Division of Physiology, Department of Basic Sciences, Faculty of Veterinary Medicine, Urmia University, Serow Highway, Urmia.
Division of Anatomy, Department of Basic Sciences, Faculty of Veterinary Medicine, Urmia University, Serow highway, Urmia, Iran.
Behav Pharmacol. 2024 Apr 1;35(2-3):66-78. doi: 10.1097/FBP.0000000000000746. Epub 2023 Aug 15.
It has been demonstrated that the nucleus accumbens (NAc) plays an important role in modulation of nociception due to its extensive connections with different regions of the brain. In addition, this nucleus receives histaminergic projections from tuberomammillary nucleus. Considering the role of the central histaminergic system in nociception, the effect of histamine and its H 2 and H 3 receptors agonist and antagonist microinjections into the NAc on orofacial formalin nociception was investigated. In male Wistar rats, using stereotaxic surgery, two guide cannulas were bilaterally implanted into the right and left sides of the NAc. Diluted formalin solution (1.5%, 50 µl) injection into the vibrissa pad led to orofacial nociception. Immediately after injection, face rubbing was observed at 3-min blocks for 45 min. Orofacial formalin nociception was characterized by a biphasic nociceptive response (first phase: 0-3 min and second phase: 15-33 min). Microinjections of histamine (0.5 and 1 μg/site), dimaprit (1 μg/site, H 2 receptor agonist) and thioperamide (2 μg/site, H 3 receptor antagonist) attenuated both phases of formalin orofacial nociception. Prior microinjection of famotidine (2 μg/site) inhibited the antinociceptive effects of dimaprit (1 μg/site). Furthermore, comicroinjection of thioperamide (2 μg/site) and immepip (1 μg/site) prevented thioperamide (2 μg/site)-induced antinociception. Naloxone (2 μg/site) also prevented histamine, dimaprit- and thioperamide-induced antinociception. The results of this study demonstrate that at the level of the NAc, histamine and its H 2 and H 3 receptors are probably involved in the modulation of orofacial nociception with an opioid system-dependent mechanism.
已经证明,伏隔核(NAc)通过与大脑不同区域的广泛连接,在调节疼痛感知中发挥重要作用。此外,该核接收来自结节乳头核的组胺能投射。鉴于中枢组胺能系统在疼痛感知中的作用,研究了将组胺及其 H2 和 H3 受体激动剂和拮抗剂微注射到 NAc 对口腔福尔马林疼痛感知的影响。在雄性 Wistar 大鼠中,通过立体定向手术,将两个导向套管双侧植入 NAc 的右侧和左侧。将稀释的福尔马林溶液(1.5%,50 μl)注射到触须垫中会导致口腔疼痛感知。注射后立即以 3 分钟为一个块观察 45 分钟的面部摩擦。口腔福尔马林疼痛感知的特征是双相疼痛反应(第一相:0-3 分钟,第二相:15-33 分钟)。组胺(0.5 和 1μg/部位)、二甲普里(1μg/部位,H2 受体激动剂)和噻哌酰胺(2μg/部位,H3 受体拮抗剂)的微注射减轻了福尔马林口腔疼痛感知的两个阶段。先前微注射法莫替丁(2μg/部位)抑制了二甲普里(1μg/部位)的抗伤害作用。此外,噻哌酰胺(2μg/部位)和 immepip(1μg/部位)的共微注射防止了噻哌酰胺(2μg/部位)引起的抗伤害作用。纳洛酮(2μg/部位)也阻止了组胺、二甲普里和噻哌酰胺引起的抗伤害作用。本研究的结果表明,在 NAc 水平,组胺及其 H2 和 H3 受体可能通过阿片系统依赖性机制参与调节口腔疼痛感知。