ABSTRACT
Introduction: Testis is an important male reproductive and endocrine organ whose structure and function are altered in diabetes complicated disorders. Aim: This study evaluated the protective effect of Moringa oleifera (MO) and Ocimum gratissimum (OG) on diabetic rat testes. Methodology: Thirty six rats, weighing between 120-180g, were divided into six groups of 6 rats each. Groups 1 and 2 representing Normal (NC) and Diabetic Control (DC) received 0.5ml of dimethylsulphoxide. Group 3 received 5IU/kg b.w insulin; groups 4, 5 and 6 received 500mg/kg b.w of MO, 500mg/kg b.w of OG and 250mg/kg b.w of each extract respectively. Fasting blood glucose (FBG), serum testosterone, luteinizing hormone (LH), follicle stimulating hormone (FSH) and histology of the testes were analysed after 28 days treatment. Results: MO, OG and the combination extract normalized the levels of FBG. Only the Moringa extract normalized the levels of testosterone, LH and FSH compared with DC. The OG extract had no effect on the level of the three sex hormones but provided a potentiating effect on the FSH level in the MO + OG group. The results were confirmed by histological studies which showed damage on the testes for the DC and OG and reversal of damage to the testes in MO and MO + OG groups. Conclusion: The combined extracts more than Moringa extract alone, had ameliorative effects on testicular architecture and spermatogenesis in diabetes and provide a cheap alternative to treating diabetes associated testicular damage and sexual dysfunction.
ABSTRACT
Aim of the Study: To evaluate the effects of ethanolic leaf extracts of Gongronema latifolium (G.L) and Nauclea latifolia (N.L) on antioxidant enzymes activity (GPx, SOD and CAT) and hormonal status (T3, T4, Insulin, c-peptide) in streptozotocin-induced diabetic Wistar rats. Material and Methods: Thirty six (36) albino Wistar rats of both sexes weighing 150-250g were divided into 6 groups of 6 rats each. Groups 1, 2 and 3 received 400mg/kg body weight (b.w) of G.L, N.L and 200mg/kg b.w each of G.L and N.L respectively while group 4 received 5 iu/kg b.w of insulin subcutaneously daily for 21 days, Groups 5 and 6 served as controls (diabetic and Normal) and received placebo. Fasting blood glucose was determined at the start of the experiment and thereafter at 72 hours interval and at the end of experimental period. The animals were sacrificed and sera preparations were used for antioxidant enzymes and hormonal assays. Results: Blood glucose in diabetic animals decreased significantly (P=.05) by 66.34%, 18.12%, 67.73% and 86.62% of initial values upon treatment with G.l, N.l, G.I plus N.I and insulin respectively. There was only a 24.44% decrease in the diabetic control. A significant decrease (P=.05) in insulin and T3 levels was observed in the diabetesinduced rats (65 and 85% respectively) compared to NC. The levels of the hormones where however significantly increased (P=.05) on treatment of the diabetic animals with G.l, N.l, G.I plus N.I and insulin. Whereas a significant decrease (P=.05) was observed in T4 level of DC rats compared to the NC, treatment with the leaf extracts and insulin did not result in any elevation of the hormone relative to DC. The C-peptide levels for all groups were much lower than the corresponding insulin levels, suggesting a type 1 diabetes in the diabetes-induced rats. A significant decrease (P=.05) in activity was observed for GPx and SOD in the DC group relative to NC. A combination of G.l and N.l gave a much higher reversal in activity (P<.01) when compared to treatments with individual leaf extracts. There was a significant increase (P=.05) in CAT activity in the DC animals relative to NC. This was potentiated in all treatment groups with the combination group showing a synergy in its potentiating effect. Conclusion: There was a reversal in the level of the hormones and the activity of the antioxidant enzymes towards normal control, and comparable to the reversals by treatment with insulin, on treatment of the diabetic animals with the leaves extracts especially in combination. The results taken together indicate a synergy that makes the combination of the two plants extracts a potent antidiabetic remedy.
ABSTRACT
Alkaloids extract of the leaf of Gnetum africanum pretreatment was investigated on the activities of aspartate amino transaminase (AST), alanine amino transaminase (ALT) and alkaline phosphatase (ALP) serum and tissue levels in rats. The alkaloids extract was soxhlet extracted following a modified standard procedure. Acute toxicity of the extract was carried out in male rats to determine two tolerated doses used in investigation. Thirty adult male rats were divided into three groups (n=10). Group one received normal saline (0.85%Nacl) as control; groups two and three received alkaloids extract of Gnetum africanium, 12 and 800mg/kg/d, for 3 and 31 days respectively. At the end of each treatment course, the rats were sacrificed 24h after last dose and blood samples collected through cardiac puncture into non-haperinized tubes, allowed to clot for 30 min and sera obtained by ultra iced-centrifugation. The biological activities of AST, ALT and ALP were measured by enzyme kits method. Histopathology of rat liver tissues of all treated groups were carried out. The alkaloids extract pretreatment for 3 days did not significantly alter serum and tissue enzymes levels of AST and ALT but significantly reduced the activity of ALP. However, subchronic treatments for 31 days significantly reversed the inhibitory effect of the extract on AST, ALT and ALP respectively. Histopathology of the rat liver morphology of all the treated groups showed no disorder. The observation allows conclusion that alkaloids extract of the leaf of Gnetum africanum is non hepatoxic.
ABSTRACT
The study evaluated the effect of combined extracts of Vernonia amygdalina (VA) and Gongronema latifolium (GL) on the pancreas of streptozotocin (STZ) induced diabetic Wistar rats. Thirty-two (32) albino rats were divided equally into 4 groups. Groups A and B which served as normal (NC) and diabetic (DC) controls respectively, received placebo treatment. The diabetic test groups C and D were respectively treated with combined extracts of VA and GL (200mg/kg b. w., p. o.) and insulin, (humulin 5 IU/kg, s.c.) for 28 days. Thereafter, the animals were sacrificed and blood and pancreas were collected for serum glucose and histological evaluation, respectively. Changes in animal weight were also measured within the period. From the results it was revealed that both the combined extracts and humulin significantly increased the animals’ body weight (p<0.05) from -10.5% reduction in the DC, to 7.6% and 8.9% respectively. In the same order, serum glucose significantly decreased (p<0.05) by 12.49% and 14.96% after the 28-day treatment compared to DC. The extent of reversal of hyperglycemia in the extract treated animals compared well with the insulin treated group. The biochemical results were corroborated with results of histological evaluations: The pancreatic β-cells of DC animals which were distorted and degenerated with shrunken cell mass as against prominent islet cells with normal exocrine pancreas of NC animals became rapidly proliferated upon intervention with the combined extracts, suggesting a possible regeneration of the islet cells. On the otherhand, intervention with humulin did not produce observable differences in the cyto-architecture of the pancreatic islets compared to the diabetic control, confirming an extra-pancreatic mechanism of insulin.