Metabolic rate, respiratory exchange ratio, and apneas during meditation

1989 ◽  
Vol 256 (3) ◽  
pp. R632-R638 ◽  
Author(s):  
J. Kesterson ◽  
N. F. Clinch
Keyword(s):  
Metabolic Rate ◽  
Respiratory Exchange Ratio ◽  
Transcendental Meditation ◽  
Interaction Effects ◽  
Co2 Production ◽  
O2 Consumption ◽  
Significant Trial ◽  
Significant Drop ◽  
Eyes Closed ◽  
Marked Decline

We tested the hypothesis that a drop in metabolic rate (MR) causes the apneas observed in some subjects during transcendental meditation (TM). We measured O2 consumption (VO2) and CO2 production (VCO2) in three groups of experienced meditators and one group of nonmeditating controls. Measurements were made before, during, and after TM for the meditators and before, during, and after eyes-closed relaxation for the nonmeditating controls. The three groups of meditators consisted of 1) those showing little change in the frequency of ventilation (f) with meditation, 2) those showing a marked decline in f, and 3) those showing numerous apneas and a marked fall in f. There were significant trial effects but no group or interaction effects for the decline in VO2. Thus we concluded that a drop in MR is not the cause of the apneas. However, there were significant trial and interaction effects for the changes in VCO2 and the respiratory exchange ratio (R), with a significant drop in R for the meditators but not for the controls. We report additional evidence and speculate that the drop in R is a consequence of mild hypoventilation.

Measurement and analysis of gas exchange during exercise using a programmable calculator

1980 ◽  
Vol 49 (3) ◽  
pp. 456-461 ◽  
Author(s):  
D. Y. Sue ◽  
J. E. Hansen ◽  
M. Blais ◽  
K. Wasserman
Keyword(s):  
Gas Exchange ◽  
Respiratory Exchange Ratio ◽  
Minute Ventilation ◽  
Co2 Production ◽  
O2 Consumption ◽  
Exercise Tests ◽  
Programmable Calculator ◽  
Arterial Blood Gas ◽  
Arterial Blood ◽  
End Tidal

Although exercise testing is useful in the diagnosis and management of cardiovascular and pulmonary diseases, a rapid comprehensive method for measurement of ventilation and gas exchange has been limited to expensive complex computer-based systems. We devised a relatively inexpensive, technically simple, and clinically oriented exercise system built around a desktop calculator. This system automatically collects and analyzes data on a breath-by-breath basis. Our calculator system overcomes the potential inaccuracies of gas exchange measurement due to water vapor dilution and mismatching of expired flow and gas concentrations. We found no difference between the calculator-derived minute ventilation, CO2 production, O2 consumption, and respiratory exchange ratio and the values determined from simultaneous mixed expired gas collections in 30 constant-work-rate exercise studies. Both tabular and graphic displays of minute ventilation, CO2 production, O2 consumption, respiratory exchange ratio, heart rate, end-tidal O2 tension, end-tidal CO2 tension, and arterial blood gas value are included for aid in the interpretation of clinical exercise tests.

Effect of metabolic rate on ventilatory roll-off during hypoxia

1994 ◽  
Vol 76 (6) ◽  
pp. 2310-2314 ◽  
Author(s):  
W. M. Gershan ◽  
H. V. Forster ◽  
T. F. Lowry ◽  
M. J. Korducki ◽  
A. L. Forster ◽  
...  
Keyword(s):  
Metabolic Rate ◽  
Minute Ventilation ◽  
Face Mask ◽  
Co2 Production ◽  
O2 Consumption ◽  
Arterial Blood Gas ◽  
Arterial Blood ◽  
Series Of Experiments ◽  
Carotid Arterial ◽  
Arterial Po2

