|Year : 2015 | Volume
| Issue : 1 | Page : 126-130
Evaluation of analgesic, antipyretic and anti-inflammatory activity on Cordia dichotoma G. Forst. Leaf
Richa Gupta, Jagjit Kaur
Department of Pharmacognosy, Amar Shaheed Baba Ajit Singh Jujhar Singh Memorial College of Pharmacy, Bela (Ropar), Punjab, India
|Date of Submission||30-May-2014|
|Date of Acceptance||13-Jul-2014|
|Date of Web Publication||17-Dec-2014|
Department of Pharmacognosy, Amar Shaheed Baba Ajit Singh Jujhar Singh Memorial College of Pharmacy, Bela (Ropar) - 140 111, Punjab
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: Cordia dichotoma G. Forst. is an important medicinal plant of family Boraginaceae. Traditionally, its leaves are used to treat fever, headache, and joint pain but its medicinal activities have not been proven by research. Objective: To evaluate the analgesic, anti-inflammatory, and antipyretic activity of C. dichotoma G. Forst. leaf extract.
Material and Methods: The various extracts of leaf powder were prepared by using soxhlet apparatus. The methanol extract was selected for pharmacological study. To evaluate analgesic activity, Eddy's hot plate method, to study anti-inflammatory activity, carageenan-induced rat paw edema method, and to study antipyretic activity, yeast-induced pyrexia method was used. SD female rats (180-200 g) were used for the study. Results: In all three tests, the methanol extract high dose (400 mg/kg) was found to be highly significant as compared to standard drug. Conclusion: This study proved the traditional uses of plant leaves and concluded the analgesic, anti-inflammatory, and antipyretic activity of the leaf methanol extract.
Keywords: Analgesic, anti-inflammatory, antipyretic, Boraginaceae, Cordia dichotoma
|How to cite this article:|
Gupta R, Kaur J. Evaluation of analgesic, antipyretic and anti-inflammatory activity on Cordia dichotoma G. Forst. Leaf. Phcog Res 2015;7:126-30
|How to cite this URL:|
Gupta R, Kaur J. Evaluation of analgesic, antipyretic and anti-inflammatory activity on Cordia dichotoma G. Forst. Leaf. Phcog Res [serial online] 2015 [cited 2021 Mar 7];7:126-30. Available from: http://www.phcogres.com/text.asp?2015/7/1/126/147227
| Introduction|| |
The genus Cordia belongs to the family Boraginaceae, with some 300 species distributed worldwide, mostly in the warmer regions of the World. According to a literature survey, several uses in traditional medicine have been reported for different Cordia species. The ethnopharmacological and chemotaxonomic importance of the genus Cordia led us to investigate one of its species, namely Cordia dichotoma G. Forst., which is a medicinal plant found widespread from northern India to southern China. Chemical screening of both the leaves and the fruits showed the presence of pyrrolizidine alkaloids, coumarins, flavonoids, terpenes, and sterols. Four flavonoid glycosides (robinin, rutin; rutoside, datiscoside, and hesperidin), a flavonoid aglycone (dihydrorobinetin), and 2 phenolic derivatives (chlorogenic acid and caffeic acid) were isolated from fruits and leaves.  The fruit used as astringent, anthelmentic, diuretic, demulcent, and expectorant. The mucilage of the fruit treats coughs and other chest complaints. It is also used to treat uterus and urethra disorders. The powder form of the fruit kernels is mixed with oil to heal tinea. The plant is also a diuretic and laxative.  The leaves used as tonic, stimulant, and febrifuge. Leaf decoction used in cough and cold.  The leaves are also used to relieve headache and treat ulcers. The present work aimed to investigate the analgesic, anti-inflammatory, and antipyretic activity of C. dichotoma G. Forst leaf.
| Materials and Methods|| |
The leaves of C. dichotoma G. Forst., family Boraginaceae were procured from Attari, Anandpur Sahib and authenticated and identified by Dr. H.B Singh, Scientist and Head, Raw material, Herbarium and museum, NISCAIR, New Delhi. The voucher specimen of the sample (NISCAIR/RHMD/Consult/-2011-12/1788/88) was deposited in herbarium of Pharmacognosy department, ASBASJSM College of pharmacy, Bela (Ropar) for future with reference no. JCD/11/03.
Chemicals and reagents
All chemicals, reagents and solvents used were of AR and HPLC grade (Loba, Himedia, Qualigen). Distilled water and precoated silica gel G plates (6 × 6 inches, 0.2 mm thickness, aluminium base, E Merck) were used.
A definite weight of crude leafy drug was taken in a soxhlet apparatus thimble after making moderately coarse and then continuous hot soxhlet extraction was done by various solvents in a sequence of increasing polarity as follows:  Petroleum ether, chloroform, methanol, and water. Before starting extraction with subsequent solvent, the marc (plant material) was dried of all its previous solvent content by spreading out on paper. The weight of the extract obtained was determined after concentration in Heidolph Rota evaporator, and the percentage of extractive value was calculated on dry weight basis.
