Table of Contents  
Year : 2012  |  Volume : 3  |  Issue : 4  |  Page : 326-328  

Hepatoprotective activity of active fractions of Thespesia lampas Dalz and Gibs (Malvaceae)

1 Research Scholar, Kerala University, Thiruvananthapuram 695 029, India
2 S. B. College of Pharmacy, Anaikuttam 626 130, Sivakasi. Tamil Nadu, India
3 Tropical Botanic Garden and Research Institute, Palode, Thiruvananthapuram 695 562, India

Date of Web Publication24-Nov-2012

Correspondence Address:
A Subramoniam
T.C. 14/80, Near KIMS, Anayara, Thiruvananthapuram 695 029, Kerala
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0976-500X.103691

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How to cite this article:
Ambrose S S, Solairaj P, Subramoniam A. Hepatoprotective activity of active fractions of Thespesia lampas Dalz and Gibs (Malvaceae). J Pharmacol Pharmacother 2012;3:326-8

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Ambrose S S, Solairaj P, Subramoniam A. Hepatoprotective activity of active fractions of Thespesia lampas Dalz and Gibs (Malvaceae). J Pharmacol Pharmacother [serial online] 2012 [cited 2022 Jan 19];3:326-8. Available from:


In the absence of satisfactory treatment using conventional medicine, treatment of liver disorders remains as one of the major medical problems. [1] Numerous medicinal plants are used in local health traditions to treat liver disorders. [1] In the recent past, studies have shown varying levels of hepatoprotective properties in traditional plants found in Kerala, India, such as Phyllanthus maderaspatensis, Phyllanthus rheedii, Thespesia populena, Momordica subangulata, Naregamia alata, Lygodium flexuosum, Cheilanthes farinosa, Physalis peruviana, and Trichopus zeylanicus.[2],[3],[4],[5],[6] However, many medicinal plants used in remote villages and tribal pockets of Kerala remain to be studied. Thespesia lampas Dalz. and Gibs (family Malvaceae) is one such plant. This plant root is used in folklore medicine to treat liver diseases in Attapadi Hills of Western Ghats, Kerala. In traditional medicine, its roots and fruits are used for treating gonorrhea, jaundice, and syphilis. Studies have shown that the plant possesses anti-microbial, antioxidant, anti-lipoxygenase, anti-hyperlipidaemic, and anthelmintic activities. The traditional use of this plant as a hepato-protective agent has not been verified. This study was carried out to get insights into the utility of T. lampas to develop a satisfactory hepatoprotective medicine.

Male albino rats of Wistar strain weighting 190 ± 10 g were used for the study. They were reared under standard conditions. The experimental protocol was approved by Institute Animal Ethics Committee controlled by Committee for the Purpose of Control and Supervision of Experiments on Animals.

The plant roots were collected from Attapadi Hills and authenticated by Dr. Mathew Dan of TBGRI. A voucher specimen (No. SAS 1450) was deposited in TBGRI.

The plant root powder was sequentially extracted with petroleum ether, ethanol, and water. The yield of ethanol extract (the most active extract) was 4.4% of the root powder. The ethanol extract (40 g) was fractionated sequentially into n-butanol, ethyl acetate, and double-distilled water (each 50 × 3 ml) fractions. The fractions were dried in a water bath at 50 °C. The yield of n-butanol fraction was 32% of the ethanol extract. The ethanol extract and n-butanol fraction were subjected to HPLC analysis.

To isolate major compounds from the ethanol extract, the extract was subjected to column chromatography (500 × 30 mm) using Merck silica gel (60-120 mesh) and increasing polarity of solvents (petroleum ether, chloroform, ethyl acetate, and methanol in different ratios) for elution. Identification of isolated compounds was done by comparison with standards in HPLC and with spectral data (IR, NMR, and mass spectra).

Hepatoprotective property of T. lampas extracts and different fractions on paracetamol-induced hepatic damage was done essentially as described. [6] Briefly, the rats were divided into indicated number of groups. The extracts were given orally for 5 days. Paracetamol was administered (single dose in 1% CME, 2 g/kg, p.o.) to all the groups except the normal control group on the third day of the experiment. The rats were sacrificed on the fifth day after blood collection under ether anesthesia by ocular puncture of retro-orbital plexus. [7] Serum was separated under cold conditions, and biochemical parameters were measured using assay kits (SPAN Diagnostics Ltd., Surat, India). Hepatoprotective activity of the butanol fraction against CCl 4 -toxicity in rats was performed as described. [4]

As shown in [Table 1], T. lampas root extracts showed varying levels of hepato-protection against paracetamol-induced liver damage. Ethanol extract showed better activity compared to water and petroleum ether extracts. All the three fractions of the ethanol extract showed varying levels of hepatoprotection (data not shown). However, n-butanol fraction (200 mg/ kg) exhibited maximum hepatoprotective activity which was concentration dependent and comparable to that of 50 mg/ kg silymarin [Table 1]. Similarly, the fraction showed hepatoprotective action against CCl 4 -induced hepatic damage also (data not shown).
Table 1: Effect of various extracts and active fraction of the alcohol extract of T. lampas roots on paracetamol-induced liver injury in rats

