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KMID : 0363120080210030179
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Korean Journal of Pain
2008 Volume.21 No. 3 p.179 ~ p.186
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Spinal α2 Adrenoceptor and Antiallodynic Effect by Clonidine after Chronic Administration of 4-Methylcatechol in Neuropathic Rat Pain Model
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Chung Kyu-Yeon
Shin Sang-Wook
Choi Bong-Soo
Kim Cheul-Hong
Kim Kyung-Hoon
Kim Hae-Kyu
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Abstract
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Background: The adrenergic nervous system in the spinal cord contributes to the development of neuropathic pain after nerve injury. Brain derived neurotrophic factor may facilitate the sympathetic change in the spinal cord and influence the state of neuropathic pain. We probed the effect of chronic repetitive administration of systemic 4-methylcatechol, which is known to be a neurotrophic factor inducer, in a spinal nerve ligation model.
Methods: We made the rat neuropathic pain model by the ligation of the L5 spinal nerve. Intraperitoneal 4-methylcatechol (10μg/kg) or the same volume of saline wasadministrated twice daily just after the operation for 7 days. The tactile allodynia was measured by using von Frey filaments and its change was followed up from 3 days after SNL. The lumbosacral enlargement of the spinal cord was taken out and the mRNA contents of the α2-adrenoceptor subtypes were measured by real time polymerase chain reaction and this was then compared with the control groups. The antiallodynic effect of intrathecal clonidine (3, 10, 30 μg) was evaluated and compared in the 4-methylcatechol treated rats and the control rats.
Results: The expression of the α2A and α2C adrenoceptor subtypes did not change after 4-methylcatechol treatment. Intrathecal clonidine showed an earlier and better effect at the highest dose (30 μg intrathecal), but not with any other doses.
Conclusions: Chronic intraperitoneal administration of 4-methylcatechol may improve the effect of intrathecal clonidine, but we could not prove the increase of α2A and α2C adrenoceptors in the spinal cord of 4-methylcatechol treated rats.
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KEYWORD
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adrenergic receptor, brain derived neurotrophic factor, neuropathic pain, spinal nerve ligation, 4-methylcatechol
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