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Addiction to conventional opioid pain analgesics is a major societal problem that is increasing at an alarming rate. New drugs to combat the effects of opioid abuse are desperately needed. Kappa-opioid agonists are efficacious in peripheral pain models but suffer from centrally-mediated effects. In this review, we discuss our efforts, as well as other’s efforts in developing peripheral kappa-based opioid receptor agonists that have the potential analgesic activity of opioids but do not manifest the negative side-effects of opioid use and abuse. Further, derivatives of the tetra peptide D-Phe-D-Phe-D-Nle-D-Arg-NH2, such as CR665, exhibit high peripheral to central selectivity in analgesic models when administered intravenously (IV); however, they are inactive when administered orally. Application of the JT Pharmaceuticals non-natural amino acid technology to CR665 produced derivatives that exhibit peripheral analgesic activity when dosed orally but do not promote CNS-based effects. Lead compound JT09 activates the kappa-opioid receptor with EC50s in the low nM range, while agonist selectivity for kappa over other peripheral opioid receptors was >33,400 fold. Results indicate that JT09 acts as efficacious as morphine in alleviating peripheral pain, while failing to produce undesired CNS-mediated activity. Additionally, JT09 did not promote other CNS-mediated effects associated with morphine (addiction, sedation, dysphoria, tolerance). Thus, we propose that JT09 has potential for development as a novel analgesic.
Keywords: Analgesic, Kappa, Opioid, Pain, Peripheral
In this review, we describe the characteristics of JT09 that demonstrate its potential for development as a novel, broad- spectrum, analgesic.
METHODS AND RESULTS
Application of the JT Pharma proprietary peptide modification strategy imparts improved stability and oral availability with most peptides evaluated thus far . In pharmacokinetic/pharmacodynamic (PK/PD) studies, JT09 displayed a potent kappa-opioid receptor selectivity versus the mu- and delta-opioid receptors of >33,400-fold; a peripheral-selectivity of >938-fold; an oral EC50 of 4.7 mg/kg; and an i.v. EC50 of 0.032 mg/kg . These PK/PD numbers are minimal estimates, since mu- or delta- activities were not detected. It was also demonstrated that JT09 does not act as a kappa-opioid receptor antagonist or an inverse agonist.
In rat pain efficacy models, JT09 was evaluated in an acetic acid writhing assay, an established measure of peripherally mediated pain, and in a hot plate assay, a measure of centrally mediated pain. In the acetic acid writhing assay, rats were orally gavage (p.o.) with JT09 (20 mg/kg), while control rats received either morphine (10 mg/kg, intraperitoneally (i.p.)) or saline (0.2 mL, p.o.). JT09 demonstrated indistinguishable efficacy when compared to morphine in the acetic acid writhing assay for peripheral pain. In the hot plate model, rats received JT09 (20 mg/kg, p.o.), while control rats received morphine (10 mg/kg, i.p.). Rats were tested for centrally-mediated pain 20 min later by measuring the latency to paw licking behavior following placement on a 53°C hot plate. In the hot plate model, JT09 did not attenuate centrally-mediated pain, thus supporting that JT09 does not cross the BBB. Behavioral assays were performed in order to assess the side effect profile associated with JT09. Addiction is a major issue associated with conventional analgesics, such as morphine and other opioid derivatives. In order to assess the abuse liability associated with JT09, rats were studied in a self-administration model, in which rats were trained to press a lever to receive an intravenous drug infusion. Rats failed to maintain lever responding when switched from sucrose to JT09 (20 mg/kg/infusion), extinguishing lever pressing behavior within five days. This finding suggests that JT09 does not promote reward seeking behavior. When switched to cocaine (50 µg/uL/infusion), rats resumed lever pressing behavior, thus proving that the rats tested were not deficient in reward processing. In order to further assess abuse liability, a conditioned place preference model was performed, where rats would receive alternate oral doses of JT09 (20 mg/kg) and saline (0.2 mL) in their respective compartment (right or left, randomly assigned). The amount of time spent in each particular compartment was used to determine if the rats developed an association of JT09 with a particular compartment, which is a sign of addictive predilection. Results demonstrated that rats did not develop a preference for JT09 over saline, further suggesting that JT09 does not promote drug seeking behavior.
The most common cause of discontinuation of centrally- acting KOA drugs, such as U50,488, enadoline, ADL 10- 0101, and ADL 10-0116, is the promotion of dysphoria and sedation . In order to assess the induction of dysphoria, a forced swim assay was performed. Depressive effects are measured by the amount of time spent immobile during the last 4 min of each trial. Administration of JT09 (20 mg/kg, p.o.) did not promote immobility beyond that of saline, whereas salvinorin A (1 mg/kg, i.p.), a centrally-acting KOA, promoted significant immobility . This finding suggests that JT09 does not promote dysphoria. In order to assess sedation, rats were studied in locomotor boxes to assess activity levels following the administration of either saline (0.2 mL, p.o.), morphine (10 mg/kg, i.p.) or JT09 (20 mg/kg, p.o.). Results indicated that there was a significant difference in the activity level of rats that received morphine when compared to JT09; however, the activity levels were indistinguishable when comparing rats that received JT09 and saline. This supports that JT09 does not promote sedative effects due to its high peripheral selectivity for the kappa receptor over the mu receptor. JT09 was assessed in a multiple dose study, where rats were dosed at their EC50 for 14 days, sacrificed, and then assessed via histological examination. On examination, rats administered JT09 did not demonstrate any gross or microscopic changes to the sampled tissues. This suggests that JT09 does not promote any noticeable toxicity in rats at the ED50 dose level. Further toxicity studies will be performed administering JT09 at higher dose levels.
