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Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi

Yıl 2021, Cilt 11, Sayı 1, 135 - 146, 15.01.2021
https://doi.org/10.17714/gumusfenbil.754474

Öz

Rodofit olarak bilinen alglerde bulunan ve kırmızı renkli bir pigment olan astaksantin (ASTA) terpeni bir tetraterpendir. Çalışmada ASTA’nın doz-süre etkileşimine bağlı olarak olası toksik ve genotoksik etkileri araştırılmıştır. ASTA’nın toksik etkisi, Drosophila melanogaster’in Oregon-R yabanıl soyunda in vivo ömür uzunluğu testi ile belirlenmiştir. Bu amaçla ergin dişi ve erkek bireyler farklı dozlarda ASTA içeren (25, 50, 100 ve 200 ppm) besiyerinde kronik olarak beslenmiştir. Kontrol grubunda ortalama ömür uzunluğu dişilerde 49.07±1.92 gün iken erkeklerde 51.01±2.12 gündür. Bu değerler en düşük ve en yüksek ASTA uygulama gruplarında (25-200 ppm) dişilerde sırasıyla 32.06±1.50 ve 27.06±1.18 gün, erkeklerde de 32.45±1.48 ve 23.52±0.92 gün olarak bulunmuştur. ASTA’nın kontrol ve uygulama gruplarına ait sonuçlar birbiriyle karşılaştırıldığı zaman hem dişi hem de erkek popülasyonunda ortalama ömür uzunluğunun doz-süre etkileşimine bağlı olarak kısaldığı gözlenmiştir (p<0.05). ASTA terpeninin genotoksik etkisi de yine D.melanogaster’de somatik mutasyon ve rekombinasyon testi (SMART) ile belirlenmiştir. SMART sonucunda elde edilen verilere göre tüm ASTA uygulama gruplarında (50, 100, 200 ve 400 ppm) konsantrasyon artışına bağlı olarak klon indüksiyon frekansında artış gözlenmiştir. Bu sonuçlar ASTA’nın somatik mutasyonları uyardığını göstermektedir.

Kaynakça

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  • Büyükleyla, M. ve Rencüzoğulları, E. (2009). The effects of thymol on sister chromatid exchange, chromosome aberration and micronucleus in human lymphocytes. Ecotoxicology and Enviromental Safety, 72(3), 943-947.
  • Calixto, J.B. (2000). Efficacy, safety, quality control, marketing and regulatory guidelines for herbal medicines (phytotherapeutic agents). Brazilian Journal of Medical and Biological Research, 33(2), 179-189.
  • Chang, H.T., Chou, C.T., Liang, W.Z., Lu, T., Kuo, D.H., Shieh, P., Ho, C.M. ve Jan, C.R. (2014). Effects of thymol on Ca²⁺ homeostasis and apoptosis in MDCK renal tubular cells. Chinese Journal of Physiology, 57(2), 90-98.
  • Cho, K.S., Lim, Y.R., Lee, K., Lee, J., Lee, J.H. ve Lee, I.S. (2017). Terpenes from forests and human health. Toxicological Research, 33(2), 97-106.
  • Clark, R.L. (2009). Embryotoxicity of the artemisinin antimalarials and potential consequences for use in women in the first trimester. Reproductive Toxicology, 28, 285-296.
  • Clarkson, P.M. ve Thompson, H.S. (2000). Antioxidants: what role do they play in physical activity and health?. The American Journal of Clinical Nutrition, 72(2), 637-646.
  • Çelik, H., Kızılet, H., Özdal, M., Gülmez, O., Algur, Ö.F. ve Uysal, H. (2018). Lactarius indigo mantarında bulunan ve ömür uzunluğunu inhibe eden guazilen’e karşı Pleurotus sajor-caju ve Pleurotus osteratus mantarları. International Eurasian Conference on Biological and Chemical Sciences 26-27 April, Ankara, Türkiye.
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  • Ding, W., Lev, D.D., Bishop, M.E., Lyn‐Cook, L.E., Kulkarni, R., Chang, C.W., Aidoo, A. and Manjanatha, M.G. (2011). Methyleugenol genotoxicity in the fischer 344 rat using the comet assay and pathway‐focused gene expression profiling. Toxicology Science, 123,103–112.
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Determination of ın vivo chronic effects of astaxanthin in different strains of drosophila melanogaster

Yıl 2021, Cilt 11, Sayı 1, 135 - 146, 15.01.2021
https://doi.org/10.17714/gumusfenbil.754474

