Heart rate control in diabetic rabbits: blunted response to isoproterenol

1988 ◽  
Vol 255 (5) ◽  
pp. E636-E641 ◽  
Author(s):  
B. E. Zola ◽  
B. Miller ◽  
G. L. Stiles ◽  
P. S. Rao ◽  
E. H. Sonnenblick ◽  
...  

To study the effects of chronic diabetes on heart rate and adrenergic responsiveness we compared unanesthetized diabetic rabbits, 10-13 mo after alloxan monohydrate injection, to age-matched controls. There were no significant differences found between groups for body or heart weight. Both resting and intrinsic heart rate (the latter obtained after atropine sulfate and propranolol HCl) were similar. In addition, serum and left ventricular epinephrine and norepinephrine concentrations as well as left ventricular beta-receptor density and affinity were unchanged in diabetic animals. Heart rate responses to isoproterenol were blunted in diabetics at the three highest doses. Base-line mean blood pressure was modestly lower in diabetic rabbits, and parallel declines in pressure for both groups were observed in response to isoproterenol. The diminished heart rate response to isoproterenol in diabetic rabbits may be due to diminished myocardial sensitivity to catecholamines, possibly combined with altered baroreceptor reflexes. These experiments may provide an explanation for the blunted heart rate response to exercise described in human diabetics.

2018 ◽  
pp. 437-445
Author(s):  
Gregory S. Thomas

The chapter Heart Rate Response to Exercise reviews the studies performed to estimate a patient’s maximum predicted heart rate. While the commonly used formula (220 – age), developed in 1971, is easy to remember, it underestimates the actual maximum heart rate in older persons. Studies of large sample size have found the maximum heart rate to be relatively independent of sex and physical fitness but to incrementally decline with age. The decrease with age is less than 1 beat per minute per year, however. A more accurate and recommended formula is [(208) – (0.7)(age)] as developed by Tanaka and colleagues.


1992 ◽  
Vol 85 (Supplement) ◽  
pp. 3S-45
Author(s):  
Allen F. Bowyer ◽  
Rosemary A. Thomas

1984 ◽  
Vol 108 (2) ◽  
pp. 316-326 ◽  
Author(s):  
Iwao Sato ◽  
Katsuro Shimomura ◽  
Yasuhiro Hasegawa ◽  
Tohru Ohe ◽  
Mokuo Matsuhisa ◽  
...  

Heart & Lung ◽  
2015 ◽  
Vol 44 (3) ◽  
pp. 246-250 ◽  
Author(s):  
Hilary F. Armstrong ◽  
Jose Gonzalez-Costello ◽  
Wilawan Thirapatarapong ◽  
Ulrich P. Jorde ◽  
Matthew N. Bartels

1959 ◽  
Vol 14 (5) ◽  
pp. 809-812 ◽  
Author(s):  
Dean L. Franklin ◽  
Richard M. Ellis ◽  
R. F. Rushmer

Instantaneous blood flow through the thoracic aorta was monitored continuously during spontaneous activity in intact dogs by means of a new, pulsed, ultrasonic flowmeter. Integrated flow per stroke, accumulated flow per unit time and heart rate were simultaneously derived by means of electronic computers. During treadmill exercise at 3 mph on a 5% grade, the heart rate increased by two- or threefold, but the aortic flow per stroke was only slightly increased. This observation was confirmed by direct measurements, of left ventricular diameter. An increase in stroke volume is not an essential feature of the cardiac response to exercise in these experiments. Submitted on December 15, 1958


1976 ◽  
Vol 41 (5) ◽  
pp. 790-796 ◽  
Author(s):  
I. Sato ◽  
Y. Hasegawa ◽  
K. Hotta

The dynamic property of the heart rate response to exercise was determined and expressed in the frequency domain to establish a method of examiningcardiovascular control function. The response of heart rate to a stimulus was measured at 5-s intervals in nine healthy young volunteers. The stimulusconsisted of several runs of two-step exercise practiced in semirandom sequence for 19 min. The weight function of the system was estimated from autocorrelation function of the input signal and cross-correlation function between the input and output signals. The weight function was transformed into a transfer function and its Bode plot diagram was drawn. From the diagram, four dynamic parameters were determined. These parameters are as follows: Kis a constant showing the theoretical steady-state increment of heart rate,and T1, T2, T3 are time constants. The values obtained in the present experiment with the healthy young males were: K 46.0 +/- 14.6 beats, T1, 2.12 +/- 0.44, T2, 1.12 +/- 0.16, and T3 0.70 +/- 0.07 min.


1999 ◽  
Vol 86 (3) ◽  
pp. 812-818 ◽  
Author(s):  
Kiminori Kato ◽  
Donald C. Chapman ◽  
Heinz Rupp ◽  
Anton Lukas ◽  
Naranjan S. Dhalla

To examine the role of changes in myocardial metabolism in cardiac dysfunction in diabetes mellitus, rats were injected with streptozotocin (65 mg/kg body wt) to induce diabetes and were treated 2 wk later with the carnitine palmitoyltransferase inhibitor (carnitine palmitoyltransferase I) etomoxir (8 mg/kg body wt) for 4 wk. Untreated diabetic rats exhibited a reduction in heart rate, left ventricular systolic pressure, and positive and negative rate of pressure development and an increase in end-diastolic pressure. The sarcolemmal Na+-K+-ATPase activity was depressed and was associated with a decrease in maximal density of binding sites (Bmax) value for high-affinity sites for [3H]ouabain, whereas Bmax for low-affinity sites was unaffected. Treatment of diabetic animals with etomoxir partially reversed the depressed cardiac function with the exception of heart rate. The high serum triglyceride and free fatty acid levels were reduced, whereas the levels of glucose, insulin, and 3,3′,-5-triiodo-l-thyronine were not affected by etomoxir in diabetic animals. The activity of Na+-K+-ATPase expressed per gram heart weight, but not per milligram sarcolemmal protein, was increased by etomoxir in diabetic animals. Furthermore, Bmax (per g heart wt) for both low-affinity and high-affinity binding sites in control and diabetic animals was increased by etomoxir treatment. Etomoxir treatment also increased the depressed left ventricular weight of diabetic rats and appeared to increase the density of the sarcolemma and transverse tubular system to normalize Na+-K+-ATPase activity. Therefore, a shift in myocardial substrate utilization may represent an important signal for improving the depressed cardiac function and Na+-K+-ATPase activity in diabetic rat hearts with impaired glucose utilization.


1989 ◽  
Vol 14 (2) ◽  
pp. 338-344 ◽  
Author(s):  
Rebecca J. Quigg ◽  
Michael B. Rocco ◽  
Diane F. Gauthier ◽  
Mark A. Creager ◽  
L. Howard Hartley ◽  
...  

1979 ◽  
Vol 11 (3) ◽  
pp. 227???233
Author(s):  
A. C.P. POWLES ◽  
J. R. SUTTON ◽  
J. R. WICKS ◽  
N. B. OLDRIDGE ◽  
N. L. JONES

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