Sains Malaysiana 46(9)(2017): 1457–1464
http://dx.doi.org/10.17576/jsm-2017-4609-14
Bioassay-Guided Fractionation of Emilia sonchifolia Extract
on the Induction of Ovarian Maturation in Fenneropenaeus merguiensis
(Pemeringkatan Bioasai
Berpandu Ekstrak Emilia sonchifolia pada Aruhan Kematangan
Ovari dalam Fenneropenaeus merguiensis)
LAMAI
MAIKAEO1,
WILAWAN
MAHABUSARAKAM1
& WILAIWAN CHOTIGEAT2*
1Department
of Molecular Biology and Bioinformatics, Faculty of Science, Prince
of Songkla University, Hat Yai, Songkhla, 90112, Thailand
2Department
of Chemistry, Faculty of Science, Prince of Songkla University
Hat
Yai, Songkhla, 90112,Thailand
Diserahkan:
31 Ogos 2016/Diterima: 17 Januari 2017
ABSTRACT
This study was carried
out to identify the active compounds of Emilia
sonchifolia on induction of ovarian maturation in Fenneropenaeus
merguiensis. The crude extracts from dichloromethane and acetone
were investigated in vitro. The crude extract from acetone
induced up-regulation of shrimp ovarian peritrophin (SOP)
and translationally controlled tumor protein (TCTP)
genes, which were highly expressed during early phase of ovarian
development higher than dichloromethane extract. Furthermore, fraction
14 (F14) from acetone extract up-regulated both of the SOP and the TCTP genes
to the greatest extent. Leading to in vivo study, the effect
of ribosomal protein L10a (RPL10a), which acts as shrimp ovarian
stimulator plus with F14 on shrimp ovarian maturation was investigated
by injection. The best result was observed in the group that received
RPL10a plus with F14 at 0.8 μg/g body weight of shrimp. The
RPL10a plus F14 enhanced the shrimp ovaries from undeveloped stage
to 57% of early developing stage within 15 days. Meanwhile, the
control group remained 100% of the undeveloped stage. Hence, F14
seems to play a positive role in the induction of shrimp ovarian
maturation. The component of F14 was identified using mass spectroscopy
and presented as 1,2-benzenedicarboxylic acid; 2,4-di-tert-butyl
phenol; 2,4,5-trimethoybenzylidene;palmitic acid; 1-heneicosyl formate;
1-heptadecanol; ethyl-4-ethoxybenzoate and stearic acid.
Keywords: E. sonchifolia; ovarian maturation; shrimp; SOP;
TCTP
ABSTRAK
Penyelidikan ini telah
dijalankan untuk mengenal pasti sebatian aktif Emilia sonchifolia pada induksi kematangan ovari dalam Fenneropenaeus
merguiensis. Ekstrak mentah daripada diklorometana dan aseton
dikaji secara in vitro. Ekstrak mentah daripada aseton meningkatkan
aruhan peritofin ovari udang (SOP) dan secara translasi mengawal gen tumor protein (TCTP)
yang dinyatakan pada fasa awal perkembangan ovari adalah lebih tinggi
daripada ekstrak diklorometana. Selain itu, pecahan 14 (F14) daripada
ekstrak aseton meningkatkan kedua-dua gen SOP dan TCTP ke
tahap terbaik. Ini membawa kepada kajian secara in vivo dengan
kesan ke atas protein ribosomal L10a (RPL10a), yang bertindak sebagai
perangsang ovari udang tambahan F14 pada kematangan ovari udang
yang dikaji melalui suntikan. Hasil terbaik yang diperhatikan dalam
kumpulan yang menerima RPL10a dicampur dengan F14 pada 0.8 μg/g
badan berat udang. RPL10a
dan F14 meningkatkan ovari udang daripada peringkat mundur ke 57% peringkat
awal pembangunan dalam masa 15 hari. Sementara itu, kumpulan kawalan
kekal 100% pada peringkat mundur. Oleh yang demikian, F14 seperti
memainkan peranan yang positif dalam aruhan kematangan ovari udang.
