Highlights
- •Opioid antinociceptive and behaviorally disruptive effects are measured concurrently.
- •The ratio of ED50 values for both measures are calculated, and differ among opioids.
- •These ratios indicate the behavioral selectivity of opioid antinociception.
- •ED50 ratios serve as preclinical estimates of therapeutic index.
- •Opioids with differing ED50 ratios may have differing scopes of clinical utility.
Abstract
Although the clinical application of opioids for pain management is often hindered
by undesired behavioral impairment, preclinical assays of antinociception typically
do not provide information regarding the behaviorally disruptive effects of opioids
that may accompany their antinociceptive effects. To address this, we modified a warm
water tail withdrawal procedure to determine concurrently the effects of opioids on
tail withdrawal latency (antinociception) and indices of food-maintained operant behavior
(rates of responding and reinforcement density) in squirrel monkeys. Six opioid agonists
were tested, and all produced dose-dependent antinociception and impairment of operant
behavior. The ratio of median effective dose (ED50) values for both measures (behavioral impairment:antinociception) was used as a quantitative
measure of therapeutic index. Nalbuphine had the highest ED50 ratio (4.88), reflecting antinociception with minimal behavioral disruption. Oxycodone,
heroin, buprenorphine, and methadone all produced similar ED50 ratios (.82–1.14), whereas butorphanol yielded a significantly lower ED50 ratio (.17) reflecting behavioral disruption at doses producing only minimal antinociception.
The antinociceptive and behaviorally disruptive effects of oxycodone and buprenorphine
were further characterized using Schild analysis to calculate apparent pA2 values for antagonism of the 2 drugs by naltrexone. These analyses suggest that µ-receptor
mechanisms likely mediate the antinociceptive as well as behaviorally disruptive effects
of oxycodone (pA2 values: 8.13 and 8.57) and buprenorphine (pA2 values: 8.6 and 7.9).
Perspective
This article presents an assay that allows for the concurrent assessment of the antinociceptive
and behaviorally disruptive effects of opioids. Our results show that the tail withdrawal
assay in squirrel monkeys can provide a useful index of the behavioral selectivity
with which opioids produce antinociception.
Key words
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to The Journal of PainAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- Morphine versus nalbuphine for open gynaecological surgery: A randomized controlled double blinded trial.Pain Res Treat. 2014; 2014 (727952)
- Some quantitative uses of drug antagonists.Br J Pharmacol Chemother. 1959; 14: 48-58
- Antinociceptive interactions between mu-opioid receptor agonists and the serotonin uptake inhibitor clomipramine in rhesus monkeys: Role of mu agonist efficacy.J Pharmacol Exp Ther. 2010; 335: 497-505
- Discriminative stimulus, reinforcing, physical dependence, and antinociceptive effects of oxycodone in mice, rats, and rhesus monkeys.Exp Clin Psychopharmacol. 2004; 12: 163-172
- Opioid complications and side effects.Pain Physician. 2008; 11: S105-S120
- Antagonism of the antinociceptive and discriminative stimulus effects of heroin and morphine by 3-methoxynaltrexone and naltrexone in rhesus monkeys.J Pharmacol Exp Ther. 2002; 302: 264-273
- Enadoline discrimination in squirrel monkeys: Effects of opioid agonists and antagonists.J Pharmacol Exp Ther. 2001; 297: 215-223
- Sex-related differences in the antinociceptive effects of opioids: Importance of rat genotype, nociceptive stimulus intensity, and efficacy at the mu opioid receptor.Psychopharmacology (Berl). 2000; 150: 430-442
