Thorn David A, Zhang Yanan, Li Jun-Xu
Department of Pharmacology and Toxicology, University at Buffalo, Buffalo, NY, USA.
Research Triangle Institute, Research Triangle Park, NC, USA.
Psychopharmacology (Berl). 2017 Jun;234(12):1871-1880. doi: 10.1007/s00213-017-4599-4. Epub 2017 Mar 17.
Emerging evidence suggests the potential utility of combining opioids with imidazoline I receptor agonists for chronic pain. However, chronic pain management requires prolonged pharmacotherapy, and the consequence of such combination therapy remains unclear.
This study examined the anti-hyperalgesic effect of the opioid oxycodone, the selective I receptor agonist phenyzoline, alone and in combination, during prolonged treatment.
Von Frey filament test was used to examine the anti-hyperalgesic effect of drugs in complete Freund's adjuvant (CFA)-induced inflammatory pain or chronic constriction injury (CCI)-induced neuropathic pain in rats. Twice-daily treatment with oxycodone and phenyzoline, alone or in combination, was continued until the development of significant tolerance (oxycodone) or as long as 19 days passed (phenyzoline).
In rats receiving CFA or CCI manipulation, mechanical hyperalgesia was dose-dependently reversed by oxycodone and phenyzoline. Twice-daily treatment with 2 × ED dose of oxycodone for 7 days led to significant antinociceptive tolerance to oxycodone but not cross-tolerance to phenyzoline. Similarly, twice-daily treatment with 2 × ED dose of phenyzoline for 19 days led to significant antinociceptive tolerance to phenyzoline but not cross-tolerance to oxycodone. Twice-daily treatment with the combined oxycodone and phenyzoline using different ratios (1:3, 1:1 and 3: 1) at the doses that were functionally equivalent to the treatment doses of oxycodone and phenyzoline for 13-19 days generally led to delayed antinociceptive tolerance.
Combination therapy with oxycodone and I receptor agonists maintains prolonged antinociceptive effectiveness with reduced propensity to develop tolerance.
新出现的证据表明,将阿片类药物与咪唑啉I受体激动剂联合用于慢性疼痛可能具有一定作用。然而,慢性疼痛管理需要长期的药物治疗,这种联合治疗的后果仍不清楚。
本研究考察了阿片类药物羟考酮、选择性I受体激动剂苯乙脒单独及联合使用在长期治疗期间的抗痛觉过敏作用。
采用von Frey细丝试验检测药物对大鼠完全弗氏佐剂(CFA)诱导的炎性疼痛或慢性缩窄性损伤(CCI)诱导的神经性疼痛的抗痛觉过敏作用。每天两次使用羟考酮和苯乙脒单独或联合给药,持续至出现显著耐受性(羟考酮)或长达19天(苯乙脒)。
在接受CFA或CCI处理的大鼠中,羟考酮和苯乙脒可剂量依赖性地逆转机械性痛觉过敏。每天两次用2×ED剂量的羟考酮治疗7天导致对羟考酮产生显著的抗伤害性耐受,但对苯乙脒无交叉耐受。同样,每天两次用2×ED剂量的苯乙脒治疗19天导致对苯乙脒产生显著的抗伤害性耐受,但对羟考酮无交叉耐受。每天两次使用不同比例(1:3、1:1和3:1)的羟考酮和苯乙脒联合给药,剂量与羟考酮和苯乙脒的治疗剂量等效,持续13 - 19天,通常会导致抗伤害性耐受延迟出现。
羟考酮与I受体激动剂联合治疗可维持长期的抗伤害性效果,且产生耐受性的倾向降低。