6 research outputs found
Malondialdehyde serum concentration in Wistar rats fed a high-fructose diet (66% fructose), treated with water (control) or hydroethanolic extract from the leaves of <i>Jacaranda decurrens</i> subsp. <i>symmetrifoliolata</i> (E-Jds, 200 mg/Kg), for 60 days by gavage.
<p>*P<0.05 <i>vs.</i> E-Jds.</p
AAPH-induced lipid peroxidation of erythrocytes. Concentration of malondialdehyde (MDA) at 180 min after adding the AAPH hemolysis inducer in 2.5% erythrocytes incubated with different concentrations of ascorbic acid and hydroethanolic extract of <i>Jacaranda decurrens</i> subsp. <i>symmetrifoliolata</i> (E-Jds) leaves compared with 5% He + AAPH.
<p>*** P < 0.001 <i>vs.</i> He+AAPH.</p
Hemolysis assessment at (A) 60, (B) 120, (C) 180 and (D) 240 min after addition of AAPH in erythrocytes at 2.5% incubated with different concentrations of ascorbic acid and E-Jds.
<p>*** P<0.001 <i>vs.</i> HE+AAPH.</p
IC<sub>50</sub> and maximum activity of DPPH free radical scavenging of standard antioxidants and the hydroethanolic extract from the leaves of <i>Jacaranda decurrens</i> subsp. <i>symmetrifoliolata</i> (E-Jds).
<p>BHT â=â butylhydroxytoluene</p><p>IC<sub>50</sub> and maximum activity of DPPH free radical scavenging of standard antioxidants and the hydroethanolic extract from the leaves of <i>Jacaranda decurrens</i> subsp. <i>symmetrifoliolata</i> (E-Jds).</p
Activity of the antioxidant enzymes glutathione peroxidase (A), superoxide dismutase (B), and catalase (C) in human erythrocyte lysates incubated with E-Jds at different concentrations.
<p>* P<0.05 and *** P<0.001 <i>vs.</i> Control.</p
Hemolysis assessment at 2.5% (He) incubated with different concentrations of E-Jds for 240 min.
<p>E-Jds â=â hydroethanolic extract from the leaves of <i>Jacaranda decurrens</i> subsp. <i>Symmetrifoliolata</i>. The data no are statistically different.</p