The various chemical tests were performed on each extract to determine presence of different phytoconstituents such as alkaloids, glycosides, flavonoids, steroids, carbohydrates, saponins, etc. , The total alkaloid,  total flavonoid,  and total phenolic content  were also determined in the crude drug sample.
The methanol extract of C. dichotoma leaves was used to evaluate its analgesic, anti-inflammatory, and antipyretic activity. SD female rats (180-200 g) were used for the present study. They were maintained under standard environmental conditions and were feed with standard pellet diet. The experimental protocol was approved by the Institution Animals Ethics Committee (IAEC) of ASBASJSM College of Pharmacy, Bela (Ropar) Punjab under the accession no. ASCB/IAEC/04/12/61. Animals were procured from NIPER, Mohali. Animals were housed in polypropylene cages (6 per cage) with dust free rice husk as a bedding material under laboratory condition with control environment of temperature (23° ± 2°C), humidity (60% ± 10%), and 12 h light/dark cycles as per guidelines of the Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA), India. They were provided standard rodent chow/feed and water ad libitum. Before subjecting them to experimentation, the animals were given a week time to get acclimatized with laboratory conditions. The animals were fasted for 18 h before the experiment. After a sufficient period of acclimatization, they were used to evaluate anti-inflammatory, anti-pyretic, and analgesic activities of C. dichotoma.
Grouping of animals
Twenty-four animals were used in all; six animals were used in each group.
- Group I: Positive control group
- Group II: Standard group
- Group III: C. dichotoma low dose level of leaf extract
- Group IV: C. dichotoma high dose level of leaf extract.
Analgesic activity was analyzed by Eddy's Hot plate method. ,,, Indomethacin (10 mg/kg per oral) was taken as standard drug. Rats were placed on hot plate and recorded the reaction time in second for licking of hind paw or jumping with cut- off time of 20 sec. The reaction time following the administration of the test extracts, reference standard drug, and control saline vehicle were measured at 0, 30, 60, 90, and 120 min.
Anti-inflammatory activity was analyzed by the carrageenan-induced rat paw edema method. ,, Indomethacin (10 mg/kg per oral) was taken as standard drug.
Antipyretic activity was analyzed by the method Yeast- induced Pyrexia. , Paracetamol (100 mg/kg per oral) was taken as standard drug. The test substance was dosed orally (0 hour), and rectal temperature was recorded at 1, 2, 3, and 4 hours. The difference in temperature between 0 hour and at the end of 4 hour was compared and analyzed.
The data was expressed in mean SEM, and the test dose was compared with control and subjected to one-way ANOVA followed by Dunnett Test. P < 0.05 was considered significant, P < 0.01 more significant, and P < 0.001 highly significant.
| Results|| |
- The [Figure 1] is showing leaves and fruits of Cordia C. dichotoma G. Forst
- Extraction process:- The percentage yield and physical appearance of various extracts of C. dichotoma leaf is shown in [Table 1]. The successive solvent extraction showed maximum yield with methanol
|Table 1: Percentage yield and physical characteristics of various extracts of Cordia dichotoma G. Forst. Leaf|
Click here to view
- Phytochemical screening: The phytochemical analysis of all extracts for presence of various chemical constituents is shown in [Table 2]
- Quantitative estimation: The estimation of total alkaloid, total flavonoid, and total phenolic content in leaves was done by standard test methods, and it was found as 2.20% w/w, 4.58 mg/ml [Figure 2], and 4.27 mg/ml [Figure 3], respectively
|Figure 2: Standard plot of quercetin for the estimation of total flavonoid content|
Click here to view
|Figure 3: Standard plot of Gallic acid for the estimation of total phenolic content|
Click here to view
- Pharmacological studies: The dose for methanol extract was selected as per OECD 423 guidelines. According the acute oral toxicity study of C. dichotoma leaf methanol extract, 2000 mg/kg was the non-toxic dose for rats. Therefore, two doses were selected,-a low dose (200 mg/kg) and a high dose (400 mg/kg)
- Evaluation of analgesic activity by Eddy's Hot plate method: The analgesic effect of different doses (200 mg/kg and 400 mg/kg) of methanol extract of C. dichotoma G. Forst leaf on rats is shown in [Table 3] and [Figure 4]
- Evaluation of anti-inflammatory activity by Carrageenan- induced rat paw edema method: The effect of different doses (200 mg/kg and 400 mg/kg) of methanol extract of C. dichotoma G. Forst leaf on Carrageenan-induced rat paw edema in rats are shown in [Table 4] and [Figure 5]
- Evaluation of anti-pyretic activity by Yeast-induced pyrexia method The effect of different doses (200 mg/kg and 400 mg/kg) of methanol extract of C. dichotoma leaf on yeast-induced pyrexia rats are shown in [Table 5] and [Figure 6].
|Table 5: Effect of the CDME on induction of yeast induces pyrexia in rats|
Click here to view
|Figure 6: Effect of the CDME on induction of yeast induced pyrexia in rats|
Click here to view
| Discussion|| |
In this study, CDME showed positive results and its high dose (400 mg/kg) was found be highly significantly effective as analgesic, anti-inflammatory, and anti-pyretic drug compared to effects of low dose. Its anti-inflammatory potential was found lesser as compared to the other two effects. The effect of high dose was increasing with time, but the maximum time limit for its effects could not be elucidated because of the limited time of the study. This is the first study showing the antipyretic potential of C. dichotoma plant leaves.
