The Effect of Deafferentation on Cerebral Blood Flow Response to Acetazolamide

Hiroshi Yamauchi; Hidehiko Okazawa; Kanji Sugimoto; Yoshihiko Kishibe; Masaaki Takahashi

Abstract

BACKGROUND AND PURPOSE: Decreased cerebral blood flow (CBF) response after acetazolamide administration may indicate increased cerebral blood volume (CBV) owing to reduced perfusion pressure from major cerebral artery steno-occlusive disease. However, decreased cerebral metabolic rate of oxygen (CMRO₂) caused by neuronal damage or deafferentation may also decrease the CBF response to acetazolamide, which adds complexity to the assessment of autoregulatory vasodilatation. The purpose of this study was to investigate the relationship between CBF response to acetazolamide and CBV or CMRO₂ in a pure form of deafferentation, crossed cerebellar diaschisis (CCD).

METHODS: We used positron emission tomography to study 17 patients with unilateral supratentorial infarct and contralateral cerebellar hypoperfusion. The CBF response to acetazolamide was assessed by measuring baseline CBF and CBF 10 minutes after an intravenous injection of acetazolamide. Multivariate analysis was used to test the independent predictive value of the CBV and CMRO₂ at baseline with respect to the change of CBF during acetazolamide administration.

RESULTS: Multivariate analysis revealed that in CCD CBV was significantly and independently associated with the percent change of CBF during acetazolamide administration (P < .0001), whereas CMRO₂ was not.

CONCLUSION: In deafferentation, changes in CBV may account for variations in CBF response to acetazolamide and decreased CMRO₂ may not affect CBF response to acetazolamide expressed as the percent change.

Evaluation of the cerebral blood flow (CBF) response to acetazolamide is widely used to evaluate the vasodilatory capacity in patients with major cerebral arterial occlusive diseases (1, 2). The CBF response to acetazolamide as assessed by quantitative CBF evaluation may be predictive of the risk of stroke, suggesting that evaluation of the CBF response to acetazolamide may be important for the treatment of patients with steno-occlusive lesions of the major cerebral arteries (3–5). Reduction of cerebral perfusion pressure due to severe atherosclerotic disease of the cerebral arteries causes autoregulatory cerebral vasodilatation, which acts to keep CBF constant. At an early stage, the CBF response to acetazolamide may be reduced according to the degree of vasodilatation that is reflected by an increase of cerebral blood volume (CBV). With further reduction in perfusion pressure, the autoregulatory capacity is exceeded, and CBF falls passively as a function of pressure. Then, the CBF response to vasodilatory stimuli may be absent, because vasodilatory capacity may be exhausted. Thus, a decrease of the CBF response to acetazolamide may reflect an increase of CBV caused by reduced perfusion pressure in patients with major cerebral artery steno-occlusive lesions (6, 7). However, a decrease in cerebral metabolic rate of oxygen (CMRO₂) caused by ischemia may also decrease the CBF response to acetazolamide by decreasing the production of carbon dioxide (CO₂) (7, 8), which adds complexity to the quantitative assessment of cerebral autoregulatory vasodilation.

In patients with major cerebral arterial occlusive diseases, the decreased CMRO₂ in the normal-appearing cerebral cortex may be caused by primary minor ischemic change, including neuronal loss or secondary metabolic change through deafferentation (9, 10). Therefore, knowledge of the effect of primary minor ischemic change or deafferentation on the CBF response to acetazolamide may make it possible to interpret the results of the acetazolamide test properly. Although it is difficult to study the region with primary minor ischemic change selectively, crossed cerebellar diaschisis (CCD) can be studied as one example of a pure form of deafferentation (11). Some supratentorial brain lesions cause a decrease in CBF and metabolism in the contralateral cerebellum without morphologic change. The main mechanism responsible for this phenomenon appears to be deafferentation through the cortico-ponto-cerebellar tract (10–12). Decreased CMRO₂ resulting from deafferentation may cause vasoconstriction, which may result in decreased CBV (12). It is not yet known how these changes in CBV and CMRO₂ affect the CBF response to acetazolamide in deafferentation. The purpose of this study was to investigate the relationship between CBF response to acetazolamide and CBV or CMRO₂ in CCD.

