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Saturday, April 9, 2022

EVALUATION OF ANTI-PSORIASIS ACTIVITY OF TEST FORMULATION(S) USING 12-O-TETRADECANOYLPHORBOL-13-ACETATE (TPA) PSORIASIS IN EXPERIMENTAL ANIMALS

                                                                
                                                                    STUDY PROTOCOL

EVALUATION OF ANTI-PSORIASIS ACTIVITY OF TEST FORMULATION(S) USING 12-O-TETRADECANOYLPHORBOL-13-ACETATE (TPA) PSORIASIS IN EXPERIMENTAL ANIMALS

1.0 INTRODUCTION

Psoriasis is a common skin disorder characterized by the focal formation of inflamed, raised plaques that shed scales from excessive growth of epithelial cells and involve, hyperplasia of epidermal keratinocytes, ectasia, infiltration of T lymphocytes, neutrophils, and other types of leukocytes in the affected skin. Vascular endothelial growth factor (VEGF) is a crucial factor that mediates the angiogenesis of blood vessels and is highly expressed in the skin lesions of psoriasis. VEGF induces microvascular alterations in the dermal papillae, which facilitates the development and persistence of psoriatic lesions.




2.0 TEST SYSTEM DETAILS:

Species : Mus musculus (Mouse)

Strain : Swiss albino or C57bl/6 or Balb/c

Age : 6-10 weeks

Body Wight : 20-25 g

Sex : Male or Female

No. of animals : 8 /Group

Total animals : 56 + 6 extra = 62

3.0 ALLOCATION OF GROUPS:

Group No.

Group Description

Disease Induction agent administered

Treatment administered

Dose Volume and Route

G1

Normal Control

None

0.5% MC, p.o., q.d

10 mL/kg, p.o.

G1

Disease Control

 

 

20 μL of TPA

solution (2.5 μg/ear of TPA dissolved in acetone) on the right pinna and 20 µL of acetone on the left pinna (This will serve as the vehicle control)

 

 

 

 

 

 

0.5% MC, p.o., q.d.+ Acetone on right pinna

Oral: 10 mL/kg

Topical application (acetone) : 20 µL

G3

Reference Control

0.5% MC, p.o. bid +  Dexamethasone - 0.2 mg (dissolved in acetone) on right ear, q.d.

Oral: 5 mL/kg

Topical application: 20 µL

G4

Treated orally with low dose of Test Formulation-1 + Topically with Oil formulation of  Test Formulation-1x

Test Formulation-1-X1 mg/kg, q.d.  in 0.5% MC  + 20 µL of  Test Formulation-1x oil on right ear, q.d.

Oral: 10 mL/kg

Topical application (Oil) : 20 µL

G5

Treated orally with intermediate dose 1 of  Test Formulation-1 +  Topically with Oil formulation of  Test Formulation-1x

Test Formulation-1 -X2 mg/kg,    q.d. in 0.5% MC + 20 µL of  Test Formulation-1x oil  on right ear,  q.d.

G6

Treated orally with  of  Test Formulation-2 +  Topically with Oil formulation of  Test Formulation-2x

Test Formulation-2 -Y1 mg/kg,   q.d. in 0.5% MC + 20 µL of  Test Formulation-2x oil  on right ear,  q.d.

G7

Treated orally with high dose of  Test Formulation-2 +  Topically with Oil formulation of  Test Formulation-2x

Test Formulation-2 -Y2 mg/kg,  q.d. in 0.5% MC + 20 µL of  Test Formulation-2x oil  on right ear,  q.d.

















Abbreviations: MC-Methyl Cellulose, p.o.-per os. q.d..: quaque die. X1, X2 and Y1, Y2 are defined as the incremental doses of the Test formulations. The dose range will be from 10 mg/kg to 1000 mg/kg, q.d. 

      

4.0 METHOD:

· Healthy animals will be selected, randomized based on body weight and divided into 7 different groups consisting of 8 animals each.

· Treatment will be given as follows:

· Group G1 will serve as normal control and treated with 0.5% MC, p.o., q.d.

