This study purposed to prove the potential of β-
1,3 / 1,6-D-Glukan (Polysaccharide Peptide) from
Miselia Ganoderma Lucidum as an antioxidant and
endothelial protective in STEMI and NSTEMI
patients with Diabetes as a risk factor. Data analysis
showed that extract of Ganoderma Lucidum could
reduce MDA levels significantly (p = 0.03), it can
significantly increase SOD (p = 0.00), decrease in
CEC levels significantly (p= 0,02), and significantly
increase in SOD level (p = 0.016). This data shows
that β-1,3 / 1,6-D-glucan (Polysaccharide Peptide)
has an antioxidant effect and increases the potential
of endothelial cells in carrying out angiogenesis even
in oxidative stress conditions and it is associated with
SOD improvement, especially MnSOD. β-1,3 / 1,6-
D-Glucan (Polysaccharide Peptide) increases the
expression of MnSOD and increases its antioxidant
activity. This increase can then reduce free radicals in
endothelial cells and increase cell resistance to
oxidative stress.
SOD has enzymatic activity to scavenge on
superoxide anion molecules (O2), through the
mechanism of redox reactions. Under oxidized
conditions, SOD will release excess electrons in
superoxid anions, and release O2 molecules. Under
reduced conditions, SOD will catalyze the reaction of
superoxid anions with hydrogen cations (2H +) to
form hydrogen peroxide (H2O2) which is more
unreactive. Determination of the form of reduced or
oxidized SOD, is determined by the amount of redox
from metal ions that are conjugated with SOD.
Furthermore, H2O2 will be catalyzed further by
enzymes catalase and glutathione peroxidase (Fukai
and Ushio-Fukai, 2011).
At high conditions of free radicals, there is an
initial response to an increase in SOD production,
specifically Cu / ZnSOD through the PI3K / Akt
transmission pathway and NF-κB transcription factor
in cells exposed to oxidants. However, in conditions
of high free radicals that continue, causing problems
in the process of SOD formation, especially in
MnSOD and EC SOD. MnSOD is made on
mitochondria, which require "mitochondrial import
machines" to be used in the cytosol and carry out their
functions. In high conditions of free radicals, there is
a disturbance in the process of important
mitochondrial, which can reduce the level of
cytosolic MnSOD (Candas and Li, 2014). In addition,
SOD scavenge metabolites, namely H2O2 can also be
the amount of functional SOD2 protein, also can be
displayed mRNA from SOD2. It can act as H2O2
affecting the amount of SOD2 protein in the post-
translational process (Candas and Li, 2014).
Malondialdehyde (MDA) is a product of lipid
peroxidation and one of the oxidant markers most
often studied. MDA is involved in many disease such
as cancer, Alzheimer’s, diabetes and heart disease
observed an increase in MDA which contribute to
heart disease. Other research states that agents that
decrease MDA and increase SOD provide benefits
and are even considered as therapeutic agents for
heart disease because they can reduce oxidative stress
in the body (Kim, Yun and Kwon, 2016).
Endothelial dysfunction is characterized by a state
of endothelial stiffness, pro inflammation, and pro
thrombi nature. This occurs in most cardiovascular
diseases, such as coronary disease, peripheral
vascular disease, hypertension, chronic heart failure,
diabetes, chronic kidney failure, and severe viral
infections. High free radicals cause oxidative stress,
and can cause endothelial dysfunction.
Cardiovascular risk factors are associated with an
increase in ROS sources such as NADPH oxidase,
xanthine oxidase, cyclooxygenase and mitochondria.
Free radicals can disrupt the balance of nitric oxide,
damage the endothelium, and if it occurs in a long
time, will affect the permeability of blood vessels,
causing toxic substances easily enter the tissues.
Oxidative stress that occurs can also cause increased
proliferation of vascular smooth muscle cells,
increase in metalloproteinase matrix and be involved
in the formation of atherosclerotic plaque (Alessio et
al., 2013).
Factors that can induce endothelial cell release
from the vascular wall include mechanical injury to
the vascular wall, after arterial or venous blood
sampling, and acute plaque rupture. ROS activity
together with prolonged inflammation that disrupts
the integrity of integrins and cadherins can also cause
endothelial cell release. In this study, the results
obtained by giving PsP of Ganoderma Lucidum, a
significant decrease in the number of CEC compared
with placebo. This indicates that PsP Ganoderma
Lucidum can improve endothelial dysfunction that
occurs in the process of atherosclerosis. CEC itself is
known that can be induced through various processes
that occur in atherosclerosis, such as persistent
inflammation and high free radical conditions
(Rajendran et al., 2013).
Protease enzymes and pro-inflammatory
cytokines produced will disrupt the integrity of
integrin and cadherin proteins that function for
endothelial cell adhesion (Schmidt, Manca and
Hoefer, 2015). The number of CECs in addition to
indicating endothelial dysfunction, also gives an idea
of the severity of the atherosclerotic process.
Sugimoto et al. reported that there was a positive