You are here

Homalothecium sericeum özütlerinin zamana bağlı olarak glioma hücrelerinin çoğalması üzerindeki etkileri

Time dependent cytotoxic role of Homalothecium sericeum extracts on glioma

Journal Name:

Publication Year:

Keywords (Original Language):

Abstract (2. Language): 
Bryophytes have been used as medicinal plants for more than 400 years in China, Europe and North America. There is also evidence confirming the antibiotic and anticancer activity of Bryophytes against, prokaryotes, fungi and different cancer cells. The purpose of the current study was to investigate cytotoxic property of Homalothecium sericeum (hedw.) schimp., which is a bryophyte, extracts on rat glioma (C6) cells for 48 hrs, in vitro. We first collected two different (acetone and A) extracts from H. sericeum by two different extraction processes. C6 cells were seeded in 96 well plates (2x104 cells/well) and incubated for 24 hrs. Following this incubation period, the medium was replaced with only medium (control) or medium with extracts at concentrations of 0.17, 1.7, 17, 85 or 170 Lig/mL for 48 hrs. Cytotoxicity was determined by using 3-(4,5-dimethylthiazol-2yl)- 2,5-diphenyltetrazolium bromide (MTT) colorimetric assay. Acetone extract of H. sericeum at 0.17, 1.7 and 17 Lig/mL concentrations did not change the survival rate of C6, but 85 and 170 Lig/mL inhibited about 16 % and 36 % after 48 hr (p<0.001), respectively. Extract A at concentration of 0.17 Lig/mL did not also affect C6 viability, but 1.7, 17 (p<0.01), 85 and 170 (p<0.001) Lig/mL decreased C6 cell viability by 6, 8, 24 and 33 % for 48 hr, respectively. Acetone and A extracts of H. sericeum showed a moderate but similar dose dependent cytotoxicity on C6. Further studies are needed to clarify the content of these extracts.
Abstract (Original Language): 
Bryofıtler 400 yıldan fazla bir süredir Çin, Avrupa ve Kuzey Amerika'da bitkisel ilaç olarak kullanılmaktadır. Bryofitlerin prokaryot, mantar türleri üzerinde antibiyotik ve farklı kanser hücreleri üzerinde antikanser etkinlik gösterdiği konusunda veriler bulunmaktadır. Bu çalışmanın amacı, bir Bryofit olan Homalothecium sericeum 'un sıçan glioma (C6) hücreleri üzerinde 48 saatlik sitotoksik etkinliğini araştırmaktır. İlk olarak, iki farklı özüt elde etme yöntemiyle aseton ve A özütlerini elde ettik. C6 hücreleri 96 kuyucuklu kültür kaplarına ekilerek (2x104 hücre/kuyucuk) 24 saat inkübe edildi. İnkübasyon süresinin ardından kuyucuklara özütlerin 0.17, 1.7, 17, 85 ve 170 Lig/mL konsantrasyonları eklenerek 48 saat muamele edildi. Sitotoksisite, MTT [3-(4,5-dimetiltiazol-2yl)- 2,5-difeniltetrazolyum bromid] yöntemi ile belirlendi. 48 saat sonunda aseton özütünün 0.17, 1.7 ve 17 Lig/mL konsantrasyonları C6 hücre canlılığını değiştirmezken, 85 ve 170 Lg/mL konsantrasyonları hücre canlılığını sırası ile %16 ve %36 oranında azalttı (p<0.001). A özütünün 0.17 Lig/mL konsantrasyonu hücre canlılığını 48 saat sonunda değiştirmezken, 1.7, 17 (p<0.01), 85 and 170 (p<0.001) Lig/mL konsantrasyonları sırası ile % 6, 8, 24 ve 33 oranında azaltmıştır. H. sericeum'un aseton ve A özütü glioma hücreleri üzerinde orta ve benzer bir şekilde doza bağımlı sitotoksik etki göstermiştir. Bu özütlerin içeriği hakkında yapılacak daha kapsamlı çalışmalara ihtiyaç duyulmaktadır.
1-4

REFERENCES

References: 

