scholarly journals The Climbing Performance, Neuromuscular Transmitter (ACHE) Activity, Reproductive Performance and Survival of Drosophila melanogaster Fed Diet with Mangifera indica Cold Aqueous Leaf Extract

Author(s):  
Etuh Monday Alexander ◽  
John Chinyere Aguiyi ◽  
Iorjiim Walter Mdekera ◽  
Ochala Sunshine Ogwu ◽  
Oyeniran Oluwatosin Imoleayo ◽  
...  

Objective: To screen the toxic effect of Mangifera indica aqueous leaf extract in Drosophila melanogaster. Materials and Methods: Phytochemical screening was carried out. 20 Adult flies were exposed to 7.5 mg, 15 mg,  30 mg, 45 mg and 100 mg /10 g diet for acute toxicity (168hrs) while 50 flies were exposed to 2.5 mg, 5 mg and 10 mg/10 g diet for sub chronic (28 days). All concentrations were prepared in 1000µl of distilled water and replicated three (3) times. Diet+1000µl of Distilled water served as control. Fecundity/developmental toxicity, Climbing and AChE activities were carried out by exposing flies to the sub-chronic concentrations for 5 days. Results: Phytochemical screening revealed the presence of alkaloids, phenols, flavonoids, tannins, saponins and terpenoids. The acute toxicity test showed 100% mortality at 100 mg/ 10 g diet and 168hrs LC50 was 72.4 mg/10 g diet. The sub chronic toxicity test showed decrease in flies survival along concentration with a least survival at 10 mg/10 g diet. There was a slight reduction and elevation in the Climbing and AChE activities respectively but not statistically significant (p>0.05) compared to control. At 5 mg and 10 mg/10 g diet there was a delay in the development with few emerged flies. Conclusion: From the Results, it can be concluded that Mangiferaindica aqueous leaf extract may be toxic at high dose from 72.4 mg/10 g diet and might have an adverse effect on the development and survival of flies at sub chronic concentration as low as 2.5 mg/10g diet.

Author(s):  
Etuh, Monday Alexander ◽  
John C. Aguiyi ◽  
Ochala, Sunshine Ogwu ◽  
Omale Simeon ◽  
Oyeniran, Oluwatosin Imoleayo ◽  
...  

Objective: To evaluate in vivo antioxidant activity of Mangifera indica cold aqueous leaf extract.  Methods: A number of 50 adult flies were exposed to graded concentrations of Mangifera indca cold aqueous leaf extract, 2.5 mg/10 g diet, 5 mg/10 g diet and 10 mg/10 g diet for 5 days. Each concentration was prepared in 200 µl of distilled water and replicated five times. 10 g diet with 200 µl distilled water served as control. Mortality reading was taken at 24 hours interval. The flies were homogenized, centrifuged and the supernatant was used to assay for Glutathione-S-transferase (GST), Catalase (CAT) and Total thiol content. Results: The % mortality of flies after 5 days showed 32.5%, 0%, 15.5% and 37% in the control (10 g diet with 200 µl of distilled water), 2.5 mg/10 g diet, 5 mg/10 g diet and 10 mg/ 10 g diet respectively. There was elevation in total thiol content and high GST and CAT activity in 2.5 mg/10 g diet and 5 mg/10 g diet treated flies. Conclusion: The 100% and 85% survival of 2.5 mg/10 g and 5 mg/10 g diet-treated flies respectively and increase of fly antioxidant system after 5 days exposure at these concentrations may suggest protective activity of Mangifera indica in D. melanogaster.


2011 ◽  
Vol 4 (4) ◽  
pp. 206-210 ◽  
Author(s):  
George Asare ◽  
Phyllis Addo ◽  
Kwasi Bugyei ◽  
Ben Gyan ◽  
Samuel Adjei ◽  
...  

Acute toxicity studies of aqueous leaf extract ofPhyllanthus niruriPhyllanthus niruriis a plant with medicinal properties. It is often used to treat mild malaria and the elimination of renal stones. However, studies on its toxicity are scarce. The study was carried out to determine if the aqueous leaf extract ofP. niruriadministered to female Sprague-Dawley rats would illicit evidence of toxicity. Fifteen female rats weighing 150-200 g were divided into 3 groups. Rats in Group 1 were given a single low dose (LD) of 2 000 mg/kg b.w. of the extract by oral gavage within 24 hrs. Rats in Group 2 were given a single high dose (HD) of 5 000 mg/kg b.w. of the extract by oral gavage within 24 hrs. Rats in Group 3 were not given any extract but drinking water and served as the control group (C). All the rats were observed for signs of toxidromes for 14 days. On the 15thday, all the rats were sacrificed. Body organs were harvested for macroscopic examination. Urine and blood samples were drawn and analyzed. Hematological tests performed included full blood count and hemoglobin. Biochemical examinations included bilirubin, alanine aminotransferase (ALT), aspartate aminotransferase (AST), total protein, albumin, globulin, alkaline phosphatse (ALP), γ-glutamyltranspeptidase (GGT), urea, and creatinine. The results of the three groups were not significantly different. Examination of the various body organs did not show any abnormality. Thus no toxicity was observed at the levels administered. The LD50of the aqueous extract is > 5 000 mg/kg. b.w.


