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Evaluation of anti-inflammatory activity
of selected medicinal plants used in
Indian traditional medication system in
vitro as well as in vivo
Rafik U. Shaikh, Mahesh M. Pund, Rajesh N. Gacche
Under the guidance
Of
Dr. Navneet Khurana
Submitted by:
Moh Aijaz
M.Pharm
(Pharmacology)
Submitted to:
Dr. Navneet Khurana
Head of the
Department
1
Contents
o INTRODUCTION
oMediators of inflammation
oMECHANISM OF INFLAMMATION
oDrugs commonly used in inflammation
oNSAIDs
oPharmacological effects of NSAIDs
oClinical uses of NSAIDs
oTradition Of Herbal Drug
oMaterials and methods
oSelected medicinal plants
oIn Vitro study COX
inhibition assay
oIn vivo study( Carrageenan-
induced rat paw edema assay)
oResults
oDiscussion
oAcknowledgment
oReferences
2
INTRODUCTION
 Inflammation is a normal, protective response
to tissue injury caused by physical trauma,
noxious chemicals or microbiological agents.
There are mainly two types of inflammation
which are as follows:-
Acute inflammation
Chronic inflammation
3
Acute inflammation :-
It is associated with increased vascular
permeability, capillary infiltration and emigration
of leukocytes.
Chronic inflammation:-
It is associated with infiltration of mononuclear
immune cells, macrophages, neutrophils, fibroblast
activation, proliferation (angiogenesis) and
fibrosis.
4
The traditional names for signs of
inflammation come from Latin:-
I. Dolor (pain)
II. Calor (heat)
III. Rubor (redness)
IV. Tumor (swelling)
V. Functio laesa (loss of function)
5
Mediators of inflammation
Prostaglandins
Bradykinin
Serotonin
Histamine
Interleukins-2 – 6, 10,
12,13
Platelet activating
factor
Gamma-Interferon
Tumor Necrosis Factor
Transforming Growth
Factor
Lymphotoxin
6
MECHANISM OF INFLAMMATION
7
Drugs commonly used in inflammation
NSAIDs – (nonsteroidal
anti-inflammatory drugs)
8
Nonselective COX inhibitors
1. Salicylates
*Acetylsalicylic acid (Aspirin)
* Salicylamide
2. Pyrazolone derivatives
*Phenylbutazone
*Metamizol (Analginum)
3. Indole derivatives
*Indomethacin
4. Propionic acid derivatives
*Ibuprofen
5. Anthranilic acid
derivatives
*Mephenamic acid
6. Aryl – acetic acid derivatives
*Diclophenac sodium
7. Oxicam derivatives
*Piroxicam
8. Dihydropyrrolizine
carboxylic acid derivative
*Ketorolac
Nonsteroidal anti-
inflammatory drugs (NSAIDs)
9
Selective COX inhibitors
Preferential COX-2 inhibitors
Nimesulide
Meloxicam
Nabumeton
Selective COX-2 inhibitors
Celecoxib
Parecoxib
Rofecoxib
NOTE:-
These drugs cause little gastric mucosa
damage, they do not inhibit platelet
aggregation!!!1
0
Pharmacological effects of NSAIDs
Anti-inflammatory
Analgesic
Antipyretic
Antiplatelet (Aspirin)
11
Clinical uses of NSAIDs
1. Pain: headache, toothache, myalgia,
backpain;
2. Fever;
3. Arthritises: rheumatoid arthritis,
osteoarthritis, gout, ankylosing spondylitis;
4. Dismenorrhoea (especially ibuprofen);
1
2
1
3
Tradition Of Herbal Drug
 Allopathic drugs which are single active components
that target one specific pathway
 Herbal medicines work in a way that depends on
an orchestral approach.
 Medicinal plants have been source of wide variety
of biologically active compounds.
 Popular due to toxicity and side-effects are less as
compare to allopathic medicines.
