Azhdari-Zarmehri Hassan, Ghasemi Elmira, Heidari-Oranjaghi Nima, Sadegh Mehdi
Department of Basic Sciences and Neuroscience Research Center, Torbat Heydariyeh University of Medical Sciences, Torbat Heydariyeh.
Cellular and Molecular Research Center, Sabzevar University of Medical Sciences, Sabzevar.
Neuroreport. 2018 Feb 7;29(3):224-228. doi: 10.1097/WNR.0000000000000964.
Repeated administration of morphine or orexin-A produces tolerance to their antinociceptive effects. We investigated the possible incidence of cross-tolerance between orexin-A and morphine. Adult male Sprague-Dawley rats (200-250 g) were used. Under deep anesthesia, a stereotaxic apparatus was used to implant a 23 G cannula into the lateral ventricle for an intracerebroventricular (ICV) microinjection. The antinociceptive effect of three different doses of orexin-A (5, 20, and 40 µM; dissolved in 5 µl sterile saline; ICV) was examined using the hot-plate test at 15, 30, 60, and 90 min after infusion. To evaluate tolerance, orexin-A (20 µM; ICV) or morphine (10 mg/kg; intraperitoneal) was administered for 7 consecutive days (twice per day) and the analgesic response was assessed at days 1, 4, and 7. Cross-tolerance was investigated at day 8 with a single injection of morphine (10 mg/kg; intraperitoneal) to the repeated orexin-A group and a single microinjection of orexin-A (20 µM; ICV) to the repeated morphine group. Analgesic responses were then examined. Administration of both orexin-A and morphine produced significant antinociception at day 1 (P<0.001 compared with the saline group). However, a significant reduction in the analgesic effects of both morphine and orexin-A appeared at day 7, following repeated administration (P<0.01). Orexin-A microinjection at day 8 in the repeated morphine group did not result in significant antinociception (P>0.05), whereas morphine injection in the repeated orexin-A group at day 8 showed a significant analgesic effect (P<0.001). These results indicate cross-tolerance to the analgesic effect of orexin-A following morphine tolerance.
重复给予吗啡或食欲素-A会使其抗伤害感受作用产生耐受性。我们研究了食欲素-A与吗啡之间可能存在的交叉耐受性发生率。使用成年雄性Sprague-Dawley大鼠(200-250克)。在深度麻醉下,使用立体定位仪将一根23G套管植入侧脑室用于脑室内(ICV)微量注射。在输注后15、30、60和90分钟,使用热板试验检测三种不同剂量的食欲素-A(5、20和40μM;溶于5μl无菌盐水中;ICV)的抗伤害感受作用。为了评估耐受性,连续7天(每天两次)给予食欲素-A(20μM;ICV)或吗啡(10mg/kg;腹腔注射),并在第1、4和7天评估镇痛反应。在第8天,对重复给予食欲素-A的组单次注射吗啡(10mg/kg;腹腔注射),对重复给予吗啡的组单次微量注射食欲素-A(20μM;ICV),以研究交叉耐受性。然后检查镇痛反应。在第1天,给予食欲素-A和吗啡均产生了显著的抗伤害感受作用(与盐水组相比,P<0.001)。然而,在重复给药后,吗啡和食欲素-A的镇痛作用在第7天均出现显著降低(P<0.01)。在第8天,对重复给予吗啡的组进行食欲素-A微量注射未产生显著的抗伤害感受作用(P>0.05),而在第8天,对重复给予食欲素-A的组注射吗啡显示出显著的镇痛作用(P<0.001)。这些结果表明,在吗啡产生耐受性后,对食欲素-A的镇痛作用存在交叉耐受性。