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Oxcarbazepine antinociception in animals with inflammatory pain or painful diabetic neuropathy
Author(s) -
Kiguchi Sumiyoshi,
Imamura Takahiro,
Ichikawa Kiyoshi,
Kojima Masami
Publication year - 2004
Publication title -
clinical and experimental pharmacology and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 103
eISSN - 1440-1681
pISSN - 0305-1870
DOI - 10.1111/j.1440-1681.2004.03950.x
Subject(s) - oxcarbazepine , medicine , diabetic neuropathy , neuropathic pain , anesthesia , nociception , pharmacology , diabetes mellitus , carbamazepine , endocrinology , receptor , psychiatry , epilepsy
Summary 1. Diabetic neuropathy is one of the most frequent complications of diabetes mellitus. However, the mechanisms underlying these disorders are not yet well defined and it has been reported that currently available analgesics have hardly any ameliorating effect on painful diabetic neuropathy. 2. The purpose of the present study was to evaluate the antinociceptive effect of oxcarbazepine (OCBZ), a keto derivative of carbamazepine (CBZ), in animal models generally used in pain research and in rats and mice with streptozotocin (STZ)‐induced diabetes. In addition, we compared the effect of OCBZ with those of CBZ, mexiletine and morphine. 3. Diabetes was induced by injection of STZ at a dose of 300 mg/kg (i.p.) in mice and 50 mg/kg (i.v.) in rats. Experiments were conducted 2 weeks after STZ injection and those animals with a serum glucose level above 400 mg/dL were used for data analysis. Antinociceptive effects of the drugs were evaluated by the paw withdrawal test (normal, STZ‐induced diabetic and carrageenin‐injected rats), tail‐flick test (normal and STZ‐induced diabetic mice) and nociceptive behaviour (formalin‐injected mice). 4. In the present study, diabetic mice showed thermal hyperalgesia and diabetic rats exhibited mechanical hyperalgesia. From these results, the STZ‐induced diabetic animals used in the present study were found to be suitable for research on painful diabetic neuropathy. In STZ‐induced diabetic animals, the antinociceptive effects of OCBZ, CBZ and mexiletine were facilitated, whereas the effect of morphine was attenuated, compared with effects in normal animals. 5. Oxcarbazepine inhibited the formalin‐induced biphasic pain responses and increased the nociceptive threshold in the case of carrageenin‐induced hyperalgesia. In view of these results, inhibition of substance P‐mediated pain transmission may be involved in the antinocieptive action of OCBZ. 6. These results indicate that OCBZ has an analgesic action and is a possible therapeutic agent for the treatment of neuropathic pain, such as occurs in painful diabetic neuropathy.