1
4
Selected medicinal plants used in Indian
traditional medication system in vitro as
well as in vivo are follows
1.Cissus quadrangularis (A-13) Veld
grape
2.Plumbago zeylanica (A-15) Chitrak
3.Terminalia bellerica (A-16) Bahera
4.Terminalia chebulla (A-17) Harad
1
5
Cissus quadrangularis Plumbago zeylanica
Terminalia bellerica Terminalia chebulla
1
6
Materials and methods
Materials
The COX-1 & 2 (human ovine) inhibitor Screening
assay kit [Catalog No. 760111]
(3- (4,5-dimethylthiazol-2-yl)
2, 5- diphenyl tetrazolium bromide)
DPPH (1, 1-diphenyl-2-picryl hydrazyl)
Phenanthroline
Phenazine methosulphate (PMS)
Nitroblue tetrazolium (NBT)
Nicotinamide Adenine Dinucleotide (NADH)
1
7
Medicinal plants
Methods for extraction of sample
The shed dried powdered plant samples (10 g)
Sequentially xtracted in
hexane, ethanol and water
upto 8 h
Extracted samples
Evaporated under
reduced pressure at room temperature
The dried extracts were preserved at 4° C in refrigerator
for further analysis
1
8
(In Vitro study)
COX inhibition assay
The assay was performed by using Colorimetric COX
(human ovine) inhibitor Screening assay kit.
Reaction mixture contains:-
150 µl of assay buffer
10 µl of heme
10 µl of enzyme (either COX-1 or COX-2)
10 µl of plant sample (1 mg/ml)
Aspirin (acetylsalicylic acid, 1mM)was used as a
standard drug
1
9
The percent COX inhibition was
calculated using following equation:-
2
0
Experimental animals
Swiss albino mice are used
Weight between 25-30 g
They were kept in rat cages and fed on standard
mice food (Amrut Feeds Ltd., Sangali (MS), India)
In vivo study
2
1
Carrageenan-induced rat paw edema assay
The Extract of selected samples were prepared in 1 % w/v gum acacia and
administered orally at a dose of 100 mg/kg and 250 mg/kg, 1 h
before carrageenan injection
Edema was induced on the right hind paw
Subplantar injection of 20 ml carrageenan (1 % w/v) in 0.9 % saline
in right hind paw
After 1 hour
2
2
A control group received vehicle only
A standard group was treated with indomethacin
(20 mg/kg, p.o.)
The volume of injected and of the contra lateral
paws was measured 1, 3,and 5 h after induction of
inflammation, using a plethysmometer
The value was expressed as the percent
reduction in volume with respect to the control
group of at different time intervals
2
3
Results
Effect of plant samples on COX inhibition
The average COX-1 & 2 inhibition was calculated by taking the
mean of COX inhibition activity in three solvent extracts
Overall it was found that:-
T. bellarica (mean activity COX-1, 61.83 % & COX-2, 73.34 %)
T. chebulla (mean activity COX-1, 52.82 % & COX-2, 74.38 %)
C. Quadrangularis (mean activity COX-1, 53.25 %
P. zeylanica (mean activity COX-2 42.86 %)
C. quadrangularis COX-1 (28.18 %), (Water extrate)
2
4
It is shown shows that the ethanol fractions
were found to be more effective COX inhibitory
agents as compared to water and hexane
extracts ( Table 1&2)
The results were compared with Aspirin (1
mM) showing COX-1 (8.54 ± 0.37 %) and COX-
2 (11.11 ± .13 %)
2
5
2
6
Profile of carrageenan induced anti-inflammatory
activity
oral administration of P. zeylanica, T. bellarica and T. chebulla
plant extracts showed promising anti-inflammatory activity by
reducing the carrageenan induced paw edema volume
carrageenan induced 69, 86, and 99 % edema formation at
1, 3 and 5 h respectively, compared with 0 h readings in
control group.
Higher dose of 250 mg/kg, T. bellarica (32.85 %) and
T.chebulla (34.28 %) showed significant decrease in edema
volume after 1 h
At the same dose of T. bellarica (22.77 %) and T. chebulla
(20.80%)
considerable reduction in the edema volume was observed
2
7
The results were compared with standard anti-inflammatory drug
such as Indomethacin (20 mg/kg) which showed effective
inhibition (51.48 %) at 5 h
2
8
Natural product, especially medicinal plants and drug
discovery has remained a very successful combination for the
inventorization of new therapeutic agents.
