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FREE PAPER PRESENTATION - Spironolactone Rx after onset of collagen induced arthritis - Dr...
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Treatment with spironolactone after the onset of collagen induced arthritis reduces joint inflammation,
cartilage destruction and bone erosion
Inderjeet VermaDoctoral Research Fellow
Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala, India &
Healing Touch City Clinic, Chandigarh
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Disclosures…
This study was supported by University Grant
Commission (UGC), New Delhi, F.No. 10-15/2007
(SA-1)
No other relevant financial involvement with any other
organization or entity with a financial interest in or financial
conflict with the subject matter or materials discussed in the
presentation apart from those disclosed.
No assistance was utilized in the production of this presentation
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AcknowledgementsDr. Javed N Agrewala
Chief Scientist, Department of Immunology,
IMTECH, Chandigarh, India.
Dr. Asif Baliyan
Junior Resident, Department of Pathology,
GMCH, Chandigarh, India.
Dr. B.N. Datta
Former Professor, Department of Pathology,
PGIMER, Chandigarh, India
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Study Background….. Synthetic DMARDs though effective but
do not produce relief in all Rheumatoid
Arthritis patients.
A number of patients have contraindications
or remain unrelieved from disease activity
& cardiovascular morbidity from these
drug. Biologic DMARDs is efficacious but has limitations.
Given the anti-inflammatory and TNF inhibiting potential of
spironolactone was first reported as 1961.1
Rev Can Biol 1961;20:82932
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Study Objective….
To evaluate the therapeutic effect
of spironolactone (SPIR) in
collagen-induced arthritis model in
mice.
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Materials and MethodsCollagen Induced Arthritis (CIA)
Male DBA/1 mice, 7–10 weeks of age
Immunized intradermal at the base of the tail with bovine collagen (CII) + CFA (4mg/ml)A booster inj. of CII + FIA was injected on day 21st. 2
IAEC No- 107/99/CPCSEA
Nat Protoc.2007; 2:1269–75.
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Experimental Groups
Group I : Normal Control Group II : Arthritic Control/Group III : SPIR 20 (mg/kg/day)Group IV : SPIR 40 (mg/kg/day)Group V : SPIR 80 (mg/kg/day)Group VI : MTX (5 mg/kg/week)Group VII : CMC ControlGroup VIII : PBS Control
Forty-eight DBA/1 mice were randomly divided into eight groups each comprising six animals.
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Outcome Parameters:
Materials and Methods
Arthritis score and paw thickness
Cytokine measurement (TNF-α & IL-6)
Oxidative markers (TBARS3 & NO4)
Histological analysis
3Anal Biochem. 1979;95: 351-358.4 Analytical Biochemsitry . 2002; 306: 79-82
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21 24 27 30 33 36 39 410
1
2
3
4
5
6
7
8
NC
PC
MTX
SPIR 20
SPIR 40
SPIR 80
Art
hriti
s sc
ore
Day after CII immunization
Results
Results were expressed in Means SEM.Error bar have been omitted for clarity of figure. NC; normal control, PC; positive/arthritis control, MTX; methotrexate control, SPIR; spironolactone (20/40/80 mg/kg/day).
Arthritis scores of CIA mice in different study groups
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Values are given as mean ± SEM (n=6), **p ≤ 0.01 and ***p ≤ 0.001 vs. arthritis control). Statistical analysis: One way ANOVA followed by a followed by post hoc analysis. It represents the paw thickness of normal and CIA mice after treatment.
Paw thickness of normal and CIA mice after treatment
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Effect of drugs on serum cytokines (TNF-α and IL-6)
All the values are the mean and SEM. *p <0.05, **p 6 0.01 compared with positive control group.Reduction of TNF-α and IL-6 level in CIA mice by SPIR and MTX treatment.
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Effect of SPIR on the levels of oxidative markers
Values are given as mean ± SEM (n=6). *p < 0.05, **p ≤ 0.01.CIA mice were treated with SPIR 20, 40 and 80 mg/kg/day and MTX 5mg/kg/week for 3 weeks. SPIR 40 and 80 mg/kg/day produced significant effect on TBARS and NO level. MTX does not have shown any significant change in TBARS. But MTX significantly reduced NO level (p <0.05).
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Histopathological images of the ankle joint of DBA1 mice
A; Normal control group: normal bone, cartilage and joint tissue. B; Arthritis control group: infiltration of inflammatory cells, erosive bone and cartilage destruction. C; Methotrexate treated group: no infiltration of inflammatory cells with minimal cartilage destruction and inflammation. D; Spironolactone 20 treated group: erosive bone and cartilage destruction showing marked infiltration of inflammatory cells in synovial tissue. E; Spironolactone 40 treated group: moderate erosive bone and cartilage destruction with moderate infiltration of inflammatory cells in synovial tissue. F; Spironolactone 80 treated group: mild infiltration of inflammatory cells in the synovial tissue. There is no bone and cartilage destruction.
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The Present study concluded that SPIR (40 ,80 mg/kg) significantly reduced the paw swelling and arthritis severity indicated by improvement in arthritis score
Improvement in antioxidant status was evident by decreased level of TBARS and NO in mice treated with SPIR (40 ,80 mg/kg) when compared with arthritis control.
Significantly decreased inflammatory cytokines TNFα and IL-6 and histopathological analysis revealed that treatment with SPIR (40 ,80 mg/kg) led to restoration of joint architecture.
Results of current study highlights that SPIR possess anti-inflammatory and immunomodulatory effect that is extremely similar to MTX, suggesting that SPIR may be a potential alternative DMARD for the treatment of human arthritis.
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Tidal wave of data: challenge and opportunity…..
THANK YOU
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