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Geriforte – An indigenous geriatric tonic in hyperlipidaemia

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[Probe, (1975): (XIV), 4, 277-280]<br />

<strong>Geriforte</strong> <strong>–</strong> <strong>An</strong> Indigenous Geriatric Tonic <strong>in</strong> Hyperlipidaemia<br />

Sahgal, V.K., M.D., Honorary Endocr<strong>in</strong>ologist<br />

and<br />

Sood, N.K., M.B.,B.S., Resident Medical Officer,<br />

Sk<strong>in</strong> Institute, New Delhi, India.<br />

INTRODUCTION<br />

The subject of disorders of the lipid metabolism especially <strong>hyperlipidaemia</strong> has assumed<br />

significance because of co-related <strong>in</strong>cidence of atherosclerosis and co-related <strong>in</strong>cidence of<br />

atherosclerosis and coronary thrombosis. Classical literature of Indian medic<strong>in</strong>e has dealt at length<br />

with this topic. Sushruta Samhita mentioned the role of fats, as well as diets hav<strong>in</strong>g sweet taste, <strong>in</strong><br />

the actio-pathogenesis of 'medaroga' or obesity.<br />

Today there is a consensus of op<strong>in</strong>ion that <strong>hyperlipidaemia</strong> should be treated though it is not known<br />

whether correction of blood levels of total lipids, neutral fats, and cholesterol will <strong>in</strong>duce<br />

amelioration <strong>in</strong> co-exist<strong>in</strong>g vascular disease. The drugs, used to br<strong>in</strong>g about normalisation of the<br />

blood lipid levels are nicot<strong>in</strong>ic acid, dextro-thyrox<strong>in</strong>e, triparanol, clofibrate, cholestyram<strong>in</strong>e and<br />

oestrogenic compounds. A number of Ayurvedic medic<strong>in</strong>es consist<strong>in</strong>g of such drugs and substances<br />

as 'Shilajeet', 'Guggul', 'Gomutra', 'Triphala', 'Loharaja', 'Rasanjana', 'Madhu', 'Yava', 'Mudga',<br />

'Koradusa', 'Syamka' and 'Uddalka' which have properties to reduce fats are prescribed as remedial<br />

agents possess<strong>in</strong>g the efficacy of cleans<strong>in</strong>g the <strong>in</strong>ternal channels …. Sushruta Sutra 15:33.<br />

<strong>Geriforte</strong> is an <strong><strong>in</strong>digenous</strong> medic<strong>in</strong>e said to be useful <strong>in</strong> <strong>hyperlipidaemia</strong> and the present study was<br />

designed to assess the efficacy of this drug.<br />

MATERIAL AND METHODS<br />

Patients attend<strong>in</strong>g the out-patients of the Sk<strong>in</strong> Institute, Delhi were screened for the presence of<br />

<strong>hyperlipidaemia</strong> by estimat<strong>in</strong>g their serum cholesterol and serum triglyceride values.<br />

Hyperlipidaemic subjects were then prescribed <strong>Geriforte</strong> 2 tablets b.d. for a period of 3 months. At<br />

the end of the period, their blood lipid profile was studied aga<strong>in</strong>. At the beg<strong>in</strong>n<strong>in</strong>g of the study and<br />

at fortnightly <strong>in</strong>tervals, a detailed questionnaire was filled <strong>in</strong> regard<strong>in</strong>g the patients' subjective<br />

observations together with f<strong>in</strong>d<strong>in</strong>gs on physical exam<strong>in</strong>ation.<br />

RESULTS<br />

Twelve patients (10 males and 2 females) with vary<strong>in</strong>g degrees of <strong>hyperlipidaemia</strong> were studied for<br />

6-12 weeks.<br />

It is seen that <strong>Geriforte</strong> <strong>in</strong>duced a fall <strong>in</strong> both the cholesterol and triglyceride fraction and the fall <strong>in</strong><br />

triglyceride values is comparable to that seen with other currently used hypolipidaemic agents<br />

(Malhotra, Ahuja and Sahgal, 1971, Malhotra & Ahuja, 1971). There is a def<strong>in</strong>ite fall <strong>in</strong> serum<br />

cholesterol, though it is not as significant. No side effects were noticed while the patients were on<br />

<strong>Geriforte</strong> Table I.<br />

DISCUSSION<br />

The <strong>in</strong>creased awareness of lipid metabolic disorders and the desirability to correct both the hypertriglyceridaemic<br />

and hyper-cholesterolaemic, arises from the work of Albr<strong>in</strong>k and Man (1959) who<br />

