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21 September 2015 Coupling of cerebral blood flow and oxygen consumption during hypothermia in newborn piglets as measured by time-resolved near-infrared spectroscopy: a pilot study
Author Affiliations +
Abstract
Hypothermia (HT) is a potent neuroprotective therapy that is now widely used in following neurological emergencies, such as neonatal asphyxia. An important mechanism of HT-induced neuroprotection is attributed to the associated reduction in the cerebral metabolic rate of oxygen (CMRO2). Since cerebral circulation and metabolism are tightly regulated, reduction in CMRO2 typically results in decreased cerebral blood flow (CBF); it is only under oxidative stress, e.g., hypoxia-ischemia, that oxygen extraction fraction (OEF) deviates from its basal value, which can lead to cerebral dysfunction. As such, it is critical to measure these key physiological parameters during therapeutic HT. This report investigates a noninvasive method of measuring the coupling of CMRO2 and CBF under HT and different anesthetic combinations of propofol/nitrous-oxide (N2O) that may be used in clinical practice. Both CBF and CMRO2 decreased with decreasing temperature, but the OEF remained unchanged, which indicates a tight coupling of flow and metabolism under different anesthetics and over the mild HT temperature range (38°C to 33°C).

1.

Introduction

Mild hypothermia (HT), in which the brain temperature is lowered to 32°C to 33°C, has been shown to be an effective neuroprotective therapy to reduce brain injury following cardiac arrest, traumatic brain injury, birth asphyxia, and ischemic encephalopathy.1 An important mechanism of HT-induced neuroprotection is the preservation of brain adenosine triphosphate levels resulting from a reduction in the cerebral metabolic rate of oxygen (CMRO2).2 Indeed, the effects of HT on cerebral blood flow (CBF) are a consequence of the tight coupling between CMRO2 and CBF.3,4 Preservation of this coupling is an important factor in the control of the cerebral circulation and metabolism, connecting the change in metabolic demands with the supply of substrates by blood flow. As a consequence of this balance between flow and metabolism, the oxygen extraction fraction (OEF) represents a sensitive marker of brain health;5 under oxidative stress, e.g., hypoxia-ischemia (HI), OEF increases from its basal value of 33% leading to cerebral venous desaturation.68

Current methods of measuring cerebral energy metabolism using positron emission tomography and magnetic resonance spectroscopy are not practical for neuromonitoring during prolonged periods of cooling and rewarming phases since therapeutic HT can last up to 72 h.9,10 By contrast, optical methods are well suited for this since they are safe, compact, portable, and can provide continuous monitoring at the bedside. We have previously developed a dynamic contrast-enhanced near-infrared spectroscopy (NIRS) technique for measuring absolute CBF and CMRO2 using the light-absorbing dye, indocyanine green (ICG), as an intravascular contrast agent in newborn piglets1115 and adult porcine model.1618 However, there has been no previous study investigating the feasibility of using time-resolved (TR) NIRS to measure CBF and CMRO2 during HT.

Although the results from a recent study have shown that neonates with hypoxic-ischemic encephalopathy have lower blood flow index and relative CMRO2 during cooling when compared to healthy neonates,19 the effect of HT on flow-metabolism coupling under different anesthetic regimes on the noninjured brain has not been studied to our knowledge. In the present study, CBF and CMRO2 were measured by TR-NIRS in healthy newborn piglets under isoflurane for induction of anesthesia and then both measurements were repeated under propofol/nitrous oxide (N2O) while the brain temperature was lowered from 38°C to 33°C.

2.

Materials and Methods

2.1.

Instrumentation

The light sources of the time-resolved system were thermoelectrically cooled picosecond pulsed diode lasers (LDH-P-C emitting at 760, 810, and 830 nm, PicoQuant, Germany) activated by a computer-controlled laser driver (SEPIA PDL 828, PicoQuant). The 760- and 830-nm emission wavelengths were chosen to quantify tissue oxyhemoglobin (HbO2) and deoxyhemoglobin (Hb) concentrations, which were used to determine the cerebral oxygen saturation, whereas the 810-nm laser coincides with the peak absorption wavelength of ICG in plasma. The output power and pulse repetition rates of the lasers were set to 1.4 mW and 27MHz, respectively. The individual pulses of the lasers were temporally separated by sharing the 80-MHz clock of the laser driver among the three lasers. Light emitted by each diode laser was attenuated by two adjustable neutral density filters (NDC-50-4M, Thorlabs, Newton, New Jersey) and coupled by a microscope objective lens (NA=0.25, magnification=10×) into one arm of a trifurcated fiber bundle (three step-index multimode fibers, NA=0.22, core 400μm; Fiber Optics Technology, Pomfret, Connecticut). The distal common end of the bundle (emission probe) was placed on the scalp of the animal and held in position by a probe holder. The average power delivered to a subject was attenuated to 20μW/laser, which is below ANSI safety limits for skin exposure.20