Methods

Patients

Seventeen patients (12 male, five female; age, 61 ± 12 years [mean ± SD]) with unilateral supratentorial infarcts were enrolled in this study. Five patients had cortical infarcts in the middle cerebral artery (MCA) territory, and 12 had purely subcortical infarcts in the MCA territory. All patients fulfilled the following criteria: 1) significant CBF asymmetry in the cerebellum as compared with normal subjects; 2) absence of clinical symptoms of ischemia in the vertebrobasilar artery territory; 3) absence of gross morphologic alterations in the cerebellum and brain stem at MR imaging; and 4) normal conventional angiographic findings in the vertebrobasilar system. The interval between ischemic event and positron emission tomography (PET) examination was 7 ± 16 months.

PET Measurements

All the subjects underwent PET with a whole-body scanner (Advance; General Electric Medical Systems, Milwaukee, WI), which permits simultaneous acquisition of 35 image sections with intersection spacing of 4.25 mm (13, 14). Written informed consent was obtained from each subject under the guidance of the Ethics Committee of the Shiga Medical Center. Performance tests showed the intrinsic resolution of the scanner to be 4.6–5.7 mm in the transaxial direction and 4.0–5.3 mm in the axial direction. As part of the scanning procedure, but before the tracer administration, ⁶⁸Ge/⁶⁸Ga transmission scanning was performed for 10 minutes for attenuation correction. For reconstruction of the PET data, images were blurred to 6.0 mm full-width half-maximum in the transaxial direction by using a Hanning filter. Functional images were reconstructed as 128 × 128 pixels, with each pixel representing an area of 2.0 mm × 2.0 mm.

The subjects were placed in the scanner with their heads immobilized with a head-holder and positioned with light beams to obtain transaxial sections parallel to the orbitomeatal line. A small cannula was placed in the left brachial artery for blood sampling. First, a baseline H₂¹⁵O study was performed (14, 15). After intravenous bolus injection of 555 MBq of H₂¹⁵O into the right antecubital vein, a 3-minute dynamic PET scan was started at the time of tracer administration with frame durations of 5 seconds × 12, 10 seconds × 6, and 20 seconds × 3. Arterial blood was continuously drawn from a catheter in the radial artery by using a minipump (AC-2120; Atto Co., Tokyo, Japan), and the concentration of radioactivity was monitored with a coincidental flow-through radioactivity detector (Pico-Count;Bioscan Inc., Washington, DC) (16) and used as an input function for data analysis.

After the baseline H₂¹⁵O study, a series of ¹⁵O-gas studies were performed. C¹⁵O₂ and ¹⁵O₂ were inhaled continuously through a mask (14). The scan time was 5 minutes, and arterial blood was sampled manually from the brachial artery three times during each scan. Each sample was collected for 10–20 seconds to average the fluctuation due to the respiratory cycle, and the radiotracer concentrations of whole blood and plasma were measured with a well counter. Inhalation of C¹⁵O with 3-minute scanning was used to measure the CBV. Arterial samples were obtained manually twice during the scanning, and the radiotracer concentration of whole blood was measured.

After the ¹⁵O-gas study, 1 g of acetazolamide was administered intravenously (15). Ten minutes after administration, a second H₂¹⁵O study was done: an intravenous bolus injection of 555 MBq of H₂¹⁵O and a 3-minute dynamic PET scan were performed in the same way as in the baseline study.

No subject showed a significant change in PaCO₂ during PET scanning, and the changes in the physiologic data during acetazolamide administration were small in all patients.

In the ¹⁵O-gas study, we calculated CBF, CMRO₂, and oxygen extraction fraction (OEF) on the basis of the steady-state method (17). CMRO₂ and OEF were corrected by the CBV (18). In the H₂¹⁵O study, CBF was calculated by using the autoradiographic method with a partition coefficient of 0.9 (mL/g) (19, 20).

Data Analysis

We analyzed images in the tomographic plane corresponding to the level of the cerebellum. We used the scan section that most satisfactorily visualized the cerebellar hemisphere. First, in the baseline H2¹⁵O-CBF image, we placed three circular regions of interest 16 mm in diameter over the gray matter of the cerebellar hemisphere ipsilateral to the supratentorial lesion. These regions of interest were then copied on the contralateral side with respect to the anteroposterior axis, which was determined in relation to the interhemispheric line in the upper section of the CBF image. We took care not to include the sinus in the regions of interest, by comparing the CBF image with the CBV image (12).