This study was done to determine 1) whether goats demonstrate the roll-off phenomenon, i.e., a secondary decrease in minute ventilation (VE), after an initial hyperventilation during various levels of hypoxia and, if so, 2) whether roll-off could be due to changes in metabolic rate. We hypothesized that roll-off occurs in the goat during hypoxia but is not due to hypometabolism. To answer question 1, eight unanesthetized adult goats were exposed to 15–20 min of hypoxia at 0.15, 0.12, and 0.09 inspired O2 fraction (FIO2), resulting in 60, 40, and 30 Torr arterial PO2, respectively. Goats were fitted with a face mask connected to a spirometer to measure VE, and arterial blood gas samples were obtained via carotid arterial catheters. Roll-off was seen with 0.15 and 0.12 FIO2, whereas VE steadily increased with 0.09 FIO2. During hypoxia, arterial PCO2 fell 2, 3, and 7 Torr at 0.15, 0.12, and 0.09 FIO2, respectively. In the second series of experiments, nine different goats were exposed to 30 min of 0.12 FIO2. O2 consumption and CO2 production were measured five times during baseline and hypoxia. VE increased to 32% above baseline values after 2 min of hypoxia and then gradually decreased by 18%. Changes in breathing frequency and tidal volume contributed to the roll-off. O2 consumption decreased (P = 0.0029, analysis of variance) and CO2 production increased (P = 0.0027) during hypoxia, although both changes were small (< 7%) compared with the eventual 18% decrease in VE. We conclude that the adult goat demonstrates the roll-off phenomenon during moderate levels of hypoxia. (ABSTRACT TRUNCATED AT 250 WORDS)

Metabolism and ventilation in acute hypoxia: a comparative analysis in small mammalian species

1992 ◽  
Vol 262 (6) ◽  
pp. R1040-R1046 ◽  
Author(s):  
P. Frappell ◽  
C. Lanthier ◽  
R. V. Baudinette ◽  
J. P. Mortola
Keyword(s):  
Comparative Analysis ◽  
Metabolic Rate ◽  
Minute Ventilation ◽  
Acute Hypoxia ◽  
Mammalian Species ◽  
Resting Metabolic Rate ◽  
Cardiovascular Responses ◽  
General Characteristic ◽  
Co2 Production ◽  
O2 Consumption

O2 consumption (VO2), CO2 production (VCO2), and minute ventilation (VE) have been measured during normoxia and hypoxia (10-20 min in 10% O2) in specimens of 27 species from 6 mammalian orders, ranging in body mass (M) from a few grams to several kilograms. In normoxia, both metabolism and VE scaled close to M3/4, VE/VO2 and VE/VCO2 therefore being independent of M. In hypoxia, VE/metabolism increased in all species (on average greater than 100%), mostly because of a drop in VO2. On average, VE was 23% above the normoxic value but in some species decreased below normoxia. VO2 dropped in all but one species, on average 35%. Body temperature decreased by variable amounts, usually more in the smallest species. The decrease in metabolism during hypoxia was positively correlated with the resting metabolic rate of the species in a manner very similar to what can be calculated from data of previously studied newborn mammals. Hence hypoxia may decrease metabolic rate by decreasing thermogenesis, with larger effects in smaller animals, whether newborns or adults, because of their higher thermogenic requirements. We conclude that 1) hypoxic hypometabolism is a general characteristic of the mammalian response to hypoxia and cannot be neglected in the interpretation of ventilatory and cardiovascular responses and 2) its magnitude is inversely related to the resting VO2 of the species and therefore could be less prominent or possibly absent in adults of larger species.

Effect of ruminal CO2 on gas exchange and ventilation in the Hereford calf

1985 ◽  
Vol 58 (5) ◽  
pp. 1481-1484 ◽  
Author(s):  
W. D. Kuhlmann ◽  
S. R. Dolezal ◽  
M. R. Fedde
Keyword(s):  
Body Temperature ◽  
Gas Exchange ◽  
Respiratory Exchange Ratio ◽  
Minute Ventilation ◽  
Gas Absorption ◽  
Co2 Production ◽  
O2 Consumption ◽  
Ventilatory Pattern ◽  
Ruminal Epithelium ◽  
Expired Gas

