Phytochemical screening and in vitro anthelmintic activity of methanolic extract of Terminalia glaucescens leaf on Haemonchus contortus eggs.

Helminth infections remain a major constraint to livestock productivity in the tropical and subtropical areas across the world, especially in the areas where extensive grazing is practiced. The development of resistance to anthelmintic drugs, scarcity and high cost of purchase especially to farmers of low income in developing countries led to the need of alternative helminth control methods. However, there is an urgent need to discover novel drugs that can cure helminthiasis. A survey was carried out among agropastoralists to elicit information on the use of Ethnoveterinary Plants (EvPs) as alternative medicine for helminthiasis. The plants used by the agropastoralists were collected and identified at the Department of Botany Herbarium, University of Ibadan. The plant part was pulverized and cold macerated successively with n-hexane, ethyl acetate, methanol and aqueous methanol to obtain crude extracts. The methanolic extract was assayed against Haemonchus contortus at test concentrations (6.25, 12.5, 25, 50 and 100 µg/mL) and Albendazole at 25µg/mL were tested for the egg hatch inhibition assay. Eggs hatched and unhatched were counted under the microscope at 48, 96 and 144 hours (h). Among the EvPs identified, Terminalia glaucescens was the least utilized plant by the agropastoralists, and thus, selected for evaluation. The preliminary phytochemical screening revealed presence of tannin, alkaloid, saponin, flavonoid, phenolic, steroids, glycosides, triterpenes and reducing sugars. At 96 h, there were significant difference (P<0.05) in egg hatch inhibition (EHI) percentage at 100ug/mL (87.55), 50µg/mL (84.29) at inhibitory concentration (IC50 value 1.07) compared to 25ug/mL (100) for the Albendazol. At 144 h, there were no significant (P>0.05) differences observed in EHI values of methanolic extract of the leaf at 100ug/mL (89.69), 50ug/mL (87.06), 25ug/mL (85.53) and 12.5µg/mL (82.89) at IC50 value 1.08 compared to 25ug/mL (100) for the Albendazol. T. glaucescens leaf is a potential source of novel anthelmintics and further investigation should be carried out on its in vivo anthelmintic activity.

(22ß,25R)-3ß-Hydroxy-spirost-5-en-7-iminoxy-heptanoic acid exhibits anti-prostate cancer activity through caspase pathway.

Prostate cancer is one of the most common cancers in men. Diosgenin and related compounds are potential cytotoxic agents. Twelve diverse analogues of long chain fatty acid/ester of diosgenin-7-ketoxime have been prepared. Six of the analogues exhibited significant anticancer activity against a panel of human cancer cell lines with IC50 ranging from 12 to 35µM. Compound 16, the best representative of the series exerted S phase arrest in DU145 prostate cancer cells and induced apoptosis through caspase pathway. Additionally, these analogues inhibited lipopolysaccharide induced pro-inflammatory cytokines (TNF-α and IL-6) up to 47.7% and 23.3% respectively. Compound 16 was found to be safe in acute oral toxicity in Swiss albino mice up to 300mg/kg dose. The anticancer and antiinflammatory properties of compound 16 are important and can further be optimized for a better anti-prostate cancer candidate.

Synthesis of novel anticancer agents through opening of spiroacetal ring of diosgenin.

Diosgenin has been modified to furostane derivatives after opening the F-spiroacetal ring. The aldehyde group at C26 in derivative 8 was unexpectedly transformed to the ketone 9. The structure of ketone 9 was confirmed by spectroscopy and finally by X-ray crystallography. Five of the diosgenin derivatives showed significant anticancer activity against human cancer cell lines. The most potent molecule of this series i.e. compound 7, inhibited cellular growth by arresting the population at G0/G1 phase of cell division cycle. Cells undergo apoptosis after exposure to the derivative 7 which was evident by increase in sub G0 population in cell cycle analysis. Docking experiments showed caspase-3 and caspase-9 as possible molecular targets for these compounds. This was further validated by cleavage of PARP, a caspase target in apoptotic pathway. Compound 7 was found non-toxic up to 1000mg/kg dose in acute oral toxicity in Swiss albino mice.

Synthesis of diosgenin analogues as potential anti-inflammatory agents.

We herein report the synthesis of diosgenin analogues from commercially available diosgenin as the starting material. The structures of newly synthesised compounds were confirmed by (1)H NMR, (13)C NMR and mass spectrometry. All analogues were evaluated for in-vitro anti-inflammatory profile against LPS-induced inflammation in primary peritoneal macrophages isolated from mice by quantification of pro-inflammatory (TNF-α, IL-6 and IL-1ß) cytokines in cell culture supernatant using the ELISA technique followed by in-vitro cytotoxicity study. Among the synthesised analogues, analogue 15 [(E) 26-(3',4',5'-trimethoxybenzylidene)-furost-5en-3ß-acetate)] showed significant anti-inflammatory activity by inhibiting LPS-induced pro-inflammatory cytokines in a dose-dependent manner without any cytotoxicity. Efficacy and safety of analogue 15 were further validated in an in-vivo system using LPS-induced sepsis model and acute oral toxicity in mice. Oral administration of analogue 15 inhibited the pro-inflammatory cytokines in serum, attenuated the liver and lung injury and reduced the mortality rate in sepsis mice. Acute oral toxicity study showed that analogue 15 is non-toxic at higher dose in BALB/c mice. Molecular docking study revealed the strong binding affinity of diosgenin analogues to the active site of the pro-inflammatory proteins. These findings suggested that analogue 15 may be a useful therapeutic candidate for the treatment of inflammatory diseases.

Antibacterial activity of Jatropha multifida roots.

Hexane, ethyl acetate, chloroform and methanol successive extracts of Jatropha multifida yellow rootbark, red rootbark and rootwood effectively inhibited the growth of B. subtilis and S. aureus at concentration of 200 microg/disk.

The antimicrobial activity of roots of Jatropha podagrica (Hook).

Hexane, chloroform and methanol extracts of the rootwood and rootbarks of Jatropha podagrica were studied for their antimicrobial activity against 18 organisms. All the extracts exhibited some broad spectrum antibacterial activity, at a concentration of 20 mg/mL. The hexane extracts were generally more active than the chloroform and methanol extracts. The hexane extract of the yellow rootbark was the most active of all the extracts and its activity was comparable to that of gentamycin but better with regard to the control of S. aureus and B. cereus. Three of the extracts, hexane extract of the yellow rootbark and hexane and methanol extracts of the rootwood showed moderate antifungal activity against the yeast fungus, Candida albicans.

Studies on the seed oils of Parkia biglobosa and Parkia bicolor.

The seed oils of Parkia biglobosa and Parkia bicolor (Mimosaceae) have been analysed for their possible edible utility and to provide some physical data on both oils. The fatty acid composition of the oils was identified. Six major fatty acids were identified in the oil of P. bicolor while five were identified in that of P. biglobosa by Gas Chromatography (GC) and Gas Chromatography-Mass Spectroscopy (GC-MS). The two oils contained five similar fatty acids in almost the same ratios. Arachidic acid was the most abundant fatty acids (greater than forty per cent) in both oils. Other fatty acids in the oils were behenic, stearic, palmitic and linoleic acids. The sixth fatty acid in P. bicolor was an odd number of carbon atom and un unsaturated fatty acid (C20H37COOH) named bicolargic acid. The oils were also found to be non toxic.