Photons emerging from the scalp were collected by another fiber bundle (multimode step-index fibers, NA=0.55, 3.6 mm diameter active area; Fiber Optics Technology, Pomfret, Connecticut). The other end of the fiber bundle was secured in front of an electromechanical shutter (SM05, Thorlabs). Light transmitted through the shutter was collected by a Peltier cooled microchannel plate photomultiplier tube (PMC-100, Becker and Hickl, Germany). Detection of single photons generated electrical pulses (amplitude of 50 to 200 mV, width=1.5ns) that were transmitted to a time-correlated single-photon counting (TCSPC) module (SPC-134, Becker and Hickl) to generate the temporal point spread function (TPSF). The TCSPC module had a dead time of 100 ns, and because of that, the maximum count rate per laser was constrained to 800kHz (i.e., one photon detected every 1.25μs) to minimize dead-time effects. This count rate, which was 3% of the laser pulse repetition rate, also minimized pileup effects.21

2.2.

Optical Properties Measurement

To quantify tissue optical properties from the measured TPSFs, the instrument response function (IRF) was measured to account for the temporal dispersion in the system.22 IRFs were measured at the start and end of each experiment at the same count rate as the TPSFs (800 kHz). Figure 1 shows a typical IRF of the TR instrument (FWHM=390ps) and a TPSF measured on a piglet’s head at a source-detector distance of 20 mm. Both TPSFs and IRF were acquired at 800 kHz at a sampling interval of 400 ms. The tissue optical properties were obtained using an analytical model of light diffusion.23 The model solution was first convolved with the measured IRF, and a nonlinear optimization routine (based on the MATLAB® function fminsearch) was used to fit the convolved model to each measured TPSF to determine the absorption coefficient (μa), reduced scattering coefficient (μs), and a scaling factor, which accounts for variations in laser power, detection gain, and coupling efficiency.22 The fitting range was set to 80% prior to the peak of the TPSF, as diffusion modeling is known to be a poor model for early photons24,25 and 20% after the peak to minimize the effects of noise. Tissue optical properties at each temperature were determined by averaging 32 TPSFs collected over 320 s. For the hemodynamics measurements, changes in light absorption caused by ICG were characterized using only μa as a fitting parameter, with μs and the scaling factor was fixed to their baseline values. Finally, the measured change in the absorption coefficient was used to compute the ICG concentration, as discussed in the following section.

Fig. 1

(a) Typical instrument response function of the time-resolved (TR) instrument with a FWHM of 390 ps and (b) a temporal point spread function acquired at the same wavelength on the piglet head at a source-detector distance of 20 mm.

NPH_2_3_035006_f001.png

2.3.

Determination of Cerebral Blood Flow

CBF was quantified using a bolus-tracking method that requires an intravenous bolus injection of ICG (1 ml, 0.2mg/kg) into a peripheral vein, followed by continuous measurement of the time-varying concentration of the dye in arterial blood and brain tissue. The arterial concentration, Ca(t), was measured noninvasively by a dye densitometer (model DDG-2001 A/K, Nihon Kohden, Tokyo, Japan) with the probe attached to a front foot of the animal. Brain tissue concentration of ICG, Ctis(t), was determined from the measured changes in μa acquired continuously for 76 s at a sampling interval of 400 ms:12

Eq. (1)

Ctis(t)=[μa(t)μa(0)]/[ln(10)×ϵICG],
where μa(0) represents the baseline absorption coefficient determined over a 10-s period prior to ICG injection and ϵICG is the extinction coefficient of ICG at 802 nm (186OD/mM/cm).26 The brain (tissue) and arterial concentrations of ICG are related by the following equation:

Eq. (2)

Ctis(t)=Ca(t)*[CBF·R(t)],
where * represents the convolution operator and CBF·R(t) is the flow-scaled impulse residue function, i.e., R(t) scaled by CBF. The function CBF·R(t) was extracted from the arterial and tissue ICG concentration curves [i.e., Eq. (2)] using a deconvolution algorithm.27 The initial height of the derived function is CBF, since by definition R(0)=1.28 Figure 2 shows typical brain and arterial ICG concentration curves measured with the TR-NIRS technique and a pulse dye densitometer under isoflurane at 38°C. The peak arterial concentration is 20 to 30 times greater than that of tissue concentration since the cerebral blood volume (CBV) is about 3% to 5% of the total brain volume.