Öz

Astaxanthine (ASTA) terpene, a red pigment found in algae known as rhodopite, is a tetraterpene. In this study, possible toxic and genotoxic effects of the ASTA were investigated depending on the dose-time interaction. The toxic effect of the ASTA was determined by in vivo longevity test in Oregon-R wild strain of Drosophila melanogaster. For this purpose, adult female and male individuals were chronically fed on media containing different doses of the ASTA (25, 50, 100 and 200 ppm). While the average life span in the control group is 49.07±1.92 days in females, it is 51.01±2.12 days in males. These values are 32.06±1.50 and 27.06±1.18 days in females in the lowest and highest ASTA application groups (25-200 ppm), 32.45±1.48 and 23.52±0.92 in males, respectively. When the results of the control and application groups of the ASTA terpene were compared, it was observed that the average life span decreased in both female and male populations depending on the dose-time interaction (p<0.05). The genotoxic effect of the ASTA terpene was also determined by the somatic mutation and recombination test (SMART) in D.melanogaster. According to the data obtained from the SMART result, an increase in clone induction frequency was observed in all the ASTA application groups (50, 100, 200 and 400 ppm) due to concentration increase. These results show that ASTA stimulates somatic mutations.

Kaynakça

  • Al-Zubairi, A.S., Abdul, A.B. ve Syam, M.M. (2010). Evaluation of the genotoxicity of zerumbone in cultured human peripheral blood lymphocytes. Toxicology In Vitro, 24, 707-712.
  • Arıca, Ş.Ç. (2017). Yaşlanma ve alglerin anti-gerontolojik etkileri. Ege Journal of Fisheries and Aquatic Sciences, 34(4), 469-474.
  • Aslan, N. (2005). Kekik tarımı ve kullanım alanları. Lisans Bitirme Tezi, Ziraat Fakültesi Tarla Bitkileri Bölümü, Dicle Üniversitesi, Diyarbakır.
  • Azqueta, A. ve Collins, A. R. (2012). Carotenoids and DNA damage. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 733(1-2), 4-13.
  • Azirak, S. ve Rencüzoğulları, E. (2008). The in vivo genotoxic effects of carvacrol and thymol in rat bone marrow cells. Environmental Toxicology, 23(6), 728-735.
  • Büyükleyla, M. ve Rencüzoğulları, E. (2009). The effects of thymol on sister chromatid exchange, chromosome aberration and micronucleus in human lymphocytes. Ecotoxicology and Enviromental Safety, 72(3), 943-947.
  • Calixto, J.B. (2000). Efficacy, safety, quality control, marketing and regulatory guidelines for herbal medicines (phytotherapeutic agents). Brazilian Journal of Medical and Biological Research, 33(2), 179-189.
  • Chang, H.T., Chou, C.T., Liang, W.Z., Lu, T., Kuo, D.H., Shieh, P., Ho, C.M. ve Jan, C.R. (2014). Effects of thymol on Ca²⁺ homeostasis and apoptosis in MDCK renal tubular cells. Chinese Journal of Physiology, 57(2), 90-98.
  • Cho, K.S., Lim, Y.R., Lee, K., Lee, J., Lee, J.H. ve Lee, I.S. (2017). Terpenes from forests and human health. Toxicological Research, 33(2), 97-106.
  • Clark, R.L. (2009). Embryotoxicity of the artemisinin antimalarials and potential consequences for use in women in the first trimester. Reproductive Toxicology, 28, 285-296.
  • Clarkson, P.M. ve Thompson, H.S. (2000). Antioxidants: what role do they play in physical activity and health?. The American Journal of Clinical Nutrition, 72(2), 637-646.
  • Çelik, H., Kızılet, H., Özdal, M., Gülmez, O., Algur, Ö.F. ve Uysal, H. (2018). Lactarius indigo mantarında bulunan ve ömür uzunluğunu inhibe eden guazilen’e karşı Pleurotus sajor-caju ve Pleurotus osteratus mantarları. International Eurasian Conference on Biological and Chemical Sciences 26-27 April, Ankara, Türkiye.
  • Çelik, H. ve Uysal H. (2019). Stimulation of longevity toxicity based on chronic application of terpenes. International Eurasian Conference on Biological and Chemical Sciences 28-29 June, Ankara, Türkiye.
  • Davinelli, S., Nielsen, M.E ve Scapagnini, G. (2018). Astaxanthin in skin health, repair, and disease: A comprehensive review. Nutrients, 10(4), 522.
  • Ding, W., Lev, D.D., Bishop, M.E., Lyn‐Cook, L.E., Kulkarni, R., Chang, C.W., Aidoo, A. and Manjanatha, M.G. (2011). Methyleugenol genotoxicity in the fischer 344 rat using the comet assay and pathway‐focused gene expression profiling. Toxicology Science, 123,103–112.
