Hepatoprotective Potential of Cordia Subcordata Lam. Against Carbon Tetra Chloride (CCL) - Induced Hepatotoxicity in Wistar Albino Rats
Hepatoprotective Potential of Cordia Subcordata Lam. Against Carbon Tetra Chloride (CCL) - Induced Hepatotoxicity in Wistar Albino Rats
Hepatoprotective Potential of Cordia Subcordata Lam. Against Carbon Tetra Chloride (CCL) - Induced Hepatotoxicity in Wistar Albino Rats
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coastal areas. In Tahiti, the leaves are Percentage yield of ethanolic extract of
used in remedies for bronchitis and Cordia subcordata was found to be 16.5
asthma where the leaves probably act as % w/w.
a purgative. The plant is also used in the Preliminary phytochemical screening
treatment of hepatic infections, cirrhosis The phytochemical examination of
of the liver and inflammation of the ethanolic (90%) extract of Cordia
lymph nodes. It is also used to treat subcordata Lam. leaves was performed
albumin present in the urine. Cook by the standard methods [10].
Islanders use the leaves in remedies for
abdominal swellings and urinary tract Animals used
infections [7-9]. Wistar albino rats (150-220g) of either
However, there are no ethnomedicinal sex were obtained from the animal house
information and scientific findings for in C.L. Baid Metha College of
the above said traditional claim for Pharmacy, Chennai. The animals were
hepatic disorders. Therefore, to justify maintained in a well-ventilated room
the traditional claims the present study with 12:12 hour light/dark cycle in
was undertaken to find out if ethanol polypropylene cages. The animals were
extract of Cordia subcordata Lam. fed with standard pellet feed (Hindustan
leaves demonstrates the hepatoprotective Lever Limited., Bangalore) and water
activity against CCl4-induced liver was given ad libitum. Ethical committee
damage in rats. Hence, the present study clearance was obtained from IAEC
was designed to verify the claims of the (Institutional Animal Ethics Committee)
native practitioners. of CPCSEA (Ref No. IAEC / XIII / 01 /
CLBMCP / 2008 - 2009).
MATERIALS AND METHODS
Plant collection Acute Toxicity Study
The Plant material of Cordia subcordata
Lam. leaves was collected from The acute toxicity of 90% ehanolic
Tirunelveli District, in the Month of extract of Cordia subcordata was
August 2008. The plant was determined as per the OECD guideline
authenticated by Dr.V.Chelladurai, no. 423 (Acute Toxic Class Method). It
Research Officer Botany. C.C.R.A.S., was observed that the test extract was
Govt. of India. The voucher specimen not mortal even at 2000mg/kg dose.
(CHE-SA-CS-08) of the plant was Hence, 1/20th (100mg/kg), 1/10th
deposited at the college for further (200mg/kg) and 1/5th (400mg/kg) of this
reference. dose were selected for further study [11].
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Fig. 1 (a): Normal control treated group Fig. 1(b): normal control treated group
on 4th day (100x) on 8th day (100x)
Fig. 2(a): CCl treated group on 4th day (100x) Fig. 2(b):CCl treated group on 8th day (100x)
4 4
Fig. 3 (a): CCl supplemented with EECS 400 Fig. 3 (b): CCl supplemented with EECS 400
4 4
treated group on 4th day (100x) treated group on 8th day (100x)
Fig. 4(a): CCl with Liv.52 (40mg/kg, p.o) Fig. 4(b): CCl with Liv.52 (40mg/kg, p.o)
4 4
treated group on 4th day (100x) treated group on 8th day (100x)
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(ACP), serum ALT were confirmed by [9] Whistler, W.A., Polynesian Herbal
histopathological studies of liver Medicine. Everbest, Hong Kong, 1992,
138-139.
sections which reveal that the normal [10] Whistler, W.A., J. Ethnopharmacol.,
liver architecture was disturbed by 1985, 13 (3), 239-280.