| Conclusion|| |
In conclusion, the present study supports the traditional use of C. dichotoma G. Forst. leaves methanol extract as analgesic, antipyretic, and anti-inflammatory drug. However, the crude extracts of this plant need to be further purified through isolation and identification of the responsible compound for these above activities. The mechanism of action of C. dichotoma G. Forst. leaves may be another interested area to work in future.
| Acknowledgements|| |
We are grateful to Dr. G. D. Gupta (Director) and college management for providing all necessary facilities and co-operation for doing this work. We also express our gratitude to whole faculty of ASBSJSM College of Pharmacy, Bela (Ropar), Punjab, for their support.
| References|| |
Patel AK, Pathak N, Trivedi H, Gavania M, Patel M, Panchal N. Phytopharmacological properties of Cordia dichotoma
as a potential medicinal tree: An overview. Int J Inst Pharm Life Sci 2011;1:40-51.
Kirtikar KR and Basu BD. Indian Medicinal Plants, edited by L. M. Basu. Allahabad: Central Council for Research in Ayurveda and Siddha (Deptt. of AYUSH, Min. of Health and Family Welfare), Govt. of India. 2 nd
ed. 1933; p. 2131-3.
Chopra RN, Nayar SL, Chopra IC. Glossary of Indian medicinal plants, National institute of Science communication and information resources. 1 st
ed. New Delhi: CSIR; 1956. p. 77.
Harborne JB. Phytochemical methods In: A guide to modern techniques of plant analysis. 3 rd
ed. UK: Chapman and Hall, ICMR; 1998. p. 89-131.
Evans WC. Trease and Evans Pharmacognosy. 16 th
ed. Saunders Elsevier; 2009. p. 135-48.
Ordon Ez AL, Gomez JD, Vattuone MA, Isla MI. Antioxidant activities of Sechium edule
(Jacq.) Swart extracts. Food Chem 2006;97:452-8.
Sengul M, Yildiz H, Gungor N, Cetin B, Eser Z, Ercisli S. Total phenolic content, antioxidant and antimicrobial activities of some medicinal plants. Pak J Pharm Sci 2009;13:102-6.
Purnima A, Koti BC, Thippeswamy AH, Jaji MS, Vishwantha AH, Kurhe YV, et al
. Anti-inflammatory, analgesic and antipyretic activities of Mimuso pselengi
Linn. Indian J Pharm Sci 2010;72:480-5.
Vogel WH, Scholkens BA, Sandow J, Muller G, Vogel WF. Drug discovery and evaluation pharmacological assays. 2 nd
ed. Berlin: Springer Verlag; 2002. p. 696, 772.
Singh S, Raheja M, Sharma S. Analgesic activity on different extracts of Cordia dichotoma
bark. Indian J Nat Prod 2008;24:21.
Mustaffa F, Indurkar J, Ismail S, Mordi MN, Ramanathan S, Mansor SM. Analgesic activity, toxicity study and phytochemical screening of standardized Cinnomomum iners
leaves methanolic extract. Pharmacognosy Res 2010;2:76-81.
Okpo SO, Fatokun F, Adeyemi OO. Analgesic and anti-inflammatory activity of Crinum glaucum
aqueous extract. J Ethnopharmacol 2001;78:207-11.
Handunnetti SM, Kumara RR, Deraniyagala SA, Ratnasooriya WD. Anti-inflammatory activity of Ixora coccinea
methanolic leaf extract. Pharmacognosy Res 2009;1:80-90.
Dutta S, Das S. A study of the anti-inflammatory effect of the leaves of Psidium guajava
Linn. on experimental animal models. Pharmacognosy Res 2010;2:313-7.
Nisar M, Khan I, Simjee SU, Gilani AH, Obaidullah, Perveen OH. Anticonvulsant, analgesic and antipyretic activities of Taxus wallichiana
Zucc. J Ethnopharmacol 2008;116:490-4.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]
|This article has been cited by|
||Traditional uses, phytochemistry and pharmacology of the medicinal species of the genus Cordia
| ||Manisha J. Oza,Yogesh A. Kulkarni |
| ||Journal of Pharmacy and Pharmacology. 2017; |
|[Pubmed] | [DOI]|
||Anti-inflammatory activity of berry fruits in mice model of inflammation is based on oxidative stress modulation
| ||GeissonMarcos Nardi,AdrianaGraziele de Farias anuário,CassioGeremia Freire,Fernanda Megiolaro,Ketlin Schneider,MarleneRaimunda Andreola Perazzoli,ScheleyRaap Do Nascimento,AnaCristina Gon,LuisaNathalia Bolda Mariano,Glauber Wagner,Rivaldo Niero,Claudriana Locatelli |
| ||Pharmacognosy Research. 2016; 8(5): 42 |
|[Pubmed] | [DOI]|