Intermittent food deprivation improves cardiovascular and neuroendocrine responses to stress in rats

被引:130
作者
Wan, RQ [1 ]
Camandola, S [1 ]
Mattson, MP [1 ]
机构
[1] NIA, Gerontol Res Ctr, Neurosci Lab, Baltimore, MD 21224 USA
关键词
energy restriction; cardiovascular disease; glucose metabolism; hypertension; sympathetic nervous system;
D O I
10.1093/jn/133.6.1921
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Stressful events may trigger disease processes in many different organ systems, with the cardiovascular system being particularly vulnerable. Five-mo-old male rats had ad libitum (AL) access to food or were deprived of food every other day [intermittent food deprivation (IF)] for 6 mo, during which time their heart rate (HR), blood pressure (BP), physical activity and body temperature were measured by radiotelemetry under nonstress and stress (immobilization or cold-water swim) conditions. IF rats had significantly lower basal HR and BP, and significantly lower increases in HR and BP after exposures to the immobilization and swim stressors. Basal levels of adrenocorticotropic hormone (ACTH) and corticosterone were greater in the IF rats. However, in contrast to large stress-induced increases in ACTH, corticosterone and epinephrine levels in AL rats, increases in these hormones in response to repeated immobilization stress sessions were reduced or absent in IF rats. Nevertheless, the IF rats exhibited robust hypothalamic/pituitary and sympathetic neuroendocrine responses to a different stress (swim). The IF treatment improved glucose metabolism, as indicated by lower basal levels of circulating glucose and insulin, but with maintenance of glucose and insulin responses to stress. We concluded that improvements in cardiovascular risk factors and cardiovascular and neuroendocrine stress adaptation occur in response to IF.
引用
收藏
页码:1921 / 1929
页数:9
相关论文
共 49 条
[21]   EFFECTS OF CALORIC RESTRICTION AND WEIGHT-LOSS ON GLYCEMIC CONTROL, INSULIN RELEASE AND RESISTANCE, AND ATHEROSCLEROTIC RISK IN OBESE PATIENTS WITH TYPE-II DIABETES-MELLITUS [J].
HUGHES, TA ;
GWYNNE, JT ;
SWITZER, BR ;
HERBST, C ;
WHITE, G .
AMERICAN JOURNAL OF MEDICINE, 1984, 77 (01) :7-17
[22]  
Kaur Jasjeet, 2002, Am J Ther, V9, P510, DOI 10.1097/00045391-200211000-00009
[23]   Exercise Effects on Muscle Insulin Signaling and Action - Selected Contribution: Modulation of insulin resistance and hypertension by voluntary exercise training in the TG( mREN2)27 rat [J].
Kinnick, TR ;
Youngblood, EB ;
O'Keefe, MP ;
Saengsirisuwan, V ;
Teachey, MK ;
Henriksen, EJ .
JOURNAL OF APPLIED PHYSIOLOGY, 2002, 93 (02) :805-812
[24]   Chronic and acute psychological risk factors for clinical manifestations of coronary artery disease [J].
Kop, WJ .
PSYCHOSOMATIC MEDICINE, 1999, 61 (04) :476-487
[25]   ROLE OF SYMPATHETIC ACTIVITY IN BLOOD-PRESSURE REDUCTION WITH LOW CALORIE REGIMEN [J].
KUSHIRO, T ;
KOBAYASHI, F ;
OSADA, H ;
TOMIYAMA, H ;
SATOH, K ;
OTSUKA, Y ;
KURUMATANI, H ;
KAJIWARA, N .
HYPERTENSION, 1991, 17 (06) :965-968
[26]   Transcriptional profiles associated with aging and middle age-onset caloric restriction in mouse hearts [J].
Lee, CK ;
Allison, DB ;
Brand, J ;
Weindruch, R ;
Prolla, TA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (23) :14988-14993
[27]   Evidence that brain-derived neurotrophic factor is required for basal neurogenesis and mediates, in part, the enhancement of neurogenesis by dietary restriction in the hippocampus of adult mice [J].
Lee, J ;
Duan, W ;
Mattson, MP .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (06) :1367-1375
[28]   Influence of aging and long-term caloric restriction on oxygen radical generation and oxidative DNA damage in rat liver mitochondria [J].
López-Torres, M ;
Gredilla, R ;
Sanz, A ;
Barja, G .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (09) :882-889
[29]   Modification of brain aging and neurodegenerative disorders by genes, diet, and behavior [J].
Mattson, MP ;
Chan, SL ;
Duan, WZ .
PHYSIOLOGICAL REVIEWS, 2002, 82 (03) :637-672
[30]  
Niedfeldt MW, 2002, AM FAM PHYSICIAN, V66, P445