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Year : 2016  |  Volume : 48  |  Issue : 4  |  Page : 394--398

Role of fosaprepitant, a neurokinin Type 1 receptor antagonist, in morphine-induced antinociception in rats

Pranav Prasoon, Shivani Gupta, Rahul Kumar, Mayank Gautam, Saroj Kaler, Subrata Basu Ray 
 Department of Anatomy, All Institute of Medical Sciences, New Delhi, India

Correspondence Address:
Subrata Basu Ray
Department of Anatomy, All India Institute of Medical Sciences, New Delhi
India

Abstract

Objectives: Opioids such as morphine form the cornerstone in the treatment of moderate to severe pain. However, opioids also produce serious side effects such as tolerance. Fosaprepitant is a substance P (SP) receptor antagonist, which is used for treating chemotherapy-induced nausea and vomiting. SP is an important neuropeptide mediating transmission of pain at the spinal level. Thus, it was hypothesized that combining morphine with fosaprepitant would increase the antinociceptive effect of morphine. The objectives were to evaluate the effect of fosaprepitant on morphine-induced antinociception in rats and to investigate its mechanism of action. Methods: Sprague-Dawley rats were injected with morphine (10 mg/kg twice daily) and/or fosaprepitant (30 mg/kg once daily) for 7 days. Pain threshold was assessed by the hot plate test. Expression of SP and calcitonin gene-related peptide (CGRP) in the spinal cords of these rats was evaluated by immunohistochemistry. Results: Morphine administration resulted in an antinociceptive effect compared to the control group (day 1 and to a lesser extent on day 4). The decreased antinociception despite continued morphine treatment indicated development of tolerance. Co-administration of fosaprepitant attenuated tolerance to morphine (days 1 and 3) and increased the antinociceptive effect compared to control group (days 1–4). Expression of SP was increased in the morphine + fosaprepitant group. Conclusions: The results show that fosaprepitant attenuates the development of tolerance to morphine and thereby, increases the antinociceptive effect. This is likely linked to decreased release of SP from presynaptic terminals.



How to cite this article:
Prasoon P, Gupta S, Kumar R, Gautam M, Kaler S, Ray SB. Role of fosaprepitant, a neurokinin Type 1 receptor antagonist, in morphine-induced antinociception in rats.Indian J Pharmacol 2016;48:394-398


How to cite this URL:
Prasoon P, Gupta S, Kumar R, Gautam M, Kaler S, Ray SB. Role of fosaprepitant, a neurokinin Type 1 receptor antagonist, in morphine-induced antinociception in rats. Indian J Pharmacol [serial online] 2016 [cited 2022 Jan 19 ];48:394-398
Available from: https://www.ijp-online.com/text.asp?2016/48/4/394/186198


Full Text

Mjority of cancer patients, particularly at an advanced stage of the disease, suffer from pain.[1] Pain management is rendered challenging by the heterogeneity in patient characteristics such as age, stage of the disease, psychological status, and social life. Superimposed on these are the incidences of “Breakthrough pain” also known as incidental or transitory pain, which are temporary flare-ups of extreme pain.[2]

Opioids such as morphine form the mainstay in the treatment of moderate to severe cancer pain.[3] However, opioids also produce adverse effects such as nausea and vomiting, excessive sedation, and tolerance. Adjuvant analgesics such as corticosteroids, anticonvulsants, and antidepressants are also frequently prescribed for better control of the pain.[4] µ-opioid receptors, which mediate the antinociceptive effect of morphine, are widely expressed in the central nervous system (CNS). In the dorsal horn of the spinal cord, these receptors are present in the primary sensory afferents and in the neurons of laminae I-II. The sensory afferents also contain substanceP(SP), an important neuropeptide concerned with transmission of pain.[5] SP predominantly binds to the neurokinin type 1 receptor (NK1r) expressed by the dorsal horn neurons.[6] NK1r is also expressed elsewhere in the CNS (e.g., corpus striatum and nucleus tractus solitarius), gastrointestinal tract, and urinary bladder. Release of SP following persistent or high-intensity nociceptive input induces synaptic plasticity in the dorsal horn neurons, leading to lowering of nociceptive threshold known as central sensitization.[7] Correspondingly, ablation of the NK1r expressing neurons by SP-Saporin complex impairs central sensitization without affecting basal pain sensitivity.[8] Thus, it was hypothesized that combining morphine with an NK1r antagonist such as fosaprepitant might attenuate the development of tolerance to morphine. The NK1r antagonist aprepitant (Emend ®) is often used for treating chemotherapy-induced nausea and vomiting.[9] Fosaprepitant (dimeglumine), a water-soluble prodrug of aprepitant, was later introduced in the market. Fosaprepitant administration gives rise to high NK1r occupancy in the CNS for a prolonged period of time (41–75% receptor occupancy at 120 h).[10] The expression of SP in the spinal cord was determined at the end of the behavioral study. Apart from SP, calcitonin gene-related peptide (CGRP) is also present in primary nociceptive afferents and takes part in the process of central sensitization.[11] Its expression was also evaluated.

