Acute And Sub-Acute Toxicity Evaluation Of Ethanolic Extract Of Leucas aspera (Lamiaceae) In Experimental Rats

K.G.Kripa1, D.Chamundeeswari*2 and J.Thanka3

1Department Of Biochemistry, School of Life Sciences, Vels University, Pallavaram, Chennai

2Faculty Of Pharmacy, Sri Ramachandra University, Porur, Chennai

3Department Of Pathology, Sri Ramachandra Medical College and Research Institute, Porur, Chennai 600116, India

Corresponding Author:
Dr. D.Chamundeeswari
Principal, Faculty of Pharmacy
Sri Ramachandra University, Porur
Chennai, India
[email protected]

Date of Submission: 10-04-2011Date of Acceptance: 22-08-2011

Citation:K.G.Kripa, D. Chamundeeswari,J. Thanka,“Acute And Sub-Acute Toxicity Evaluation Of Ethanolic Extract Of Leucas aspera (Lamiaceae) In Experimental Rats”, Int. J. Drug Dev. & Res., Jul-Sep 2011, 3(3): 339-347

Copyright:© 2010 IJDDR, K.G.Kripa et al. This is an open access paper distributed under the copyright agreement with Serials Publication, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.



The present study aimed to evaluate the acute (14 days) and sub-acute (28 days) oral toxicity of ethanolic extract of Leucas aspera (EELA) on albino mice and adult Wistar rats. Acute dosage was 2000mg/kg body weight while sub-acute dosage was 100, 200 and 400 mg/kg b.w. per day of the extract. All morphological, biochemical, hematological changes, in addition to mortality and body weight changes were recorded. Histopathological study was done on vital organs. EELA did not show mortality up to 2g/kg b.w. in the acute toxicity studies. The sub-acute toxicity study demonstrated no significant changes in body weight, food, and water intake. Hematological parameters and biochemical analytes inclusive of glucose, urea, creatinine, total cholesterol, total protein and total bilirubin did not show statistically significant differences between the control and treated groups while the activities of aminotransferases was slightly increased in group IV (P < 0.001) animals. No morphological changes were observed in the histopathological analysis of the major vital organs (liver, kidney, heart, spleen, lungs and brain) tested. In conclusion, the results of this study suggest the non-toxic nature of the ethanolic extract of Leucas aspera at normal therapeutic doses.


Leucas aspera, Sub-acute toxicity, Traditional medicine, Ethanolic extract, Phytotherapy.


Leucas R.Br. (Lamiaceae) is a large genus of herbs distributed throughout the tropical regions of the whole world with two main centers, one in eastern tropical Africa, the other in Asia, with its largest diversity in India. About forty three species occur in India. [1] Some of the species which have been proved for their medicinal values are L. aspera, L. biflora, L. cephalotes, L. ciliata, L. lanata, L. lavendulaefolia, L. linifolia, L. martini cenesis, L. stelligra, L. urticaefolia and L. zeylanica. Leucas aspera (thumbai) grows as an herbaceous, muchbranched, erect or diffuse annual, 30 to 60 cm high weed on wastelands. The plant is used as an insecticide and indicated in traditional medicine for coughs, colds, painful swellings and chronic skin eruptions. In traditional medicine, the leaves find their use in chronic rheumatism and juice for skin eruptions. [2] Literature survey shows the plant to have anti-fungal, anti-microbial, anti-ulcer and hepatoprotective effects. The analgesic, antiinflammatory and anti-pyretic efficacies of Leucas aspera have also been proved. The root parts of Leucas aspera showed the plant to have antinociceptive, antioxidant and cytotoxic activities. Pharmacognostical evaluation of the plant collected from various regions of northern India has been reported. Some of the compounds isolated from Leucas aspera include a hydroxyl tetra triacontan-4- one, aliphatic ketones, nicotine, alpha-farnesene, alpha–thujene, menthol, amyl propionate and isoamyl propionate. [3] Baicalin and Baicalein isolated from the flowers of Leucas aspera were found to stabilize RBC membrane integrity in hypotonicity induced hemolysis. [4] Prostaglandin inhibitory and in vitro antioxidant activity guided fractionation of shoots of Leucas aspera yielded eight lignans and four flavonoids inclusive of acacetin, apigenin, chrysoeriol, coumaryl –D-glucoside, nectandrin B, meso- dihydroguaiaretic acid, macelignan. [5] Characterisation of leucasin isolated from L. aspera leaves for free radical-scavenging showed that leucasin has the ability to chelate metal ions and inhibit oxidation of lipids by breaking the chain reaction due to Fe3+. [6] Despite the use of the plant in traditional medicine for ages, there is limited scientific evidence regarding the safety and efficacy to support the continued therapeutic application of these herbal remedies. Our study was therefore undertaken to determine the toxicity profile of Leucas aspera on rats. To the best of our knowledge, there is no record in the literature of the toxicity profile of Leucas aspera. The acute and sub-acute toxicity data may be required to predict the safety and effects of long term exposure to a particular medicinal plant. This study therefore seeks to assess Leucas aspera for its toxic effects using hematology, serum chemistry, and histopathological changes as toxicity indices.