Fig. 2

Samples (a) tissue ICG concentration curve measured with the TR near-infrared spectroscopy (NIRS) technique and (b) arterial ICG concentration curve obtained with the pulse dye densitometer from indocyanine green (ICG) bolus injection under isoflurane at brain temperature of 38°C. Both tissue and arterial curves were measured simultaneously over a period of 50 s during injection of 1.0 ml of ICG solution at a concentration of 0.1mg/ml.

NPH_2_3_035006_f002.png

2.4.

Determination of Cerebral Oxygen Metabolism and Extraction Fraction

CMRO2 was calculated using Fick’s principle:11

Eq. (3)

CMRO2=CBF([O2]a[O2]v).

The difference between the arterial oxygen concentration, [O2]a, and the cerebral venous concentration of oxygen, [O2]v, is commonly referred to as the arteriovenous oxygen difference and is the difference between the O2 concentration of the arterial blood feeding the tissue of interest and O2 concentration of the venous blood draining the tissue. Equation (3) can be further expanded as follows:29

Eq. (4)

CMRO2=CBF1.39[tHb](SaO2SvO2),
where [tHb] is total hemoglobin concentration, which can be measured from blood samples. SaO2 and SvO2 are arterial and venous O2 saturation, respectively. The constant 1.39 is the O2 carrying capacity of hemoglobin measured in milliliters per gram of Hb. Note that the dye densitometer also provides continuous measurements of SaO2, whereas SvO2 was determined indirectly from the TR-NIRS measurements of the cerebral blood oxygen saturation, StisO2. This technique relies on the assumption that there exists a stable arterial-venous blood ratio in the CBV:30,31

Eq. (5)

StisO2=αSaO2+(1α)SvO2,
where α represents the fraction of arterial blood in CBV. The relative distribution of arterial and venous compartments is generally accepted to be 25% and 75% of the total CBV; therefore, α was set to 0.25.30,31 To obtain tissue cerebral blood oxygen saturation, i.e., StisO2, cerebral hemoglobin (HbO2, Hb) concentrations were calculated from the TR-NIRS measurements. These hemoglobin concentrations were determined by fitting the tissue absorption coefficients to the extinction coefficients of Hb and HbO2, assuming a stable concentration of 85% water in the brain.32 A least-square optimization algorithm (MATLAB function fminsearch) was used to extract the concentrations of oxy- and deoxyhemoglobin from the absorption coefficients measured at the three wavelengths. StisO2 was then calculated as follows:

Eq. (6)

StisO2=HbO2HbO2+Hb.

Using this relationship, a new expression for CMRO2 can be derived that is independent of SvO2:

Eq. (7)

CMRO2=CBF1.39[tHb](SaO2StisO21α).
The fraction of oxygen extracted from arterial blood into the brain, OEF, was also calculated using the method described by Brown et al.:11

Eq. (8)

OEF=CMRO2CBF[O2]a.
The tight coupling of CBF and CMRO2 in the normal brain leads to a stable level of OEF around 33%.33 A decoupling of the two signifies oxidative stress and can lead to an increase in OEF beyond the normal value.7

2.5.

