Research Article

Antihypercholesterolemic and Antioxidative Potential of an Extract of the Plant, Piper betle, and Its Active Constituent, Eugenol, in Triton WR-1339-Induced Hypercholesterolemia in Experimental Rats

Table 2

Mean serum levels of hepatic marker enzymes in* Wistar rats.

Parameters testedGroup I
(control)
Group II
hypercholesterolemic,
saline treated
Group III
hypercholesterolemic,
lovastatin treated
Group IV
hypercholesterolemic,
Piper betle extract treated
Group V
hypercholesterolemic,
eugenol treated

AST
ALT
ALP
LDH

Sampling done 10 days after induction of hypercholesterolemia and 7 days after start of treatment.
Values represent the mean ± SD for observations made on five rats in each group.
Units: aspartate and alanine aminotransferases: µmoles × 10−2 of pyruvate liberated/min/mg protein.
Alkaline phosphatase: µmoles × 10−2 of phenol liberated/min/mg protein.
Lactate dehydrogenase: µmoles × 10−1 of pyruvate formed/minute/mg protein.
Statistical analysis: one-way analysis of variance (ANOVA), where significant, post hoc testing (least significant difference) done for intergroup comparisons.
AST: aspartate aminotransferase, ALT: alanine aminotransferase, ALP: alkaline phosphatase, LDH: lactate dehydrogenase.
aStatistically significant difference ( ) when compared with group I values.
bStatistically significant difference ( ) when compared with group II values.
cStatistically significant difference ( ) when compared with group III values.
dStatistically significant difference ( ) when compared with group IV values.