Uji Toksisitas Daun Kelor ( Moringa Oleifera) Terhadap Sel Fibroblas Gingiva Menggunakan Uji MTT Assay
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ABSTRACT
Background: The oral cavity's health is one of the most important factors in determining the quality of human life. Oral cancer is a type of disease that can fataly change the quality of human life if not properly handle. Among all the cancer treatment, chemotherapy is oftenly done. However, chemotherapy has some side effects that can exacerbate the patient's state. Alternative care has become another promising option besides chemotherapy. One of them is Moringa oleifera or as known as kelor leaves. The active compound content of Moringa oleifera extract especially isothiocianate has good potential in cancer therapy. But, any materials used in human care must passed the toxicity test. Purpose: This research was conducted to find out the toxicity of Moringa oleifera extract with isothiocianate to primary cell gingival fibroblast.Method: Experimental laboratory study with the post test only group control design. There are 4 types of concentration group from kelor leaves extract which is 3,125%, 1,625%, 0,812%, and 0,406% and there are also the media control and cell control. Each sample were put in 96 well that already contain fibroblast cell culture with 6 times replication for each group. And then, it was tested with MTT assay. Results: The concentration group from 3,125% until 0,406% has the percentage of living cells above 100%. Conclusion: The results of this research is that the kelor leaves (Moringa oleifera) extract with isothiocyanate is not toxic against primary cell culture fibroblast.
Keywords: Moringa oleifera extract, isothiocyanate , toxicity.
Latar Belakang: Kesehatan rongga mulut merupakan salah satu faktor penting yang berperan dalam menentukan kualitas hidup manusia. Kanker rongga mulut merupakan salah satu penyakit yang dapat mengubah kualitas hidup manusia dan berkaibat fatal apabila tidak ditangani dengan tepat. Salah satu pengobatan kanker yang sering dilakukan adalah kemoterapi. Meskipun demikian, kemoterapi memiliki beberapa efek samping yang dapat berakibat buruk kepada pasien kanker. Perawatan alternatif pun menjadi pilihan lain selain kemoterapi. Salah satunya adalah dengan daun kelor (Moringa oleifera) . Kandungan aktif dari daun kelor memiliki manfaat yang baik sebagai terapi kanker. Namun, semua bahan yang akan digunakan pada manusia harus melawati uji toksisitas. Tujuan: Tujuan dilakukan penelitian ini yaitu untuk mengetahui hasil toksisitas ekstrak daun kelor (Moringa oleifera) dengan kandungan isotiosianat terhadap cell line fibroblas. Metode: Penelitian eksperimental laboratoris dengan post test only group design. Terdapat 4 macam kelompok konsentrasi dari ekstrak daun kelor yaitu 3,125%, 1,625%, 0,812%, dan 0,406% disertai dengan kontrol media dan kontrol sel. Setiap perlakuan diletakkan pada plate 96 well yang telah berisi kultur sel fibroblas dengan 6 kali replika untuk setiap kelompok. Kemudian dilakukan uji MTT assay. Hasil: Kelompok konsentrasi 3,125% hingga 0,812% memiliki jumlah persentase sel hidup diatas 100%. Kesimpulan: Hasil penelitian ini menunjukkan bahwa ekstrak daun kelor (Moringa oleifera) dengan kandungan isotiosianat tidak bersifat toksik terhadap kultur sel primer fibroblas.
Kata Kunci : Ekstrak daun kelor (Moringa oleifera), isotiosianat, uji toksisitas.
DAFTAR PUSTAKA
Aminah, S, Ramdhan, T, & Yanis, M, 2015, Kandungan Nutrisi dan Sifat Fungsional Tanaman Kelor (Moringa oleifera), Buletin Pertanian Perkotaan Vol 5, pp.37-39
Anusavice, KJ, 2013, Phillips' Science of Dental Materials, 12th ed, Elsevier Saunders, Missouri, pp. 150
Andrianus, Edmondo, 2014, Potensi Ekstrak Daun Rumput Mutiara (Hedyotis corymbosa (L) Lamk) terhadap Apoptosis Sel Kanker Rongga Mulut pada Tikus Wistar Jantan yang diinduksi Benzo(A)pirene, Skripsi,Fakultas Kedokteran Gigi Universitas Airlangga, pp.10-11
Anwar, F, Latif, S, & Ashraf, M, 2007, Moringa oleifera : A Food Plant with Multiple Medicinal Uses, Wiley Interscience, pp.20-21.
Bose, CK, 2007, Possible role of Moringa Oleifera L. root in epithelial ovarian cancer, MedGenMed, pp.4-5
Barrientos, S, Stojadinovic, O, Golinko, MS, et al, 2008,Growth factor and Cytokines in wound healing, wound reapir and regeneration,Wound Repair Reagen, Vol. 16(5), pp. 585-601
Budhy, TI, Wulandari, Erawati, & Mooduto, Latief, 2007, Uji Sitotoksisitas Ekstrak Air Asam Jawa 5% Terhadap Cell Line BHK 21, Indonesian Journal of Dentistry, pp.19
Freshney, R, 2011,Animal cell Culture , A practical approach, 6th edition, IRI, Press : Washington DC, pp.113-114
Ghantous, Y, 2017, Global Incidence and Risk Factors Of Oral Cancer, National Institutes of Health, pp.1
Gibco, 2015, Cell Culture Basic Handbook, Thermo Fisher Scientific, pp.2.