From the absolute values of the PET variables, we calculated the percent difference between the contralateral (CL) and ipsilateral (IL) cerebellar cortex (asymmetry index) as AI (%) = (CL − IL)/IL × 100. We assumed that the resulting values reflected the percent changes caused by CCD. We also studied seven younger healthy subjects (mean age 46 ± 6 years) by using the ¹⁵O-gas steady state method, and calculated the AI between the right (R) and left (L) cerebellar cortex as AI − L (%) = (R − L)/L × 100 and AI − R (%) = (L − R)/R × 100. AI − L and AI − R for CBF in the healthy subjects (mean ± SD) were −0.01 ± 2.07% and 0.14 ± 2.06%, respectively. Patients with significant cerebellar CBF asymmetry (ie, with an individual value of AI below −6.30% for a left supratentorial stroke or below −6.04% for a right supratentorial stroke, the respective means −3 SD in normal subjects) were selected as the study subjects.

In each hemisphere, we calculated the absolute and percent differences between the values obtained after acetazolamide administration and the values at baseline (Δ and Δ%) as Δ = CBF value (acetazolamide) − CBF value (baseline) and Δ% = Δ/(CBF value [baseline]) × 100 (%). We assumed that the resulting values reflected the absolute and percent changes caused by acetazolamide administration.

Statistical Analysis

We compared the results, except for CBF, in each cerebellar cortex by using the Wilcoxon signed-rank test. Differences were considered significant at P < .05.

Spearman rank correlation was used to analyze the relationship of CBV or CMRO₂ to the change of CBF during acetazolamide administration (Δ and Δ%). A P value of <.05 was regarded as indicating statistical significance. We also used multiple linear regression analysis to test the independent predictive value of CBV or CMRO₂ with respect to the change of CBF during acetazolamide administration (Δ and Δ%). We applied this analysis by using the hemispheric values of the change of CBF (Δ or Δ%) in each hemisphere (34 hemispheres) as the dependent variable and the baseline value of CBV or CMRO₂ as the independent variable. We adopted the two hemispheric values for each patient because of the suspected hemispheric difference of baseline hemodynamics and metabolism in each patient, although the data are not independent of each other.

Results

In the group as a whole, in the cerebellar cortex contralateral to the supratentorial infarction, significant decreases of CMRO₂ and CBV and an increase of OEF were found, as compared with the respective values in the ipsilateral cerebellar cortex. The absolute change of CBF during acetazolamide administration in the contralateral cerebellar cortex was significantly less than that in the ipsilateral cortex, whereas the percent change of CBF showed no significant difference between the two cortices (Table 1).

View this table:

TABLE 1:

Baseline values of PET variables and CBF response to acetazolamide in the cerebellar hemispheres contralateral and ipsilateral to the supratentorial infarction

In univariate analysis, the absolute change of CBF during acetazolamide administration was significantly and negatively correlated with CBV, whereas the percent change of CBF was significantly and negatively correlated with both CBV and CMRO₂ (Fig 1). At baseline, CBV was significantly and positively correlated with CMRO₂ (Spearman correlation coefficient, ρ = 0.66; P < .001).

Fig 1.

Scatterplots relating the absolute (upper row) or percent (lower row) change in CBF during acetazolamide administration to the values of CBV (left panels) or CMRO₂ (right panels) at baseline in the cerebellar hemispheres on both sides.

The positive relationships between CMRO₂ and the absolute change of CBF during acetazolamide administration became significant after controlling for the effect of CBV by using multiple linear regression analysis (model 2 in Table 2). This model, which included the values of CBV and CMRO₂, accounted for a significant proportion of the variance of the absolute change of CBF (P < .0001; R² = 0.53). CBV accounted for 20.5% of the variance of the change of CBF, whereas CMRO₂ accounted for 32.5% of the variance.

View this table:

TABLE 2:

Multiple linear regression analysis of the absolute change of CBF during acetazolamide administration as the dependent variable

The negative relationship between CMRO₂ and the percent change of CBF during acetazolamide administration, which was significant in univariate analysis, became insignificant after controlling for the effect of CBV by using multiple linear regression analysis (Table 3, model 2). The CBV was a significant independent predictor of the percent change of CBF and accounted for 62.3% of the variance.

