Madison Caitlin A, Wellman Paul J, Eitan Shoshana
Behavioral and Cellular Neuroscience, Department of Psychological and Brain Sciences, Texas A&M University, College Station, Texas, USA.
Behav Pharmacol. 2020 Apr;31(2&3):293-307. doi: 10.1097/FBP.0000000000000552.
Social environment influences the trajectory of developing opioid use disorder (OUD). Thus, the present study tested the hypothesis that sociability levels will affect the responses to opioids. Mice were tested for their baseline sociability, anxiety levels, pain sensitivities, and their acute locomotor response to 5 mg/kg opioids. Then, they were administered repeatedly with saline, hydrocodone, or morphine (20 mg/kg for 5 days, and then 40 mg/kg for 5 days). Subsequently, they were examined for the expression of locomotor sensitization and retested for the effects of opioids on their sociability, anxiety levels, and pain sensitivity. On the basis of their baseline sociability level, mice were divided into socially avoiding and socially exploring. Socially avoiding and socially exploring mice did not differ in their baseline weight and anxiety sensitivities. Socially avoiding mice had slightly higher baseline heat sensitivity than those in socially exploring mice. Repeated administration of opioids had differential effects in socially avoiding and socially exploring mice. In both social groups, repeated morphine administration had overall stronger effects compared with hydrocodone. Morphine-treated socially exploring mice developed greater locomotor sensitization than those in morphine-treated socially avoiding mice. Morphine-treated socially avoiding mice, but not socially exploring mice, spent more time in the center zone of the open-field test and in the light zone of light/dark boxes, and developed heat hyperalgesia. This study suggests that socially exploring animals are more sensitive to the sensitizing effects of opioids. In contrast, opioids have greater effects on the stress and pain systems of socially avoiding animals. Thus, the underlying mechanisms for developing OUD might differ in individuals with various sociability levels.
社会环境会影响阿片类物质使用障碍(OUD)的发展轨迹。因此,本研究检验了社交能力水平会影响对阿片类药物反应这一假设。对小鼠进行基线社交能力、焦虑水平、疼痛敏感性以及对5毫克/千克阿片类药物的急性运动反应测试。然后,给它们反复注射生理盐水、氢可酮或吗啡(20毫克/千克,持续5天,然后40毫克/千克,持续5天)。随后,检测它们运动敏化的表达情况,并再次测试阿片类药物对其社交能力、焦虑水平和疼痛敏感性的影响。根据基线社交能力水平,将小鼠分为社交回避型和社交探索型。社交回避型和社交探索型小鼠在基线体重和焦虑敏感性方面没有差异。社交回避型小鼠的基线热敏感性略高于社交探索型小鼠。阿片类药物的反复给药对社交回避型和社交探索型小鼠有不同影响。在两个社交组中,与氢可酮相比,反复注射吗啡的总体效果更强。吗啡处理的社交探索型小鼠比吗啡处理的社交回避型小鼠产生更大的运动敏化。吗啡处理的社交回避型小鼠,而非社交探索型小鼠,在旷场试验的中央区域和明暗箱的亮区花费更多时间,并出现热痛觉过敏。本研究表明,社交探索型动物对阿片类药物的敏化作用更敏感。相比之下,阿片类药物对社交回避型动物的应激和疼痛系统有更大影响。因此,不同社交能力水平个体发生OUD的潜在机制可能不同。