 Methods



Male Sprague-Dawley rats (n = 24) weighing approximately 250 g were used for the study. Permission for the experimental work was obtained from the Institutional Animal Ethics Committee (767/IAEC/13 dated 1-1-2014). Rats were divided into 4 equal groups and injected physiological saline (twice daily subcutaneously in morning and evening; Group I), morphine sulfate (10 mg/kg twice daily subcutaneously; Group II), fosaprepitant (30 mg/kg once by intraperitoneal route; Group III), and finally, the last group was co-administered both morphine and fosaprepitant (Group IV) in the same doses as in Group II and III, respectively, for a week. In the last group, fosaprepitant was injected 30 min before the morphine injection. The dose of fosaprepitant (30 mg/kg) was higher than that used in an earlier study (25 mg/kg).[12] The approximate LD50 is >200 mg/kg in rats. The rationale for selecting a higher dose was the rapid conversion of fosaprepitant to aprepitant (half-life ~30 min) in the rat compared to dogs and humans. Hot plate latency or the thermal escape behaviour was determined in the morning, 40 min after saline (Group I), fosaprepitant (Group III), or morphine injection (Group II and IV). This time point was previously standardized as corresponding with maximum antinociceptive effect of morphine. Testing for latency was done at 24 h intervals. The hot plate test is commonly employed for screening the putative antinociceptive property of drugs. The advantages of this test are the brief nature of the nociceptive stimulus, which does not produce any tissue damage and that multiple testing can be done in the same animal.[13],[14] The predictability of this test to clinical situations is high for morphine and related opioid substances.[15]

Animals were initially acclimatized to the testing chamber for 15 min at room temperature. Testing was done in a quiet room with the ambient temperature between 22°C and 25°C. On the day of the experiment, the testing platform of the hot plate apparatus (Stoelting, USA) was set at a constant temperature of 52.5°C. The rats were placed on the hot plate, and the behavioral end points were either licking of the hindpaw or jumping.[15] The test was repeated thrice at 5–7 min intervals and the average of these values was the latency period (sec). A 40 s, cut-off was fixed to prevent damage to the completely analgesic paw after morphine injection. Transformation of these values was done by calculating the percent maximum possible effect (%MPE) as follows:

([Drug induced latency − basal response time]/[40 s − basal response time]) ×100

On day 8 (morning), rats were anesthetized by pentobarbital injection (100 mg/kg intraperitoneal). This was followed by intracardiac perfusion with 4% paraformaldehyde solution in 0.1 M phosphate buffer saline. The cervical enlargement (upper part) was isolated after laminectomy. Transverse sections of the spinal cord (20 µm thick) were obtained in a cryostat and processed for immunohistochemical localization of SP and CGRP using specific antibodies (anti-SP antibody, Abcam, UK; anti-CGRP antibody, Calbiochem, USA; 1:500 titer) using the Avidin-Biotin complex method (Vector Labs, USA).[16] Representative sections (3/rat; systematic random sampling) were later viewed under a microscope and the images captured. The expression of SP and CGRP in the superficial laminae (Rexed's laminae I-II) of the gray matter was quantitated by Image J software (NIH, USA). Specific expression was obtained after deducting background staining in the white matter (lateral funiculus) from the total value obtained from the superficial laminae. Some of the cryostat sections were stained with 0.5% Cresyl violet for localization of neurons in the dorsal horn.

Statistical evaluation of data was done by GraphPad Prism version 5 (GraphPad software, La Jolla, San Diego, USA). Values of latency period of the different groups of animals were independently analyzed at each time point by one-way analysis of variance followed by Bonferroni multiple comparison test. P < 0.05 was considered statistically significant. Values are represented as mean ± standard error of mean. Each experimental group had 6 animals.

 Results



The various groups of rats had different baseline values, which affected the subsequent comparison of the antinociceptive effect of the drugs [Figure 1]a. Hence, normalization of the data was done by calculating the %MPE [Figure 1]b. The %MPE values of control and the fosaprepitant-treated groups did not show any statistically significant change during the experiment. Morphine injection produced significantly higher antinociceptive effect on day 1 (P< 0.001) and to a lesser extent day 4 (P< 0.05) compared to the control group. The sharp decrease in the antinociceptive effect from day 2 in the morphine treated group indicated the development of tolerance. Morphine + fosaprepitant combination delayed the onset of tolerance in comparison to morphine treated group on days 1 (P< 0.01) and 3 (P< 0.001). Compared to control, antinociception was higher between days 1 and 4 (P< 0.001) for this group.{Figure 1}

Cresyl violet staining showed the dorsal horn neurons arranged in various laminae [Figure 2]. Immunohistochemical study revealed the expression of SP and CGRP over the superficial laminae (laminae I-II) of the dorsal horn [Figure 2]. Quantitative image analysis revealed increased SP expression in the morphine + fosaprepitant treated group compared to others [Figure 3]. Statistically significant difference was present between morphine and morphine + fosaprepitant co-treatment groups (P< 0.001). CGRP expression was not significantly altered.{Figure 2}{Figure 3}