View this table:

TABLE 3:

Multiple linear regression analysis of the percent change of CBF during acetazolamide administration as the dependent variable

Discussion

This study showed that, in deafferentation, variations in the CBF response to acetazolamide are accounted for by changes in CBV and a decrease in CMRO₂ does not affect the CBF response to acetazolamide expressed as the percent change. We found that both the absolute and percent changes of CBF during acetazolamide administration were significantly and negatively correlated with the baseline CBV value in CCD. In multivariate analysis, although both CBV and CMRO₂ were independent predictors of the absolute change of CBF, only CBV was an independent predictor of the percent change. For the absolute CBF response, CBV accounted for 20.5% of the variance and CMRO₂ accounted for 32.5%. As expected from the mechanism of the vasodilatory effect of acetazolamide, CMRO₂ was positively correlated with the CBF change. On the other hand, only CBV accounted for a significant proportion of the variance of the percent change of CBF (62.3%). The CBF response to acetazolamide expressed as the percent change can thus be used to estimate CBV in CCD because of the minor contribution of CMRO₂.

Several studies using various methods to measure CBF investigated the acetazolamide reactivity in CCD and showed inconsistent results (21–25). Two recent studies in which CBF response to acetazolamide was assessed by quantitative CBF by using PET showed no significant difference between the cerebellar hemispheres in the CBF response to acetazolamide expressed as the percent change (24, 25), in agreement with the findings of the present study. Because CBV was reduced in CCD, CBF response to acetazolamide should be increased if acetazolamide reactivity indicates vasodilatory capacity. In CCD, however, CMRO₂ is also reduced, and reduced CMRO₂ may cause a reduction of the CBF response to acetazolamide. The vasodilatory effect of acetazolamide probably occurs through inhibition of carbonic anhydrase in circulating red blood cells, which interferes with CO₂ clearance from the brain because of conversion of the CO₂ to circulating bicarbonate (1, 8). Consequently, increased levels of CO₂ around cerebral vessels cause cerebral vasodilatation. Thus, the vasodilatory effect of acetazolamide may depend on the level of the production of CO₂, which may be associated with baseline CMRO₂. In the patients studied here, CBV was positively correlated with CMRO₂. Therefore, the positive effect of the decreased CBV on the CBF response to acetazolamide may have been counterbalanced by the negative effect of the decrease of CMRO₂, resulting in the lack of hemispheric difference in the CBF response expressed as the percent change. For the CBF response expressed as the absolute change, the negative effect of the decrease of CMRO₂ was large, which caused a hemispheric difference in the CBF response.

Previous studies using PET showed a negative correlation between the change of CBF during acetazolamide administration and the baseline value of CBV in patients with major cerebral arterial occlusive disease, which supports the notion that evaluation of the CBF response to acetazolamide may be useful for estimating the degree of cerebral autoregulatory vasodilatation in response to reduced perfusion pressure (6, 7). This correlation, however, was shown to be weakened by the confounding effect of a decrease in CMRO₂ on the CBF response to acetazolamide (7). In patients with major cerebral arterial occlusive disease and cerebral infarcts, neuronal damage or deafferentation may cause decreased CMRO₂ in the normal-appearing cerebral cortex (10). In the present study, the CBF response to acetazolamide expressed as the percent change was shown to be correlated only with the CBV in CCD, which suggests that any decreases in the CMRO₂ resulting from deafferentation may not affect the CBF response to acetazolamide. In patients with major cerebral arterial occlusive diseases, if CMRO₂ reduction correlates with CBF response to acetazolamide, it is not deafferentation, but neuronal damage, that is confounding the CBF response, on the assumption that similar relationships exist in the cerebral cortical areas. Therefore, the evaluation of the neuronal integrity may be needed to interpret the results of the acetazolamide test properly. This can be done by visualizing the distribution of central-type benzodiazepine receptors (9, 26). If neuronal integrity is preserved in the cerebral cortex ipsilateral to the major cerebral arterial lesion, the CBF response to acetazolamide could be used as an index of preexisting vasodilatation. In our study, no patients showed atrophy of the cerebellar cortex contralateral to the supratentorial infarction. Neuronal damage due to transneuronal degeneration would cause a severe decrease of CMRO₂ that might contribute to reduced CBF response to acetazolamide.

Conclusion

In deafferentation, variations in the CBF response to acetazolamide may be accounted for by changes in CBV, and a reduction in CMRO₂ may not affect the CBF response expressed as the percent change. Evaluation of the CBF response to acetazolamide may be useful for estimating CBV in regions with secondary metabolic depression caused by deafferentation.

