HYPOGLYCAEMIC AND ANTIDIABETIC EFFECT OF ROOT EXTRACTS OF CEIBA PENTANDRA IN NORMAL AND DIABETIC RATS
The effect of the root bark extract of Ceiba pentandra (Linn) in normal and streptozotocin-induced diabetic rats was studied. Blood glucose levels were determined after oral administration of graded doses of C. pentandra (40, 75,150 and 300 mg/kg) in fasted normal and diabetic groups. In both grou...
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Published in | African journal of traditional, complementary, and alternative medicines Vol. 3; no. 1 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Nigeria
African Ethnomedicines Network
15.12.2005
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Subjects | |
Online Access | Get full text |
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Summary: | The effect of the root bark extract of Ceiba pentandra (Linn)
in normal and streptozotocin-induced diabetic rats was studied. Blood
glucose levels were determined after oral administration of graded
doses of C. pentandra (40, 75,150 and 300 mg/kg) in fasted normal and
diabetic groups. In both groups, 40 and 75 mg/kg of the extract,
significantly reduced blood glucose levels 8 h after administration,
which was consistent and time-dependent. C. pentandra at the lower dose
of 40mg/kg produced blood -glucose-lowering effect of 40.0% and 48.9%,
in normal and diabetic rats respectively when compared with control
rats. The higher doses of 150 and 300 mg/kg did not affect
significantly the blood glucose levels. In multiple dose studies, the
diabetic rats were treated orally by gavages, twice a day for 3 days.
On day 3, C. pentandra (40 and 75mg/kg) significantly decreased blood
and urine glucose levels as compared to initial values. The 14 h
fasting blood glucose concentration was lowered by 59.8 % and 42.8% at
the doses of 40 and 75 mg/kg and the corresponding urine glucose levels
reductions were 95.7% and 63.6%, respectively. The results indicated
that C. pentandra possessed hypoglycaemic effect. The plant extract was
capable of ameliorating at lower doses, hyperglycaemia in
streptozotocin-induced diabetic rats and could be a potential source
for isolation of new orally active agent(s) for anti-diabetic therapy. |
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ISSN: | 0189-6016 0189-6016 |
DOI: | 10.4314/ajtcam.v3i1.31147 |