1,381
Views
19
CrossRef citations to date
0
Altmetric
Research Article

Biological activity of HPLC-characterized ethanol extract from the aerial parts of Haplophyllum tuberculatum

, , &
Pages 151-156 | Received 17 Jan 2013, Accepted 22 Jun 2013, Published online: 19 Sep 2013

Figures & data

Figure 1. HPLC–MS profile of the polyphenols obtained from ethanol extract of Haplophyllum tuberculatum aerial parts at 254 nm, 280 nm and 340 nm.

Figure 1. HPLC–MS profile of the polyphenols obtained from ethanol extract of Haplophyllum tuberculatum aerial parts at 254 nm, 280 nm and 340 nm.

Figure 2. Effect of Haplophyllum tuberculatum ethanol extract on cell viability. U373-MG cells were treated with plant extract (range of concentrations from 0.025 to 250 µg/mL) for 24 h. Triton X-100 was employed as negative control. Results were expressed as mean of the percentage of control cells (100%) ± standard deviation (S.D.). *p < 0.05 versus control cells; $p < 0.05 versus ethanol extracts at all assayed concentrations.

Figure 2. Effect of Haplophyllum tuberculatum ethanol extract on cell viability. U373-MG cells were treated with plant extract (range of concentrations from 0.025 to 250 µg/mL) for 24 h. Triton X-100 was employed as negative control. Results were expressed as mean of the percentage of control cells (100%) ± standard deviation (S.D.). *p < 0.05 versus control cells; $p < 0.05 versus ethanol extracts at all assayed concentrations.

Figure 3. Protective effect of Haplophyllum tuberculatum ethanol extract against H2O2-induced loss in viability. U373-MG cells were treated with plant extract (range of concentrations from 0.025 to 250 µg/mL) for 24 h, prior to 1 mM H2O2 exposure (30 min). Triton X-100 was employed as negative control. Results were expressed as a mean of the percentage of control cells (100%) ± standard deviation (S.D.). *p < 0.05 versus control cells; #p < 0.05 versus H2O2.

Figure 3. Protective effect of Haplophyllum tuberculatum ethanol extract against H2O2-induced loss in viability. U373-MG cells were treated with plant extract (range of concentrations from 0.025 to 250 µg/mL) for 24 h, prior to 1 mM H2O2 exposure (30 min). Triton X-100 was employed as negative control. Results were expressed as a mean of the percentage of control cells (100%) ± standard deviation (S.D.). *p < 0.05 versus control cells; #p < 0.05 versus H2O2.

Figure 4. Protective effect of Haplophyllum tuberculatum ethanol extract against H2O2-induced intracellular ROS production. U373-MG cells were treated with plant extract (0.025, 0.25 and 0.025 µg/mL) for 24 h, prior to 1 mM H2O2 exposure (30 min). Results were expressed as a mean of the percentage of control cells (100%) ± standard deviation (S.D.). *p < 0.05 versus H2O2.

Figure 4. Protective effect of Haplophyllum tuberculatum ethanol extract against H2O2-induced intracellular ROS production. U373-MG cells were treated with plant extract (0.025, 0.25 and 0.025 µg/mL) for 24 h, prior to 1 mM H2O2 exposure (30 min). Results were expressed as a mean of the percentage of control cells (100%) ± standard deviation (S.D.). *p < 0.05 versus H2O2.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.