Ochi Takehiro, Ohkubo Yoshitaka, Mutoh Seitaro
Department of Immunology and Inflammation, Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., 1-6, Kashima 2-chome, Yodogawa-ku, Osaka, 532-8514, Japan.
Neurosci Lett. 2003 Oct 16;350(1):29-32. doi: 10.1016/s0304-3940(03)00835-8.
We investigated the anti-hyperalgesic effect of FR140423, 3-(difluoromethyl)-1-(4-methoxyphenyl-5-[4-(methylsulfinyl)phenyl]pyrazole, in a rat model of postoperative pain. Oral administration of FR140423 at doses between 1 and 100 mg/kg after surgery dose dependently attenuated the punctate mechanical hyperalgesia caused by an incision of the plantar surface of the hind paw with an ED50 value of 59 mg/kg. The anti-hyperalgesic effect of systematically administered FR140423 was blocked by naloxone, a non-selective opioid receptor antagonist. Furthermore, the delta-opioid receptor antagonist naltrindole (0.2 mg/kg) reversed anti-hyperalgesia induced by FR140423. Naloxonazine and nor-binaltorphimine failed to antagonize the anti-hyperalgesic effect of FR140423. The action of FR140423 differs from the naloxonazine-reversible anti-hyperalgesia induced by morphine. The present findings suggest that delta-opioid systems play a role in the rat anti-hyperalgesia produced by FR140423 for postoperative pain characterized by mechanical hyperalgesia.
我们在大鼠术后疼痛模型中研究了3-(二氟甲基)-1-(4-甲氧基苯基)-5-[4-(甲基亚磺酰基)苯基]吡唑(FR140423)的抗痛觉过敏作用。术后口服剂量为1至100 mg/kg的FR140423可剂量依赖性地减轻后爪足底表面切开引起的点状机械性痛觉过敏,其半数有效剂量(ED50)值为59 mg/kg。系统性给予FR140423的抗痛觉过敏作用被非选择性阿片受体拮抗剂纳洛酮阻断。此外,δ-阿片受体拮抗剂纳曲吲哚(0.2 mg/kg)可逆转FR140423诱导的抗痛觉过敏。纳洛酮嗪和去甲二氢吗啡酮未能拮抗FR140423的抗痛觉过敏作用。FR140423的作用不同于吗啡诱导的可被纳洛酮嗪逆转的抗痛觉过敏。目前的研究结果表明,δ-阿片系统在FR140423对以机械性痛觉过敏为特征的大鼠术后疼痛产生的抗痛觉过敏中发挥作用。