Animal Preparation and Experimental Procedure

Experiments were conducted on five newborn piglets. All animal experiments were approved by the Animal Use Subcommittee of the Canadian Council on Animal Care at our institution. Newborn Duroc cross piglets were obtained from a local supplier on the morning of the experiment. Anesthesia was induced with 1% to 2% isoflurane, which was increased to 3% to 4% during preparatory surgery. A tracheotomy was performed and the piglet was ventilated with oxygen and medical air mixture. A femoral artery was catheterized to monitor heart rate (HR) and mean arterial blood pressure (MAP) and to intermittently collect arterial blood samples for gas (paCO2, paO2), pH, and glucose concentration analysis. A cannula was inserted into an ear vein for infusion of propofol (AstraZeneca Pharmaceuticals, Inc., Canada) and ICG injection (Sigma-Aldrich, Saint Louis, Missouri). After surgery, piglets were maintained on 1% to 2% isoflurane at normothermia (NT38°C). Arterial CO2 tension (paCO2) was monitored throughout the experiment, either directly by blood gas measurements or by the end-tidal CO2 tension, and maintained at normocapnia between 37 and 40 mmHg by adjusting the breathing rate and ventilation volume. Arterial oxygen tension (paO2) was maintained at a level between 90 and 130 mmHg by adjusting the ratio of oxygen to medical air. Blood glucose was monitored intermittently and if it fell below 4.5mmol/l, then a 1 to 2 ml infusion of 25% dextrose solution was administered intravenously. Brain temperature was also measured with a thermocouple probe. The needle thermocouple probe was inserted laterally into the brain to a depth of 2 cm vertical from the brain surface and 0.5 cm posterior to the bregma. Animals were placed in the prone position and a custom-made probe holder was strapped to the head to hold the TR-NIRS emission and detection probes 2 cm apart, parasagittally, 1.5cm dorsal to the eyes. Figure 3 shows a schematic of a piglet’s head with the locations of the emission and detection probes as well as the needle thermocouple. The experiments started after a delay of 60 min to allow time for the animal to stabilize following surgery. This delay was also sufficient for the TR instrument to reach a quasiequilibrium to minimize drift artifacts induced by temperature fluctuations in the TR-NIRS instrument.34

Fig. 3

Schematic of a piglet head showing the location of the detection, emission probes, and approximate position of the needle thermocouple probe to measure brain temperature. The emission-detector distance was 2 cm.

NPH_2_3_035006_f003.png

After the stabilization period, CBF and CMRO2 were first measured under isoflurane (1% to 2%) and then under intravenous infusion of propofol (9 to 22.4mg/kg/h) and ventilation with 70% nitrous oxide (N2O70%) and 30% oxygen (O230%) while brain temperature was lowered from normothermia (38°C) to HT (35° and 33°C). For propofol (10mg/ml) infusion, the rate was adjusted according to the animal’s response to pain stimuli and change in vital signs such as blood pressure and HR with a mean infusion rate of 2.51±1.15ml/h. For normothermia, a heated water blanket was used to maintain rectal and brain temperature between 38°C to 38.5°C. HT was induced by placing plastic ice bags on the surface of the piglet’s body. Each experiment was completed within 5 h and after the last measurement, the animal was euthanized with intravenous potassium chloride (1 to 2ml/kg, 2mEq/ml) infusion. The time-limiting factor of the proposed CBF method is the necessity for ICG to be cleared from the blood stream by the liver. Since that takes about 10 to 15 min, CBF measurement can only be acquired every 15 min. Figure 4 illustrates the experimental workflow; tissue oxygen saturation (Stis) and CBF were acquired in two blocks during each condition. All data sets for each condition were acquired within 15min.

Fig. 4

Experimental workflow: the solid boxes are distinctive steps, whereas the dotted box is recurring for each induced condition.

NPH_2_3_035006_f004.png

2.6.

Statistical Analysis

SPSS 17.0.0 (SPSS, Inc, Chicago, Illinois) was used for all statistical analyses. Wilcoxon test was used to determine statistical differences between measurements acquired under normothermia (38°C) when the anesthetic was switched from isoflurane to propofol/N2O. Comparisons between temperature-based measurements were performed using the Friedman test. Statistical significance was based on p-value <0.05. All data are presented as mean±standard deviation unless otherwise noted.

3.

Results

Experiments were conducted on five piglets (three females and two males), with an average age of 34±6h and an average weight of 1.4±0.3kg. Table 1 presents a summary of the physiological parameters (MAP, HR, paCO2, paO2, pH, SaO2, [O2]a and StisO2) for the different anesthetic groups and brain temperatures. When the anesthetic was switched from isoflurane (baseline) to propofol/N2O, there were statistically significant increases in HR and MAP (p<0.05) compared to baseline; however, HR started to decrease immediately after initiation of cooling. Additionally, a statistically significant (p<0.05) decrease in paO2 was observed when the temperature fell below 35°C. There were no significant changes in paCO2, SaO2, [O2]a, tHb, pH, and StisO2 with temperature.