<strong>in</strong>dicated the relationship between serum triglyceride and cholesterol and the pathogenesis of<br />

coronary artery disease. The crucial level cholesterol is 330 mg and triglycerides 150 mg. The effect<br />

of available drugs on serum lipid is not universal. Their cont<strong>in</strong>ued and prolonged use may be<br />

precluded because of the possibility of development of tolerance to them. The effect of <strong>Geriforte</strong> on


oth serum cholesterol and triglycerides makes it a useful addition to the list of hypolipidaemic<br />

agents and merits further study, especially as the mechanism of action is so far purely conjectural.<br />

Perhaps the effect is dose related, and this facet also needs to be studied further.<br />

Table 1<br />

Sl<br />

No.<br />

Name<br />

At the onset<br />

Cholesterol Triglyceride<br />

After 6-12 weeks<br />

Cholesterol Triglyceride<br />

Percentage fall<br />

Cholesterol Triglyceride<br />

1 M.S.V. 296 133 239 117 19 15<br />

2 C.L.M. 280 134 242 116 13 23<br />

3 K.L. 296 136 252 106 15 24<br />

4 S.N. 444 216 364 156 18 29<br />

5 R.S. 335 176 284 156 15 11<br />

6 Mrs. J.R. 358 136 312 101 13 27<br />

7 P.J. 410 156 396 140 4 10<br />

8 M.J. 380 138 346 127 9 7<br />

9 Par J. 456 216 426 198 7 7<br />

10 Mr. J. 392 144 368 122 6 16<br />

11 Ra J. 410 138 372 118 10 14<br />

12 Prem J. 274 136 254 119 7 12<br />

* Studied for one month only.<br />

ERRATUM<br />

To Table II, article entitled "<strong>Geriforte</strong> <strong>–</strong> <strong>An</strong> Indigenous Tonic <strong>in</strong> Hyperlipidaemia"<br />

By V.K. Sahgal and N.K. Sood, published <strong>in</strong> PROBE (1975): 4, 279.<br />

Table II: Effect of hypolipidaemic agents on serum lipid fractions <strong>in</strong> different cl<strong>in</strong>ical trials<br />

Authors Drugs & Doses<br />

No. of<br />

patients<br />

Duration<br />

of trial <strong>in</strong><br />

weeks<br />

Cholesterol<br />

Fall <strong>in</strong><br />

TriglyceridePhospholipid<br />

Berge et al (1961) Nicot<strong>in</strong>ic Acid<br />

(3 to 3.9 g)<br />

51 24 - 36 24% <strong>–</strong> 14%<br />

Parson & Madison (1961) Nicot<strong>in</strong>ic Acid<br />

(3-6 g)<br />

50 50 - 186 23% 29% <strong>–</strong><br />

Hashim & Van Itallie (1965) Cholestyram<strong>in</strong>e<br />

(3-13 g)<br />

9 4 - 60 21% 50% <strong>–</strong><br />

Fallon & Woods (1968) Cholestyram<strong>in</strong>e<br />

(3-16 g)<br />

21 5 - 60 0% 24% <strong>–</strong><br />

Starr et al (1960) Sod. D-Thyrox<strong>in</strong>e<br />

(2-16 mg)<br />

45 4 - 76 15% 40% <strong>–</strong><br />

W<strong>in</strong>ters & Soloff (1962) Sod. D-Thyrox<strong>in</strong>e<br />

(4-12 mg)<br />

36 24 25% 53% <strong>–</strong><br />

Berkowitz (1965) Clofibrate<br />

(2.0 g)<br />

35 16 26% 40% <strong>–</strong><br />

Orga<strong>in</strong> et al (1967) Clofibrate<br />

24 20 8.2 to 47% <strong>–</strong><br />

(2 g)<br />

25.4%<br />

Hartman & Forster (1969) Ciba 13437 S.U.<br />

(200-300 mg)<br />

88 4 - 30 15-29% 31-73% 11-28%<br />

Malhotra, Ahuja and Sahgal Clofibrate (0.5 g)<br />

12 6 - 34 22% 36% 13%<br />

(1971)<br />

t.d.s.<br />

Ciba 13437 S.U.<br />

(100 mg) t.d.s<br />

12 6-34 38% 19% 32%<br />

Gum Gugglu Fraction A<br />

(0.5 g) b.d.<br />

20 6-34 29% 31% 16%<br />

Malhotra & Ahuja (1971) Clofibrate<br />

(0.5 g) t.d.s<br />

12 6 - 34 24% 40% 14%<br />

Ciba 13437 S.U.<br />

(100g) t.d.s.<br />

12 6-34 46% 21% 30%<br />

Gum Gugglu Fraction A<br />

(0.5 g) b.d.<br />

20 6-34 27% 29% 18%


SUMMARY<br />

The cl<strong>in</strong>ical efficacy of <strong>Geriforte</strong>, an <strong><strong>in</strong>digenous</strong> preparation, was evaluated as a hypolipidaemic<br />

agent. 12 patients with <strong>hyperlipidaemia</strong> were studied from 6 to 12 weeks. A significant lower<strong>in</strong>g of<br />

both serum cholesterol and triglyceride levels took place. No side-effects were noticed.<br />

