Forced and voluntary diving in ducks: cardiovascular adjustments and their control

1988 ◽  
Vol 66 (1) ◽  
pp. 75-83 ◽  
Author(s):  
David R. Jones ◽  
R. A. Furilla ◽  
M. R. A. Heieis ◽  
G. R. J. Gabbott ◽  
F. M. Smith

Diving ducks submerge voluntarily for less than 1 min yet, in forced dives in the laboratory, redhead ducks can endure at least 8 min underwater. This is much longer than a dabbling duck of the same body mass can endure and is a result of the quicker onset of oxygen-conserving cardiovascular responses in divers. Oxygen conservation during forced dives is indicated by a profound bradycardia as blood flow is restricted to cerebral and central cardiovascular areas. In voluntary dives, on the other hand, heart rate is frequently above resting rates, and blood flow is preferentially directed to the working muscles of the hind limbs. Profound bradycardia only occurs in unrestrained ducks when they are trapped underwater. Since leg movements cease within 30 s after ducks are trapped, blood flow must at that time be directed away from the working muscles, as in the "classical" oxygen-conserving dive response. Cardiovascular adjustments to forced diving are caused by stimulation of nasal receptors in diving ducks. In dabblers, arterial chemoreceptor stimulation is crucial to the response, although an intact barostatic system may be necessary for development of profound bradycardia. Baroreceptors are essential for the cardiac response observed when dabblers are trained to dive for food, although neither baro-, chemo-, nor naso-receptors appear to have much to do with the cardiac adjustments to voluntary submergence in diving ducks. Nevertheless, in divers, cardiac adjustments to dabbling and forced, voluntary, and trapped dives are linearly related on a plot of dive (trapped) against the logarithm of predive (pretrap) heart rate. This relationship is due to a similar increase in vagal activity, of some 50% of maximum, in all types of diving manoeuvers. Phychogenic factors, long thought to be important in cardiac responses to forced diving, would appear to underpin this relationship.

1986 ◽  
Vol 121 (1) ◽  
pp. 227-238 ◽  
Author(s):  
R. A. Furilla ◽  
D. R. Jones

In restrained redhead ducks, forced submergence caused heart rate to fall from 100 +/− 3 beats min-1 (mean +/− S.E.M., N = 12) to a stable underwater rate of 35 +/− 4 beats min-1 (N = 12) within 5 s after submergence. Bradycardia was unaffected by breathing oxygen before a dive, but was virtually eliminated by local anaesthesia of the narial region. In contrast, in a dabbling duck (Anas platyrhynchos) bradycardia in short dives was eliminated by breathing oxygen before a dive. In unrestrained diving, on a man-made pond, heart rate in redheads diving voluntarily (y) was related to pre-dive heart rate (x) by the equation y = 76 + 0.29 +/− 0.05x +/− 17 (r2 = 0.71). Chasing, to induce submergence, had variable effects on this relationship. Local anaesthesia of the narial region inhibited voluntary diving but heart rates in chase-induced dives after nasal blockade were significantly higher, by 10–30%, than those obtained from untreated ducks in chase-induced dives. Breathing oxygen before voluntary dives had no apparent effect on heart rate after 2–5 s submergence. Voluntary head submersion by dabbling ducks caused no change in heart rate. We conclude that nasal receptors make only a minor contribution to cardiac responses in unrestrained dives, compared with forced dives, in diving ducks. Furthermore, these results show that little can be learned about cardiac responses in free diving ducks from studies of forced dives in dabblers or divers.


