ANTI-DIABETIC ACTIVITY OF EPIPREMNUM AUREUM.L IN NORMAL AND ALLOXAN-INDUCED DIABETIC RATS

Authors

Abstract

ABSTRACT
Objective: The study was carried out with the objective of phytochemical screening and to evaluate the anti-diabetic activity of aqueous and alcoholic
extract of E. aureum.
Methods: The anti-diabetic activity was determined alloxan-induced diabetic rats. A total of 24 albino Wistar rats of either sex weighing 200-250 g
were divided into 4 groups consisting of 4 rats in each group. Group-1 served as control, Group-2 received standard drug, Group-3 received test drug
aqueous extract of E. aureum, and Group-4 received test drug alcoholic extract of E. aureum.
Results: Phytochemical investigation of aqueous and alcoholic extracts of E. aureum revealed the presence of alkaloids, tannins, saponins, terpenoids,
and flavonoids as secondary metabolites. The both aqueous and alcoholic extracts of E. aureum showed a significant reduction in blood glucose levels
due to the presence of phytochemicals such as flavonoids, terpenoids, and alkaloids in both extracts of E. aureum. The administration of drug (IP) was
continued upto 15 days.
Conclusion: Extracts of E. aureum have shown the great potential of anti-diabetic activity in normal and alloxan-induced rats. Flavonoids might be
producing hypoglycemic effect by a mechanism independent from insulin secretion, e.g. by the inhibition of endogenous glucose production or by
the inhibition of intestinal glucose absorption. This study E. aureum of both aqueous and alcoholic extracts was showed significant effect on alloxaninduced
rats.
Keywords: Epipremnum aureum, Anti-diabetic activity, Alloxan-induced diabetic rats, Glucometer.

Downloads

Download data is not yet available.

Author Biography

Abhinayani G, JNTU

pharmacology

References

REFERENCES

Amos AF, Mc Carty DJ, Zimmet P. The rising global burden of diabetes

and its complications: Estimates and projections to the year 2010.

Diabet Med 1997;14 Suppl 5:S1-5.

th

Bajaj JS, Madan R. Diabetes in tropics and developing countries. IDF

Bull 1995;38(2):5-6.

Nathan DM. The pathophysiology of diabetic complications: How much

does the glucose hypothesis explain? Ann Intern Med 1996;124:86-9.

Dixit VP, Joshi SC. Antiatherosclerotic effects of alfalfa meal ingestion

in chicks: A biochemical evaluation. Indian J Physiol Pharmacol

;29(1):47-50.

Eshrat MH. Effect of Coccinia indica (L.) and Abroma augusta (L.)

on glycemia, lipid profile and on indicators of end-organ damage

in streptozotocin induced diabetic rats. Indian J Clin Biochem

;18(2):54-63.

Punitha R, Vasudevan K, Manoharan S. Effect of Pogamia pinnata

flowers on blood glucose and oxidative stress in alloxan induced

diabetic rats. Indian J Pharmacol 2006;38(1):62-3.

Chopra RN, Chopra IL, Honda KL, Kapur LD. Indigenous Drugs of

India. 2

day in normal rats

Treatment Dose (mg/kg) Blood glucose level (mg/dl)

hour 0.5 hour 1 hour 1.5 hour 2 hour

Normal control - 101±2 142±4 132±2 118±2 98±2

Diabetic control 10 259±3 383±5 339±2 290±2 281±2

Std (Glibenclamide) 10 107±2 125±2 115±2 112±1 88±1

AQEEa 200 156±1 102±4 122±2 102±1 94±1

ALEEa 200 158±2 148±3 145±1 111±4 75±2

Values are expressed as mean±S.E.M. n=3. Significant values were compared with p<0.01. Normal control versus all groups. Parenthesis indicates % reduction in BGL

nd

ed. Calcutta: U.N. Dhar and Sons Ltd.; 1958. p. 300-29.

Abhinayani G, Shanker VS, Benazir F. Evaluation of antidiabetic

activity of alcoholic extract of Aloe barbadensis, Momardica Charantia,

Trigonella Foenum-Graecum and their combinations used in alloxan

induced diabetic rats. World J Pharm Pharm Sci 2015;4(11):1380-9.

Macwan CP, Patel MA. Antioxidant potential of dried powder of

Capparis zeylanica Linn. Int J Pharm Pharm Sci 2010;2(3):58-60.

Khandelwal KR. Practical Pharmacognosy Techniques and

Experiments. Pune: Nirali Prakashan; 2003. p. 149-56.

Chanda S, Dave R, Kaneria M, Shukla V. Acute oral toxicity of

Polyalthia longifolia var. Pendula leaf extract in Wistar albino rats.

Pharm Biol 2012;50(11):1408-15.

OECD. Guideline for Testing of Chemicals. Acute Oral Toxicity-Up

and Down Procedure. Paris: OECD; 2001. p. 425.

Pareek H, Sharma S, Khajja BS, Jain K, Jain GC. Evaluation of

hypoglycemic and anti-hyperglycemic potential of Tridax procumbens

(Linn.). BMC Complement Altern Med 2009;9:48.

Vats V, Grover JK, Rathi SS. Evaluation of anti-hyperglycemic and

hypoglycemic effect of Trigonella foenum graecum Linn, Ocimum

sanctum Linn and Pterocarpus marsupium Linn in normal and

alloxanized diabetic rats. J Ethnopharmacol 2002;79(1):95-100.

Khosla P, Gupta DD, Nagpal RK. Effect of Trigonella foenum graecum

(Fenugreek) on blood glucose in normal and diabetic rats. Indian J

Physiol Pharmacol 1995;39(2):173-4.

Abdel-Barry JA, Abdel-Hassan IA, Al-Hakiem MH. Hypoglycaemic

and antihyperglycaemic effects of Trigonella foenum-graecum leaf

in normal and alloxan induced diabetic rats. J Ethnopharmacol

;58(3):149-55.

Published

01-07-2016

How to Cite

G, A., N. Kishore R, F. Benazir, and P. Agarwal. “ANTI-DIABETIC ACTIVITY OF EPIPREMNUM AUREUM.L IN NORMAL AND ALLOXAN-INDUCED DIABETIC RATS”. Asian Journal of Pharmaceutical and Clinical Research, vol. 9, no. 4, July 2016, pp. 89-92, https://journals.innovareacademics.in/index.php/ajpcr/article/view/11387.

Issue

Section

Original Article(s)