Effects of aging on cardiac output, regional blood flow, and body composition in Fischer-344 rats.

The purpose of this study was to determine the effects of maturation and aging on cardiac output, the distribution of cardiac output, tissue blood flow (determined by using the radioactive-microsphere technique), and body composition in conscious juvenile (2-mo-old), adult (6-mo-old), and aged (24-mo-old) male Fischer-344 rats. Cardiac output was lower in juvenile rats (51 +/- 4 ml/min) than in adult (106 +/- 5 ml/min) or aged (119 +/- 10 ml/min) rats, but cardiac index was not different among groups. The proportion of cardiac output going to most tissues did not change with increasing age. However, the fraction of cardiac output to brain and spinal cord tissue and to skeletal muscle was greater in juvenile rats than that in the two adult groups. In addition, aged rats had a greater percent cardiac output to adipose tissue and a lower percent cardiac output to cutaneous and reproductive tissues than that in juvenile and adult rats. Differences in age also had little effect on mass-specific perfusion rates in most tissues. However, juvenile rats had lower flows to the pancreas, gastrointestinal tract, thyroid and parathyroid glands, and kidneys than did adult rats, and aged rats had lower flows to the white portion of rectus femoris muscle, spleen, thyroid and parathyroid glands, and prostate gland than did adult rats. Body mass of juvenile rats was composed of a lower percent adipose mass and a greater fraction of brain and spinal cord, heart, kidney, liver, and skeletal muscle than that of the adult and aged animals. Relative to the young adult rats, the body mass of aged animals had a greater percent adipose tissue mass and a lower percent skeletal muscle and skin mass. These data demonstrate that maturation and aging have a significant effect on the distribution of cardiac output but relatively little influence on mass-specific tissue perfusion rates in conscious rats. The old-age-related alterations in cardiac output distribution to adipose and cutaneous tissues appear to be associated with the increases in percent body fat and the decreases in the fraction of skin mass, respectively, whereas the decrease in the portion of cardiac output directed to reproductive tissue of aged rats appears to be related to a decrease in mass-specific blood flow to the prostate gland.

[1]  L. Birnbaum,et al.  Age-related changes in dermal absorption of 2,3,7, 8-tetrachlorodibenzo-p-dioxin and 2,3,4,7,8-pentachlorodibenzofuran. , 1990, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[2]  R. Tuma,et al.  Age-related change in skeletal muscle blood flow in the rat. , 1987, Journal of gerontology.

[3]  R. Armstrong,et al.  A method for using microspheres to measure muscle blood flow in exercising rats. , 1982, Journal of applied physiology: respiratory, environmental and exercise physiology.

[4]  J. Docherty Cardiovascular responses in ageing: a review. , 1990, Pharmacological reviews.

[5]  E. Frohlich,et al.  Reference sample microsphere method: cardiac output and blood flows in conscious rat. , 1980, The American journal of physiology.

[6]  J. Willoughby,et al.  Activation of 5-HT 1 serotonin receptors in the medial basal hypothalamus stimulates prolactin secretion in the unanaesthetized rat. , 1988, Neuroendocrinology.

[7]  G Olivetti,et al.  Myocyte cell loss and myocyte cellular hyperplasia in the hypertrophied aging rat heart. , 1990, Circulation research.

[8]  P R Biondetti,et al.  Subcutaneous and visceral fat distribution according to sex, age, and overweight, evaluated by computed tomography. , 1986, The American journal of clinical nutrition.

[9]  R. Schwartz,et al.  The importance of body composition to the increase in plasma norepinephrine appearance rate in elderly men. , 1987, Journal of gerontology.

[10]  W. Hoffman,et al.  Cardiovascular and Regional Blood Flow Changes during Halothane Anesthesia in the Aged Rat , 1982, Anesthesiology.

[11]  J. Fleg,et al.  Role of muscle loss in the age-associated reduction in VO2 max. , 1988, Journal of applied physiology.

[12]  J. Stern,et al.  Regional blood flow of exercise-trained younger and older cold-exposed rats. , 1989, The American journal of physiology.