References

↵
Vorstrup S. Tomographic cerebral blood flow measurements in patients with ischemic cerebrovascular disease and evaluation of the vasodilatory capacity by the acetazolamide test. Acta Neurol Scand Suppl 1988;114:1–48
PubMed
↵
Yonas H, Pindzola RR. Physiological determination of cerebrovascular reserves and its use in clinical management. Cerebrovasc Brain Metab Rev 1994;6:325–340
PubMed
↵
Yonas H, Smith HA, Durham SR, et al. Increased stroke risk predicted by compromised cerebral blood flow reactivity. J Neurosurg 1993;79:483–489
CrossRef PubMed
Kuroda S, Houkin K, Kamiyama H, et al. Long-term prognosis of medically treated patients with internal carotid or middle cerebral artery occlusion: can acetazolamide test predict it? Stroke 2001;32:2110–2116
Abstract/FREE Full Text
↵
Ogasawara K, Ogawa A, Terasaki K, et al. Use of cerebrovascular reactivity in patients with symptomatic major cerebral artery occlusion to predict 5-year outcome: comparison of xenon-133 and iodine-123-IMP single-photon emission computed tomography. J Cereb Blood Flow Metab 2002;22:1142–1148
CrossRef PubMed
↵
Nariai T, Suzuki R, Hirakawa K, et al. Vascular reserve in chronic cerebral ischemia measured by the acetazolamide challenge test: comparison with positron-emission tomography. AJNR Am J Neuroradiol 1995;16:563–570
Abstract
↵
Yamauchi H, Okazawa H, Kishibe Y, et al. Reduced blood flow response to acetazolamide reflects pre-existing vasodilation and decreased oxygen metabolism in major cerebral arterial occlusive disease. Eur J Nucl Med 2002;29:1349–1356
CrossRef
↵
Gotoh F, Meyer JS, Tomita M. Carbonic anhydrase inhibition and cerebral venous blood gases and ions in man. Arch Intern Med 1966;117:39–46
CrossRef PubMed
↵
Garcia JH, Lassen NA, Weiller C, et al. Ischemic stroke and incomplete infarction. Stroke 1996;27:761–765
Abstract/FREE Full Text
↵
Feeney DM, Baron JC. Diaschisis. Stroke 1986;17:817–830
FREE Full Text
↵
Baron JC, Bousser MG, Comar D, Castaigne P. Crossed cerebellar diaschisis in human supratentorial brain infarction. Trans Am Neurol Assoc 1980;105:459–461
↵
Yamauchi H, Fukuyama H, Kimura J. Hemodynamic and metabolic changes in crossed cerebellar hypoperfusion. Stroke 1992;23:855–860
Abstract/FREE Full Text
↵
DeGardo T, Turkington T, Williams J, et al. Performance characteristics of a whole-body PET scanner. J Nucl Med 1994;35:1398–1406
Abstract/FREE Full Text
↵
Okazawa H, Yamauchi H, Sugimoto K, et al. Quantitative comparison of the bolus and steady-state methods for measurement of cerebral perfusion and oxygen metabolism: positron emission tomography study using ¹⁵O gas and water. J Cereb Blood Flow Metab 2001;21:793–803
CrossRef PubMed
↵
Okazawa H, Yamauchi H, Sugimoto K, et al. Effects of acetazolamide on cerebral blood flow, blood volume, and oxygen metabolism: a positron emission tomography study with healthy volunteers. J Cereb Blood Flow Metab 2001;21:1472–1479
CrossRef PubMed
↵
Votaw JR, Shulman SD. Performance evaluation of the pico-count flow-through detector for use in cerebral blood flow PET studies. J Nucl Med 1998;39:509–515
Abstract/FREE Full Text
↵
Frackowiak RSJ, Lenzi GL, Jones T, Heather JD. Quantitative measurement of regional cerebral blood flow and oxygen metabolism in man using ¹⁵O and positron emission tomography: theory, procedure, and normal values. J Comput Assist Tomogr 1980;4:727–736
CrossRef PubMed
↵
Lammertsma AA, Jones T. Correction for the presence of intravascular oxygen-15 in the steady-state technique for measuring regional oxygen extraction ratio in the brain. 1. Description of the method. J Cereb Blood Flow Metab 1983;3:416–424
PubMed
↵
Herscovitch P, Markham J, Raichle ME. Brain blood flow measured with intravenous H2(15)O. I. Theory and error analysis. J Nucl Med 1983;24:782–789
Abstract/FREE Full Text
↵
Raichle ME, Martin WRW, Herscovitch P, et al. Brain blood flow measured with intravenous H2(15)O. II. Implementation and validation. J Nucl Med 1983;24:790–798
Abstract/FREE Full Text
↵
Bogsrud TV, Rootwelt K, Russell D, Nyberg-Hansen R. Acetazolamide effect on cerebellar blood flow in crossed cerebral-cerebellar diaschisis. Stroke 1990;21:52–55
Abstract/FREE Full Text
Matsuda H, Tsuji S, Sumiya H, et al. Acetazolamide effect on vascular response in areas with diaschisis as measured by Tc-99m HMPAO brain SPECT. Clin Nucl Med 1992;17:581–586
CrossRef PubMed
Sakashita Y, Matsuda H, Kakuda K, Takamori M. Hypoperfusion and vasoreactivity in the thalamus and cerebellum after stroke. Stroke 1993;24:84–87
Abstract/FREE Full Text
↵
Kuwabara Y, Ichiya Y, Sasaki M, et al. Cerebellar vascular response to acetazolamide in crossed cerebellar diaschisis: a comparison of ^99mTc- HMPAO single-photon emission tomography with ¹⁵O-H2O positron emission tomography. Eur J Nucl Med 1996;23:683–689
PubMed
↵
Ito H, Kanno I, Shimosegawa E, et al. Hemodynamic changes during neuronal deactivation in human brain: a positron emission tomography study of crossed cerebellar diaschisis. Ann Nucl Med 2002;16:249–254
CrossRef PubMed
↵
Dong Y, Fukuyama H, Nabatame H, et al. Assessment of benzodiazepine receptors using iodine-123-labeled iomazenil single-photon emission computed tomography in patients with ischemic cerebrovascular disease: a comparison with PET study. Stroke 1997;28:1776–1782
Abstract/FREE Full Text