Abe, K., Matsuki, N., 2000. Measurement of cellular 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenytetrazolium bromide (MTT) reduction activity and lactate dehydrogenase release using MTT. Neuroscience Research. 38: 325-29.
Asakawa, Y. 2001. Recent advances in phytochemistry of bryophytes-acetogenins, terpenoids and bis (bibenzyl)s from selected Japanese, Taiwanese, New Zealand, Argentinean and European liverworts. Phytochemistry. 56: 297-312.
4
Biological Diversity and Conservation - 5 /1 (2012)
Basile,
A.
, Sorbo, S., Giordano, S., Lavitola, A., Castaldo-Cobianchi, R. 1998. Antibacterial activity in Pleurochaete
squarrosa extract (Bryophyta). International Journal of Antimicrobial Agents. 10: 169-172. Basile, A., Giordano, S., Lopez-Saez, J.A., Castaldo-Cobianchi, R. 1999. Antibacterial activity of pure flavonoids
isolated from mosses. Phytochemistry. 52: 1479-1482. Collet, B., Guitton, N., Saikali, S., Avril, T., Pineau, C., Hamlat, A., Mosser, J., Quillien, V. 2011. Differential analysis
of glioblastoma multiforme proteome by a 2D-DIGE approach. Proteome Science. 9/1: 1-26. Ezer, T., Kara, R., Düzenli, A. 2010. The life strategies of bryophytes which form epiphytic vegetation on Mount
Musa/Turkey. Biological Diversity and Conservation. 3/3: 75-84. Hahn, H., Seeger, T., Geiger, H., Zinsmeister, H.Z., Markham, K.R., Wong, H. 1995. The first biaurone, a triflavone
and biflavonoids from two Aulacomnium species. Phytochemistry. 40: 573-576. Ivanova, V., Kolarova, M., Aleksieva, K., Dornberger, K.J., Haertl, A.. , Moellmann, U., Dahse, H.M., Chipev, N.,
2007. Sanionins: Anti-inflammatory and antibacterial agents weak cytotoxicity from the Antarctic Moss Sanionia
georgico-uncinata. Preparative Biochemistry and Biotechnology. 37: 343-352. Krzaczkowski, L., Wright, M., Reberioux, D., Massiot, G., Etievant, C., Gairin, J.E. 2009. Pharmacological screening
of bryophyte extracts that inhibit growth and induce abnormal phenotypes in human HeLa cancer cells. Fundamental
& Clinical Pharmacology. 23/4: 473-482. Liu, K.W., Feng, H., Bachoo, R., Kazlauskas, A., Smith, E.M., Symes, K., Hamilton, R.L., Nagane, M., Nishikawa, R.,
Hu,
B.
, Cheng, S.Y. 2011. SHP-2/PTPN11 mediates gliomagenesis driven by PDGFRA and INK4A/ARF
aberrations in mice and humans. The Journal of Clinical Investigation. 121/3: 905-917. Matsuo, A., Sato, A. 1991. Sterols of Mosses. Phytochemistry. 30: 2305-2306.
Mossmann, T. 1983. Rapid colorimetric assay of cellular growth and survival: application to proliferation and
cytotoxicity assay. Journal Immunology Method. 65: 55-63. Oztopcu-Vatan, P., Savaroglu, F., Filik-Iscen, C., Kabadere, S., Ilhan, S., Uyar, R. 2011. Antimicrobial and
antiproliferative activities of Homalothecium sericeum (Hedw.) Schimp. extracts. Phresenius Environmental
Bulletin. 20: 461-466.
Sabovljevic, A., Sokovic, M., Sabovljevic, M., Grubisic, D. 2006. Antimicrobial activity of Bryum argenteum.
Fitoterapia. 77: 144-145.
Salford, L.G., Siesjö, P., Skagerberg, G., Persson, B.R.R., Larsson, E.M., Lindvall, M., Visse, E., Widegren, B. 2002.
Search for effective therapy against glioblastoma multiforme-clinical immunisation with autologous glioma cells
transduced with the human interferon-g gene. International Congress Series. 1247: 211-220. Saritas, Y., Sonwa, M.M., Iznaguen, H., König, W.A., Muhle, H., Mues, R. 2001. Volatile constituents in mosses
(Musci). Phytochemistry. 57: 443-457. Savaroglu, F., Filik-Iscen, C., Oztopcu-Vatan, P., Kabadere, S., Ilhan, S., Uyar, R. 2011. Determination of antimicrobial
and antiproliferative activities of the aquatic moss Fontinalis antipyretica Hedw. Turkish Journal of Biology. 35:
361-369.
Singh, M., Rawat, A.K.S., Govindarajan, R. 2007. Antimicrobial activity of some Indian mosses. Fitoterapia. 78: 156¬158.
Yamada, P., Isoda, H., Han, J.K., Talorete, T.P., Yamaguchi, T., Abe, Y. 2007. Inhibitory effect of fulvic acid extracted
from Canadian sphagnum peat on chemical mediator release by RBL-2H3 and KU812 cells. Bioscience,
Biotechnology and Biochemistry. 71: 1294-1305. Zinsmeister, H.D., Mues, R. 1987. Moose als Reservoir bemerkenswerter sekundaerer Inhaltsstoffe. GIT
Fachzeitscchrift für das Laboratorium. Gıt Verlag. 31: 499-512. Zinsmeister, H.D., Becker, H., Eicher, T. 1991. Bryophytes, a source of biologically active, naturally occurring
material. Angewandte Chemie-International Edition in English. 30: 130-147.

Thank you for copying data from http://www.arastirmax.com