  • Edwards, J.A., Bellion, P., Beilstein, P., Rümbeli, R. ve Schierle, J. (2016). Review of genotoxicity and rat carcinogenicity investigations with astaxanthin. Regulatory Toxicology and Pharmacology, 75, 5-19.
  • Eichorn, S.E. ve Evert, R.F. (2016). Raven bitki biyolojisi. (Çeviri Editörü: İsmail Türkan), Palme Yayıncılık.
  • Erdem, S. ve Eren, P.A. (2009). Tedavi amacıyla kullanılan bitkiler ve bitkisel ürünlerin yan etkileri. Türk Hijyen ve Deneysel Biyoloji Dergisi, 133.
  • Fassett, R.G. ve Coombes, J.S. (2011). Astaxanthin: a potential therapeutic agent in cardiovascular disease. Marine Drugs, 9(3), 447-465.
  • Frei, H. ve Würgler, F.E. (1988). Statistical Methods to decide whether mutagenicity test data from Drosophila assays indicate a positive, negative or inconclusive result. Mutation Research, 203, 297-308.
  • Gil Da Costa, R.M., Oliveira, P.A., Bastos, M.M., Lopes, C.C. ve Lopes, C. (2014). Ptaquiloside-induced early-stage urothelial lesions show increased cell proliferation and intact Β-Catenin and E-Cadherin expression. Environmental Toxicolog, 29, 763-769.
  • Goulart, M., Batoreu, M.C., Rodrigues, A.S., Laires, A. ve Rueff, J. (2005). Lipoperoxidation products and thiol antioxidants in chromium exposed workers. Mutagenesis, 20, 311315.
  • Gören, A.C. (2002). Bazı Sideritis (Sideritis argyrea, Sideritis dichotoma, Sideritis trojana) türlerinin diterpenik bileşenlerinin izolasyonu ve yapılarının tayini. Doktora Tezi, Balıkesir Üniversitesi, Fen Bilimleri Enstitüsü, Kimya Anabilim Dalı, Balıkesir.
  • Graf, U., Abraham, S.K., Guzmán-Rincón, J. ve Würgler, F.E. (1998). Antigenotoxicity studies in Drosophila melanogaster. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 402(1-2), 203-209.
  • Guzman-Rincon, J. and Graf, U. (1995). Drosophila melanogaster somatic mutation and recombination test as a biomonitor. Environmental Science Research, 50, 169-182.
  • Güneş, E. and Danacıoğlu, D.A. (2018). The effect of olive (Olea europaea L.) phenolics and sugar on Drosophila melanogaster’s development. Animal Biology,68(4), 367-385.
  • Hammer, K. A., Carson, C.F. ve Riley, T.V. (1999). Antimicrobial activity of essential oils and other plant extracts. Journal of Applied Microbiology, 86, 985-990.
  • Huangfu, J., Liu, J., Sun, Z., Wang, M., Jiang, Y., Chen, Z. Y. ve Chen, F. (2013). Antiaging effects of astaxanthin-rich alga Haematococcus pluvialis on fruit flies under oxidative stress. Journal of Agricultural and Food Chemistry, 61(32), 7800-7804.
  • Hussein, G., Goto, H., Oda, S., Sankawa, U., Matsumoto, K. ve Watanabe, H. (2006). Antihypertensive potential and mechanism of action of astaxanthin: III. antioxidant and histopathological effects in spontaneously hypertensive rats. Biological and Pharmaceutical Bulletin, 29(4), 684-688.
  • İpek, E., Zeytinoglu, H., Okay, S., Tuylu, B.A., Kurkcuoglu, M. ve Baser, K.H.C. (2005). Genotoxicity and antigenotoxicity of Origanum oil and carvacrol evaluatedby ames Salmonella/Microsomal test. Food and Chemistry, 93, 551-556.
  • Kamaya, Y., Tokita, N. ve Suzuki, K. (2005). Effects of dehydroabietic acid and abietic acid on survival, reproduction, and growth of the crustacean Daphnia magna. Ecotoxicology and Environmental Safety, 61(1), 83-88.
  • Kasımoğlu, C. ve Uysal, H. (2016). Farklı test sistemleri ile somatik hücrelerde profenofos genotoksisitesine karşı kuşburnu (Rosa canina L.) ekstrelerinin doğal bir antigenotoksik ajan olarak kullanılması. Cumhuriyet Üniversitesi Fen Fakültesi Fen Bilimleri Dergisi, 37, 1.
  • Kırbağ, S. ve Bağcı, E. (2000). Piceae abies (L.) karst. ve Picea orientalis (L.) link uçucu yağlarının antimikrobiyal aktivitesi üzerine bir araştırma. Journal of Quafqaz Universty, 3(1), 183-1882.
  • Kırca, A., Özkan, M. ve Cemeroğlu, B. (2006). Stability of black carrot anthocyanins in various fruit juices and nectars. Food Chemistry, 97, 598-605.
  • Koh, T., Machino, M.,Murakami, Y.,Umemura, N. and Sakagami, H. (2013). Cytotoxicity of dental compounds towards human oral squamous cell carcinoma and normal oral cells. In Vivo, 27, 85– 95.
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Ayrıntılar

