of the new endothelial cells into a blood vessel.
When the process of angiogenesis interupted it will
efect the distribution of nutrition to the body part of
the embryo that can efect the development of body
weight and thickness.
2 MATERIALS AND METHOD
The tools used in this research include egg
incubator, egg tray, petri dish, Effendorf tube, vortex
mixer, scales, organ pots, dispossible 1 cc onemade,
dispossible 5 cc Onemade, object glass, cover glass,
tweezers, Scissors, egg shell punch, autoclaves,
staining jar, masking tape, glove, pipette, camera,
digital scales and calipers. The materials used in this
study include the unincubated chicken eggs,
turmeric rhizome simplisia powder, ringer's lactate
solution, NaCl 0.9% liquid and DMSO 100% liquid.
Preparation of the turmeric rhizome simplisia
with making a solution of DMSO 2% by dissolving
DMSO 100% into the solution of NaCl 0.9%.
Turmeric rhizomes simplisia powder as much as
0.48 mg/gr eggs for the treatment group of P1 and
0.96 mg/gr eggs for group treatment P2 diluted with
DMSO 2% to reach the volume of 1.25 mL then
homogenized using a vortex mixer.
The location of the egg sack was marked by a
pencil, as well as on the top of a egg sack for the
spot to punch the eggs. The next step was to
punched the egg as wide as the syringe needle in the
marked part and then injected the turmeric rhizome
simplisia as much as 0.25 mL in the P1 group and as
much as 0.25 mL in the P2 group. The hole where
was the injection done than be closed using masking
tape and the egg labeled.
The incubation of eggs was done in incubators
with a temperature of 38°C for 72 hours then carried
out the injection of the turmeric rhizome simplisia
and incubated at the temperature of 38°C until the
embryo reaches the 10th days old. The position of
the egg in the incubation was vertically with the egg
sack located above.
The egg shells are broken down by knocking
the egg sack using tweezers without cange the
position of the eggs. The embryo from the egg
caried out into the petri dish then the embryo are
taken and soaked in ringer's lactate solution while
shake several times to remove the remaining egg
yolks. A clean embryo was measured the body
weight by digital scale and the thickness by calipers.
The body weight was measured to within 0.1g
using electronic scales while the body width was
taken across the widest point of the abdomen in
embryos (Browne, 2006).
3 RESULT
The results showed that the turmeric rhizome
simplisia at dose of 0,48 mg/gr caused died in one of
incubated chicken egg and at dose of 0.96 mg/gr
caused two of five incubated chicken egg was died.
The factor that caused died in incubated egg with
inoculation of trumeric rhizome simplisia was not
known exactly, however, the embryos have been
death when we hasvest it. We suggest that apoptosis
is probably a cause of death of chicken embryos that
was inoculated with turmeric rhizome simplisia.
Piwocka et al (2001) said that curcumin a yellow
pigment from Curcuma longa, curcumin may induce
apoptosis in normal and cancer cells, it induces
nonclassical apoptosis via a still-unrecognized
mechanism, which leads to chromatin degradation
and high-molecular-weight DNA fragmentation. In
the other hand, research that conducted by Chen et al
(2010) showed that curcumin induces apoptotic
injury effects on mouse blastocysts through ROS
generation, and further promotes mitochondria-
dependent apoptotic signaling processes to impair
sequent embryonic development. The left eggs from
group of dose 0.48 mg/gr (P1) and 0.98 mg/gr (P2)
have decreased of body weight and thicness
compared with negative control group (K-) (Figure 1
and 2).
Figure 1. Body weight of Chicken Embryo Inoculated
with Turmeric Rhizome Simplisia and Incubated for 10
Days.