1987 ◽  
Vol 127 (1) ◽  
pp. 333-348 ◽  
Author(s):  
R. A. FURILLA ◽  
DAVID R. JONES

Dive heart rate was plotted against pre-dive heart rate in forced and voluntary dives and dabbles by restrained and free ducks. The relationship between pre-dive heart rate and the cardiac interval occurring just before or coincident with submersion (first cardiac interval) and the heart rate after 2–5 s submergence (stabilized heart rate) was emphasized. Stabilized heart rate in forced dives by restrained ducks at rest and at the end of a bout of exercise, and heart rate in voluntary dives and dabbles were linearly related on a plot of dive heart rate against the logarithm of predive heart rate. Even the heart rate occurring 2–5 s after ducks were ‘trapped’ under water, compared with the rate immediately before ‘trapping’, fitted on this line. The line was described by the equation y = - 451 + 2461ogx where y is dive (or trapped) and × is pre-dive (or pre-trap) heart rate (r2 = 0.98). The relationship was unaltered by β-blockade with propranolol. Furthermore, nasal blockade with Xylocaine, O2 breathing before submersion, and arterial baroreceptor denervation had no marked effect on the relationship in voluntary and trapped dives. Implantation of stimulating electrodes bilaterally on the cut distal ends of vagal and cardiac sympathetic nerves suggested that in all these dives there is a similar increase in the level of efferent vagal activity during submersion. However, the first cardiac interval in voluntary dives represents a much lower heart rate and therefore higher level of vagal activity. The present data suggest that there is considerable psychogenic modulation of cardiac responses in voluntary diving and only in forced dives, by restrained animals, is cardiac control largely reflexogenic.


1963 ◽  
Vol 18 (5) ◽  
pp. 987-990 ◽  
Author(s):  
Shanker Rao

Reports of cardiovascular responses to head-stand posture are lacking in literature. The results of the various responses, respectively, to the supine, erect, and head-stand posture, are as follows: heart rate/min 67, 84, and 69; brachial arterial pressure mm Hg 92, 90, and 108; posterior tibial arterial pressure mm Hg 98, 196, and 10; finger blood flow ml/100 ml min 4.5, 4.4, and 5.2; toe blood flow ml/100 ml min 7.1, 8.1, and 3.4; forehead skin temperature C 34.4, 34.0 and 34.3; dorsum foot skin temperature C 28.6, 28.2, and 28.2. It is inferred that the high-pressure-capacity vessels between the heart level and posterior tibial artery have little nervous control. The high-pressure baroreceptors take active part in postural adjustments of circulation. The blood pressure equating mechanism is not as efficient when vital tissues are pooled with blood as when blood supply to them is reduced. man; heart rate; blood flow; skin temperature Submitted on January 3, 1963


1973 ◽  
Vol 51 (4) ◽  
pp. 249-259 ◽  
Author(s):  
G. P. Biro ◽  
J. D. Hatcher ◽  
D. B. Jennings

The participation of the aortic chemoreceptors in the reflex cardiac responses to acute hypoxia is suggested only by the indirect evidence of pharmacological stimulation of these receptors. In order to assess their role more directly, the response to a 15 min period of hypoxia was determined after surgical denervation of the aortic chemoreceptors (A.D.), and compared with the response of sham-operated (S.O.) dogs, anesthetized with morphine–pentobarbital. In the control period, while breathing room air, the cardiovascular and respiratory parameters measured in the A.D. animals were not different from those of the S.O. dogs. Hypoxia (partial pressure of oxygen approximately 30 mm Hg) in the S.O. dogs was associated with a statistically significant rise in the heart rate (+71 ± 7 min−1, mean ± S.E.M.) and of the cardiac output (+25 ± 10 ml kg−1 min−1). In the A.D. animals, the significantly smaller increment in heart rate (+29 ± 6 min−1) was associated with a fall of the cardiac output (−16 ± 12 ml kg−1 min−1). The hypoxia-induced changes in heart rate and cardiac output in the S.O. animals were different (p < 0.05) from those in the A.D. group. The minute volume of ventilation was significantly augmented in both groups, and to a comparable extent. These findings indicate that the aortic chemoreceptors play a significant role in the cardiac response to hypoxia, but they do not affect, to a significant extent, the respiratory response.