Komponen F14 dikenal pasti menggunakan spektroskopi jisim sebagai
asid 1,2-benzenadikarboksilik; 2,4-di-tert-butil fenol; 2,4,5-trimetoibenziliden;
asid palmitik; format 1-heneicosil; 1-heptadekanol; etil-4-etoksibenzoat
dan asid stearik.
Kata kunci:
E.
sonchifolia; kematangan ovari; SOP; TCTP; udang
RUJUKAN
Babu,
M.M., Sivaram, V., Immanuel, G., Citarasu, T. & Punitha, S.M.J.
2008. Effects of herbal enriched artemia supplementation over the
reproductive performance and larval quality in spent spawners of
the Tiger shrimp (Penaeus monodon). Turkish Journal of
Fisheries and Aquatic Sciences 8: 301-307.
Benzie,
J.A.H. 1998. Penaeid genetics and biotechnology. Aquaculture
164: 23-47.
Chen,
X-W., Wei, Y-Y., Zhou, W-P., Pan, M-J. & Li, J-S. 2009. Study
on separations and the antimicrobial effects of the total flavonoids
of Emilia sonchifolia. Food Science and Technology 1:
163-169.
Cheng,
D. & Röder, E. 1986. Pyrrolizidine alkaloids from Emilia
sonchifolia. Planta Medica 6: 484-486.
Citarasu,
T., Sekar, R., Babu, M. & Marian, M. 2002. Developing artemia
enriched herbal diet for producing quality larvae in Penaeus
monodon. Asian Fisheries Science 15: 21-32.
Devi,
L. 1995. Effect of Asparagus racemous to improve the survival
and reproductive performance in Artemia parthenogenetica.
M. Phil Dissertation, Manonmaniam Sundaranar University (Unpublished).
Gao,
J.J., Cheng, D.L. & Liu, X.P. 1993. Chemical constituents of
Emilia sonchifolia (L.) DC. Zhongguo Zhongyao Zazhi 18:
102-103.
Harrison,
K.E. 1990. The role of nutrition in maturation, reproduction and
embryonic development of decapod crustaceans: A review. Journal
Shellfish Research 9: 1-28.
Hilda,
K.M. 1992. Performance evaluation of Reprostim on the survival,
growth and reproduction of Artemia franciscana. M.Sc. Dissertation,
Manonmaniam Sundaranar University (Unpublished).
Lee,
S.O., Jeon, J.M., Oh, C.W., Kim, Y.M., Kang, C.K., Lee, D.S., Mykles,
D.L. & Kim, H.W. 2011. Two juvenile hormone esterase-like carboxylesterase
cDNAs from a Pandalus shrimp (Pandalopsis japonica): Cloning,
tissue expression, and effects of eyestalk ablation. Comparative
Biochemistry and Physiology Part B: Biochemistry and Molecular Biology
159(3): 148-156.
Lee,
F.Y. & Chang, C.F. 1997. The concentrations of vitellogenin
(vitellin) and protein in hemolymph, ovary and hepatopancreas in
different ovarian stages of the freshwater prawn, Macrobrachium
rosenbergii. Comparative Biochemistry Physiology A Physiology
117(4): 433-439.
Lo,
T.S., Cui, Z., Mong, J.L.Y., Wong, Q.W.L., Chan, S.M., Kwan, H.S.
& Chu, K.H. 2007. Molecular coordinated regulation of gene expression
during ovarian development in the Penaeid shrimp. Marine Biotechnology
9(4): 459-468.
Loongyai,
W., Phongdara, A. & Chotigeat, W. 2007. Cloning and expression
of a TCTP homolog from the ovaries of banana prawn. Marine Biology
150: 455-462.
Maikaeo,
L., Chotigeat, W. & Mahabusarakam, W. 2015. Emilia sonchifolia
extract activity against white spot syndrome virus and yellow
head virus in shrimp cell cultures. Disease of Aquatic Organism
115(2): 157-164.
