Abstract

Votucalis is a biologically active protein in tick (R. appendiculatus) saliva, which specifically binds histamine with high affinity and, therefore, has the potential to inhibit the host’s immunological responses at the feeding site. We hypothesized that scavenging of peripherally released endogenous histamine by Votucalis results in both anti-itch and anti-nociceptive effects. To test this hypothesis, adult male mice were subjected to histaminergic itch, as well as peripheral nerve injury that resulted in neuropathic pain. Thus, we selected models where peripherally released histamine was shown to be a key regulator. In these models, the animals received systemic (intraperitoneal, i.p.) or peripheral transdermal (subcutaneous, s.c. or intraplantar, i.pl.) administrations of Votucalis and itch behavior, as well as mechanical and thermal hypersensitivity, were evaluated. Selective histamine receptor antagonists were used to determine the involvement of histamine receptors in the effects produced by Votucalis. We also used the spontaneous object recognition test to confirm the centrally sparing properties of Votucalis. Our main finding shows that in histamine-dependent itch and neuropathic pain models peripheral (s.c. or i.pl.) administration of Votucalis displayed a longer duration of action for a lower dose range, when compared with Votucalis systemic (i.p.) effects. Stronger anti-itch effect was observed after co-administration of Votucalis (s.c.) and antagonists that inhibited peripheral histamine H1 and H2 receptors as well as central histamine H4 receptors indicating the importance of these histamine receptors in itch. In neuropathic mice, Votucalis produced a potent and complete anti-nociceptive effect on mechanical hypersensitivity, while thermal (heat) hypersensitivity was largely unaffected. Overall, our findings further emphasize the key role for histamine in the regulation of histaminergic itch and chronic neuropathic pain. Given the effectiveness of Votucalis after peripheral transdermal administration, with a lack of central effects, we provide here the first evidence that scavenging of peripherally released histamine by Votucalis may represent a novel therapeutically effective and safe long-term strategy for the management of these refractory health conditions.

Highlights

  • Histamine [2-(4-imidazolyl)-ethylamine], that can be found in almost all tissues of the mammalian body (Haas et al, 2008), is synthesised and stored primarily in cytosolic granules of the peripheral and central tissues, mast cells, basophils, eosinophils, platelets, basophiles, histaminergic neurons and enterochromaffin cells (Benly, 2015; Branco et al, 2018)

  • Dose-dependent significant inhibition of itch behaviour resulting from systemic (i.p.) treatment with Votucalis was only observed in histamine-dependent itch induced by compound 48/80 (Figure 1A; drug effect: F(5,339) = 6.4, p < 0.0001)

  • We demonstrated that Votucalis, a novel CNS-sparing and high-affinity recombinant histamine binding protein, produced both anti-pruritic and anti-nociceptive effects in mouse models of acute itch and chronic neuropathic pain following both systemic and peripheral administration, which represent commonly used routes of drug applications in clinical practice

Read more

Summary

Introduction

Histamine [2-(4-imidazolyl)-ethylamine], that can be found in almost all tissues of the mammalian body (Haas et al, 2008), is synthesised and stored primarily in cytosolic granules of the peripheral and central tissues, mast cells, basophils, eosinophils, platelets, basophiles, histaminergic neurons and enterochromaffin cells (Benly, 2015; Branco et al, 2018). Given its wide distribution in multiple cell types, histamine has been shown to regulate many physiologic and pathologic conditions, including pruritus/itch (Baron et al, 2001) and chronic pain (Obara et al, 2020). Histamine produces these regulatory effects via four G protein-coupled histamine receptors: H1, H2, H3 and H4 receptors that are expressed in both the central and peripheral nervous system (CNS and PNS, respectively) (Lindskog, 2017). Histamine as well as histamine receptors have long been attractive targets for therapeutic interventions in conditions where itch and pain are symptoms requiring treatment (O’Donoghue and Tharp, 2005; Obara et al, 2020). The therapeutic potential of histamine modulation still requires clarification

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call