Background and Objectives: Platanus orientalis also called Oriental plane or Chinar or Boonyi (Platanaceae) is a large, deciduous tree, known for its longevity and spreading crown. The present work describes determination of antioxidant, anti-inflammatory and total phenol content of Platanus orientalis. Materials and Methods: Different extracts of the plant such as stem, root and leaves were prepared in different solvents such as chloroform, methanol and water. Results: Total phenol content in this plant reveal that methanol extract of Platanus orientalis root showed maximum free radical scavenging activity followed by methanol wood extract. Antioxidant activity of the plant extracts in this study reveal that it is methanol and chloroform extracts which showed above 50% inhibition in contrast to aqueous extracts. Anti-inflammatory activity of Platanus orientalis showed that aqueous wood extract of Platanus orientalis showed maximum activity in contrast to other extracts. With the help of acute toxicity test it was found that all the extracts are nontoxic at 2 g kg 1 b.wt. to Wistar rats. Conclusion: These finding provides some biological value of different extracts of Platanus orientalis for the use as antioxidant and anti-inflammatory agents. However, further investigation on isolation and purification of the bio-active molecules is needed to explore the exact mechanism of action of the Platanus orientalis extracts.
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From ancient times, traditional system of medicine is being used for the treatment of various diseases. To maintain a good health, this system of medicine is being widely used in most developing countries1. These plants possess active compounds that owe them their medicinal value. The active compounds produce various physiological actions in human and animal body2.
The preliminary screening of extracts through Standard Operating Procedures (SOPs) is a must before leading to deepened phytochemical investigation. So this investigation is on those lines to illustrate the pharmacological evaluation of Oriental plane (Platanus orientalis). Platanus orientalis (Plantanaceae) is a native of Eastern Mediterranean region of world. It is commonly cultivated and highly valued as an ornamental tree in Kashmir3. This is a part of study, in accordance with Quality by design approach of medicinal and aromatic plants (MAPs) of Western Himalayas undertaken by our centre.
Platanus is a unique living member of Platanaceae family. It is a small genus of trees that is known in English as plane trees. The principal use of plane trees are as ornamental trees, especially by roadsides and parks4, 5. The plane trees are widely planted to improve the microclimate6. The plane leaves commonly known in Iran as "Barge chenar", have been used in concentrated aromatic liquids, herbal remedies and Iranian traditional medicine to treat several disorders. They are used in Iranian folk and traditional medicines for treating some dermatological, gastrointestinal, rheumatic and inflammatory diseases7-9. Some Persian scientists and hakims such as Avicenna and Hakim Momen were also familiar with this tree and mentioned its medicinal uses like teeth pain killer and analgesic and antiinflammtory effects for knee pain and inflammation in their books7,8. The plane leaves contain flavonoids, pentacyclic triterpenoids, tannins and caffeic acid9-13. Many pharmacological activities such as cytotoxic, cytostatic, astringent, antimicrobial and antiseptic effects have been attributed to the Platanus species. Platanus orientalis is the major species of Platanus in Iran and is widely distributed in northern and central parts of the country13,14,15.
MATERIALS AND METHODS
Collection of plant material and preparation of the extracts: The plant viz. Platanus orientalis collected from Shopian region of Kashmir in the month of May-July, 2007 and identified by Centre of Plant Taxonomy (COPT) University of Kashmir. The plant parts i.e., stem and leave, after collection were cleaned and dried under shade for few days, cut into small pieces and then powdered in a wood grinder under sterilized conditions. The colour of the powder was stem (yellowish) leaves (dark green) and roots (reddish).
Animals: Randomly bred closed colony Wistar rats (12-16 weeks old and weighing 120-160 g) reared in animal house laboratory (CSIR-Indian Institute of Integrative Medicine Jammu) were used. Rats were housed in groups of 5-10 in plastic cages. They were given pellet diet ad libitum during the course of experimentation. Twelve hour light cycle was automatically controlled (on at 7.00 AM and off at 7.00 PM) and the room temperature was regulated at 26±1°C. Before the experimentation, animals were housed in these conditions for 3-4 days to become acclimatized.