Received April 2, 2003.
Accepted after revision July 3, 2003.

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Crossed Cerebellar Diaschisis in Acute Stroke Detected by Dynamic Susceptibility Contrast MR Perfusion Imaging

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[1] ↵
Vorstrup S. Tomographic cerebral blood flow measurements in patients with ischemic cerebrovascular disease and evaluation of the vasodilatory capacity by the acetazolamide test. Acta Neurol Scand Suppl 1988;114:1–48
PubMed

[2] ↵
Yonas H, Pindzola RR. Physiological determination of cerebrovascular reserves and its use in clinical management. Cerebrovasc Brain Metab Rev 1994;6:325–340
PubMed

[3] ↵
Yonas H, Smith HA, Durham SR, et al. Increased stroke risk predicted by compromised cerebral blood flow reactivity. J Neurosurg 1993;79:483–489
CrossRef PubMed

[4] Kuroda S, Houkin K, Kamiyama H, et al. Long-term prognosis of medically treated patients with internal carotid or middle cerebral artery occlusion: can acetazolamide test predict it? Stroke 2001;32:2110–2116
Abstract/FREE Full Text

[5] ↵
Ogasawara K, Ogawa A, Terasaki K, et al. Use of cerebrovascular reactivity in patients with symptomatic major cerebral artery occlusion to predict 5-year outcome: comparison of xenon-133 and iodine-123-IMP single-photon emission computed tomography. J Cereb Blood Flow Metab 2002;22:1142–1148
CrossRef PubMed

[6] ↵
Nariai T, Suzuki R, Hirakawa K, et al. Vascular reserve in chronic cerebral ischemia measured by the acetazolamide challenge test: comparison with positron-emission tomography. AJNR Am J Neuroradiol 1995;16:563–570
Abstract

[7] ↵
Yamauchi H, Okazawa H, Kishibe Y, et al. Reduced blood flow response to acetazolamide reflects pre-existing vasodilation and decreased oxygen metabolism in major cerebral arterial occlusive disease. Eur J Nucl Med 2002;29:1349–1356
CrossRef

[8] ↵
Gotoh F, Meyer JS, Tomita M. Carbonic anhydrase inhibition and cerebral venous blood gases and ions in man. Arch Intern Med 1966;117:39–46
CrossRef PubMed

[9] ↵
Garcia JH, Lassen NA, Weiller C, et al. Ischemic stroke and incomplete infarction. Stroke 1996;27:761–765
Abstract/FREE Full Text