 Discussion



The Aδ and C groups of nerve fibers carry pain from the periphery to the spinal cord. Majority of these fibers end in laminae I and II of the dorsal horn. The peptidergic subgroup of these nerve fibers contains neuropeptides such as SP and CGRP, which are released into the synaptic cleft following noxious stimulation. These neuropeptides diffuse to the postsynaptic terminal, where they bind to the corresponding receptors. Morphine-induced antinociception is linked to decreased release of glutamate, SP, CGRP, etc., from presynaptic terminals and greater postsynaptic hyperpolarization due to the activation of inwardly rectifying potassium channels.[17] Both these effect decrease onward neurotransmission of pain signals. Co-administration of fosaprepitant possibly interfered with the binding of SP to the NK1rs expressed by postsynaptic neurons in the spinal cord. The results of this study show that combining morphine with fosaprepitant (Group IV) delayed the development of morphine tolerance and concurrently increased the antinociceptive effect compared to the control group. As mentioned earlier, this could be due to decreased binding of SP to the NK1r. Evidence from electrophysiological experiments indicates that noxious stimuli produce slow and prolonged excitatory potentials in postsynaptic dorsal horn neurons, which are inhibited by NK1r antagonist.[18] Since fosaprepitant treatment (Group III) alone did not result in an antinociceptive effect, the interaction between morphine and fosaprepitant is likely synergistic in nature. Previously, injection of a bifunctional peptide having both µ-opioid receptor agonist and NK1r antagonist properties relieved pain in neuropathic rats without producing tolerance.[19] In a different study, Tumati et al. reported that intrathecal administration of both morphine and a NK1r antagonist reduced subsequent opioid withdrawal-induced hyperalgesia.[20] Paradoxically, a SP-opioid receptor agonist chimera inhibited development of opioid tolerance.[21] Pharmacokinetic interaction between fosaprepitant/aprepitant and morphine could also contribute to the enhanced antinociceptive effect. Aprepitant is mainly metabolized by CYP3A4 enzyme.[22] N-Demethylation of morphine by CYP3A4 is an important biotransformation pathway in rodents. Hence, morphine concentration in the nervous system could be increased by concurrent administration of these drugs.

Significant alterations in the expression of SP and CGRP were not observed except in the group treated with morphine + fosaprepitant combination (Group IV). This was unexpected because prevailing evidence suggests that NK1r does not regulate the release of SP in the spinal cord. However, contrary to this, NK1r has been recently reported to be crucial for release of SP from dorsal root ganglion neurons.[23] Thus, a possibility exists that fosaprepitant decreased release of SP from presynaptic terminals. Moreover, it has been speculated that there could be SP autoreceptors on presynaptic terminals, which can modulate SP release.[24] But, fosaprepitant treatment alone did not increase SP immunoreactivity in the present work. As noted earlier, morphine inhibits the release of SP under acute conditions but rats chronically treated with morphine in our study did not show a statistically significant increase in SP expression. Presumably, both NK1 autoreceptors as well as morphine-induced inhibition of SP release might have contributed to the increased SP expression in Group IV [Figure 4]. A limitation of this study was that the expression of SP and CGRP was evaluated at the end of the observation period and not between days 1 and 4, when the antinociceptive effect was maximum. Another limitation was the use of a fixed-dose combination of morphine and fosaprepitant.{Figure 4}

The antinociceptive effect of morphine decreased rapidly following daily administration, indicating development of tolerance. Morphine tolerance has been reported to develop even after a single dose. The antinociceptive effect of morphine is likely due to decreased release of pronociceptive neurotransmitters such as glutamate and neuropeptides such as SP from presynaptic nerve terminals which could be lost during tolerance.[17] One of the factors responsible for tolerance could be counter-adapting processes, which maintains the status quo in the spinal cord. Similarly, the potentiation of the antinociceptive effect of morphine by fosaprepitant is also lost on continued administration (day 5 onward). Identical result was reported with a chimera possessing both opioid agonist and NK1r antagonist properties.[25] Morphine tolerance is a complex phenomenon with several factors contributing to it.[26],[27] Moreover, the factors can differ depending upon the specific µ-opioid receptor agonist used for producing the tolerance.[28]

 Conclusion



The results indicate that addition of fosaprepitant to morphine can delay morphine tolerance for a limited period of time. This information could be used to treat breakthrough pain in cancer patients. To the best of our knowledge, this is the first report on the novel antinociceptive effect of morphine + fosaprepitant combination. Further studies are required to further elucidate this novel antinociceptive effect of morphine + fosaprepitant combination.

Acknowledgement

Financial support was provided by the Department of Biotechnology (BT-PR14279Med/30/452/2010), Government of India.

Financial Support and Sponsorship

Nil.

Conflicts of Interest

There are no conflicts of interest.

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