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ISSN : 2153-2435
Pharmaceutica Analytica Acta
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Evaluation of Ethanolic Extract of Desmodium Gyrans DC Leaves on Wound Healing Activity in Rats

Gopalakrishnan S* and Rajameena R

Senior Professor and Head Department of Pharmaceutical Chemistry, Manonmaniam Sundaranar University, Tirunelveli, India

*Corresponding Author:
Gopalakrishnan S
Senior Professor and Head Department of Pharmaceutical Chemistry
Manonmaniam Sundaranar University
Tirunelveli, India
Tel: 09443172243

Received date: July 26, 2012; Accepted date: September 20, 2012; Published date: September 25, 2012

Citation: Gopalakrishnan S, Rajameena R (2012) Evaluation of Ethanolic Extract of Desmodium gyrans DC Leaves on Wound Healing Activity in Rats. Pharmaceut Anal Acta 3:169. doi: 10.4172/2153-2435.1000169

Copyright: © 2012 Gopalakrishnan S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Desmodium gyrans DC is a well-known herb for its antidote, cardiac-tonic and wound healing activities. The present study was aimed for wound healing potential of the ethanol extract of Desmodium gyrans leaves in the form of simple ointment using two types of wound models in rats, viz. excision wound and dead space wound. The results were comparable to standard drug ciphadin ointment, in terms of wound contraction, tensile strength, histopathological and hydroxy proline content. Histopathological study showed significant increase in fibroblast cells, collagen fibres and blood vessels formation. All parameters were observed significant (p<0.01) in comparison to control group.


Desmodium gyrans; Wound healing; Excision wound; Dead space wound; Histopathological; Fibroblast cells


The world health organization (WHO) urged researchers to examine whether traditional medicines produced any beneficial clinical results [1]. The plant kingdom represents a largely unexplored reservoir of biologically active compounds not only as drugs, but also as unique templates that could serve as a starting point for synthetic analogs and an interesting tool that can be applied for a better understanding of biological processes. Folkloric uses are supported by a long history of human experience. Numerous biologically active plants are discovered by evaluation of ethnopharmacological data, and these plants may offer the local population immediately accessible therapeutic products [2].

Some of these plants are used in the management of fresh wounds, while others for the treatment chronic wounds. The common ways of the treatment are either direct application of crushed fresh plant on the wound or repeated wash of the wound with a plant decoction. Despite the wide spread use of local plants in wound healing, only few of them have been investigated for their potential usefulness using excision and incision wound models by rats [3,4].

Wound healing involves continuous cell-cell and cell-matrix interactions that allow the process to proceed in three overlapping phase’s viz. inflammation, cellular proliferation and remodeling.

Phase 1 is a coagulation and inflammatory phase (0-3 days) and this involves migration of neutrophils at margin of incision, moving towards the fibrin clot.

Phase 2 is a proliferative phase (3-12 days) in which the neutrophils are largely replaced by the macrophages. Granulation tissue progressively invades the incision space and the incisional space is filled with granulation tissue. Collagen fibrils become more abundant and begin to bridge the incision.

Phase 3 is a remodeling phase (3-6 months), involving continuous accumulation of collagen and proliferation of fibroblasts. There is marked reduction in leukocyte infiltration and edema. The phase involves synthesis of collagen fibers, leading to increase in tensile strength of the skin [5].

Reports about medicinal plants affecting various phases of the wound healing process, such as coagulation, inflammation, fibroplasia, collagenation, epithelization and wound contraction are abundant in the scientific literature [6-9]. Still, one should keep in mind that plants have not only beneficial effects in promoting the healing process of wounds and burns or protecting the skin from fungal and bacterial infection or anti-tumor activists against skin cancer, they can be involved in different allergic, photo allergic and irritant skin reactions [10].

Desmodium gyrans DC (Fam. Fabaceae) is commonly known as “Thozhukanni” in Tamil “Namaskari” in Sanskrit. Traditionally Desmodium gyrans DC is used as antidote, cardiac-tonic and wound healing drug. The genus, Desmodium, of the Fabaceae family, includes about 350 species distributed in tropical and subtropical zones worldwide; some of them can be used as herbal medicines. For example, Desmodium gangeticum has been demonstrated to possess antioxidant, anti-nociceptive, anti-inflammatory [11,12], anti-emetic [13], cardio-protective [14], and anti-ulcer effects [15]. Phytochemical studies have progressively isolated gangetin [16], salicylic acid, rutin [17], Desmodin, gangetinin [18], chlorogenic acid and caffeic acid from Desmodium gangeticum [19]. Desmodium triflorum has been reported to possess antioxidant [20], analgesic and anti-inflammatory activities [21].