The contribution of ruminal CO2 to gas exchange measurements and ventilation was determined in four rumen-fistulated Hereford steers at rest and during exercise. The calves were exercised at 1.4 and 2.2m X s-1 under three treatments: 1)full rumen with fistula sealed, 2) full rumen with fistula open, and 3) empty rumen. Measurements also were made at rest while flushing the empty rumen with either 100% N2 or a mixture of 50% CO2–50% N2. O2 consumption, CO2 production (Mco2), and ventilation were measured by collecting the expired gas. Absorption across the ruminal epithelium during rest increased Mco2 by 3%, whereas absorption and eructation together increased Mco2 by 15%. The respiratory exchange ratio (R) was significantly different among the three treatments at rest, but no differences were observed in R among the treatments during exercise. No changes were observed in minute ventilation among the three conditions, but a decrease in respiratory frequency and an increase in tidal volume occurred when the rumen was empty. These changes in ventilatory pattern may have been due to a decrease in body temperature when the rumen was empty. When the empty rumen was flushed with 50% CO2, Mco2 was increased 21% over the value observed when flushing with 100% N2. CO2 of fermentation origin is added to the expired gas by both eructation and absorption and has a significant effect on R in the resting animal, but no effect on R during exercise.

Metabolic-ventilatory interaction in conscious rats: effect of hypoxia and ambient temperature

1994 ◽  
Vol 76 (4) ◽  
pp. 1594-1599 ◽  
Author(s):  
C. Saiki ◽  
T. Matsuoka ◽  
J. P. Mortola
Keyword(s):  
Blood Pressure ◽  
Metabolic Rate ◽  
Ambient Temperature ◽  
Blood Gases ◽  
Male Rats ◽  
Co2 Production ◽  
O2 Consumption ◽  
Arterial Pco2 ◽  
Open Flow ◽  
Arterial Po2

Previous studies have indicated that the hypometabolic response to hypoxia depends on ambient temperature (Ta), being more pronounced in the cold. If metabolic rate were an important contributor to the level of ventilation (VE), the magnitude of the hyperpneic response to hypoxia should also depend on Ta. We tested this hypothesis on adult conscious male rats. In normoxia, a drop in Ta from 25 to 10 degrees C increased O2 consumption and CO2 production (VO2 and VCO2, respectively, measured by an open-flow technique) and VE (measured with the barometric method) by 80 and 60%, respectively, with no changes in blood gases. At both Ta, hypoxia (10% inspired O2, 33–35 Torr arterial PO2) induced the same degree of hyperventilation, i.e., the same drop in arterial PCO2 (about -13 Torr). The hyperventilation at 25 degrees C Ta was achieved exclusively by an increase in VE, whereas at 10 degrees C Ta the hyperpnea was minimal (+15%) and accompanied by a drop (-30%) in VO2 and VCO2. Diaphragmatic electromyograms confirmed the VE results. Changes in blood pressure were similar at both Ta. Addition of 3% CO2 to the inspired air further increased VE, indicating that the hypoxic rat was not breathing at its maximal VE at either Ta. We conclude that, in the rat, changes in metabolic rate play an important role in the VE response to hypoxia and that Ta influences the response because of its effect on the degree of hypoxic hypometabolism.

Alterations of energy and substrate metabolism in rats with large and sustained changes in daily food intake

1995 ◽  
Vol 269 (6) ◽  
pp. R1475-R1480 ◽  
Author(s):  
J. F. Wang ◽  
H. S. Koopmans
Keyword(s):  
Food Intake ◽  
Energy Expenditure ◽  
Metabolic Rate ◽  
Weight Control ◽  
Acid Synthesis ◽  
Co2 Production ◽  
O2 Consumption ◽  
Daily Food Intake ◽  
Daily Food ◽  
Body Weight Control

Energy expenditure was measured in one-way crossed-intestine rats by use of indirect calorimetry to examine the role of energy metabolism in body weight control. The intestinal surgery was done according to Koopmans (Brain Res. Bull. 14: 595-603, 1985). The food-losing rats increased daily food intake from 70.8 to 126.3 g/day, whereas their partners decreased intake from 67.1 to 38.7 g/day (P < 0.001). Compared with levels before surgery, the food-losing rats showed slightly increased O2 consumption (1.31 vs. 1.28 1.h-1.kg-1) and metabolic rate (6.62 vs. 6.39 kcal.h-1.kg-1) and largely increased CO2 production (1.31 vs. 1.22 l.h-1.kg-1, P < 0.01), whereas in their food-gaining partners O2 consumption (1.12 vs. 1.25 l.h-1.kg-1, P < 0.01) and metabolic rate (5.76 vs. 6.26 kcal.h-1.kg-1) were significantly decreased. Respiratory quotients were higher in the food-gaining rats than in their partners (1.076 vs. 0.999, P < 0.01), indicating more fatty acid synthesis. These results suggest that daily food intake and energy expenditure increase and decrease together, despite the fact that about the same amount of food has been absorbed from the intestines of each rat.

