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Effects of Excitatory Amino Acid Receptor Antagonists on Pulpal Blood Flow of the Rat Mandibular Incisor

S. Hofman,*, J. Azérad, and Y. Boucher

Laboratoire de Physiologie de la Manducation, Université Paris 7—Denis Diderot, 2 Place Jussieu, Bât. A, 2ème étage, 75005 Paris, France;



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Figure 1. Examples of pulpal blood flow (PBF) recordings in control vs. stimulated tooth. (A) Example of recording curves (15-minute sweeps) when bipolar electrical stimulation (10 sec, 50 µA, 2 ms, 20 Hz) was performed on 1 rat mandibular incisor. PBF changes of stimulated tooth (top), PBF of contralateral incisor that was monitored as control (second), and differential PBF, which we calculated by subtracting the values measured on control tooth from those measured on the stimulated tooth (third), are shown. Mean arterial blood pressure (BP) was monitored in parallel (bottom). Values are expressed in percentages of baseline levels. (B) Example of PBF monitoring (15-minute sweeps) on both mandibular incisors of 1 animal during intravenous injection of an EAA receptor antagonist (here MPPG, 0.15 mg/kg); differential PBF evolution is also shown.

 


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Figure 2. Differential pulpal blood flow (PBF) changes induced by bipolar electrical stimulation (10 sec, 50 µA, 2 ms, 20 Hz) of 1 rat mandibular incisor after systemic administration of ionotropic GluR antagonists. (A) Amplitude and duration of initial pulpal neurogenic blood flow decrease. (B) Amplitude and duration of late pulpal neurogenic blood flow increase. {square} Control group, MK 801 group, {blacksquare} Ketamine group, Gyki 52466 group. Control rats were injected i.v. with 200 µL of physiological saline (vehicle). Amplitude is expressed in percentage of variation of differential PBF from baseline level (difference between stimulated and control teeth). Duration is expressed in sec. Values are means ± SEM. Differences among experimental groups were evaluated by one-way ANOVA. For the immediate blood flow decrease and for the late blood flow increase, no statistical differences were found among groups.

 


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Figure 3. Differential pulpal blood flow (PBF) changes induced by bipolar electrical stimulation (10 sec, 50 µA, 2 ms, 20 Hz) of 1 rat mandibular incisor after systemic administration of metabotropic GluRs antagonists. (A) Amplitude and duration of initial pulpal neurogenic blood flow decrease. (B) Amplitude and duration of late pulpal neurogenic blood flow increase. {square} Control group, MCPG 2.2 mg/kg group, {blacksquare} MCPG 7.5 mg/kg group, MPPG 0.15 mg/kg group, MPPG 2.18 mg/kg group. Control rats were injected i.v. with 200 µL of a mix of 1M NaOH (105 µL/kg) and physiological saline (vehicle). Amplitude is expressed in percentage of variation of differential PBF from baseline level (difference between stimulated and control teeth). Duration is expressed in sec. Values are means ± SEM. Differences among experimental groups were evaluated by one-way ANOVA; **indicates differences that were significant for both amplitude and duration of initial blood flow decrease for animals injected with MCPG 7.5 mg/kg compared with vehicle-treated animals (p < 0.05, n = 5). For the late blood flow increase, no statistical differences were found among groups.

 





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