Birincil Dil Türkçe
Konular Mühendislik
Bölüm Makaleler
Yazarlar

Handan UYSAL (Sorumlu Yazar)
ATATÜRK ÜNİVERSİTESİ, FEN FAKÜLTESİ
0000-0002-4290-8223
Türkiye


Hatice ÇELİK
ATATÜRK ÜNİVERSİTESİ, FEN FAKÜLTESİ
0000-0003-2531-6020
Türkiye

Destekleyen Kurum Atatürk Üniversitesi Bilimsel Araştırma Projeleri Yönetim Birimi
Proje Numarası FHD–2019-7000
Teşekkür Atatürk Üniversitesi Bilimsel Araştırma Projeleri Yönetim Birimi Başkanlığı'na destekleri için teşekkür ederiz.
Yayımlanma Tarihi 15 Ocak 2021
Yayınlandığı Sayı Yıl 2021, Cilt 11, Sayı 1

Kaynak Göster

Bibtex @araştırma makalesi { gumusfenbil754474, journal = {Gümüşhane Üniversitesi Fen Bilimleri Dergisi}, issn = {2146-538X}, eissn = {2146-538X}, address = {}, publisher = {Gümüşhane Üniversitesi}, year = {2021}, volume = {11}, pages = {135 - 146}, doi = {10.17714/gumusfenbil.754474}, title = {Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi}, key = {cite}, author = {Uysal, Handan and Çelik, Hatice} }
APA Uysal, H. & Çelik, H. (2021). Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi . Gümüşhane Üniversitesi Fen Bilimleri Dergisi , 11 (1) , 135-146 . DOI: 10.17714/gumusfenbil.754474
MLA Uysal, H. , Çelik, H. "Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi" . Gümüşhane Üniversitesi Fen Bilimleri Dergisi 11 (2021 ): 135-146 <https://dergipark.org.tr/tr/pub/gumusfenbil/issue/59602/754474>
Chicago Uysal, H. , Çelik, H. "Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi". Gümüşhane Üniversitesi Fen Bilimleri Dergisi 11 (2021 ): 135-146
RIS TY - JOUR T1 - Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi AU - Handan Uysal , Hatice Çelik Y1 - 2021 PY - 2021 N1 - doi: 10.17714/gumusfenbil.754474 DO - 10.17714/gumusfenbil.754474 T2 - Gümüşhane Üniversitesi Fen Bilimleri Dergisi JF - Journal JO - JOR SP - 135 EP - 146 VL - 11 IS - 1 SN - 2146-538X-2146-538X M3 - doi: 10.17714/gumusfenbil.754474 UR - https://doi.org/10.17714/gumusfenbil.754474 Y2 - 2020 ER -
EndNote %0 Gümüşhane Üniversitesi Fen Bilimleri Dergisi Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi %A Handan Uysal , Hatice Çelik %T Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi %D 2021 %J Gümüşhane Üniversitesi Fen Bilimleri Dergisi %P 2146-538X-2146-538X %V 11 %N 1 %R doi: 10.17714/gumusfenbil.754474 %U 10.17714/gumusfenbil.754474
ISNAD Uysal, Handan , Çelik, Hatice . "Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi". Gümüşhane Üniversitesi Fen Bilimleri Dergisi 11 / 1 (Ocak 2021): 135-146 . https://doi.org/10.17714/gumusfenbil.754474
AMA Uysal H. , Çelik H. Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi. Gümüşhane Üniversitesi Fen Bilimleri Dergisi. 2021; 11(1): 135-146.
Vancouver Uysal H. , Çelik H. Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi. Gümüşhane Üniversitesi Fen Bilimleri Dergisi. 2021; 11(1): 135-146.
IEEE H. Uysal ve H. Çelik , "Drosophila melanogaster’in farklı soylarında astaksantin’in in vivo kronik etkilerinin belirlenmesi", Gümüşhane Üniversitesi Fen Bilimleri Dergisi, c. 11, sayı. 1, ss. 135-146, Oca. 2021, doi:10.17714/gumusfenbil.754474