The present study was carried out to determine the effect of the ethanolic extract of Desmodium gyrans leaves on wound healing activity by excision and dead space wound healing models in rats.

Materials and Methods

Plant materials

The plant was collected in the month of September from Trivandrum, Kerala, India and was identified by Dr. V. Chelladurai, Research Officer (Botany). Central Council of Research in Ayurveda and Siddha, Government Siddha Medical College, Palayamkottai, Tamil Nadu, India. A voucher specimen (MSU/PHAR/HER-140) has been preserved in the Herbarium of the Department of Pharmaceutical Chemistry, Manonmaniam Sundaranar University, Tirunelveli - 627 012.

Extraction of plant material

The leaves of Desmodium gyrans DC were dried under shade and powdered. The dried powder (500 g) was successively extracted using petroleum ether (40-60°C), benzene, chloroform, ethanol and water by using a Soxhlet apparatus. The last trace of the solvent was removed under reduced pressure by rotary evaporator. The dried crude ethanolic extract has been used for the study [22].


Wistar albino rats either sex weighing between 180 g and 200 g were selected for the acute toxicity and wound healing activity studies. The study was approved by the Institutional Ethics Committee for animal experimentation KMCH college of Pharmacy, Coimbatore. The animals were stabilized for 1 week. They were maintained in standard conditions at room temperature, 60 ± 5% relative humidity and 12 h light dark cycle. They were given standard pellet diet supplied by Hindustan Lever Co., Mumbai and water ad libitum throughout the course of the study.

Acute toxicity studies

Albino rats of either sex received ethanolic extract of Desmodium gyrans leaves starting at 2 g/kg bw orally by gavage. The animals were observed for toxic symptoms continuously for the first 4 h after dosing. Finally, the number of survivors was noted after 24 h and these animals were then maintained for further 13 days with observations made daily [23].

Selection of doses

For assessment of excision wound healing activity ethanolic extract was formulated in ointment by using simple ointment BP as base. 2%(w/w) ointment was applied where 2 g of the ethanolic extract was incorporated in 100 g of simple ointment base BP. 0.2 g of each of the extract ointment and ciphadin ointment was applied once daily to treat different groups of animals, respectively.

For the assessment of wound healing activity by dead space wound model, three dose levels were chosen in such a way that, middle dose was approximately one-tenth of the maximum dose during acute toxicity studies, and a low dose, which was 50% of the one tenth dose, and a high dose, which was twice that of one-tenth dose (100 mg/kg bw, 200 mg/kg bw and 400 mg/kg bw).

In Vivo Wound healing activity

Excision wound model: The animals were divided into three groups of six rats each (Table 1)

     Days              Control              Standard (Ciphadin)              Ethanol extract
   Wound area % of wound contraction    Wound area % of wound contraction    Wound area % of wound contraction
0day 535 ± 18.3 (0.0%) -  508 ± 38.5 (0.0%) - 520 ± 34.3 (0.0%) -
3day 508 ± 21.0 (5.04%) 94.9  450 ± 34.4 (11.42%) 88.5 406 ± 29.1 (21.93%) 78.0
5day 460 ± 17.6 (14.01%) 85.9  320 ± 28.8a  (37.00%) 62.9 326 ± 32.8a (37.31%) 62.6
7day 400 ± 12.0 (25.23%) 74.7  264 ± 31.5a (48.03%) 51.9 194 ± 31.0b (62.69%) 37.3
9day 369 ± 16.5 (31.02%) 68.9 186 ± 25.2a (63.38%) 36.6 82 ± 35.4b (84.23%) 15.7
11day 309 ± 14.5 (42.24%) 57.7 104 ± 22.0b (79.52%) 20.4 48 ± 28.2b (90.77%) 9.2
13day 278 ± 13.3 (48.03%) 51.9 80 ± 18.4b (84.25%) 15.7 16 ± 10.4b (96.92%) 3.0
15day 208 ± 12.7 (61.12%) 38.8 46 ± 21.8b (90.94%) 9.0 6 ± 8.1b (98.85%) 1.1
17day 172 ± 10.2 (67.85%) 32.1 8 ± 7.1b (98.42%) 1.5 0.0b (100%) 0
19day 166.12.0 (68.97%) 31.0 0.0b (100%) 0 0.0b (100%) 0
Epithelization time (days)                  23                  17                  15

Table 1: Effect of the ethanol extract of the leaves of Desmodium gyrans and standard ointment on percentage wound contraction and epithelialization period of excision wound model in rats.