The main intention of the present study was to perform the COX
activity guided standardization of selected medicinal plants with
focus on antioxidant and cytotoxicity profile.
Discussion
2
9
The results of the COX inhibition studies focus the importance
of selected botanicals as an important resource for the isolation
and identification of new COX-2 selective anti-inflammatory
agents.
The medicinal plants such as T. bellarica and T. chebulla are
one of the major constituents of a popular ayurvedic formulation
‘Triphala’
‘Triphala’ strengthens and activates different tissues of the body,
prevents ageing and promotes health.
3
0
Acknowledgment
The study was supported by University Grant Commission
(UGC), New Delhi (India), F. No. 33-157/2007 (SR).
Authors are thankful to the Director, School of Life
Sciences, S.R.T.M. University,
Nanded for providing necessary laboratory facilities to
carry out present work.
3
1
References
1. Limongelli V, Bonomi M, Marinelli L, et al. Molecular basis of cyclooxygenase
enzymes (COXs) selective inhibition. Proc Nat Acad Sci. 2010;107:5411-5416.
2. Cao H, Yu R, Choi Y, et al. Discovery of cyclooxygenase inhibitors from
medicinal
plants used to treat inflammation. Pharmacol Res. 2010;61:519-524.
3. Hwang IK, Yi SS, Yoo KY, et al. Effects of treadmill exercise on
cyclooxygenase-2
in the hippocampus in type 2 diabetic rats: correlation with the neuroblasts.
Brain Res. 2010;1341:84-92.
4. Chen YJ, Quilley J. Fenofibrate treatment of diabetic rats reduces nitrosative
stress, renal cyclooxygenase-2 expression, and enhanced renal prostaglandin
release. J Pharmacol Exp Ther. 2008;324:658-663.
5. Jianhua F, Eliana L, Gregor F, et al. Cardiac remodeling hinders activation of
cyclooxygenase-2, diminishing protection by delayed pharmacological
preconditioning:
role of HIF1a and CREB. Cardiovasc Res. 2008;78:98-107.
6. Scott DL, Wolfe F, Huizinga TW. Rheumatoid arthritis. Lancet. 2010;376:
1094-1108. 7. Lubberts E. Th17 cytokines and arthritis. Semin Immunopathol.
2010;32:43-53.
8. Sabat R. IL-10 family of cytokines. Cytokine Growth Factor Rev. 2010;21:
315-324.
3
2
10. Bishop A. Role of oxygen in wound healing. J Wound Care. 2008;17:399-402.
11. Schafer FQ, Quian SY, Buettner GR. Iron and free radical oxidations in cell
membranes. Cell Mol Bio. 2000;46:657-662.
12. Wallace JL, Ferraz JG. New pharmacologic therapies in gastrointestinal
disease.
Gastroenterol Clin North Am. 2010;39:709-720.
13. Marnett LJ. The COXIB experience: a look in the rearview mirror. Annu Rev
Pharmacol Toxicol. 2009;49:265-290.
14. Inotai A, Hanko B, Meszaro A. Trends in the non-steroidal anti-inflammatory
drug market in six central-eastern european countries based on retail information.
Pharmacoepidemiol Drug Saf. 2010;19:183-190.
15. Vonkeman HE, van de Laar MA. Nonsteroidal anti-inflammatory drugs: adverse
effects and their prevention. Semin Arthritis Rheum. 2010;39:294-312.
16. Garcia Rodriguez LA, Tacconelli S, Patrignani P. Role of dose potency in the
prediction of risk of myocardial infarction associated with nonsteroidal
antiinflammatory
drugs in the general population. J Am Coll Cardiol. 2008;52:
1628-1636.
17. John LW, Linda V. NSAID-induced gastrointestinal damage and the design of
GI-sparing NSAIDs. Curr Opin Invest Drugs. 2008;9:1151-1156.
18. Laine L, Connors L, Griffin M, Curtis S, Kaur A, Cannon C. Prescription rates of
protective co-therapy for NSAID users at high GI risk and results of attempts to
improve adherence to guidelines. Aliment Pharmacol Ther. 2009;30:767-774.