scholarly journals Heat Stress Reduces Metabolic Rate While Increasing Respiratory Exchange Ratio in Growing Pigs

Animals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 215
Author(s):  
Dane W. Fausnacht ◽  
Kellie A. Kroscher ◽  
Ryan P. McMillan ◽  
Luciane S. Martello ◽  
Lance H. Baumgard ◽  
...  
Keyword(s):  
Heat Stress ◽  
Energy Expenditure ◽  
Metabolic Rate ◽  
Respiratory Exchange Ratio ◽  
Muscle Growth ◽  
Growing Pigs ◽  
Metabolic Phenotype ◽  
Substrate Regulation ◽  
Enclosed Chamber ◽  
Muscle Biopsies

Heat stress (HS) diminishes animal production, reducing muscle growth and increasing adiposity, especially in swine. Excess heat creates a metabolic phenotype with limited lipid oxidation that relies on aerobic and anaerobic glycolysis as a predominant means of energy production, potentially reducing metabolic rate. To evaluate the effects of HS on substrate utilization and energy expenditure, crossbred barrows (15.2 ± 2.4 kg) were acclimatized for 5 days (22 °C), then treated with 5 days of TN (thermal neutral, 22 °C, n = 8) or HS (35 °C, n = 8). Pigs were fed ad libitum and monitored for respiratory rate (RR) and rectal temperature. Daily energy expenditure (DEE) and respiratory exchange ratio (RER, CO2:O2) were evaluated fasted in an enclosed chamber through indirect calorimetry. Muscle biopsies were obtained from the longissimus dorsi pre/post. HS increased temperature (39.2 ± 0.1 vs. 39.6 ± 0.1 °C, p < 0.01) and RER (0.91 ± 0.02 vs. 1.02 ± 0.02 VCO2:VO2, p < 0.01), but decreased DEE/BW (68.8 ± 1.7 vs. 49.7 ± 4.8 kcal/day/kg, p < 0.01) relative to TN. Weight gain (p = 0.80) and feed intake (p = 0.84) did not differ between HS and TN groups. HS decreased muscle metabolic flexibility (~33%, p = 0.01), but increased leucine oxidation (~35%, p = 0.02) compared to baseline values. These data demonstrate that HS disrupts substrate regulation and energy expenditure in growing pigs.

GASEOUS METABOLISM IN PREMATURE INFANTS AT 32-34°C AMBIENT TEMPERATURE

PEDIATRICS ◽  
1964 ◽  
Vol 33 (1) ◽  
pp. 75-82
Author(s):  
Forrest H. Adams ◽  
Tetsuro Fujiwara ◽  
Robert Spears ◽  
Joan Hodgman
Keyword(s):  
Carbon Dioxide ◽  
Oxygen Consumption ◽  
Premature Infants ◽  
Rectal Temperature ◽  
Respiratory Quotient ◽  
Carbon Dioxide Production ◽  
Open Circuit ◽  
Co2 Production ◽  
O2 Consumption ◽  
Rate Of Increase

Thirty-four measurements of oxygen consumption, carbon dioxide production, respiratory quotient, and rectal temperature were made on 22 premature infants with ages ranging from 2½ hours to 18 days. The studies were conducted at 32-34°C utilizing an open circuit apparatus and a specially designed climatized chamber. Oxygen consumption and carbon dioxide production were lowest in the first 12 hours and increased thereafter. The rate of increase in O2 consumption was greater than that of CO2 production, with a consequent fall in respiratory quotient during the first 76 hours of life. A reverse relation of O2 consumption and CO2 production was found following the 4th day of life with a consequent rise in respiratory quotient. There was a close correlation between O2 consumption and rectal temperature regardless of age. A respiratory quotient below the value of 0.707 for fat metabolism was observed in 7 premature infants with ages ranging from 24 to 76 hours.

