This study aimed to determine the potential activity of standardized ethanolic extract of red spinach as prevention against atherosclerosis based on the level of Low-Density Lipoprotein (LDL) and histopathological feature of aorta in male Sprague-Dawley rats induced by high-fat, high-cholesterol diet. A total of 42 animals was divided into 6 groups: normal control group, negative control group, positive control group (0.9 mg/kgBW of simvastatin), first intervention group (200 mg/kgBW of red spinach extract), second intervention group (400 mg/kgBW of red spinach extract), and third intervention group (800 mg/kgBW of red spinach extract). From the first day up to the 66th day, all the groups, except the normal control group and negative control group, were administered simvastatin (positive control) and extract of amaranth (intervention). Then, from the eighth day until Day 66, induction of high-fat and high-cholesterol diet was given in two hours after the simvastatin and red spinach extract administration. The determination of LDL parameters was conducted on Day 0, Day 35, and Day 67. On the 67th day, the animals were dissected to examine the aortic histopathological parameters. The results showed that the ethanolic extract of red spinach with a dose of 200 mg/kgBW, 400 mg/kgBW, and 800 mg/kgBW statistically demonstrated a significant difference (p<0.05). The histopathological feature of the aorta in the treatment indicated the absence of fat in the blood vessel walls or even of foam cells supporting thereby the result of LDL level. This means there was a significant effect of ethanolic extract of red spinach on the prevention against atherosclerosis based on the level of Low-Density Lipoprotein and the histopathological feature of aorta in male Sprague-Dawley rats.

1.
R.
Jannah
,
Widodo
,
J. F.
Putri
,
S.
Rahman
and
M.
Lukitasari
,
J. Biotropica
1
,
2
,
62
65
(
2013
).
2.
Anonymous
,
Household Health Survey
(
Indonesia’s Health Ministry
,
Jakarta
,
2012
) (accessed in www.depkes.go.id, Mei 14th 2016).
3.
Anonymous
,
Central Data and Information The Condition of Heart Health
(
Indonesia’s Health Ministry
,
Jakarta
,
2014
) p.
2
(accessed Mei 14th 2016).
4.
Anonymous
,
Farmakope Herbal Indonesia Edisi 1
(
Indonesia’s Health Ministry
,
Jakarta
,
2009
), pp.
15
20
.
5.
J. T. R.
Clark
,
A Clinical Guide To Inherited Metabolic Disease
(
Cambridge University Press
,
Cambridge
,
1996
), pp.
136
141
.
6.
Alam
and
S.
Rao
,
Asian Journal of Pharmacology and Toxicology
1
,
1
,
12
16
(
2013
).
7.
D. A.
Pradana
,
F. S.
Rahmah
and
T.
Setyaningrum
,
Jurnal Sains Farmasi & Klinis
2
,
2
,
122
128
(
2016
).
8.
J.
Jabbar
,
I.
Siddiqui
and
Q.
Reza
,
JPMA
56
,
2
(
2006
).
9.
Anonymous
,
Materia Medika Indonesia Jilid V
(
Indonesia’s Health Ministry
,
Jakarta
,
1989
), p.
27
.
10.
Anonymous
,
General Standard of the Drug Plant of Extract
(
Indonesia’s Health Ministry
,
Jakarta
,
2000
), p.
13
.
11.
Widaningrum, Miskiyah and Suismono
,
Buletin Teknologi Pascapanen
3
,
18
25
(
2007
).
12.
Anonymous
,
Determination Of Limit Microbial Contamination And Chemicals in Food
(
Regulatory Agency Of Drug And Food Republic Of Indonesia
,
Jakarta
,
2009
), p.
9
.
13.
14.
Y. Q.
Zhu
,
Y.
Huang
and
Z. Y.
Chen
,
J. Nutr Biochem
11
,
14
21
(
2000
).
15.
Y.
Desmiaty
and
H.
Ratih
,
Artocarpus.
8
,
2
,
106
9
(
2008
).
16.
Yanuartono
,
J. Sain Vet.
25
,
1
,
1
10
, (
2007
).
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