(Stroke. 2004;35:1985.)
© 2004 American Heart Association, Inc.
Original Contributions |
From the Department of Neuroscience (P.A.L., J.A.Z.), University of California San Diego; the Veterans Administration San Diego Healthcare System (P.A.L., J.W., J.A.Z.), San Diego, Calif; and the Veterans Medical Research Foundation (P.A.L., J.W., J.A.Z.), San Diego, Calif.
Correspondence to Dr Paul A. Lapchak, University of California San Diego, Department of Neuroscience, MTF 316, 9500 Gilman Drive, La Jolla, CA 92093-0624. E-mail plapchak{at}ucsd.edu
| Abstract |
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Methods In this study, the behavioral and physiological effects of laser treatment were measured. The RSCEM was used to assess whether low-energy laser treatment (7.5 or 25 mW/cm2) altered clinical rating scores (behavior) when given to rabbits beginning 1 to 24 hours postembolization. Behavioral analysis was conducted from 24 hours to 21 days after embolization, allowing for the determination of the effective stroke dose (P50) or clot amount (mg) that produces neurological deficits in 50% of the rabbits. Using the RSCEM, a treatment is considered beneficial if it significantly increases the P50 compared with the control group.
Results In the present study, the P50 value for controls were 0.97±0.19 mg to 1.10±0.17 mg; this was increased by 100% to 195% (P50=2.02±0.46 to 2.98±0.65 mg) if laser treatment was initiated up to 6 hours, but not 24 hours, postembolization (P50=1.23±0.15 mg). Laser treatment also produced a durable effect that was measurable 21 days after embolization. Laser treatment (25 mW/cm2) did not affect the physiological variables that were measured.
Conclusions This study shows that laser treatment improved behavioral performance if initiated within 6 hours of an embolic stroke and the effect of laser treatment is durable. Therefore, transcranial laser treatment may be useful to treat human stroke patients and should be further developed.
Key Words: laser neuroprotection embolism stroke, acute stroke, ischemic clinical trials
| Introduction |
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| Materials and Methods |
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Embolic Strokes
For the RSCEM, microclots were prepared from blood drawn from a donor rabbit and allowed to clot at 37°C, as described in detail previously.912 The microclots were resuspended in phosphate-buffered saline, then washed and allowed to settle, followed by aspiration of the supernatant and spiking of the particles with tracer quantities of 15-µm radiolabeled microspheres. The specific activity of the particles was determined by removing an aliquot, after which appropriate volumes of phosphate-buffered saline solution were added so that a predetermined weight of clot could be rapidly injected through the catheter. After the injection, the syringe and catheter were flushed with normal saline.
Quantal DoseResponse Analysis
To evaluate the quantitative relationship between clot dose and behavioral deficits, logistic (S-shaped) curves are fitted by computer to the quantal doseresponse data as described in detail previously.912 A wide range of lesion volumes is induced to generate normal and abnormal animals with various behavioral deficits. Using 3 or more different doses of microclots generated each quantal analysis curve. In the absence of treatment, we find the low end of the curve (small numbers of microclots cause no grossly apparent neurologic dysfunction) and the high end (large numbers of microclots invariably cause encephalopathy or death). Each animal is rated as either normal or abnormal (including dead animals), and interrater variability is very low (<5%). Behaviorally normal rabbits did not have any signs of impairment, whereas behaviorally abnormal rabbits had loss of balance, head leans, circling, seizure-type activity, or limb paralysis. With this simple rating system, the composite result for a group of animals is quite reproducible. Briefly, to evaluate the quantitative relationship between numbers of clots in the brain and neurological deficits (coma or death), logistic (S-shaped) curves are fitted by computer to the quantal doseresponse data. These parameters are measures of the amount of microclots (in mg) that produce neurologic dysfunction in 50% of a group of animals (P50).912 A separate curve is generated for each treatment condition and a statistically significant increase in the P50 value compared with control is indicative of a behavioral improvement. For these studies, rabbits were randomly allocated into treatment groups before embolization, with concealment of the randomization sequence until all behavioral and postmortem analyses were complete. The data were analyzed using the t test, which included the Bonferroni correction when appropriate.
Laser Treatment
Rabbits were placed in a Plexiglas restrainer for the duration of the treatment. The laser probe was placed in direct contact with the skin. An ACCULASER (PhotoThera, Inc) low-energy laser fitted with an OZ Optics Ltd fiber optic cable and laser probe measuring 2 cm in diameter was used (wavelength of 808±5 nm).13 Instrument design studies showed that these specifications would allow for laser penetration of the rabbit skull and brain to a depth of 2.5 to 3 cm, and that the laser beam would encompass the majority of the brain if placed on the skin surface posterior to bregma on the midline. Although the surface skin temperature below the probe was elevated by up to 3°C, the focal brain temperature directly under the laser probe was increased by 0.8°C to 1.8°C during the 10-minute laser treatment using the 25 mW/cm2 energy setting. Focal brain temperature returned to normal within 60 minutes of laser treatment.
Physiological Measurements
To determine if laser treatment alters physiological variables, 14 rabbits were randomly divided into 2 groups, a control group and a laser-treated group (25mW/cm2 for 10 minutes). Blood glucose levels were measured for all embolized rabbits using a Bayer Elite XL 3901B Glucometer, and body temperature was measured using a Braun Thermoscan Type 6013 digital thermometer as described previously by Lapchak et al.14
| Results |
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We also investigated whether a longer duration of laser treatment at a higher power density would have a beneficial effect on behavioral function. For this, we used a laser with energy settings of 25 mW/cm2 and treatment duration of 10 minutes. When initiated 1 or 6 hours postembolization, this laser treatment also significantly increased behavioral performance (P50=2.02±0.46 mg; n=18; and 2.98±0.65 mg; n=26, respectively) compared with controls (Table 1; Figures 1B and 2
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Physiological Variables
Blood glucose levels and body temperature were measured to determine if laser treatment (25mW/cm2 for 10 minutes) affected either measure after a small-clot embolic stroke. Table 2 presents the results of the blood glucose measurements. For these measurements, 7 rabbits were included in each group. They were embolized with small clot after establishing baseline body temperatures and blood glucose levels. Postmortem analysis showed that the control group was embolized using 5.68±0.41 mg of clots, whereas the laser-treated group received 5.52±0.52 mg of clots. In the laser-treated group, 6 of 7 rabbits survived 24 hours, whereas only 4 of 7 of the control rabbits survived 24 hours. Within 60 minutes of embolization, there was an increase in blood glucose levels in both groups that was maintained for the 2 hours postembolization observation time. Blood glucose levels returned to control levels by 24 hours, regardless of the extent of stroke-induced behavioral deficits. Laser treatment did not significantly affect glucose levels at any time. Neither embolization nor laser treatment significantly affected body temperature in either group of rabbits (Table 3).
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| Discussion |
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Although our studies indicate that laser treatment may attenuate stroke-induced behavioral deficits in rabbits, additional preclinical device development studies are required to evaluate the safety aspects of laser therapy. The use of lasers for the treatment of stroke should be approached with caution in light of findings that laser treatment can regulate a wide range of genes and induce translation of pre-existing mRNA species into their corresponding proteins.7 Because the mechanisms involved in laser-induced behavioral improvements remain unknown, studies are underway to determine if laser treatment increases neuronal survival after embolic strokes and to elucidate the cellular mechanism involved in the process.
| Conclusion |
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| Acknowledgments |
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Received February 4, 2004; revision received April 14, 2004; accepted April 22, 2004.
| References |
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