Comparative Cardiotonic Activity of Sida cordifolia Linn with Digoxin on Perfused Frog Heart.

 

Dama Ganesh Y.*., Jori Mayuri P., Joshi Prajakta P., Deore Sumit R. and Bidkar Jayant S.

Department of Pharmacognosy, Sharadchandra Pawar College of Pharmacy, Dumbarwadi, Otur, Pune, Maharashtra, India.

*Corresponding Author E-mail: gydama2008@rediffmail.com

 

ABSTRACT:

The present study was undertaken to evaluate the cardiotonic activity of the infusion of roots of Sida cordifolia Linn belonging to family Malvaceae which is common throughout the tropical and subtropical plains all over India and Ceylon growing wild along roadside. The cardiotonic effect of infusion of roots of Sida cordifolia Linn was studied by using perfused frog heart assembly. In the present work infusion, dilution 1:1 (Infusion: Distilled water), 1:2 (Infusion: Distilled water), 1:4 (Infusion: Distilled water), are used to evaluate cardiac activity on isolated frog heart and labeled as A1, A2, A3, A4, respectively and compared with Digoxin B1-25µg/ml, B2-50µg/ml as a standard. Present preliminary studies confirm better cardiotonic activity of Sida cordifolia Linn than digoxin. A significant increase in height of force of contraction (positive ionotropic effect) and decrease in heart rate (negative chronotropic effect) was observed.

 

KEYWORDS: Sida cordifolia Linn, Digoxin, cardiotonic activity.

 

 


INTRODUCTION:

Numbers of deaths in industrial world are increasing due to cardiac diseases are emerging as a single largest contributors for morbidity in India1. The cardiovascular system includes spleen, lymphatic tissues and vessels the main function of this system is to maintain homeostasis by acting as transportation system that carries needed materials to cells and removes waste materials from cells. The conduction system functions by initiating the heart beat, conducting message around the heart, coordinating beats between the atria and ventricles2.  Various diseases related to cardiovascular system are aneurysm, atherosclerosis, cardiac arrhythmia, congestive heart failure, hypertension, myocardial infarction, phlebitis and angina pectoris etc3-6.

 

Sida cordifolia Linn (Family: Malvaceae) is a shrubby, branched and common throughout the tropical and subtropical plains all over India and Ceylon growing wild along roadside. It is used in the folk medicine for several purposes: Root infusion is used as cardiotonic, nervous diseases, asthma, piles, and urinary diseases7, 8. It has reported to posses’ antioxidant9, antistress10, adaptogenic10, antiinflammatory11,12,13, analgesic11,12,13, hypoglycaemic13, liver regeneration14.

 

The whole plant contains alkaloids, fatty oil, phytosterol, mucin, potassium nitrate and the alkaloid was identified is ephedrine7, 8, 15. The cardiovascular effect of Sida cordifolia Linn leaves by using mammalian heart model was reported16, but there was no scientific data available regarding cardiotonic activity of Sida cordifolia Linn roots.

 

Material and method1, 2, 17, 18

Drug: Root infusion of Sida cordifolia Linn

Chemical: Digoxin, Ringer solution

Animal: Frog

Instrument: Sherington rotating drum

 

Plant collection and preparation of infusion:

Plant was collected from western ghat and identified in Pharmacognosy department, Shardchandra Pawar College of Pharmacy, Otur, Pune. The root was washed, dried and powdered. The infusion was prepared by putting 1gm of powdered drug in 100ml warm water. The material was filtered through whatman filter paper no. 40 and filtrate was collected. The filtrate was diluted with the help of distilled water in varying proportion and labelled as follows,

A1- undiluted

A2- 1:1 Filtrate: distilled water

A3- 1:2 Filtrate: distilled water

A4- 1:4 Filtrate: distilled water

All the preparations were evaluated for their cardiotonic activity by using perfused frog heart assembly. The rate and force of contraction was determined.

Preparation of Digoxin:

The marketed digoxin (Sunpharma Ltd.) ampoules were obtained from local market. Various different dilutions were made with distilled water and labelled as follows B1- 25µg/ml, B2- 50µg/ml. The above prepared samples were evaluated for their cardiotonic activity and treated as standard.

 

Preparation of hypodynamic ringer solution:

Hypodynamic ringer solution was prepared by using standard method.

