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Medicinus - Dexa Medica

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NF-kB, TNFα, VCAM-1 and P-selectin. These markers<br />

were important in inflammation related to atherosclerosis.<br />

RAW 264.7 cells were able to down-regulate<br />

the expressions of NF-kB by 45% (Fig. 1a), TNFα by<br />

22% (Fig. 1b), VCAM-1 by 22% (Fig. 1c) and P-selectin<br />

(Fig. 1d) by 20%. To ascertain the effect of DLBS1033<br />

on macrophage, a macrophage binding assay to Vascular<br />

Smooth Muscle Cells (VSMC) was conducted. As<br />

seen in Fig.2, the attachment of monocytic RAW264.7<br />

to VSMC was reduced to a level 10% of the control<br />

cells. This suggested that reduction in expression of<br />

adhesion molecules V-CAM and P-Selectine, were<br />

able to reduce binding macrophage to VSMC.<br />

Effects of DLBS1033 on Plaque Stabilization Marker<br />

Plaque stabilization is also related to prevention of<br />

acute CVD events. Suppression of about 25-50% in<br />

the expression of MMP-9, a marker of plaque instability<br />

was seen after treatment with DLBS1033 (Fig.<br />

3) suggesting that this bioactive protein fraction has<br />

the ability to control plaque stabilization.<br />

Effects of DLBS1033 on Smooth Muscle Cells Viability<br />

and Migration<br />

We observed the effects of DLBS1033 on VSMC cell<br />

viability. As can be inferred in Fig. 4a, DLBS1033, was<br />

able to inhibit the proliferation of the VSMC significantly.<br />

In addition, after 4 hours following administration<br />

of DLBS1033, VSMC migration in the presence<br />

of Angiotensin II was significantly reduced to a level<br />

2-fold lower when compared to that of Angiotensin<br />

II alone (Fig. 4b). The data suggested that DLBS1033<br />

had a positive effect on smooth muscle cells viability<br />

and migration. Thus reducing the potentiality of<br />

plaque enlargement via intimal medial thickness<br />

and/or plaque stability. In addition, the expression of<br />

original article<br />

Control DLBS1033<br />

Figure 2. Effect of DLBS1033 on the attachment of monocytic RAW246.7 cells to Vascular Smooth Muscle Cells (VSMC).<br />

research<br />

growth signal JAK1 (Fig. 5a) and STAT1 (Fig. 5b) were<br />

also reduced in the presence of DLBS1033 signifying<br />

the growth arresting effect of DLBS1033 on VSMC.<br />

Figure 3. Effect of 0.5 μg/ml DLBS1033 on expression of MMP-9.<br />

MEDICINUS 24(1), January 2011 21

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