3
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Anti-inflammatory activity of selected medicinal plants

  • 1. Evaluation of anti-inflammatory activity of selected medicinal plants used in Indian traditional medication system in vitro as well as in vivo Rafik U. Shaikh, Mahesh M. Pund, Rajesh N. Gacche Under the guidance Of Dr. Navneet Khurana Submitted by: Moh Aijaz M.Pharm (Pharmacology) Submitted to: Dr. Navneet Khurana Head of the Department 1
  • 2. Contents o INTRODUCTION oMediators of inflammation oMECHANISM OF INFLAMMATION oDrugs commonly used in inflammation oNSAIDs oPharmacological effects of NSAIDs oClinical uses of NSAIDs oTradition Of Herbal Drug oMaterials and methods oSelected medicinal plants oIn Vitro study COX inhibition assay oIn vivo study( Carrageenan- induced rat paw edema assay) oResults oDiscussion oAcknowledgment oReferences 2
  • 3. INTRODUCTION  Inflammation is a normal, protective response to tissue injury caused by physical trauma, noxious chemicals or microbiological agents. There are mainly two types of inflammation which are as follows:- Acute inflammation Chronic inflammation 3
  • 4. Acute inflammation :- It is associated with increased vascular permeability, capillary infiltration and emigration of leukocytes. Chronic inflammation:- It is associated with infiltration of mononuclear immune cells, macrophages, neutrophils, fibroblast activation, proliferation (angiogenesis) and fibrosis. 4
  • 5. The traditional names for signs of inflammation come from Latin:- I. Dolor (pain) II. Calor (heat) III. Rubor (redness) IV. Tumor (swelling) V. Functio laesa (loss of function) 5
  • 6. Mediators of inflammation Prostaglandins Bradykinin Serotonin Histamine Interleukins-2 – 6, 10, 12,13 Platelet activating factor Gamma-Interferon Tumor Necrosis Factor Transforming Growth Factor Lymphotoxin 6
  • 8. Drugs commonly used in inflammation NSAIDs – (nonsteroidal anti-inflammatory drugs) 8
  • 9. Nonselective COX inhibitors 1. Salicylates *Acetylsalicylic acid (Aspirin) * Salicylamide 2. Pyrazolone derivatives *Phenylbutazone *Metamizol (Analginum) 3. Indole derivatives *Indomethacin 4. Propionic acid derivatives *Ibuprofen 5. Anthranilic acid derivatives *Mephenamic acid 6. Aryl – acetic acid derivatives *Diclophenac sodium 7. Oxicam derivatives *Piroxicam 8. Dihydropyrrolizine carboxylic acid derivative *Ketorolac Nonsteroidal anti- inflammatory drugs (NSAIDs) 9
  • 10. Selective COX inhibitors Preferential COX-2 inhibitors Nimesulide Meloxicam Nabumeton Selective COX-2 inhibitors Celecoxib Parecoxib Rofecoxib NOTE:- These drugs cause little gastric mucosa damage, they do not inhibit platelet aggregation!!!1 0
  • 11. Pharmacological effects of NSAIDs Anti-inflammatory Analgesic Antipyretic Antiplatelet (Aspirin) 11
  • 12. Clinical uses of NSAIDs 1. Pain: headache, toothache, myalgia, backpain; 2. Fever; 3. Arthritises: rheumatoid arthritis, osteoarthritis, gout, ankylosing spondylitis; 4. Dismenorrhoea (especially ibuprofen); 1 2
  • 13. 1 3
  • 14. Tradition Of Herbal Drug  Allopathic drugs which are single active components that target one specific pathway  Herbal medicines work in a way that depends on an orchestral approach.  Medicinal plants have been source of wide variety of biologically active compounds.  Popular due to toxicity and side-effects are less as compare to allopathic medicines. 1 4
  • 15. Selected medicinal plants used in Indian traditional medication system in vitro as well as in vivo are follows 1.Cissus quadrangularis (A-13) Veld grape 2.Plumbago zeylanica (A-15) Chitrak 3.Terminalia bellerica (A-16) Bahera 4.Terminalia chebulla (A-17) Harad 1 5
  • 16. Cissus quadrangularis Plumbago zeylanica Terminalia bellerica Terminalia chebulla 1 6
