. 2013 Sep 26;2(4):194–205. doi: 10.3390/antiox2040194

Table 5.

Lipid and protein damage in rat cerebellum, cerebral cortex, hippocampus and liver cells treated with L. alba.

Treatments	Lipid damage (nmol of TBARS/mg of protein)				Protein damage (nmol of DNPH/mg of protein)
Treatments	Cerebellum	Cerebral Cortex	Hippocampus	Liver	Cerebellum	Cerebral Cortex	Hippocampus	Liver
Control	12.85 ± 0.90 ^b	7.17 ± 0.41 ^c	26.80 ± 1.67 ^c	14.14 ± 1.26 ^c	0.76 ± 0.01 ^c	0.58 ± 0.01 ^c	0.11 ± 0.01 ^b	0.26 ± 0.02 ^b
H₂O₂	24.05 ± 1.46 ^a	43.73 ± 3.75 ^a	76.32 ± 5.36 ^a	36.75 ± 0.89 ^a	2.06 ± 0.03 ^a	1.63 ± 0.03 ^a	0.18 ± 0.01 ^a	0.64 ± 0.02 ^a
L. alba	11.46 ± 0.99 ^b^,c	8.12 ± 0.57 ^b^,c	25.48 ± 1.92 ^c	13.67 ± 0.73 ^c	0.21 ± 0.02 ^d	0.50 ± 0.03 ^d	0.08 ± 0.01 ^c	0.24 ± 0.01 ^b
L. alba + H₂O₂	9.90 ± 0.89 ^c	10.73 ± 0.27 ^b	38.87 ± 0.98 ^b	27.57 ± 1.18 ^b	0.92 ± 0.03 ^b	1.36 ± 0.01 ^b	0.10 ± 0.01 ^b^,c	0.29 ± 0.01 ^b

Tissues were incubated for 30 min in the presence of the Lippia alba extract (10 μg/mL) followed by 1 h in the presence of H₂O₂. Different letters correspond to values significantly different using analysis of variance (ANOVA) and Tukey’s post hoc test for p ≤ 0.05 for each tissue evaluated.