 

Evaluation of cardiotonic activity:

1.        The frog of species Rana tigrina was pithed and pinned it to the frog board.

2.        A midline incision was given on the abdomen, the pectoral girdle was removed and the heart was exposed.

3.        The pericardium was carefully removed and put a few drops of hypodynamic frog ringer over the heart.

4.        The inferior venacava was traced, put a thread around it and given a small cut in order to insert the venous cannula which is in turn connected to a perfusion bottle containing hypodynamic frog ringer solution. The cannula was inserted in the vein and the thread to assure the cannula in place.

5.        A small cut in one of the aorta was given for the perfusate to come out.

6.        A proper venous pressure of 2-4cm was given by altering the height of perfusion bottle. The effective venous pressure is the height in cms from level of the venous cannula and the ringer level in the perfusion bottle.

7.        A thin pin hook was passed through the tip of the ventricle and with the help of a fine thread attached to the hook; it was tied to the free limb of the universal lever which is fixed to a stand. A proper tension and magnification was adjusted by altering the height of the lever. The normal heart rate was noted. All test samples that is A1, A2, A3, A4, B1 and B2 were administered in different doses viz. 0.1ml, 0.2ml, 0.3ml respectively. The rate and force of heart contraction were noted. (Table 1-6, Figure 1-6).

 

Observations:-


 

Fig:1 Effect of A1- undiluted on hypodynamic heart

 

Fig:2 Effect of A2- 1:1 Filtrate: distilled water on hypodynamic heart

 

Fig:3 Effect of A3- 1:2 Filtrate: distilled water on hypodynamic heart

 

Fig:4 Effect  of A4- 1:4 Filtrate: distilled water on hypodynamic heart

 

Fig:5 Effect  of B1-25µg/ml Digoxin on  hypodynamic heart

 

Fig:6 Effect  of B2-50µg/ml Digoxin on hypodynamic heart

 


 

Table 1: Hypodynamic Heart

Sr. No.

Drug

Dose(in ml)

Beats/min.

Change in Force

1

.....

Normal

25

Normal

2

A1

0.1

24

Increase

3

A1

0.2

24

Slight increase

4

A1

0.3

22

No change

 

Table 2: Hypodynamic Heart

Sr. No.

Drug

Dose(in ml)

Beats/min.

Change in Force

1

.....

Normal

30

Normal

2

A2

0.1

25

Increase

3

A2

0.2

27

Slight increase

4

A2

0.3

24

Rapid Increase

 

Table 3: Hypodynamic Heart

Sr. No.

Drug

Dose(in ml)

Beats/min.

Change in Force

1

.....

Normal

34

Normal

2

A3

0.1

30

Increase

3

A3

0.2

28

Increase

4

A3

0.3

26

Slight decrease

 

Table 4: Hypodynamic Heart

Sr. No.

Drug

Dose(in ml)

Beats/min.

Change in Force

1

.....

Normal

31

Normal

2

A4

0.1

27

Increase

3

A4

0.2

28

No change

4

A4

0.3

23

Slight decrease

 

Table 5: Hypodynamic Heart

Sr. No.

Drug

Dose(in ml)

Beats/min.

Change in Force

1

.....

Normal

35

Normal

2

B1

0.1

31

Increase

3

B1

0.2

29

Decrease

4

B1

0.3

30

Increase

 

Table 6: Hypodynamic Heart

Sr. No.

Drug

Dose(in ml)

Beats/min.

Change in Force

1

.....

Normal

32

Normal

2

B2

0.1

28

Increase

3

B2

0.2

35

Slight decrease

4

B2

0.3

25

Sudden cardiac block

 

RESULTS AND DISCUSSION:

From the above observations, the infusion of Sida cordifolia Linn was found to restore cardiac activity of the hypodynamic frog heart, which means it increases the rapidity and force of contraction of the myocardial muscles of the perfused frog heart. The sample A1 i.e. the undiluted filtrate has shown the results with rapid increase in force of contraction at 0.1 and 0.2  and the maximum heartbeats/ min were found to be 24 beats / min at dose of 0.1 and 0.2ml the force of contraction was also increased at this dose. Another sample A2 i.e. the filtrate diluted with distilled water in the ratio 1:1 shown significant activity. It also restored the cardiac potentials in the dose dependent manner, the maximum heartbeats/min was found at the dose of 0.2ml. The sample A3 i.e. the filtrate diluted with distilled water in the ratio 1:2 has given satisfactory results with rapid increase in force of contraction at 0.1ml and 0.2ml of dose respectively. The sample A4 i.e. the filtrate diluted with distilled water in the ratio 1:4 has given significant results with increase in force of contraction at 0.1ml. As the digoxin was used as standard drug, the sample B1 i.e. 0.25 µg/ml solution of digoxin shown effective results but the sample B2 i.e. 50 µg/ml solution shown significant activity.

