Kate Jocel D. Barroga,
Diana C. Castillo, and Evaristo A. Abella, from the different institute of Philippines.
wrote a Reseach Article about, Sea Urchin Methanolic Extract Shows
Antibacterial Activity Against E. coli and S. aureus. Entitled, Pharmacological
activity of the methanolic extract of sea urchins against Escherichia coli and
Staphylococcus aureus. This research paper published by the International Journal of Biosciences (IJB). an open access scholarly research journal
on Biosciences. under the affiliation of the International Network
For Natural Sciences| INNSpub. an open access multidisciplinary research
journal publisher.
Abstract
This study elucidated
the pharmacological potential of sea urchins using methanol as extracting
medium. The antibacterial potential was evaluated using the paper disc method
and zone of inhibition against Escherichia coli and Staphylococcus
aureus was measured. Antioxidant properties of sea urchins were evaluated
using DPPH radical scavenging assay. Three species of sea urchin randomly
collected along the intertidal zone of Diguisit, Baler Aurora were identified
using diagnostic keys by the National Museum of the Philippines and they were
identified as follows; Echinothrix diadema, Echinometra mathaei, and Echinometra
oblonga. E. diadema recorded the highest diameter zone of inhibition
against E. coli and S. aureus after 24 hours of incubation
with 11.03 ± 1.75mm and 13.52 ± 1.13mm respectively while E. mathaei only
inhibited S. aureus with zone of inhibition of 9.27 ± 2.06mm in 24
hours of incubation as well. As the zone of inhibition prolongs, the zone of
inhibition decreases as observed in 48 hours of incubation. E.
oblonga did not show inhibitoy effect, however it recorded the highest
radical scavenging activity with 64.46% among the three species of sea urchins.
This was followed by E. mathaei (51.52%) and E. diadema (37.38%).
All collected species manifested antioxidant potential. Based on the results,
the collected species of sea urchins has a pharmacological potential.
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Introduction
Marine invertebrates are excellent sources of bioactive compounds with antibacterial and antioxidant dynamics. Recent discovery on pharmacological dynamics has stimulated the search for natural agents or natural sources that will lead to a desirable antibacterial and secondary metabolites (Abubakar et al., 2012).
The diversity of marine organisms in our ecosystem, secondary metabolites has been identified as one of very important compound available produced in marine organisms. Sea urchins are small, spiny, globular animals belong to the class Echinoidea of the echinoderm phylum (Shankarlal et al., 2011). Additionally, sea urchins have orbicular bodies coated with a strict shell and thoroughly covered with many sharp spines (Amarowicz et al., 2012).
As stated in the study of Bich et al., (2004), echinoderms have pharmacologically active secondary metabolites. The antibacterial activity of sea urchin is generally assayed through various extracts with different solvents. Methanol extract of Tripneustes gratilla showed highest antimicrobial activity against Pseudomonas aeruginosa (Abubakar et al., 2012). Also, methanol extract of Diadema setosum exhibited higher zone of inhibition against Salmonella typhimurium, Staphylococcus epidermidis, Citrobacter freundii, and Klebsiella pneumoniae (Rahman et al., 2015).
An investigation report of Bragadeeswaran et al. (2013) on the bioactive compounds of sea urchin Temnopleurus toreumaticus showed remarkable hemolytic and cytotoxic activities. The spines of purple sea urchin Strongylocentrotus nudus showed excellent activity by using DPPH scavenging activity indicating the presence of PHNQ as potential sources of natural antioxidants (Zhou et al., 2011).
The present work focused on the screening of the antibacterial and
antioxidant activity of whole globular body and tissues of Echinothrix diadema,
Echinometra mathaei, and Echinometra oblonga collected from the intertidal zone
of the coastal ecosystem of Barangay Diguisit, Baler, Aurora, Philippines.
Reference
Abubakar LA, Mwangi CM,
Uku JU, Ndirangu SN. 2011. Antimicrobial activity of various extracts of
the sea urchin Tripneustes gratilla (Echinoidea). African Journal of
Pharmacology and Therapeutics 1(1).
