Effects of aldehyde dehydrogenase-2 genotype on cardiovascular and endocrine responses to alcohol in young Japanese subjects

被引:33
作者
Nishimura, FT
Fukunaga, T
Kajiura, H
Umeno, K
Takakura, H
Ono, T
Nishijo, H
机构
[1] Kirin Brewery Co Ltd, Cent Labs Key Technol, Yokohama, Kanagawa 2360004, Japan
[2] Mie Univ, Sch Med, Dept Forens Med & Sci, Tsu, Mie 5148507, Japan
[3] Toyama Med & Pharmaceut Univ, Fac Med, Dept Physiol, Toyama 9300194, Japan
来源
AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL | 2002年 / 102卷 / 1-2期
关键词
alcohol; acetaldehyde; adlehyde dehydrogenase-2; heart rate variability; blood pressure variability; blood flow; catecholamines; pituitary-adrenal hormones; sympathetic activity; parasympathetic activity;
D O I
10.1016/S1566-0702(02)00206-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The present study was designed to investigate the effects of aldehyde dehydrogenase-2 (ALDH2) genotype on cardiovascular and endocrine responses to alcohol ingestion in young, healthy Japanese subjects. For this purpose, we monitored changes in the electrocardiogram (ECG), blood pressure (BP), finger blood flow (BF) and facial skin temperature (FST) during and after alcohol ingestion (0.4 ml/kg body weight). Spectral analyses of beat-to-beat variations of heart rate (HR), BP and BF were applied. Two major spectral components were examined at low frequency (LF: 0.04-0.15 Hz) and high frequency (HF: 0.15-10.4 Hz) bands for HR and BP variability (BPV). Significant effects for ALDH2 genotype were observed in HR variability (HRV) analysis; HF power of HRV was markedly depressed and the LF/HF ratio was significantly higher with alcohol in ALDH2-deficient (ND) subjects, while ALDH2-normal (NN) subjects did not display such changes. Analysis of BP variability showed increased LF and HF power after alcohol ingestion in the NN subjects, but there were no significant differences between genotypic groups. We also examined BF variability (BFV) in six major spectral components; power of the 0.8-2.2 Hz frequency band was significantly affected by genotype and higher power was observed in the ND subjects. Plasma concentrations of both epinephrine and norepinephrine increased after alcohol ingestion only in the ND subjects. Furthermore, plasma concentrations and urinary excretion of epinephrine, but not norepinephrine, were higher after alcohol ingestion in the ND than in the NN subjects. Blood acetaldehyde levels were about 10-fold higher in the ND than in the NN subjects although blood alcohol levels similarly increased in the ND and NN subjects. Our results also indicated that alcohol ingestion increased secretion of pituitary-adrenal hormones including ACTH, beta-endorphin and cortisol in the ND subjects. The present results along with previous studies suggest that alcohol-induced tachycardia in the ND subjects was probably mediated by acetaldehyde-induced rise in epinephrine secretion from the adrenal medulla and/or changes in the autonomic nervous system. Alcohol-induced relative predominance of cardiac sympathetic activity in the ND subjects might be ascribed partly to increased norepinephrine secretion from sympathetic nerve terminals. Effects of acetaldehyde on these cardiovascular and endocrine systems were discussed in terms of their effects on the central nervous system. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:60 / 70
页数:11
相关论文
共 33 条
  • [1] HEMODYNAMIC REGULATION - INVESTIGATION BY SPECTRAL-ANALYSIS
    AKSELROD, S
    GORDON, D
    MADWED, JB
    SNIDMAN, NC
    SHANNON, DC
    COHEN, RJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 249 (04): : H867 - H875
  • [2] POWER SPECTRUM ANALYSIS OF HEART-RATE FLUCTUATION - A QUANTITATIVE PROBE OF BEAT-TO-BEAT CARDIOVASCULAR CONTROL
    AKSELROD, S
    GORDON, D
    UBEL, FA
    SHANNON, DC
    BARGER, AC
    COHEN, RJ
    [J]. SCIENCE, 1981, 213 (4504) : 220 - 222
  • [3] ACETALDEHYDE ON VASCULAR SMOOTH-MUSCLE - POSSIBLE ROLE IN VASODILATOR ACTION OF ETHANOL
    ALTURA, BM
    CARELLA, A
    ALTURA, BT
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1978, 52 (01) : 73 - 83
  • [4] ALTURA BM, 1983, NEUROBEH TOXICOL TER, V5, P211
  • [5] PHARMACOLOGY OF ACETALDEHYDE
    BRIEN, JF
    LOOMIS, CW
    [J]. CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1983, 61 (01) : 1 - 22
  • [6] AUTONOMIC CARDIAC CONTROL .2. NONINVASIVE INDEXES AND BASAL RESPONSE AS REVEALED BY AUTONOMIC BLOCKADES
    CACIOPPO, JT
    BERNTSON, GG
    BINKLEY, PF
    QUIGLEY, KS
    UCHINO, BN
    FIELDSTONE, A
    [J]. PSYCHOPHYSIOLOGY, 1994, 31 (06) : 586 - 598
  • [7] BAROREFLEX MODULATION OF BLOOD-PRESSURE AND HEART-RATE VARIABILITIES IN RATS - ASSESSMENT BY SPECTRAL-ANALYSIS
    CERUTTI, C
    BARRES, C
    PAULTRE, C
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (05): : H1993 - H2000
  • [8] THE DETERMINATION OF ACETALDEHYDE IN HUMAN-BLOOD BY THE PERCHLORIC-ACID PRECIPITATION METHOD - THE CHARACTERIZATION AND ELIMINATION OF ARTEFACTUAL ACETALDEHYDE FORMATION
    ERIKSSON, CJP
    MIZOI, Y
    FUKUNAGA, T
    [J]. ANALYTICAL BIOCHEMISTRY, 1982, 125 (02) : 259 - 263
  • [9] GENOTYPING OF MITOCHONDRIAL ALDEHYDE DEHYDROGENASE IN BLOOD-SAMPLES USING ALLELE-SPECIFIC OLIGONUCLEOTIDES - COMPARISON WITH PHENOTYPING IN HAIR ROOTS
    GOEDDE, HW
    SINGH, S
    AGARWAL, DP
    FRITZE, G
    STAPEL, K
    PAIK, YK
    [J]. HUMAN GENETICS, 1989, 81 (04) : 305 - 307
  • [10] GOEDDE HW, 1979, HUM GENET, V51, P331