- 75 years of opioid research: The exciting but vain quest for the Holy Grail.Br J Pharmacol. 2006; 147: S153-S162
- Effects of naloxone, diprenorphine, buprenorphine and etorphine on unpunished and punished food-reinforced responding in the squirrel monkey.J Pharmacol Exp Ther. 1984; 228: 669-675
- Differential cross-tolerance to opioid agonists in morphine-tolerant squirrel monkeys responding under a schedule of food presentation.Eur J Pharmacol. 1989; 174: 171-180
- Behavioral effects of buprenorphine and diprenorphine under a multiple schedule of food presentation in squirrel monkeys.J Pharmacol Exp Ther. 1983; 226: 317-323
- A tail withdrawal procedure for assessing analgesic activity in rhesus monkeys.J Pharmacol Methods. 1986; 15: 263-269
- Butorphanol-mediated antinociception in mice: partial agonist effects and mu receptor involvement.J Pharmacol Exp Ther. 1997; 282: 1253-1261
- Antinociceptive and respiratory effects of nalbuphine in rhesus monkeys.J Pharmacol Exp Ther. 1994; 271: 993-999
- Acute and chronic effects of naltrexone and naloxone on schedule-controlled behavior of squirrel monkeys and pigeons.J Pharmacol Exp Ther. 1981; 216: 500-509
- Agonist and antagonist actions of morphine-like drugs on the guinea-pig isolated ileum.Br J Pharmacol Chemother. 1966; 27: 514-527
- Determination of receptors that mediate opiate side effects in the mouse.Br J Pharmacol. 1983; 79: 731-736
- Ethanol reversal of tolerance to the antinociceptive effects of oxycodone and hydrocodone.J Pharmacol Exp Ther. 2017; 362: 45-52
- Operant nociception in nonhuman primates.Pain. 2014; 155: 1821-1828
- Diltiazem enhances the analgesic but not the respiratory depressant effects of morphine in rhesus monkeys.Eur J Pharmacol. 2000; 397: 85-92
- Differentiation of kappa opioid agonist-induced antinociception by naltrexone apparent pA2 analysis in rhesus monkeys.J Pharmacol Exp Ther. 1998; 285: 518-526
- In vivo profiling of seven common opioids for antinociception, constipation and respiratory depression: No two opioids have the same profile.Br J Pharmacol. 2015; 172: 532-548
- Animal models of nociception.Pharmacol Rev. 2001; 53: 597-652
- Comparison of morphine, meperidine, anileridine, and alphaprodine on schedule-controlled responding and analgesia.Pharmacol Biochem Behav. 1980; 12: 797-801
- Evidence that nalorphine, butorphanol and oxilorphan are partial agonists at a kappa-opioid receptor.Eur J Pharmacol. 1983; 86: 467-470
- Respiratory effects of opioid full and partial agonists in rhesus monkeys.J Pharmacol Exp Ther. 1996; 277: 462-472
- Buprenorphine: A unique drug with complex pharmacology.Curr Neuropharmacol. 2004; 2: 395-402
- Interactions between mu-opioid receptor agonists and cannabinoid receptor agonists in rhesus monkeys: Antinociception, drug discrimination, and drug self-administration.J Pharmacol Exp Ther. 2013; 345: 354-362
- Anatomy of CNS opioid receptors.Trends Neurosci. 1988; 11: 308-314
- Current challenges in translational pain research.Trends Pharmacol Sci. 2012; 33: 568-573
- The effects of morphine- and nalorphine- like drugs in the nondependent and morphine-dependent chronic spinal dog.J Pharmacol Exp Ther. 1976; 197: 517-532
- Buprenorphine effects on food-maintained responding in Macaque monkeys.Pharmacol Biochem Behav. 1985; 23: 1037-1044
- The contribution of intrinsic activity to the action of opioids in vitro.Br J Pharmacol. 1986; 87: 595-601
- Effects of mixed agonist-antagonist opioids on the acquisition of conditional discriminations in monkeys.J Pharmacol Exp Ther. 1987; 240: 74-81
- Effects of opioids on accuracy of a fixed-ratio discrimination in monkeys and rats.J Pharmacol Exp Ther. 1984; 230: 541-549
