Dergiler / Turkish Journal of Medical Sciences / 2010 / Cilt: 40 - Sayı: 6

Effects of aqueous garlic extract on oxidant/antioxidant status in 32D and 32Dp210 cell lines

Sayfa
881–888
Yayın Tarihi
2022-11-05
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

We think that the oxidant potential of garlic extract might play a part in its possible anticancer potential, previously supposed by several investigators.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:To investigate the possible effects of aqueous garlic extract on the oxidant/antioxidant status and apoptosis in 32D (wild type mouse myeloid cell = normal) and 32Dp210 (BCR-ABL fusion gene (+) mouse myeloid cell = Chronic Myelocytic Leukemia cells) cell lines.
📊
Temel Bulgular & Veri:Materials and methods: Aqueous garlic extract (10% w/v) was added into the cell line media with 2 different final concentrations (0.4% and 1%).
💡
Sonuç & Katkı:We think that the oxidant potential of garlic extract might play a part in its possible anticancer potential, previously supposed by several investigators.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Key words: Garlic · mouse myeloid cell line · oxidant/antioxidant status

Özet

To investigate the possible effects of aqueous garlic extract on the oxidant/antioxidant status and apoptosis in 32D (wild type mouse myeloid cell = normal) and 32Dp210 (BCR-ABL fusion gene (+) mouse myeloid cell = Chronic Myelocytic Leukemia cells) cell lines. Materials and methods: Aqueous garlic extract (10% w/v) was added into the cell line media with 2 different final concentrations (0.4% and 1%). At 0 h and at 24, 48, and 72 h later, the oxidant (malondialdehyde (MDA) level, and xanthine oxidase (XO) enzyme activity) and antioxidant (superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) enzyme activities) parameters were measured in the cell lines. Results: It was observed that the garlic extract caused no change in the XO and antioxidant enzyme activities, but it increased the MDA level in the 32D cell line. However, significant increases were found in the MDA level, XO, and antioxidant enzyme activities in the 32Dp210 cell line treated by the garlic extract. Additionally, it was shown that garlic extract had antiproliferative and apoptotic effects on both cell lines. The most effective apoptotic dose was found to be 0.4% (w/v), and at this concentration the death risk of the 32Dp210 cell line was calculated at 2.08 times higher than that of the 32D cell line. Conclusion: It has been suggested that garlic directly causes oxidant stress in the 32D cell line owing to its own oxidant ingredients, and that the oxidant stress created by garlic in the 32Dp210 cell line might occur through increased XO activity and/or its oxidant ingredients. Additionally, antioxidant enzyme activities were found to increase in the 32Dp210 cell line; it would seem that this compensatory change could not prevent the oxidant stress created. We think that the oxidant potential of garlic extract might play a part in its possible anticancer potential, previously supposed by several investigators.

Abstract

To investigate the possible effects of aqueous garlic extract on the oxidant/antioxidant status and apoptosis in 32D (wild type mouse myeloid cell = normal) and 32Dp210 (BCR-ABL fusion gene (+) mouse myeloid cell = Chronic Myelocytic Leukemia cells) cell lines. Materials and methods: Aqueous garlic extract (10% w/v) was added into the cell line media with 2 different final concentrations (0.4% and 1%). At 0 h and at 24, 48, and 72 h later, the oxidant (malondialdehyde (MDA) level, and xanthine oxidase (XO) enzyme activity) and antioxidant (superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) enzyme activities) parameters were measured in the cell lines. Results: It was observed that the garlic extract caused no change in the XO and antioxidant enzyme activities, but it increased the MDA level in the 32D cell line. However, significant increases were found in the MDA level, XO, and antioxidant enzyme activities in the 32Dp210 cell line treated by the garlic extract. Additionally, it was shown that garlic extract had antiproliferative and apoptotic effects on both cell lines. The most effective apoptotic dose was found to be 0.4% (w/v), and at this concentration the death risk of the 32Dp210 cell line was calculated at 2.08 times higher than that of the 32D cell line. Conclusion: It has been suggested that garlic directly causes oxidant stress in the 32D cell line owing to its own oxidant ingredients, and that the oxidant stress created by garlic in the 32Dp210 cell line might occur through increased XO activity and/or its oxidant ingredients. Additionally, antioxidant enzyme activities were found to increase in the 32Dp210 cell line; it would seem that this compensatory change could not prevent the oxidant stress created. We think that the oxidant potential of garlic extract might play a part in its possible anticancer potential, previously supposed by several investigators.

