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Brilaroxazine lipogel displays antipsoriatic activity in imiquimod-induced mouse model.
- Source :
-
Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) [Skin Res Technol] 2024 Feb; Vol. 30 (2), pp. e13606. - Publication Year :
- 2024
-
Abstract
- Background: Dopamine (D) and serotonin (5-HT) pathways contribute to psoriasis pathobiology. Disruptions incite increased inflammatory mediators, keratinocyte activation and deterioration, and worsening symptoms. Brilaroxazine (RP5063), which displays potent high binding affinity to D <subscript>2/3/4</subscript> and 5-HT <subscript>1A/2A/2B/7</subscript> receptors and a moderate affinity to serotonin transporter (SERT), may affect the underlying psoriasis pathology.<br />Methods: An imiquimod-induced psoriatic mouse model (BALB/c) evaluated brilaroxazine's activity in a topical liposomal-aqueous gel (Lipogel) formulation. Two of the three groups (n = 6 per) underwent induction with 5% imiquimod, and one group received topical brilaroxazine Lipogel (Days 1-11). Assessments included (1) Psoriasis Area and Severity Index (PASI) scores (Days 1-12), skin histology for Baker score based on H&E stained tissue (Day 12), and serum blood collection for serum cytokine analysis (Day 12). One-way ANOVA followed by post hoc Dunnett's t-test evaluated significance (p < 0.05).<br />Results: Imiquimod-induced animal Baker scores were higher versus Sham non-induced control's results (p < 0.001). Brilaroxazine Lipogel had significantly (p = 0.003) lower Baker scores versus the induced Psoriasis group. Brilaroxazine PASI scores were lower (p = 0.03) versus the induced Psoriasis group (Days 3-12), with the greatest effect in the last 3 days. The induced Psoriasis group showed higher Ki-67 and TGF-β levels versus non-induced Sham controls (p = 0.001). The brilaroxazine Lipogel group displayed lower levels of these cytokines versus the induced Psoriasis group, Ki-67 (p = 0.001) and TGF-β (p = 0.008), and no difference in TNF-α levels versus Sham non-induced controls.<br />Conclusion: Brilaroxazine Lipogel displayed significant activity in imiquimod-induced psoriatic animals, offering a novel therapeutic strategy.<br /> (© 2024 Reviva Pharmaceuticals Inc. Skin Research and Technology published by John Wiley & Sons Ltd.)
- Subjects :
- Animals
Mice
Imiquimod adverse effects
Ki-67 Antigen metabolism
Serotonin metabolism
Serotonin pharmacology
Serotonin therapeutic use
Skin pathology
Cytokines metabolism
Cytokines pharmacology
Cytokines therapeutic use
Transforming Growth Factor beta metabolism
Transforming Growth Factor beta pharmacology
Transforming Growth Factor beta therapeutic use
Disease Models, Animal
Psoriasis chemically induced
Psoriasis drug therapy
Dermatologic Agents pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1600-0846
- Volume :
- 30
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI)
- Publication Type :
- Academic Journal
- Accession number :
- 38363081
- Full Text :
- https://doi.org/10.1111/srt.13606