- An examination of the interactions between the antinociceptive effects of morphine and various mu-opioids: the role of intrinsic efficacy and stimulus intensity.Anesth Analg. 1999; 88: 407-413
- Contribution of individual differences to discriminative stimulus, antinociceptive and rate-decreasing effects of opioids: importance of the drug's relative intrinsic efficacy at the mu receptor.Behav Pharmacol. 1996; 7: 261-284
- Analysis of opioid efficacy, tolerance, addiction and dependence from cell culture to human.Br J Pharmacol. 2011; 164: 1322-1334
- Characterization of the antinociceptive effects of the individual isomers of methadone after acute and chronic administrations.Behav Pharmacol. 2011; 22: 548-557
- Acute and chronic morphine administration: Effects of mixed-action opioids in rats and squirrel monkeys responding under a schedule of food presentation.J Pharmacol Exp Ther. 1991; 257: 8-18
- Buprenorphine and opioid antagonism, tolerance, and naltrexone-precipitated withdrawal.J Pharmacol Exp Ther. 2011; 336: 488-495
- Methadone and heroin antinociception: Predominant delta-opioid-receptor responses in methadone-tolerant mice.Jpn J Pharmacol. 2002; 88: 319-331
- Characteristics of older adults receiving opioids in primary care: Treatment duration and outcomes.Pain Med. 2010; 11: 1063-1071
- United States worker's compensation and disability.in: Ballantyne J. Tauben D. Expert decision making on opioid treatment. Oxford University Press, New York2013: 103-114
- Buprenorphine: Differential interaction with opiate receptor subtypes in vivo.J Pharmacol Exp Ther. 1982; 223: 157-162
- Discriminative effects of cyclazocine in the squirrel monkey.J Pharmacol Exp Ther. 1978; 205: 291-301
- Morphine-like stimulus effects in the monkey: Opioids with antagonist properties.Pharmacol Biochem Behav. 1981; 14: 241-245
- Nalbuphine.Drug Alcohol Depend. 1985; 14: 339-362
- Nalbuphine vs morphine as part of intravenous post cardiac surgery.J Anesth Clin Res. 2014; 5: 463
- Opioid interactions in rhesus monkeys: Effects of delta + mu and delta + kappa agonists on schedule-controlled responding and thermal nociception.J Pharmacol Exp Ther. 2003; 307: 1054-1064
- Kappa-opioid receptor effects of butorphanol in rhesus monkeys.J Pharmacol Exp Ther. 1999; 290: 259-265
- Subjective, psychomotor, and physiological effects of cumulative doses of mixed-action opioids in healthy volunteers.Psychopharmacology (Berl). 2001; 155: 362-371
- In vivo apparent pA2 analysis for naltrexone antagonism of discriminative stimulus and analgesic effects of opiate agonists in rats.J Pharmacol Exp Ther. 1994; 271: 959-968
- Buprenorphine antagonism of mu opioids in the rhesus monkey tail-withdrawal procedure.J Pharmacol Exp Ther. 1995; 273: 1345-1352
- Behavioral characterization of opioid mixed agonist-antagonists.Drug Alcohol Depend. 1987; 20: 303-315
- Reinforcing and discriminative stimulus properties of mixed agonist-antagonist opioids.J Pharmacol Exp Ther. 1984; 229: 118-126
- A comparison of nalbuphine with morphine for analgesic effects and safety: Meta-analysis of randomized controlled trials.Sci Rep. 2015; 5: 10927
- Synthesis and binding affinity of novel mono- and bivalent morphinan ligands for kappa, mu, and delta opioid receptors.Bioorg Med Chem. 2011; 19: 2808-2816
Article info
Publication history
Published online: February 22, 2018
Accepted:
February 13,
2018
Received in revised form:
January 10,
2018
Received:
October 3,
2017
Footnotes
This work was supported by National Institutes of Health (RO1-DA035857).
The authors have no conflicts of interest to declare.
Identification
Copyright
© 2018 by the American Pain Society