Table 1

Physiological parameters measured at different brain temperatures. SaO2, oxygen saturation of arterial blood; paO2, partial pressure of oxygen in arterial blood; MAP, mean arterial pressure; HR, heart rate; tHb, total hemoglobin concentration in arterial blood; paCO2, partial pressure of carbon dioxide in arterial blood; [O2]a, arterial concentration of oxygen; StisO2, tissue cerebral blood oxygen saturation;

VariableBaseline (isoflurane)Cooling (propofol-N2O)
(38°C)(38°C)(35°C)(33°C)
Baseline/Cooling
MAP (mmHg)(Isoflurane/propofol-N2O)42±456±6*52±2*50±11*
HR (bpm)(Isoflurane/propofol-N2O)148±5226±41*195±8*138±28
paCO2 (mmHg)(Isoflurane/propofol-N2O)40±241±241±140±2
paO2 (mmHg)(Isoflurane/propofol-N2O)155±40210±49136±4*85±16*
pH(Isoflurane/propofol-N2O)7.4±0.17.4±0.17.3±0.17.3±0.1
tHb (μmol/l)(Isoflurane/propofol-N2O)8.1±0.38.3±0.88.5±1.18.4±1.2
SaO2 (%)(Isoflurane/propofol-N2O)10097±298±197±1
[O2]a (ml/dl)(Isoflurane/propofol-N2O)11±111±211±211±1
StisO2 (%)(Isoflurane/propofol-N2O)0.69±0.010.69±0.010.69±0.010.69±0.01
*A statistically significant (p<0.05) difference compared to the baseline.

Figure 5(a) displays CBF and CMRO2 measurements under isoflurane at normothermia (38°C) and under propofol/N2O mixture at three different brain temperatures. At normothermia, both CBF and CMRO2 decreased from 50.4±13.1 to 31.3±8.8mlmin1100g1 and 2.4±0.6 to 1.5±0.4mlO2min1100g1, respectively, when the anesthetic was switched from isoflurane to propofol/N2O. There was also a progressive reduction in CBF from 31.3±8.8 to 24.1±5.9mlmin1100g1 and CMRO2 from 1.5±0.4 to 1.1±0.1mlO2min1100g1 when brain temperature decreased from 38°C to 33°C under propofol/N2O. The OEF values under the different anesthetics and brain temperatures are displayed in Fig. 5(b). It shows that OEF did not deviate from its basal value under the different anesthetic and temperature combinations, confirming the tight coupling between CBF and CMRO2; any change in metabolic demand was met by a corresponding change in substrate delivery via CBF modulation.

Fig. 5

(a) Cerebral blood flow (CBF) and oxygen metabolic rate (CMRO2); and (b) oxygen extraction fraction (OEF) at each brain temperature under isoflurane or propofol/N2O anesthesia (N=5). Values are shown as mean±SD; *p<0.05 versus at 38°C with isoflurane (baseline).

NPH_2_3_035006_f005.png

Figure 6 shows the relationships between CMRO2 and CBF under the different anesthetic groups at baseline and during HT; there is a strong linear dependence of CBF on CMRO2 for both anesthetic groups. This result shows that brain temperatures and anesthetics did not alter the CBF and CMRO2 coupling in the healthy brain; however, this might not be the case for an injured brain.

Fig. 6

Plot of CBF and CMRO2 during cooling under different anesthetic conditions. Each symbol type represents data for each anesthetic group. The lines indicate the line of regression associated with each group.

NPH_2_3_035006_f006.png

4.

Discussion

We investigated the relationship between CMRO2 and CBF under normothermia (38°C) and mild whole body HT (35°C or 33°C) with two different anesthetics, isoflurane (1%to2%)/(N266%,O233%), and propofol/(N2O70%,O230%), which is representative of what may be used in clinical practice.35 Previous studies have shown that the temperature range associated with better neurological outcomes is between 33°C and 35°C.36 However, cooling the whole body below 34°C can induce severe complications including shivering, skin erythema, renal failure, coagulopathy, pulmonary hypertension, reducing cardiac, and increased mortality.37,38 Consequently, to limit the deleterious effects of whole body cooling, only mild HT, in which the brain temperature is decreased to 33°C, has been applied in this study. Our results showed that compared to normothermia, mild HT decreases both CBF and CMRO2 with preserved flow-metabolism coupling shown by constant OEF under different anesthetics. Flow-metabolism coupling within the brain is a complex physiologic process that is regulated by a combination of metabolic, glial, neural, and vascular factors.5,39,40 In the normal brain, autoregulated CBF is cerebrovascular and metabolic reactivity induced by changes in arterial carbon dioxide tension operate to maintain a tight coupling between CBF and CMRO2. However, during cerebral ischemic insults, alterations of cerebral hemodynamic and metabolism are highly dynamic. As cerebral perfusion pressure (CPP) falls, CBF is maintained by autoregulation41 through vasodilatation of resistance arterioles, but when the capacity for compensatory vasodilation is exceeded, autoregulation fails and CBF falls as a function of CPP. When oxygen supply is diminished due to decreasing CBF, OEF increases in an effort to compensate for the reduced CBF to maintain CMRO2 commensurate with metabolic demand and preserve neuronal function and cellular integrity.5 If CPP continues to fall, CBF will progressively decline until the increase in OEF is no longer sufficient to supply the necessary oxygen to meet metabolic demand; energy failure will result and permanent tissue damage follows. Therefore, increased OEF from its basal value may be a sensitive and specific marker of oxidative stress that can lead to cerebral dysfunction.