[13]  R. Tuma,et al.  Age-related changes in regional blood flow in the rat. , 1985, The American journal of physiology.

[14]  A Tremblay,et al.  Regional distribution of body fat, plasma lipoproteins, and cardiovascular disease. , 1990, Arteriosclerosis.

[15]  K. Hongo,et al.  Effects of aging and hypertension on endothelium-dependent vascular relaxation in rat carotid artery. , 1988, Stroke.

[16]  J. Marín Age-related changes in vascular responses: a review , 1995, Mechanisms of Ageing and Development.

[17]  R. Armstrong,et al.  Distribution of cardiac output during diurnal changes of activity in rats. , 1991, The American journal of physiology.

[18]  G. Haidet,et al.  Reduced exercise capacity in senescent beagles: an evaluation of the periphery. , 1991, The American journal of physiology.

[19]  R. Tuma,et al.  Age-related alterations in the arterial microvasculature of skeletal muscle. , 1992, Journal of gerontology.

[20]  B. Saltin,et al.  Influence of age on the local circulatory adaptation to leg exercise. , 1974, Scandinavian journal of clinical and laboratory investigation.

[21]  A. Svanborg,et al.  Physiology of cardiovascular aging. , 1993, Physiological Reviews.

[22]  D. Heistad,et al.  Effects of aging on responses of cerebral arterioles. , 1990, The American journal of physiology.

[23]  R. Wallace,et al.  Aging and the central nervous system. , 1976, Experimental aging research.

[24]  H. Drexler,et al.  Multiple simultaneous determinations of hemodynamics and flow distribution in conscious rat. , 1984, Journal of pharmacological methods.

[25]  G. L. Coleman,et al.  Pathological Changes During Aging in, Barrier-Reared Fischer 344 Male Rats1 , 1977, Journal of gerontology.

[26]  E. Hasser,et al.  Rat aortic vasoreactivity is altered by old age and hindlimb unloading. , 1995, Journal of applied physiology.

[27]  R. Armstrong,et al.  Blood flow in normal and denervated muscle during exercise in conscious rats. , 1988, The American journal of physiology.

[28]  D. Heistad,et al.  Effects of aging on mechanics and composition of cerebral arterioles in rats. , 1990, Circulation research.

[29]  Z. Q. Morris,et al.  Dextran as a radioactive microsphere suspending agent: severe hypotensive effect in rat. , 1978, The American journal of physiology.

[30]  M. Delp,et al.  Physiological Parameter Values for Physiologically Based Pharmacokinetic Models , 1997, Toxicology and industrial health.

[31]  A. H. Norris,et al.  Effect of muscle mass decrease on age-related BMR changes. , 1977, Journal of applied physiology: respiratory, environmental and exercise physiology.

[32]  M. Creager,et al.  Aging progressively impairs endothelium-dependent vasodilation in forearm resistance vessels of humans. , 1996, Hypertension.

[33]  T. G. Coleman,et al.  Hemodynamic disturbances in the rat as a function of the number of microspheres injected. , 1983, The American journal of physiology.

[34]  P. Hutchins,et al.  Decreases in cerebral microvasculature with age are associated with the decline in growth hormone and insulin-like growth factor 1. , 1997, Endocrinology.

[35]  A N Peiris,et al.  Biology of regional body fat distribution: relationship to non-insulin-dependent diabetes mellitus. , 1989, Diabetes/metabolism reviews.

[36]  M. Sugimachi,et al.  Effects of Age on Endothelium‐Dependent Vasodilation of Resistance Coronary Artery by Acetycholine in Humans , 1993, Circulation.

[37]  Y. Ishida,et al.  Age-related decrease in endothelium-dependent dilator response to histamine in rat mesenteric artery. , 1986, European journal of pharmacology.

[38]  T. Lüscher,et al.  Aging differentially affects direct and indirect actions of endothelin‐1 in perfused mesenteric arteries of the rat , 1990, British journal of pharmacology.