Orexin receptor type-1 antagonist SB-334867 decreases morphine-induced antinociceptive effect in formalin test

被引:24
作者
Azhdari-Zarmehri, Hassan [1 ,2 ]
Esmaeili, Mohammad-Hossein [1 ,2 ]
Sofiabadi, Mohammad [1 ,2 ]
Haghdoost-Yazdi, Hashem [1 ,2 ]
机构
[1] Qazvin Univ Med Sci, Cellular & Mol Res Ctr, Qazvin, Iran
[2] Qazvin Univ Med Sci, Dept Physiol, Qazvin, Iran
基金
美国国家科学基金会;
关键词
Orexin receptor type-1; Morphine; Formalin test; Rat; LATERAL HYPOTHALAMIC-STIMULATION; SPINAL-CORD; ENHANCED ANTINOCICEPTION; PERIAQUEDUCTAL GRAY; HYPOCRETIN OREXIN; NEUROPATHIC PAIN; RAT-BRAIN; HOT PLATE; ANALGESIA; DISINHIBITION;
D O I
10.1016/j.pbb.2013.09.018
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
010107 [宗教学]; 030301 [社会学]; 070906 [古生物学及地层学(含古人类学)];
摘要
Orexin-A and orexin-B are two neuropeptides selectively synthesized in the lateral hypothalamus (LH), a region involved in morphine induced analgesia and pain modulation. Furthermore, orexin-A has been reported to produce an analgesic effect in pain models, which was blocked by orexin-1 receptor antagonist SB-334867, but not naloxone. We studied the effects of intracerebroventricular (ICV) injection of SB-334867, a selective orexin receptor type-1 antagonist, on morphine-induced antinociceptive effect in formalin test in rats. Morphine injection at a dose of 1.5 mg/kg caused a significant decrease in the formalin-induced nociceptive behaviors in phase 1, interphase, and phase 2A, whereas at doses of 3, 6, and 10 mg/kg, a significant reduction in the formalin-induced nociceptive behaviors was observed in all phases. The ICV injection of SB-334867 alone had no effect on the formalin-induced nociceptive behaviors. Pre-treatment with SB-334867 at a dose of 0.5 nmol significantly attenuated the analgesia induced by morphine (at dose 1.5 mg/kg of morphine; interphase and phase 2B and at dose 3 mg/kg of morphine just phase 2B of formalin test). Also, pre-treatment with SB-334867 at a dose of 5 nmol considerably attenuated the morphine-induced analgesia (at dose 1.5 mg/kg of morphine; phase 1, interphase, and phase 2, at dose 3 and 6 mg/kg of morphine just phase 2 of formalin test). Pre-treatment with SB-334867 at a dose of 50 nmol remarkably attenuated the morphine-induced analgesia (at dose 1.5 and 3 mg/kg of morphine; in phase 1, interphase, and phase 2 and also at dose 6 mg/kg of morphine; phase 1 and phase 2B of formalin test). These data suggest that the antinociceptive effects of morphine in formalin test might be associated with orexin receptor type-1. Our findings reveal a new role for the lateral hypothalamus orexin neuron's in the morphine-induced analgesia. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:64 / 70
页数:7
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