Airway resistance due to alveolar gas compression measured by barometric plethysmography in mice

2005 ◽  
Vol 98 (6) ◽  
pp. 2204-2218 ◽  
Author(s):  
Stephen J. Lai-Fook ◽  
Yih-Loong Lai
Keyword(s):  
Body Temperature ◽  
Room Temperature ◽  
Airway Resistance ◽  
Pressure Amplitude ◽  
Sinusoidal Analysis ◽  
Time Curve ◽  
Gas Compression ◽  
Pressure Time ◽  
Residual Capacity ◽  
Compression Effects

We developed a method for measuring airway resistance (Raw) in mice that does not require a measurement of airway flow. An analysis of Raw induced by alveolar gas compression showed the following relationship for an animal breathing spontaneously in a closed box: Raw = AbtVb/[Vt (Ve + 0.5Vt)]. Here Abt is the area under the box pressure-time curve during inspiration or expiration, Vb is box volume, Vt is tidal volume, and Ve is functional residual capacity (FRC). In anesthetized and conscious unrestrained mice, from experiments with both room temperature box air and body temperature humidified box air, the contributions of gas compression to the box pressure amplitude were 15 and 31% of those due to the temperature-humidity difference between box and alveolar gas. We corrected the measured Abt and Vt for temperature-humidity and gas compression effects, respectively, using a sinusoidal analysis. In anesthetized mice, Raw averaged 4.3 cmH2O·ml−1·s, fourfold greater than pulmonary resistance measured by conventional methods. In conscious mice with an assumed FRC equal to that measured in the anesthetized mice, the corrected Raw at room temperature averaged 1.9 cmH2O·ml−1·s. In both conscious mice and anesthetized mice, exposure to aerosolized methacholine with room temperature box air significantly increased Raw by around eightfold. Here we assumed that in the conscious mice both Vt and FRC remained constant. In both conscious and anesthetized mice, body temperature humidified box air reduced the methacholine-induced increase in Raw observed at room temperature. The method using the increase in Abt with bronchoconstriction provides a conservative estimate for the increase in Raw in conscious mice.

scholarly journals Airway constriction measured from tantalum bronchograms in conscious mice in response to methacholine

2008 ◽  
Vol 105 (3) ◽  
pp. 933-941
Author(s):  
Stephen J. Lai-Fook ◽  
Pamela K. Houtz
Keyword(s):  
Elastic Recoil ◽  
X Ray ◽  
Airway Constriction ◽  
Reduced Frequency ◽  
Gas Compression ◽  
Pressure Cycle ◽  
Residual Capacity ◽  
Compression Effects ◽  
Limiting Values ◽  
Minimum Points

A single-projection X-ray technique showed an increase in functional residual capacity (FRC) in conscious mice in response to aerosolized methacholine (MCh) with little change in airway resistance (Raw) measured using barometric plethysmography (Lai-Fook SJ, Houtz PK, Lai Y-L. J Appl Physiol 104: 521–533, 2008). The increase in FRC presumably prevented airway constriction by offsetting airway contractility. We sought a more direct measure of airway constriction. Anesthetized Balb/c mice were intubated with a 22-G catheter, and tantalum dust was insufflated into the lungs to produce a well-defined bronchogram. After overnight recovery, the conscious mouse was placed in a sealed box, and bronchograms were taken at maximum and minimum points of the box pressure cycle before (control) and after 1-min exposures to 25, 50, and 100 mg/ml MCh aerosol. After overnight recovery, each mouse was studied under both room and body temperature box air conditions to correct for gas compression effects on the control tidal volume (Vt) and to determine Vt and Raw with MCh. Airway diameter ( D), FRC, and Vt were measured from the X-ray images. Compared with control, D decreased by 24%, frequency decreased by 35%, FRC increased by 120%, and Raw doubled, to reach limiting values with 100 mg/ml MCh. Vt was unchanged with MCh. The limiting D occurred near zero airway elastic recoil, where the maximal contractility was relatively small. The conscious mouse adapted to MCh by breathing at a higher lung volume and reduced frequency to reach a limit in constriction.