Materials and Methods

Plant material

The aerial parts of the plant Leucas aspera were collected from Kanchipuram district of Tamilnadu. It was taxonomically identified by Dr. N.Jayaraman, Director, National Institute of Herbal Science, Plant Anatomy Research Center, Tambaram, Chennai India. Voucher specimen (PARC/2007/362) has been deposited in our college herbarium for reference.

Preparation of plant extract

Shade dried and coarsely powdered aerial parts of Leucas aspera (1 kg) was subjected to successive, exhaustive cold maceration in solvents of increasing polarity (n-hexane, chloroform, ethyl acetate and ethanol) for 72, 48, and 24 h respectively. The solvents were filtered, distilled under vacuum and dried in a vacuum dessicator to obtain four different extracts which were utilized for further studies.

In vitro antioxidant studies

The ability of the various extracts to scavenge DPPH radicals in vitro based on the method of Sreejayan and Rao, 1996 [7] was studied and percentage inhibition calculated. Based on these results, the ethanolic extract of Leucas aspera (EELA) which exhibited maximum free radical scavenging activity was selected for in vivo efficacy studies.

In vivo efficacy studies

The anti-inflammatory and antioxidant efficacy of EELA in CFA (complete Freund’s adjuvant) induced arthritis was studied on female Wistar rats. [8]

In vivo toxicity studies


Female swiss albino mice (25-30g) were utilized for the acute toxicity studies performed in accordance with OECD 423 [9] guidelines. Male and female Wistar rats (125–150 g) were used for subacute toxicity studies (OECD 407). [10] They were reared at the animal house of Vel’s University. Animals were kept in rat cages and fed on commercial pellets (Hindustan Lever Ltd, Mumbai, India) and allowed free access to fresh water ad libitum. The experimental protocols were approved by the Committee for the purpose of Control and Supervision of experiments on animals (CPCSEA), New Delhi, India (290/CPCSEA/PH04/17.10.07).

Preliminary acute toxicity studies

Swiss albino mice were divided into two groups of three each. Vehicle control group received 0.2% CMC and second group 2000 mg/kg b.w. of EELA suspended in 0.2% CMC. Immediately after the dose, animals were observed for first 4 h and next 14 days to record mortality. Animals were also observed for the presence of toxic symptoms such as weakness, aggressiveness, refusal of food, loss of weight, diarrhoea, noisy breathing, and fluid discharge from eyes and ears. [11]

Sub-acute toxicity studies

The rats were divided at random into a control group and three experimental groups with six animals in each group. The vehicle control group received 0.2% Carboxy methyl cellulose (CMC), whereas the experimental groups received EELA (100, 200, and 400 mg/kg body weight, p.o.), administered by means of bulbed steel needle for 28 days. Body weights were recorded on days 1 and 28 of the experiment, and daily observations were made for physiological and behavioral responses.