Group I served as control

Group II served as standard (ciphadin) treated with ointment topically

Group III served as test treated with Desmodium gyrans ethanol extract ointment

All animals in each group were anaesthetized by the open mask method with anaesthetic ether before wound creation. An excision wound was inflicted by cutting away a 500 mm2 full thickness of skin from a predetermined area, the wound was left undressed to the open environment and the wound contraction and wound closure time was monitored. Wound contraction was measured as percentage contraction in each 2 days after wound formation from the healed wound, a specimen sample of tissue was isolated from each rat for histopathological examination [24].

Dead space wound model: The animals were divided into five groups of six rats each and kept in separate cages (Table 2)

             Groups        Doses            Granuloma (mg) Granuloma breaking strength (g) Hydroxyproline content (µg/ml)
    Wet wt     Dry wt
Control - 68.1 ± 8.9 24.9 ± 3.4 256.8 ± 2.15 1.868 ± 0.03
Standard (Ciphadin) 50 mg/animal 146.4 ± 4.43* 54.9 ± 3.19* 347.8 ± 3.8* 5.267 ± 0.02*
Desmodium gyrans ethanol extract 100 mg/kg bw 73 ± 4.16* 27.67 ± 2.33* 283.3 ± 2.7* 3.825 ± 0.04*
Desmodium gyrans ethanol extract 200 mg/kg bw 91.33 ± 2.33* 34.33 ± 0.88* 335.0 ± 4.46* 4.847 ± 0.04*
Desmodium gyrans ethanol extract 400 mg/kg bw 92.67 ± 2.33* 37 ± 2.65* 383.2 ± 3.34* 5.143 ± 0.03*

Table 2: Effect of the ethanol extract and starndard ointment on various parameters of dead space wound model in rats.

Group I served as control

Group II served as standard (ciphadin) treated with ointment topically

Group III was treated with ethanolic extract of Desmodium gyrans DC (100 mg/kg bw)

Group IV was treated with ethanolic extract of Desmodium gyrans DC (200 mg/kg bw)

Group V was treated with ethanolic extract of Desmodium gyrans DC (400 mg/kg bw)

The model was used for the study of granuloma tissue. Animals were anaesthetized by light ether and wound was made by implantation of two polypropylene tubes (2.0×0.5 cm) one on either side, in the lumber region on the dorsal surface in each animal on the ninth postwounding day, granuloma tissue formed on an implanted tube was dissected out carefully. Granuloma tissue from one tube was dried (60°C) and stored in 10% formalin for the biochemical parameters and histopathological study. While the other part of granuloma tissue was used for determination of tensile strength [25,26].

Wound healing evaluation parameters

Wound contraction and epithelialization time: An excision wound margin was traced after wound creation by using transparent paper and area measured by graph paper. Wound contraction was measured in each 2 days interval, until complete wound healing and expressed in percentage of healing wound area. The epithelialization time was measured from initial day [27] (Figure 1).


Figure 1: Albino rats dorsal wound area photographed at 17 days after application of the ethanolic extract of Desmodium gyrans leaves by Excision model. a) Excision wound on the 0 day b) wound healed treatment (control) c) wound healed treatment standard d) wound healed treatment (ethanol extract 2%w/w).


Figure 2: Photomicroscopic view of histopathological characteristics of 9-day-old wound tissue section by Excision and Dead space model (Hematoxylin and eosin×40). a) Wound tissue treated with control b) Wound tissue treated with standard c) Wound tissue treated with ethanol extract d) Dead space model with ethanol extract (100 mg/kg) e) Dead space model with ethanol extract (200 mg/kg) f) ead space model with ethanol extract (400 mg/kg).