  • 17. Materials and methods Materials The COX-1 & 2 (human ovine) inhibitor Screening assay kit [Catalog No. 760111] (3- (4,5-dimethylthiazol-2-yl) 2, 5- diphenyl tetrazolium bromide) DPPH (1, 1-diphenyl-2-picryl hydrazyl) Phenanthroline Phenazine methosulphate (PMS) Nitroblue tetrazolium (NBT) Nicotinamide Adenine Dinucleotide (NADH) 1 7 Medicinal plants
  • 18. Methods for extraction of sample The shed dried powdered plant samples (10 g) Sequentially xtracted in hexane, ethanol and water upto 8 h Extracted samples Evaporated under reduced pressure at room temperature The dried extracts were preserved at 4° C in refrigerator for further analysis 1 8
  • 19. (In Vitro study) COX inhibition assay The assay was performed by using Colorimetric COX (human ovine) inhibitor Screening assay kit. Reaction mixture contains:- 150 µl of assay buffer 10 µl of heme 10 µl of enzyme (either COX-1 or COX-2) 10 µl of plant sample (1 mg/ml) Aspirin (acetylsalicylic acid, 1mM)was used as a standard drug 1 9
  • 20. The percent COX inhibition was calculated using following equation:- 2 0
  • 21. Experimental animals Swiss albino mice are used Weight between 25-30 g They were kept in rat cages and fed on standard mice food (Amrut Feeds Ltd., Sangali (MS), India) In vivo study 2 1
  • 22. Carrageenan-induced rat paw edema assay The Extract of selected samples were prepared in 1 % w/v gum acacia and administered orally at a dose of 100 mg/kg and 250 mg/kg, 1 h before carrageenan injection Edema was induced on the right hind paw Subplantar injection of 20 ml carrageenan (1 % w/v) in 0.9 % saline in right hind paw After 1 hour 2 2
  • 23. A control group received vehicle only A standard group was treated with indomethacin (20 mg/kg, p.o.) The volume of injected and of the contra lateral paws was measured 1, 3,and 5 h after induction of inflammation, using a plethysmometer The value was expressed as the percent reduction in volume with respect to the control group of at different time intervals 2 3
  • 24. Results Effect of plant samples on COX inhibition The average COX-1 & 2 inhibition was calculated by taking the mean of COX inhibition activity in three solvent extracts Overall it was found that:- T. bellarica (mean activity COX-1, 61.83 % & COX-2, 73.34 %) T. chebulla (mean activity COX-1, 52.82 % & COX-2, 74.38 %) C. Quadrangularis (mean activity COX-1, 53.25 % P. zeylanica (mean activity COX-2 42.86 %) C. quadrangularis COX-1 (28.18 %), (Water extrate) 2 4
  • 25. It is shown shows that the ethanol fractions were found to be more effective COX inhibitory agents as compared to water and hexane extracts ( Table 1&2) The results were compared with Aspirin (1 mM) showing COX-1 (8.54 ± 0.37 %) and COX- 2 (11.11 ± .13 %) 2 5
  • 26. 2 6
  • 27. Profile of carrageenan induced anti-inflammatory activity oral administration of P. zeylanica, T. bellarica and T. chebulla plant extracts showed promising anti-inflammatory activity by reducing the carrageenan induced paw edema volume carrageenan induced 69, 86, and 99 % edema formation at 1, 3 and 5 h respectively, compared with 0 h readings in control group. Higher dose of 250 mg/kg, T. bellarica (32.85 %) and T.chebulla (34.28 %) showed significant decrease in edema volume after 1 h At the same dose of T. bellarica (22.77 %) and T. chebulla (20.80%) considerable reduction in the edema volume was observed 2 7
  • 28. The results were compared with standard anti-inflammatory drug such as Indomethacin (20 mg/kg) which showed effective inhibition (51.48 %) at 5 h 2 8
  • 29. Natural product, especially medicinal plants and drug discovery has remained a very successful combination for the inventorization of new therapeutic agents. The main intention of the present study was to perform the COX activity guided standardization of selected medicinal plants with focus on antioxidant and cytotoxicity profile. Discussion 2 9 The results of the COX inhibition studies focus the importance of selected botanicals as an important resource for the isolation and identification of new COX-2 selective anti-inflammatory agents.