🔖

Bu Makaleye Atıf Yap

VAROL, N., DEVRİM, E., DURAK, İ., SUNGUROĞLU, A., AVCI, A., ERGÜDER, İ. B., AKAY, G. G., BAYDIN, Ö. P. (2022). Effects of aqueous garlic extract on oxidant/antioxidant status in 32D and 32Dp210 cell lines. Turkish Journal of Medical Sciences, Cilt: 40 - Sayı: 6, 881–888. https://ajindex.com/articles/611513

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (13)

  1. Kahkonen MP, Hopia AI, Vuorela HJ, Rauha JP, Pihlaja K and Kujala TS et al. Antioxidant activity of plant extracts containing phenolic compounds, J Agric Food Chem. 1999; 47: 3954-3962
  2. Sattler M, Griffin JD. Molecular mechanisms of transformation by the BCR-ABL oncogene. Semin Hematol 2003; 40: 4-10
  3. Kim SM, Kubota K, Kobayashi A. Antioxidative activity of sulfur-containing flavor compounds in garlic, Biosci Biotechnol Biochem 1997; 61: 1482-85
  4. Kodera Y, Suzuki A, Imada O, Kasuga S, Sumioka I, Kazenawa A et al. Physical, chemical, and biological properties of Sallylcysteine, an amino acid derived from garlic, J Agric Food Chem 2002; 50: 622-632
  5. Yu FS, Yu CS, Lin JP, Chen SC, Lai WW, Chung JG. Diallyl disulfide inhibits N-acetyltransferase activity and gene expression in human esophagus epidermoid carcinoma CE 81T/VGH cells, Food Chem Toxicol 2005; 43: 1029-36
  6. Schaffer EM, Liu JZ, Green J, Dangler CA and Milner JA. Garlic and associated allyl sulfur components inhibit N-methyl-Nnitrosourea-induced rat mammary carcinogenesis, Cancer Lett 1996; 102: 199-204
  7. Singh A and Shukla Y. Antitumour activity of diallyl sulfide on polycyclic aromatic hydrocarbon induced mouse skin carcinogenesis, Cancer Lett 1998; 131: 209-214
  8. Hosono T, Fukao T, Ogihara J, Ito Y, Shiba H, Seki T et al. Diallyl trisulfide suppresses the proliferation and induces apoptosis of human colon cancer cells through oxidative modification of {beta}-tubulin, J Biol Chem 2005; 280: 41487-493
  9. Ameen M, Musthapa MS, Abidi P, Ahmad I, Rahman Q. Garlic attenuates chrysotile-mediated pulmonary toxicity in rats by altering the phase I and phase II drug metabolizing enzyme system, J Biochem Mol Toxicol 2003; 17: 366-371
  10. Munday R, Munday CM. Low doses of diallyl disulfide, a compound derived from garlic, increase tissue activities of quinone reductase and glutathione transferase in the gastrointestinal tract of the rat, Nutr Cancer 1999; 34: 2-8
  11. Hashimoto S. A new spectrophotometric assay method of xanthine oxidase in crude tissue homogenate. Anal Biochem 1974; 62: 425-435
  12. Durak I, Canbolat O, Kavutcu M, Öztürk HS, Yurtaslanı Z. Activities of total, cytoplasmic and mitochondrial superoxide dismutase enzymes in sera and pleural fluids from patients with lung cancer. J Clin Lab Anal 1996; 10: 17-20
  13. Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erytrocyte glutathione peroxidase. J Lab Clin Med 1967; 70: 158-169. 14