Blood sampling methodology is crucial for precise measurement of plasma catecholamines concentrations in mice

被引:74
作者
Grouzmann, E [1 ]
Cavadas, C
Grand, D
Moratel, M
Aubert, JF
Brunner, HR
Mazzolai, L
机构
[1] CHU Vaudois, Div Clin Pharmacol & Toxicol, CH-1011 Lausanne, Switzerland
[2] CHU Vaudois, Div Hypertens & Vasc Med, CH-1011 Lausanne, Switzerland
[3] Univ Coimbra, Pharmacol Lab, Fac Pharm, P-3000 Coimbra, Portugal
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2003年 / 447卷 / 02期
关键词
blood sampling; cold stress; epinephrine; mice; norepinephrine; retro-orbital;
D O I
10.1007/s00424-003-1140-x
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Epinephrine (E) and norepinephrine (NE) play a major role in regulating metabolism and cardiovascular physiology. Both are secreted in response to stress and their measurement in plasma allows the study of sympathoadrenal function. Several studies investigating sympathoadrenal physiology are conducted using mice. Review of the literature revealed that basal mouse NE and E plasma concentrations range within 4-140 nM depending on the blood sampling method. Such variability doesn't allow study comparison and may conceal catecholamine variations in response to stress. Therefore, our aim was to determine a reliable sampling method to measure mouse plasma catecholamine concentrations. Results showed that arterial catheterization is the most accurate sampling method: E and NE basal levels were similar to those found in humans (1.1+/-0.3 nM and 4.1+/-0.5 nM, respectively). Retro-orbital bleeding led to analogous results. On the contrary, decapitation was stressful for mice and consequently NE and E concentrations were high (24.6+/-2.7 nM and 27.3+/-3.8 nM, respectively). These different bleeding methods were compared in terms of their ability to detect sympathoadrenal system stimulation (cold-pressure test). With catheter and retro-orbital samplings the expected increase in NE and E levels was easily perceived. In contrast, with decapitation no significant change in E was detected. In conclusion, arterial-catheter and retro-orbital blood sampling methods appear to be the most accurate procedures for studying the sympathetic nervous system in mice in both unstressed and stressed conditions.
引用
收藏
页码:254 / 258
页数:5
相关论文
共 17 条
[1]   PENTOBARBITAL EFFECTS ON PLASMA-CATECHOLAMINES - TEMPERATURE, HEART-RATE, AND BLOOD-PRESSURE [J].
BAUM, D ;
HALTER, JB ;
TABORSKY, GJ ;
PORTE, D .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (01) :E95-E100
[2]   Deletion of tyrosine hydroxylase gene reveals functional interdependence of adrenocortical and chromaffin cell system in vivo [J].
Bornstein, SR ;
Tian, H ;
Haidan, A ;
Böttner, A ;
Hiroi, N ;
Eisenhofer, G ;
McCann, SM ;
Chrousos, GP ;
Roffler-Tarlov, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) :14742-14747
[3]   Increased body fat mass and suppression of circulating leptin levels in response to hypersecretion of epinephrine in phenylethanolamine-N-methyltransferase (PNMT)-overexpressing mice [J].
Böttner, A ;
Haidan, A ;
Eisenhofer, G ;
Kristensen, K ;
Castle, AL ;
Scherbaum, WA ;
Schneider, H ;
Chrousos, GP ;
Bornstein, SR .
ENDOCRINOLOGY, 2000, 141 (11) :4239-4246
[4]   EFFECTS OF DIETHYL-ETHER, HALOTHANE, KETAMINE AND URETHANE ON SYMPATHETIC ACTIVITY IN THE RAT [J].
CARRUBA, MO ;
BONDIOLOTTI, G ;
PICOTTI, GB ;
CATTERUCCIA, N ;
DAPRADA, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1987, 134 (01) :15-24
[5]   Interactions between phospholamban and β-adrenergic drive may lead to cardiomyopathy and early mortality [J].
Dash, R ;
Kadambi, VJ ;
Schmidt, AG ;
Tepe, NM ;
Biniakiewicz, D ;
Gerst, MJ ;
Canning, AM ;
Abraham, WT ;
Hoit, BD ;
Liggett, SB ;
Lorenz, JN ;
Dorn, GW ;
Kranias, EG .
CIRCULATION, 2001, 103 (06) :889-896
[6]  
Grouzmann E, 2001, CLIN CHEM, V47, P1075
[7]   Two functionally distinct α2-adrenergic receptors regulate sympathetic neurotransmission [J].
Hein, L ;
Altman, JD ;
Kobilka, BK .
NATURE, 1999, 402 (6758) :181-184
[8]   Changes in organ perfusion after brain death in the rat and its relation to circulating catecholamines [J].
Herijgers, P ;
Leunens, V ;
TjandraMaga, TB ;
Mubagwa, K ;
Flameng, W .
TRANSPLANTATION, 1996, 62 (03) :330-335
[9]   Lower weight loss and food intake in protein-deprived, corticotropin releasing hormone-deficient mice correlate with glucocorticoid insufficiency [J].
Jacobson, L .
ENDOCRINOLOGY, 1999, 140 (08) :3543-3551
[10]   Impaired basal and restraint-induced epinephrine secretion in corticotropin-releasing hormone-deficient mice [J].
Jeong, KH ;
Jacobson, L ;
Pacàk, K ;
Widmaier, EP ;
Goldstein, DS ;
Majzoub, JA .
ENDOCRINOLOGY, 2000, 141 (03) :1142-1150