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


1989 ◽  
Vol 256 (6) ◽  
pp. R1340-R1347 ◽  
Author(s):  
T. Kitanaka ◽  
R. D. Gilbert ◽  
L. D. Longo

To determine the maternal cardiovascular responses to long-term hypoxemia, we studied three groups of animals: 1) pregnant ewes (n = 20) at 110-115 days gestation subjected to hypoxia for up to 28 days; 2) pregnant ewes (n = 4) that served as normoxic controls; and 3) nonpregnant ewes (n = 6) subjected to hypoxemia for up to 28 days. We measured mean arterial pressure, heart rate, uterine blood flow, and uterine vascular resistance continuously for 1 h/day while the ewe was exposed to an inspired O2 fraction of 12-13% for at least 17 days. Arterial PO2, O2 saturation, hemoglobin, arteriovenous O2 difference, and uterine O2 uptake were measured daily while blood volume and erythropoietin concentration were measured weekly. In the pregnant hypoxic group arterial PO2 decreased from a control value of 101.5 +/- 5.1 to 59.2 +/- 5.1 Torr within a few minutes, where it remained throughout the study. The hemoglobin concentration increased from 8.9 +/- 0.5 to 10.0 +/- 0.5 g/dl within 24 h where it remained, whereas erythropoietin concentration increased from 16.6 +/- 2.1 to 39.1 +/- 7.8 mU/ml at 24 h but then returned to near-control levels. Arterial glucose concentration, mean arterial pressure, and cardiac output decreased slightly but insignificantly. In contrast, body weight, heart rate, blood volume, uterine blood flow, uterine O2 flow, uteroplacental O2 uptake, and the concentrations of catecholamines and cortisol remained relatively constant. Thus both pregnant and nonpregnant sheep experience relatively minor cardiovascular and hematologic responses in response to long-term hypoxemia of moderate severity.


1993 ◽  
Vol 265 (6) ◽  
pp. R1458-R1468 ◽  
Author(s):  
O. A. Smith ◽  
C. A. Astley ◽  
F. A. Spelman ◽  
E. V. Golanov ◽  
V. G. Chalyan ◽  
...  

Heart rate, arterial blood pressure, and renal and mesenteric or femoral blood flow were telemetered from 11 Papio hamadryas in an untethered free-ranging situation. The animals' behavior was recorded on videotape, and the cardiovascular (CV) data were recorded on the audio channels of the tape. The behavior was coded, and the codes were linked to the CV data via a time-code generator and computer control. The CV data were digitized into 1-s intervals, and the static relations between CV measures and the postures/locomotions (P/Ls) associated with the behavior were analyzed. The total frequency distributions for heart rate, blood pressure, and renal conductance approximated Gaussian distributions, whereas femoral conductance was positively skewed. The distribution for renal conductance suggested that during normal waking conditions the kidney is not maximally dilated and may increase or decrease its blood flow. All distributions were highly influenced by the Sit category, which occupied 80% of the total time. The CV measures for all P/Ls had wide ranges, and the CV values associated with each P/L overlapped those for the other P/Ls. The heart rate and renal conductance associated with the various P/Ls showed the largest deviations from the grand means and therefore contributed the most to the ability to discriminate one P/L from another. Blood pressure varied little from one P/L to another. The patterns of CV variables served to distinguish particular P/Ls very effectively. The frequency distributions were separated best when they were parceled on the basis of the intensity of behavior associated with a particular P/L. These variations in intensity were the major cause of the overlaps in the frequency distributions associated with P/Ls.


Behaviour ◽  
1980 ◽  
Vol 74 (1-2) ◽  
pp. 101-112 ◽  
Author(s):  
Patricia G. Parker ◽  
Helmut C. Mueller

AbstractNaive mallard ducklings were exposed to overflights of a silhouette of either a hawk or a goose on one day and the other configuration on the next day. An audio record of the heart rate was recorded utilizing a small transducer. Most of the ducklings (14 of 20) showed a greater variance in heart rate in response to the hawk than to the goose (p<0.01 ). These results indicate that the ducklings without prior, specific experience can differentiate between a goose and a hawk and show a greater emotional response to the latter. This constitutes evidence for the recognition of configurational stimulus without prior, pertinent experience. The use of cardiac responses as a measure of emotionality or fear is discussed, as are the merits of various measures of changes in heart rate. We conclude that variance in heart rate is an excellent measure of emotional response to a stimulus.


