Dr.T Venkata Reddy

Dr.T VENKATA REDDY

CLINICAL EVALUATIONOFALURETIC
AN INDIGENOUS DIURETIC COMPOUND

by
Dr.T VENKATA REDDY, G.C.I.M. Superintendent;
Dr. AchantaLaxmipathi Govt. Ayurvedic Hospital
Dr. K. NISHTESWAR, M.D. (Ayurveda), D Sc., Lecturer/Medical Officer
Dr. N.R.S. Govt. Ayurvedic College/ Hospital, Vijaywada

 

Journal of NIMA, PP 9-10, Sept. 1993

INTRODUCTION:

The use of substances producing increase in urine output can be traced back to the dawn of medicine. Ayurveda, the oldest medical system of India mentioned several medicinal plants in the man­agement of odema, ascites and urinary disorders. During the early phase of this century some attempts have been made to study indigenous drugs on scien­tific lines. Beginning with the work of Sir R. N. Chopra in 1923, a large number of plant extracts have been studied in experimental animals. In 1955 Gujral et al., undertook a systemic study of 33 different medicinal plants selected from Ayurvedic classics for diuretic property. Aqueous extracts were prepared and sc­reening was carried out in rats according to the method of lipcnitx. Urine was collected in metabolic cage for the period of 5 hours. Urea was used as a standard for comparison. According to this study Saccharum efficinarum (Ikshumul), Tribulus terestris (Gokshura), Glycyrrhiza glabra (Yashtimadhu), Achyranthes aspera (Apamarga) and Pinus deodara (Devdar) showed good diuretic activity 1. * It was also concluded that the diuretic activity of Gokshura and Punarnava was due to their high potassium content.

A controlled clinical trial of Punarnava has been done in 40 patients suffering from Nephrotic syn­drome. It induced notable degree of diuresis. The diuretic effect was slow but prolonged. Besides relief in clinical oedema the patients also showed over-all improvement such as decrease in albuminuria, rise in serum protein and fall in serum cholesterol level 2

Juice of leaves ofAzadirachataindica (Neem leaf) has been reputed to possess diuretic activity (Chopra et al.). 3* In a preliminary study Berberine al­kaloid (Daruharidra) showed moderate diuretic activ­ity both in rats and unanesthetized dogs when com­pared with hydrochlorthiazide 4*. The diuretic activity of Oleo-resin ofGuggulu was reported by Gujral et al;5* At the dose of 6.25 mg/100 gm. of rat weighttheoleo-resin cited moderate degree of diuretic action.

In an experimental study it was observed that the alcoholic extract of Pashanabhed has no effect inpreventing the stone formation in rats but it is helpful in dissolving the preformed stones. 7*

The drug Guduchi (T. cordifolia) has been proved to possess anti-rheumatic and diuretic properties (Sesodia and - Lashminarayana, 1966). Rai and Gupta (1966) have carried out experimental evalua­tion of Guduchi for dissolution of urinary calculi. In 22 rats the stone formation was induced by implanting Zinc pellets into the bladder. The deposition of sec­ondary salts over the Zinc pellets was inhibited by aqueous extracts of T. cordifolia. 8*

ALURETIC is a compound medicine evolved by Alarsin Pharmaceuticals which consists of some of the above reviewed safe herbal diuretics. It has been reported that ALURETIC is highly efficacious as a step 1 drug in the management of mild to moderate hypertension. 9*

CONTENTS OF ALURETIC

CONTENTS OF ALURETIC:

 

Punarnava

20 mg.

Erandamul

10mg

Gokshura

20 mg.

Kavachmul

10 mg

Ikshumul

20 mg.

Guggulu

30 mg

Jesthimadhu

20 mg.

Shilajit

30 mg.

Anantamul

20 mg.

Daruharidra

20 mg

Guduchi

20 mg.

Deodar

20 mg

Apamarga

10 mg.

Nimpan

10 mg

Pashanbhed

10mg.

Haritaki

20 mg

Haldi

20 mg.

Saunf

20 mg

Sunthi

20 mg.

Bharangimul

20 mg

Kalakadu

10 mg.

Nirgundi

10 mg

Amala

10 mg.

Dusparsha

10 mg

Vidanga

10 mg.

Sahianjan

10 mg


Shankhapushpi


10 mg.