 

Thus, regarding the results obtained we can say that, all the dilutions of Sida cordifolia Linn restore cardiac activity of hypodynamic frog heart i.e. it increases rapidity and force of contraction. It was found that sample A2- 1:1 Filtrate: distilled water showed better response as compared to other samples. It is interesting to know that Sida cordifolia Linn has rapid onset of action compared to digoxin.

 

CONCLUSION:

These preliminary studies confirm the better cardiotonic activity of Sida cordifolia Linn and thus we can conclude that roots of Sida cordifolia Linn are having cardiotonic activity somewhat similar to that of digoxin a well known life saving cardiotonic drug.

 

REFERENCES: -

1.        Pai PT, Adnaik RS, Mule SN, Naikwade NS and  Magdum CS. Evaluation of cardiotonic activity of leaves of Vitex negundo Linn, International Journal of green Pharmacy, October-December 2009; 306-309.

2.        Awari DM, Mute CS and Thube BB. Cardiotonic activity from the fruit juice of Punica granatum, Journal of Pharmacy research, February 2009; 2(2): 182-184.

3.        Harsh Mohan, Textbook of Pathophysiology, Jaypee Brothers Medical Publishers, 2000; 4th Edn.: 278-325.

4.        Hardman JG and Limbird LE. Goodman and Gillman, The Pharmacological Basis of Therapeutics, McGraw Hill Publications, 1996; 9th Edn.: 810-820.

5.        Tripathi KD. Essentials of Medical Pharmacology, Jaypee Brothers Medical Publishers, New Delhi, 2003; 5th Edn.: 457-467.

6.        Barar FSK. Essentials of Pharmacotherapeutics, S. Chand Publications, New Delhi, 1985; 1st Edn.: 253-254.

7.        Nadkarni KM.The Indian Materia Medica, Vol. 1, Bombay popular publication, 1954; 3rd Edn.: 1134-1137.

8.        Kiritikar KR and Basu BD. Indian Medicinal plants, Vol. 2, Oriental enterprises, 2nd Edn.: 428-429.

9.        Dhalwal K, Deshpande YS, Purohit AP and Kadam SS. Evaluation of the Antioxidant Activity of Sida cordifolia, Pharmaceutical Biology, 2005; 43(9):754-761.

10.     Sumanth M and Mustafa SS. Antistress, Adoptogenic Activity of Sida cordifolia Roots in Mice, Indian Journal of Pharm Science, May–Jun 2009; 71(3): 323–324.

11.     Sutradhar RK, Rahman AM, Ahmad M, Bachar SC, Saha A and Guha SKU. Bioactive Alkaloid from Sida cordifolia Linn. With Analgesic and Anti-Inflammatory Activities, Iranian Journal of Pharmacology and Therapeutics, July 2006; 5(2): 175-178.

12.     Sutradhar RK, Matior Rahman AKM, Ahmad MU, Datta BK, Bachar SC and Saha A. Analgesic and antiinflammatory activity of Sida cordifolia Linn,  Indian Journal of Pharmacology, June 2006; 38(3): 207-08.

13.     Kanth VR and Diwan PV. Analgesic, Antiinflammatory and Hypoglycaemic Activities of Sida cordifolia, Phytotherapy Research, 1999; 13:75–77.

14.     Silva RL, de Melo GB, de Melo VA, Antoniolli AR, Michellone PRT, Zucoloto SM, Picinato ANC, Franco CFF, Mota GA and Silva OC. Effect of the aqueous extract of Sida cordifolia on liver regeneration after partial hepatectomy, Acta Cirurgica. Brasileria , Săo Paulo 2006; 21(1 ).

15.     Dr. Singh AP. Bala (Sida cordifolia L.)- Is It Safe Herbal Drug? Ethnobotanical Leaflets, 2006; 10: 336-341.

16.     Medeiros IA, Santos MRV, Nascimento NMS and Duarte JC, Cardiovascular effects of Sida cordifolia leaves extract in rats, Fitoterapia, 2006; 77: 19– 27.

17.     Campbell TJ and MacDonald PS Digoxin in heart failure and cardiac arrhythmias, MJA  2003; 179(2): 98-102.

18.     Kulkarni SK. Handbook of Experimental Pharmacology, Vallabh Prakashan, 1993; 2nd Edn.: 74-76.

 

 

 

 

 

Received on 22.12.2010          Modified on 20.01.2011

Accepted on 27.01.2011         © RJPT All right reserved

Research J. Pharm. and Tech. 4(6): June 2011; Page 913-916