A reevaluation of the validity of unrestrained plethysmography in mice

2002 ◽  
Vol 93 (4) ◽  
pp. 1198-1207 ◽  
Author(s):  
Lennart K. A. Lundblad ◽  
Charles G. Irvin ◽  
Andy Adler ◽  
Jason H. T. Bates
Keyword(s):  
Tidal Volume ◽  
Functional Residual Capacity ◽  
Airway Resistance ◽  
Ambient Conditions ◽  
Closed Chamber ◽  
Time Integral ◽  
Gas Compression ◽  
Compression And Expansion ◽  
Residual Capacity ◽  
Gas Conditioning

Presently, unrestrained plethysmography is widely used to assess bronchial responsiveness in mice. An empirical quantity known as enhanced pause is derived from the plethysmographic box pressure [Pb( t), where t is time] and assumed to be an index of bronchoconstriction. We show that Pb( t) is determined largely by gas conditioning when normal mice breathe spontaneously inside a closed chamber in which the air is at ambient conditions. When the air in the chamber is heated and humidified to body conditions, the changes in Pb( t) are reduced by about two-thirds. The remaining changes are thus due to gas compression and expansion within the lung and are amplified when the animals breathe through increased resistances. We show that the time integral of Pb( t) over inspiration is accurately predicted by a term containing airway resistance, functional residual capacity, and tidal volume. We conclude that unrestrained plethysmography can be used to accurately characterize changes in airway resistance only if functional residual capacity and tidal volume are measured independently and the chamber gas is preconditioned to body temperature and humidity.

ADAPTATION OF WHITE MICE (MUS MUSCULUS) TO REPEATED COOLING

1967 ◽  
Vol 45 (3) ◽  
pp. 321-327 ◽  
Author(s):  
David M. Ogilvie
Keyword(s):  
Body Temperature ◽  
Rectal Temperature ◽  
Cold Exposure ◽  
Mus Musculus ◽  
Room Temperature ◽  
The Body ◽  
Progressive Decrease

The effects, on the body temperature of white mice, of repeated short exposures to cold were investigated using two methods of restraint. Animals held in a flattened posture became hypothermic at room temperature, cooled more than five times as fast at −10 °C as mice that could adopt a heat-conserving posture, and continued to cool for some time after they were removed from the cold. With repeated tests, cooling at room temperature decreased, and an improvement in re warming ability was observed. In addition, with lightly restrained mice, the fall in rectal temperature during cold exposure showed a progressive decrease, a phenomenon not observed with severely restrained animals.

scholarly journals Temperature dependence of the rigid amorphous fraction of poly(butylene succinate)

RSC Advances ◽  
2021 ◽  
Vol 11 (41) ◽  
pp. 25731-25737
Author(s):  
Maria Cristina Righetti ◽  
Maria Laura Di Lorenzo ◽  
Patrizia Cinelli ◽  
Massimo Gazzano
Keyword(s):  
Body Temperature ◽  
Temperature Dependence ◽  
Human Body ◽  
Room Temperature ◽  
Rigid Amorphous Fraction ◽  
Butylene Succinate ◽  
Amorphous Fraction ◽  
Human Body Temperature ◽  
Rigid Amorphous

At room temperature and at the human body temperature, all the amorphous fraction is mobile in poly(butylene succinate).

scholarly journals The Atmosphere of the Underground Electric Railways of London: A Study of its Bacterial Content in 1920

1923 ◽  
Vol 22 (2) ◽  
pp. 123-155 ◽  
Author(s):  
J. Graham Forbes
Keyword(s):  
Body Temperature ◽  
Room Temperature ◽  
The Mean ◽  
Bacterial Content ◽  
The City

1. The bacterial content of the air of the Underground Railways, when the average of all results of the bacteriological investigations is taken, does not numerically compare unfavourably with the outside air of London.2. The ratio of the number of organisms growing at room temperature appears to be about 14 for railway air to 10 outside air. For those growing at body temperature the ratio is considerably higher, namely 2 to 1 respectively. The mean per litre, for room temperature organisms, is about 9 in railway air, 6·3 in the outside air; for body temperature organisms 4·6 for railway air, 2·2 for outside air.3. The bacterial content of platform air, except on the City and South London Railway, would appear to be higher than that of carriage air; the total mean for platform air being 52 and for carriage air 42·8 organisms per 5 litres, or a ratio of 16·4 and 13·5 respectively to 10 of the open air. The higher proportion in platform air is generally speaking to be accounted for by the greater amount of draught and dust disturbance.4. The ratios of the total bacterial content of railway carriage air and carriage and platform air on the six lines to open air are estimated in the following proportions:

End-expiratory and tidal volumes measured in conscious mice using single projection x-ray images

2008 ◽  
Vol 104 (2) ◽  
pp. 521-533 ◽  
Author(s):  
Stephen J. Lai-Fook ◽  
Pamela K. Houtz ◽  
Yih-Loong Lai
Keyword(s):  
Body Temperature ◽  
Lung Volume ◽  
Airway Resistance ◽  
X Rays ◽  
Airway Closure ◽  
Exposure Phase ◽  
X Ray ◽  
Total Lung Volume ◽  
Aerosol Exposure ◽  
Lung Area