Collection of blood and serum samples

Animals from sub-acute tests were fasted overnight after the dosage period, anaesthetized with ketimine, and then decapitated. Paired blood samples were collected into heparinized and nonheparinized tubes. The heparinized blood was used for hematological evaluation; the non-heparinized blood was allowed to coagulate, contents centrifuged, and the serum separated was analyzed for biochemical parameters.

Determination of hematological and serum biochemical parameters

The hematological and serum biochemical parameters were determined. Hematological parameters assayed included red blood cell (RBC) and white blood cell (WBC) counts inclusive of polymorpho nuclear leucocytes and lymphocytes, platelets, hematocrit, and hemoglobin (Hb) estimation. Erythrocyte indices (mean corpuscular volume (MCV), mean corpuscular hemoglobin concentration (MCHC), and mean corpuscular hemoglobin (MCH)) were determined from values obtained from red blood cell (RBC) count, Hb concentration, and packed cell volume (PCV) values. Serum was assayed for glucose, cholesterol, creatinine, urea, asparate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP) and protein.


Immediately after collection of blood samples, animals were opened up and various body organs such as liver, lungs, heart, kidney, spleen and brain were removed, weighed individually, and fixed in 10% buffered formalin in labeled bottles. Tissues were processed routinely and embedded in paraffin wax. Sections of 5 μm thick were stained with hematoxylin and eosin (HE) and examined under the light microscope. Stomach was cut open and observed for the presence of gross morphological changes.

Statistical analysis

The results are reported as mean ± SD for body weights, hematology, blood biochemistry, and organ weight data. The significant differences were assessed using one-way analysis of variance (ANOVA) using SPSS software package. P values less than 0.05 were considered significant.


Acute toxicity study

There was no mortality or toxicity observed after oral administration of EELA up to a dose level of 2000 mg/kg body weight.

Sub-acute toxicity studies

Effect of EELA on the general behavior of rats

The oral administration of EELA caused no noticeable change in the general behavior of the rats and there were no significant changes in body weight (Table I) or food intake of the rats as compared to the control group. Both the control and treated groups appeared relatively healthy during the period of study. There were no deaths reported in any of the groups.

Weight Control 100 mg/kg EELA
200 mg/kg
400 mg/kg
Initial b.w.(kg) 152±9.7 147±8.9* 155±10.6 NS 148±8.6*
Final b.w. (kg) 302±11.5 295±12.1* 288±14.2* 289±10.5*
Heart (g) 0.69 ±0.06 0.58±0.11** 0.60±0.09** 0.59±0.04**
Liver (g) 4.52±0.52 4.19±0.41* 4.92±0.60* 4.82±0.45*
Lung (g) 0.7±0.04 0.65±0.06** 0.72±0.05* 0.68±0.1*
Spleen (g) 0.64±0.12 0 .69±0.04* 0.71±0.06* 0.66±0.05 NS
Kidney (g) 1.09±0.3 1.01±0.04* 1.96±0.2** 1.42±0.05 NS
Testis (g) 1.02±0.03 0.98±0.05** 0.92±0.04** 0.94±0.03**
Ovary (g) 0.04±0.00 0.04±0.01 NS 0.04±0.00 NS 0.04±0.02 NS

Table I: Effects of EELA on body weight and relative organ weights of treated rats.

Effect of EELA on hematological parameters of rats

The hematological analysis (Table II) showed no significant differences in any of the parameters examined in either the control or treated groups of both sexes. All the values remained within normal limits throughout the experimental period.

