Gold nanoparticle-assisted enhancement in bioactive properties of Australian native plant extracts, Tasmannia lanceolata and Backhousia citriodora

2020 ◽  
Vol 112 ◽  
pp. 110922 ◽  
Author(s):  
Roshanak Khandanlou ◽  
Vinuthaa Murthy ◽  
Hao Wang
Data in Brief ◽  
2016 ◽  
Vol 7 ◽  
pp. 848-867 ◽  
Author(s):  
Damian H. Adams ◽  
Qingyao Shou ◽  
Hans Wohlmuth ◽  
Allison J. Cowin

2014 ◽  
Vol 30 (6) ◽  
pp. 1755-1762 ◽  
Author(s):  
Bita Zaferanloo ◽  
Trung D. Quang ◽  
Smita Daumoo ◽  
Mahmood M. Ghorbani ◽  
Peter J. Mahon ◽  
...  

Planta Medica ◽  
2019 ◽  
Vol 85 (16) ◽  
pp. 1242-1252
Author(s):  
Yun-Chae Lee ◽  
Sung-Gook Cho ◽  
Sang-Woo Kim ◽  
Jeong Nam Kim

AbstractNumerous chemically synthesized compounds are widely used in oral hygiene products. However, due to their potential risk, there is a need to improve the safety and quality of dental care by seeking alternative control agents such as those naturally found in plant materials. Here we assessed antibacterial potentials of extracts from 100 species of Korean native plants against Streptococcus mutans on cariogenesis. Among those, extracts from five plants (Arctii Fructus, Caryopteris incana, Aralia continentalis, Symplocarpus renifolius, and Lamium amplexicaule) showed a growth inhibition of S. mutans. The five extracts were further individually evaluated for their minimal inhibitory concentration and minimal bactericidal concentration. Interestingly, a synergistic antibacterial activity was observed with the combination of sodium fluoride and the plant extracts. To determine the anti-biofilm activity of plant extracts, S. mutans was treated with increasing concentrations of the extracts in the range from 1250 to 3750 µg/mL. When S. mutans was grown in the defined biofilm medium containing the individual extracts of 47 species, the biofilm amount markedly decreased compared to that of a negative control. Notably, the extract of S. renifolius significantly downregulated the gtf and spaP genes for synthesis of glucan and adhesive proteins in S. mutans, and L. amplexicaule decreased the expression of gtfD gene. Therefore, these results demonstrate that the five plant extracts modulate survival and pathogenesis of S. mutans by growth inhibition and downregulation of the gene(s) implicated in biofilm formation.


2010 ◽  
Vol 50 (6) ◽  
pp. 449 ◽  
Author(s):  
P. G. Hutton ◽  
Z. Durmic ◽  
P. E. Vercoe

The Australian native plant Eremophila glabra was tested as a potential agent for preventing lactic acidosis in sheep after it was observed to be effective against acidosis in vitro. Ruminally fistulated wethers were infused via rumen cannula with single doses of kibbled wheat (14 g/kg bodyweight) and either virginiamycin (Eskalin500; AB, 80 mg/kg of wheat plus 100 g milled oaten hay/kg of wheat, n = 6), E. glabra (EG, 100 g freeze-dried and milled leaf material per kg of wheat, n = 10) or milled oaten hay (Control, 100 g milled oaten hay/kg of wheat, n = 16). Rumen samples were collected immediately before infusion and then 2, 4, 6, 8, 12, 16 and 24 h after the infusion. The samples were analysed for pH, D-lactate, volatile fatty acids (VFA) and osmolality. Rumen pH and D-lactate values indicative of acidosis were detected in the Control and EG groups. The pH nadir of the rumen was 12 h after the wheat infusion, at which time the values in the EG (pH = 4.87) and Control (pH = 5.09) groups were lower (P < 0.05) than in the AB group (pH = 5.63) and the D-lactate concentrations were higher (P < 0.05) in the EG and Control groups (24 mmol/L and 15 mmol/L, respectively) than in the AB group (0.9 mmol/L). At the same time, total VFA concentration was higher (P < 0.05) in the AB group (102 mmol/L) than in the Control (65 mmol/L) and the EG (14 mmol/L) groups. Rumen osmolality did not differ between groups. Virginiamycin was effective at preventing lactic acidosis. However, the inclusion of dried leaves from E. glabra at a similar level that was effective in vitro did not prevent lactic acidosis in vivo, and the reasons behind this remain unclear. The study demonstrates the difficulty in converting in vitro results to in vivo and highlights the need to test the plant at higher doses in vivo.


Taxon ◽  
1988 ◽  
Vol 37 (4) ◽  
pp. 932
Author(s):  
R. S. Cowan ◽  
Peter J. Langkamp

2012 ◽  
Vol 27 (6) ◽  
pp. 471-481 ◽  
Author(s):  
H.E. Smyth ◽  
J.E. Sanderson ◽  
Y. Sultanbawa

2011 ◽  
Vol 61 (2) ◽  
pp. 234-246 ◽  
Author(s):  
K. B. Ireland ◽  
D. Hüberli ◽  
B. Dell ◽  
I. W. Smith ◽  
D. M. Rizzo ◽  
...  

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