Respiratory Exchange and Body Size in the Aldabra Giant Tortoise

1971 ◽  
Vol 55 (3) ◽  
pp. 651-665 ◽  
Author(s):  
G. M. HUGHES ◽  
R. GAYMER ◽  
MARGARET MOORE ◽  
A. J. WOAKES
Keyword(s):  
Body Weight ◽  
Body Size ◽  
Metabolic Rate ◽  
Relative Proportion ◽  
The Body ◽  
O2 Consumption ◽  
Weight Range ◽  
Testudo Hermanni ◽  
The Mean ◽  
Good Agreement

1. The O2 consumption and CO2 release of nine giant tortoises Testudo gigantea (weight range 118 g-35·5 kg) were measured at a temperature of about 25·5°C. Four European tortoises Testudo hermanni (weight range 640 g-2·16 kg) were also used. The mean RQ values obtained were 1·01 for T. gigantea and 0·97 for T. hermanni. These values were not influenced by activity or size. 2. The data was analysed by plotting log/log regression lines relating body weight to O2 consumption. Both maximum and minimum metabolic rates recorded for each individual T. gigantea showed a negative correlation with body weight. For active rates the relation was O2 consumption = 140·8W0·97, whereas for inactive animals O2 consumption = 45·47W0·82. 3. The maximum rates were obtained from animals that were observed to be active in the respirometer and the minimum rates from animals that remained quiet throughout. The scope for activity increased with body size, being 82 ml/kg/h for animals of 100 g and 103 ml/kg/h for 100 kg animals. The corresponding ratio between maximum and minimum rates increases from about 2 to 6 for the same weight range. 4. Values for metabolic rate in T. hermanni seem to be rather lower than in T. gigantea. Analysis of the relative proportion of the shell and other organs indicates that the shell forms about 31% of the body weight in adult T. hermanni but only about 18% in T. gigantea of similar size. The shell is not appreciably heavier in adult T. gigantea (about 20%). 5. Data obtained for inactive animals is in good agreement with results of other workers using lizards and snakes. Previous evidence suggesting that chelonians show no reduction in metabolic rate with increasing size is not considered to conflict with data obtained in the present work.

Measurements of metabolic rate in rats: a comparison of techniques

1988 ◽  
Vol 65 (2) ◽  
pp. 964-970 ◽  
Author(s):  
T. I. Musch ◽  
A. Bruno ◽  
G. E. Bradford ◽  
A. Vayonis ◽  
R. L. Moore
Keyword(s):  
Metabolic Rate ◽  
Maximal Exercise ◽  
Ambient Air ◽  
Open Circuit ◽  
Submaximal Exercise ◽  
Co2 Production ◽  
Arterial Blood ◽  
In Series ◽  
Series Of Experiments ◽  
Four Levels

Two different open-circuit techniques of measuring metabolic rate were examined in rats at rest and during exercise. With one technique ambient air was drawn through a tightly fitting mask that was secured to the rat's head, whereas with the other technique the rat was placed into and ambient air was drawn through a Plexiglas box. Two series of experiments were performed. In series I, two groups were studied that consisted of rats that had received myocardial infarctions produced by coronary arterial ligations and rats that had received sham operations. In this series of experiments O2 uptake (VO2) and CO2 production (VCO2) were measured at rest, during four levels of submaximal exercise, and during maximal treadmill exercise in the same group of rats by use of both techniques in random order. VO2, VCO2, and the calculated respiratory exchange ratio (R) were similar at rest, during the highest level of submaximal exercise (20% grade, 37 m/min), and during maximal exercise; however, VO2 and VCO2 were significantly lower with the metabolic box technique compared with the mask technique during the three lowest work loads (5% grade, 19 m/min; 10% grade, 24 m/min; and 15% grade, 31 m/min). These differences appeared to be associated with a change in gait produced when the mask was worn. In series II, the arterial blood gas and acid-base responses to both submaximal and maximal exercise were measured using both techniques in a group of instrumented rats that had a catheter placed into the right carotid artery.(ABSTRACT TRUNCATED AT 250 WORDS)

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