hepatotoxin (CCl4) intoxication. In the [11] Harbone, J.P., Phytochemical Methods,
liver sections of the rats treated with A Guide to modern technique of plant
EECS extract for 7 days, the normal analysis, (Chapmann and Hall,
London), 1973, pp. 1-271.
cellular architecture was retained as [12] OECD, 2002. Acute oral toxicity. Acute
compared to Liv.52, thereby further oral toxic class method guideline 423
confirming the potent hepatoprotective adopted 23.03.1996. In: Eleventh
effect of Cordia subcordata leaves. Addendum to the, OECD, guidelines for
Further research is needed to isolate and the testing of chemicals organisation for
economical co-operation and
purify the active principle involved in development, Paris, June, 2000.
hepatoprotection of this plant as well as [13] Visweswaram, D., Rajeswara Rao, P.,
to confirm the mechanisms responsible Satyanarayana, S., Indian J Pharmacol.,
for hepatoprotective activity. The 1994, 26, 301 303.
present finding provides scientific [14] Reitman, S., Frankel, S., Am J Clin
Path., 1957, 28, 56-62.
evidence to the ethnomedicinal use of [15] Kind, P.R.N., King, E.J., J. Clin. Path.,
Cordia subcordata in treating hepatic 1954, 7, 132-136.
disorders. [16] Malloy, H.T., Evelyn, K.A., J Biol
Acknowledgement Chem, 1937, 119, 481-485.
Authors are sincerely thankful to Dr. S. [17] Bousquet, B.F., Julien, R., Bon, R.,
Dreux, C., Ann Biol Clin., 1971, 29,
Venkatraman, M.Sc., M.D., Ph.D., 415.
Director and Mr.P.Muralidharan, [18] Luna, L.G., Methods of Armed Forces
M.Pharm. (Ph.D), Department of Institute of Pathology, London, 1966,
Pharmacology, C.L. Baid Metha pp131.
Foundation for Pharmaceutical [19] Galigher, A.E., and Kozloff, E.N.,
Essential Practical Microtechnique, 2nd
Education and Research, for their edn, Lea and Febiger, Philadelphia
contribution and facilities provided 1971, 77210.
regarding our Research work. [20] Kiso, Y., Tohkin, M., Hikino, H.,
Planta Med., 1983, 49, 222225.
REFERENCES [21] Allis, J.W., Ward, T.R., Seely, J.C.,
[1] Wolf, P.L., Indian Journal of Clinical Simmons, J.E., Fundamental Appl
Biochemistry 1999, 14, 5990. Toxicol., 1990, 15, 558570.
[2] Handa, S.S., Sharma, A., and [22] Cornelius, C.E., Animal Models in
Chakraborti, K.K., Fitoterapia 1986, Liver Research. San Diego: Academic
57, 307-45. Press; 1993, 37, 341.
[3] Venkateswaran, S., Pari, L., [23] Recknagel, R.O., Glende, E.A., Jr,
Viswanathan, P., Menon, V.P., J Dolak, J.A., Waller, R.L., Pharmacol
Ethnopharmacol, 1997, 57, 161167. Ther., 1989, 43, 139154.
[4] Latha, U., Rajesh, M.G,, Latha, M.S., [24] Plaa, G., Charbonneau, M., In: Hayes,
Ind Drugs, 1999, 36, 470473. A.W. (Ed.), Principles and Methods of
[5] Lupper, S., Altern Med Rev, 1999, 4, Toxicology. Raven Press, New York,
179189. 1994, pp 841846.
[6] Mitra, S.K., Venkataranganna, M.V., [25] Wachstein, M., Gastroenterol., 1959,
Sundaram, R., and Gopumadhavan, S., 37, 525- 37.
[7] J. Ethnopharmacol, 1998, 63, 181-186. [26] Max Wachstein., Elizabeth Meisel., and
[8] Weiner, M.A., Secrets of Fijian Carmen Falcon., Am J Pathol., 1962,
Medicine. Govt. Printer, Suva, Fiji, 40(2), 219241.
1984, 70. [27] Sallie, R., Tredger, J.M., William, R.,
Biopharm Drug Disp., 1991, 12, 251-
259.
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