· Group G2 will serve as disease control and treated with 0.5% MC, p.o., q.d., and acetone (20 µL) on the right ear.

· Animals of group G3 will be treated with dexamethasone, which will be solubilized in acetone and will be topically applied at the dose of 0.2 mg in a total volume of 20 µL on the right pinna. They will additionally receive 0.5 % MC, p.o., q.d.

· Mice of Group G4 to G5 will be treated with TF-1 at dose levels ranging from 10 to 1000 mg/kg, p.o. q.d. They will be additionally administered the oil formulation of TF-1x , topically in a total volume of 20 µL.

· Animals allocated to groups G6 to G7 will be treated with TF-2 at dose levels ranging from 10 to 1000 mg/kg, p.o. q.d. They will be additionally administered the oil formulation of TF-2x, topically in a total volume of 20 µL.

· For the induction of disease 20 µL of TPA solution prepared in acetone will be applied topically on the right ear of the animal at the concentration of 2.5 mg/ear every alternate day till the 10th day by using a micropipette. Acetone will be applied topically on the left ear of the animal, which will serve as the vehicle control.

· Ear thickness will be measured every day using a digital Vernier caliper

· Animals will receive the treatments for ten consecutive days.

· At the end of the experiment (i.e. on day 10), mice will be killed by an overdose of thiopentone, 6 hours after the last drug treatment, and punch biopsies will be taken from the pinnae and weighed in order to measure edema.

· Punch biopsies will be then fixed in formalin for histopathological analysis.

· Alternatively, biopsies will be frozen in liquid N2 and homogenized. Cytokines in skin homogenates were measured by ELISA according to the manufacturer’s specifications, and eicosanoids and MPO.


5.0 ENDPOINT PARAMETER(S):

· Ear Thickness

· Ear Biopsy weight

· MPO activity in ear tissue

· Cytokines in the ear homogenates: IFN-γ, IL-6, IL-1β, IL-17A, IL-17C, IL-17 E, IL-22, TNF-α.

· Gene Expression in ear homogenates: Expression of IFN-γ, IL-1, IL-4, IL-6, IL-22, IL-23, MCP-1,     GM-CSF, KRT-17. 

· Histopathology of skin tissue



6.0 REFERENCE(S):

6.1 Rosa M. Andre´s, M. Carmen Montesinos, Pedro Navalo´n, Miguel Paya´ and M. Carmen Terencio. NF-kB and STAT3 Inhibition as a Therapeutic Strategy in Psoriasis: In Vitro and In Vivo Effects of BTH. Journal of Investigative Dermatology. Volume 133, Issue 10, October 2013, Pages 2362-2371.

6.2 Mikiro Takaishia , Masayuki Ishizakib , Keisuke Suzukic , Takashi Isobeb , Takaichi Shimozatob , Shigetoshi Sanoa. Oral administration of a novel RORgt antagonist attenuates psoriasis-like skin lesions of two independent mouse models through the neutralization of IL-17. Journal of Dermatological Science 85 (2017) 12–19.

6.3 Marie Madsen, Peter Riis Hansen, Lars Bo Nielsen, Karsten Hartvigsen, Anders Elm Pedersen, Jan Pravsgaard Christensen4 , Annemarie Aarup1 and Tanja Xenia Pedersen. Effect of 12-O-tetradecanoylphorbol-13- acetate-induced psoriasis-like skin lesions on systemic inflammation and atherosclerosis in hypercholesterolaemic apolipoprotein E deficient mice. BMC Dermatology (2016) 16:9 DOI 10.1186/s12895-016-0046-1

6.4 Leslie van der Fits, Sabine Mourits, Jane S. A. Voerman, Marius Kant, Louis Boon, Jon D. Laman, Ferry Cornelissen, Anne-Marie Mus, Edwin Florencia, Errol P. Prens and Erik Lubberts. Imiquimod-Induced Psoriasis-Like Skin Inflammation in Mice Is Mediated via the IL-23/IL-17 Axis. J Immunol 2009; 182:5836-5845; doi: 10.4049/jimmunol.0802999. doi: 10.4049/jimmunol.0802999.

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