Measurement of tensile strength: Tensile strength is the resistance to breaking under tension. It indicates how much the repaired tissue resists to breaking under tension and may indicate in part the quality of repaired tissue. Sutures were removed on the day 9 after wound creation and the tensile strength was measured with the help of tensiometer, which is based on method of Kuwano [27]. In this method, wound breaking strength was measured as the weight of water at the time of wound breaking per area of the specimen.

Histopathological studies: Wound tissue specimens from control, test and standard groups were taken after complete healing excision and dead space wound and after usual processing. 6 mm thick sections were cut and stained with haematoxylin and eosin [28]. Sections were qualitatively assessed under the light microscope and observed in respect of fibroblast proliferation, collagen formation, angiogenesis, epithelialization, and hydroxy proline estimation. Tissues were dried in a hot air oven at 60-70°C to constant weight and were hydrolysed in 6N HCl at 130°C for 4 h in sealed tubes. The hydrolysate was neutralized to pH 7.0 and was subjected to chloramines-T oxidation for 20 min. the reaction was determinated by addition of 0.4M perchloric acid and colour was developed with the help of Ehrlich reagent at 60°C [29] and measured at 557 nm using a spectrophotometer.

Statistical analysis: Treated group was compared with the control group. The results were analysed statistically using Dunnet’s ‘t’-test to identify the differences between the treated and control groups. The data were considered significant at p<0.01.


Wound contraction

The percentage wound contraction was determined using the following formula:-

Wound area was measured by tracing the wound margin using a transparent paper in each 2 days interval and healed area calculated by subtracting from the original wound area. On day 15, the wound contraction of standard and ethanol extract ointment treated groups was found to be significant (p<0.01) in comparison to simple ointment base treated group. On day 17 ethanol extract ointment treated wound was completely healed while standard ointment treated group was also almost at complete healing stage, and simple ointment base treated group showed 67.85% healing. It was also observed that epithelialization period of treated and standard group were less in comparison to simple ointment base treated group (Table 1).

Effect of the ethanol extract of Desmodium gyrans and standard (ciphadin) ointment in wistar rats excision and dead space type of wounds showed significant healing as in epithelialization, collagenation (C), fibrablasts cells (F) and angiogenesis (BV).

Tensile strength of dead space wound

Tensile strength for the treated group on day 17 was found to be significant (p<0.05) than control group as shown in Table 2.

Hydroxy proline and granuloma weight

Treated group showed significant increased hydroxy proline level when compared to that of the control group (p<0.05) (Table 2). Granuloma weight of treated animal groups was found to be increased when compared with that of the control group.


Wound healing process consists of different phases such as granulation, collagenation, collagen maturation and scar maturation which are concurrent but independent to each other. Hence in this study two different models were used to assess the effect of ethanolic extract of Desmodium gyrans on various phases.

The results showed that the ethanolic extract ointment possesses a definite prohealing action. In excision wound healing model the ethanolic extract of the leaves of Desmodium gyrans showed significant increase in percentage closure of excision wounds by enhanced epithelization significant increase, (p<0.01) in tensile strength, granuloma tissue and hydroxy proline content, which was further supported by histopathological studies and gain in granuloma breaking strength. This indicated improved collagen maturation by increased cross linking. An increase in dry granuloma weight indicated higher protein content.

The preliminary phytochemical analysis of the alcoholic extract of the Desmodium gyrans leaves showed the presence of flavonoids, phenolic compounds, steroid and alkaloids. These phytochemical constituents may be responsible for the wound healing activity. The Desmodium plant extracts possessed a wide range of pharmacological properties, including improving cardiovascular and cerebrovascular functions and regulating immune system as well as anti-inflammatory, cytotoxic, antiparasitic, antidiabetic, antinephrolithic, antibacterial, and nootropic activites [30].


The study showed that the ethanol extract ointment of Desmodium gyrans effectively stimulates wound contraction, increases tensile strength of dead space wounds as compared to the control group. These findings justify the inclusion of this plant in the management of wound healing.


One of the authors, R. Rajameena thanks the Manonmaniam Sundaranar University, Tirunelveli for the University Stipendiary Research Fellowship (USRF) and Dr. A.Rajasekaran, Principal, KMCH college of Pharmacy, Coimbatore for providing facilities to carryout the pharmacological studies.


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