Determination of antioxidant activity
General free radical scavenging-DPPH assay: This is the primary method in which the free radical i.e., DPPH which is purple in colour is reduced by the antioxidant to yellow colour based on efficacy of the antioxidant. In this method 3 mL of mixture was prepared by adding 1 mL DPPH (5% in methanol) 200-100 μL of extract and respective solvent, the mixture was incubated at room temperature for 30 min and formation of yellow coloured complex was read at 517 nm spectrophotometrically. Ascorbic acid was taken as positive control and reaction solvent with DPPH as negative:
Superoxide anion scavenging-riboflavin photo oxidation method: Univalent reduction of oxygen causes production of superoxide anion, which interacts with hydrogen peroxide leading to the generation of highly reactive and toxic hydroxyl radicals. Superoxide anion is thus the first reduction product of oxygen, which reacts with lipids, DNA and directly affects intercellular enzymes. In this method, the photo oxidation of riboflavin leads to the generation of riboflavin radicals which then oxidizes and generates superoxide radicals. The reaction mixture 1.7 mL was made by adding 300 μL of EDTA (0.1 M) 500 μL NBT (1.5 mM) 0.067 M phosphate buffer and 200 μL of different concentrations of extracts (25 mg mL1). The tubes were incubated at 37°C for 5-8 min. Then, 200 μL of riboflavin was added and were kept in sunlight for 10-12 min. Until colour change was observed (purple). The absorbance was then read at 560 nm. Reaction medium devoid of extract was taken as negative control and ascorbic acid as positive controls (C1 and C2; one having H2O2 and other without it):
Hydroxyl radical scavenging-deoxyribose assay: The highly reactive radical i.e., hydroxyl radical (OH) is generated by the reaction of H2O2 with ferrous ions, which cleaves covalent bonds in proteins, carbohydrates, causes lipid per oxidation and destroys cell membrane. The assay was done by two ways in first one, 1 mL of reaction mixture was prepared by adding 500 μL DNA (500 mg 50 mL1), 100 μL ferric nitrate (20 mM), 100 μL ascorbic acid (500 mM), different volumes of Tris HCl buffer (0.001 M) and 100 μL of different concentrations of extracts. The reaction mixture was incubated at 37°C for 24 h in water bath. Then, 1 mL TCA (20%) was added and centrifuged at 5000 rpm for 5 min. To the supernatant was added 1 mL TBA (1.68%) kept in boiling water for 20 min and cooled under tap water. In the second method, 30 μL H2O2 was added after ferric nitrate to make total of 1 mL volume and the rest procedure was same as first one. The reddish pink colour complex was red at 535 nm in both. Reaction medium without extract act as negative control and ascorbic acid as positive control:
Determination of acute inflammatory test in Wistar rats: The test was performed by standard procedure. Oedema was induced in Wistar rats in groups of four by injecting 0.1 mL of carrageenan (1% w/v) solution in normal saline into sub plantar region of the left hind paw after 45 min of extract administration (250 mg kg1 b.wt.). Paw volume was immediately measured and after 4 h of carrageenan injection. Ibuprofen was used as positive control and normal distilled water as negative control. The inflammation was measured by volumetric differential meter.
Determination of preliminary toxicity test: The test was performed accordingly as used15. In this method few groups of animals were made, each group containing two Wistar rats and normal or negative control which was given normal double distilled water. Extract was solubilised in water and administered orally as a single dose of 5 mg kg1 b.wt. These animals were observed for 72 h period. The number of deaths was expressed as percentile and preliminary toxicity test observed.
RESULTS AND DISCUSSION
Platanus orientalis contains various tannins and polyphenols, including flavonoids such as quercetin, kaempferol and their glycosides10,11,14. It has been reported that these flavonoids have potent anti-inflammatory and analgesic actions on inflammation and pain16-18. Depending on the chemical substitutions on the flavone-skeleton, flavonoids can play a modulating, biphasic and regulatory action on inflammation and immunity. Flavonoids exert their properties both as plant extracts and as purified aglycone molecules16. Also caffeic acid is found in the plant leaves and it has been reported that this compound has anti-inflammatory activity19,20. It seems these natural compounds in the polyphenolic and total extracts of the plant leaves have been partly associated with our pharmacological findings, although it is not clear whether these plant constituents are the only contributing components of this extract.
Total yield of plant extracts: Hot extraction of plant in different solvent systems yielded different amount of extracts. Platanus orientalis chloroform wood extract (10.12%) fallowed methanol root extract (8.06%). Methanol extract of Platanus orientalis root (≈ 400 ppm) and wood (≈ 360 ppm) showed higher polyphenol content in comparison to other extracts (Table 1).
DPPH radical scavenging assay of Platanus orientalis extracts: Methanol, chloroform and aqueous extracts of Platanus orientalis wood, root and leaves were evaluated for their antioxidant activity. From the present study it was elucidated that the chloroform extracts of wood and root and also methanol extract of leaves showed maximum activity in contrast to control (Table 2).
