine clearance, PRA, and PAC were unmodified. Finally, whereas lean Zucker rats (n = 8) responded very similarly to the Sprague-Dawley animals, the natriuretic effect of the hormone was attenuated in the obese Zucker groups. At 400 mu g/kg (n = 8) no natriuresis was elicited, but at 1,600 mu g/kg(n = 8) a modest but significant two- to threefold increment in sodium excretion was observed in the obese rats. In both Zucker groups, MAP, creatinine clearance, PRA, and PAC were unchanged. Collectively, these results demonstrate a significant natriuretic effect of exogenous leptin in the normal rat and a blunted saluretic response in hypertension and obesity. It is suggested that leptin may be a potential salt-excretory factor in normal rats and may function pathophysiologically in obesity and hypertension.
引用
收藏
页码:R2056 / R2060
页数:5
相关论文
共 32 条
[21]   LEPTIN LEVELS IN HUMAN AND RODENT - MEASUREMENT OF PLASMA LEPTIN AND OB RNA IN OBESE AND WEIGHT-REDUCED SUBJECTS [J].
MAFFEI, M ;
HALAAS, J ;
RAVUSSIN, E ;
PRATLEY, RE ;
LEE, GH ;
ZHANG, Y ;
FEI, H ;
KIM, S ;
LALLONE, R ;
RANGANATHAN, S ;
KERN, PA ;
FRIEDMAN, JM .
NATURE MEDICINE, 1995, 1 (11) :1155-1161
[22]  
Misra A, 1996, J INVEST MED, V44, P540
[23]   Leptin receptor missense mutation in the fatty Zucker rat [J].
Phillips, MS ;
Liu, QY ;
Hammond, HA ;
Dugan, V ;
Hey, PJ ;
Caskey, CT ;
Hess, JF .
NATURE GENETICS, 1996, 13 (01) :18-19
[24]   DIETARY-SODIUM CHLORIDE INCREASES BLOOD-PRESSURE IN OBESE ZUCKER RATS [J].
REDDY, SR ;
KOTCHEN, TA .
HYPERTENSION, 1992, 20 (03) :389-393
[25]  
Reisin E, 1995, Curr Opin Nephrol Hypertens, V4, P67, DOI 10.1097/00041552-199501000-00010
[26]   Relation between plasma leptin levels and measures of body fat in identical twins discordant for obesity [J].
Ronnemaa, T ;
Karonen, SL ;
Rissanen, A ;
Koskenvuo, M ;
Koivisto, VA .
ANNALS OF INTERNAL MEDICINE, 1997, 126 (01) :26-31
[27]   RENAL INJURY IN OBESE ZUCKER RATS - GLOMERULAR HEMODYNAMIC-ALTERATIONS AND EFFECTS OF ENALAPRIL [J].
SCHMITZ, PG ;
ODONNELL, MP ;
KASISKE, BL ;
KATZ, SA ;
KEANE, WF .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (03) :F496-F502
[28]   Chronic leptin infusion increases arterial pressure [J].
Shek, EW ;
Brands, MW ;
Hall, JE .
HYPERTENSION, 1998, 31 (01) :409-414
[29]   Molecular cloning of rat leptin receptor isoform complementary DNAs - Identification of a missense mutation in Zucker fatty (fa/fa) rats [J].
Takaya, K ;
Ogawa, Y ;
Isse, N ;
Okazaki, T ;
Satoh, N ;
Masuzaki, H ;
Mori, K ;
Tamura, N ;
Hosoda, K ;
Nakao, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (01) :75-83
[30]   Identification and expression cloning of a leptin receptor, OB-R [J].
Tartaglia, LA ;
Dembski, M ;
Weng, X ;
Deng, NH ;
Culpepper, J ;
Devos, R ;
Richards, GJ ;
Campfield, LA ;
Clark, FT ;
Deeds, J ;
Muir, C ;
Sanker, S ;
Moriarty, A ;
Moore, KJ ;
Smutko, JS ;
Mays, GG ;
Woolf, EA ;
Monroe, CA ;
Tepper, RI .
CELL, 1995, 83 (07) :1263-1271