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Acta Physiologica Congress

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Acta Physiologica 2012; Volume 206, Supplement 693
Joint FEPS and Spanish Physiological Society Scientific Congress 2012
9/8/2012-9/11/2012
Santiago de Compostela, Spain


GLUCOSAMINE-INDUCED SUPPRESSION OF TOOTH PULPAL NOCICEPTIVE RESPONSES IN THE RAT
Abstract number: P63

Kaida1 K, Hayashi2 Y, Yamashita3 H, Kimoto4 M, Toda3 K

1Cariology, Integrative Sensory Physiology, Nagasaki University,
2Cariology, Nagasaki University,
3Integrative Sensory Physiology, Nagasaki University,
4Integrative Sensory Physiology, Physiologocal Laboratory, Nagasaki University, Japan Women's University

Objectives: 

D-glucosamine hydrochloride (DGL) has a variety of biological activities. Although, it has been reported that DGL has a significant pain relief effect in treating osteoarthritis et al, little is known about the effect on dental pain. To evaluate the applicability of DGL as a medicament to control pain in tooth is not yet reported. In this study, using an in vitro rat mandible-inferior alveolar nerve preparation (jaw-nerve preparation), we examined the effect of DGL on nociceptive responses in the tooth pulpal nerve.

Materials: 

We evaluated the effect of DGL on nociceptive responses for twenty Male Wistar albino rats by using an in vitro jaw-nerve preparation. Bradykinin(BK) was used as a chemical nociceptive stimulant which was poured near the exposed tooth pulp. Sixty second after BK application, the surface of the exposed pulp was applied with DGL solution in the DGL group, while in the control group, with physiological saline.

Results: 

The frequency in the control group was 2.06 ± 0.21 Hz (n = 10) after 5 minutes of saline application, while that in the DGL group was 0.76 ± 0.16 Hz (n = 10) after 5 minutes of DGL application. The DGL group showed significantly lower frequency than the control groups (t-test, p<0.05).

Conclusions: 

BK-induced nociceptive responses were fairly suppressed by direct application of DGL. Our results suggest that DGL might have a pain relief effect in dental pain.

To cite this abstract, please use the following information:
Acta Physiologica 2012; Volume 206, Supplement 693 :P63

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