  • 30. The medicinal plants such as T. bellarica and T. chebulla are one of the major constituents of a popular ayurvedic formulation ‘Triphala’ ‘Triphala’ strengthens and activates different tissues of the body, prevents ageing and promotes health. 3 0
  • 31. Acknowledgment The study was supported by University Grant Commission (UGC), New Delhi (India), F. No. 33-157/2007 (SR). Authors are thankful to the Director, School of Life Sciences, S.R.T.M. University, Nanded for providing necessary laboratory facilities to carry out present work. 3 1
  • 32. References 1. Limongelli V, Bonomi M, Marinelli L, et al. Molecular basis of cyclooxygenase enzymes (COXs) selective inhibition. Proc Nat Acad Sci. 2010;107:5411-5416. 2. Cao H, Yu R, Choi Y, et al. Discovery of cyclooxygenase inhibitors from medicinal plants used to treat inflammation. Pharmacol Res. 2010;61:519-524. 3. Hwang IK, Yi SS, Yoo KY, et al. Effects of treadmill exercise on cyclooxygenase-2 in the hippocampus in type 2 diabetic rats: correlation with the neuroblasts. Brain Res. 2010;1341:84-92. 4. Chen YJ, Quilley J. Fenofibrate treatment of diabetic rats reduces nitrosative stress, renal cyclooxygenase-2 expression, and enhanced renal prostaglandin release. J Pharmacol Exp Ther. 2008;324:658-663. 5. Jianhua F, Eliana L, Gregor F, et al. Cardiac remodeling hinders activation of cyclooxygenase-2, diminishing protection by delayed pharmacological preconditioning: role of HIF1a and CREB. Cardiovasc Res. 2008;78:98-107. 6. Scott DL, Wolfe F, Huizinga TW. Rheumatoid arthritis. Lancet. 2010;376: 1094-1108. 7. Lubberts E. Th17 cytokines and arthritis. Semin Immunopathol. 2010;32:43-53. 8. Sabat R. IL-10 family of cytokines. Cytokine Growth Factor Rev. 2010;21: 315-324. 3 2
  • 33. 10. Bishop A. Role of oxygen in wound healing. J Wound Care. 2008;17:399-402. 11. Schafer FQ, Quian SY, Buettner GR. Iron and free radical oxidations in cell membranes. Cell Mol Bio. 2000;46:657-662. 12. Wallace JL, Ferraz JG. New pharmacologic therapies in gastrointestinal disease. Gastroenterol Clin North Am. 2010;39:709-720. 13. Marnett LJ. The COXIB experience: a look in the rearview mirror. Annu Rev Pharmacol Toxicol. 2009;49:265-290. 14. Inotai A, Hanko B, Meszaro A. Trends in the non-steroidal anti-inflammatory drug market in six central-eastern european countries based on retail information. Pharmacoepidemiol Drug Saf. 2010;19:183-190. 15. Vonkeman HE, van de Laar MA. Nonsteroidal anti-inflammatory drugs: adverse effects and their prevention. Semin Arthritis Rheum. 2010;39:294-312. 16. Garcia Rodriguez LA, Tacconelli S, Patrignani P. Role of dose potency in the prediction of risk of myocardial infarction associated with nonsteroidal antiinflammatory drugs in the general population. J Am Coll Cardiol. 2008;52: 1628-1636. 17. John LW, Linda V. NSAID-induced gastrointestinal damage and the design of GI-sparing NSAIDs. Curr Opin Invest Drugs. 2008;9:1151-1156. 18. Laine L, Connors L, Griffin M, Curtis S, Kaur A, Cannon C. Prescription rates of protective co-therapy for NSAID users at high GI risk and results of attempts to improve adherence to guidelines. Aliment Pharmacol Ther. 2009;30:767-774. 3 3