Abstract

Analgesic drugs in a combination-form can achieve greater efficacy with lesser side effects compared to either drug alone. The combination of drugs acting at different targets or mechanisms of action has been recognized as an alternative approach for achieving optimal analgesia. In this study, the analgesic effects of pregabalin (30, 60, 100, 200 mg/kg), curcumin (15, 30, 60, 100, 120 mg/kg), and 1:1 fixed-dose ratio of the pregabalin-curcumin combination were assessed using two acute nociceptive pain models, the acetic acid-induced writhing and tail-flick tests in mice. The pregabalin-curcumin combination produced a dose-dependent decrease in mean of writhes and an increase in the percentage of antinociception by the acetic acid-induced writhing test. In the tail-flick test, the combination also showed an improvement in antinociception indicated by the tail-flick latency, % antinociception, and area under the curve (AUC). Isobolographic analysis of interactions demonstrated a significant synergistic interaction effect between pregabalin and curcumin in both acute nociceptive pain models with the experimental ED50 below the predicted additive line and the combination index < 1. These findings demonstrate that the combination of pregabalin and curcumin exhibits a synergistic interaction in mouse models of acute nociceptive pain.

Highlights

  • Pain is a nociceptor response to noxious and non-noxious stimuli that, in turn, stimulates the central nervous system to perceive pain [1]

  • All indicated doses used in this study did not display any effects on motor performances at the time points tested at 90 min post-treatment (Figure 4). These results indicate that the fixed ratio combination (1:1) in tail‐flick test. g Combination index (γ) of pregabalin and curcumin combination

  • Previous reports support the potential roles of either pregabalin or curcumin to be used

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Summary

Introduction

Pain is a nociceptor response to noxious and non-noxious stimuli that, in turn, stimulates the central nervous system to perceive pain [1]. Current pharmacotherapy for acute pain includes acetaminophen, steroids, non-steroidal anti-inflammatory drugs (NSAIDs), and opioids. Their side effects, such as gastrointestinal bleeding, Molecules 2020, 25, 4172; doi:10.3390/molecules25184172 www.mdpi.com/journal/molecules. One of the potent targets for pain treatment is the calcium channel [4]. The α2-δ subunits of voltage-gated calcium channels (VGCCs) are distributed and expressed in the peripheral nerves of the dorsal root ganglia and the central nervous system (CNS) [5,6]. Pregabalin treatment reduced acute postoperative pain in humans, which might be attributed to its antinociceptive activity [11]

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