Guha, N, Boffeta, P, Shangina, ,et al, 2007, Oral Health and Risk of Squamous Cell Carcinoma of the Head and Neck and Esophagus: Results of Two Multicentic Case- Control Studies, American Journal of Epidemiology, pp.1159-1160.
Harborne, JB, 1987, Metode Fitokimia, Penuntun Cara Modern Menganalisis Tumbuhan, Penerjemah: Kosasih P., Iwang S.Terbitn kedua, Bandung:Penerbit ITB, pp.152-153.
Istindiah, HN & Auerkari, EL, 2001, Mekanisme Kontrol Siklus Sel (Suatu Tinjauan Khusus Peran Protein Regulator Pada Jalur Retinoblastoma (Rb) ), Jurnal Kedokteran Gigi Universitas Indonesia vol 8(1) pp.40
Kayanoki, Y, Fujii, J, Suzuki, K,et al, 1994, Suppression of Antioxidatve Enzym Expression by Transforming Growth Factor-β1 in Rat Hepatocytes, The Journal of Biological Chemistry, pp.15488
Krisnadi, Dudi, 2015, Kelor Super Nutrisi.Pusat Informasi dan Pengembangan Tanaman Kelor Indonesia Lembaga Swadaya Masyarakat – Media Peduli Lingkungan(LSM-Mepeling), pp.8-12, 36-37,63-64.
Kumar S & Pandey AK,Chemistry and Biological Activities of Flavonoids: An Overview, Review Article, The Scientific World Journal, Vol 2013, Article ID 162750, pp 1-16.
Kousholt, A, Menzel, T, & Sorensen, C, 2012, Pathways for Genome Integrity in G2 Phase of the Cell Cycle, Biomolecules, pp. 2.
Laborde, E, 2010, Glutathine Transferase as mediators of Signalling Pathway Involved in Cell Proliferation and Cell Death, pp.3-4.
Loprinzi, C, Bensinger, W, & Peterson, D, 2014, Understanding and Managing Chemotherapy Side Effects, Cancer Care, pp.4-7.
Ma'at, Suprapto, 2011,Teknik Dasar Kultur Sel, Surabaya: Airlangga University, pp.9-10
Marthur, B, 2005, Moringa oleifera, Treesforlife, pp.11
Provost, J, 1998, MTT Proliferatoin Assay Protocol.Investigating the Biochemistry & Cellular Physiology of NHE1,Provost & Wallert Research pp.15-16.
Putra, Wayan DP, Dharmayudha, Anak AGO, & Sudimartini, LM, 2016, Identifikasi Senyawa Kimia Ekstrak Etanol Daun Kelor (Moringa oleifera L) di Bali, Indonesia Medicus Veterinus, pp.466-467.
Redha, Abdhi, 2010, Flavonoid:Struktur, Sifat Antioksidatif dan Peranannya dalam sistem biologis, Jurnal Belian vol 9, pp.197-199.
Ricci, P, 2008,Environmental and Health Risk Assessment and Management: Principles and Practices, Netherlands:Springer, pp.213.
Sayuti, Kesuma & Yenrina, Rina, 2015, Antioksidan, alami dan sintetik, Padang:AU Press, pp.10-17
Saxena, M, Nema, R, & Gupta, A, 2013, Phytochemistry of Medicinal Plants, Joural of Pharmacognosy and Phytochemistry, pp.168.
Shentilreja, P & Kathiresan, K, 2015, In Vitro Cytotoxicity MTT Assay in Vero, HepG2 and MCF-7 Cell study of Marine Yeast, Journal of Applied Phamaceutical Science Vol.5, pp.081-082.
Srivastava, S& Singh, S, 2004, Cell cycle arrest,apoptosis induction and inhibition of nuclear factor kappa B activation in anti-proliferatic activity of benzyl isothiocyanate against human pancreatic cancer cells, Carcinogenesis:Departement of Pharmacology and University of Pittsburg Cancer Institute, pp.1701-1704
Tiara, 2010, Curcumin sebagai Terapi Pendamping untuk Kanker.Jurnal Medika Kedokteran Indonesia vol XXXV, pp.1-2.
Toma, A& Deno, S, 2014, Phytochemistry and Pharmacological Activities of Moriga oleifera, Internatioinal Journal of Biological Chemistry, pp.223-227.
Veal, E, Toone, M, Jones, N, Morgan, B, 2002, Distinct Roles for Gluthatione S-Transferase in the Oxidative Stress Response in Schizosaccharomyces pombe, Journal of Biological Chemistry, pp.1.
Warnakulasuriya, S, 2008, Global Epidemiology of Oral and Ooropharyngeal Cancer, Department of Oral Medicine and Experimental Oral Pathology, London:Elsevier, pp.309
Walton, R& Toerbinejed, 2008, Prinsip dan Praktik Ilmu Endodonsia 3th ed, Jakarta:EGC, pp.15.
Yousef, A, 2011, Isothiocyanate Glycoside, Phytotherapy, pp. 1.
Yulianti, T, 2009, Biofumigan Untuk Pengendalian Patogen Tular Tanah Penyebab Penyakit Tanaman Yang Ramah Lingkungan, Pengembangan Inovasi Pertanian, pp.156-160.
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