2006 ◽  
Vol 101 (3) ◽  
pp. 771-777 ◽  
Author(s):  
Adnan Cutuk ◽  
Eli R. Groppo ◽  
Edward J. Quigley ◽  
Klane W. White ◽  
Robert A. Pedowitz ◽  
...  

The purpose of this study is to assess cardiovascular responses to lower body positive pressure (LBPP) and to examine the effects of LBPP unloading on gait mechanics during treadmill ambulation. We hypothesized that LBPP allows comfortable unloading of the body with minimal impact on the cardiovascular system and gait parameters. Fifteen healthy male and female subjects (22–55 yr) volunteered for the study. Nine underwent noninvasive cardiovascular studies while standing and ambulating upright in LBPP, and six completed a gait analysis protocol. During stance, heart rate decreased significantly from 83 ± 3 beats/min in ambient pressure to 73 ± 3 beats/min at 50 mmHg LBPP ( P < 0.05). During ambulation in LBPP at 3 mph (1.34 m/s), heart rate decreased significantly from 99 ± 4 beats/min in ambient pressure to 84 ± 2 beats/min at 50 mmHg LBPP ( P < 0.009). Blood pressure, brain oxygenation, blood flow velocity through the middle cerebral artery, and head skin microvascular blood flow did not change significantly with LBPP. As allowed by LBPP, ambulating at 60 and 20% body weight decreased ground reaction force ( P < 0.05), whereas knee and ankle sagittal ranges of motion remained unaffected. In conclusion, ambulating in LBPP has no adverse impact on the systemic and head cardiovascular parameters while producing significant unweighting and minimal alterations in gait kinematics. Therefore, ambulating within LBPP is potentially a new and safe rehabilitation tool for patients to reduce loads on lower body musculoskeletal structures while preserving gait mechanics.


1988 ◽  
Vol 75 (4) ◽  
pp. 389-394 ◽  
Author(s):  
I. W. Fellows ◽  
I. A. MacDonald ◽  
T. Bennett ◽  
D. P. O'Donoghue

1. On two separate occasions, at least 1 week apart, seven young healthy male subjects received intravenous infusions of either adrenaline [0.27 nmol (50 ng) min−1 kg−1] or saline (154 mmol/l NaCl), plus ascorbic acid (5.68 mmol/l), over 30 min. 2. On each occasion, the subjects were exposed to distal body subatmospheric pressure (DBSP), 0 to 50 mmHg (0 to 6.65 kPa) in 10 mmHg (1.33 kPa) steps, before infusion, during the final 15 min of the infusion, and at 15 min and 30 min after the cessation of the infusion. 3. Venous adrenaline concentrations of 2.85 ±0.22 nmol/l were achieved during the adrenaline infusion, compared with 0.49 ± 0.07 nmol/l during the saline infusion (P < 0.001). At 15 min and at 30 min after cessation of the adrenaline infusion, venous adrenaline concentrations had fallen to levels similar to those achieved after the cessation of the saline infusion. 4. Heart rate rose significantly from 58 ±4 beats/min to 67 ±4 beats/min during the adrenaline infusion (P < 0.05), but there was no further significant change in response to 50 mmHg (6.65 kPa) DBSP. At 30 min after the cessation of the adrenaline infusion, heart rate rose from 60 ± 4 beats/min to 78 ± 7 beats/min in response to 50 mmHg DBSP. This increase was significantly greater than that observed before the adrenaline infusion [58 ± 4 beats/min to 69 ±7 beats/min during 50 mmHg (6.65 kPa) DBSP; P < 0.01]. 5. During the infusion of adrenaline, systolic arterial blood pressure rose and diastolic arterial blood pressure fell, but the blood pressure responses to DBSP were unaffected. 6. Forearm blood flow increased significantly during adrenaline infusion but there was no significant difference in the fall in forearm blood flow during DBSP compared with the values before infusion. At 15 min after the cessation of the adrenaline infusion, forearm vascular resistance rose proportionately more in response to DBSP than it had before the adrenaline infusion (P < 0.05). 7. These results are consistent with adrenaline-mediated facilitation of sympathetic neuronal release of noradrenaline in the heart and in the forearm vascular bed.


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