The vasodilating effects of isoflurane have limited its use as a sedative agent in the neurosurgical intensive care unit (NICU) because of the fear of a potential increase in intracranial pressure (ICP) caused by the increase in CBF.42 By contrast, propofol is being used more frequently in the NICU, particularly for head-injury cases.43 Propofol is known to decrease CBF while preserving brain flow-metabolism coupling and acts as a global central nervous system depressant.42 It has been shown that a typical anesthetic induction dose of propofol reduces blood pressure by 30% resulting from a decrease in sympathetic activity, direct vasodilation, and myocardial depression.44,45 When the anesthetic was switched from isoflurane to propofol, there was a statistically significant increase in HR, suggesting that decrease in peripheral vascular resistance induced by propofol was partially compensated by an increase in HR.42

In the present study, TR-NIRS was used to separate the effects of tissue scattering from absorption and measure both endogenous and exogenous tissue chromophore concentrations.46 Although quantitative and mobile, a limitation with the TR-NIR technique is the need to inject a bolus of ICG every time CBF is measured. However, this is a minimally invasive procedure since ICG is injected into a peripheral vein and the time-dependent arterial ICG concentration curve can be measured noninvasively by pulse dye densitometry. Furthermore, ICG is approved for clinical use in North America and the incidence of allergic reactions to the dye is very low (1250,000) in both adults and newborns.47 Recently, Verdecchia et al. have shown that TR-NIRS can be combined with diffuse correlation spectroscopy to provide a quasicontinuous quantitative assessment of CBF and CMRO2.14 With this approach, only infrequent injections of ICG are needed to calibrate the continuous measurement of changes in CBF and CMRO2 into absolute values.

The superficial layer on the newborn head (scalp and skull) is relatively thin (about 1 to 2 mm) so that the contribution of the extracerebral tissue layer to the signal is relatively small. Consequently, the TPSFs were analyzed using the solution to the diffusion equation for a semi-infinite homogeneous medium.12 Extracerebral contamination is a major issue in the adult studies because of the greater thickness of the scalp and skull;16 however, depth-resolved approaches enable the separation superficial contributions and deep components on the basis that light penetration increases with source-detector distance. Furthermore, TR-NIRS has the ability to distinguish early from late arriving photons. Since photons with extended time-of-flight have a higher probability of probing deeper tissue, TR-NIRS can discriminate superficial from deep tissue absorption from measurements acquired at a single source-detector.48

A potential concern with our experimental procedure is that anesthesia was initiated with isoflurane during preparatory surgery and at normothermia. Besides being an easy to use anesthetic agent to induce anesthesia, isoflurane increases CBF relative to propofol/nitrous oxide and affords the condition to investigate whether autoregulation responses (flow metabolism coupling) remain intact at low-dose isoflurane at normothermia.49 Understanding how the combination of HT under different anesthetics may alter flow-metabolism coupling or OEF from its basal values in the healthy brain is critical before extending these neuroprotective strategies to the injured brain. Therefore, it might be worth trying different anesthetic induction agents in future studies. As well, rewarming is a critical phase of therapeutic HT in which too fast rewarming rates may retrigger destructive processes at the cellular level.50 Rapid rewarming of the injured brain commonly leads to a mismatch between cerebral metabolism and perfusion (hence increased OEF) and can cause rebound ICP elevations, cerebral venous desaturation, and brain ischemia. It is suggested that controlling the rewarming rate to as low as 0.1°C to 0.4°C/h is preferred to reduce the neurological risks.51 Therefore, monitoring for possible deleterious effects of rewarming via TR-NIRS measurement of OEF as developed in this study is important for guaranteeing HT treatment efficacy.

