Diosmin nanocrystal gel alleviates imiquimod-induced psoriasis in rats via modulating TLR7,8/NF-κB/micro RNA-31, AKT/mTOR/P70S6K milieu, and Tregs/Th17 balance

Inflammopharmacology. 2023 Jun;31(3):1341-1359. doi: 10.1007/s10787-023-01198-w. Epub 2023 Apr 3.

Abstract

Diosmin is a flavonoid with promising anti-inflammatory and antioxidant properties. However, it has difficult physicochemical characteristics since its solubility demands a pH level of 12, which has an impact on the drug's bioavailability. The aim of this work is the development and characterization of diosmin nanocrystals using anti-solvent precipitation technique to be used for topical treatment of psoriasis. Results revealed that diosmin nanocrystals stabilized with hydroxypropyl methylcellulose (HPMC E15) in ratio (diosmin:polymer; 1:1) reached the desired particle size (276.9 ± 16.49 nm); provided promising colloidal properties and possessed high drug release profile. Additionally, in-vivo assessment was carried out to evaluate and compare the activities of diosmin nanocrystal gel using three different doses and diosmin powder gel in alleviating imiquimod-induced psoriasis in rats and investigating their possible anti-inflammatory mechanisms. Herein, 125 mg of 5% imiquimod cream (IMQ) was applied topically for 5 consecutive days on the shaved backs of rats to induce psoriasis. Diosmin nanocrystal gel especially in the highest dose used offered the best anti-inflammatory effect. This was confirmed by causing the most statistically significant reduction in the psoriasis area severity index (PASI) score and the serum inflammatory cytokines levels. Furthermore, it was capable of maintaining the balance between T helper (Th17) and T regulatory (Treg) cells. Moreover, it tackled TLR7/8/NF-κB, miRNA-31, AKT/mTOR/P70S6K and elevated the TNFAIP3/A20 (a negative regulator of NF-κB) expression in psoriatic skin tissues. This highlights the role of diosmin nanocrystal gel in tackling imiquimod-induced psoriasis in rats, and thus it could be a novel promising therapy for psoriasis.

Keywords: AKT/mTOR/P70S6K trajectory; Diosmin nanocrystal gel; Imiquimod-induced psoriasis; TLR7/8/NF-KB/miR-31 trajectory; Th17/Treg balance.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / therapeutic use
  • Diosmin* / adverse effects
  • Disease Models, Animal
  • Imiquimod / adverse effects
  • Mice
  • Mice, Inbred BALB C
  • MicroRNAs*
  • NF-kappa B / metabolism
  • Nanoparticles*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Psoriasis* / chemically induced
  • Psoriasis* / drug therapy
  • Rats
  • Ribosomal Protein S6 Kinases, 70-kDa / metabolism
  • Ribosomal Protein S6 Kinases, 70-kDa / pharmacology
  • Ribosomal Protein S6 Kinases, 70-kDa / therapeutic use
  • Signal Transduction
  • Skin
  • TOR Serine-Threonine Kinases / metabolism
  • Toll-Like Receptor 7 / metabolism
  • Toll-Like Receptor 7 / therapeutic use

Substances

  • NF-kappa B
  • Imiquimod
  • Proto-Oncogene Proteins c-akt
  • Toll-Like Receptor 7
  • Diosmin
  • Ribosomal Protein S6 Kinases, 70-kDa
  • TOR Serine-Threonine Kinases
  • Anti-Inflammatory Agents
  • MicroRNAs
  • mTOR protein, rat
  • TLR7 protein, rat