Deoxyribose assay of extracts: Methanol, chloroform and aqueous extracts of Platanus orientalis wood, root and leaves were evaluated for their antioxidant activity.
From the present study it was elucidated that methanol extract of all showed comparable activity (Table 3).
NBT (superoxide scavenging) assay: Methanol, chloroform and aqueous extracts of Platanus orientalis wood, root and leaves were evaluated for their antioxidant activity. Methanol extract of leaves showed the maximum activity (Table 4).
Anti-inflammatory activity evaluation of Platanus orientalis leaves extract by carrageenan induced paw oedema: Aqueous, methanol and chloroform extracts were administrated at a dose level of 250 mg kg1 b.wt. in five group of rats four each group in which one as positive and other negative control. Present study shows methanol and chloroform solvent system extracts showed negative results. Whereas aqueous showed (6.38%) inhibition. Ibuprofen administrated at 100 mg kg1 b.wt., showed (72.76%) inhibition (Table 5).
Anti-inflammatory activity evaluation of Platanus orientalis roots extract by carrageenan induced paw oedema: Aqueous, methanol and chloroform extracts were administrated at a dose level of 250 mg kg1 b.wt. in five group of rats four each group in which one as positive and other negative control. Present study shows methanol and chloroform solvent system extracts showed negative results. Whereas aqueous showed (1.88%) inhibition. Ibuprofen administrated at 100 mg kg1 b.wt., showed (75.84%) inhibition (Table 5).
Anti-inflammatory activity evaluation of Platanus orientalis wood extract by carrageenan induced paw oedema: Aqueous, methanol and chloroform extracts were administrated at a dose level of 250 mg kg1 b.wt., in five group of rats four each group in which one as positive and other negative control.
Present study shows aqueous extract (21.18%) inhibition, chloroform extract (15.90%) inhibition fallowed by methanol extract (9.09%) inhibition. Ibuprofen administrated at 100 mg kg1 b.wt. showed (70.90%) inhibition (Table 5).
Preliminary toxicity test: This test was done for 17 extracts and sub-fractions i.e., of Platanus orientalis of which anti-inflammatory activity was done. The animals under consideration did not died for the stipulated time of 72 h and also not showed any conditions of increased diuresis, convulsion, ataxy, diarrhoea or weight loss.
Successful analysis of botanical compounds from the plant material is largely dependent on the type of solvent used in the extraction procedures. Traditional healers use primarily water as solvent but in present study, it was found that plant extract in organic solvent was found such chloroform and methanol provided more convenient activity as compared to aqueous extracts. In this study, it was found that it is the wood of Platanus orientalis which showed the whole activities in maximum, so it is to be concluded that most of the bioactive materials are concentrated in the wood whatever the solvent system. Total phenol content was found accordingly root extract>wood extract>leaves extract or in accordance with, MeOH extract>CHCl3 extract>aqueous extract, so it is the methanol extract of Platanus orientalis root (≈ 400 ppm) and wood (≈ 360 ppm) which showed maximum phenol content. Antioxidant activity was found accordingly: Wood extract>root extract>leaves extract or as MeOH extract>CHCl3 extract>aqueous extract. Anti-inflammatory activity of Platanus orientalis was observed accordingly as aqueous extract>CHCl3 extract>MeOH extract or as wood extract>leaves extract>root extract. The results of the present study shows that, in Platanus orientalis wood, aqueous extract; chloroform extract and methanol extract inhibition of inflammation is 21.18, 15.90 and 9.09%, respectively. In Platanus orientalis leaves, methanol and chloroform solvent system extracts showed negative results, whereas aqueous extracts showed (6.38%) inhibition. In Platanus orientalis root, methanol and chloroform solvent system extracts showed negative results, whereas aqueous extract showed (1.88%) inhibition. These finding provides some biological value of different extracts of Platanus orientalis for the use as antioxidant and anti-inflammatory agents. However, further investigation on isolation and purification of the bio-active molecules is needed to explore the exact mechanism of action of the Platanus orientalis extracts.
In conclusion, the pharmacological activities of the plant leaves showed moderate antioxidant and anti-inflammatory effects and further pharmacological and biological studies are needed to elucidate the mechanisms of its action.
The financial support from the Centre Council for Research in Unani Medicine (CCRUM) and Council of Scientific and Industrial Research (CSIR) New Delhi, India, as Pool Officer under the Grant No. IA-27401 is gratefully acknowledged.
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