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阿片类药物和非阿片类药物对人类对应激的反应的影响。

Effects of opioid- and non-opioid analgesics on responses to psychosocial stress in humans.

机构信息

Interdisciplinary Scientist Training Program, University of Chicago, Chicago, IL, USA; Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, IL, USA.

Interdisciplinary Scientist Training Program, University of Chicago, Chicago, IL, USA.

出版信息

Horm Behav. 2018 Jun;102:41-47. doi: 10.1016/j.yhbeh.2018.04.009. Epub 2018 Apr 24.

Abstract

Both preclinical and clinical evidence suggests that the endogenous opioid system is involved in responses to stress. For example, in animal models opioid agonists reduce isolation distress whereas opioid antagonists increase isolation distress. We recently reported that the mixed mu agonist and kappa antagonist buprenorphine dampened responses to acute psychosocial stress in humans. Now we extend this to study the effects of a pure mu-opioid agonist, hydromorphone, and a non-opioid analgesic, acetaminophen, on response to social stress. We compared the effect of hydromorphone (2 and 4 mg), acetaminophen (1000 mg) to a placebo using a between subject design. Healthy adult volunteers were randomly assigned to receive placebo (N = 13), 2 mg hydromorphone (N = 12), 4 mg hydromorphone (N = 12), or 1000 mg acetaminophen (paracetamol; N = 13) under double-blind conditions before undergoing a stress task or a control task on two separate sessions. The stress task, consisting of a standardized speaking task and the non-stressful control task were presented in counterbalanced order. Dependent measures included mood ratings, subjective appraisal of the stress (or no-stress) task, salivary cortisol, pupil diameter, heart rate, and blood pressure. The stress task produced its expected increase in heart rate, blood pressure, salivary cortisol, pupil diameter, and subjective ratings of anxiety and negative mood. Hydromorphone dose-dependently dampened cortisol responses to stress, and decreased ratings of how "challenging" participants found the task. Acetaminophen did not affect physiological responses, but, like hydromorphone, decreased ratings of how "challenging" the task was. The hydromorphone results support the idea that the mu-opioid system is involved in physiological responses to acute stress in humans, in line with results from preclinical studies. The non-opioid analgesic acetaminophen did not dampen physiological responses, but did reduce some components of psychological stress. It remains to be determined how both opioid and non-opioid systems mediate the complex physiological and psychological responses to social stress.

摘要

临床前和临床证据表明,内源性阿片系统参与了应激反应。例如,在动物模型中,阿片类激动剂减轻了隔离痛苦,而阿片类拮抗剂则增加了隔离痛苦。我们最近报道,混合 μ 激动剂和 κ 拮抗剂丁丙诺啡可减轻人类对急性心理社会应激的反应。现在,我们将其扩展到研究纯 μ 阿片类激动剂氢吗啡酮和非阿片类镇痛药对乙酰氨基酚对社会应激反应的影响。我们使用受试者间设计比较了氢吗啡酮(2 和 4mg)、对乙酰氨基酚(1000mg)和安慰剂的效果。健康成年志愿者随机分为安慰剂组(N=13)、2mg 氢吗啡酮组(N=12)、4mg 氢吗啡酮组(N=12)或 1000mg 对乙酰氨基酚(扑热息痛;N=13)组,在两次单独的会议上,在接受一项应激任务或一项非应激任务之前,接受双盲条件下的治疗。应激任务包括标准化演讲任务和非应激控制任务,以平衡顺序呈现。因变量包括情绪评分、对应激(或无应激)任务的主观评估、唾液皮质醇、瞳孔直径、心率和血压。应激任务导致心率、血压、唾液皮质醇、瞳孔直径和焦虑和负面情绪的主观评分增加。氢吗啡酮剂量依赖性地抑制了皮质醇对压力的反应,并降低了参与者对任务的“挑战性”评价。对乙酰氨基酚不影响生理反应,但与氢吗啡酮一样,降低了对任务的“挑战性”评价。氢吗啡酮的结果支持这样的观点,即μ 阿片系统参与了人类对急性应激的生理反应,与临床前研究的结果一致。非阿片类镇痛药对乙酰氨基酚没有抑制生理反应,但确实减少了一些心理压力成分。阿片类和非阿片类系统如何介导对社会应激的复杂生理和心理反应仍有待确定。

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