The evaluation of airway resistance (Raw) in conscious mice requires both end-expiratory (Ve) and tidal volumes (Vt) (Lai-Fook SJ and Lai YL. J Appl Physiol 98: 2204–2218, 2005). In anesthetized BALB/c mice we measured lung area (AL) from ventral-to-dorsal x-ray images taken at FRC (Ve) and after air inflation with 0.25 and 0.50 ml (ΔVL). Total lung volume (VL) described by equation: VL = ΔVL + VFRC = KAL1.5 assumed uniform (isotropic) inflation. Total VFRC averaged 0.55 ml, consisting of 0.10 ml tissue, 0.21 ml blood and 0.24 ml air. K averaged 1.84. In conscious mice in a sealed box, we measured the peak-to-peak box pressure excursions (ΔPb) and x-rays during several cycles. K was used to convert measured AL1.5 to VL values. We calculated Ve and Vt from the plot of VL vs. cos(α − φ). Phase angle α was the minimum point of the Pb cycle to the x-ray exposure. Phase difference between the Pb and VL cycles (φ) was measured from ΔPb values using both room- and body-temperature humidified box air. A similar analysis was used after aerosol exposures to bronchoconstrictor methacholine (Mch), except that φ depended also on increased Raw. In conscious mice, Ve (0.24 ml) doubled after Mch (50–125 mg/ml) aerosol exposure with constant Vt, frequency (f), ΔPb, and Raw. In anesthetized mice, in addition to an increased Ve, repeated 100 mg/ml Mch exposures increased both ΔPb and Raw and decreased f to apnea in 10 min. Thus conscious mice adapted to Mch by limiting Raw, while anesthesia resulted in airway closure followed by diaphragm fatigue and failure.

Hypoxia-induced changes in shivering and body temperature

1987 ◽  
Vol 62 (6) ◽  
pp. 2477-2484 ◽  
Author(s):  
H. Gautier ◽  
M. Bonora ◽  
S. A. Schultz ◽  
J. E. Remmers
Keyword(s):  
Central Nervous System ◽  
Body Temperature ◽  
Room Temperature ◽  
Co2 Concentration ◽  
Hypoxic Conditions ◽  
O2 Concentration ◽  
The Central Nervous System ◽  
Induced Changes ◽  
Maintain Body Temperature ◽  
Ambient Hypoxia

Experiments were carried out on conscious cats to evaluate the general characteristics and modes of action of hypoxia on thermoregulation during cold stress. Intact and carotid-denervated (CD) conscious cats were exposed to ambient hypoxia (low inspired O2 fraction) or CO hypoxia in prevailing laboratory (23–25 degrees C) or cold (5–8 degrees C) environments. In the cold, both groups promptly decreased shivering and body temperature when exposed to either type of hypoxia. Small increases in CO2 concentration reinstituted shivering in both groups. At the same inspired concentration of O2, CD animals decreased shivering and body temperature more than intact cats. While this difference resulted, in part, from a lower alveolar PO2 in CD cats, a difference between intact and CD cats was apparent when the two groups were compared at the same alveolar PO2. During more prolonged hypoxia (45 min), shivering returned but did not reach normoxic levels, and body temperature tended to stabilize at a hypothermic value. Exposure to various levels of hypoxia produced graded suppression of shivering, with the result that the change in body temperature varied directly with inspired O2 concentration. Hypoxia appears to act on the central nervous system to suppress shivering and sinus nerve afferents appear to counteract this direct effect of hypoxia. In intact cats, this counteraction appears to be sufficient to maintain body temperature under hypoxic conditions at room temperature but not in the cold.

Gas-phase oxidation of butene-2

1958 ◽  
Vol 244 (1238) ◽  
pp. 331-344 ◽  
Keyword(s):  
Gas Phase ◽  
Pressure Change ◽  
Reaction Products ◽  
Peroxide Formation ◽  
Time Curve ◽  
Pressure Time ◽  
Initial Oxygen ◽  
Gas Phase Oxidation ◽  
Reactive Radicals ◽  
Reaction Processes

The gas-phase thermal oxidation of butene-2 has been examined over the temperature range 289 to 395°C. No difference in behaviour of the cis and trans forms could be detected. At the higher temperatures the reaction resembled that of the oxidation of propylene in the shape of the pressure-time curve and in the identity of many of the reaction products. At the lower temperatures a decrease in pressure partly due to peroxide formation followed the induction period, and by the end of this time much of the initial oxygen had been consumed. At all temperatures excess olefin produced an apparent inhibiting effect manifested by a decreased yield of carbon monoxide and a fall-off in the maximum rate of pressure change and total pressure change. Reaction processes are discussed, and it is suggested that a peroxide precedes the formation of acetaldehyde. Branching occurs largely through reaction of acetyl radicals produced from the acetaldehyde. The inhibiting effects produced by excess olefin are attributed to the replacement of reactive radicals by the less reactive allylic-type radicals, and the addition reactions of olefin at higher olefin concentrations lead to polymerization and a low or negative overall pressure change.

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