Balanites Aegyptiaca Fruit extract for managing sugarcane woolly aphid

2019 ◽  
Vol 81 (1) ◽  
pp. 163
Author(s):  
S. S. Nalge ◽  
A. S. Wabale
2016 ◽  
Vol 5 (1) ◽  
pp. 35-37
Author(s):  
Gereziher Geremedhin Sibhat ◽  
◽  
Mebrahtom Gebrelibanos Hiben ◽  

Prescription and/or over the counter medications when taken together with certain foods or herbal substances, leads to either increase or decrease a drug’s therapeutic out comes or adverse effects. It has been reported that a number of plant materials alter some pharmacokinetic parameters of chloroquine when administered concurrently. In some malarious areas of Ethiopia like Tigray region where chloroquine is used as antimalarial drug, medicinal and/or food plants are commonly consumed as herbal medicines or as food items. Thus, this study was aimed to evaluate the potential consequence of oral co-administration of hydroalcoholic fruit extract of Balanites aegyptiaca and leaf latex of Aloe camperi on the antimalarial effectiveness of chloroqine. Extract alone and extract in combination with chloroquine were tested against plasmodium berghie infected mice using peters four day suppressive method. Acute toxicity study was also carried out. The present study revealed that concurrent administrations of leaf extract of Balanites aegyptiaca and leaf leatx of Aloe camperi was found to increase parasitemia suppression potential of chloroquine. From the study it can be concluded that Balanites aegyptiaca and leaf leatx of Aloe camperi can potentiate malaria suppression of chloroquine.


2020 ◽  
Vol 10 (2) ◽  
pp. 45-52
Author(s):  
Idi Audu Wakawa ◽  
Abubakar Chiroma

Chemicals have been used to anaesthetize fish but due to their hazardous effects on the environment, fish and humans environmentally friendly plant anaesthetics are being sought. Fruit of Desert date (Balanites aegyptiaca) is nontoxic to humans but has been reported to have anaesthetic potentials on fish. This study investigates anaesthetic effect of aqueous crude fruit extract of B. aegyptiaca on African catfish (Clarias gariepinus) fingerlings. Phytochemical and proximate compositions of the fruit were screened. Exactly 120 C. gariepinus fingerlings (mean weight 32.13±2.43g and mean total length 23.88±2.11cm) were used for the experiment. A total of 10 fingerlings were exposed to each of 2.00, 2.50, 3.00, 3.50 and 4.00g/L concentrations of aqueous crude fruit extract of B. aegyptiaca and a control in 6 plastic tanks (45x28x25cm) filled with 10L of tap water. Setup was arranged in randomized block design and replicated. Temperature, dissolved oxygen, pH, free carbon dioxide and total alkalinity were monitored. Results revealed long mean induction (25.05±3.35 min) and recovery (108.35±2.45 min) times with resultant mortalities (40%) of C. gariepinus fingerlings. significant correlation (P<0.01) exists between concentration of the fruit extract and induction time as well as between fruit extract concentrations and survival of fingerlings. Aqueous crude fruit extract of B. aegyptiaca is, therefore, not effective for anaesthetization of C. gariepinus fingerlings hence should be avoided. Keywords: Anaesthetic, Balanites aegyptiaca, Clarias gariepinus


Author(s):  
Thecan Caesar-Ton That ◽  
Lynn Epstein

Nectria haematococca mating population I (anamorph, Fusarium solani) macroconidia attach to its host (squash) and non-host surfaces prior to germ tube emergence. The macroconidia become adhesive after a brief period of protein synthesis. Recently, Hickman et al. (1989) isolated N. haematococca adhesion-reduced mutants. Using freeze substitution, we compared the development of the macroconidial wall in the wild type in comparison to one of the mutants, LEI.Macroconidia were harvested at 1C, washed by centrifugation, resuspended in a dilute zucchini fruit extract and incubated from 0 - 5 h. During the incubation period, wild type macroconidia attached to uncoated dialysis tubing. Mutant macroconidia did not attach and were collected on poly-L-lysine coated dialysis tubing just prior to freezing. Conidia on the tubing were frozen in liquid propane at 191 - 193C, substituted in acetone with 2% OsO4 and 0.05% uranyl acetate, washed with acetone, and flat-embedded in Epon-Araldite. Using phase contrast microscopy at 1000X, cells without freeze damage were selected, remounted, sectioned and post-stained sequentially with 1% Ba(MnO4)2 2% uranyl acetate and Reynold’s lead citrate. At least 30 cells/treatment were examined.


Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
S Mahattanadul ◽  
S Nima ◽  
S Kasiwong ◽  
S Tewtrakul ◽  
P Tansakul

2012 ◽  
Vol 2 (12) ◽  
pp. 58-59
Author(s):  
suvarna M N Vinay ◽  
◽  
Ramesh B S Ramesh B S ◽  
Venkatachalapathy R Venkatachalapathy R ◽  
Makari Hanumantappa K ◽  
...  

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