SIGNIFICANCEThere are many pharmacological and non-pharmacological treatments of chronic pain; however, very few treatment modalities have proven to demonstrate sustainable efficacy. In particular, mu-opioid receptor agonists (MOAs) provide sufficient analgesia acutely in many patients, yet suffer from untoward side effects, such as those mentioned above. Given the significant burden of current opioid and non-opioid medications used in pain management, there remains a significant need for a novel class of analgesics that lacks abuse liability and has a diminished side effect profile. Much like the well-known MOAs, kappa-opioid agonists (KOAs)
have significant analgesic properties; however, KOAs potentiate negative side effects such as sedation, hallucinations and dysphoria, thus limiting their development as a viable therapeutic. Developing a KOA with limited CNS penetration would provide analgesic coverage against chronic pain without the aforementioned negative side effects associated with the agonism of centrally located kappa opioid receptors. Pre-clinical and clinical studies show that peptide-derived, peripherally- restricted, orally active kappa opioid agonists such as JT09, CR845, and ICI 204,448 offer promising qualities and could potentially be the solution to this problem. Further, application of the JT Pharma peptide modification strategy to CR665 imparted oral bioavailability, while enhancing the potency and PK/PD properties of the parent compound. CR845, a derivative of CR665 under development by Cara Therapeutics, demonstrated 15% oral bioavailability in Phase I clinical trials following reformulation to improve oral delivery. Given our preliminary results in pre-clinical studies, we suspect that JT09 will demonstrate significantly improved oral bioavailability without the specific need for reformulation. Additionally, JT09 does not promote sedation, whereas IC 204,448 demonstrated significant depression of locomotor activity .
On average, 115 people a day die from an opioid-induced drug overdose, thus emphasizing the potential ground breaking nature of developing an orally-active non-addictive analgesic with retained efficacy . In comparison, 44 people died per day during the peak of the HIV/AIDs crisis, further outlining the significance of this public health epidemic. A possible solution to this issue is the peripherally-restricted kappa opioid agonist, JT09. The oral EC50 of JT09 in rats appears to be druggable when extrapolated to human doses, while retaining the efficacy of morphine. Further, we have established that JT09 does not promote CNS-mediated effects associated with centrally mediated KOAs or commonly used opioids such as morphine (i.e. sedation, dysphoria, tolerance, addiction, etc.). Thus, we propose that JT09 has potential for development as a novel analgesic.
A full report of this letter is in press at Advances in Pharmacology and Clinical Trials.
The authors are grateful for the contributions by Ghee SM, Bhadsavle SS and Kopfman ML, for helping conduct experiments; Woster PM and Kumarasinghe IR for synthesizing experimental compounds; and Helke KL for performing histological studies. This work was supported by NIH grants DA-036398, NS-090629 and MH-65099 to Dix TA and by a grant from SCE&G to Beck TC.
This work was supported by NIH grants DA-036398, NS- 090629 and MH-65099 to Thomas A. Dix and a grant from SCE&G to Tyler C. Beck. The authors confirm that this article content has no conflicts of interest.
- American Society of Addiction Medicine (2016) Opioid addiction 2016: Facts and figures.
- Beck TC, Reichel CM, Ghee SM, Helke KL, Bhadsavle SS, et al. (2018) Development of a peptide-derived orally-active kappa opioid agonist for peripheral pain: Preclinical results in rats. Adv Pharmacol Clin Trials.
- DeHaven-Hudkins DL, Dolle RE (2004) Peripheral restricted opioid agonists and novel analgesic agents. Curr Pharm Des 10: 743-757.
- Gaskin DJ, Richard P (2011) The economic costs of pain in the United States. Institute of Medicine (US) Committee on Advancing Pain Research, Care and Education. Appendix C.
- Goldberg D, McGee S (2011) Pain as a global health priority. BMC Public Health 11: 770.
- Hughes FM Jr, Shaner BE, Brower JO, Woods RJ, Dix TA (2013) Development of a peptide-derived orally available kappa-opioid agonist targeting peripheral pain. J Med Chem 7: 16-22.
- Kumar N (2014) Kappa opioid receptor agonists: New targets in treatment of pain. University of Wellington. Retrieved from: http://hdl.handle.net/10063/4963
- Lundquist JT, Dix TA (1998) Asymmetric synthesis of [omega]-bromo-2(S)-azido acids as precursors for the synthesis of novel amino acids. Tetrahedron Lett 39: 775-778.
- MacPherson RD (2000) The pharmacological basis of contemporary pain management. Pharmacol Ther 88: 163-185.
- Peart JN, Gross ER, Gross GJ (2004) Effect of Exogenous kappa-opioid receptor activation in rat model of myocardial infarction. J Cardiovasc Pharmacol 43: 410-415.
- Riviere PJM (2004) Peripheral kappa-opioid agonists for visceral pain. Br J Pharmacol 141: 1331-1334.
- Stein SC, Clark JD, Oh U, Vasko MR, Wilcox GL, et al. (2008) Peripheral mechanisms of pain and analgesia. Brain Res Rev 60: 90.
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