Effect of EELA on biochemical parameters of rats

Blood Indices Control 100 mg/kg EELA200 mg/kg 400 mg/kg
RBC (x106/mm3) 4.98±0.41 4.95±0.43 NS 4. 82±0.33 NS 4.92±0.18 NS
Hemoglobin (g/dl) 14.90±0.5 14.4±0.82 NS 14.62±0.44 NS 14.83±0.28
PCV (%) 44.67±2.1 43.17±2.23 NS 42.17±2.56** 42.17±3.19 NS
MCV (fl) 84.78±4.7 87.64±7.03 NS 87.63±3.26 NS 85.89±7.63 NS
MCH (pg) 28.69±1.7 29.20±1.99 NS 30.41±1.26 NS 30.19±0.92*
MCHC (g/dl) 33.86±0.7 33.36±0.93 NS 34.73±1.44 NS 35.36±3.02 NS
Platelets (x105/µl) 1.18±0.13 1.52±0.07** 1.45±0.27* 1.57±0.20**
WBC (x103/mm3) 3.533±0.4 3.383±0.51 NS 2.866±0.320** 2.746±0.329*
PMNL 50.67±1.5 49.00±6.13 NS 47.33±2.34* 45.50±4.04*
Lymphocytes 47.00±0.6 48.17±4.58 NS 48.83±1.47* 50.67±3.01*

Table II: Effect of EELA on hematological parameters of treated rats

EELA caused no significant changes in blood glucose, urea, plasma creatinine, total proteins, total bilirubin and cholesterol whilst there was a limited increase in the activities of liver marker enzymes ALT and AST in group IV animals (Table III).

Parameters Control 100 mg/kg EELA
200 mg/kg
400 mg/kg
Glucose (mg/dl) 102±13.4 90±10.6 * 105± 18.7 NS 113±15.52*
Cholesterol (mg/dl) 72±2.1 78.11±9.6* 80.23±8.12* 82.64±5.2**
Protein (g/dl) 5.10±0.40 5.23±0.43 NS 4.82±0.32* 4.98±0.35 NS
Bilirubin (mg/dl) 0.63±0.19 0.73±0.24 * 0.71±0.31 NS 0.69±0.12 NS
Urea (mg/dl) 30.67±4.3 37.67±4.3** 38.00±5.6** 34.50±4.68 NS
Creatinine (mg/dl) 0.93±0.15 0.73±0.26 * 1.05±0.38 * 0.95±0.36NS
ALP (IU/L) 61±4.42 63.17±7.6 NS 57.17±5.4 NS 70.0±4.68***
AST (IU/L) 84.00±5.2 90.33±9.55* 89.50±6.09 * 93.8±7.22***
ALT (IU/L) 69.83±7.4 73.33±6.4NS 81.2±7.15 ** 92.5±7.55 ***

Table III: Effect of EELA on biochemical parameters of treated rats

Histopathological Studies

Histopathological analysis has shown all tissues apart from liver of the treated groups to be morphologically similar to that of the negative control groups.

Liver-The normal liver showed polygonal hepatocytes with a rounded nucleus, arranged in cords with the portal tract exhibiting a normal structure. In the treated groups, rats of groups II and III also exhibit normal morphological features whilst that of Group IV showed mild focal portal inflammation with lymphocytes, the structure of hepatocytes being normal and intact with no necrosis (Fig 1a, 1b, 1c and 1d).

Fig 1 - Histology of rat liver, lung and kidney from the control and treated groups (100x magnification).

Lungs- Sections of lung tissue of control and treated groups showed normal alveoli (Fig 1e, 1f, 1g and 1h). Kidney-The kidney of the control group consists of normal cortex and medulla. The glomeruli and renal tubules namely the proximal and distal convoluted tubules exhibit a normal structure. The treated groups also exhibited a normal architecture indicating the absence of renal toxicity (Fig1i, 1j, 1k and 1l).

Heart –The histological features of control and Groups II, III and IV showed a normal myocardium at 100 x magnification (Fig 2a, 2b, 2c and 2d). Spleen – The spleen of the control rats showed the white pulp containing lymphocytes surrounded by a red pulp. The spleen of EELA treated groups also exhibited the same structural features (Fig 2e, 2f, 2g and 2h).

Fig 2 - Histology of rat heart, spleen, cerebellum and cerebrum from the control and treated groups (100x magnification).

Brain- Brain appears to be normal in the negative control group. Cerebrum and cerebellum are normal. The cerebellum (Fig 2i, 2j, 2k and 2l) and and cerebrum (Fig 2m, 2n, 2o and 2p) also had similar structural features.