5.

Conclusion

We have measured the cerebral metabolic activity (CMRO2) and CBF at different temperatures in a neonatal animal model. Both CBF and CMRO2 decreased with lowering of the brain temperature but the OEF remained unchanged, which indicates a tight coupling of flow and metabolism over the mild HT temperature range (38°C to 33°C). This tight coupling might not be preserved leading to increased OEF above the normal values when oxidative stress occurs as in the ischemic brain. Furthermore, rewarming is a critical phase of therapeutic HT to monitor for oxidative stress.10,52 Rapid rewarming of the injured brain commonly leads to a mismatch between cerebral metabolism and perfusion10 (hence increased OEF) and can cause rebound ICP elevations,53 cerebral venous desaturation,52 and brain ischemia. It is suggested that controlling the rewarming rate to as low as 0.1°C to 0.4°C/h is preferred to reduce the neurological risks.54 Therefore, monitoring for possible deleterious effects of rewarming via TR-NIRS measurement of OEF as developed in this study is important for guaranteeing HT treatment efficacy. Although the results from this pilot study were encouraging, more animal experiments will be required to evaluate flow-metabolism coupling in the injured brain, e.g., in HI.

Acknowledgments

The authors would like to thank Jennifer Hadway for her help in conducting the animal experiments. This study was funded in part through support from the Canadian Institutes of Health Research and the Heart and Stroke Foundation of Canada.

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Biography

Mohammad Fazel Bakhsheshi received his PhD in medical biophysics from Western University, Canada, in 2014. He received his BSc degree in mechanical engineering from the University of Tehran, Iran, and MSc degree in mechanical engineering from Western University, Canada. He is currently a postdoctoral researcher at Robarts Research Institute. His research interests include application of optics in brain temperature monitoring and developing of selective brain cooling methods to induce hypothermia.

Mamadou Diop obtained a PhD in physics from the Center for Optics, Photonics, and Lasers at Laval University (Quebec). He then took a two-year postdoctoral position at the Institute for Microsctructural Sciences of the National Research Council (NRC) of Canada in Ottawa. After completion of his postdoc, he moved to London (Ontario) to become a research associate at the Lawson Health Research Institute (LHRI). He is currently a research scientist with the imaging program of the LHRI at St. Joseph’s Hospital, where he develops noninvasive optical instruments and algorithms for medical applications.

Laura B. Morrison received an associate degree in veterinary technology from the University of Guelph (Ridgetown) and became a registered veterinary technician in 2005. She graduated from the University of Guelph in 2008 with a Bachelor of Science in animal science. She started working in imaging research at Lawson Health Research Institute in 2010 and acquired registered laboratory animal technician status through the Canadian Association for Laboratory Animal Science in 2012. She continues to work passionately with many biomedical imaging research projects and has been a previously published co-author.

Keith St. Lawrence is an associate professor in medical biophysics at the University of Western Ontario and a scientist at the LHRI. His research focuses on the development and application of imaging modalities, including optical methods, for mapping brain function and assessing cerebrovascular health. He is currently supported by a personnel award from the Heart and Stroke Foundation, Ontario Provincial Office, to develop optical techniques for detecting cerebral ischemia in critical-care patients.

Ting-Yim Lee is director of PET/CT imaging research at Lawson Health Research Institute, a scientist with Robarts Research Institute, and a professor of medical imaging at the University of Western Ontario. His research focuses on the use of imaging to study physiological processes in diseases. His lab has pioneered a method of using x-ray dye and CT scanning to measure blood flow in various tissues, including the brain, tumors, and the heart.

© 2015 Society of Photo-Optical Instrumentation Engineers (SPIE) 2329-423X/2015/$25.00 © 2015 SPIE
Mohammad Fazel Bakhsheshi, Mamadou Diop, Laura B. Morrison, Keith St. Lawrence, and Ting-Yim Lee "Coupling of cerebral blood flow and oxygen consumption during hypothermia in newborn piglets as measured by time-resolved near-infrared spectroscopy: a pilot study," Neurophotonics 2(3), 035006 (21 September 2015). https://doi.org/10.1117/1.NPh.2.3.035006
Published: 21 September 2015
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