Amarowicz R, Synowiecki
J, Shahidi F. 2012. Chemical composition of shells from red (Strongylocentrotus
franciscanus) and green (Strongylocentrotus droebachiensis) sea urchin. Journal
of Food Chemistry 133, 822-826.
Bich D, Chung D, Chuong
B, Dong N, Dam D, Hien P, Lo V, Mai P, Man P, Nhu D. 2004. The medicinal
plants and animals in Vietnam. Hanoi Science and Technology Publication 1.
Bragadeeswaran S, Sri
Kumaran N, Prasath Sankar P, Prabahar R. 2013. Bioactive potential of sea
urchin Temnopleurus toreumaticus from Devanampattinam, Southeast
coast of India. Journal of Pharmacy and Alternative Medicine 2(3), 9-18.
Brasseur L, Hennebert
E, Fievez L, Caulier G, Bureau F, Tafforeau L, Eeckhaut I. 2017. The roles
of spinochromes in four shallow water tropical sea urchins and their potential
as bioactive pharmacological agents. Marine drugs 15(6), 179.
Horton, J. 2012.
Invertebrates of the Coral Sea: Echinometra mathaei. Published
at the University of Queensland, Australia.
Kazemi S. Heidari B,
Rassa M. 2016. Antibacterial and hemolytic effects of aqueous and organic
extracts from different tissues of sea urchin Echinometra mathaei on
pathogenic streptococci. International Aquatatic Research 8(4), 299-308.
Lalitha, M. K. 2004.
Manual on Antimicrobial Susceptibility Testing. New Delhi, India. Indian
Association of Medical Microbiologists.
Lebedev AV, Ivanova MV,
Levitsky DO. 2003. Iron chelators and free radical scavengers in naturally
occurring polyhydroxylated 1, 4-naphthoquinones. Hemoglobin 32(1-2), 165-179.
Minh CV, Kiem PV, Huong
LM, Kim YH. 2004. Cytotoxic constituents of Diadema setosum. Archives
of Pharmacal Research 27(7), 734-737.
Mokhlesi A, Saeidnia S,
Gohari AR, Shahverdi AR, Nasrolahi A, Farahani F, Es’haghi N. 2012.
Biological activities of the sea cucumber Holothuria leucospilota. Asian
Journal of Animal and Veterinary Advances 7, 243-249.
Pettit GR, Ode RH. 1979.
Phenols, quinones, and related compounds. Phenols, quinones, and related
compounds. In: Biosynthetic Products for Cancer Chemotherapy.
Rahman MA, Amin SMN,
Yussof FM, Kupan P, Sham-Sudi MN. 2012. Length weight relationships and
fecun-dity estimates of long-spined sea urchin, Diadema setosum, fron
Pulau Pangkor, Peninsular Malaysia. Aquatic Ecosystem Health Manage 15, 311-315.
Schoppe S. 2001.
Echinoderms of the Philippines: A guide to common shallow water sea stars,
brittle stars, sea urchins, sea cucumbers and feather star. VISCA-GTZ Program
on Applied Tropical Ecology, Visayas State College of Agriculture, Leyte,
Philippines.
Shankarlal S, Prabu K,
Natarajan E. 2011. Antimicrobial and antioxidant activity of purple sea
urchin shell (Salmacis virgulata L. Agassiz and Desor 1846).
American-Eurasian Journal of Science Research 6(3), 178-181.
Silhavy TJ, Kahne D,
Walker S. 2010. The bacterial cell envelope. Biosynthetic Products for
Cancer Chemotherapy 127-143.
Yasmin. 2015.
Developmental biology of sea urchin, Echinometra oblonga (Blainville,
1825) And Its Larval Settlement Behavior in Response to Chemical Cues.
Zhou DY, Zhu BW, Wang
XD, Tan H, Yang J, Li DM, Dong XP, Wu HT, Sun L, Li XL, Murata Y. 2011.
Extraction and antioxidant property of polyhydroxylated naphthoquinone pigments
from spines of purple sea urchin Strongylocentrotus nudus. Food
Chemistry (129), 1591-1597.
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