Herbal drugs have received greater attention as an alternative to clinical therapy and the demand for these herbal remedies has greatly increased recently. Their utilization is often based on long-term clinical experience. Despite the usage of plants in folk medicine over ages, only lately has pharmacology and toxicity of these plants begun to receive attention from scientists. With the upsurge in the use of herbal remedies in the last two decades, there is need for a thorough scientific evaluation of these medicinal plants. Hence to validate their claimed pharmacological properties and investigate their possible toxicity, preclinical toxicity studies were carried out on the ethanolic extract of Leucas aspera in mice and rat models.

In the present study, during acute toxicity evaluation, none of the animals died at the dose administered indicating that the LD 50 of EELA was much higher than 2000 mg/kg b.w. for the acute toxicity studies. Natural products usually do not present toxicity, and the arousal of toxic effects if any can be attributed to their use only when the effects occur immediately after administration. Further, there were no significant changes in food and water consumption. The determination of these parameters is important in the study of safety of a therapeutic product, as proper intake of nutrients and water are essential to the physiological status of the animals and to the accomplishment of proper response to the drug tested. [12] Body weight and organ weight changes serve as an indicator of adverse side effects since animals that survive cannot lose more than 10% of the initial body weight. [13] In the present study, in body weight evaluation, no significant difference was found, suggesting that EELA had no effect on the normal growth of rats, justifying the doses chosen.

This study has also shown that sub-acute treatment with the extract did not cause any change in hematological parameters. Hematological changes such as anemia are often accompaniments of bone marrow toxicity and analysis of blood parameters with respect to animal studies have a high relevance and predictive value for humans. [14] Further, the lack-of-effect on PMNL levels indicate that the extract may not have induced any inflammatory process since these cells are usually elevated in the course of inflammations. The anti-inflammatory role of EELA in adjuvant induced arthritis has already been established. [8]

In biochemical evaluation, there were no significant treatment related changes in blood glucose and serum cholesterol levels. Among the other parameters evaluated, AST and ALT are well known enzymes which serve as biomarkers capable of predicting toxicity. AST is present in a wide variety of tissues which includes heart, kidney, skeletal muscle and liver whereas ALT is primarily localized in the liver. [15] Both ALT and AST levels of groups II and III were not statistically different from that of control whereas the activities were slightly increased (P<0.001) in group IV animals. AST and ALT are often diagnostic of underlying cellular injuries. The analysis of these parameters is important since there are several reports of liver toxicity related to the use of phytotherapeutic products. [16] Histopathological examination of the selected organs from treated animals showed normal architecture in the groups II and III. Group IV animals exhibited mild infiltration of lymphocytes, but the hepatocyte structure was nomal and intact with no necrosis thus establishing the hepatoprotective role of EELA.

The insignificant difference in urea and creatinine levels between the treated groups and the control group probably indicate that the extract did not interfere with the renal capacity to excrete the metabolite. Indeed, creatinine is known as a good levels is only observed if there is marked damage to indicator of renal function. Any rise in creatinine levels is only observed if there is marked damage to functional nephrons. [17] Histopathological slides of kidney structure showed normal structural features suggesting the preserved renal integrity of EELA treated rats. Heart, lung, brain and spleen of the treated rats also did not demonstrate significant changes in morphology indicating the protective effect of EELA on these tissues. Further, stomach parts of treated animals did not show the development of ulcerative spots. The antiulcerogenic activity of L. aspera has earlier been recognized in the study of Reddy et al, 1992. [18]


Since, there were no significant adverse effects on the hematological and biochemical parameters, it may be concluded that the ethanolic extract of Leucas aspera did not induce any noteworthy damage to the vital organs. In conclusion, the present investigation demonstrates that at doses consumed in the traditional medicine, the ethanolic extract of Leucas aspera may be considered as relatively safe, as it did not cause either mortality or produce severe toxicological effects on selected body organs, biochemical indices and hematological markers of rats during the acute and sub-acute periods of study.


The authors are grateful to DST for financial grant.


Conflict of Interest: NIL

Source of Support: NONE

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