We examined the role of the vanilloid VR1 receptor in the thermal hyperalge
sia and allodynia seen in diabetic mice. Tail-flick latencies at source vol
tages of 35 and 50 V for a 50-W projection bulb in diabetic mice were signi
ficantly shorter than those in non-diabetic mice. Tail-flick latencies at 3
5 and 50 V in diabetic mice were increased by pretreatment with anti-vanill
oid VR1 receptor serum. Intrathecal(i.t.) injection of anti-VR1 serum resul
ted in a significant increase in the tail-flick latency at 50 V in non-diab
etic mice. However, i.t. pretreatment with anti-vanilloid VR1 receptor seru
m did not affect the tail-flick latency at a heat intensity of 35 V in non-
diabetic mice. Thus. it seems likely that thermal allodynia and hyperalgesi
a in diabetic mice may be due to the sensitization of vanilloid VR1 recepto
rs in primary sensory neurons in the spinal cord. (C) 2001 Elsevier Science
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