ACKNOWLEDGEMENT<br />

We are grateful to the Himalaya Drug Company, for the generous supply of <strong>Geriforte</strong> tablets and<br />

other facilities and Dr. P.N. Behl, the Director, Sk<strong>in</strong> Institute, New Delhi, for allow<strong>in</strong>g us to carry<br />

out this study.<br />

REFERENCES<br />

1. Abell, L.L., Levy, B.B., Brodie, B.B. and Kendell, F.E., A simplified method for the<br />

estimation of total serum cholesterol <strong>in</strong> serum and demonstration of its specificity, J. Biol.<br />

Chem. (1952): 195, 357.<br />

2. Albr<strong>in</strong>k, M.J. and Man, E.B., Serum triglycerides <strong>in</strong> coronary artery disease, Arch. Int. Med.<br />

(1959): 103, 4.<br />

3. Albr<strong>in</strong>k, M., Meig, J. and Man, E., Serum lipids, hypertension and coronary heart disease,<br />

Am. J. Med. (1961): 31, 4.<br />

4. Berge, K.G., Achor, R.W.P., Christensen, N.A., Mason, H.L. and Barker, N.W.,<br />

Hypercholesterolemia and nicot<strong>in</strong>ic acid, Am. J. Med. (1961): 31, 24.<br />

5. Berkowitz, D., The effect of chlorophenoxyisobutyrate with and without androsterone on<br />

serum lipids fat <strong>in</strong>tolerance and uricacid metabolism. Metabolism, (1965): 14, 966.<br />

6. Fallon, H.J. and Woods, J.W., Response of hyperlipoprote<strong>in</strong>emia to cholestyram<strong>in</strong>e res<strong>in</strong>. J.<br />

Am. med. Assoc. (1968): 204, 1161.<br />

7. Hartmann, G and Forster, G., Cl<strong>in</strong>ical evaluation of a new hypolipidaemic drug, J.<br />

Atheroscler. Res. (1969): 10, 235.<br />

8. Hashim, S.A. and Van Itallie, T.B., Cholestyram<strong>in</strong>e res<strong>in</strong> therapy for hypercholesteremia, J.<br />

Am. med. Assoc. (1965): 192,289.<br />

9. Malhotra, S.C., Ahuja, M.M.S. and Sahgal, V.K., Comparative hypolipidaemic effectiveness<br />

of gum Guggul (Commiphora mukul) Fraction A, Ethyl-p-chlorophenoxy-isobutyrate and<br />

Ciba-13437 Su-Sem<strong>in</strong>ar on disorders of lipid metabolism. CCRIMH - AIIMS, (1971): New<br />

Delhi.<br />

10. Malhotra, S.C. and Ahuja, M.M.S., Comparative hypolipidaemic effectiveness of gum<br />

Guggul. Fraction A Ethyl-p-chlorophenoxy-isobutyrate and Ciba-13437 Su. Ind. J. med. Res.<br />

(1971): 1621,59.<br />

11. Orga<strong>in</strong>, E.S., Bogdonoff, M.D. and Ca<strong>in</strong>, C., Clofibrate and androsterone effect on serum<br />

lipids, Archs. Intern. med. (1967): 119, 80.<br />

12. Parson, Jr., W.B. and Madison, W., Treatment of Hypercholesteraemia by nicot<strong>in</strong>ic acid,<br />

Archs. Intern. Med. (1961): 107, 639.


13. Starr, P., Roen, P., Freibrun, L. and Schleissner, Reduction of serum cholesterol by sodium<br />

dextrothyrox<strong>in</strong>-E. Archs. Intern. med. (1960): 105, 830.<br />

14. Sushruta Samhita: Sutra 15, 33.<br />

15. Van Handle, E.B. and Zilversmit, Micro-method for direct determ<strong>in</strong>ation of serum<br />

triglycerides, J. Lab. Cl<strong>in</strong>. med. (1957): 50, 152.<br />

16. W<strong>in</strong>ters, W.L. and Soloff, L.A., Observation on sodium D-thyrox<strong>in</strong>e as a hypocholestercmic<br />

agent <strong>in</strong> persons with hypercholesteracmia with and without ischaemic heart disease, Am. J.<br />

med. Sci. (1962): 243, 458.

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