2021 ◽  
Vol 12 (1) ◽  
pp. 95
Author(s):  
Millicent Umaru ◽  
Kabiru Abubakar ◽  
Gabriel Uyaiabasi ◽  
Giaze Tijjani ◽  
Yusuf Alkali ◽  
...  

Author(s):  
Ezekiel E. Ben ◽  
Asuquo E. Asuquo ◽  
D. U. Owu

Background: The endocrinal abnormalities in diabetes mellitus as one of the numerous metabolic disorders is associated with derangement in exocrine functions of the pancreas and ultimately influences blood glucose regulation. Aim: The study was aimed at assessing the role of alpha-amylase and glycogen synthase in anti-diabetic potential of Terminalia catappa in diabetic rats.  Materials and Methods: Thirty five (35) Wistar rats were assigned to 5 groups of 7 animals each. Group 1 served as the control administered distilled water at 5ml/kg bodyweight and group 2 was a non diabetic group given orally, 130/kg body weight of aqueous leaf extract of Terminalia catappa.  Groups 3, 4 and 5 received a single dose of 150mg/kg body weight of alloxan solution intraperitoneally to induce diabetes and rats with blood glucose levels ≥200mg/dl after 72 hours were considered diabetic. This was followed by oral administration of 5ml/kg bodyweight of distilled water, 130mg/kg body weight of Terminalia catappa leaf extract orally and subcutaneous administration of insulin, 0.75U/kg body weight to groups 3 (diabetic), 4(diabetic + extract) and 5 (diabetic + insulin) respectively. Results: The results showed significant (P<.05) increase in serum level of alpha-amylase and glycogen synthase in both non-diabetic extract treated and diabetic groups when compared to control. But these enzymes significantly (P<.05) reduced in diabetic extract and insulin treated groups when compared to the diabetic group.  Conclusion: Therefore the hypoglycaemic potential of Terminalia catappa leaf extract could be attributed to its ability to reduce alpha-amylase level while lowered glycogen synthase might be secondary to reduction in blood glucose.


2016 ◽  
Vol 8 ◽  
pp. 22
Author(s):  
Elizabeth FB ◽  
Obikili E.N ◽  
Esom A. E ◽  
Anyanwu G.E

<p><strong>Background:</strong> Different parts of plants possess variable phytochemical compounds and LD<sub>50</sub>. <em>Crinum giganteum</em> (Gadalli) is one of the plants most commonly consumed in parts of Africa for its various medicinal values. Despite this popularity, the phytochemical screening and the toxicity of the leaf extracts were yet to be evaluated. This study was designed to identify    the bioactive agents and estimate the LD<sub>50</sub> for the aqueous leaf extract of gadalli. <strong>Method</strong>: Phytochemical screening was done using standard methods. Each bioactive agent and the LD<sub>50</sub> were estimated by Arithmetic methods of Karber. <strong>Results: </strong>Phytochemical analysis revealed high presence of alkaloids,  saponins, and slight presence of glycosides while the oral LD<sub>50 </sub>was found to be 200 mg/kg. <strong>Conclusion: </strong>The major active ingredients of<strong> </strong>aqueous leaf extract of gadalli are alkaloids and saponins. It is observed to be unsafe at 200mg/kg and above.</p><p><strong>Keywords: </strong>Phytochemicals, <em>Crinum Giganteum</em>, LD<sub>50</sub>, Alkaloids, Saponins, Glycosides</p><p> </p>


2015 ◽  
Vol 14 (7) ◽  
pp. 1231 ◽  
Author(s):  
OJ Sharaibi ◽  
OT Ogundipe ◽  
OA Magbagbeola ◽  
MI Kazeem ◽  
AJ Afolayan

2015 ◽  
Vol 5 (1) ◽  
pp. 52-57
Author(s):  
M. Dangambo ◽  
H. Kabara ◽  
A. Alhassan ◽  
M. Sule ◽  
M. Atiku ◽  
...  

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