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HPLC chromatogram of the ethanol extract showed the presence of nine peaks and two very minor peaks [Figure 1]a. Four compounds were isolated from the ethanol extract by column chromatography. One of the two major compounds was identified as ellagic acid and the other (retention time: 6.81 min) was an unidentified phenolic compound. Other compounds identified were rutin and tannic acid. As judged from retention time-matching with standards in HPLC, quercetin and gallic acid were detected as very minor compounds [Figure 1]a.
Figure 1: HPLC chromatogram of the ethanol extract and butanol fraction of the ethanol extract of T. lampas. (a) Ethanol extract. (b) Butanol fraction. Mobile phase: acetonitrile– methanol– 25 mM KH2PO4 (10:5:85 v/v) pH 2.5. Column: Grace C18 (250 × 4.6) mm; particle size: 5 μm; wavelength: 261 nm; flow: 1.0 mL/min; injection volume: 20 μl from 500 μg/mL sample

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In the HPLC profile of the n-butanol fraction of the ethanol extract, one major peak and 4 minor peaks were seen [Figure 1]b. The major peak (retention time: 6.81 min) was the unidentified phenolic compound purified from the ethanol extract. Other peaks were rutin, ellagic acid, tannic acid, and an unidentified compound [Figure 1]b.

During the course of our study, a preliminary report appeared on the hepatoprotective property of T. lampas root against CCl 4 -toxicity in rats. In that study, the water extract of the plant root was reported to have more hepatoprotective activity than the methanol extract. [8] In this study, the ethanol extract was found to be better than the water extract.

We show for the first time that T. lampas contains three known hepatoprotective compounds (tannic acid, ellagic acid, and rutin) and a major unidentified hepatoprotective phenolic compound. Tannic acid is the active principle in the plant Polygonum bistorta which shows protection against paracetamol-induced liver damage in rats. [9] Ellagic acid is known to have hepatoprotective, anti-oxidant, and anticancer activities. [10] Rutin (20 mg/kg) prevents paracetamol-induced liver damage. [11]

The ethanol extract contained more amount of the known hepatoprotective compounds, ellagic acid in particular, whereas relative concentrations of these compounds were low in the n-butanol fraction. However, the hepato-protective activity of the n-butanol fraction was higher compared to the ethanol extract. The n-butanol fraction contained the major unidentified phenolic compound which could be the major active principle. We have tentatively identified this compound as geraniin. Studies are in progress to confirm the same.

T. lampas root is used in traditional medicine without any recorded or known toxicity. Further, in our preliminary investigation the root powder was well tolerated in rats up to 5 g/kg tested.

Since the active extract and fraction contain several bio-active compounds, they may perhaps act against the toxic chemicals by additive or synergistic actions. Low doses of several phytochemicals with hepato-protective and other beneficial effects could probably serve as a better and safer hepato-protective medicine. T. lampas is very promising for the development of safe and effective hepatoprotective phytomedicine and/or conventional medicine.

   Acknowledgments Top

The authors are thankful to Dr. Rangamoopan Vaithyan, Goolikadavu in Attapadi Hills in Kerala for help in plant collection. Dr. Mathew Dan of TBGRI for the authentication of plant species.

   References Top

1.Subramoniam A, Pushpangadan P. Development of phytomedicines for liver diseases. Indian J Pharmacol 1999;31:166-75.  Back to cited text no. 1
  Medknow Journal  
2.Asha VV, Akhila S, Wills PJ, Subramoniam A. Further studies on the hepatoprotective activity of Phyllanthus maderaspatensis Linn. J Ethnopharmacol 2004;92:67-70.  Back to cited text no. 2
3.Suresh V, Asha VV. Preventive effect of ethanol extract of Phyllanthus rheedii Wight. on D-galactoseamine induced hepatic damage in Wistar rats. J Ethnopharmacol 2008;116:447-53.  Back to cited text no. 3
4.Yuvaraj P, Subramoniam A. Hepatoprotective property of Thespesia populena against carbon tetrachloride induced liver damage in rats. J Basic Clin Physiol Pharmacol 2009;20:28-32.  Back to cited text no. 4
5.Krishna RN, Sreejith PS, Asha VV. Cytotoxic and apoptotic activity of Chilanthes farinose (Forsk.) Kaulf against human hepatoma, Hep 3B cells. J Ethnopharmacol 2010;128:166-71.  Back to cited text no. 5
6.Subramoniam A, Evans DA, Rajasekharan S, Pushpangadan P. Hepatoprotective activity of Trichopus zeylanicus extract against paracetamol-induced hepatic damage in rats. Indian J Exp Biol 1998;36:385-9.  Back to cited text no. 6
7.Parasuraman S, Raveendran R, Kesavan R. Blood sample collection in small laboratory animals. J Pharmacol Phamacother 2010;2:87-93.  Back to cited text no. 7
8.Sangameswaran B, Chumbhale D, Balakrishnan BR, Jayakar B. Hepatoprotective effects of Thespesia lampas Dalz. and Gibson in CCl 4 induced liver injury in rats. Dhaka University J Pharm Sci 2008;7:11-3.  Back to cited text no. 8
9.Mittal DK, Joshi D, Shukla S. Protective effect of Polygonum bistorta Linn. and its active principle against acetaminophen-induced toxicity in rats. Asian J Exp Biol 2010;1:951-8.  Back to cited text no. 9
10.Singh K, Khanna AK, Chander R. Hepatoprotective activity of ellagic acid against carbon tetrachloride-induced hepatotoxicity in rats. Indian J Exp Biol 1999;37:1025-6.  Back to cited text no. 10
11.Khalid HJ, Sheikh AS, Anwar HG. Protective effect of rutin on paracetamol and CCl4 -induced hepatotoxicity in rodents. Fitoterapia 2002;73:557-63.  Back to cited text no. 11


  [Figure 1]

  [Table 1]

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