Patola

10 mg

 

Aim of the study: To assess the diuretic effects of ALURETIC (ALARSIN) in oedematous conditions.

METHODS AND MATERIALS:

In the present study 10 patients suffering from oedema of various origins have been included as­sociated with the following symptoms/signs.

1. Swelling of legs
2. Swelling of abdomen
3. Swelling of face.
4. Swelling all over the body.
5. Breathlessness on exertion
6. Cough
7. Flatulence
8. Anemia
9. Hypertension
10. Giddiness

The patients attending'O.P. at Dr. A. L. Government Ayurvedic Hospital, Vijayawada were selected and taken up for complete clinical assessment. Routine investigations like urinary cytology, urinary analysis, HB%, R.B.C. count, TC, ESR and X-ray were done before and after treatment.

The clinically evaluated cases were given ALURETIC-2 tablets three times a day for a period of six weeks. The response of the drug has been graded as follows:

1.             Good: relief noticed at the end one-week treat­ment.

2.             Fair: relief noticed at the end of two weeks treat­ment.

3.             Poor: relief obtained at the end of six weeks treat­ment.

Out of 10 subjects 5 were males and 5 were females. The minimum age was 40 years and the maximum age was 69 years. The following diseases were diagnosed as causative factors for oedema.

1.             Ascites (due to cirrhosis of     liver)    2

2.             Congestive cardiac failure      7

3.           Anemia1

RESULTS & DISCUSSION:

In the present study 10 patients with oedematous state were administered ALURETIC 2 tablets at a time, thrice a day for a period of six weeks for evaluating diuretic action. Blood pressure was also recorded in sitting posture at weekly intervals. 9 out of 10 patients were having mild to moderate hyper­tension. (mild hypertension: diastolic BP 90-100 mm/Hg. moderate hypertension: diastolic BP 100­-105 mm/Hg). The response was good in 8 patients suffering from Ascites. (2 cases) and congestive car­diac failure (6 cases), fair in one patient (suffering from CCF) and poor in one case (Anemia). Appreci­able reduction in blood pressure was observed only after 2 weeks. The diuretic response was noticed evi­dently after 24 hours and no side effects were re­ported in this study. Symptoms of Hypokalaemia like muscular weakness, constipation and anorexia were not complained by the patients during the trial periods. 10* So it is deemed that Aluretic can be classified as potassium sparing diuretic. Since the Alureticcontains the drugs namely Goskhura and Punarnava which are having large quantities of potassium, the loss of potassium through diuresis will almost be near to nil. Aluretic contains the drugs namely Guduchi which is useful in preventing stone formation and Pashanbhed which helps in dissolving preformed stone in the bladder or kidney. Hence it can also be indicated in urolithiasis. The follow up study was carried out upto 2 months and it was observed that the effect of Aluretic is temporary.

To sum up ALURETIC is found to be the most ef­fective diuretic in the management of oedema due to cardiac, renal and hepatic disorders. It can be ad­ministered as an adjuvant therapy in HypertensionandUrolithiasis

Acknowledgement: The authors are thankful to Alarsin Pharmaceuticals, Bombay for the generous supply of samples of ALURETIC tablets.

REFERENCES:

1.             Heravey K. S.. A Preliminary Experimental study of the diuretic activity of some Indigenous drugs, In­dian Journal of Medical Research, 54, 774-778, 1966.

2.             Udupa K. N. Chaturvedi G. N & Tripathi S. N ; Ad­vances in Research in Indian Medicine, Banaras Hindu University, 1970.

3.             Singh R. H. &Udupa'K. N. Journal of Research in Indian Medicine, Vol. VII, No. 3.

4.             Chopra R. N. & Chopra I. C., A review of works on Indian Medicinal Plants, ICMR, 1955.

5.             Advances in research in Indian Medicine, 1970.

6.             Journal of Indian Medical Association, 25, 49, 1955.

7.             Journal of research in Indian Medicine, Vol. IX, No 2, 1974.

8.             Indian Journal of Physiology and Pharmacology,10:12,2:21,

9.             Somasundarum H. Clinical efficacy of tablets ALURETIC in the management of mild to moderate essential Hypertension, current Medical Practice, Vol. 36, No. 4, April 1992.

10.           D. R. Laurence & P. N. Bennett, Clinical Pharmacology, 1980