[10] ↵
Feeney DM, Baron JC. Diaschisis. Stroke 1986;17:817–830
FREE Full Text

[11] ↵
Baron JC, Bousser MG, Comar D, Castaigne P. Crossed cerebellar diaschisis in human supratentorial brain infarction. Trans Am Neurol Assoc 1980;105:459–461

[12] ↵
Yamauchi H, Fukuyama H, Kimura J. Hemodynamic and metabolic changes in crossed cerebellar hypoperfusion. Stroke 1992;23:855–860
Abstract/FREE Full Text

[13] ↵
DeGardo T, Turkington T, Williams J, et al. Performance characteristics of a whole-body PET scanner. J Nucl Med 1994;35:1398–1406
Abstract/FREE Full Text

[14] ↵
Okazawa H, Yamauchi H, Sugimoto K, et al. Quantitative comparison of the bolus and steady-state methods for measurement of cerebral perfusion and oxygen metabolism: positron emission tomography study using ¹⁵O gas and water. J Cereb Blood Flow Metab 2001;21:793–803
CrossRef PubMed

[15] ↵
Okazawa H, Yamauchi H, Sugimoto K, et al. Effects of acetazolamide on cerebral blood flow, blood volume, and oxygen metabolism: a positron emission tomography study with healthy volunteers. J Cereb Blood Flow Metab 2001;21:1472–1479
CrossRef PubMed

[16] ↵
Votaw JR, Shulman SD. Performance evaluation of the pico-count flow-through detector for use in cerebral blood flow PET studies. J Nucl Med 1998;39:509–515
Abstract/FREE Full Text

[17] ↵
Frackowiak RSJ, Lenzi GL, Jones T, Heather JD. Quantitative measurement of regional cerebral blood flow and oxygen metabolism in man using ¹⁵O and positron emission tomography: theory, procedure, and normal values. J Comput Assist Tomogr 1980;4:727–736
CrossRef PubMed

[18] ↵
Lammertsma AA, Jones T. Correction for the presence of intravascular oxygen-15 in the steady-state technique for measuring regional oxygen extraction ratio in the brain. 1. Description of the method. J Cereb Blood Flow Metab 1983;3:416–424
PubMed

[19] ↵
Herscovitch P, Markham J, Raichle ME. Brain blood flow measured with intravenous H2(15)O. I. Theory and error analysis. J Nucl Med 1983;24:782–789
Abstract/FREE Full Text

[20] ↵
Raichle ME, Martin WRW, Herscovitch P, et al. Brain blood flow measured with intravenous H2(15)O. II. Implementation and validation. J Nucl Med 1983;24:790–798
Abstract/FREE Full Text

[21] ↵
Bogsrud TV, Rootwelt K, Russell D, Nyberg-Hansen R. Acetazolamide effect on cerebellar blood flow in crossed cerebral-cerebellar diaschisis. Stroke 1990;21:52–55
Abstract/FREE Full Text

[22] Matsuda H, Tsuji S, Sumiya H, et al. Acetazolamide effect on vascular response in areas with diaschisis as measured by Tc-99m HMPAO brain SPECT. Clin Nucl Med 1992;17:581–586
CrossRef PubMed

[23] Sakashita Y, Matsuda H, Kakuda K, Takamori M. Hypoperfusion and vasoreactivity in the thalamus and cerebellum after stroke. Stroke 1993;24:84–87
Abstract/FREE Full Text

[24] ↵
Kuwabara Y, Ichiya Y, Sasaki M, et al. Cerebellar vascular response to acetazolamide in crossed cerebellar diaschisis: a comparison of ^99mTc- HMPAO single-photon emission tomography with ¹⁵O-H2O positron emission tomography. Eur J Nucl Med 1996;23:683–689
PubMed

[25] ↵
Ito H, Kanno I, Shimosegawa E, et al. Hemodynamic changes during neuronal deactivation in human brain: a positron emission tomography study of crossed cerebellar diaschisis. Ann Nucl Med 2002;16:249–254
CrossRef PubMed

[26] ↵
Dong Y, Fukuyama H, Nabatame H, et al. Assessment of benzodiazepine receptors using iodine-123-labeled iomazenil single-photon emission computed tomography in patients with ischemic cerebrovascular disease: a comparison with PET study. Stroke 1997;28:1776–1782
Abstract/FREE Full Text

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The Effect of Deafferentation on Cerebral Blood Flow Response to Acetazolamide

Abstract