Makkapan,
W., Maikaeo, L., Miyazaki, T. & Chotigeat, W. 2011. Molecular
mechanism of serotonin via methyl farnesoate in ovarian development
of white shrimp: Fenneropenaeus merguiensis de Man. Aquaculture
321(1-2): 101-107.
Maurício,
E., Gerard, C., Maite, M., Miguel, A., Elsa, N., Gilberto, J., Ilie,
R. & Gabriela, G. 2012. Reproductive performance, biochemical
composition and fatty acid profile of wild-caught and 2nd generation
domesticated Farfantepenaeus duorarum (Burkenroad, 1939)
broodstock. Aquaculture 344-349: 194-204.
Meunpol,
O., Iam-Pai, S., Suthikrai, W. & Piyatiratitivorakul, S. 2007.
Identification of progesterone and 17α-hydroxyprogesterone
in polychaetes (Perinereis sp.) and the effects of hormone
extracts on penaeid oocyte development in vitro. Aquaculture
270(1-4): 485-492.
Navakanitworakul,
R., Deachamag, P., Wonglapsuwan, M. & Chotigeat, W. 2012. The
roles of ribosomal protein S3a in ovarian development of Fenneropenaeus
merguiensis (De Man). Aquaculture 338-341: 208-215.
Ouraji,
H., Fereidoni, A.E., Shayegan, M. & Asil, S.M. 2011. Comparison
of fatty acid composition between farmed and wild Indian white shrimps,
Fenneropenaeus indicus. Food and Nutrition Sciences 2:
824-829.
Palasin,
K., Makkapan, W., Thongnoi, T. & Chotigeat, W. 2014. Stimulation
of ovarian development in white shrimp, Fenneropenaeus merguiensis
De Man, with a recombinant ribosomal protein L10a. Aquaculture
432: 38-45.
Sambhu,
C. & Jayaprakas, V. 2001. Livol (IHF-1000), a new herbal growth
promoter in white prawn, Penaeus indicus (Crustacea). Indian
Journal of Geo-Marine Science 30: 38-43.
Shylesh,
B., Nair, S.A. & Subramoniam, A. 2005. Induction of cell-specific
apoptosis and protection from Dalton’s lymphoma challenge in
mice by an active fraction from Emilia sonchifolia. Indian
Journal of Phamacology 37(4): 232-237.
Shylesh,
B.S. & Padikkala, J. 1999. Antioxidant and anti-inflammatory
activity of Emilia sonchifolia. Fitoterapia 70(3):
275-278.
Srinivasan,
K.K. & Subramanian, S.S. 1980. Chemical investigation of Emilia
sonchifolia. Fitoterapia 51: 241-243.
Teshima,
S., Kanazawa, A., Koshio, S. & Herinouchi, K. 1998. Lipid methabolism
in destalked prawn Penaeus japonicus: Induced maturation
and accumulation of the lipid in the ovary. Nippon Suisan Gakk
54(7): 1115-1122.
Wonglapsuwan,
M., Miyazaki, T., Loongyai, W. & Chotigeat, W. 2010. Characterization
and biological activity of the ribosomal protein L10a of the white
Shrimp: Fenneropenaeus merguiensis de Man during vitellogenesis.
Marine Biotechnology 12: 230-240.
Wonglapsuwan,
M., Phongdara, A. & Chotigeat, W. 2009. Dynamic changes in gene
expression during vitellogenic stages of the white shrimp: Fenneropenaeus
merguiensis de Man. Aquaculture Research 40(6): 633-643.
Xu,
X.L., Ji, W.J., Castell, J.D. & O’Dor, R.K. 1994. Essential
fatty acid requirement of the Chinese prawn, Penaeus chinensis.
Aquaculture 127(1): 29-40.
Yadava,
R.N. & Mamta, R. 2012. Antiviral activity of a new flavone glycoside
from Emilia sonchifolia DC. Indian Journal Chemistry 15B:
635-638.
*Pengarang untuk surat-menyurat;
email: wilaiwan58@hotmail.com
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