Effect of chronic hypoxia on leptin, insulin, adiponectin, and ghrelin

被引:27
作者
Chaiban, Joumana T. [1 ]
Bitar, Fadi F. [3 ]
Azar, Sami T. [2 ]
机构
[1] Amer Univ Beirut, Med Ctr, Dept Internal Med, Div Endocrinol, Beirut 11072020, Lebanon
[2] Amer Univ Beirut, Med Ctr, Dept Physiol, Beirut 11072020, Lebanon
[3] Amer Univ Beirut, Med Ctr, Dept Pediat, Beirut 11072020, Lebanon
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2008年 / 57卷 / 08期
关键词
hypoxia; adiponectin; insulin; leptin; ghrelin;
D O I
10.1016/j.metabol.2007.02.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The endocrine system plays an important role in the adaptation to hypoxia. The aim of this study was to assess the effect of chronic hypoxia on insulin, adiponectin, leptin, and ghrelin levels in a neonatal animal model. Sprague-Dawley rats were placed in a normobaric hypoxic environment at birth. Controls remained in room air. Rats were killed at 2 and 8 weeks of life. Insulin, adiponectin, leptin, and ghrelin were measured. At 2 weeks of life, there was no significant difference in insulin, adiponectin, and leptin levels between the hypoxic and control rats. The only statistically significant difference was found in ghrelin levels, which were lower in the hypoxic group (3.19 +/- 3.35 vs 24.52 +/- 5.09 pg/mL; P < .05). At 8 weeks of life, insulin was significantly higher in the hypoxic group (0.72 +/- 0.14 vs 0.44 +/- 0.26 ng/mL; P < .05) and adiponectin was significantly lower (1257.5 +/- 789.5 vs 7817.3 +/- 8453.7 ng/mL; P < .05). Leptin and ghrelin did not show significant difference in this age group, but leptin level per body weight was higher in the hypoxic group. Finally, we conclude that 2 weeks of continuous neonatal hypoxic exposure leads to a decrease in plasma ghrelin only with no significant change in insulin, adiponectin, and leptin and that 8 weeks of hypoxia leads to a decrease in adiponectin with an increase in insulin despite a significant decrease in weight. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1019 / 1022
页数:4
相关论文
共 34 条
[1]   Transcriptional activation of the human leptin gene in response to hypoxia - Involvement of hypoxia-inducible factor 1 [J].
Ambrosini, G ;
Nath, AK ;
Sierra-Honigmann, MR ;
Flores-Riveros, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (37) :34601-34609
[2]   BETA-ADRENERGIC RECEPTOR DYSFUNCTION IN HYPOXIC INHIBITION OF INSULIN RELEASE [J].
BAUM, D ;
PORTE, D .
ENDOCRINOLOGY, 1976, 98 (02) :359-366
[3]   EFFECT OF ACUTE HYPOXIA ON CIRCULATING INSULIN LEVELS [J].
BAUM, D ;
PORTE, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1969, 29 (07) :991-+
[4]   A role for leptin and its cognate receptor in hematopoiesis [J].
Bennett, BD ;
Solar, GP ;
Yuan, JQ ;
Mathias, J ;
Thomas, GR ;
Matthews, W .
CURRENT BIOLOGY, 1996, 6 (09) :1170-1180
[5]   Modulation of ceramide content and lack of apoptosis in the chronically hypoxic neonatal rat heart [J].
Bitar, FF ;
Bitar, H ;
El Sabban, M ;
Nasser, M ;
Yunis, KA ;
Tawil, A ;
Dbaibo, GS .
PEDIATRIC RESEARCH, 2002, 51 (02) :144-149
[6]   EFFECT OF EARLY VERSUS DELAYED HYPOXIC ENVIRONMENT ON NEONATAL RABBITS [J].
BITAR, FF ;
FELDBAUM, DM ;
KOHMAN, LJ ;
LITOVSKY, S ;
VEIT, LJ .
JOURNAL OF SURGICAL RESEARCH, 1994, 57 (02) :264-267
[7]   Plasma leptin levels are increased in survivors of acute sepsis: Associated loss of diurnal rhythm in cortisol and leptin secretion [J].
Bornstein, SR ;
Licinio, J ;
Tauchnitz, R ;
Engelmann, L ;
Negrao, AB ;
Gold, P ;
Chrousos, GP .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (01) :280-283
[8]  
Braun B, 2001, J APPL PHYSIOL, V91, P623
[9]   Serum immunoreactive leptin concentrations in normal-weight and obese humans [J].
Considine, RV ;
Sinha, MK ;
Heiman, ML ;
Kriauciunas, A ;
Stephens, TW ;
Nyce, MR ;
Ohannesian, JP ;
Marco, CC ;
McKee, LJ ;
Bauer, TL ;
Caro, JF .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (05) :292-295
[10]   Uremic hyperleptinemia: Adaptive or maladaptive? [J].
Dagogo-Jack, S .
KIDNEY INTERNATIONAL, 1998, 54 (03) :997-998